Lima, Fabio V; Koutrolou-Sotiropoulou, Paraskevi; Yen, Tzyy Yun M; Stergiopoulos, Kathleen
2016-01-01
Ebstein anomaly is an uncommon congenital cardiac lesion that may be associated with cyanosis, arrhythmias and right heart dysfunction. Investigation into patient characteristics and outcomes in pregnant women with Ebstein anomaly has been limited. To characterize patient characteristics and clinical events for pregnant women with Ebstein anomaly during hospitalization for delivery in the USA; also, to determine the effect of Ebstein anomaly on maternal clinical outcomes and individual predictors of poor outcome at time of delivery. We screened the Healthcare Cost and Utilization Project's National Inpatient Sample for hospital admissions of pregnant women for delivery (vaginal or caesarean section) in the USA from 2003-2012, and identified a cohort of 7,850,381. Clinical characteristics and maternal outcomes were identified in those with and without Ebstein anomaly. The primary outcome of interest was major adverse cardiac events (MACE), a composite of in-hospital death, acute myocardial infarction, cerebrovascular events, embolic events, cardiac complications of labour and delivery heart failure or arrhythmia. Our study population consisted of 82 hospitalizations of pregnant women with Ebstein anomaly and 7,850,299 without. The Ebstein cohort more frequently had ostium secundum-type atrial septal defect and/or patent foramen ovale and anomalous atrioventricular excitation (P<0.001 for both). The MACE rate was significantly higher among Ebstein patients (P<0.001). Preterm delivery, postpartum haemorrhage and caesarean delivery occurred more frequently among the Ebstein cohort (19.5% vs 7.2%, 8.5% vs 2.8% and 47.6% vs 31.1%, respectively; P≤0.001). In a multivariable analysis, anomalous atrioventricular excitation (odds ratio [OR] 21.75, 95% confidence interval [CI] 1.03-457.91) and preterm delivery (OR 11.71, 95% CI 1.39-98.89) were associated with MACE among those with Ebstein anomaly. Pregnant women with Ebstein anomaly are at higher risk of MACE during pregnancy and delivery. Preterm delivery occurred more frequently in women with Ebstein anomaly. Copyright © 2016 Elsevier Masson SAS. All rights reserved.
[A case report of Ebstein's anomaly treated with Hetzer's procedure].
Sako, H; Hadama, T; Shigemitsu, O; Miyamoto, S; Anai, H; Wada, T; Iwata, E; Mori, Y; Soeda, T; Takakura, K
2001-02-01
A 27-year-old male who had been diagnosed with Ebstein's anomaly was admitted with uncontrollable congestive heart failure. The echocardiogram revealed severe tricuspid valve incompetence and the electrocardiogram showed atrial fibrillation. He underwent Hetzer's repair procedure for tricuspid valve incompetence and Minzioni's right atrial isolation technique to restore sinus rhythm. His congestive heart failure quickly disappeared and sinus rhythm was restored after operation. He was discharged 3 weeks postoperatively and remains well 22 months after his operation. Hetzer's technique for tricuspid valve repair in Ebstein's anomaly restructures the valve mechanism at the level of the true tricuspid anulus by using the most mobile leaflet for valve closure without plication of the atrialized chamber. We conclude that Hetzer's procedure is an effective operation for Ebstein's anomaly.
Ebstein's anomaly in pregnancy: maternal and neonatal outcomes.
Chopra, Seema; Suri, Vanita; Aggarwal, Neelam; Rohilla, Meenakshi; Vijayvergiya, Rajesh; Keepanasseril, Anish
2010-04-01
Ebstein's anomaly is a rare congenital cardiac abnormality, associated with cyanosis and arrhythmia. Patients often reach childbearing age and pregnant women pose a challenge to the treating physician. We describe the course and outcome of pregnancy in women with Ebstein's anomaly and discuss the related management issues. Analysis of pregnancies in four women with Ebstein's anomaly was carried out in a referral institute in northern India. Data of two women were analyzed retrospectively and the other two women were prospectively followed in their pregnancies during the study period. The course of the pregnancy, disease and perinatal outcome in each woman were analyzed. Four women had eight pregnancies all resulting in vaginal deliveries. There were two premature deliveries. The mean birth weight was 2.54 + or - 0.88 kg. Of the eight babies, six did not have any cardiac anomalies; one was an unexplained neonatal death and for another, no data was available. Pregnancy was well tolerated in two patients, while one had right heart failure during early pregnancy, and one had arrhythmia during labor, which was managed medically; one patient had arrhythmia in the postpartum period, which was managed medically. When a woman with Ebstein's anomaly reaches childbearing age, fertility is not affected, even in cyanotic women. Under close supervision by the woman's obstetrician and cardiologist, the pregnancy outcome is usually favorable.
Bauser-Heaton, Holly; Nguyen, Charles; Tacy, Theresa; Axelrod, David
2015-01-01
This is the first report of the use of veno-venous extracorporeal membrane oxygenation in a neonate with severe Ebstein's anomaly. The report suggests the use of veno-venous extracorporeal membrane oxygenation in the immediate neonatal period may be a useful therapy in severe Ebstein's anomaly. By providing adequate oxygenation independent of the patient's native pulmonary blood flow, veno-venous extracorporeal membrane oxygenation allows the pulmonary vascular resistance to decrease and may promote right ventricular recovery.
Sasikumar, Navaneetha; Krishna Manohar, Soman R; Philip, Saji; Cherian, Kottoorathu Mammen; Suresh Kumar, Raghavannair
2013-08-01
A 20 year-old male was diagnosed to have Ebstein's anomaly with severe right ventricular dysfunction. He was taken up for 1.5 ventricle repair. Post procedure, there was difficulty in weaning from cardiopulmonary bypass due to progressive right ventricular dilatation compromising the systemic output. An atrial septectomy did not help. Progressive right ventricular dilatation compressing the left ventricle, demonstrated on transoesophageal echocardiogram, prompted us to perform a right ventricular exclusion and univentricular palliation. The patient was successfully weaned off cardiopulmonary bypass and had a smooth postoperative recovery. Judicious use of right ventricular exclusion and univentricular palliation could be an effective bailout strategy in difficult surgical scenarios in Ebstein's anomaly. Copyright © 2012 Australian and New Zealand Society of Cardiac and Thoracic Surgeons (ANZSCTS) and the Cardiac Society of Australia and New Zealand (CSANZ). Published by Elsevier B.V. All rights reserved.
Influence of pregnancy on cardiac function and hemodynamics in women with Ebstein's anomaly.
Kanoh, Miki; Inai, Kei; Shinohara, Tokuko; Shimada, Eriko; Shimizu, Mikiko; Tomimatsu, Hirofumi; Ogawa, Masaki; Nakanishi, Toshio
2018-05-16
We examined the perinatal outcomes and right ventricular function before pregnancy, during pregnancy, and after delivery in women with Ebstein's anomaly. We retrospectively investigated the clinical course and mode of delivery and monitored hemodynamic parameters throughout pregnancy in 17 women with Ebstein's anomaly, who delivered at our institution during the period of 1995-2015. Eight women, including nine pregnancies, underwent elective cesarean section, and nine women, including 14 pregnancies, underwent vaginal delivery. Elective cesarean section was performed in cases with significant heart failure or arrhythmias and in the presence of more than 2 of the following: cardiothoracic ratio ≥60%, moderate or severe tricuspid valve regurgitation, or tricuspid valve regurgitation pressure gradient ≥35 mmHg during pregnancy. The cardiothoracic ratio and tricuspid valve regurgitation pressure gradient significantly increased during pregnancy compared to pre-pregnancy values. New York Heart Association classification deteriorated from class I to class II or III in five cases during pregnancy. Although pregnancy was relatively safe among women with Ebstein's anomaly, some women developed cyanosis, arrhythmia, and heart failure, leading to elective cesarean section. Monitoring clinical and hemodynamic changes throughout pregnancy is advised in order to minimize maternal cardiac risk and select the appropriate mode of delivery. This article is protected by copyright. All rights reserved. This article is protected by copyright. All rights reserved.
Ebstein's anomaly in children: a single-center study in Angola.
Manuel, Valdano; Morais, Humberto; Magalhães, Manuel Pedro; Nunes, Maria Ana Sampaio; Leon, Gilberto; Ferreira, Manuel; Filipe Júnior, António Pedro
2015-10-01
Ebstein's anomaly is a rare complex congenital heart defect of the tricuspid valve. We aimed to describe the frequency, clinical profile, and early and short-term post-operative results in patients under the age of 18 years operated for this anomaly in a tertiary center in Angola. A retrospective cross-sectional study was conducted over a period of 37 months. We analyzed all patients diagnosed with congenital heart defects. Of the 1362 patients studied, eight (0.6%) had Ebstein's anomaly; six patients (75%) were female. Mean age was 69±59 months. Five patients were in NYHA functional class III or IV. Mean cardiothoracic index was 0.72. Seven patients (87.5%) had severe tricuspid regurgitation and five (62.5%) had another associated congenital heart defect. All patients were operated: two had complications and one (12.5%) died in the early post-operative period. The mean follow-up time was 1.22±0.6 years, and mortality during follow-up was 12.5% (n=1). At the end of the study, of the five patients in whom cone reconstruction was performed, four (80%) were in functional class I. Mean cardiothoracic index decreased to 0.64. Three patients had mild and two had moderate tricuspid regurgitation. The patient who underwent cone reconstruction and a Glenn procedure was in functional class I. The frequency of Ebstein's anomaly was similar to that in other centers. Cone reconstruction was viable in the majority of patients, with good early and short-term results. Copyright © 2015 Sociedade Portuguesa de Cardiologia. Published by Elsevier España. All rights reserved.
Tanimura, Kazuki; Miura, Yukiko; Ishii, Hisanari
2016-02-01
An 18-year-old female patinet with Ebstein anomaly underwent surgical repair of scoliosis under total intravenous anesthesia. In addtition to normal monitors, we used transesophageal echocardiography (TEE) and EV1000 (Edwards Lifesciences, Irvine, USA), which show stroke volume variation and stroke volume index simultaneously in a rectangular coordinates. TEE detected reversal of intracardiac shunt which caused SpO2 decrease during fixing screws at thoracic vertebrae, then manual ventilation with oxygen unproved SpO2. Because of a high venous pressure due to Ebstein anomaly, surgical bleeding seemed to be larger than usual. By using EV1000, volume status and cardiac contractility were estimated and adequate volume loading and inoptrope injection were performed to stabilize circulatory condition. The operation was completed without any cardiac and respiratory complications.
Hösch, Olga; Sohns, Jan Martin; Nguyen, Thuy-Trang; Lauerer, Peter; Rosenberg, Christina; Kowallick, Johannes Tammo; Kutty, Shelby; Unterberg, Christina; Schuster, Andreas; Faßhauer, Martin; Staab, Wieland; Paul, Thomas; Lotz, Joachim; Steinmetz, Michael
2014-07-01
The classification of clinical severity of Ebstein anomaly still remains a challenge. The aim of this study was to focus on the interaction of the pathologically altered right heart with the anatomically-supposedly-normal left heart and to derive from cardiac magnetic resonance (CMR) a simple imaging measure for the clinical severity of Ebstein anomaly. Twenty-five patients at a mean age of 26±14 years with unrepaired Ebstein anomaly were examined in a prospective study. Disease severity was classified using CMR volumes and functional measurements in comparison with heart failure markers from clinical data, ECG, laboratory and cardiopulmonary exercise testing, and echocardiography. All examinations were completed within 24 hours. A total right/left-volume index was defined from end-diastolic volume measurements in CMR: total right/left-volume index=(RA+aRV+fRV)/(LA+LV). Mean total right/left-volume index was 2.6±1.7 (normal values: 1.1±0.1). This new total right/left-volume index correlated with almost all clinically used biomarkers of heart failure: brain natriuretic peptide (r=0.691; P=0.0003), QRS (r=0.432; P=0.039), peak oxygen consumption/kg (r=-0.479; P=0.024), ventilatory response to carbon dioxide production at anaerobic threshold (r=0.426; P=0.048), the severity of tricuspid regurgitation (r=0.692; P=0.009), tricuspid valve offset (r=0.583; P=0.004), and tricuspid annular plane systolic excursion (r=0.554; P=0.006). Previously described severity indices ([RA+aRV]/[fRV+LA+LV]) and fRV/LV end-diastolic volume corresponded only to some parameters. In patients with Ebstein anomaly, the easily acquired index of right-sided to left-sided heart volumes from CMR correlated well with established heart failure markers. Our data suggest that the total right/left-volume index should be used as a new and simplified CMR measure, allowing more accurate assessment of disease severity than previously described scoring systems. © 2014 American Heart Association, Inc.
A modified repair technique for tricuspid incompetence in Ebstein's anomaly.
Hetzer, R; Nagdyman, N; Ewert, P; Weng, Y G; Alexi-Meskhisvili, V; Berger, F; Pasic, M; Lange, P E
1998-04-01
A modified technique for tricuspid valve repair in Ebstein's anomaly restructures the valve mechanism at the level of the true tricuspid anulus by using the most mobile leaflet for valve closure without plication of the atrialized chamber. Midterm results of this therapeutic approach for patients with Ebstein's anomaly and tricuspid valve incompetence are reported. Between October 1988 and April 1997, the incompetent tricuspid valve was repaired with our technique in 19 patients (12 female, 7 male; 2 to 54 years, mean 21 years). The indication for operation was congestive heart failure of various degrees in all patients. Tricuspid incompetence was grade II in two patients, grade III in 14, and grade IV in three. Associated congenital malformations were simultaneously repaired (interatrial communication in 18, ventricular septal defect in two, pulmonary stenosis in two, mitral valve prolapse in one). Follow-up ranged between 10 and 103 months (median 28 months) and was complete for all patients. There were no operative deaths. One patient with active endocarditis and pulmonary abscess died 2 months after the operation of recurrent sepsis; there were no late deaths. During follow-up, New York Heart Association functional class improved from 2.8 before the operation to 1.9 without recurrent cyanosis, and tricuspid incompetence decreased from a mean grade of 3.1 to one of 0.9, without any echocardiographic deterioration of the tricuspid valve function or right ventricular dilation. Our technique allows tricuspid valve repair in patients with Ebstein's anomaly, even in cases usually reserved for primary valve replacement, without late functional deterioration.
Holst, Kimberly A; Dearani, Joseph A; Said, Sameh M; Davies, Ryan R; Pizarro, Christian; Knott-Craig, Christopher; Kumar, T K Susheel; Starnes, Vaughn; Kumar, S Ram; Pasquali, Sara K; Thibault, Dylan P; Meza, James M; Hill, Kevin D; Chiswell, Karen; Jacobs, Jeffrey P; Jacobs, Marshall L
2018-05-16
Ebstein anomaly (EA) encompasses a broad spectrum of morphology and clinical presentation. Those who are symptomatic early in infancy are generally at highest risk, but there are limited data regarding multi-centric practice patterns and outcomes. We analyzed multi-institutional data concerning operations and outcomes in neonates and infants with EA. Index operations reported in the STS Congenital Heart Surgery Database (2010-2016) were potentially eligible for inclusion. Analysis was limited to patients with diagnosis of Ebstein anomaly and less than 1 year of age at time of surgery (neonates ≤30 days, infants 31-365 days). The study population included 255 neonates and 239 infants (at 95 centers). Among neonates, median age at operation was 7 days (IQR 4-13) and the majority required preoperative ventilation (61.6%, 157). The most common primary operation performed among neonates was Ebstein repair (39.6%, 101) followed by systemic to pulmonary shunt (20.4%, 52) and tricuspid valve closure (9.4%, 24). Overall neonatal operative mortality was 27.4% (70) with composite morbidity-mortality of 51.4% (48). For infants, median age at operation was 179 days (6 months); the most common primary operation for infants was superior cavopulmonary anastomosis (38.1%, 91) followed by Ebstein repair (15.5%, 37). Overall operative mortality for infants was 9.2% (22) with composite morbidity-mortality of 20.1% (48). Symptomatic EA in early infancy is very high risk and a variety of operative procedures were performed. A dedicated prospective study is required to more fully understand optimal selection of treatment pathways to guide a systematic approach to operative management. Copyright © 2018. Published by Elsevier Inc.
Oki, T; Fukuda, N; Tabata, T; Yamada, H; Manabe, K; Fukuda, K; Abe, M; Iuchi, A; Ito, S
1997-03-01
We describe a patient with Ebstein's anomaly in whom Doppler echocardiography was used to clarify the mechanism responsible for 'sail sound' and tricuspid regurgitation associated with this condition. Phonocardiography revealed an additional early systolic heart sound, consisting of a first low-amplitude component (T1) and a second high-amplitude component (T2, 'sail sound'). In simultaneous recordings of the tricuspid valve motion using M mode echocardiography and phonocardiography, the closing of the tricuspid valve occurred with T1 which originated at the tip of the tricuspid leaflets, while T2 originated from the body of the tricuspid leaflets. Using color Doppler imaging, the tricuspid regurgitant signal was detected during pansystole, indicating a blue signal during the phase corresponding to T1 and a mosaic signal during the phase corresponding to T2 at end-systole. Thus, 'sail sound' in patients with Ebstein's anomaly is not simply a closing sound of the tricuspid valve, but a complex closing sound which includes a sudden stopping sound after the anterior and/or other tricuspid leaflets balloon out at systole.
Renilla, Alfredo; Santamarta, Elena; Corros, Cecilia; Martín, María; Barreiro, Manuel; de la Hera, Jesús
2013-01-01
To establish the etiology of heart failure in patients with congenital heart disease can be challenging. Multiple concomitant anomalies that can be missed after an initial diagnosis could be seen in these patients. In patients with congenital heart disease, a more accurate evaluation of cardiac morphology and left ventricular systolic function could be evaluated by recent non-invasive cardiac imaging techniques. We present a rare case where multimodal cardiac imaging was useful to establish the final diagnosis of left ventricular non-compaction associated with Ebstein's anomaly. Copyright © 2012 Instituto Nacional de Cardiología Ignacio Chávez. Published by Masson Doyma México S.A. All rights reserved.
... Kliegman RM, Stanton BF, St. Geme JW, Schor NF. Cyanotic congenital heart lesions. In: Kliegman RM, Stanton BF, St. Geme JW, Schor NF, eds. Nelson Textbook of Pediatrics . 20th ed. Philadelphia, ...
Theron, Alexis; Pinard, Amélie; Riberi, Alberto; Zaffran, Stéphane
2016-07-01
Congenital tricuspid valve disease is a rare defect that includes regurgitation, stenosis and Ebstein's anomaly. We report a case of severe tricuspid regurgitation associated with functional mitral regurgitation in a 47-year-old man with congestive heart failure. Transthoracic echocardiography (TTE) ruled out any Ebstein's anomaly. Three-dimensional TTE revealed a 'tricuspid hole' into the anterior leaflet that was only attached to the tricuspid annulus next to both anteroseptal and anteroposterior commissures. There was no sign of leaflet tear or perforation. The surgical repair of the tricuspid and mitral valves was performed with an optimal result. No sign of endocarditis or rheumatic disease was observed during the intervention. Sequence analysis of GATA4, HEY2 and ZFPM2 genes was performed, but no causative mutation was identified. © The Author 2015. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery. All rights reserved.
Im, Yu-Mi; Park, Chun Soo; Park, Jeong-Jun; Yun, Tae-Jin
2016-03-01
Surgical techniques currently used for the repair of Ebstein's anomaly comprise reconstruction of the tricuspid valve mechanism at the level of the true annulus with or without plication of the atrialized right ventricle. However, performing this procedure for patients with a dysmorphic anterior leaflet (i.e., insufficient leaflet tissue and decreased mobility due to tethering) may necessitate technical modifications. A retrospective review was performed of 31 patients (seven males and 24 females, median age at operation 31 years) with Ebstein's anomaly, who underwent tricuspid valve repair between March 2002 and December 2014. The original Hetzer technique (annulus to annulus approximation) was employed for six patients with a well-formed anterior leaflet. In 25 patients, the tricuspid valve mechanism was restored at the displaced septal leaflet by approximating the anterior leaflet attachment in the true annulus to the displaced septal leaflet attachment in the mid-septum. A bidirectional superior cavopulmonary anastomosis was added in 27 of 31 (87%) patients. No early or late death occurred during the median follow-up of 66 months (1-138 months). Immediate postoperative tricuspid regurgitation was trivial to mild in 22 patients, and the median preoperative, immediate postoperative, and last follow-up tricuspid regurgitation jet areas in 21 adult patients were 23.3 cm2, 10.4 cm2, and 7.0 cm2, respectively. Two patients underwent reoperation at 81 and 119 months postoperatively. Five-year freedom from severe tricuspid regurgitation or reoperation was 93.2%. Restoration of the tricuspid valve mechanism at the level of displaced septal leaflet leads to excellent long-term outcomes. The addition of the bidirectional superior cavopulmonary anastomosis has contributed to the success of this technique. © 2016 Wiley Periodicals, Inc.
Balakrishnan, K G; Sapru, R P; Sasidharan, K; Venkitachalam, C G
1982-01-01
The clinical, haemodynamic and angiographic features of 18 patients with right ventricular endomyocardial fibrosis (RVEMF) and 8 patients with Ebstein's anomaly of the tricuspid valve (EATV) have been compared. Diagnosis was confirmed by selective angiography. The position of the tricuspid annulus was identified from selective right ventricular angiograms and confirmed by selective right coronary angiography. In 83% of RVEMF patients the tricuspid annulus was displaced to the left of the spine. A false impression of displacement of the tricuspid leaflet can thus be created. However, a tricuspid leaflet displaced away from the tricuspid annulus was found only in patients with EATV. A considerable overlap exists between the wide spectrum of clinical presentations of the two conditions. Helpful distinguishing features that favour EATV were, the presence of a scratchy diastolic murmur and polyphasic QRS complexes in the ECG. Atrial fibrillation in the ECG, and myocardial calcification or pericardial effusion, whenever present, favour RVEMF.
Modified repair in patients with Ebstein's anomaly.
Nagdyman, Nicole; Ewert, Peter; Komoda, Takeshi; Alexi-Meskisvili, Vladimir; Weng, Yuguo; Berger, Felix; Hetzer, Roland
2010-05-01
Since 1988, a modified repair technique has been used at the authors' institution to treat patients with Ebstein's anomaly. This technique restructures the valve mechanism at the level of the true tricuspid annulus by using the most mobile leaflet for valve closure, without plication of the atrialized chamber. A total of 19 patients had additional attachment of the anterior right ventricular wall to the interventricular septum (Sebening's stitch) and reconstruction of the tricuspid valve as a double-orifice valve. The long-term results of the study are presented. Between 1988 and 2008, tricuspid valve repair was performed in 50 patients with Ebstein's anomaly (33 females, 17 males; median age 22 years; range: 0.6 to 60 years), at the authors' institution. The median follow up was 68 months (range: 5 to 238) months. Details of the survival rate, reoperations, NYHA class, maximal VO2, right ventricular function (velocity-time integral pulmonary artery (VTI-PA)), and tricuspid valve insufficiency were documented. No patient deaths occurred during surgery; the early mortality was 7.1%, and late mortality 2.4%. Those patients who died were all aged > 50 years, and in NYHA class III or IV. No additional patient deaths have occurred since 2004. Four reoperations were necessary. Both, the NYHA class and tricuspid valve insufficiency were improved significantly (from 3.1 to 1.8; p < 0.001 and from 3.2 to 1.9; p < 0.001, respectively). The VTI-PA was increased significantly, with a stable heart rate (p = 0.01). No aneurysm of the right ventricle was observed. The long-term follow up demonstrated good clinical results in tricuspid repair, without plication of the right ventricle, even in cases where tricuspid valve replacement was discussed. Modifications seemed to support these results. Surgery in older patients with a progressive NYHA class seemed to carry a higher operative mortality.
[Ebstein's "like" anomaly ventricular double inlet. A rare association].
Muñoz Castellanos, Luis; Kuri Nivon, Magdalena
The association of univentricular heart with double inlet and Ebstein's "like" anomaly of the common atrioventricular valve is extremely rare. Two hearts with this association are described with the segmental sequential system which determine the atrial situs, the types of atrioventricular and ventriculoarterial connections and associated anomalies. Both hearts had atrial situs solitus, and a univentricular heart with common atrioventricular valve, a foramen primum and double outlet ventricle with normal crossed great arteries. In the fiefirst heart the four leaflets of the atrioventricular valve were displaced and fused to the ventricular walls, from the atrioventricular union roward the apex with atrialization of the inlet and trabecular zones and there was stenosis in the infundibulum and in the pulmonary valve. In the second heart the proximal segment of the atrioventricular valve was displaced and fused to the ventricular whith shot atrialization and the distal segment was dysplastic with fibromixoid nodules and tendinous cords short and thick; the pulmonary artery was dilate. Both hearts are grouped in the atrioventricular univentricular connection in the segmental sequential system. The application of this method in the diagnosis of congenital heart disease demonstrates its usefulness. The associations of complex anomalies in these hearts show us the infinite spectrum of presentation of congenital heart disease which expands our knowledge of pediatric cardiology. Copyright © 2016 Instituto Nacional de Cardiología Ignacio Chávez. Publicado por Masson Doyma México S.A. All rights reserved.
Meloni, Luigi; Abbruzzese, Piero A.; Pirisi, Raimondo; Cherchi, Angelo
1997-01-01
We describe a case of a 50-year-old woman with congenitally corrected transposition of the great vessels, in whom severe left-sided tricuspid (systemic atrioventricular) valve insufficiency was the only associated anomaly. The tricuspid valve was dysplastic and abnormally oriented toward the interventricular septum, without the downward displacement of Ebstein's anomaly. The mechanism of atrioventricular regurgitation was unusual in that it consisted of the rupture of chordae tendineae of both the anterior and septal leaflets. The left-sided tricuspid valve was replaced with a St. Jude prosthesis and the postoperative course was uneventful.
Identification of clinically relevant phenotypes in patients with Ebstein anomaly.
Cabrera, Rodrigo; Miranda-Fernández, Marta Catalina; Huertas-Quiñones, Victor Manuel; Carreño, Marisol; Pineda, Ivonne; Restrepo, Carlos M; Silva, Claudia Tamar; Quero, Rossi; Cano, Juan David; Manrique, Diana Carolina; Camacho, Camila; Tabares, Sebastián; García, Alberto; Sandoval, Néstor; Moreno Medina, Karen Julieth; Dennis Verano, Rodolfo José
2018-03-01
Ebstein anomaly (EA) is a heterogeneous congenital heart defect (CHD), frequently accompanied by diverse cardiac and extracardiac comorbidities, resulting in a wide range of clinical outcomes. Phenotypic characterization of EA patients has the potential to identify variables that influence prognosis and subgroups with distinct contributing factors. A comprehensive cross-sectional phenotypic characterization of 147 EA patients from one of the main referral institutions for CHD in Colombia was carried out. The most prevalent comorbidities and distinct subgroups within the patient cohort were identified through cluster analysis. The most prevalent cardiac comorbidities identified were atrial septal defect (61%), Wolff-Parkinson-White syndrome (WPW; 27%), and right ventricular outflow tract obstruction (25%). Cluster analysis showed that patients can be classified into 2 distinct subgroups with defined phenotypes that determine disease severity and survival. Patients in cluster 1 represented a particularly homogeneous subgroup with a milder spectrum of disease, including only patients with WPW and/or supraventricular tachycardia (SVT). Cluster 2 included patients with more diverse cardiovascular comorbidities. This study represents one of the largest phenotypic characterizations of EA patients reported. The data show that EA is a heterogeneous disease, very frequently associated with cardiovascular and noncardiovascular comorbidities. Patients with WPW and SVT represent a homogeneous subgroup that presents with a less severe spectrum of disease and better survival when adequately managed. This should be considered when searching for genetic causes of EA and in the clinical setting. © 2018 Wiley Periodicals, Inc.
Bar-Cohen, Yaniv; Khairy, Paul; Morwood, James; Alexander, Mark E; Cecchin, Frank; Berul, Charles I
2006-07-01
ECG algorithms used to localize accessory pathways (AP) in patients with Wolff-Parkinson-White (WPW) syndrome have been validated in adults, but less is known of their use in children, especially in patients with congenital heart disease (CHD). We hypothesize that these algorithms have low diagnostic accuracy in children and even lower in those with CHD. Pre-excited ECGs in 43 patients with WPW and CHD (median age 5.4 years [0.9-32 years]) were evaluated and compared to 43 consecutive WPW control patients without CHD (median age 14.5 years [1.8-18 years]). Two blinded observers predicted AP location using 2 adult and 1 pediatric WPW algorithms, and a third blinded observer served as a tiebreaker. Predicted locations were compared with ablation-verified AP location to identify (a) exact match for AP location and (b) match for laterality (left-sided vs right-sided AP). In control children, adult algorithms were accurate in only 56% and 60%, while the pediatric algorithm was correct in 77%. In 19 patients with Ebstein's anomaly, diagnostic accuracy was similar to controls with at times an even better ability to predict laterality. In non-Ebstein's CHD, however, the algorithms were markedly worse (29% for the adult algorithms and 42% for the pediatric algorithms). A relatively large degree of interobserver variability was seen (kappa values from 0.30 to 0.58). Adult localization algorithms have poor diagnostic accuracy in young patients with and without CHD. Both adult and pediatric algorithms are particularly misleading in non-Ebstein's CHD patients and should be interpreted with caution.
Asada, Dai; Ikeda, Kazuyuki; Yamagishi, Masaaki
2017-04-01
There are a few reports of successful replacement of the left-sided systemic tricuspid valve with a mechanical valve in small infants with congenitally corrected transposition of the great arteries having Ebstein's anomaly. Tricuspid valve replacement is the preferred option when pulmonary artery banding, performed as a prelude to performing the double-switch operation, is not feasible because of severe heart failure caused by tricuspid regurgitation.
Congenital heart defects in Williams syndrome.
Yuan, Shi-Min
2017-01-01
Yuan SM. Congenital heart defects in Williams syndrome. Turk J Pediatr 2017; 59: 225-232. Williams syndrome (WS), also known as Williams-Beuren syndrome, is a rare genetic disorder involving multiple systems including the circulatory system. However, the etiologies of the associated congenital heart defects in WS patients have not been sufficiently elucidated and represent therapeutic challenges. The typical congenital heart defects in WS were supravalvar aortic stenosis, pulmonary stenosis (both valvular and peripheral), aortic coarctation and mitral valvar prolapse. The atypical cardiovascular anomalies include tetralogy of Fallot, atrial septal defects, aortic and mitral valvular insufficiencies, bicuspid aortic valves, ventricular septal defects, total anomalous pulmonary venous return, double chambered right ventricle, Ebstein anomaly and arterial anomalies. Deletion of the elastin gene on chromosome 7q11.23 leads to deficiency or abnormal deposition of elastin during cardiovascular development, thereby leading to widespread cardiovascular abnormalities in WS. In this article, the distribution, treatment and surgical outcomes of typical and atypical cardiac defects in WS are discussed.
Ergenoglu, Mehmet U; Yerebakan, Halit; Ozveren, Olcay; Koner, Ozge; Kalangos, Afksendiyos; Demirsoy, Ergun
2011-10-01
Congenitally corrected transposition of the great arteries, which is characterized by atrioventricular and ventriculoarterial discordance, is a rare congenital heart disease. Most of the cases are diagnosed in childhood, owing to associated cardiac anomalies, such as ventricular septal defect, pulmonary stenosis or pulmonary atresia, and Ebstein-like malformation of the tricuspid valve. We present a patient with congenitally corrected transposition of the great arteries who underwent surgical replacement of the tricuspid valve with a bioprosthesis and reconstruction of the left ventricular outflow tract with bovine conduit.
Kühn, Andreas; Meierhofer, Christian; Rutz, Tobias; Rondak, Ina-Christine; Röhlig, Christoph; Schreiber, Christian; Fratz, Sohrab; Ewert, Peter; Vogt, Manfred
2016-08-01
Ebstein's anomaly (EA) is often associated with right ventricular (RV) dysfunction. Data on echocardiographic quantification of RV function are, however, rare. The aim of this study was to determine how non-volumetric echocardiographic indices and qualitative assessment of global systolic RV function correlate with cardiovascular magnetic resonance (CMR)-derived RV ejection fraction (EF). We compared six echocardiographic indices and qualitative assessment of RV function with the gold standard CMR. A total of 49 unoperated patients with EA and a mean age of 32 ± 18 years were examined. Tricuspid annular plane systolic excursion, tissue Doppler myocardial velocities (peak S and IVA) and 2D strain and strain rate measures for the RV were compared with CMR-derived EF. Only 2D global longitudinal strain (2D-GLS), out of the six parameters investigated, showed a weak, although statistically significant correlation with CMR-derived RVEF (R = -0.4, P = 0.01). Using a cut-off value of -20.15, 2D-GLS sensitivity (77%) and specificity (46%) in detecting patients with a CMR-derived EF of <50% were comparable with qualitative assessment (sensitivity 77%, specificity 45%). Overall echocardiographic parameters of RV function correlate poorly with CMR-derived EF in patients with EA. Only 2D global longitudinal RV strain correlated weakly with CMR-derived RVEF. However, the sensitivity and specificity for detecting RV dysfunction using 2D strain imaging were comparable with qualitative RV functional assessment. Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2015. For permissions please email: journals.permissions@oup.com.
Ergul, Yakup; Koca, Serhat; Akdeniz, Celal; Tuzcu, Volkan
2018-06-07
In Ebstein's anomaly (EA), tachycardia substrates are complex, and accessory pathway (AP) ablations are often challenging. This study demonstrates the utility of the EnSite Velocity system (St. Jude Medical, St Paul, MN) in the catheter ablation of supraventricular tachycardia in children with EA. Twenty patients [Female/Male = 8/12, median age 11.5 years (2.6-18)] with EA who underwent catheter ablation guided by the EnSite Velocity system between December 2011 and December 2016 were retrospectively evaluated. Five patients had severe EA, and two of them were at Fontan palliation pathway. The most common indications for ablations were palpitations/syncope and treatment-resistant arrhythmias. Thirty-one tachycardia substrate foci (21 manifest AP, 2 concealed AP, 4 Mahaim AP, 3 focal atrial tachycardias, and 1 typical atrioventricular nodal reentrant tachycardia) were detected in 20 patients. There were multiple tachycardia substrates in 11 patients (55%). The patient-based acute procedure success rate was 19/20 (95%), and the tachycardia-based success rate was 30/31 (97%). The mean procedure time was 170 ± 43 min (90-265). Fluoroscopy was not used in 15 (75%) patients. The mean fluoroscopy time in the remaining five patients was 3.6 ± 2.9 min (0.7-7.8). During a mean follow-up of 35.1 ± 20.3 months (6-60), tachycardia recurred in four patients (4/19, 21%). No complications were seen. Catheter ablation of arrhythmias can be performed effectively and safely in pediatric EA patients by using a limited fluoroscopic approach with the help of electroanatomical mapping systems. However, the rate of tachycardia recurrence at follow-up remains high.
Nathan, A T; Marino, B S; Dominguez, T; Tabbutt, S; Nicolson, S; Donaghue, D D; Spray, T L; Rychik, J
2010-01-01
Congenital tricuspid valve disease (Ebstein's anomaly, tricuspid valve dysplasia) with severe tricuspid regurgitation and cardiomegaly is associated with poor prognosis. Fetal echocardiography can accurately measure right atrial enlargement, which is associated with a poor prognosis in the fetus with tricuspid valve disease. Fetal lung volumetric assessments have been used in an attempt to predict viability of fetuses using ultrasonogram and prenatal MRI. We describe a fetus with tricuspid dysplasia, severe tricuspid regurgitation, right atrial enlargement and markedly reduced lung volumes. The early gestational onset of cardiomegaly with bilateral lung compression raised the possibility of severe lung hypoplasia with decreased broncho-alveolar development. Use of fetal echocardiography with measurement of pulmonary artery size combined with prenatal MRI scanning of lung volumes resulted in an improved understanding of this anomaly and directed the management strategy towards a successful Fontan circulation. 2010 S. Karger AG, Basel.
Schidlow, David N; Donofrio, Mary T
2018-01-01
Maternal hyperoxygenation (MH) during fetal ultrasound can characterize fetal pulmonary vasoreactivity (PVr) and its associations with postnatal physiology. We explored MH testing to facilitate perinatal risk stratification for fetuses with congenital heart disease (CHD). MH was performed in 12 fetuses: 2 with Ebstein anomaly, 2 with total anomalous pulmonary venous connection (TAPVC), 4 with hypoplastic left heart syndrome (HLHS) with (a) restrictive atrial septum (RAS) or (b) intact atrial septum (IAS) with decompressing vertical vein (VV), and 4 with D-loop transposition of the great arteries (TGA). PVr and physiologic and anatomic changes with MH and outcomes were recorded. Among Ebstein fetuses, pulmonary blood flow with MH mirrored postnatal findings. Among TAPVC fetuses, MH VV gradients correlated with postnatal gradients. One HLHS/IAS/VV fetus had no PVr and decreased pulmonary vein forward to reverse velocity time integral ratio with MH. Shortly after delivery, the infant experienced severe low cardiac output and required urgent atrial septoplasty. The remaining HLHS fetuses had PVr and underwent routine Stage 1 Norwood. Among TGA fetuses, septum primum position, foramen ovale flow, and the presence or absence of PVr with MH reflected postnatal findings. MH may help identify fetuses with CHD at risk for perinatal compromise. Additional study may yield insights into fetal PVr and elucidate predictors of perinatal outcomes. Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.
Early Evaluation of the Fetal Heart.
Hernandez-Andrade, Edgar; Patwardhan, Manasi; Cruz-Lemini, Mónica; Luewan, Suchaya
2017-01-01
Evaluation of the fetal heart at 11-13 + 6 weeks of gestation is indicated for women with a family history of congenital heart defects (CHD), a previous child with CDH, or an ultrasound finding associated with cardiac anomalies. The accuracy for early detection of CHD is highly related to the experience of the operator. The 4-chamber view and outflow tracts are the most important planes for identification of an abnormal heart, and can be obtained in the majority of fetuses from 11 weeks of gestation onward. Transvaginal ultrasound is the preferred route for fetal cardiac examination prior to 12 weeks of gestation, whereas, after 12 weeks, the fetal heart can be reliably evaluated by transabdominal ultrasound. Cardiac defects, such as ventricular septal defects, tetralogy of Fallot, Ebstein's anomaly, or cardiac tumors, are unlikely to be identified at ≤14 weeks of gestation. Additional ultrasound techniques such as spatiotemporal image correlation and the evaluation of volumes by a fetal-heart expert can improve the detection of congenital heart disease. The evaluation of the fetal cardiac function at 11-13 + 6 weeks of gestation can be useful for early identification of fetuses at risk of anemia due to hemoglobinopathies, such as hemoglobin Bart's disease. © 2017 S. Karger AG, Basel.
Armanni-Ebstein phenomenon and hypothermia.
Zhou, Chong; Byard, Roger W
2011-03-20
Retrospective review was undertaken of 46 cases of lethal hypothermia for the presence of subnuclear vacuolization of renal tubular epithelial cells. Fifteen of the 46 cases (33%) had renal tubular vacuolization typical of the Armanni-Ebstein phenomenon. The age range was 30-87 years (average 59 years) with a male to female ratio of 6:9. Nine of the 15 cases with Armanni-Ebstein changes (60%) had a history of diabetes mellitus, and in seven of these vitreous humour biochemical analyses were performed, all of which revealed diabetic ketoacidosis (vitreous glucose levels = 32.9-85.3 mmol/L; β-hydroxybutyrate = 7.4-20 mmol/L). This study has confirmed the association between hypothermia and renal tubular epithelial vacuolization, but in addition raises the prospect that this may be contributed to in some cases by underlying diabetic ketoacidosis. Hypothermic deaths should, therefore, raise the possibility of diabetes mellitus and initiate postmortem biochemical measurement of vitreous humor glucose and β-hydroxybutyrate levels. Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.
Lu, Chun-Wei; Wu, Mei-Hwan; Chen, Hui-Chi; Kao, Feng-Yu; Huang, San-Kuei
2014-07-01
The prevalence of Wolff-Parkinson-White (WPW) syndrome varies between 0.68 and 1.7/1000. The epidemiological profile may be modified after the introduction of transcatheter interventions. The aim of this study is to investigate the epidemiological trends of the WPW syndrome in a general population during a period with available and reimbursed transcatheter ablation. Data of WPW patients <50 years old were retrieved from our national database (2000-2010). We identified 6086 (61% male) patients, accounting for an overall prevalence of 0.36/1000 with a peak of 0.61/1000 in ages 20-24 years. The risk of death and sudden death was 0.071% and 0.02% per patient-year, respectively. The 42 deaths occurred at a median age of 29 years. Associated congenial heart disease was noted in 158 (2.6%) patients, including 42 with Ebstein's anomaly that increased the mortality risk (P=0.001, OR=8.5). In those without congenital heart disease, myocardial dysfunction occurred in 115 (1.9%) patients and increased the risk of death (P<0.001, OR=10.6) and sudden death. Radiofrequency catheter ablation was performed in 2527 patients at a median age of 25.7 years (4.54% per patient-year, discharge mortality 0.16%); 11 (0.4%) before the age of 5, and 2231 (88%) after the age of 15. Whereas repeated ablation procedures accounted for 6.0% of the procedures, those in Ebstein's patients were 25%. Radiofrequency catheter ablation is already a common treatment for WPW patients, particularly during young adulthood, which accounts for a lower prevalence. Myocardial dysfunction and associated congenital heart disease remain as risks of mortality. Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.
Contemporary management of tricuspid regurgitation: an updated clinical review.
Taylor, Joshua T; Chidsey, Geoffrey; Disalvo, Thomas G; Byrne, John G; Maltais, Simon
2013-01-01
Tricuspid regurgitation (TR) is a complex and insidious valvular pathology that represents a complex decision and management algorithm for patients. TR is present in a significant proportion of the population and is especially prevalent in patients with advanced heart failure. Patients with TR have been demonstrated to have a decreased survival even with normal left heart function. TR can be a result of pathology that directly affects the valvular structure (i.e., Ebstein anomaly) or as a result of increased forward pressures (ie, pulmonary hypertension, left heart failure). Conservative management of patients with TR is primarily symptomatic relief. Definitive therapy involves surgical repair of the tricuspid valve. Furthermore, as more patients develop advanced heart failure, the management of TR in patients with left ventricular assist devices has become necessary because of the evidence of increased in-hospital morbidity and a trend toward decreased survival.
Baker, Kimberly; Sanchez-de-Toledo, Joan; Munoz, Ricardo; Orr, Richard; Kiray, Shareen; Shiderly, Dana; Clemens, Michele; Wearden, Peter; Morell, Victor O; Chrysostomou, Constantinos
2012-01-01
Objective. Infants with critical congenital heart disease (CHD) can have genetic and other extracardiac malformations, which add to the short- and long-term risk of morbidity and perhaps mortality. We sought to examine our center's practice of screening for extracardiac anomalies and to determine the yield of these tests among specific cardiac diagnostic categories. Design. Retrospective review of infants admitted to the cardiac intensive care unit with a new diagnosis of CHD. Subjects were categorized into six groups: septal defects (SD), conotruncal defects (CTD), single-ventricle physiology (SV), left-sided obstructive lesions (LSO), right-sided obstructive lesions (RSO), and "other" (anomalous pulmonary venous return, Ebstein's anomaly). Screening modalities included genetic testing (karyotype and fluorescent in situ hybridization for 22q11.2 deletion), renal ultrasound (RUS), and head ultrasound (HUS). Results. One hundred forty-one patients were identified. The incidence of cardiac anomalies was: CTD (36%), SD (18%), SV (18%), LSO (14%), RSO (3%), and "other" (8%). Overall 14% had an abnormal karyotype, 5% had a deletion for 22q11.2, 28% had an abnormal RUS and 22% had abnormal HUS. Patients in SD and SV had the highest incidence of abnormal karyotype (36% and 17%); 22q11.2 deletion was present only in CTD and LSO groups (9% and 7%, respectively); abnormal RUS and HUS were seen relatively uniformly in all categories. Premature infants had significantly higher incidence of renal 43% vs. 24%, and intracranial abnormalities 46% vs. 16%. Conclusion. Infants with critical CHD and particularly premature infants have high incidence of genetic and other extracardiac anomalies. Universal screening for these abnormalities with ultrasonographic and genetic testing maybe warranted because early detection could impact short and long-term outcomes. © 2011 Wiley Periodicals, Inc.
Kobza, R; Kurz, D J; Oechslin, E N; Prêtre, R; Zuber, M; Vogt, P; Jenni, R
2004-03-01
To define the entity of tricuspid regurgitation caused by tethering of the tricuspid valve leaflets by aberrant tendinous chords. Retrospective study. Tertiary care centre (university teaching hospital). 10 patients with unexplained severe tricuspid regurgitation. The last 13 500 echocardiographic studies from our facility were reviewed to identify patients with severe unexplained tricuspid regurgitation. Tethering was defined by the presence of aberrant tendinous chords to the tricuspid valve leaflets limiting the mobility of the tricuspid leaflet and resulting in incomplete coaptation and apical displacement of the regurgitant jet origin. Aberrant tendinous chords were defined as those inserting at the clear zone of the tricuspid leaflet and not originating from the papillary muscle. Patients fulfilling the diagnostic criteria for Ebstein's anomaly were excluded. 10 patients with aberrant tendinous chords tethering one or more tricuspid valve leaflets were identified. There were short non-aberrant tendinous chords in seven patients, five of whom also had right ventricular or tricuspid annulus dilatation. Tethering of the tricuspid valve leaflets by aberrant tendinous chords can be the sole mechanism of congenital tricuspid regurgitation. It is often associated with short non-aberrant tendinous chords, which may develop secondary to right ventricular or tricuspid annulus dilatation. Awareness of tethering as a cause of tricuspid regurgitation may be important in planning reconstructive surgery.
Congenital Heart Defects in Adults : A Field Guide for Cardiologists
Romfh, Anitra; Pluchinotta, Francesca Romana; Porayette, Prashob; Valente, Anne Marie; Sanders, Stephen P.
2013-01-01
Advances in cardiology and cardiac surgery allow a large proportion of patients with congenital heart defects to survive into adulthood. These patients frequently develop complications characteristic of the defect or its treatment. Consequently, adult cardiologists participating in the care of these patients need a working knowledge of the more common defects. Occasionally, patients with congenital heart defects such as atrial septal defect, Ebstein anomaly or physiologically corrected transposition of the great arteries present for the first time in adulthood. More often patients previously treated in pediatric cardiology centers have transitioned to adult congenital heart disease centers for ongoing care. Some of the more important defects in this category are tetralogy of Fallot, transposition of the great arteries, functionally single ventricle defects, and coarctation. Through this field guide, we provide an overview of the anatomy of selected defects commonly seen in an adult congenital practice using pathology specimens and clinical imaging studies. In addition, we describe the physiology, clinical presentation to the adult cardiologist, possible complications, treatment options, and outcomes. PMID:24294540
The Blalock-Taussig shunt revisited: a contemporary experience.
McKenzie, E Dean; Khan, Muhammad S; Samayoa, Andres X; Vener, Daniel S; Ishak, Youstina M; Santos, Alexia B; Heinle, Jeffrey S; Fraser, Charles D
2013-04-01
The Blalock-Taussig shunt (BTS) was introduced 68 years ago before open repair of cyanotic congenital heart disease (CHD) was possible. The originally described technique has undergone many modifications but remains an integral component of the management of cyanotic CHD. We report our contemporary, single institution experience with the BTS. We performed a retrospective review of all patients treated with a BTS from June 1995 to December 2011. There were 730 BTS performed in 712 patients; 727 (99.6%) by interposition graft (modified). The BTS was predominantly right-sided (n = 657, 90%). Median age and weight at palliation were 8 days (range 0 days to 18.5 years) and 3.2 kg (1.5 to 51 kg). Median hospital length of stay was 16 days (range 0 to 347 days). There were 241 (33%) BTS performed as initial palliation for ultimate 2-ventricle (2V) circulation, 471 (65%) as part of staged palliation for patients with functionally univentricular lesions (1V), 6 (1%) as a part of 1.5-ventricle palliation, and 12 (1%) for Ebstein's anomaly. There were 473 (65%) BTS placed via sternotomy and the most common site of BTS was the right subclavian to right pulmonary artery (PA; n = 452, 62%). Hospital mortality was higher for BTS in 1V patients (1V 15% vs 2V 3%, p < 0.0001). Overall, 536 (73%) patients were bridged to complete repair or the second stage of 1V palliation after a median duration of 6.5 months (0 days to 15.3 years). Multivariable regression showed that sternotomy approach, use of cardiopulmonary bypass, innominate artery-PA shunt, and diagnosis of Ebstein's were risk factors for in-hospital mortality (p < 0.05). Although the BTS remains an important component of the surgical treatment of cyanotic congenital heart disease, patients with single ventricle circulation still face significant ongoing risk of mortality. Copyright © 2013 American College of Surgeons. Published by Elsevier Inc. All rights reserved.
Morphologic-echocardiographic correlates of Ebstein's malformation.
Rusconi, P G; Zuberbuhler, J R; Anderson, R H; Rigby, M L
1991-07-01
The cross-sectional echocardiographic findings were analysed retrospectively in 26 patients with Ebstein's malformation in the light of studies of autopsied specimens from different patients showing this lesion. The salient anatomical feature in diagnosis is the finding of the hinge point of the septal and mural leaflets of the valve within the inlet component of the right ventricle rather than at the atrioventricular junction. The other important feature is the nature of the distal attachment of the leaflets, particularly the anterosuperior one, which can either be in focal or linear fashion. The hinge point of the septal leaflet was noted echocardiographically to be displaced in 19 patients but, significantly, the leaflet was absent in the other seven. Also significant was that the hinge point of the mural leaflet at the crux had been visualized in only 15 of the patients. The anterosuperior leaflet had a distal linear attachment in 20 of the patients, with the anteroseptal commissure becoming a keyhole in six of these through which blood passed to the functional right ventricle. The valve remained a competent structure, even though closing at the junction of atrialized and functional components of the right ventricle rather than at the atrioventricular junction. Cross-sectional echocardiography is the technique of choice with which to display the salient morphological features of Ebstein's malformation.
Pediatric Pulmonary and Cardiovascular Complications of Vertically Transmitted HIV Infection (P2C2)
2016-04-13
Acquired Immunodeficiency Syndrome; Lung Diseases; Cardiovascular Diseases; Heart Diseases; Heart Failure; HIV Infections; Cytomegalovirus Infections; Pneumocystis Carinii Infections; Ebstein-Barr Virus Infections
The right atrium: gateway to the heart--anatomic and pathologic imaging findings.
Malik, Sachin B; Kwan, Damon; Shah, Amar B; Hsu, Joe Y
2015-01-01
Knowledge of right atrial anatomic and pathologic imaging findings and associated clinical symptoms is important to avoid false-positive diagnoses and missed findings. Complete evaluation of the heart often requires a multimodality approach that includes radiography, echocardiography, computed tomography (CT), magnetic resonance (MR) imaging, and invasive angiography. In general, CT provides the highest spatial resolution of these modalities at the cost of radiation exposure to the patient. Echocardiography and MR imaging offer complementary and detailed information for functional evaluation without added radiation exposure. The advantages and disadvantages of each modality for the evaluation of right atrial anatomic structure, size, and pathologic findings are discussed. Cardiac MR imaging is the reference standard for evaluation of right atrial size and volume but often is too time consuming and resource intensive to perform in routine clinical practice. Therefore, established reference ranges for two-dimensional transthoracic echocardiography are often used. Right atrial pathologic findings can be broadly categorized into (a) congenital anomalies (cor triatriatum dexter, Ebstein anomaly, and aneurysm), (b) disorders of volume (tricuspid regurgitation, pathologic mimics such as a pseudoaneurysm, and atrial septal defect), (c) disorders of pressure (tricuspid stenosis, restrictive cardiomyopathy, and constrictive pericarditis), and (d) masses (pseudomasses, thrombus, lipomatous hypertrophy of the interatrial septum, lipoma, myxoma, sarcoma, and metastatic disease). Familiarity with each pathologic entity and its treatment options is essential to ensure that appropriate imaging modalities are selected. Online supplemental material is available for this article. RSNA, 2015
One and a half ventricular repair as an alternative for hypoplastic right ventricle.
Maluf, Miguel Angel; Carvalho, Antonio Carlos; Carvalho, Werther Brunow
2010-01-01
Patients with complex congenital heart disease, characterized by right ventricle hypoplasia, had a palliative surgical option with one and a half ventricular repair. From July 2001 to March 2009, nine patients (mean age 5.2 years, range 3 to 9 years) with hypoplastic right ventricle, underwent correction with one and a half ventricle technique. Preoperative diagnoses included: pulmonary atresia with intact ventricular septum, in six and Ebstein's anomaly, in three cases. Six patients had bidirectional cavo-pulmonary shunt (Glenn operation) previously. The surgical approach was performed with cardiopulmonary bypass to correct intracardiac defects: atrial septal defect closure (nine cases); right ventricle outlet tract reconstruction with porcine pulmonary prosthesis (seven cases); tricuspid valvuloplasty (three cases). There was one (11.1%) hospital death. All the patients left the hospital in good clinical conditions. One patient presented pulmonary stenosis at distal prosthesis anastomosis and needed surgical correction. There was one (12.5%) late deaths after reoperation. At mean follow-up of 39.8 months (range 16 months to 8.4 years) seven patients are alive in functional class I (NYHA). Surgical treatment of congenital cardiac anomalies in the presence of a hypoplastic right ventricle by means of one and a half ventricle repair has the advantages of reducing the surgical risk of biventricular repair compared to the Fontan circulation; it maintains a low right atrium pressure, a pulsatile pulmonary blood flow and improves the systemic oxygen saturation with short and medium-term promising results. Longer follow-up is needed to prove the efficacy of such a repair in the long term.
Potential implications of the helical heart in congenital heart defects.
Corno, Antonio F; Kocica, Mladen J
2007-01-01
The anatomic and functional observations made by Francisco Torrent-Guasp, in particular his discovery of the helical ventricular myocardial band (HVMB), have challenged what has been taught to cardiologists and cardiac surgeons over centuries. A literature debate is ongoing, with interdependent articles and comments from supporters and critics. Adequate understanding of heart structure and function is obviously indispensable for the decision-making process in congenital heart defects. The HVMB described by Torrent-Guasp and the potential impact on the understanding and treatment of congenital heart defects has been analyzed in the following settings: embryology, ventriculo-arterial discordance (transposition of great arteries), Ebstein's anomaly, pulmonary valve regurgitation after repair of tetralogy of Fallot, Ross operation, and other congenital heart defects. The common structural spiral feature is only one of the elements responsible for the functional interaction of right and left ventricles, and understanding the form/function relationship in congenital heart defects is more difficult than for acquired heart disease because of the variety and complexity of congenital heart defects. Individuals involved in the care of patients with congenital heart defects have to be stimulated to consider further investigations and alternative surgical strategies.
The Double-Orifice Valve Technique to Treat Tricuspid Valve Incompetence.
Hetzer, Roland; Javier, Mariano; Delmo Walter, Eva Maria
2016-01-01
A straightforward tricuspid valve (TV) repair technique was used to treat either moderate or severe functional (normal valve with dilated annulus) or for primary/organic (Ebstein's anomaly, leaflet retraction/tethering and chordal malposition/tethering, with annular dilatation) TV incompetence, and its long-term outcome assessed. A double-orifice valve technique was employed in 91 patients (mean age 52.6 ± 23.2 years; median age 56 years; range: 0.6-82 years) with severe tricuspid regurgitation. Among the patients, three had post-transplant iatrogenic chordal rupture, five had infective endocarditis, 11 had mitral valve insufficiency, 23 had Ebstein's anomaly, and 47 had isolated severe TV incompetence. The basic principle was to reduce the distance between the coapting leaflets, wherein the most mobile leaflet could coapt to the opposite leaflet, by creating two orifices, ensuring valve competence. The TV repair was performed through a median sternotomy or right anterior thoracotomy in the fifth intercostal space under cardiopulmonary bypass. The degree and extent of creating a double-valve orifice was determined by considering the minimal body surface area (BSA)-related acceptable TV diameter. Repair was accomplished by passing pledgeted mattress sutures from the middle of the true anterior annulus to a spot on the opposite septal annulus, located approximately two-thirds of the length of the septal annulus to avoid injury to the bundle of His. The annular apposition divides the TV into a larger anterior and a smaller posterior orifices, enabling valve closure, on both sides. In adults, the diameter of the anterior valve orifice should be 23-25 mm, and the posterior orifice 15-18 mm; thus, the total valve orifice area is 5-6 cm2. In children, the total valve orifice should be a standard deviation of 1.7 mm for a BSA of <1. 0m2, and 1.5 mm for a BSA of >1.0m2. During a mean follow up of 8.7 ± 1.34 years (median 10 years; range: 1.5-25.9 years) there have been no reoperations for TV insufficiency or stenosis. Reoperations on three patients (mean age 42.5 ± 8.7 years) were indicated for aortic valve replacement at 14 months postoperatively (n = 1) and for assist device implantation (n = 2) who eventually underwent heart transplant at 18 and 20 months after TV repair, respectively. The cumulative 12-year survival rate was 86.9%. This double-orifice technique is technically a straightforward repair to abolish TV incompetence with highly satisfactory results, particularly in patients with severe annular dilatation or with leaflet and chordal tethering. In the present series, the technique provided no pitfalls (if the location of the conduction system was borne in mind), requiring only a gentle placement of sutures. It also led to no residual regurgitation or reoperation during the follow up period.
Defining Ebstein's malformation using three-dimensional echocardiography.
Vettukattil, Joseph J; Bharucha, Tara; Anderson, Robert H
2007-12-01
Ebstein's malformation is difficult to visualise, for both the echocardiographer and the surgeon. The essence of the problem in Ebstein's malformation is the deviation of the hingepoints of the leaflets towards the junctions of the inlet and apical trabecular parts of the right ventricle. Three-dimensional echocardiography offers new insights into the morphology and function of malformed valves, and allows elucidation of all the features. It allows clear visualisation of the valve leaflets, showing the precise morphology of the valve leaflets, the extent of their formation, the level of their attachment, and their degree of coaptation. Visualisation of the mechanism of regurgitation or stenosis is possible, as is more accurate quantification of the regurgitant jet or jets. Subchordal apparatus may be seen more clearly using three-dimensional echocardiography, and their functional anatomy understood. The multiplanar review modality allows examination of the three-dimensional data set even in patients with sub-optimal echocardiographic imaging. Previously, much of this information could only be well-understood at the time of surgery or post mortem, meaning that the majority of the specimens fully examined were at the poorly functioning end of the spectrum. This information is of use in furthering our understanding of this complex lesion as it functions in vivo, and demonstrating which anatomical pathology is significant in producing functional and physiological consequences. It is also of use for the clinician in selecting which patients are amenable to surgical intervention, for either single or biventricular repair, and for the surgeon in planning how to approach the operation. Correlation between three-dimensional echocardiographic findings and surgical findings has already been established, but the effect of this enhanced anatomical knowledge on surgical planning and surgical outcome requires further investigation.
Nominal dysphasia and euphoria caused by EBV encephalitis
Carman, Kursat Bora; Yakut, Ayten; Ekici, Arzu; Isikay, Sedat
2013-01-01
Encephalitis is an uncommon neurological complication of Ebstein-Barr virus (EBV) infection and usually presents with confusion, decreased level of consciousness, fever, epileptic seizure, emotional instability and chorea. We present a patient with EBV encephalitis, characterised by nominal dysphasia, euphoria and personality changes. PMID:23307455
[Fetal echocardiography efficiency. Clinical experience].
San Luis Miranda, Raúl; Arias Monroy, Laura Guadalupe; Gutiérrez González, Gladis Alicia; León Avila, José Luis; Cruz Rodríguez, Armando; Osornio Correa, Porfirio Rafael
2008-12-01
Congenital heart disease diagnostic has a high diagnostic precision with fetal echocardiography. This study has been reported in populations with high risk and with a sensibility of 86 to 99% and specificity of 91 to 100%. To know sensibility and specificity of fetal echocardiography in high-risk pregnancies, and to describe types and frequency of congenital heart disease in utero. 229 files of pregnant women with high-risk factors, more than 15 weeks of gestation, and at birth cardiovascular exam were analyzed. This analysis was made by means of simple frequencies, sensibility, specificity, positive and negative predictive value, and truth index calculation. We found 62 (27%) cases with fetal heart disease. Mean of maternal age was 27 +/- 5.5 years, and of gestational age 31 +/- 5 weeks. Risk factors that require study were: four-chamber abnormality in routine ultrasound, dysmorphy, fetal bradicardia, and poll and oligohydramnios. There were 55 (88.7%) high-risk heart diseases, and most frequent were Ebstein's anomaly, unique ventricle, hypoplastic left ventricle syndrome, and tumors. Sensibility was 98.41%, specificity was 97.59%, positive prognostic value was 97.59%, and negative prognostic value was 99.39%. Fetal echocardiography has a high diagnosis certainty in our hospital unit, thus, it has to be a normal prenatal exam in pregnant women with high-risk factors.
Corno, Antonio F; Kocica, Mladen J; Torrent-Guasp, Francisco
2006-04-01
The new concepts of cardiac anatomy and physiology, based on the observations made by Francisco Torrent-Guasp's discovery of the helical ventricular myocardial band, can be useful in the context of the surgical strategies currently used to manage patients with congenital heart defects. The potential impact of the Torrent-Guasp's Heart on congenital heart defects have been analyzed in the following settings: ventriculo-arterial discordance (transposition of the great arteries), double (atrio-ventricular and ventriculo-arterial) discordance (congenitally corrected transposition of the great arteries), Ebstein's anomaly, pulmonary valve regurgitation after repair of tetralogy of Fallot, Ross operation, and complex intra-ventricular malformations. The functional interaction of right and left ventricles occurs not only through their arrangements in series but also thanks to the structural spiral features. Changes in size and function of either ventricle may influence the performance of the other ventricle. The variety and complexity of congenital heart defects make the recognition of the relationship between form and function a vital component, especially when compared to acquired disease. The new concepts of cardiac anatomy and function proposed by Francisco Torrent-Guasp, based on his observations, should stimulate further investigations of alternative surgical strategies by individuals involved with the management of patients with congenital heart defects.
El-Said, Howaida; Hegde, Sanjeet; Moore, John
2014-01-01
The patient was a male infant with L-transposition of great arteries (L-TGA), Ebstein's anomaly of the tricuspid valve, subvalvar aortic stenosis, ventricular septal defect (VSD), hypoplastic right ventricle, arch hypoplasia, and congenital complete heart block. He underwent a Norwood procedure, aortic arch repair, permanent pacemaker implantation, and a 3.5-mm aortopulmonary shunt at 4 days of age. At the time of his surgery, left ventricular function was in the normal range (ejection fraction [EF] = 67%). However by 3 months of age, he was noted to have developed moderate-severe biventricular dysfunction (left ventricular ejection fraction [LVEF] = 34%). Atresia of the coronary sinus with a small left superior venacava (LSVC) and a bridging vein was discovered during cardiac catheterization at this time. The coronary sinus mean pressure was 17 mm Hg, and the common atrial mean pressure was 6 mmHg. We opened the atretic coronary sinus ostium using radiofrequency ablation and stent placement. There was dramatic improvement in ventricular function observed over a 2-month period. Follow-up cardiac catheterization 5 months later revealed the stent in the coronary sinus to be widely patent with no intimal buildup, and the ventricular function was normal (LVEF = 58%). The patient had a bidirectional Glenn procedure with an uncomplicated postoperative course and is currently awaiting Fontan completion. © 2013 Wiley Periodicals, Inc.
Pothineni, Koteswara R; Duncan, Kurt; Yelamanchili, Pridhvi; Nanda, Navin C; Patel, Vinod; Fan, PoHoey; Burri, Manjula V; Singh, Anurag; Panwar, Sadik R
2007-05-01
Twenty-nine patients with different tricuspid valve (TV) pathologies were studied by both two-dimensional transthoracic (2DTTE) and live/real time three-dimensional transthoracic echocardiography (3DTTE). A major contribution of 3DTTE over 2DTTE was the en face visualization of all three leaflets of the TV in all patients. This allowed accurate assessment of TV orifice area in patients with TV stenosis and carcinoid disease. Loss of TV leaflet tissue, defects in TV leaflets and size of TV systolic non-coaptation could also be delineated and resulted in identifying the mechanism of tricuspid regurgitation (TR) in patients with Ebstein's anomaly and rheumatic heart disease. Prolapse of TV leaflets could also be well visualized and enabled us to develop a schema for systematic assessment of individual segment prolapse which could help in surgical planning. The exact sites of chordae rupture in patients with flail TV as well as right ventricular papillary muscle rupture could be well seen by 3DTTE. 3DTTE also permitted sectioning of various TV masses for more specific diagnosis of their nature. In addition, color Doppler 3DTTE provided an estimate of quantitative evaluation of TR severity, since the exact shape and size of the vena contracta could be accurately assessed. In conclusion, our preliminary experience with 3DTTE has demonstrated substantial incremental value over 2DTTE in the assessment of various TV pathologies.
Kikuchi-Fujimoto disease and systemic lupus erythematosus: the EBV connection?
Gionanlis, Lazaros; Katsounaros, Marios; Bamihas, Gerasimos; Fragidis, Stelios; Veneti, Panagiota; Sombolos, Kostas
2009-01-01
Kikuchi-Fujimoto disease (KFD) is a benign and self-limited disease of unknown etiology that affects mainly young women. It presents with localized lymphadenopathy, usually cervical, accompanied with fever, night sweats, and leucopenia. KFD has been rarely described in association with autoimmune disorders, mainly systemic lupus erythematosus (SLE). We report the case of a young patient presenting with KFD coinciding with SLE. The association of KFD and SLE is reviewed. Moreover, a possible pathogenetic role of Ebstein-Barr virus linking the two clinical entities is discussed.
Jordan, Christopher P; Freedenberg, Vicki; Wang, Yongfei; Curtis, Jeptha P; Gleva, Marye J; Berul, Charles I
2014-12-01
In 2010, the National Cardiovascular Data Registry enhanced pediatric, nonatherosclerotic structural heart disease and congenital heart disease (CHD) data collection. This report characterizes CHD and pediatric patients undergoing implantable cardioverter defibrillator implantation. In this article, we report implantable cardioverter defibrillator procedures (April 2010 to December 2012) in the registry for 2 cohorts: (1) all patients with CHD (atrial septal defect, ventricular septal defect, tetralogy of Fallot, Ebstein anomaly, transposition of the great vessels, and common ventricle) and (2) patients <21 years. We evaluated indications and characteristics to include transvenous and nontransvenous lead implants, CHD type, and New York Heart Association class. There were 3139 CHD procedures, 1601 for patients <21 years and 126 for CHD <21 years. Implantable cardioverter defibrillator indications for patients with CHD were primary prevention in 1943 (61.9%) and secondary prevention in 1107 (35.2%). Pediatric patients had 935 (58.4%) primary prevention and 588 (36.7%) secondary prevention devices. Primary prevention had higher New York Heart Association class. Nontransvenous age (35.9 ± 23.2 versus 40.1 ± 24.6 years; P=0.05) and nontransvenous height (167.1 ± 18.9 cm; range, 53-193 cm versus 170.4 ± 13.1 cm; range, 61-203 cm; P<0.01) were lower than for transvenous patients. CHD and pediatrics had similar rates of transvenous (97%) and nontransvenous (3%) leads and did not differ from the overall registry. Transposition of the great vessels and common ventricle had higher rates of nontransvenous leads. Primary prevention exceeds secondary prevention for CHD and pediatrics. Nontransvenous lead patients were younger, with higher rates of transposition of the great vessels and common ventricle patients compared with transvenous lead patients. © 2014 American Heart Association, Inc.
Successful cardiac transplantation outcomes in patients with adult congenital heart disease.
Menachem, Jonathan N; Golbus, Jessica R; Molina, Maria; Mazurek, Jeremy A; Hornsby, Nicole; Atluri, Pavan; Fuller, Stephanie; Birati, Edo Y; Kim, Yuli Y; Goldberg, Lee R; Wald, Joyce W
2017-09-01
The purpose of our study is (1) to characterise patients with congenital heart disease undergoing heart transplantation by adult cardiac surgeons in a large academic medical centre and (2) to describe successful outcomes associated with our multidisciplinary approach to the evaluation and treatment of adults with congenital heart disease (ACHD) undergoing orthotopic heart transplantation (OHT). Heart failure is the leading cause of death in patients with ACHD leading to increasing referrals for OHT. The Penn Congenital Transplant Database comprises a cohort of patients with ACHD who underwent OHT between March 2010 and April 2016. We performed a retrospective cohort study of the 20 consecutive patients. Original cardiac diagnoses include single ventricle palliated with Fontan (n=8), dextro-transposition of the great arteries after atrial switch (n=4), tetralogy of Fallot (n=4), pulmonary atresia (n=1), Ebstein anomaly (n=1), unrepaired ventricular septal defect (n=1) and Noonan syndrome with coarctation of the aorta (n=1). Eight patients required pretransplant inotropes and two required pretransplant mechanical support. Nine patients underwent heart-liver transplant and three underwent heart-lung transplant. Three patients required postoperative mechanical circulatory support. Patients were followed for an average of 38 months as of April 2016, with 100% survival at 30 days and 1 year and 94% overall survival (19/20 patients). ACHD-OHT patients require highly specialised, complex and multidisciplinary healthcare. The success of our programme is attributed to using team-based, patient-centred care including our multidisciplinary staff and specialists across programmes and departments. © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.
Budde, Birgit S; Binner, Priska; Waldmüller, Stephan; Höhne, Wolfgang; Blankenfeldt, Wulf; Hassfeld, Sabine; Brömsen, Jürgen; Dermintzoglou, Anastassia; Wieczorek, Marcus; May, Erik; Kirst, Elisabeth; Selignow, Carmen; Rackebrandt, Kirsten; Müller, Melanie; Goody, Roger S; Vosberg, Hans-Peter; Nürnberg, Peter; Scheffold, Thomas
2007-12-26
Noncompaction of the ventricular myocardium (NVM) is the morphological hallmark of a rare familial or sporadic unclassified heart disease of heterogeneous origin. NVM results presumably from a congenital developmental error and has been traced back to single point mutations in various genes. The objective of this study was to determine the underlying genetic defect in a large German family suffering from NVM. Twenty four family members were clinically assessed using advanced imaging techniques. For molecular characterization, a genome-wide linkage analysis was undertaken and the disease locus was mapped to chromosome 14ptel-14q12. Subsequently, two genes of the disease interval, MYH6 and MYH7 (encoding the alpha- and beta-myosin heavy chain, respectively) were sequenced, leading to the identification of a previously unknown de novo missense mutation, c.842G>C, in the gene MYH7. The mutation affects a highly conserved amino acid in the myosin subfragment-1 (R281T). In silico simulations suggest that the mutation R281T prevents the formation of a salt bridge between residues R281 and D325, thereby destabilizing the myosin head. The mutation was exclusively present in morphologically affected family members. A few members of the family displayed NVM in combination with other heart defects, such as dislocation of the tricuspid valve (Ebstein's anomaly, EA) and atrial septal defect (ASD). A high degree of clinical variability was observed, ranging from the absence of symptoms in childhood to cardiac death in the third decade of life. The data presented in this report provide first evidence that a mutation in a sarcomeric protein can cause noncompaction of the ventricular myocardium.
Arrhythmias in Adults with Congenital Heart Disease: What Are Risk Factors for Specific Arrhythmias?
Loomba, Rohit S; Buelow, Matthew W; Aggarwal, Saurabh; Arora, Rohit R; Kovach, Joshua; Ginde, Salil
2017-04-01
An increasing number of patients with congenital heart disease are now surviving into adulthood. This has also led to the emergence of complications from the underlying congenital heart disease, related surgical interventions, and associated combordities. While the prevalence of particular arrhythmias with specific congenital heart disease has been previously described, a detailed analysis of all lesions and a large number of comorbidities has not been previously published. Admissions with congenital heart disease were identified in the National Inpatient Sample. Associated comorbidities were also identified for these patients. Univariate analysis was done to compare those risk factors associated with specific arrhythmias in the setting of congenital heart disease. Next, regression analysis was done to identify what patient characteristics and comorbidities were associated with increased risk of specific arrhythmias. A total of 52,725,227 admissions were included in the analysis. Of these, 109,168 (0.21%) had congenital heart disease. Of those with congenital heart disease, 27,088 (25%) had an arrhythmia at some point. The most common arrhythmia in those with congenital heart disease was atrial fibrillation, which was noted in 86% of those with arrhythmia followed by atrial flutter which was noted in 20% of those with congenital heart disease. The largest burden of arrhythmia was found to be in those with tricuspid atresia with a 51% prevalence of arrhythmia in this group followed by Ebstein anomaly which had an arrhythmia prevalence of 39%. Increasing age, male gender, double outlet right ventricle, atrioventricular septal defect, heart failure, obstructive sleep apnea, transposition of the great arteries, congenitally corrected transposition, and tetralogy of Fallot were frequently noted to be independent risk factors of specific arrhythmias. Approximately, 25% of adult admissions with congenital heart disease are associated with arrhythmia. The burden of arrhythmia varies by the specific lesion and other risk factors as well. Understanding of these can help in risk stratification and can help devise strategies to lower this risk. © 2016 Wiley Periodicals, Inc.
Photiadis, J; Sinzobahamvya, N; Arenz, C; Sata, S; Haun, C; Schindler, E; Asfour, B; Hraska, V
2011-08-01
The Aristotle score quantifies the complexity involved in congenital heart surgery. It defines surgical performance as complexity score times hospital survival. We studied how expected and observed surgical performance evolved over time. 2312 main procedures carried out between 2006 and 2010 were analyzed. The Aristotle basic score, corresponding hospital survival and related observed surgical performance were estimated. Expected survival was based on the mortality risks published by O'Brien and coauthors. Observed performance divided by expected performance was called the standardized ratio of performance. This should trend towards a figure above 100%. Survival rates and performance are given with 95% confidence intervals. The mean Aristotle basic score was 7.88 ± 2.68. 51 patients died: observed hospital survival was 97.8 % (97.1 %-98.3%). 115 deaths were anticipated: expected survival was 95.2% (93.5%-96.3%). Observed and expected surgical performance reached 7.71 (7.65-7.75) and 7.49 (7.37-7.59), respectively. Therefore the overall standardized ratio of performance was 102.94%. The ratio increased from 2006 (ratio = 101.60%) to 2009 (103.92%) and was 103.42% in 2010. Performance was high for the repair of congenital corrected transposition of the great arteries and ventricular septal defect (VSD) by atrial switch and Rastelli procedure, the Norwood procedure, repair of truncus arteriosus, aortic arch repair and VSD closure, and the Ross-Konno procedure, with corresponding standardized ratios of 123.30%, 116.83%, 112.99%, 110.86% and 110.38%, respectively. With a ratio of 82.87%, performance was low for repair of Ebstein's anomaly. The standardized ratio of surgical performance integrates three factors into a single value: procedure complexity, postoperative observed survival, and comparison with expected survival. It constitutes an excellent instrument for quality monitoring of congenital heart surgery programs over time. It allows an accurate comparison of surgical performance across institutions with different case mixes. © Georg Thieme Verlag KG Stuttgart · New York.
Howley, Lisa W; Khoo, Nee Scze; Moon-Grady, Anita J; Patel, Sonali S; Alrais, Fayeza; Tworetzky, Wayne; Colen, Timothy; Brooks, Paul; Trines, Jean; Ojala, Tiina; Hornberger, Lisa K
2017-06-01
In severe right heart obstruction (RHO), redistribution of cardiac output to the left ventricle (LV) is well tolerated by the fetal circulation. Although the same should be true of severely regurgitant tricuspid valve disease (rTVD) with reduced or no output from the right ventricle, affected fetuses more frequently develop hydrops or suffer intrauterine demise. We hypothesized that right atrium (RA) function is altered in rTVD but not in RHO, which could contribute to differences in outcomes. Multi-institutional retrospective review of fetal echocardiograms performed over a 10-year period on fetuses with rTVD (Ebstein's anomaly, tricuspid valve dysplasia) or RHO (pulmonary atresia/intact ventricular septum, tricuspid atresia) and a healthy fetal control group. Offline velocity vector imaging and Doppler measurements of RA size and function and LV function were made. Thirty-four fetuses with rTVD, 40 with RHO, and 79 controls were compared. The rTVD fetuses had the largest RA size and lowest RA expansion index, fractional area of change, and RA indexed filling and emptying rates compared with fetuses with RHO and controls. The rTVD fetuses had the shortest LV ejection time and increased Tei index with a normal LV ejection fraction. RA dilation (odds ratio, 1.27; 95% CI, 1.05-1.54) and reduced indexed emptying rate (odds ratio, 2.49; 95% CI, 1.07-5.81) were associated with fetal or neonatal demise. Fetal rTVD is characterized by more severe RA dilation and dysfunction compared with fetal RHO and control groups. RA dysfunction may be an important contributor to reduced ventricular filling and output, potentially playing a critical role in the worsened outcomes observed in fetal rTVD. Copyright © 2017 American Society of Echocardiography. Published by Elsevier Inc. All rights reserved.
The New Concept of Univentricular Heart
Frescura, Carla; Thiene, Gaetano
2014-01-01
The concept of univentricular heart moved from hearts with only one ventricle connected with atria [double inlet ventricle or absent atrioventricular (AV) connection] to hearts not amenable to biventricular repair, namely hearts with two ventricles unable to sustain separately pulmonary and systemic circulations in sequence. In the latter definition, even hearts with one hypoplastic ventricle are considered “functional” univentricular hearts. They include pulmonary/aortic atresia or severe stenosis with hypoplastic ventricle, and rare conditions like huge intramural cardiac tumors and Ebstein anomaly with extreme atrialization of right ventricular cavity. In this setting, the surgical repair is univentricular with “Fontan” operation, bypassing the ventricular mass. In other words, functionally univentricular heart is a condition in which, after surgery, only one ventricle sustain systemic circulation. Univentricular hearts (double inlet or absent AV connection) almost invariably show two ventricular chambers, one main and one accessory, which lacks an inlet portion. The latter is located posteriorly when morphologically left and anteriorly when morphologically right. As far as double inlet left ventricle, this is usually associated with discordant ventriculo-arterial (VA) connection (transposition of the great arteries) and all the blood flow to the aorta, which takes origin from the hypoplastic anterior right ventricle, is ventricular septal defect (bulbo-ventricular foramen) dependent. If restrictive, an aortic arch obstruction may be present. Double inlet left ventricle may be rarely associated with VA concordance (Holmes heart). As far as double inlet right ventricle with posterior hypoplastic left ventricular cavity, ventriculo-arterial connection is usually of double outlet type; thus the term double inlet–outlet right ventricle may be coined. Absent right or left AV connection may develop in the setting of both d- or l-loop, whatever the situs. In this condition, the contra-lateral patent AV valve may be either mitral or tricuspid in terms of morphology and the underlying ventricle (main chamber) either morphologically left or right. Establishing the loop, whatever right or left (also called right or left ventricular topology), is a fundamental step in the segmental-sequential analysis of congenital heart disease. PMID:25072035
Tricuspid regurgitation: contemporary management of a neglected valvular lesion.
Irwin, Richard Bruce; Luckie, Matthew; Khattar, Rajdeep S
2010-11-01
Right-sided cardiac valvular disease has traditionally been considered less clinically important than mitral or aortic valve pathology. However, detectable tricuspid regurgitation (TR) is common and recent data suggest that significant TR can lead to functional impairment and reduced survival, particularly in patients with concomitant left-sided valvular disease. The tricuspid valve is a complex anatomical structure and advances in three dimensional echocardiography and cardiac MRI have contributed to a greater understanding of tricuspid valve pathology. These imaging techniques are invaluable in determining the aetiology and severity of TR, and provide an assessment of right ventricular function and pulmonary artery pressure. TR is more prevalent in women and those with a history of myocardial infarction and heart failure. It also occurs in about 10% of patients with rheumatic heart disease. Chronic severe TR may have a prolonged clinical course culminating in the development of fatigue and poor exercise tolerance due to a reduced cardiac output. Approximately 90% of cases of TR are secondary to either pulmonary hypertension or intrinsic right ventricular pathology and about 10% are due to primary tricuspid valve disease. Primary causes such as Ebstein's anomaly, rheumatic disease, myxomatous changes, carcinoid syndrome, endomyocardial fibrosis, and degenerative disease have characteristic morphological features readily identifiable by echocardiography. Ascertaining an accurate right ventricular systolic pressure is important in separating primary from secondary causes as significant TR with a pressure <40 mm Hg implies intrinsic valve disease. Cardiac MRI may be indicated in those with inadequate echocardiographic images and is also the gold standard for the evaluation of right ventricular function and morphology. The assessment of leaflet morphology, annular dimensions, and pulmonary artery pressure are particularly important for determining subsequent management. Along with appropriate treatment of the underlying cause of TR and pulmonary hypertension, management guidelines indicate a move towards more aggressive treatment of TR. In those undergoing left-sided valve surgery, tricuspid valve repair is universally recommended in the presence of severe coexistent TR; in those with isolated severe TR, surgery is recommended in the presence of symptoms or progressive right ventricular dilatation or dysfunction.
Right ventricular outflow tract obstruction in complicated monochorionic twin pregnancy.
Eschbach, S J; Boons, L S T M; Van Zwet, E; Middeldorp, J M; Klumper, F J C M; Lopriore, E; Teunissen, A K K; Rijlaarsdam, M E; Oepkes, D; Ten Harkel, A D J; Haak, M C
2017-06-01
Severe right ventricular outflow tract obstruction (RVOTO) is a potential complication in recipient twins of twin-to-twin transfusion syndrome (TTTS) that requires postnatal follow-up or treatment. We aimed to evaluate pregnancy characteristics of neonates with RVOTO from complicated monochorionic twin pregnancies, determine the incidence of RVOTO in TTTS cases and construct a prediction model for its development. This was an observational cohort study of all complicated monochorionic twin pregnancies with a postnatal diagnosis of RVOTO examined at our center. Cases were referred for evaluation of the need for fetal therapy or intervention because of TTTS, selective intrauterine growth restriction (sIUGR) or multiple congenital malformations in one of the twins. Ultrasound data were retrieved from our monochorionic twin database. Among liveborn TTTS recipients treated prenatally with laser therapy, those with RVOTO were compared with those without RVOTO (controls). We describe four additional cases with RVOTO that were not TTTS recipients. A total of 485 twin pregnancies received laser therapy for TTTS during the study period. RVOTO was diagnosed in 3% (11/368) of liveborn TTTS recipients, of whom two showed mild Ebstein's anomaly. Before laser therapy, pericardial effusion was seen in 45% (5/11) of RVOTO cases (P < 0.01) and abnormal A-wave in the ductus venosus (DV) in 73% (8/11) (P = 0.03), significantly higher proportions than in controls. Mean gestational age at laser therapy was 17 + 3 weeks in RVOTO cases compared with 20 + 3 weeks in controls (P = 0.03). A prediction model for RVOTO was constructed incorporating these three significant variables. One TTTS donor had RVOTO after the development of transient hydrops following laser therapy. Three larger twins in pregnancies complicated by sIUGR developed RVOTO, the onset of which was detectable early in the second trimester. RVOTO occurs in TTTS recipient twins but can also develop in TTTS donors and larger twins of pregnancies complicated by sIUGR. Abnormal flow in the DV, pericardial effusion and early gestational age at onset of TTTS are predictors of RVOTO in TTTS recipients, which suggests increased vulnerability to hemodynamic imbalances in the fetal heart in early pregnancy. These findings could guide diagnostic follow-up protocols after TTTS treatment. Copyright © 2016 ISUOG. Published by John Wiley & Sons Ltd. Copyright © 2016 ISUOG. Published by John Wiley & Sons Ltd.
A 2-year-old boy with circulatory failure owing to streptococcal toxic shock syndrome: case report.
Keenswijk, Werner; Vande Walle, Johan
2017-04-20
A 2-year-old boy presented with severe hypotension and acute kidney injury after a prodrome of non-bloody diarrhoea and fever in the preceding 3 days. He had a mild Ebstein cardiac anomaly but otherwise a normal past history and growth. On examination, he looked ill, his temperature was 37.5 °C, circulation was poor, and there were several purpuric lesions on the face, hands and scrotum. Haemoglobin was 7.8 g/dL (11-14), total white cell count 27 × 10 9 /L, platelets 62 × 10 9 /L, blood urea nitrogen 20.7 mmol/L (4.2-17.1), serum creatinine 95.4 μmol/L (21.2-36.2), CRP 154 mg/L (<5), AST 296 U/L (11-50), ALT 909 U/L (7-40) and C 3 component of complement 0.8 g/L (0.9-1.8). Activated partial thromboplastin time (APTT) and prothrombin time (PT) were prolonged and fibrinogen level was 1.0 g/L (2-4). He received immediate fluid resuscitation (IV 0.9% saline solution, 2 × 10 ml/kg boluses, followed by glucose 5/0.45% sodium chloride solution, 2 × 10 ml/kg) and antibiotics (ciprofloxacin and amikacin) but circulation continued to deteriorate with development of decreased consciousness. He was placed on mechanical ventilation and vasopressor agents were added. Despite improved circulation over the next 2 days, he developed oliguria, progressive fluid overload, generalised oedema and a right-sided pleural effusion. Dialysis was commenced on day 3 of admission. Differential diagnosis included sepsis, atypical haemolytic uraemic syndrome and lupus nephritis. Blood and urine cultures remained negative but an anti-streptolysin O titre of 1318 (<200) IU/mL led to the diagnosis of streptococcal toxic shock syndrome which is rare in early childhood and associated with high mortality. Haemodialysis was commenced and continued for 10 days with successful treatment of fluid overload and subsequent extubation. Renal function was completely restored over the following 6 weeks and he was discharged in good clinical condition about 2 months after intial admission. The clinical course and outcome are discussed, and the importance of timely initiation of dialysis when there is fluid overload is emphasised.
Mahjour, Seyed Babak; Ghaffarpasand, Fariborz; Fattahi, Mohammad Javad; Ghaderi, Abbas; Fotouhi Ghiam, Alireza; Karimi, Mehran
2010-12-01
To investigate the seroprevalence of Herpes Simplex Viruses (HSV1 and HSV2), Ebstein-Barr Virus (EBV) and Hepatitis B Virus (HBV) in children with acute lymphoblastic leukemia (ALL) in southern Iran. 90 patients with ALL and 90 age-sex matched healthy participants were enrolled in this study. Antibodies (IgG) against HBsAg, HSV1, HSV2, EBV different antigens including Epstein-Barr nuclear antigen-1 (EBNA-1), viral capsid antigen (VCA) and early antigen (EA) were measured by enzyme-linked immunosorbent assay (ELISA). There were 54 (60%) male and 36 (40%) female in both study groups with mean age of 8.47 ± 3.61 and 8.61 ± 2.84 years in case and control group respectively (P = 0.812). The prevalence of antibodies against HBsAg (P = 0.002), HSV1 (P < 0.0001), VCA (P = 0.021) and EA (P < 0.0001) antigens of EBV were significantly higher in ALL patients. With the results of this study, we could not exclude a connection between these viral infections and later leukemogenesis in childhood ALL, although nor latent infection nor congenital infection cannot be excluded by this method.
Distribution of branchial anomalies in a paediatric Asian population.
Teo, Neville Wei Yang; Ibrahim, Shahrul Izham; Tan, Kun Kiaang Henry
2015-04-01
The objective of the present study was to review the distribution and incidence of branchial anomalies in an Asian paediatric population and highlight the challenges involved in the diagnosis of branchial anomalies. This was a retrospective chart review of all paediatric patients who underwent surgery for branchial anomalies in a tertiary paediatric hospital from August 2007 to November 2012. The clinical notes were correlated with preoperative radiological investigations, intraoperative findings and histology results. Branchial anomalies were classified based on the results of the review. A total of 28 children underwent surgery for 30 branchial anomalies during the review period. Two children had bilateral branchial anomalies requiring excision. Of the 30 branchial anomalies, 7 (23.3%) were first branchial anomalies, 5 (16.7%) were second branchial anomalies, 3 (10.0%) were third branchial anomalies, and 4 (13.3%) were fourth branchial anomalies (one of the four patients with fourth branchial anomalies had bilateral branchial anomalies). In addition, seven children had 8 (26.7%) branchial anomalies that were thought to originate from the pyriform sinus; however, we were unable to determine if these anomalies were from the third or fourth branchial arches. There was inadequate information on the remaining 3 (10.0%) branchial anomalies for classification. The incidence of second branchial anomalies appears to be lower in our Asian paediatric population, while that of third and fourth branchial anomalies was higher. Knowledge of embryology and the related anatomy of the branchial apparatus is crucial in the identification of the type of branchial anomaly.
Distribution of branchial anomalies in a paediatric Asian population
Teo, Neville Wei Yang; Ibrahim, Shahrul Izham; Tan, Kun Kiaang Henry
2015-01-01
INTRODUCTION The objective of the present study was to review the distribution and incidence of branchial anomalies in an Asian paediatric population and highlight the challenges involved in the diagnosis of branchial anomalies. METHODS This was a retrospective chart review of all paediatric patients who underwent surgery for branchial anomalies in a tertiary paediatric hospital from August 2007 to November 2012. The clinical notes were correlated with preoperative radiological investigations, intraoperative findings and histology results. Branchial anomalies were classified based on the results of the review. RESULTS A total of 28 children underwent surgery for 30 branchial anomalies during the review period. Two children had bilateral branchial anomalies requiring excision. Of the 30 branchial anomalies, 7 (23.3%) were first branchial anomalies, 5 (16.7%) were second branchial anomalies, 3 (10.0%) were third branchial anomalies, and 4 (13.3%) were fourth branchial anomalies (one of the four patients with fourth branchial anomalies had bilateral branchial anomalies). In addition, seven children had 8 (26.7%) branchial anomalies that were thought to originate from the pyriform sinus; however, we were unable to determine if these anomalies were from the third or fourth branchial arches. There was inadequate information on the remaining 3 (10.0%) branchial anomalies for classification. CONCLUSION The incidence of second branchial anomalies appears to be lower in our Asian paediatric population, while that of third and fourth branchial anomalies was higher. Knowledge of embryology and the related anatomy of the branchial apparatus is crucial in the identification of the type of branchial anomaly. PMID:25917471
Associated congenital anomalies among cases with Down syndrome.
Stoll, Claude; Dott, Beatrice; Alembik, Yves; Roth, Marie-Paule
2015-12-01
Down syndrome (DS) is the most common congenital anomaly widely studied for at least 150 years. However, the type and the frequency of congenital anomalies associated with DS are still controversial. Despite prenatal diagnosis and elective termination of pregnancy for fetal anomalies, in Europe, from 2008 to 2012 the live birth prevalence of DS per 10,000 was 10. 2. The objectives of this study were to examine the major congenital anomalies occurring in infants and fetuses with Down syndrome. The material for this study came from 402,532 consecutive pregnancies of known outcome registered by our registry of congenital anomalies between 1979 and 2008. Four hundred sixty seven (64%) out of the 728 cases with DS registered had at least one major associated congenital anomaly. The most common associated anomalies were cardiac anomalies, 323 cases (44%), followed by digestive system anomalies, 42 cases (6%), musculoskeletal system anomalies, 35 cases (5%), urinary system anomalies, 28 cases (4%), respiratory system anomalies, 13 cases (2%), and other system anomalies, 26 cases (3.6%). Among the cases with DS with congenital heart defects, the most common cardiac anomaly was atrioventricular septal defect (30%) followed by atrial septum defect (25%), ventricular septal defect (22%), patent ductus arteriosus (5%), coarctation of aorta (5%), and tetralogy of Fallot (3%). Among the cases with DS with a digestive system anomaly recorded, duodenal atresia (67%), Hirschsprung disease (14%), and tracheo-esophageal atresia (10%) were the most common. Fourteen (2%) of the cases with DS had an obstructive anomaly of the renal pelvis, including hydronephrosis. The other most common anomalies associated with cases with DS were syndactyly, club foot, polydactyly, limb reduction, cataract, hydrocephaly, cleft palate, hypospadias and diaphragmatic hernia. Many studies to assess the anomalies associated with DS have reported various results. There is no agreement in the literature as to which associated anomalies are most common in cases with DS with associated anomalies. In this study we observed a higher percentage of associated anomalies than in the other reported series as well as an increase in the incidence of duodenal atresia, urinary system anomalies, musculoskeletal system anomalies, and respiratory system anomalies, and a decrease in the incidence of anal atresia, annular pancreas, and limb reduction defects. In conclusion, we observed a high prevalence of total congenital anomalies and specific patterns of malformations associated with Down syndrome which emphasizes the need to evaluate carefully all cases with Down syndrome for possible associated major congenital anomalies. Copyright © 2015 Elsevier Masson SAS. All rights reserved.
1982-03-01
gravity anomaly values computed from measured gravity at discrete points (x,y) within the 10 x 10 area. If the Ag are Bouguer gravity anomalies, the Ag is...a 10 x 10 mean Bouguer anomaly. If the Ag are free-air gravity anomalies, the Ag is a 10 x 10 mean free-air gravity anomaly. Either anomaly form can...it requires less subjective judgment. Predictions in continental areas always are made using Bouguer gravity anomalies because this anomaly form is
Prevalence and distribution of selected dental anomalies among saudi children in Abha, Saudi Arabia.
Yassin, Syed M
2016-12-01
Dental anomalies are not an unusual finding in routine dental examination. The effect of dental anomalies can lead to functional, esthetic and occlusal problems. The Purpose of the study was to determine the prevalence and distribution of selected developmental dental anomalies in Saudi children. The study was based on clinical examination and Panoramic radiographs of children who visited the Pediatric dentistry clinics at King Khalid University College of Dentistry, Saudi Arabia. These patients were examined for dental anomalies in size, shape, number, structure and position. Data collected were entered and analyzed using statistical package for social sciences version. Of the 1252 children (638 Boys, 614 girls) examined, 318 subjects (25.39%) presented with selected dental anomalies. The distribution by gender was 175 boys (27.42%) and 143 girls (23.28%). On intergroup comparison, number anomalies was the most common anomaly with Hypodontia (9.7%) being the most common anomaly in Saudi children, followed by hyperdontia (3.5%). The Prevalence of size anomalies were Microdontia (2.6%) and Macrodontia (1.8%). The prevalence of Shape anomalies were Talon cusp (1.4%), Taurodontism (1.4%), Fusion (0.8%).The prevalence of Positional anomalies were Ectopic eruption (2.3%) and Rotation (0.4%). The prevalence of structural anomalies were Amelogenesis imperfecta (0.3%) Dentinogenesis imperfecta (0.1%). A significant number of children had dental anomaly with Hypodontia being the most common anomaly and Dentinogenesis imperfecta being the rare anomaly in the study. Early detection and management of these anomalies can avoid potential orthodontic and esthetic problems in a child. Key words: Dental anomalies, children, Saudi Arabia.
Prevalence and distribution of selected dental anomalies among saudi children in Abha, Saudi Arabia
2016-01-01
Background Dental anomalies are not an unusual finding in routine dental examination. The effect of dental anomalies can lead to functional, esthetic and occlusal problems. The Purpose of the study was to determine the prevalence and distribution of selected developmental dental anomalies in Saudi children. Material and Methods The study was based on clinical examination and Panoramic radiographs of children who visited the Pediatric dentistry clinics at King Khalid University College of Dentistry, Saudi Arabia. These patients were examined for dental anomalies in size, shape, number, structure and position. Data collected were entered and analyzed using statistical package for social sciences version. Results Of the 1252 children (638 Boys, 614 girls) examined, 318 subjects (25.39%) presented with selected dental anomalies. The distribution by gender was 175 boys (27.42%) and 143 girls (23.28%). On intergroup comparison, number anomalies was the most common anomaly with Hypodontia (9.7%) being the most common anomaly in Saudi children, followed by hyperdontia (3.5%). The Prevalence of size anomalies were Microdontia (2.6%) and Macrodontia (1.8%). The prevalence of Shape anomalies were Talon cusp (1.4%), Taurodontism (1.4%), Fusion (0.8%).The prevalence of Positional anomalies were Ectopic eruption (2.3%) and Rotation (0.4%). The prevalence of structural anomalies were Amelogenesis imperfecta (0.3%) Dentinogenesis imperfecta (0.1%). Conclusions A significant number of children had dental anomaly with Hypodontia being the most common anomaly and Dentinogenesis imperfecta being the rare anomaly in the study. Early detection and management of these anomalies can avoid potential orthodontic and esthetic problems in a child. Key words:Dental anomalies, children, Saudi Arabia. PMID:27957258
Domain Anomaly Detection in Machine Perception: A System Architecture and Taxonomy.
Kittler, Josef; Christmas, William; de Campos, Teófilo; Windridge, David; Yan, Fei; Illingworth, John; Osman, Magda
2014-05-01
We address the problem of anomaly detection in machine perception. The concept of domain anomaly is introduced as distinct from the conventional notion of anomaly used in the literature. We propose a unified framework for anomaly detection which exposes the multifaceted nature of anomalies and suggest effective mechanisms for identifying and distinguishing each facet as instruments for domain anomaly detection. The framework draws on the Bayesian probabilistic reasoning apparatus which clearly defines concepts such as outlier, noise, distribution drift, novelty detection (object, object primitive), rare events, and unexpected events. Based on these concepts we provide a taxonomy of domain anomaly events. One of the mechanisms helping to pinpoint the nature of anomaly is based on detecting incongruence between contextual and noncontextual sensor(y) data interpretation. The proposed methodology has wide applicability. It underpins in a unified way the anomaly detection applications found in the literature. To illustrate some of its distinguishing features, in here the domain anomaly detection methodology is applied to the problem of anomaly detection for a video annotation system.
Prevalence and distribution of selected developmental dental anomalies in an Indian population.
Gupta, Saurabh K; Saxena, Payal; Jain, Sandhya; Jain, Deshraj
2011-06-01
The purpose of this study was to determine the prevalence of developmental dental anomalies in an Indian population and to statistically analyze the distribution of these anomalies. The study was based on clinical examination, evaluation of dental casts, and panoramic radiographs of 1123 Indian subjects (572 males, 551 females), who visited the outpatient clinic at Government Dental College, Indore between November 2009 and September 2010, after obtaining their informed consent. These patients were examined for the following developmental dental anomalies: shape anomalies (microdontia, talon cusp, dens evaginatus, fusion, taurodontism), number anomalies (hypodontia, oligodontia, anodontia), structural anomalies (amelogenesis imperfecta, dentinogenesis imperfecta) and positional anomalies (ectopic eruption, rotation, impaction). The percentages of these anomalies were assessed for the whole group and compared using statistical analysis. Among the 1123 subjects, a total of 385 individuals (34.28%) presented with the selected developmental dental anomalies. The distribution by sex was 197 males (34.44%), and 188 females (34.06%). Out of the total 1123 individuals, 351 (31.26%) exhibited at least one anomaly, 28 (2.49 %) showed two anomalies and 6 (0.53%) displayed more than two anomalies. P values indicated that the dental anomalies were statistically independent of sex. On intergroup comparison, positional anomalies were significantly most prevalent (P < 0.05) in the Indian population. The most common developmental dental anomaly was rotation (10.24%), followed by ectopic eruption (7.93%). The next common group was number anomalies. The most common number anomaly was hypodontia (4.19%), which had a higher frequency than hyperdontia (2.40%). Analyzing the next prevalent group of shape anomalies, microdontia (2.58%) was found to be the most common, followed by taurodontism (2.49%), dens evaginatus (2.40%) and talon cusp (0.97%). Dentinogenesis imperfecta (0.09%) was the rarest, followed by amelogenesis imperfecta (0.27%) and fusion (0.27%).
MAGSAT anomaly map and continental drift
NASA Technical Reports Server (NTRS)
Lemouel, J. L. (Principal Investigator); Galdeano, A.; Ducruix, J.
1981-01-01
Anomaly maps of high quality are needed to display unambiguously the so called long wave length anomalies. The anomalies were analyzed in terms of continental drift and the nature of their sources is discussed. The map presented confirms the thinness of the oceanic magnetized layer. Continental magnetic anomalies are characterized by elongated structures generally of east-west trend. Paleomagnetic reconstruction shows that the anomalies found in India, Australia, and Antarctic exhibit a fair consistency with the African anomalies. It is also shown that anomalies are locked under the continents and have a fixed geometry.
Distribution of female genital tract anomalies in two classifications.
Heinonen, Pentti K
2016-11-01
This study assessed the distribution of Müllerian duct anomalies in two verified classifications of female genital tract malformations, and the presence of associated renal defects. 621 women with confirmed female genital tract anomalies were retrospectively grouped under the European (ESHRE/ESGE) and the American (AFS) classification. The diagnosis of uterine malformation was based on findings in hysterosalpingography, two-dimensional ultrasonography, endoscopies, laparotomy, cesarean section and magnetic resonance imaging in 97.3% of cases. Renal status was determined in 378 patients, including 5 with normal uterus and vagina. The European classification covered all 621 women studied. Uterine anomalies without cervical or vaginal anomaly were found in 302 (48.6%) patients. Uterine anomaly was associated with vaginal anomaly in 45.2%, and vaginal anomaly alone was found in 26 (4.2%) cases. Septate uterus was the most common (49.1%) of all genital tract anomalies, followed by bicorporeal uteri (18.2%). The American classification covered 590 (95%) out of the 621 women with genital tract anomalies. The American system did not take into account vaginal anomalies in 170 (34.7%) and cervical anomalies in 174 (35.5%) out of 490 cases with uterine malformations. Renal abnormalities were found in 71 (18.8%) out of 378 women, unilateral renal agenesis being the most common defect (12.2%), also found in 4 women without Müllerian duct anomaly. The European classification sufficiently covered uterine and vaginal abnormalities. The distribution of the main uterine anomalies was equal in both classifications. The American system missed cervical and vaginal anomalies associated with uterine anomalies. Evaluation of renal system is recommended for all patients with genital tract anomalies. Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.
Invesigation of prevalence of dental anomalies by using digital panoramic radiographs.
Bilge, Nebiha Hilal; Yeşiltepe, Selin; Törenek Ağırman, Kübra; Çağlayan, Fatma; Bilge, Osman Murat
2017-09-21
This study was performed to evaluate the prevalence of all types and subtypes of dental anomalies among 6 to 40 year-old patients by using panoramic radiographs. This cross-sectional study was conducted by analyzing digital panoramic radiographs of 1200 patients admitted to our clinic in 2014. Dental anomalies were examined under 5 types and 16 subtypes. Dental anomalies were divided into five types: (a) number (including hypodontia, oligodontia and hyperdontia); (b) size (including microdontia and macrodontia); (c) structure (including amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia); (d) position (including transposition, ectopia, displacement, impaction and inversion); (e) shape (including fusion-gemination, dilaceration and taurodontism); RESULTS: The prevalence of dental anomalies diagnosed by panoramic radiographs was 39.2% (men (46%), women (54%)). Anomalies of position (60.8%) and shape (27.8%) were the most common types of abnormalities and anomalies of size (8.2%), structure (0.2%) and number (17%) were the least in both genders. Anomalies of impaction (45.5%), dilacerations (16.3%), hypodontia (13.8%) and taurodontism (11.2%) were the most common subtypes of dental anomalies. Taurodontism was more common in the age groups of 13-19 years. The age range of the most frequent of all other anomalies was 20-29. Anomalies of tooth position were the most common type of dental anomalies and structure anomalies were the least in this Turkish dental population. The frequency and type of dental anomalies vary within and between populations, confirming the role of racial factors in the prevalence of dental anomalies. Digital panoramic radiography is a very useful method for the detection of dental anomalies.
[Mass anomalies of the extremities in anurans].
Kovalenko, E E
2000-01-01
The author analyses literature data on anomalies of limbs in Anura. It is shown that published data is usually not enough to discuss either conditions of appearance or the causes of anomalies. Traditional statistical methods does not adequately characterise the frequency of anomalies. The author suggests a new criteria for ascertaining the fact of appearance of mass anomalies. A number of experimental data don't correspond to current theoretical ideas about the nature of anomalies. It is considered to distinguish "background" and "mass" anomalies. "Background" anomalies can not be a good indicator of unfavourable condition of development.
Yamunadevi, Andamuthu; Selvamani, M; Vinitha, V; Srivandhana, R; Balakrithiga, M; Prabhu, S; Ganapathy, N
2015-08-01
To record the prevalence rate of dental anomalies in Dravidian population and analyze the percentage of individual anomalies in the population. A cluster sample analysis was done, where 244 subjects studying in a dental institution were all included and analyzed for occurrence of dental anomalies by clinical examination, excluding third molars from analysis. 31.55% of the study subjects had dental anomalies and shape anomalies were more prevalent (22.1%), followed by size (8.6%), number (3.2%) and position anomalies (0.4%). Retained deciduous was seen in 1.63%. Among the individual anomalies, Talon's cusp (TC) was seen predominantly (14.34%), followed by microdontia (6.6%) and supernumerary cusps (5.73%). Prevalence rate of dental anomalies in the Dravidian population is 31.55% in the present study, exclusive of third molars. Shape anomalies are more common, and TC is the most commonly noted anomaly. Varying prevalence rate is reported in different geographical regions of the world.
Ristivojević, Andjelka; Djokić, Petra Lukić; Katanić, Dragan; Dobanovacki, Dušanka; Privrodski, Jadranka Jovanović
2016-05-01
According to the World Health Organization (WHO) definition, congenital anomalies are all disorders of the organs or tissues, regardless of whether they are visible at birth or manifest in life, and are registered in the International Classification of Diseases. The aim of this study was to compare the incidence and structure of prenatally detected and clinically manifested congenital anomalies in the newborns in the region of Novi Sad (Province of Vojvodina, Serbia) in the two distant years (1996 and 2006). This retrospective cohort study included all the children born at the Clinic for Gynecology and Obstetrics (Clinical Center of Vojvodina) in Novi Sad during 1996 and 2006. The incidence and the structure of congenital anomalies were analyzed. During 1996 there were 6,099 births and major congenital anomalies were found in 215 infants, representing 3.5%. In 2006 there were 6,628 births and major congenital anomalies were noted in 201 newborns, which is 3%. During 1996 there were more children with anomalies of musculoskeletal system, urogenital tract, with anomalies of the central nervous system and chromosomal abnormalities. During the year 2006 there were more children with cardiovascular anomalies, followed by urogenital anomalies, with significant decline in musculoskeletal anomalies. The distribution of the newborns with major congenital anomalies, regarding perinatal outcome, showed the difference between the studied years. In 2006 the increasing number of children required further investigation and treatment. There is no national registry of congenital anomalies in Serbia so the aim of this study was to enlight this topic. In the span of ten years, covering the period of the NATO campaign in Novi Sad and Serbia, the frequency of major congenital anomalies in the newborns was not increased. The most frequent anomalies observed during both years implied the musculosketelal, cardiovascular, urogenital and central nervous system. In the year 2006 there was a significant eruption of cardiovascular anomalies and a significant decrease of musculoskeletal anomalies, chromosomal abnormalities and central nervous system anomalies, while the number of urogenital anomalies declined compared to the year 1996.
Relationships between Rwandan seasonal rainfall anomalies and ENSO events
NASA Astrophysics Data System (ADS)
Muhire, I.; Ahmed, F.; Abutaleb, K.
2015-10-01
This study aims primarily at investigating the relationships between Rwandan seasonal rainfall anomalies and El Niño-South Oscillation phenomenon (ENSO) events. The study is useful for early warning of negative effects associated with extreme rainfall anomalies across the country. It covers the period 1935-1992, using long and short rains data from 28 weather stations in Rwanda and ENSO events resourced from Glantz (2001). The mean standardized anomaly indices were calculated to investigate their associations with ENSO events. One-way analysis of variance was applied on the mean standardized anomaly index values per ENSO event to explore the spatial correlation of rainfall anomalies per ENSO event. A geographical information system was used to present spatially the variations in mean standardized anomaly indices per ENSO event. The results showed approximately three climatic periods, namely, dry period (1935-1960), semi-humid period (1961-1976) and wet period (1977-1992). Though positive and negative correlations were detected between extreme short rains anomalies and El Niño events, La Niña events were mostly linked to negative rainfall anomalies while El Niño events were associated with positive rainfall anomalies. The occurrence of El Niño and La Niña in the same year does not show any clear association with rainfall anomalies. However, the phenomenon was more linked with positive long rains anomalies and negative short rains anomalies. The normal years were largely linked with negative long rains anomalies and positive short rains anomalies, which is a pointer to the influence of other factors other than ENSO events. This makes projection of seasonal rainfall anomalies in the country by merely predicting ENSO events difficult.
Shokri, Abbas; Poorolajal, Jalal; Khajeh, Samira; Faramarzi, Farhad; Kahnamoui, Hanieh Mogaver
2014-03-01
This study was performed to evaluate the prevalence of all types and subtypes of dental anomalies among 7- to 35-year-old patients by using panoramic radiographs. This cross-sectional study was conducted on 1649 people in Hamadan City, in 2012-2013. The prevalence of four types and 12 subtypes of dental anomalies was evaluated by two observers separately by using panoramic radiography. Dental anomalies were divided into four types: (a) shape (including fusion, taurodontism, and dens invagination); (b) number (including hypodontia, oligodontia, and hyperdontia); (c) structure (including amelogenesis imperfecta, dentinogenesis imperfecta, and dentin dysplasia); and (d) position (including displacement, impaction, and dilacerations). The reliability between the two observers was 79.56% according to the Kappa statistics. The prevalence of dental anomalies diagnosed by panoramic radiographs was 29%. Anomalies of position and number were the most common types of abnormalities, and anomalies of shape and structure were the least in both genders. Anomalies of impaction (44.76%), dilacerations (21.11%), hypodontia (15.88%), taurodontism (9.29%), and hyperdontia (6.76%) were the most common subtypes of dental anomalies. The anomalies of shape and number were more common in the age groups of 7-12 years and 13-15 years, respectively, while the anomalies of structure and position were more common among the other age groups. Anomalies of tooth position were the most common type of dental anomalies, and structure anomalies were the least in this Iranian population. The frequency and type of dental anomalies vary within and between populations, confirming the role of racial factors in the prevalence of dental anomalies.
Upper Lithospheric Sources of Magnetic and Gravity Anomalies of The Fennoscandian Shield
NASA Astrophysics Data System (ADS)
Korhonen, J. V.; Koistinen, T.; Working GroupFennoscandian Geophysical Maps
Magnetic total intensity anomalies (DGRF-65), Bouguer anomalies (d=2670 kg/m3) and geological units from 3400 Ma to present of the Fennoscandian Shield have been digitally compiled and printed as maps 1:2 000 000. Insert maps 1:15,000,000 com- pare anomaly components in different source scales: pseudogravimetric anomaly ver- sus Bouguer anomaly, DGRF-65 anomaly versus pseudomagnetic anomaly, magnetic vertical derivative versus second derivative of Bouguer anomaly. Data on bulk density, total magnetisation and lithology of samples have been presented as scatter diagrams and distribution maps of the average petrophysical properties in space and time. In sample level, the bulk density correlates with the lithology and, together with mag- netisation, establishes four principal populations of petrophysical properties. The av- erage properties, calculated for 5 km x 5 km cells, correlate only weakly with av- erage Bouguer-anomaly and magnetic anomaly, revealing major deep seated sources of anomalies. Pseudogravimetric and Bouguer anomalies correlate only locally with each other. The correlation is negative in the area of felsic Palaeoproterozoic rocks in W- and NW-parts of the Shield. In 2D models the sources of gravity anomalies are explained by lateral variation of density in upper and lower crust. Smoothly varying regional components are explained by boundaries of the lower crust, the upper mantle and the astenosphere. Magnetic anomalies are explained by lateral variation of magnetisation in the upper crust. Re- gional components are due to the lateral variation of magnetisation in the lower crust and the boundaries of lower crust and mantle and the Curie isotherm of magnetite.
System for closure of a physical anomaly
Bearinger, Jane P; Maitland, Duncan J; Schumann, Daniel L; Wilson, Thomas S
2014-11-11
Systems for closure of a physical anomaly. Closure is accomplished by a closure body with an exterior surface. The exterior surface contacts the opening of the anomaly and closes the anomaly. The closure body has a primary shape for closing the anomaly and a secondary shape for being positioned in the physical anomaly. The closure body preferably comprises a shape memory polymer.
Orbital debris hazard insights from spacecraft anomalies studies
NASA Astrophysics Data System (ADS)
McKnight, Darren S.
2016-09-01
Since the dawning of the space age space operators have been tallying spacecraft anomalies and failures then using these insights to improve the space systems and operations. As space systems improved and their lifetimes increased, the anomaly and failure modes have multiplied. Primary triggers for space anomalies and failures include design issues, space environmental effects, and satellite operations. Attempts to correlate anomalies to the orbital debris environment have started as early as the mid-1990's. Early attempts showed tens of anomalies correlated well to altitudes where the cataloged debris population was the highest. However, due to the complexity of tracing debris impacts to mission anomalies, these analyses were found to be insufficient to prove causation. After the fragmentation of the Chinese Feng-Yun satellite in 2007, it was hypothesized that the nontrackable fragments causing anomalies in LEO would have increased significantly from this event. As a result, debris-induced anomalies should have gone up measurably in the vicinity of this breakup. Again, the analysis provided some subtle evidence of debris-induced anomalies but it was not convincing. The continued difficulty in linking debris flux to satellite anomalies and failures prompted the creation of a series of spacecraft anomalies and failure workshops to investigate the identified shortfalls. These gatherings have produced insights into why this process is not straightforward. Summaries of these studies and workshops are presented and observations made about how to create solutions for anomaly attribution, especially as it relates to debris-induced spacecraft anomalies and failures.
ANOMALY STRUCTURE OF SUPERGRAVITY AND ANOMALY CANCELLATION
DOE Office of Scientific and Technical Information (OSTI.GOV)
Butter, Daniel; Gaillard, Mary K.
2009-06-10
We display the full anomaly structure of supergravity, including new D-term contributions to the conformal anomaly. This expression has the super-Weyl and chiral U(1){sub K} transformation properties that are required for implementation of the Green-Schwarz mechanism for anomaly cancellation. We outline the procedure for full anomaly cancellation. Our results have implications for effective supergravity theories from the weakly coupled heterotic string theory.
Analysis of pre-earthquake ionospheric anomalies before the global M = 7.0+ earthquakes in 2010
NASA Astrophysics Data System (ADS)
Yao, Y. B.; Chen, P.; Zhang, S.; Chen, J. J.; Yan, F.; Peng, W. F.
2012-03-01
The pre-earthquake ionospheric anomalies that occurred before the global M = 7.0+ earthquakes in 2010 are investigated using the total electron content (TEC) from the global ionosphere map (GIM). We analyze the possible causes of the ionospheric anomalies based on the space environment and magnetic field status. Results show that some anomalies are related to the earthquakes. By analyzing the time of occurrence, duration, and spatial distribution of these ionospheric anomalies, a number of new conclusions are drawn, as follows: earthquake-related ionospheric anomalies are not bound to appear; both positive and negative anomalies are likely to occur; and the earthquake-related ionospheric anomalies discussed in the current study occurred 0-2 days before the associated earthquakes and in the afternoon to sunset (i.e. between 12:00 and 20:00 local time). Pre-earthquake ionospheric anomalies occur mainly in areas near the epicenter. However, the maximum affected area in the ionosphere does not coincide with the vertical projection of the epicenter of the subsequent earthquake. The directions deviating from the epicenters do not follow a fixed rule. The corresponding ionospheric effects can also be observed in the magnetically conjugated region. However, the probability of the anomalies appearance and extent of the anomalies in the magnetically conjugated region are smaller than the anomalies near the epicenter. Deep-focus earthquakes may also exhibit very significant pre-earthquake ionospheric anomalies.
On the origin of the Bangui magnetic anomaly, central African empire
NASA Technical Reports Server (NTRS)
Marsh, B. D.
1977-01-01
A large magnetic anomaly was recognized in satellite magnetometer data over the Central African Empire in central Africa. They named this anomaly the Bangui magnetic anomaly due to its location near the capital city of Bangui, C.A.E. Because large crustal magnetic anomalies are uncommon, the origin of this anomaly has provoked some interest. The area of the anomaly was visited to make ground magnetic measurements, geologic observations, and in-situ magnetic susceptibility measurements. Some rock samples were also collected and chemically analyzed. The results of these investigations are presented.
Temilola, Dada Oluwaseyi; Folayan, Morenike Oluwatoyin; Fatusi, Olawunmi; Chukwumah, Nneka Maureen; Onyejaka, Nneka; Oziegbe, Elizabeth; Oyedele, Titus; Kolawole, Kikelomo Adebanke; Agbaje, Hakeem
2014-10-16
The study of dental anomalies is important because it generates information that is important for both the anthropological and clinical management of patients. The objective of this study is to determine the prevalence and pattern of presentation of dental hard-tissue developmental anomalies in the mix dentition of children residing in Ile-Ife, a suburban region of Nigeria. Information on age, sex and socioeconomic status was collected from 1,036 children aged four months to 12 years through a household survey. Clinical examination was conducted to assess the presence of dental anomalies. Associations between age, sex, socioeconomic status, prevalence, and pattern of presentation of the developmental hard-tissue dental anomalies were determined. Two hundred and seventy six (26.6%) children had dental anomalies. Of these, 23.8% had one anomaly, 2.5% had two anomalies, and 0.3% had more than two anomalies. Of the children with anomalies, 49.3%were male, 50.7%were female, and 47.8%, 28.6% and 23.6% were children from low, middle and high socioeconomic classes, respectively. More anomalies were seen in permanent than primary dentition. Anomalies of tooth structure were most prevalent (16.1%); anomalies which affect tooth number were least prevalent (1.3%). Dens evaginatus, peg-shaped lateral, macrodontia, and talon cusp were more prevalent in the permanent dentition, and dens evaginatus peg-shaped lateral and macrodontia were more prevalent in the maxilla. There were significantly more macrodontia anomalies in males and in children of high socioeconomic status. This large survey of dental hard-tissue anomalies found in the primary dentition and mixed dentition of children in Nigeria provides anthropological and clinical data that may aid the detection and management of dental problems of children in Nigeria.
Impact of moisture variations on the circulation of the south-west monsoon
NASA Astrophysics Data System (ADS)
Kishtawal, C. M.; Pal, P. K.; Narayanan, M. S.; Manna, S. K.; Sharma, O. P.; Agarwal, Sangeeta; Upadhyaya, H. C.
1993-12-01
The impact of moisture anomalies on the circulation of the south-west Indian monsoon has been studied with a general circulation model. Newtonian relaxation is adopted to subject the model atmosphere under sustained moisture anomalies. The impact of negative anomalies of moisture was seen as a divergent circulation anomaly, while the positive anomaly was a stronger convergent anomaly. Although the humidity fields display a resilient behaviour, and relax back to normal patterns 1-2 days after the forcing terms in humidity are withdrawn, the circulation anomalies created by the moisture variation keeps growing. A feedback between positive moisture anomalies and low level convergence exists, which is terminated in the absence of external forcings.
Upper mantle heterogeneity: Comparisons of regions south of Australia with Philippine Basin
NASA Technical Reports Server (NTRS)
1982-01-01
The nature of mass anomalies that occur beneath the regions of negative residual depth anomalies were identified. Residual geoid anomalies with negative residual depth anomalies are identified in the Philippine Basin (negative) and in the region south of Australia (positive and negative). In the latter region the geoid anomalies are eastward and the depth anomaly is northeast. It is suggested that the negative depth anomaly and the compensating mass excess in the uppermost mantle developed in the Eocene as the lithosphere of the west Philippine basin formed. Heating of the deeper upper mantle which causes slow surface wave velocities and negative gravity and geoid anomalies may be a younger phenomenon which is still in progress.
Analysis of GEO spacecraft anomalies: Space weather relationships
NASA Astrophysics Data System (ADS)
Choi, Ho-Sung; Lee, Jaejin; Cho, Kyung-Suk; Kwak, Young-Sil; Cho, Il-Hyun; Park, Young-Deuk; Kim, Yeon-Han; Baker, Daniel N.; Reeves, Geoffrey D.; Lee, Dong-Kyu
2011-06-01
While numerous anomalies and failures of spacecraft have been reported since the beginning of the space age, space weather effects on modern spacecraft systems have been emphasized more and more with the increase of their complexity and capability. However, the relationship between space weather and commercial satellite anomalies has not been studied extensively. In this paper, we investigate the geostationary Earth orbit (GEO) satellite anomalies archived by Satellite News Digest during 1997-2009 in order to search for possible influences of space weather on the anomaly occurrences. We analyze spacecraft anomalies for the Kp index, local time, and season and then compare them with the tendencies of charged particles observed by Los Alamos National Laboratory (LANL) satellites. We obtain the following results: (1) there are good relationships between geomagnetic activity (as measured by the Kp index) and anomaly occurrences of the GEO satellites; (2) the satellite anomalies occurred mainly in the midnight to morning sector; and (3) the anomalies are found more frequently in spring and fall than summer and winter. While we cannot fully explain how space weather is involved in producing such anomalies, our analysis of LANL data shows that low-energy (<100 keV) electrons have similar behaviors with spacecraft anomalies and implies the spacecraft charging might dominantly contribute to the GEO spacecraft anomalies reported in Satellite News Digest.
Dental anomalies in primary dentition and their corresponding permanent teeth.
Gomes, R R; Fonseca, J A C; Paula, L M; Acevedo, A C; Mestrinho, H D
2014-05-01
The objectives of this paper are to estimate the prevalence of dental anomalies in primary dentition in a sample of 2- to 5-year-old Brazilian preschool children, determine their distribution, and investigate their occurrence in the succedaneous teeth of the sample compared with a control group of children with no dental anomalies in the primary dentition. The one-stage sample comprised 1,718 two to five-year-old children with fully erupted primary dentition clinically examined for dental anomalies. All children presenting dental anomalies underwent panoramic radiographs. Descriptive statistics were performed for the studied variables. A control group matched by sex and age was studied to compare the prevalence ratio for dental anomalies in the permanent dentition. The prevalence of dental anomalies in the primary dentition was 1.8 %, with no significant statistical difference between sexes. Double teeth were the most frequently observed. Dental anomalies on the succedaneous permanent teeth were diagnosed in 54.8 % of the children with affected primary dentition. The prevalence ratio (PR) for dental anomalies in the succedaneous permanent teeth was 17.1 (confidence interval (CI) 5.33-54.12) higher compared with the control group, higher in children with bilateral anomalies (PR = 31.2, CI 10.18-94.36). An association between anomalies of the permanent dentition and the presence of dental anomalies in primary teeth was observed, especially when they occur bilaterally. The results in the present study have a clinical relevance in the diagnosis of children with dental anomalies in primary dentition. Early identification of these anomalies can aid the dentist in planning dental treatment at the appropriate time.
Decomposing Worldwide Complete Spherical Bouguer Gravity Anomaly Using 2-D Empirical Method
NASA Astrophysics Data System (ADS)
Firdaus, Ruhul; Mey Ekawati, Gestin
2017-04-01
Currently available worldwide gravity anomaly data provides a high-resolution (2’×2’) of Complete Spherical Bouguer Anomaly (CSBA) based on the available information of the Earth gravity field from surface and satellite measurements. The data has not only been provided and processed thoroughly but it also has been claimed to be appropriate for various geophysical applications. Therefore, the analysis of gravity anomaly is becoming increasingly significant for the earth sciences as a whole and assisting both shallow and deep geological problems. Earth gravity anomaly has to be analyzed carefully as it has very complex data due to anomaly mixing of the density masses spread over the Earth horizontally and vertically. The bigger the spatial coverage of data (e.g. global scale data), the more severe the data from anomaly mixing due to various wavelength. BEMD is an empirical method supposedly suitable with highly oscillation-mixing data. It can effectively isolate each local anomaly in details and is analogized as successively reverse moving average with local windowing. BEMD is designed to reduce multi-component, non-linear gravity field data to a series of single local anomaly contributions. Anomaly from a single body was assumed as a mono-component signal. The main advantage of BEMD processing techniques is to present the subtle details in the data which are not clearly identified in anomaly maps, without specifying any prior information about the nature of the source bodies. As the result, we have identified regional anomalies due to the drift of continental and oceanic masses considered as crust-regional anomaly (CRA). We remove the CRA from the CBA to provide surface-residual anomaly (SRA) where shallow geologic bodies reveal. Meanwhile, the CRA itself can be used as reference to reduce this high magnitude anomaly from any measurement data to exhibit only shallow body anomaly. Further analysis can be carried out to build a general understanding of the details and parameters of the shallower or deeper causative body distributions.
NASA Technical Reports Server (NTRS)
Kim, Jeong-Hee; Rapp, Richard H.
1990-01-01
In June 1986 a 1 x 1 deg/mean free-air anomaly data file containing 48955 anomalies was completed. In August 1986 a 30 x 30 min mean free-air anomaly file was defined containing 31787 values. For the past three years data has been collected to upgrade these mean anomaly files. The primary emphasis was the collection of data to be used for the estimation of 30 min means anomalies in land areas. The emphasis on land areas was due to the anticipated use of 30 min anomalies derived from satellite altimeter data in the ocean areas. There were 10 data sources in the August 1986 file. Twenty-eight sources were added based on the collection of both point and mean anomalies from a number of individuals and organizations. A preliminary 30 min file was constructed from the 38 data sources. This file was used to calculate 1 x 1 deg mean anomalies. This 1 x 1 deg file was merged with a 1 x 1 deg file which was a merger of the June 1986 file plus a 1 x 1 deg file made available by DMA Aerospace Center. Certain bad 30 min anomalies were identified and deleted from the preliminary 30 min file leading to the final 30 min file (the July 1989 30 min file) with 66990 anomalies and their accuracy. These anomalies were used to again compute 1 x 1 deg anomalies which were merged with the previous June 86 DMAAC data file. The final 1 x 1 deg mean anomaly file (the July 89 1 x 1 deg data base) contained 50793 anomalies and their accuracy. The anomaly data files were significantly improved over the prior data sets in the following geographic regions: Africa, Scandinavia, Canada, United States, Mexico, Central and South America. Substantial land areas remain where there is little or no available data.
Toward Baseline Software Anomalies in NASA Missions
NASA Technical Reports Server (NTRS)
Layman, Lucas; Zelkowitz, Marvin; Basili, Victor; Nikora, Allen P.
2012-01-01
In this fast abstract, we provide preliminary findings an analysis of 14,500 spacecraft anomalies from unmanned NASA missions. We provide some baselines for the distributions of software vs. non-software anomalies in spaceflight systems, the risk ratings of software anomalies, and the corrective actions associated with software anomalies.
DSCS II. Battery Anomaly Investigation Satellites 9437 and 9438.
1980-04-25
Chronology Prior to Identifying the Anomaly 2-1 3 . ANOMALY OBSERVATIONS 3 -1 3.1 Satellite 9437 3 -1 3.1.1 State of the Batteries Prior to the Anomaly...Observation 3 -1 3.1.2 Anomalous Behavior 3 -1 3.2 Satellite 9438 3 -6 3.2.1 State of the Batteries Prior to the Anomaly Observation 3 -6 3.2.2 Anomalous...Behavior 3 -6 4. ANOMALY INVESTIGATIONS 4-1 4.1 Scope 4-1 4.2 Postulated Causes of the Anomaly 4-1 4.3 Cell Short Circuits 4-2 4.3.1 Evidence in Support of
The life cycles of persistent anomalies and blocking over the North Pacific
NASA Technical Reports Server (NTRS)
Dole, Randall M.
1986-01-01
The evolution of persistent anomaly patterns over the central North Pacific is investigated. Composite time evolution fields of the 500-mbar anomaly patterns are constructed from low-pass and unfiltered height anomaly data; the time scales for the development and decay of these persistent anomalies are analyzed. The relationship between zonal flow in the Pacific jet region and the development of the anomaly patterns is examined. The effect of baroclinic instabilities on the development of the anomalies is studied. The vertical structure and synoptic characteristics of the evolution of the anomalies are described. It is noted that the initial rapid growth of the main center may be associated with a propagating, intensifying, synoptic-scale disturbance which originates in the midlatitudes over eastern Asia.
NASA Technical Reports Server (NTRS)
Acker, James G.
2006-01-01
The availability of climatological chlorophyll-a concentration data products from the SeaWiFS mission spanning the eight-year mission period allowed the creation of a climatological anomaly analysis function in Giovanni, the GES DISC Interactive Online Visualization and ANalysis Infrastructure. This study utilizes the Giovanni anomaly analysis function to examine mesoscale anomalies in the North Atlantic Ocean during the springtime North Atlantic Bloom. This examination indicates that areas exhibiting positive anomalies and areas exhibiting negative anomalies are coherent over significant spatial scales, with relatively abrupt boundaries between areas with positive and negative anomalies. Year-to-year variability in anomaly "intensity" can be caused by either variability in the temporal occurrence of the bloom peak or by variability in the peak chlorophyll concentration in a particular area. The study will also discuss the feasibility of combining chlorophyll anomaly analysis with other data types.
Coexistence of bilateral first and second branchial arch anomalies
Thakur, J S; Shekar, Vidya; Saluja, Manika; Mohindroo, N K
2013-01-01
Branchial arch anomalies are one of the most common congenital anomalies that are usually unilateral and bilateral presentation is rare. The simultaneous presence of bilateral second branchial arch anomalies along with bilateral first arch anomalies is extremely rare, with only three such cases reported in the literature. We present two non-syndromic cases of coexisting bilateral first and second arch anomalies. Developmental anomalies of the branchial apparatus account for 17% of all paediatric cervical masses and are the most common type of congenital cervical mass. They usually present in the paediatric age group. About 96–97% of these anomalies are unilateral. Bilateral presentation is seen in 2–3% having a strong familial association. Congenital syndromes also have been associated with first and second branchial arch anomalies. Thorough clinical examination and investigations should be done to rule out these syndromes. PMID:23580675
Chemistry of the Apollo 11 highland component
NASA Technical Reports Server (NTRS)
Laul, J. C.; Papike, J. J.; Simon, S. B.; Shearer, C. K.
1983-01-01
Thirty-eight Apollo 11 lunar highland fragments from coarse fines 10085 have been subjected to petrologic and chemical study. Six major chemical groups are identified: (a) high-K KREEP; (b) anorthosite with a 10X chondrite positive Eu anomaly and anorthosite with 30X positive Eu anomaly; (c) ANT; (d) LKFM; (e) anorthositic gabbro with no Eu anomaly, with a positive Eu anomaly, and with a negative Eu anomaly; and (f) dominant Highland component, 2X-10X chondrite with a positive 10X-14X Eu anomaly. Newly recognized groups are presented based on the REE patterns: (a) ANT group with 5X La and a 22X positive Eu anomaly; (b) 10X flat with 14X positive Eu anomaly; and (c) 2-3X flat with a 10X positive Eu anomaly. The highland suite is very low in K and REE, and is overall quite similar to the Apollo 16 suite.
Prevalence of dental anomalies in Saudi orthodontic patients.
Al-Jabaa, Aljazi H; Aldrees, Abdullah M
2013-07-01
This study aimed to investigate the prevalence of dental anomalies and study the association of these anomalies with different types of malocclusion in a random sample of Saudi orthodontic patients. Six hundred and two randomly selected pretreatment records including orthopantomographs (OPG), and study models were evaluated. The molar relationship was determined using pretreatment study models, and OPG were examined to investigate the prevalence of dental anomalies among the sample. The most common types of the investigated anomalies were: impaction followed by hypodontia, microdontia, macrodontia, ectopic eruption and supernumerary. No statistical significant correlations were observed between sex and dental anomalies. Dental anomalies were more commonly found in class I followed by asymmetric molar relation, then class II and finally class III molar relation. No malocclusion group had a statistically significant relation with any individual dental anomaly. The prevalence of dental anomalies among Saudi orthodontic patients was higher than the general population. Although, orthodontic patients have been reported to have high rates of dental anomalies, orthodontists often fail to consider this. If not detected, dental anomalies can complicate dental and orthodontic treatment; therefore, their presence should be carefully investigated during orthodontic diagnosis and considered during treatment planning.
Dwijendra, K S; Parikh, Vishal; George, Soja Sara; Kukkunuru, Gururam Tej; Chowdary, Gali Nagarjuna
2015-06-01
The study is planned to correlate the existence of dental anomalies with different types of malocclusion as the occurrence of anomalies is common in malocclusion. The present study was conducted among 430 patients with different types of malocclusion as 161 patients having Class I, 203 with Class II, and 66 with Class III malocclusion. The age of the patients ranged from 12 to 15 years. Diagnosis was done on the basis of history, clinical, cephalometric, radiographs, and dental cast examination. The level of significance was set at P = 0.05. Most common anomaly was rotation of teeth (18.80%), followed by hypodontia (10.90%), and least occurring was gemination, fusion, talon's cusp, and dilacerations. 31.4% showed one dental anomaly, whereas 11.9% exhibited two or more dental anomalies. The highest mean value of all the dental anomalies was seen with severe cases of malocclusion and also significant differences were observed according to gender. The present study investigated various dental anomalies in relation to malocclusion. It was found that 31.4% showed one dental anomaly, whereas 11.9% exhibited two or more dental anomalies. Hence, careful prior investigation of dental anomalies is necessary for better orthodontic treatment planning to reduce the complications.
Dental and oral anomalies in incontinentia pigmenti: a systematic review.
Minić, Snežana; Trpinac, Dušan; Gabriel, Heinz; Gencik, Martin; Obradović, Miljana
2013-01-01
Incontinentia pigmenti (IP) is an X-linked genodermatosis caused by a mutation of the IKBKG gene. The objective of this study was to present a systematic review of the dental and oral types of anomalies, to determine the total number and sex distribution of the anomalies, and to analyze possible therapies. We analyzed the literature data from 1,286 IP cases from the period 1993-2010. Dental and/or oral anomalies were diagnosed for 54.38% of the investigated IP patients. Most of the anomaly types were dental, and the most frequent of these were dental shape anomalies, hypodontia, and delayed dentition. The most frequent oral anomaly types were cleft palate and high arched palate. IKBKG exon 4-10 deletion was present in 86.36% of genetically confirmed IP patients. According to the frequency, dental and/or oral anomalies represent the most frequent and important IP minor criteria. The most frequent mutation was IKBKG exon 4-10 deletion. The majority of dental anomalies and some of the oral anomalies could be corrected. Because of the presence of cleft palate and high arched palate in IP patients, these two anomalies may be considered as diagnostic IP minor criteria as well.
NASA Technical Reports Server (NTRS)
Yuan, D. W.
1984-01-01
Magnetic anomalies of the South American continent are generally more positive and variable than the oceanic anomalies. There is better correlation between the magnetic anomalies and the major tectonic elements of the continents than between the anomalies and the main tectonic elements of the adjacent oceanic areas. Oceanic areas generally show no direct correlation to the magnetic anomalies. Precambrian continental shields are mainly more magnetic than continental basins and orogenic belts. Shields differ markedly from major aulacogens which are generally characterized by negative magnetic anomalies and positive gravity anomalies. The Andean orogenic belt shows rather poor correlation with the magnetic anomalies. The magnetic data exhibit instead prominent east-west trends, which although consistent with some tectonic features, may be related to processing noise derived from data reduction procedures to correct for external magnetic field effects. The pattern over the Andes is sufficiently distinct from the generally north trending magnetic anomalies occurring in the adjacent Pacific Ocean to separate effectively the leading edge of the South American Plate from the Nazea Plate. Eastern South America is characterized by magnetic anomalies which commonly extend across the continental margin into the Atlantic Ocean.
Total electron content anomalies associated with global VEI4 + volcanic eruptions during 2002-2015
NASA Astrophysics Data System (ADS)
Li, Wang; Guo, Jinyun; Yue, Jianping; Shen, Yi; Yang, Yang
2016-10-01
In previous studies, little attention has been paid to the total electron content (TEC) anomalies preceding the volcanic eruption. We analyze the coupling relationship between volcanic eruption and TEC anomalies, and discuss the spatial distribution of TEC anomalies associated with volcanic geographical location. We utilize the global ionosphere map (GIM) data from the Center for Orbit Determination in Europe (CODE) to analyze TEC variations before the global volcanic eruptions indicated by VEI (Volcanic Explosivity Index) 4 + from 2002 to 2015 with the sliding interquartile range method. The results indicate the occurrence rate of TEC anomalies before great volcanic eruptions is related with the volcanic type and geographical position. The occurrence rate of TEC anomalies before stratovolcano and caldera eruptions is higher than that before shield and pyroclastic shield eruptions, and the occurrence rate of TEC anomalies has a descending trend from low latitudes to high latitudes. The TEC anomalies before the volcanic eruptions in low-mid latitudes are within the volcanic affected areas, but do not coincide with the volcanic foci. The corresponding TEC anomalies could be observed in the conjugated region, and all the TEC anomalies in the volcanic affected areas are usually close to bounds of equatorial anomaly zones. However, the TEC anomalies preceding these eruptions in high latitudes usually surround the volcano, and no TEC anomalies appear in the conjugated region. These conclusions have potential applications to the prediction of great volcanic eruptions in the future.
The use of Compton scattering in detecting anomaly in soil-possible use in pyromaterial detection
DOE Office of Scientific and Technical Information (OSTI.GOV)
Abedin, Ahmad Firdaus Zainal; Ibrahim, Noorddin; Zabidi, Noriza Ahmad
The Compton scattering is able to determine the signature of land mine detection based on dependency of density anomaly and energy change of scattered photons. In this study, 4.43 MeV gamma of the Am-Be source was used to perform Compton scattering. Two detectors were placed between source with distance of 8 cm and radius of 1.9 cm. Detectors of thallium-doped sodium iodide NaI(TI) was used for detecting gamma ray. There are 9 anomalies used in this simulation. The physical of anomaly is in cylinder form with radius of 10 cm and 8.9 cm height. The anomaly is buried 5 cm deep in the bed soil measuredmore » 80 cm radius and 53.5 cm height. Monte Carlo methods indicated the scattering of photons is directly proportional to density of anomalies. The difference between detector response with anomaly and without anomaly namely contrast ratio values are in a linear relationship with density of anomalies. Anomalies of air, wood and water give positive contrast ratio values whereas explosive, sand, concrete, graphite, limestone and polyethylene give negative contrast ratio values. Overall, the contrast ratio values are greater than 2 % for all anomalies. The strong contrast ratios result a good detection capability and distinction between anomalies.« less
Shape memory polymer foams for endovascular therapies
Wilson, Thomas S.; Maitland, Duncan J.
2017-03-21
A system for occluding a physical anomaly. One embodiment comprises a shape memory material body wherein the shape memory material body fits within the physical anomaly occluding the physical anomaly. The shape memory material body has a primary shape for occluding the physical anomaly and a secondary shape for being positioned in the physical anomaly.
Shape memory polymer foams for endovascular therapies
Wilson, Thomas S [Castro Valley, CA; Maitland, Duncan J [Pleasant Hill, CA
2012-03-13
A system for occluding a physical anomaly. One embodiment comprises a shape memory material body wherein the shape memory material body fits within the physical anomaly occluding the physical anomaly. The shape memory material body has a primary shape for occluding the physical anomaly and a secondary shape for being positioned in the physical anomaly.
Shape memory polymer foams for endovascular therapies
Wilson, Thomas S.; Maitland, Duncan J.
2015-05-26
A system for occluding a physical anomaly. One embodiment comprises a shape memory material body wherein the shape memory material body fits within the physical anomaly occluding the physical anomaly. The shape memory material body has a primary shape for occluding the physical anomaly and a secondary shape for being positioned in the physical anomaly.
NASA Technical Reports Server (NTRS)
Bowin, C.
1982-01-01
A negative free-air gravity anomaly which occurs in the central part of the Philippine Sea was examined to determine the distribution and nature of possible regional mass excesses or deficiencies. Geoid anomalies from GEOS-3 observation were positive. A negative residual geoid anomaly consistent with the area of negative free-air gravity anomalies were found. Theoretical gravity-topography and geoid-topography admittance functions indicated that high density mantle at about 60 km dept could account for the magnitudes of the gravity and residual geoid anomaly and the 1 km residual water depth anomaly in the Philippine Sea. The negative residual depth anomaly may be compensated for by excess density in the uppermost mantle, but the residual geoid and regional free-air gravity anomalies and a slow surface wave velocity structure might result from low-density warm upper mantle material lying beneath the zone of high-density uppermost mantle. From a horizontal disk approximation, the depth of the low-density warm mantle was estimated to be on the order of 200 km.
ISHM Anomaly Lexicon for Rocket Test
NASA Technical Reports Server (NTRS)
Schmalzel, John L.; Buchanan, Aubri; Hensarling, Paula L.; Morris, Jonathan; Turowski, Mark; Figueroa, Jorge F.
2007-01-01
Integrated Systems Health Management (ISHM) is a comprehensive capability. An ISHM system must detect anomalies, identify causes of such anomalies, predict future anomalies, help identify consequences of anomalies for example, suggested mitigation steps. The system should also provide users with appropriate navigation tools to facilitate the flow of information into and out of the ISHM system. Central to the ability of the ISHM to detect anomalies is a clearly defined catalog of anomalies. Further, this lexicon of anomalies must be organized in ways that make it accessible to a suite of tools used to manage the data, information and knowledge (DIaK) associated with a system. In particular, it is critical to ensure that there is optimal mapping between target anomalies and the algorithms associated with their detection. During the early development of our ISHM architecture and approach, it became clear that a lexicon of anomalies would be important to the development of critical anomaly detection algorithms. In our work in the rocket engine test environment at John C. Stennis Space Center, we have access to a repository of discrepancy reports (DRs) that are generated in response to squawks identified during post-test data analysis. The DR is the tool used to document anomalies and the methods used to resolve the issue. These DRs have been generated for many different tests and for all test stands. The result is that they represent a comprehensive summary of the anomalies associated with rocket engine testing. Fig. 1 illustrates some of the data that can be extracted from a DR. Such information includes affected transducer channels, narrative description of the observed anomaly, and the steps used to correct the problem. The primary goal of the anomaly lexicon development efforts we have undertaken is to create a lexicon that could be used in support of an associated health assessment database system (HADS) co-development effort. There are a number of significant byproducts of the anomaly lexicon compilation effort. For example, (1) Allows determination of the frequency distribution of anomalies to help identify those with the potential for high return on investment if included in automated detection as part of an ISHM system, (2) Availability of a regular lexicon could provide the base anomaly name choices to help maintain consistency in the DR collection process, and (3) Although developed for the rocket engine test environment, most of the anomalies are not specific to rocket testing, and thus can be reused in other applications.
Solomon, Benjamin D.; Raam, Manu S.; Pineda-Alvarez, Daniel E.
2010-01-01
Purpose The goal of this study was to describe a novel pattern of genitourinary (GU) anomalies in VACTERL association, which involves congenital anomalies affecting the vertebrae, anus, heart, trachea and esophagus, kidneys, and limbs. Procedures We collected clinical data on 105 patients diagnosed with VACTERL association and analyzed a subset of 89 patients who met more stringent inclusion criteria. Findings Twenty-one percent of patients have GU anomalies, which are more severe (but not more frequent) in females. Anomalies were noted in patients without malformations affecting the renal, lower vertebral, or lower gastrointestinal systems. Conclusions There should be a high index of suspicion for the presence of GU anomalies even in patient who do not have spatially similar malformations. PMID:21235632
Solomon, Benjamin D; Raam, Manu S; Pineda-Alvarez, Daniel E
2011-06-01
The goal of this study was to describe a novel pattern of genitourinary (GU) anomalies in VACTERL association,which involves congenital anomalies affecting the vertebrae,anus, heart, trachea and esophagus, kidneys, and limbs.We collected clinical data on 105 patients diagnosed with VACTERL association and analyzed a subset of 89 patients who met more stringent inclusion criteria. Twenty-one percent of patients have GU anomalies, which are more severe (but not more frequent) in females. Anomalies were noted in patients without malformations affecting the renal, lower vertebral, or lower gastrointestinal systems. There should be a high index of suspicion for the presence of GU anomalies even in patients who do not have spatially similar malformations.
Neonate with VACTERL Association and a Branchial Arch Anomaly without Hydrocephalus.
Velazquez, Danitza; Pereira, Elaine; Havranek, Thomas
2016-03-01
VACTERL (vertebral anomalies, anal atresia, cardiac defect, tracheoesophageal fistula, renal anomaly, limb anomalies) is an association of anomalies with a wide spectrum of phenotypic expression. While the majority of cases are sporadic, there is evidence of an inherited component in a small number of patients as well as the potential influence of nongenetic risk factors (maternal diabetes mellitus). Presence of hydrocephalus has been reported in VACTERL patients (VACTERL-H) in the past, with some displaying branchial arch anomalies. We report the unique case of an infant of diabetic mother with VACTERL association and a branchial arch anomaly-in the absence of hydrocephalus.
Gravitational parity anomaly with and without boundaries
NASA Astrophysics Data System (ADS)
Kurkov, Maxim; Vassilevich, Dmitri
2018-03-01
In this paper we consider gravitational parity anomaly in three and four dimensions. We start with a re-computation of this anomaly on a 3D manifold without boundaries and with a critical comparison of our results to the previous calculations. Then we compute the anomaly on 4D manifolds with boundaries with local bag boundary conditions. We find, that gravitational parity anomaly is localized on the boundary and contains a gravitational Chern-Simons terms together with a term depending of the extrinsic curvature. We also discuss the main properties of the anomaly, as the conformal invariance, relations between 3D and 4D anomalies, etc.
Fernandez, Nicolas; Escobar, Rebeca; Zarante, Ignacio
2016-01-01
Hypospadias is a congenital abnormality of the penis, in which there is incomplete development of the distal urethra. There are numerous reports showing na increase of prevalence of hypospadias. Association of craniofacial malformations in patients diagnosed with hypospadias is rare. The aim of this study is to describe the association between hypospadias and craniofacial congenital anomalies. A retrospective review of the Latin-American collaborative study of congenital malformations (ECLAMC) data was performed between January 1982 and December 2011. We included children diagnosed with associated hypospadias and among them we selected those that were associated with any craniofacial congenital anomaly. Global prevalence was 11.3 per 10.000 newborns. In this population a total of 809 patients with 1117 associated anomalies were identified. On average there were 1.7 anomalies per patient. Facial anomalies were present in 13.2%. The most commonly major facial anomaly associated to hypospadias was cleft lip/palate with 52 cases. We identified that 18% have an association with other anomalies, and found an association between craniofacial anomalies and hypospadias in 0.59 cases/10.000 newborns. Hypospadias is the most common congenital anomaly affecting the genitals. Its association with other anomalies is rare. It has been reported that other malformations occur in 29.3% of the cases with hypospadias. The more proximal the meatus, the higher the risk for having another associated anomaly. Associated hypospadias are rare, and it is important to identify the concurrent occurrence of craniofacial anomalies to better treat patients that might need a multidisciplinary approach. Copyright© by the International Brazilian Journal of Urology.
Fernandez, Nicolas; Escobar, Rebeca; Zarante, Ignacio
2016-01-01
ABSTRACT Introduction: Hypospadias is a congenital abnormality of the penis, in which there is incomplete development of the distal urethra. There are numerous reports showing an increase of prevalence of hypospadias. Association of craniofacial malformations in patients diagnosed with hypospadias is rare. The aim of this study is to describe the association between hypospadias and craniofacial congenital anomalies. Materials and Methods: A retrospective review of the Latin-American collaborative study of congenital malformations (ECLAMC) data was performed between January 1982 and December 2011. We included children diagnosed with associated hypospadias and among them we selected those that were associated with any craniofacial congenital anomaly. Results: Global prevalence was 11.3 per 10.000 newborns. In this population a total of 809 patients with 1117 associated anomalies were identified. On average there were 1.7 anomalies per patient. Facial anomalies were present in 13.2%. The most commonly major facial anomaly associated to hypospadias was cleft lip/palate with 52 cases. We identified that 18% have an association with other anomalies, and found an association between craniofacial anomalies and hypospadias in 0.59 cases/10.000 newborns. Discussion: Hypospadias is the most common congenital anomaly affecting the genitals. Its association with other anomalies is rare. It has been reported that other malformations occur in 29.3% of the cases with hypospadias. The more proximal the meatus, the higher the risk for having another associated anomaly. Conclusion: Associated hypospadias are rare, and it is important to identify the concurrent occurrence of craniofacial anomalies to better treat patients that might need a multidisciplinary approach. PMID:27564292
Cloud-Radiative Driving of the Madden-Julian Oscillation as Seen by the A-Train
NASA Technical Reports Server (NTRS)
Del Genio, Anthony; Chen, Yonghua
2015-01-01
Cloud and water vapor radiative heating anomalies associated with convection may be an effective source of moist static energy driving the Madden-Julian Oscillation (MJO). In this paper five years of radiative heating profiles derived from CloudSat radar and Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation data are analyzed to document radiative heating anomalies during the MJO. Atmospheric shortwave absorption and surface longwave radiation anomalies are of opposite sign and 10-20% as large as top-of-atmosphere outgoing longwave radiation (OLR) anomalies, confirming that OLR provides a useful estimate of the total column radiative heating anomaly. Positive anomalies generally peak about one week before the MJO peak and are smallest over the Indian Ocean. Anomalies over the Maritime Continent are strongest, and coincident with the MJO peak. Shortwave heating profile anomalies are about half as large as longwave anomalies in the active region of the MJO but generally of opposite sign; thus shortwave heating damps the longwave destabilization of the lower troposphere. The exception is the onset phase of the MJO, where shortwave and longwave heating anomalies due to thin cirrus are both positive in the upper troposphere and exert a stabilizing influence. Specific humidity anomalies in the middle troposphere reach 0.5 g kg(exp. -1), but the associated clear sky heating anomaly is very small. Radiative enhancement of column moist static energy becomes significant about 10 days before the MJO peak, when precipitation anomalies are still increasing, and then remains high after the MJO peak after precipitation has begun to decline.
Revised estimation of 550-km times 550-km mean gravity anomalies
NASA Technical Reports Server (NTRS)
Williamson, M. R.
1977-01-01
The calculation of 550-km x 550-km mean gravity anomalies from 1 degree x 1 degree mean free-air gravimetry data is discussed. The block estimate procedure developed by Kaula is used to obtain 1,504 of the 1,654 possible mean block anomalies. The estimated block anomalies calculated from 1 deg x 1 deg mean anomalies referred to the reference ellipsoid and from 1 degree x 1 degree mean anomalies referred to a 24th-degree-and-order field are compared.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Solaimani, Mohiuddin; Iftekhar, Mohammed; Khan, Latifur
Anomaly detection refers to the identi cation of an irregular or unusual pat- tern which deviates from what is standard, normal, or expected. Such deviated patterns typically correspond to samples of interest and are assigned different labels in different domains, such as outliers, anomalies, exceptions, or malware. Detecting anomalies in fast, voluminous streams of data is a formidable chal- lenge. This paper presents a novel, generic, real-time distributed anomaly detection framework for heterogeneous streaming data where anomalies appear as a group. We have developed a distributed statistical approach to build a model and later use it to detect anomaly. Asmore » a case study, we investigate group anomaly de- tection for a VMware-based cloud data center, which maintains a large number of virtual machines (VMs). We have built our framework using Apache Spark to get higher throughput and lower data processing time on streaming data. We have developed a window-based statistical anomaly detection technique to detect anomalies that appear sporadically. We then relaxed this constraint with higher accuracy by implementing a cluster-based technique to detect sporadic and continuous anomalies. We conclude that our cluster-based technique out- performs other statistical techniques with higher accuracy and lower processing time.« less
Prevalence of dental developmental anomalies: a radiographic study.
Ezoddini, Ardakani F; Sheikhha, M H; Ahmadi, H
2007-09-01
To determine the prevalence of developmental dental anomalies in patients attending the Dental Faculty of Medical University of Yazd, Iran and the gender differences of these anomalies. A retrospective study based on the panoramic radiographs of 480 patients. Patients referred for panoramic radiographs were clinically examined, a detailed family history of any dental anomalies in their first and second degree relatives was obtained and finally their radiographs were studied in detail for the presence of dental anomalies. 40.8% of the patients had dental anomalies. The more common anomalies were dilaceration (15%), impacted teeth (8.3%) and taurodontism (7.5%) and supernumerary teeth (3.5%). Macrodontia and fusion were detected in a few radiographs (0.2%). 49.1% of male patients had dental anomalies compared to 33.8% of females. Dilaceration, taurodontism and supernumerary teeth were found to be more prevalent in men than women, whereas impacted teeth, microdontia and gemination were more frequent in women. Family history of dental anomalies was positive in 34% of the cases.. Taurodontism, gemination, dens in dente and talon cusp were specifically limited to the patients under 20 year's old, while the prevalence of other anomalies was almost the same in all groups. Dilaceration, impaction and taurodontism were relatively common in the studied populaton. A family history of dental anomalies was positive in a third of cases.
Effect of attractive interactions on the water-like anomalies of a core-softened model potential.
Pant, Shashank; Gera, Tarun; Choudhury, Niharendu
2013-12-28
It is now well established that water-like anomalies can be reproduced by a spherically symmetric potential with two length scales, popularly known as core-softened potential. In the present study we aim to investigate the effect of attractive interactions among the particles in a model fluid interacting with core-softened potential on the existence and location of various water-like anomalies in the temperature-pressure plane. We employ extensive molecular dynamic simulations to study anomalous nature of various order parameters and properties under isothermal compression. Order map analyses have also been done for all the potentials. We observe that all the systems with varying depth of attractive wells show structural, dynamic, and thermodynamic anomalies. As many of the previous studies involving model water and a class of core softened potentials have concluded that the structural anomaly region encloses the diffusion anomaly region, which in turn, encloses the density anomaly region, the same pattern has also been observed in the present study for the systems with less depth of attractive well. For the systems with deeper attractive well, we observe that the diffusion anomaly region shifts toward higher densities and is not always enclosed by the structural anomaly region. Also, density anomaly region is not completely enclosed by diffusion anomaly region in this case.
Application of isostatic gravity anomaly in the Yellow Sea area
NASA Astrophysics Data System (ADS)
Hao, Z.; Qin, J.; Huang, W.; Wu, X.
2017-12-01
In order to study the deep crustal structure of the Yellow Sea area, we used the Airy-Heiskanen model to calculate the isostatic gravity anomaly of this area. Based on the Bouguer gravity anomaly and water depth data of this area, we chose the calculating parameters as standard crustal thickness 30 km, crust-mantle density difference 0.6g/cm3and grid spacing 0.1°×0.1°. This study reveals that there are six faults and four isostatic negative anomalies in the study area. The isostatic anomalies in much of Yellow Sea areas give priority to those with positive anomalies. The isostatic anomalies in North Yellow Sea are higher than South Yellow Sea with Jiashan-Xiangshui fault as the boundary. In the north of the study area, isostatic anomalies are characterized by large areas of positive anomaly. The change is relatively slow, and the trends give priority to the trend NE or NEE. In the middle of the north Yellow Sea basin, there is a local negative anomaly, arranged as a string of beads in NE to discontinuous distribution. Negative anomaly range is small, basically corresponds to the region's former Cenozoic sedimentary basin position. To the south of Jiashan-Xiangshui fault and west of Yellow Sea eastern margin fault, including most of the south Yellow Sea and Jiangsu province, the isostatic anomalies are lower. And the positive and negative anomalies are alternative distribution, and negative anomaly trap in extensive development. The trends give priority to NE, NEE, both to the NW. On the basis of the characteristics of isostatic gravity anomalies, it is concluded that the Yellow Sea belongs to continental crustal isostatic area whose isostatic anomalies is smooth and slow. ReferencesHeiskanen, W. A., F. A. V. Meinesz, and S. A. Korff (1958), The Earth and Its Gravity Field, McGraw-Hill, New York. Meng, X. J., X. H. Zhang, and J. Y. Yang (2014), Geophysical survey in eastern China seas and the characteristics of gravity and magnetic fields, Marine Geoglogy & Quaternary Geology, 34(6), 127-134.
Fourth Branchial Anomaly Presenting with a Lateral Neck Mass in a Neonate
Yoo, Tae-Kyung; Kim, Soo-Hong; Kim, Ha-Shin; Park, Kwi-Won
2014-01-01
Branchial cleft anomalies are an important differential diagnosis in congenital neck masses in infants. The third and fourth branchial anomalies are rare branchial cleft anomalies, which are hard to differentiate. We report here an uncommon case of the fourth branchial anomaly that was presented as an asymptomatic neck mass in a neonate. PMID:26023505
Fourth branchial anomaly presenting with a lateral neck mass in a neonate.
Yoo, Tae-Kyung; Kim, Soo-Hong; Kim, Ha-Shin; Kim, Hyun-Young; Park, Kwi-Won
2014-01-01
Branchial cleft anomalies are an important differential diagnosis in congenital neck masses in infants. The third and fourth branchial anomalies are rare branchial cleft anomalies, which are hard to differentiate. We report here an uncommon case of the fourth branchial anomaly that was presented as an asymptomatic neck mass in a neonate.
Anomaly Trends for Missions to Mars: Mars Global Surveyor and Mars Odyssey
NASA Technical Reports Server (NTRS)
Green, Nelson W.; Hoffman, Alan R.
2008-01-01
The long term flight operations of the Mars Global Surveyor and Mars Odyssey spacecraft give us an excellent chance to examine the operations of two long lived spacecraft in orbit around Mars during overlapping time periods. This study examined the anomalies for each mission maintained for NASA at the Jet Propulsion Laboratory. By examining the anomalies each mission encountered during their multiyear missions, trends were identified related to when anomalies occurred during each mission, the types of anomalies encountered, and corrective actions taken to mitigate the effects of the anomalies. As has been discovered in previous studies the numbers of anomalies directly correlate with mission activity and show a decreasing trend with elapsed mission time. Trend analysis also identified a heavy emphasis on software as the source or solution to anomalies for both missions.
6d, Coulomb branch anomaly matching
NASA Astrophysics Data System (ADS)
Intriligator, Kenneth
2014-10-01
6d QFTs are constrained by the analog of 't Hooft anomaly matching: all anomalies for global symmetries and metric backgrounds are constants of RG flows, and for all vacua in moduli spaces. We discuss an anomaly matching mechanism for 6d theories on their Coulomb branch. It is a global symmetry analog of Green-Schwarz-West-Sagnotti anomaly cancellation, and requires the apparent anomaly mismatch to be a perfect square, . Then Δ I 8 is cancelled by making X 4 an electric/magnetic source for the tensor multiplet, so background gauge field instantons yield charged strings. This requires the coefficients in X 4 to be integrally quantized. We illustrate this for theories. We also consider the SCFTs from N small E8 instantons, verifying that the recent result for its anomaly polynomial fits with the anomaly matching mechanism.
Berger, Katherine H; Zhu, Bao-Ping; Copeland, Glenn
2003-09-01
Congenital anomalies are a leading cause of infant deaths, accounting for almost a fifth of all infant deaths. Few studies have researched the survival experience of infants born with congenital anomalies past the infant stage. Using birth and death files routinely linked to the Michigan Birth Defects Registry, we identified all singleton infants during calendar years 1992 through 1998 with reportable congenital anomalies for our study. A comparative file of children born without congenital anomalies during the same time period was developed using linked birth and death files. The mortality data were assessed by age at death (through age six) and race to determine mortality rates, relative risks, hazard ratios, and survival trends. Throughout early childhood, children born with congenital anomalies had a high risk of mortality compared with all other children. The overall 7-year hazard ratio comparing children with congenital anomalies with all other children was 7.2. Overall mortality rates for black children were significantly higher than white children through the age of seven, irrespective of whether they had congenital anomalies. Among children with congenital anomalies, this disparity disappeared after adjusting for birth weight, sex, mother's age, mother's education, and number of organ systems affected. Compared with children without congenital anomalies, children born with congenital anomalies had a higher risk of mortality well beyond the infant period. Racial disparities in mortality rates among children with congenital anomalies were due to confounding factors.
Influence of Western Tibetan Plateau Summer Snow Cover on East Asian Summer Rainfall
NASA Astrophysics Data System (ADS)
Wang, Zhibiao; Wu, Renguang; Chen, Shangfeng; Huang, Gang; Liu, Ge; Zhu, Lihua
2018-03-01
The influence of boreal winter-spring eastern Tibetan Plateau snow anomalies on the East Asian summer rainfall variability has been the focus of previous studies. The present study documents the impacts of boreal summer western and southern Tibetan Plateau snow cover anomalies on summer rainfall over East Asia. Analysis shows that more snow cover in the western and southern Tibetan Plateau induces anomalous cooling in the overlying atmospheric column. The induced atmospheric circulation changes are different corresponding to more snow cover in the western and southern Tibetan Plateau. The atmospheric circulation changes accompanying the western Plateau snow cover anomalies are more obvious over the midlatitude Asia, whereas those corresponding to the southern Plateau snow cover anomalies are more prominent over the tropics. As such, the western and southern Tibetan Plateau snow cover anomalies influence the East Asian summer circulation and precipitation through different pathways. Nevertheless, the East Asian summer circulation and precipitation anomalies induced by the western and southern Plateau snow cover anomalies tend to display similar distribution so that they are more pronounced when the western and southern Plateau snow cover anomalies work in coherence. Analysis indicates that the summer snow cover anomalies over the Tibetan Plateau may be related to late spring snow anomalies due to the persistence. The late spring snow anomalies are related to an obvious wave train originating from the western North Atlantic that may be partly associated with sea surface temperature anomalies in the North Atlantic Ocean.
Johnson, Carole D.; Dawson, C.B.; Belaval, Marcel; Lane, John W.
2002-01-01
A surface-geophysical investigation to characterize the hydrogeology and contaminant distribution of the former landfill area at the University of Connecticut in Storrs, Connecticut, was conducted in 2000 to supplement the preliminary hydrogeologic assessment of the contamination of soil, surface water, and ground water at the site. A geophysical-toolbox approach was used to characterize the hydrogeology and contaminant distribution of the former landfill. Two-dimensional direct-current resistivity, inductive terrain-conductivity, and seismic-refraction surface-geophysical data were collected and interpreted in an iterative manner with exploratory drilling, borehole geophysics, and hydraulic testing. In this investigation, a geophysical-toolbox approach was used to 1) further define previously identified conductive anomalies and leachate plumes; 2) identify additional leachate plumes, possible fracture zones, and (or) conductive lithologic layers in the bedrock; and 3) delineate bedrock-surface topography in the drainage valleys north and south of the landfill. Resistivity and terrain-conductivity surveys were used to further delineate previously identified geophysical anomalies to the north and southwest of the landfill. A conductive anomaly identified in the terrain-conductivity survey to the north of the landfill in 2000 had a similar location and magnitude as an anomaly identified in terrain-conductivity surveys conducted in 1998 and 1999. Collectively, these surveys indicated that the magnitude of the conductive anomaly decreased with depth and with distance from the landfill. These anomalies indicated landfill leachate in the overburden and shallow bedrock. Results of previous surface-geophysical investigations southwest of the landfill indicated a shallow conductive anomaly in the overburden that extended into the fractured-bedrock aquifer. This conductive anomaly had a sheet-like geometry that had a north-south strike, dipped to the west, and terminated abruptly about 450 feet southwest of the landfill. The sheet-like conductive anomaly was interpreted as a fractured, conductive lithologic feature filled with conductive fluids. To further delineate this anomaly, two two-dimensional resistivity profiles were collected west of the sheet-like conductive anomaly to assess the possibility that the sheet-like conductive anomaly continued to the west in its down-dip direction. Each of the north-south oriented resistivity profiles showed bullet-shaped rather than linear-shaped anomalies, with a relatively smaller magnitude of conductivity than the sheet-like conductive anomaly to the east. If these bullet-like features are spatially connected, they may represent a linear, or pipe-like, conductive anomaly in the bedrock with a trend of N290?E and a plunge of 12?. Additional surveys were conducted to assess the apparent southern termination of the sheet-like conductive feature. Terrain-conductivity surveys indicated the sheet-like feature was not continuous to the south. A two-dimensional resistivity line and a coincident terrain-conductivity profile indicated the presence of a steep, eastward dipping, low magnitude, electrically conductive anomaly on the eastern end of the profile. Although the sheet-like conductive anomaly apparently did not continue to the south, the survey conducted in 2000 identified an isolated, weak conductive anomaly south of the previously identified anomaly. Inductive terrain-conductivity surveys performed north of the sheet-like conductive anomaly and west of the landfill indicated the anomaly did not extend to the north into the area of the former chemical-waste disposal pits. No conductive plumes or conductive features were observed in the subsurface bedrock west of the landfill. A conductive anomaly was identified in the southern section of the new terrain-conductivity grid. The magnitude and distribution of the apparent conductivity of this anomaly was identified as a nearly vertica
Thottam, Prasad John; Bathula, Samba S; Poulik, Janet M; Madgy, David N
2014-01-01
Branchial cleft anomalies make up 30% of all pediatric neck masses, but complete second branchial cleft anomalies are extremely rare. We report an unusual case of a complete second branchial cleft anomaly that presented as a draining neck fistula and a tonsillar cyst in an otherwise healthy 3-month-old girl. At the age of 7 months, the patient had been experiencing feeding difficulties, and there was increasing concern about the risk of persistent infections. At that point, the anomaly was excised in its entirety. Our suspicion that the patient had a complete second branchial cleft anomaly was confirmed by imaging, surgical excision, and histopathologic analysis.
Germanakis, Ioannis; Matsui, Hikoro; Gardiner, Helena M
2012-01-01
To compare myocardial deformation patterns in fetuses with congenital heart disease (CHD) with our reference range using speckle tracking echocardiography. We prospectively stored and analyzed 4-chamber loops of 28 fetuses with CHD (median gestation 27 weeks, range 20.9-37.0). The peak longitudinal left (LVs) and right (RVs) ventricular free wall Lagrangian strain and LV/RV strain ratio were measured from Syngo VVI software- (Siemens) derived original coordinates. Strain values from the first examination were compared with normative data from the same population using ANOVA with post hoc tests and serial examinations described in 14 fetuses. Simple shunt lesions (0.82) and shunts with pulmonary stenosis or atresia (0.93) had reduced mean LV/RV strain ratios compared to normal fetuses (1.01; 95% CI 0.97-1.05). Fetuses with hypoplastic left heart had the lowest (0.29), and those with Ebstein the highest (1.55), LV:RV ratio. Serial measurements showed increased LVs in aortic coarctation and aortic stenosis, but not in one developing important mitral regurgitation. Increased right ventricular loading in a fetus developing pulmonary regurgitation was associated with increasing RVs. Myocardial strain reflects the changing physiology of fetal CHD. Speckle tracking might be a useful tool to study the progress of myocardial function in affected fetuses. Copyright © 2012 S. Karger AG, Basel.
Scherzer, Pnina; Katalan, Shachaf; Got, Gay; Pizov, Galina; Londono, Irene; Gal-Moscovici, Anca; Popovtzer, Mordecai M.; Ziv, Ehud
2011-01-01
The Psammomys obesus lives in natural desert habitat on low energy (LE) diet, however when maintained in laboratory conditions with high energy (HE) diet it exhibits pathological metabolic changes resembling those of type 2 diabetes. We have evaluated and correlated the histopathology, metabolic and functional renal alterations occurring in the diabetic Psammomys. Renal function determined by measuring glomerular filtration rate (GFR), protein excretion, protein/creatinine ratio and morpho-immunocytochemical evaluations were performed on HE diet diabetic animals and compared to LE diet control animals. The diabetic animals present a 54% increase in GFR after one month of hyperglycemic condition and a decrease of 47% from baseline values after 4 months. Protein excretion in diabetic animals was 5 folds increased after 4 months. Light microscopy showed an increase in glomeruli size in the diabetic Psammomys, and electron microscopy and immunocytochemical quantitative evaluations revealed accumulation of basement membrane material as well as frequent splitting of the glomerular basement membrane. In addition, glycogen-filled Armanni-Ebstein clear cells were found in the distal tubules including the thick ascending limbs of the diabetic animals. These renal complications in the Psammomys, including changes in GFR with massive proteinuria sustained by physiological and histopathological changes, are very similar to the diabetic nephropathy in human. The Psamommys obesus represents therefore a reliable animal model of diabetic nephropathy. PMID:22025969
Spacecraft Environmental Anomalies Handbook
1989-08-01
1989 4. TITLE AND SUBTITLE S. FUNDING NUMBERS SPACECRAFT ENVIRONMENTAL ANOMALIES HANDBOOK 282201AA PE: 63410F 6. AUTHOR(S) Paul A. Robinson, Jr 7...engineering solutions for mitigating the effects of environmental anomalies have been developed. Among the causes o, spacecraft anomalies are surface...have been discovered after years of investig!:tion, and engineering solutions for mitigating the effccts of environmental anomalies have been developed
Prevalence and distribution of dental anomalies in orthodontic patients.
Montasser, Mona A; Taha, Mahasen
2012-01-01
To study the prevalence and distribution of dental anomalies in a sample of orthodontic patients. The dental casts, intraoral photographs, and lateral panoramic and cephalometric radiographs of 509 Egyptian orthodontic patients were studied. Patients were examined for dental anomalies in number, size, shape, position, and structure. The prevalence of each dental anomaly was calculated and compared between sexes. Of the total study sample, 32.6% of the patients had at least one dental anomaly other than agenesis of third molars; 32.1% of females and 33.5% of males had at least one dental anomaly other than agenesis of third molars. The most commonly detected dental anomalies were impaction (12.8%) and ectopic eruption (10.8%). The total prevalence of hypodontia (excluding third molars) and hyperdontia was 2.4% and 2.8%, respectively, with similiar distributions in females and males. Gemination and accessory roots were reported in this study; each of these anomalies was detected in 0.2% of patients. In addition to genetic and racial factors, environmental factors could have more important influence on the prevalence of dental anomalies in every population. Impaction, ectopic eruption, hyperdontia, hypodontia, and microdontia were the most common dental anomalies, while fusion and dentinogenesis imperfecta were absent.
Magnetic anomalies in the Cosmonauts Sea, off East Antarctica
NASA Astrophysics Data System (ADS)
Nogi, Y.; Hanyu, T.; Fujii, M.
2017-12-01
Identification of magnetic anomaly lineations and fracture zone trends in the Southern Indian Ocean, are vital to understanding the breakup of Gondwana. However, the magnetic spreading anomalies and fracture zones are not clear in the Southern Indian Ocean. Magnetic anomaly lineations in the Cosmonauts Sea, off East Antarctica, are key to elucidation of separation between Sri Lanka/India and Antarctica. No obvious magnetic anomaly lineations are observed from a Japanese/German aerogeophysical survey in the Cosmonauts Sea, and this area is considered to be created by seafloor spreading during the Cretaceous Normal Superchron. Vector magnetic anomaly measurements have been conducted on board the Icebreaker Shirase mainly to understand the process of Gondwana fragmentation in the Indian Ocean. Magnetic boundary strikes are derived from vector magnetic anomalies obtained in the Cosmonauts Sea. NE-SW trending magnetic boundary strikes are mainly observed along the several NW-SE oriented observation lines with magnetic anomaly amplitudes of about 200 nT. These NE-SW trending magnetic boundary strikes possibly indicate M-series magnetic anomalies that can not be detected from the aerogeophysical survey with nearly N-S observation lines. We will discuss the magnetic spreading anomalies and breakup process between Sri Lanka/India and Antarctica in the Cosmonauts Sea.
Mangione, Francesca; Nguyen, Laure; Foumou, Nathalie; Bocquet, Emmanuelle; Dursun, Elisabeth
2018-03-01
Prevalence of dental anomalies in cleft patients is higher than that in general population. The objectives of this study were to assess the prevalence of dental anomalies and their coexistence in French children with cleft and, then, to investigate the relation between the dental anomalies and the cleft type. Seventy-four non-syndromic cleft patients (6-16 years old) from Lille Regional University and Mondor-Chenevier Hospitals (France) were included. Clefts were classified as right/left unilateral cleft lip and palate (UCLP), bilateral cleft lip and palate (BCLP) and cleft palate (CP). Dental anomalies were investigated on panoramic radiographs and categorized as agenesis, supernumerary teeth, incisor rotations, impacted canines and shape anomalies. Prevalence and gender distribution of dental anomalies, mean number of affected teeth per patient, agenesis occurrence and location, and coexistence of dental anomalies were analysed by cleft type. 96.0% of patients presented at least one dental anomaly (agenesis 83.8%, incisor rotations 25.7%, shape anomalies 21.6%, impacted canines 18.9%, supernumerary teeth 8.1%). BCLP patients had a higher number of affected teeth, and left UCLP patients had a higher one compared to right UCLP patients. Distribution of inside (45.3%) and outside (54.7%) cleft region agenesis was similar. Adjacent (31.8%) and not adjacent (33.3%) combined dental anomalies were often encountered. Dental anomalies were localized inside as well as outside cleft region and were often associated with each other. BCLP patients were more affected. Early radiographic evaluation allows a comprehensive diagnosis of inside and outside cleft region anomalies, required for the multidisciplinary dental treatment.
NASA Technical Reports Server (NTRS)
Srivastava, Ashok, N.; Akella, Ram; Diev, Vesselin; Kumaresan, Sakthi Preethi; McIntosh, Dawn M.; Pontikakis, Emmanuel D.; Xu, Zuobing; Zhang, Yi
2006-01-01
This paper describes the results of a significant research and development effort conducted at NASA Ames Research Center to develop new text mining techniques to discover anomalies in free-text reports regarding system health and safety of two aerospace systems. We discuss two problems of significant importance in the aviation industry. The first problem is that of automatic anomaly discovery about an aerospace system through the analysis of tens of thousands of free-text problem reports that are written about the system. The second problem that we address is that of automatic discovery of recurring anomalies, i.e., anomalies that may be described m different ways by different authors, at varying times and under varying conditions, but that are truly about the same part of the system. The intent of recurring anomaly identification is to determine project or system weakness or high-risk issues. The discovery of recurring anomalies is a key goal in building safe, reliable, and cost-effective aerospace systems. We address the anomaly discovery problem on thousands of free-text reports using two strategies: (1) as an unsupervised learning problem where an algorithm takes free-text reports as input and automatically groups them into different bins, where each bin corresponds to a different unknown anomaly category; and (2) as a supervised learning problem where the algorithm classifies the free-text reports into one of a number of known anomaly categories. We then discuss the application of these methods to the problem of discovering recurring anomalies. In fact the special nature of recurring anomalies (very small cluster sizes) requires incorporating new methods and measures to enhance the original approach for anomaly detection. ?& pant 0-
Popoola, Bamidele O; Onyejaka, Nneka; Folayan, Morenike O
2016-07-07
Developmental dental hard tissue anomalies are often associated with oral health problems. This study determined the clinical prevalence of developmental dental hard tissue anomalies in the permanent dentition of children resident in southwestern Nigeria and its association with dental caries and poor oral hygiene status. This was a cross-sectional study recruiting 1565 school children, 12 to 15 year old attending schools in Ibadan, Oyo State and Ile-Ife, Osun State. All eligible study participants had oral examinations conducted to determine presence of developmental hard dental tissue anomalies, caries and oral hygiene status. The prevalence of developmental dental hard tissue anomalies was determined. Logistic Poisson regression was used to determine the association of between developmental dental hard tissue anomalies, caries and oral hygiene status. Only 65 (4.2 %) children had clinically diagnosed developmental dental hard tissue anomalies. The most prevalent anomaly was enamel hypoplasia (2.2 %). More females (p = 0.003) and more children with middle socioeconomic class (p = 0.001) had enamel hypoplasia. The probability of having poor oral hygiene was significantly increased for children with developmental dental anomalies (APR: 0.07; 95 % CI: 0.03 - 0.12; p = 0.002). The probability of having caries was insignificantly increased for children with developmental dental hard tissue anomalies (APR: 0.005; 95 % CI: -0.03 - 0.04; p = 0.08). The most prevalence clinically detectable developmental dental hard tissue anomalies for the study population was enamel hypoplasia. The presence of developmental dental hard tissue anomalies significantly increased the chances of having poor oral hygiene but not caries. Further studies are required to understand if poor oral hygiene is associated with dental caries in children with developmental dental hard tissue anomalies.
Associated anomalies in cases with esophageal atresia.
Stoll, Claude; Alembik, Yves; Dott, Beatrice; Roth, Marie-Paule
2017-08-01
Esophageal atresia (EA) is a common type of congenital anomaly. The etiology of esophageal atresia is unclear and its pathogenesis is controversial. Infants with esophageal atresia often have other non-EA associated congenital anomalies. The purpose of this investigation was to assess the prevalence and the types of these associated anomalies in a defined population. The associated anomalies in cases with EA were collected in all livebirths, stillbirths, and terminations of pregnancy during 29 years in 387,067 consecutive births in the area covered by our population-based registry of congenital malformations. Of the 116 cases with esophageal atresia, representing a prevalence of 2.99 per 10,000, 54 (46.6%) had associated anomalies. There were 9 (7.8%) cases with chromosomal abnormalities including 6 trisomies 18, and 20 (17.2%) nonchromosomal recognized dysmorphic conditions including 12 cases with VACTERL association and 2 cases with CHARGE syndrome. Twenty five (21.6%) of the cases had multiple congenital anomalies (MCA). Anomalies in the cardiovascular, the digestive, the urogenital, the musculoskeletal, and the central nervous systems were the most common other anomalies. The anomalies associated with esophageal atresia could be classified into a recognizable malformation syndrome or pattern in 29 out of 54 cases (53.7%). This study included special strengths: each affected child was examined by a geneticist, all elective terminations were ascertained, and the surveillance for anomalies was continued until 2 years of age. In conclusion the overall prevalence of associated anomalies, which was close to one in two cases, emphasizes the need for a thorough investigation of cases with EA. A routine screening for other anomalies may be considered in infants and in fetuses with EA. © 2017 Wiley Periodicals, Inc.
Springett, Anna; Wellesley, Diana; Greenlees, Ruth; Loane, Maria; Addor, Marie-Claude; Arriola, Larraitz; Bergman, Jorieke; Cavero-Carbonell, Clara; Csaky-Szunyogh, Melinda; Draper, Elizabeth S; Garne, Ester; Gatt, Miriam; Haeusler, Martin; Khoshnood, Babak; Klungsoyr, Kari; Lynch, Catherine; Dias, Carlos Matias; McDonnell, Robert; Nelen, Vera; O'Mahony, Mary; Pierini, Anna; Queisser-Luft, Annette; Rankin, Judith; Rissmann, Anke; Rounding, Catherine; Stoianova, Sylvia; Tuckerz, David; Zymak-Zakutnia, Natalya; Morris, Joan K
2015-12-01
The aim of this study was to examine the prevalence of trisomies 18 and 13 in Europe and the prevalence of associated anomalies. Twenty-five population-based registries in 16 European countries provided data from 2000-2011. Cases included live births, fetal deaths (20+ weeks' gestation), and terminations of pregnancy for fetal anomaly (TOPFAs). The prevalence of associated anomalies was reported in live births. The prevalence of trisomy 18 and trisomy 13 were 4.8 (95%CI: 4.7-5.0) and 1.9 (95%CI: 1.8-2.0) per 10,000 total births. Seventy three percent of cases with trisomy 18 or trisomy 13 resulted in a TOPFA. Amongst 468 live born babies with trisomy 18, 80% (76-83%) had a cardiac anomaly, 21% (17-25%) had a nervous system anomaly, 8% (6-11%) had esophageal atresia and 10% (8-13%) had an orofacial cleft. Amongst 240 Live born babies with trisomy 13, 57% (51-64%) had a cardiac anomaly, 39% (33-46%) had a nervous system anomaly, 30% (24-36%) had an eye anomaly, 44% (37-50%) had polydactyly and 45% (39-52%) had an orofacial cleft. For babies with trisomy 18 boys were less likely to have a cardiac anomaly compared with girls (OR = 0.48 (0.30-0.77) and with trisomy 13 were less likely to have a nervous system anomaly [OR = 0.46 (0.27-0.77)]. Babies with trisomy 18 or trisomy 13 do have a high proportion of associated anomalies with the distribution of anomalies being different in boys and girls. © 2015 Wiley Periodicals, Inc.
New Data Bases and Standards for Gravity Anomalies
NASA Astrophysics Data System (ADS)
Keller, G. R.; Hildenbrand, T. G.; Webring, M. W.; Hinze, W. J.; Ravat, D.; Li, X.
2008-12-01
Ever since the use of high-precision gravimeters emerged in the 1950's, gravity surveys have been an important tool for geologic studies. Recent developments that make geologically useful measurements from airborne and satellite platforms, the ready availability of the Global Positioning System that provides precise vertical and horizontal control, improved global data bases, and the increased availability of processing and modeling software have accelerated the use of the gravity method. As a result, efforts are being made to improve the gravity databases publicly available to the geoscience community by expanding their holdings and increasing the accuracy and precision of the data in them. Specifically the North American Gravity Database as well as the individual databases of Canada, Mexico, and the United States are being revised using new formats and standards to improve their coverage, standardization, and accuracy. An important part of this effort is revision of procedures and standards for calculating gravity anomalies taking into account the enhanced computational power available, modern satellite-based positioning technology, improved terrain databases, and increased interest in more accurately defining the different components of gravity anomalies. The most striking revision is the use of one single internationally accepted reference ellipsoid for the horizontal and vertical datums of gravity stations as well as for the computation of the calculated value of theoretical gravity. The new standards hardly impact the interpretation of local anomalies, but do improve regional anomalies in that long wavelength artifacts are removed. Most importantly, such new standards can be consistently applied to gravity database compilations of nations, continents, and even the entire world. Although many types of gravity anomalies have been described, they fall into three main classes. The primary class incorporates planetary effects, which are analytically prescribed, to derive the predicted or modeled gravity, and thus, anomalies of this class are termed planetary. The most primitive version of a gravity anomaly is simply the difference between the value of gravity predicted by the effect of the reference ellipsoid and the observed gravity anomaly. When the height of the gravity station increases, the ellipsoidal gravity anomaly decreases because of the increased distance of measurement from the anomaly- producing masses. The two primary anomalies in geophysics, which are appropriately classified as planetary anomalies, are the Free-air and Bouguer gravity anomalies. They employ models that account for planetary effects on gravity including the topography of the earth. A second class of anomaly, geological anomalies, includes the modeled gravity effect of known or assumed masses leading to the predicted gravity by using geological data such as densities and crustal thickness. The third class of anomaly, filtered anomalies, removes arbitrary gravity effects of largely unknown sources that are empirically or analytically determined from the nature of the gravity anomalies by filtering.
Analysis of spacecraft anomalies
NASA Technical Reports Server (NTRS)
Bloomquist, C. E.; Graham, W. C.
1976-01-01
The anomalies from 316 spacecraft covering the entire U.S. space program were analyzed to determine if there were any experimental or technological programs which could be implemented to remove the anomalies from future space activity. Thirty specific categories of anomalies were found to cover nearly 85 percent of all observed anomalies. Thirteen experiments were defined to deal with 17 of these categories; nine additional experiments were identified to deal with other classes of observed and anticipated anomalies. Preliminary analyses indicate that all 22 experimental programs are both technically feasible and economically viable.
Apollo experience report: Flight anomaly resolution
NASA Technical Reports Server (NTRS)
Lobb, J. D.
1975-01-01
The identification of flight anomalies, the determination of their causes, and the approaches taken for corrective action are described. Interrelationships of the broad range of disciplines involved with the complex systems and the team concept employed to ensure timely and accurate resolution of anomalies are discussed. The documentation techniques and the techniques for management of anomaly resolution are included. Examples of specific anomalies are presented in the original form of their progressive documentation. Flight anomaly resolution functioned as a part of the real-time mission support and postflight testing, and results were included in the postflight documentation.
Vascular Anomalies (Part I): Classification and Diagnostics of Vascular Anomalies.
Sadick, Maliha; Müller-Wille, René; Wildgruber, Moritz; Wohlgemuth, Walter A
2018-06-06
Vascular anomalies are a diagnostic and therapeutic challenge. They require dedicated interdisciplinary management. Optimal patient care relies on integral medical evaluation and a classification system established by experts in the field, to provide a better understanding of these complex vascular entities. A dedicated classification system according to the International Society for the Study of Vascular Anomalies (ISSVA) and the German Interdisciplinary Society of Vascular Anomalies (DiGGefA) is presented. The vast spectrum of diagnostic modalities, ranging from ultrasound with color Doppler, conventional X-ray, CT with 4 D imaging and MRI as well as catheter angiography for appropriate assessment is discussed. Congenital vascular anomalies are comprised of vascular tumors, based on endothelial cell proliferation and vascular malformations with underlying mesenchymal and angiogenetic disorder. Vascular tumors tend to regress with patient's age, vascular malformations increase in size and are subdivided into capillary, venous, lymphatic, arterio-venous and combined malformations, depending on their dominant vasculature. According to their appearance, venous malformations are the most common representative of vascular anomalies (70 %), followed by lymphatic malformations (12 %), arterio-venous malformations (8 %), combined malformation syndromes (6 %) and capillary malformations (4 %). The aim is to provide an overview of the current classification system and diagnostic characterization of vascular anomalies in order to facilitate interdisciplinary management of vascular anomalies. · Vascular anomalies are comprised of vascular tumors and vascular malformations, both considered to be rare diseases.. · Appropriate treatment depends on correct classification and diagnosis of vascular anomalies, which is based on established national and international classification systems, recommendations and guidelines.. · In the classification, diagnosis and treatment of congenital vascular anomalies, radiology plays an integral part in patient management.. · Sadick M, Müller-Wille R, Wildgruber M et al. Vascular Anomalies (Part I): Classification and Diagnostics of Vascular Anomalies. Fortschr Röntgenstr 2018; DOI: 10.1055/a-0620-8925. © Georg Thieme Verlag KG Stuttgart · New York.
Branchial anomalies in children.
Bajaj, Y; Ifeacho, S; Tweedie, D; Jephson, C G; Albert, D M; Cochrane, L A; Wyatt, M E; Jonas, N; Hartley, B E J
2011-08-01
Branchial cleft anomalies are the second most common head and neck congenital lesions seen in children. Amongst the branchial cleft malformations, second cleft lesions account for 95% of the branchial anomalies. This article analyzes all the cases of branchial cleft anomalies operated on at Great Ormond Street Hospital over the past 10 years. All children who underwent surgery for branchial cleft sinus or fistula from January 2000 to December 2010 were included in this study. In this series, we had 80 patients (38 female and 42 male). The age at the time of operation varied from 1 year to 14 years. Amongst this group, 15 patients had first branchial cleft anomaly, 62 had second branchial cleft anomaly and 3 had fourth branchial pouch anomaly. All the first cleft cases were operated on by a superficial parotidectomy approach with facial nerve identification. Complete excision was achieved in all these first cleft cases. In this series of first cleft anomalies, we had one complication (temporary marginal mandibular nerve weakness. In the 62 children with second branchial cleft anomalies, 50 were unilateral and 12 were bilateral. In the vast majority, the tract extended through the carotid bifurcation and extended up to pharyngeal constrictor muscles. Majority of these cases were operated on through an elliptical incision around the external opening. Complete excision was achieved in all second cleft cases except one who required a repeat excision. In this subgroup, we had two complications one patient developed a seroma and one had incomplete excision. The three patients with fourth pouch anomaly were treated with endoscopic assisted monopolar diathermy to the sinus opening with good outcome. Branchial anomalies are relatively common in children. There are three distinct types, first cleft, second cleft and fourth pouch anomaly. Correct diagnosis is essential to avoid inadequate surgery and multiple procedures. The surgical approach needs to be tailored to the type of anomaly of origin of the anomaly. Complete excision is essential for good outcomes. Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.
Bižić, Marta R; Cvetinović, Nataša; Majstorović, Marko J; Radojčić, Zoran; Vukadinović, Vojkan; Krstić, Zoran; Djordjević, Miroslav L
2012-01-01
Urogenital congenital anomalies are among the most common congenital anomalies and very frequent pathology in paediatric urology. Health care systems strive to shorten the duration and reduce the costs of hospitalization, while maintaining treatment effectiveness. To evaluate the duration of hospital stay of surgically treated patients with congenital urogenital anomalies and estimate the possibility of using fast track surgery principles in paediatric urology in the local settings of a developing country. Retrospective non-randomized study included 552 patients who had been surgically treated at the Urology Department of the University Children's Hospital, during 2010. In line with their congenital anomalies, all patients were classified in one of four groups: I--upper urinary tract anomalies (252 patients); II--genital anomalies (164 patients); III--testicular anomalies (76 patients) and IV--associated anomalies (60 patients). We analyzed the total duration of stay as well as pre- and post-operative stay in the hospital. The average duration of hospitalization was 4.7 +/- 4.0 days. Patients with testicular anomalies stayed for the shortest period (2.3 +/- 1.9 days) (p < 0.01) and patients with associated anomalies stayed in the hospital the longest (6.5 +/- 4.7 days) (p < 0.01). Modern methods of surgical treatment allow reduction of hospitalization, financial savings to the healthcare system and greater comfort for patients. Our results showed that this is also possible to apply in our environment.
NASA Astrophysics Data System (ADS)
Liu, Wenjing; Xu, Liang
2017-07-01
Based on Center of Orbit Determination in Europe (CODE) global ionospheric map (GIM) data, a statistical analysis of local total electron content (TEC) anomalies before 121 low-depth ( D ≤ 100 km) strong ( M w ≥ 7.0) earthquakes has been made using the sliding median differential calculation method combining with a new approach of image processing technique. The results show that significant local TEC anomalies could be observed 0-6 days before 80 earthquakes, about 66.1% out of the total. The positive anomalies occur more often than negative ones. For 26 cases, both positive and negative anomalies are observed before the shock. The pre-earthquake TEC anomalies show local time recurrence for 38 earthquakes, which occur around the same local time on different days. The local time distribution of the pre-earthquake TEC anomalies mainly concentrates between 19 and 06 LT, roughly from the sunset to sunrise. Most of the pre-earthquake TEC anomalies do not locate above the epicenter but shift to the south. The pre-earthquake TEC anomalies could be extracted near the magnetic conjugate point of the epicenter for 40 events, which is 50% out of the total 80 cases with significant local TEC anomalies. In general, the signs of the anomalies around epicenter and its conjugate point are the same, but the abnormal magnitude and lasting time are not.
Prevalence of dental anomalies in the permanent dentition of children with Down syndrome.
Sekerci, Ahmet Ercan; Cantekin, Kenan; Aydinbelge, Mustafa; Ucar, Faruk İzzet
2014-01-01
The purpose of this study was to evaluate the prevalence of various congenital dental anomalies in the permanent dentition of Turkish children with Down syndrome. The sample consisted of 216 diagnostic records of children diagnosed with Down syndrome. All subjects had a clinical examination as well as radiographs and photographs taken. Anomalies in the permanent dentition were documented. There was a high incidence of dental anomalies, the most frequent being taurodontism (81 percent), rotation (28 percent), hypodontia (26 percent), tooth impaction (18 percent), ectopic eruption (14 percent), microdontia (13 percent), and hyperdontia (9 percent). Differences in prevalence of congenitally missing teeth, structural anomalies, and positional anomalies reached a statistically significant level regarding gender (P<.05). Turkish children with Down syndrome presented a high incidence of anomalies affecting the permanent dentition, and, in most cases, individuals presented with more than one anomaly.
Satellite GN and C Anomaly Trends
NASA Technical Reports Server (NTRS)
Robertson, Brent; Stoneking, Eric
2003-01-01
On-orbit anomaly records for satellites launched from 1990 through 2001 are reviewed to determine recent trends of un-manned space mission critical failures. Anomalies categorized by subsystems show that Guidance, Navigation and Control (GN&C) subsystems have a high number of anomalies that result in a mission critical failure when compared to other subsystems. A mission critical failure is defined as a premature loss of a satellite or loss of its ability to perform its primary mission during its design life. The majority of anomalies are shown to occur early in the mission, usually within one year from launch. GN&C anomalies are categorized by cause and equipment type involved. A statistical analysis of the data is presented for all anomalies compared with the GN&C anomalies for various mission types, orbits and time periods. Conclusions and recommendations are presented for improving mission success and reliability.
Blaser, Nicole; Guskov, Sergei I; Entin, Vladimir A; Wolfer, David P; Kanevskyi, Valeryi A; Lipp, Hans-Peter
2014-11-15
The gravity vector theory postulates that birds determine their position to set a home course by comparing the memorized gravity vector at the home loft with the local gravity vector at the release site, and that they should adjust their flight course to the gravity anomalies encountered. As gravity anomalies are often intermingled with geomagnetic anomalies, we released experienced pigeons from the center of a strong circular gravity anomaly (25 km diameter) not associated with magnetic anomalies and from a geophysical control site, equidistant from the home loft (91 km). After crossing the border zone of the anomaly--expected to be most critical for pigeon navigation--they dispersed significantly more than control birds, except for those having met a gravity anomaly en route. These data increase the credibility of the gravity vector hypothesis. © 2014. Published by The Company of Biologists Ltd.
NASA Astrophysics Data System (ADS)
Greene, John A.; Tominaga, Masako; Miller, Nathaniel C.; Hutchinson, Deborah R.; Karl, Matthew R.
2017-11-01
To investigate the oceanic lithosphere formation and early seafloor spreading history of the North Atlantic Ocean, we examine multiscale magnetic anomaly data from the Jurassic/Early Cretaceous age Eastern North American Margin (ENAM) between 31 and 40°N. We integrate newly acquired sea surface magnetic anomaly and seismic reflection data with publicly available aeromagnetic and composite magnetic anomaly grids, satellite-derived gravity anomaly, and satellite-derived and shipboard bathymetry data. We evaluate these data sets to (1) refine magnetic anomaly correlations throughout the ENAM and assign updated ages and chron numbers to M0-M25 and eight pre-M25 anomalies; (2) identify five correlatable magnetic anomalies between the East Coast Magnetic Anomaly (ECMA) and Blake Spur Magnetic Anomaly (BSMA), which may document the earliest Atlantic seafloor spreading or synrift magmatism; (3) suggest preexisting margin structure and rifting segmentation may have influenced the seafloor spreading regimes in the Atlantic Jurassic Quiet Zone (JQZ); (4) suggest that, if the BSMA source is oceanic crust, the BSMA may be M series magnetic anomaly M42 ( 168.5 Ma); (5) examine the along and across margin variation in seafloor spreading rates and spreading center orientations from the BSMA to M25, suggesting asymmetric crustal accretion accommodated the straightening of the ridge from the bend in the ECMA to the more linear M25; and (6) observe anomalously high-amplitude magnetic anomalies near the Hudson Fan, which may be related to a short-lived propagating rift segment that could have helped accommodate the crustal alignment during the early Atlantic opening.
Dental anomalies associated with cleft lip and palate in Northern Finland.
Lehtonen, V; Anttonen, V; Ylikontiola, L P; Koskinen, S; Pesonen, P; Sándor, G K
2015-12-01
Despite the reported occurrence of dental anomalies of cleft lip and palate, little is known about their prevalence in children from Northern Finland with cleft lip and palate. The aim was to investigate the prevalence of dental anomalies among patients with different types of clefts in Northern Finland. Design and Statistics: patient records of 139 subjects aged three years and older (with clefts treated in Oulu University Hospital, Finland during the period 1996-2010 (total n. 183) were analysed for dental anomalies including the number of teeth, morphological and developmental anomalies and their association with the cleft type. The analyses were carried out using Chi-square test and Fisher's exact test. Differences between the groups were considered statistically significant at p values < 0.05. More than half of the patients had clefts of the hard palate, 18% of the lip and palate, and 13% of the lip. At least one dental anomaly was detected in 47% of the study population. Almost one in three (26.6%) subjects had at least one anomaly and 17.9% had two or three anomalies. The most common type of anomaly in permanent teeth were missing teeth followed by supernumerary teeth. Supernumerary teeth were significantly more apparent when the lip was involved in the cleft compared with palatal clefts. Missing teeth were less prevalent among those 5 years or younger. The prevalence of different anomalies was significantly associated with the cleft type in both age groups. Dental anomalies are more prevalent among cleft children than in the general population in Finland. The most prevalent anomalies associated with cleft were missing and supernumerary teeth.
Greene, John A.; Tominaga, Masako; Miller, Nathaniel; Hutchinson, Deborah; Karl, Matthew R.
2017-01-01
To investigate the oceanic lithosphere formation and early seafloor spreading history of the North Atlantic Ocean, we examine multiscale magnetic anomaly data from the Jurassic/Early Cretaceous age Eastern North American Margin (ENAM) between 31 and 40°N. We integrate newly acquired sea surface magnetic anomaly and seismic reflection data with publicly available aeromagnetic and composite magnetic anomaly grids, satellite-derived gravity anomaly, and satellite-derived and shipboard bathymetry data. We evaluate these data sets to (1) refine magnetic anomaly correlations throughout the ENAM and assign updated ages and chron numbers to M0–M25 and eight pre-M25 anomalies; (2) identify five correlatable magnetic anomalies between the East Coast Magnetic Anomaly (ECMA) and Blake Spur Magnetic Anomaly (BSMA), which may document the earliest Atlantic seafloor spreading or synrift magmatism; (3) suggest preexisting margin structure and rifting segmentation may have influenced the seafloor spreading regimes in the Atlantic Jurassic Quiet Zone (JQZ); (4) suggest that, if the BSMA source is oceanic crust, the BSMA may be M series magnetic anomaly M42 (~168.5 Ma); (5) examine the along and across margin variation in seafloor spreading rates and spreading center orientations from the BSMA to M25, suggesting asymmetric crustal accretion accommodated the straightening of the ridge from the bend in the ECMA to the more linear M25; and (6) observe anomalously high-amplitude magnetic anomalies near the Hudson Fan, which may be related to a short-lived propagating rift segment that could have helped accommodate the crustal alignment during the early Atlantic opening.
Case report: a branchial cleft anomaly presenting as an oropharyngeal mass.
Mullin, David; Merz, Meredith
2011-12-01
Branchial anomalies are common cervical pathologic entities encountered in the field of otolaryngology and are typical in the pediatric and young adult populations. In most cases, these anomalies present as a cyst, sinus, or fistula in a rather stereotypical fashion. When a branchial anomaly deviates from the classic presentation, an improper diagnosis and inadequate management are more likely to occur, leading to an increased recurrence rate. We present a case of a 6-year-old girl with an incidental finding of a right posterior oropharyngeal wall mass, distinctly separate from the tonsillar fossa, which was found on pathologic analysis to be a branchial cleft anomaly. The theories regarding the pathogenesis of branchial anomalies are presented, along with other cases of atypical branchial anomalies.
Preliminary correlations of MAGSAT anomalies with tectonic features of Africa
Hastings, David A.
1982-01-01
An overview of the MAGSAT scalar anomaly map for Africa has suggested a correlation of MAGSAT anomalies with major crustal blocks of uplift or depression and different degrees of regional metamorphism. The strongest MAGSAT anomalies in Africa are closely correlated spatially with major tectonic features. Although a magnetic anomaly caused by a rectangular crustal block would be offset from the block's center by the effects of magnetic inclination, an anomaly caused by real crustal blocks of varying uplift, depression, and degree of regional metamorphism would be located nearer to the locus of greatest vertical movement and highest grade of metamorphism. Thus, the Bangui anomaly may be caused by a central old Precambrian shield, flanked to the north and south by two relatively young sedimentary basins.
Damaske, D.; Läufer, A.L.; Goldmann, F.; Möller, H.-D.; Lisker, F.
2007-01-01
An aeromagnetic survey was flown over the offshore region northeast of Cape Adare and the magnetic anomalies compared to onshore structures between Pennell Coast and Tucker Glacier. The magnetic anomalies show two nearly orthogonal major trends. NNW-SSE trending anomalies northeast of Cape Adare represent seafloor spreading within the Adare Trough. A connection of these anomalies to the Northern Basin of the Ross Sea is not clear. Onshore faults are closely aligned to offshore anomalies. Main trends are NW-SE to NNW-SSE and NE-SW to NNESSW. NNW-SSE oriented dextral-transtensional to extensional faults parallel the Adare Peninsula and Adare Trough anomalies. NE-SW trending normal faults appear to segment the main Hallett volcanic bodies.
Presentation and Treatment of Poland Anomaly.
Buckwalter V, Joseph A; Shah, Apurva S
2016-12-01
Background: Poland anomaly is a sporadic, phenotypically variable congenital condition usually characterized by unilateral pectoral muscle agenesis and ipsilateral hand deformity. Methods: A comprehensive review of the medical literature on Poland anomaly was performed using a Medline search. Results: Poland anomaly is a sporadic, phenotypically variable congenital condition usually characterized by unilateral, simple syndactyly with ipsilateral limb hypoplasia and pectoralis muscle agenesis. Operative management of syndactyly in Poland anomaly is determined by the severity of hand involvement and the resulting anatomical dysfunction. Syndactyly reconstruction is recommended in all but the mildest cases because most patients with Poland anomaly have notable brachydactyly, and digital separation can improve functional length. Conclusions: Improved understanding the etiology and presentation of Poland anomaly can improve clinician recognition and management of this rare congenital condition.
NASA Astrophysics Data System (ADS)
Fucugauchi, J. U.; Lopez-Loera, H.; Rebolledo-Vieyra, M.
2011-12-01
We present the initial results of a low-altitude high-resolution aeromagnetic study over the Yucatan peninsula. Area surveyed extends from 86W to 91W and 18N to 21N, covering the peninsula and adjacent continental margin of Gulf of Mexico and Caribbean Sea. Aeromagnetic surveys are integrated into a regional map, and regional and residual anomalies are separated using spectral and least-squares methods. For the study, aeromagnetic field was reduced to the pole and several data filtering techniques were used, including first and second vertical derivatives, analytical signal, and upward and downward analytical continuations. The region is characterized by large amplitude broad elongated magnetic anomalies oriented north-south in the northern sector of the continental shelf, and northwest-southeast and northeast-southwest over the western and eastern sides of the peninsula, respectively. Major regional anomalies extend from the continental shelf into the peninsula, whereas other anomaly trends in the central northern sector, at northeast limit of Chicxulub crater, are restricted to the shelf. Largest anomaly on the east extends over the Holbox fracture zone. At its southern end, south of Chetumal a parallel trend extends over the Rio Hondo fault zone between Quintana Roo and Belize. On the western peninsula the anomaly is characterized by two parallel trends offset between Yucatan and Campeche. The central zone of Chicxulub is characterized by a semi-circular anomaly pattern, surrounded by long wavelength small amplitude anomalies extending to the east on the peninsula and shelf, isolated from the regional broad anomalies. To the south of Chicxulub anomaly, there is an elongated low with a central high extending southward from the terrace zone inside the crater rim. The elongated magnetic anomaly correlates with a broad gravity low, which is apparent south of the concentric zone of anomalies. To the north of Chicxulub anomaly, a magnetic high inside the crater is followed by a low outside, which extend to the north and northwest. The regional broad anomalies crossing the peninsula and shelf are interpreted as crustal structures on the Yucatan block related to pre- and rifting deformation, which include basement uplift. The southward elongated magnetic anomaly and gravity low may correspond to a pre-impact structure. From analysis of residual anomalies, we found no clear indication of secondary craters or multiple impacts.
Clinical Study of Second Branchial Cleft Anomalies.
Lee, Dong Hoon; Yoon, Tae Mi; Lee, Joon Kyoo; Lim, Sang Chul
2018-03-30
The objective of this study was to review the clinical characteristics and surgical treatment outcomes of second branchial cleft anomalies, and to evaluate the usefulness and accuracy of preoperative fine-needle aspiration cytology (FNAC) in the diagnosis of branchial cleft cysts. A retrospective chart review was performed at Chonnam National University Hwasun Hospital from January 2010 to December 2016. Among 25 patients with second branchial cleft anomalies, in 23 patients (92.0%), these anomalies presented as cysts, and in the remaining 2 patients (8.0%), these anomalies presented as fistulas. Fine-needle aspiration cytology had a diagnostic sensitivity of 100%, a positive-predictive value of 100%, and accuracy of 100% for diagnosing second branchial cleft cyst. All patients of second branchial cleft anomalies were treated surgically under general anesthesia. No recurrence of second branchial cleft anomalies was observed. Branchial cleft cysts were the most common type of second branchial cleft anomalies. Preoperative FNAC is a useful and accurate method for preoperative evaluation of branchial cleft cysts. Surgical excision of second branchial cleft anomalies is the treatment of choice without any complications and with no recurrence.
Cervical vertebral anomalies in patients with anomalies of the head and neck.
Manaligod, J M; Bauman, N M; Menezes, A H; Smith, R J
1999-10-01
Congenital head and neck anomalies can occur in association with vertebral anomalies, particularly of the cervical vertebrae. While the former are easily recognized, especially when part of a syndrome, the latter are often occult, thereby delaying their diagnosis. The presence of vertebral anomalies must be considered in pediatric patients with head and neck abnormalities to expedite management of select cases and to prevent neurologic injury. We present our experience with 5 pediatric patients who were referred to the Department of Otolaryngology-Head and Neck Surgery at the University of Iowa with a variety of syndromic anomalies of the head and neck. Each patient was subsequently also found to have a vertebral anomaly. The relevant embryogenesis of the anomalous structures is discussed, with highlighting of potential causes such as teratogenic agents and events and germ-line mutations. A review of syndromes having both head and neck and vertebral anomalies is presented to heighten awareness of otolaryngologists evaluating children with syndromic disorders. Finally, the findings on radiographic imaging studies, particularly computed tomography, are discussed to facilitate the prompt diagnosis of vertebral anomalies.
Improved global prediction of 300 nautical mile mean free air anomalies
NASA Technical Reports Server (NTRS)
Cruz, J. Y.
1982-01-01
Current procedures used for the global prediction of 300nm mean anomalies starting from known values of 1 deg by 1 deg mean anomalies yield unreasonable prediction results when applied to 300nm blocks which have a rapidly varying gravity anomaly field and which contain relatively few observed 60nm blocks. Improvement of overall 300nm anomaly prediction is first achieved by using area-weighted as opposed to unweighted averaging of the 25 generated 60nm mean anomalies inside the 300nm block. Then, improvement of prediction over rough 300nm blocks is realized through the use of fully known 1 deg by 1 deg mean elevations, taking advantage of the correlation that locally exists between 60nm mean anomalies and 60nm mean elevations inside the 300nm block. An improved prediction model which adapts itself to the roughness of the local anomaly field is found to be the model of Least Squares Collocation with systematic parameters, the systematic parameter being the slope b which is a type of Bouguer slope expressing the correlation that locally exists between 60nm mean anomalies and 60nm mean elevations.
NASA Astrophysics Data System (ADS)
Ko, H.; Scheeres, D.
2014-09-01
Representing spacecraft orbit anomalies between two separate states is a challenging but an important problem in achieving space situational awareness for an active spacecraft. Incorporation of such a capability could play an essential role in analyzing satellite behaviors as well as trajectory estimation of the space object. A general way to deal with the anomaly problem is to add an estimated perturbing acceleration such as dynamic model compensation (DMC) into an orbit determination process based on pre- and post-anomaly tracking data. It is a time-consuming numerical process to find valid coefficients to compensate for unknown dynamics for the anomaly. Even if the orbit determination filter with DMC can crudely estimate an unknown acceleration, this approach does not consider any fundamental element of the unknown dynamics for a given anomaly. In this paper, a new way of representing a spacecraft anomaly using an interpolation technique with the Thrust-Fourier-Coefficients (TFCs) is introduced and several anomaly cases are studied using this interpolation method. It provides a very efficient way of reconstructing the fundamental elements of the dynamics for a given spacecraft anomaly. Any maneuver performed by a satellite transitioning between two arbitrary orbital states can be represented as an equivalent maneuver using an interpolation technique with the TFCs. Given unconnected orbit states between two epochs due to a spacecraft anomaly, it is possible to obtain a unique control law using the TFCs that is able to generate the desired secular behavior for the given orbital changes. This interpolation technique can capture the fundamental elements of combined unmodeled anomaly events. The interpolated orbit trajectory, using the TFCs compensating for a given anomaly, can be used to improve the quality of orbit fits through the anomaly period and therefore help to obtain a good orbit determination solution after the anomaly. Orbit Determination Toolbox (ODTBX) is modified to adapt this technique in order to verify the performance of this interpolation approach. Spacecraft anomaly cases are based on either single or multiple low or high thrust maneuvers and the unknown thrust accelerations are recovered and compared with the true thrust acceleration. The advantage of this approach is to easily append TFCs and its dynamics to the pre-built ODTBX, which enables us to blend post-anomaly tracking data to improve the performance of the interpolation representation in the absence of detailed information about a maneuver. It allows us to improve space situational awareness in the areas of uncertainty propagation, anomaly characterization and track correlation.
Climate Analysis of Evaporation Ducts in the South China Sea
2013-12-01
variations that involve anomalies in extratropical and tropical atmospheric longwave patterns. Figure 43 shows the 200 mb GPH anomalies for the extreme...where the two figures overlap, especially in the extratropics (but with the 200 mb anomalies being slightly further to the west than those at 850 mb...barotropic structure. The global anomalies (Figure 43) show clear anomalous extratropical wave trains (e.g., the alternating positive and negative anomalies
Clustering and Recurring Anomaly Identification: Recurring Anomaly Detection System (ReADS)
NASA Technical Reports Server (NTRS)
McIntosh, Dawn
2006-01-01
This viewgraph presentation reviews the Recurring Anomaly Detection System (ReADS). The Recurring Anomaly Detection System is a tool to analyze text reports, such as aviation reports and maintenance records: (1) Text clustering algorithms group large quantities of reports and documents; Reduces human error and fatigue (2) Identifies interconnected reports; Automates the discovery of possible recurring anomalies; (3) Provides a visualization of the clusters and recurring anomalies We have illustrated our techniques on data from Shuttle and ISS discrepancy reports, as well as ASRS data. ReADS has been integrated with a secure online search
Tectonically Induced Anomalies Without Large Earthquake Occurrences
NASA Astrophysics Data System (ADS)
Shi, Zheming; Wang, Guangcai; Liu, Chenglong; Che, Yongtai
2017-06-01
In this study, we documented a case involving large-scale macroscopic anomalies in the Xichang area, southwestern Sichuan Province, China, from May to June of 2002, after which no major earthquake occurred. During our field survey in 2002, we found that the timing of the high-frequency occurrence of groundwater anomalies was in good agreement with those of animal anomalies. Spatially, the groundwater and animal anomalies were distributed along the Anninghe-Zemuhe fault zone. Furthermore, the groundwater level was elevated in the northwest part of the Zemuhe fault and depressed in the southeast part of the Zemuhe fault zone, with a border somewhere between Puge and Ningnan Counties. Combined with microscopic groundwater, geodetic and seismic activity data, we infer that the anomalies in the Xichang area were the result of increasing tectonic activity in the Sichuan-Yunnan block. In addition, groundwater data may be used as a good indicator of tectonic activity. This case tells us that there is no direct relationship between an earthquake and these anomalies. In most cases, the vast majority of the anomalies, including microscopic and macroscopic anomalies, are caused by tectonic activity. That is, these anomalies could occur under the effects of tectonic activity, but they do not necessarily relate to the occurrence of earthquakes.
Orbital Anomalies in Goddard Spacecraft for Calendar Year 1994
NASA Technical Reports Server (NTRS)
Thomas, Walter B.
1996-01-01
This report summarizes and updates the annual on-orbit performance between January I and December 31, 1994, for spacecraft built by or managed by the Goddard Space Flight Center (GSFC). During 1994, GSFC had 27 active orbiting satellites and I Shuttle-launched and retrieved 'free flyer.' There were 310 reported anomalies among 21 satellites and one GSFC instrument (TOMS). GOES-8 accounted for 66 anomalies, and SAMPES reported 155 'anomalies'. Of the 155 anomalies reported for all but SAMPEX, only 4 affected the spacecraft missions 'substantially' or greater, that is, presented a loss of more than 33% of the total missions. The most frequent subsystem anomalies were Instrument/Payload(44), Timing Command and Control(40), and Attitude Control Systems(33). Of the non-SAMPEX anomalies, 29% had no effect on the missions and 28% caused subsystem or instrument degradation and, for another 28%, no anomaly effect on the mission could be determined. Fifty-three percent of non-SAMPEX anomalies could not be classified according to 'type'; the other most common types were 'systemic'(35), 'random'(19), and 'normal or expected operation'(15). Forty percent of the anomalies were not classified according to failure category; the remaining most frequent occurrences were 'design problems'(50) and 'other known problems'(35).
DOE Office of Scientific and Technical Information (OSTI.GOV)
Rostron, B.; Toth, J.
Lenticular reservoirs are accompanied by diagnostic pore-pressure anomalies when situated in a field of formation-fluid flow. Computer simulations have shown that these anomalies depend on the size and shape of the lens, the direction and intensity of flow, and the hydraulic conductivity contrast between the lens and the surrounding rock. Furthermore, the anomalies reflect the position of the petroleum-saturated portion of a lens since hydraulic conductivity is related to hydrocarbon content. Studies to date have shown that for an oil-free lens a pair of oppositely directed, symmetrical pressure anomalies exists. Each pair consists of a positive and a negative anomaly,more » respectively, at the downstream and upstream ends of the lens. A 2000-m long lens could generate a 200-kPa anomaly in a commonly occurring gravity-flow field. A lens that is filled with hydrocarbons will create a lower conductivity reservoir thus causing negative anomalies at the downstream and positive anomalies at the upstream ends of the lens. The paired anomaly for a partially full lens falls in between these two end members. Pore-pressure distributions from drill-stem tests in mature, well-explored regions can be compared to computer-simulated pore-pressure anomaly patterns. Results can be interpreted in terms of the lens geometry and degree of hydrocarbon saturation.« less
FRaC: a feature-modeling approach for semi-supervised and unsupervised anomaly detection.
Noto, Keith; Brodley, Carla; Slonim, Donna
2012-01-01
Anomaly detection involves identifying rare data instances (anomalies) that come from a different class or distribution than the majority (which are simply called "normal" instances). Given a training set of only normal data, the semi-supervised anomaly detection task is to identify anomalies in the future. Good solutions to this task have applications in fraud and intrusion detection. The unsupervised anomaly detection task is different: Given unlabeled, mostly-normal data, identify the anomalies among them. Many real-world machine learning tasks, including many fraud and intrusion detection tasks, are unsupervised because it is impractical (or impossible) to verify all of the training data. We recently presented FRaC, a new approach for semi-supervised anomaly detection. FRaC is based on using normal instances to build an ensemble of feature models, and then identifying instances that disagree with those models as anomalous. In this paper, we investigate the behavior of FRaC experimentally and explain why FRaC is so successful. We also show that FRaC is a superior approach for the unsupervised as well as the semi-supervised anomaly detection task, compared to well-known state-of-the-art anomaly detection methods, LOF and one-class support vector machines, and to an existing feature-modeling approach.
Patek, Kyla J; Kline-Fath, Beth M; Hopkin, Robert J; Pilipenko, Valentina V; Crombleholme, Timothy M; Spaeth, Christine G
2012-01-01
The purpose of this study was to describe the relationship between intracranial and extracranial anomalies and neurodevelopmental outcome for fetuses diagnosed with a posterior fossa anomaly (PFA) on fetal MRI. Cases of Dandy-Walker malformation, vermian hypogenesis/hypoplasia, and mega cisterna magna (MCM) were identified through the Fetal Care Center of Cincinnati between January 2004 and December 2010. Parental interview and retrospective chart review were used to assess neurodevelopmental outcome. Posterior fossa anomalies were identified in 59 fetuses; 9 with Dandy-Walker malformation, 36 with vermian hypogenesis/hypoplasia, and 14 with MCM. Cases with isolated PFAs (14/59) had better outcomes than those with additional anomalies (p = 0.00016), with isolated cases of MCM all being neurodevelopmentally normal. Cases with additional intracranial anomalies had a worse outcome than those without intracranial anomalies (p = 0.00017). The presence of extracranial anomalies increased the likelihood of having a poor outcome (p = 0.00014) as did the identification of an abnormal brainstem (p = 0.00018). Intracranial and extracranial anomalies were good predictors of neurodevelopmental outcome in this study. The prognosis was poor for individuals with an abnormal brainstem, whereas those with isolated MCM had normal neurodevelopmental outcome. © 2012 John Wiley & Sons, Ltd.
NASA Technical Reports Server (NTRS)
Lee, Shihyan; McIntire, Jeff; Oudari, Hassan
2012-01-01
The Visible/Infrared Imager Radiometer Suite (VIIRS) contains six dual gain bands in the reflective solar spectrum. The dual gain bands are designed to switch gain mode at pre-defined thresholds to achieve high resolution at low radiances while maintaining the required dynamic range for science. During pre-launch testing, an anomaly in the electronic response before transitioning from high to low gain was discovered and characterized. On-orbit, the anomaly was confirmed using MODIS data collected during Simultaneous Nadir Overpasses (SNOs). The analysis of the Earth scene data shows that dual gain anomaly can be determined at the orbital basis. To characterize the dual gain anomaly, the anomaly region and electronic offsets were tracked per week during the first 8 month of VIIRS operation. The temporal analysis shows the anomaly region can drift 20 DN and is impacted by detectors DC Restore. The estimated anomaly flagging regions cover 2.5 % of the high gain dynamic range and are consistent with prelaunch and on-orbit LUT. The prelaunch results had a smaller anomaly range (30-50 DN) and are likely the results of more stable electronics from the shorter data collection time. Finally, this study suggests future calibration efforts to focus on the anomaly's impact on science products and possible correction method to reduce uncertainties.
FRaC: a feature-modeling approach for semi-supervised and unsupervised anomaly detection
Brodley, Carla; Slonim, Donna
2011-01-01
Anomaly detection involves identifying rare data instances (anomalies) that come from a different class or distribution than the majority (which are simply called “normal” instances). Given a training set of only normal data, the semi-supervised anomaly detection task is to identify anomalies in the future. Good solutions to this task have applications in fraud and intrusion detection. The unsupervised anomaly detection task is different: Given unlabeled, mostly-normal data, identify the anomalies among them. Many real-world machine learning tasks, including many fraud and intrusion detection tasks, are unsupervised because it is impractical (or impossible) to verify all of the training data. We recently presented FRaC, a new approach for semi-supervised anomaly detection. FRaC is based on using normal instances to build an ensemble of feature models, and then identifying instances that disagree with those models as anomalous. In this paper, we investigate the behavior of FRaC experimentally and explain why FRaC is so successful. We also show that FRaC is a superior approach for the unsupervised as well as the semi-supervised anomaly detection task, compared to well-known state-of-the-art anomaly detection methods, LOF and one-class support vector machines, and to an existing feature-modeling approach. PMID:22639542
Midlatitude atmosphere-ocean interaction during El Nino. Part I. The north Pacific ocean
DOE Office of Scientific and Technical Information (OSTI.GOV)
Alexander, M.A.
Atmosphere-ocean modeling experiments are used to investigate the formation of sea surface temperature (SST) anomalies in the North Pacific Ocean during fall and winter of the El Nino year. Experiments in which the NCAR Community Climate Model (CCM) surface fields are used to force a mixed-layer ocean model in the North Pacific (no air-sea feedback) are compared to simulations in which the CCM and North Pacific Ocean model are coupled. Anomalies in the atmosphere and the North Pacific Ocean during El Nino are obtained from the difference between simulations with and without prescribed warm SST anomalies in the tropical Pacific.more » In both the forced and coupled experiments, the anomaly pattern resembles a composite of the actual SST anomaly field during El Nino: warm SSTs develop along the coast of North America and cold SSTs form in the central Pacific. In the coupled simulations, air-sea interaction results in a 25% to 50% reduction in the magnitude of the SST and mixed-layer depth anomalies, resulting in more realistic SST fields. Coupling also decreases the SST anomaly variance; as a result, the anomaly centers remain statistically significant even though the magnitude of the anomalies is reduced. Three additional sensitivity studies indicate that air-sea feedback and entrainment act to damp SST anomalies while Ekman pumping has a negligible effect on mixed-layer depth and SST anomalies in midatitudes.« less
Linburg-Comstock: Is Overuse an Etiological Factor?
Bulut, Tugrul; Tahta, Mesut; Ozturk, Tahir; Zengin, Eyup Cagatay; Ozcan, Cem; Sener, Muhittin
2017-11-01
Linburg-Comstock anomaly is typically defined as a tenosynovial interconnection between flexor pollicis longus and flexor digitorum profundus tendon of the second finger. There are several studies stating that the current anomaly is congenital or acquired. The aim of this study is to reveal whether overuse, which is mostly reported as an acquired etiologic factor, effective in development of the current anomaly. Three hundred thirteen medical secretaries who work with computer keyboard at least 6 hours a day were defined as study group. Three hundred twenty-three volunteers without jobs who necessitate continuous and repetitive hand and finger activities were defined as control group. All individuals were examined by an orthopaedic surgeon. Additionally, cases with Linburg-Comstock anomaly were evaluated in respect of forearm pain and subjective findings of carpal tunnel syndrome. Linburg-Comstock anomaly was determined in 27.8% cases of medical secretary group and in 32.2% of healthy control group. In medical secretaries with Linburg-Comstock anomaly, 25.3% had forearm pain and 5.7% had findings of carpal tunnel syndrome. In control group with Linburg-Comstock anomaly, 21.2% had forearm pain and 13.5% had findings of carpal tunnel syndrome. No relationship was found between overuse of the hand and Linburg-Comstock anomaly and the symptoms accompanying the anomaly. The current study reveals that overuse is not an etiologic factor in Linburg-Comstock anomaly existence and related symptoms. We think that the current anomaly develops on congenital basis rather than acquired factors.
ERIC Educational Resources Information Center
Online-Offline, 1999
1999-01-01
This theme issue on anomalies includes Web sites, CD-ROMs and software, videos, books, and additional resources for elementary and junior high school students. Pertinent activities are suggested, and sidebars discuss UFOs, animal anomalies, and anomalies from nature; and resources covering unexplained phenonmenas like crop circles, Easter Island,…
NASA Technical Reports Server (NTRS)
Shukla, J.; Moura, A. D.
1980-01-01
The monthly mean sea surface temperature anomalies over tropical Altantic and rainfall anomalies over two selected stations for 25 years (1948-1972) were examined. It is found that the most severe drought events are associated with the simultaneous occurrence of warm sea surface temperature anomalies over north and cold sea surface temperature anomalies over south tropical Atlantic. Simultaneous occurrences of warm sea surface temperature anomaly at 15 deg N, 45 deg W and cold sea surface temperature anomaly at 15 deg S, 5 deg W were always associated with negative anomalies of rainfall, and vice versa. A simple primitive equation model is used to calculate the frictionally controlled and thermally driven circulation due to a prescribed heating function in a resting atmosphere.
NASA Astrophysics Data System (ADS)
Fathrio, Ibnu; Manda, Atsuyoshi; Iizuka, Satoshi; Kodama, Yasu-Masa; Ishida, Sachinobu
2018-05-01
This study presents ocean heat budget analysis on seas surface temperature (SST) anomalies during strong-weak Asian summer monsoon (southwest monsoon). As discussed by previous studies, there was close relationship between variations of Asian summer monsoon and SST anomaly in western Indian Ocean. In this study we utilized ocean heat budget analysis to elucidate the dominant mechanism that is responsible for generating SST anomaly during weak-strong boreal summer monsoon. Our results showed ocean advection plays more important role to initate SST anomaly than the atmospheric prcess (surface heat flux). Scatterplot analysis showed that vertical advection initiated SST anomaly in western Arabian Sea and southwestern Indian Ocean, while zonal advection initiated SST anomaly in western equatorial Indian Ocean.
Presentation and Treatment of Poland Anomaly
Buckwalter V, Joseph A.; Shah, Apurva S.
2016-01-01
Background: Poland anomaly is a sporadic, phenotypically variable congenital condition usually characterized by unilateral pectoral muscle agenesis and ipsilateral hand deformity. Methods: A comprehensive review of the medical literature on Poland anomaly was performed using a Medline search. Results: Poland anomaly is a sporadic, phenotypically variable congenital condition usually characterized by unilateral, simple syndactyly with ipsilateral limb hypoplasia and pectoralis muscle agenesis. Operative management of syndactyly in Poland anomaly is determined by the severity of hand involvement and the resulting anatomical dysfunction. Syndactyly reconstruction is recommended in all but the mildest cases because most patients with Poland anomaly have notable brachydactyly, and digital separation can improve functional length. Conclusions: Improved understanding the etiology and presentation of Poland anomaly can improve clinician recognition and management of this rare congenital condition. PMID:28149203
Barisic, Ingeborg; Odak, Ljubica; Loane, Maria; Garne, Ester; Wellesley, Diana; Calzolari, Elisa; Dolk, Helen; Addor, Marie-Claude; Arriola, Larraitz; Bergman, Jorieke; Bianca, Sebastiano; Doray, Berenice; Khoshnood, Babak; Klungsoyr, Kari; McDonnell, Bob; Pierini, Anna; Rankin, Judith; Rissmann, Anke; Rounding, Catherine; Queisser-Luft, Annette; Scarano, Gioacchino; Tucker, David
2014-01-01
Oculo-auriculo-vertebral spectrum is a complex developmental disorder characterised mainly by anomalies of the ear, hemifacial microsomia, epibulbar dermoids and vertebral anomalies. The aetiology is largely unknown, and the epidemiological data are limited and inconsistent. We present the largest population-based epidemiological study to date, using data provided by the large network of congenital anomalies registries in Europe. The study population included infants diagnosed with oculo-auriculo-vertebral spectrum during the 1990–2009 period from 34 registries active in 16 European countries. Of the 355 infants diagnosed with oculo-auriculo-vertebral spectrum, there were 95.8% (340/355) live born, 0.8% (3/355) fetal deaths, 3.4% (12/355) terminations of pregnancy for fetal anomaly and 1.5% (5/340) neonatal deaths. In 18.9%, there was prenatal detection of anomaly/anomalies associated with oculo-auriculo-vertebral spectrum, 69.7% were diagnosed at birth, 3.9% in the first week of life and 6.1% within 1 year of life. Microtia (88.8%), hemifacial microsomia (49.0%) and ear tags (44.4%) were the most frequent anomalies, followed by atresia/stenosis of external auditory canal (25.1%), diverse vertebral (24.3%) and eye (24.3%) anomalies. There was a high rate (69.5%) of associated anomalies of other organs/systems. The most common were congenital heart defects present in 27.8% of patients. The prevalence of oculo-auriculo-vertebral spectrum, defined as microtia/ear anomalies and at least one major characteristic anomaly, was 3.8 per 100 000 births. Twinning, assisted reproductive techniques and maternal pre-pregnancy diabetes were confirmed as risk factors. The high rate of different associated anomalies points to the need of performing an early ultrasound screening in all infants born with this disorder. PMID:24398798
First branchial cleft anomalies: otologic manifestations and treatment outcomes.
Shinn, Justin R; Purcell, Patricia L; Horn, David L; Sie, Kathleen C Y; Manning, Scott C
2015-03-01
This study describes the presentation of first branchial cleft anomalies and compares outcomes of first branchial cleft with other branchial cleft anomalies with attention to otologic findings. Case series with chart review. Pediatric tertiary care facility. Surgical databases were queried to identify children with branchial cleft anomalies. Descriptive analysis defined sample characteristics. Risk estimates were calculated using Fisher's exact test. Queries identified 126 subjects: 27 (21.4%) had first branchial cleft anomalies, 80 (63.4%) had second, and 19 (15.1%) had third or fourth. Children with first anomalies often presented with otologic complications, including otorrhea (22.2%), otitis media (25.9%), and cholesteatoma (14.8%). Of 80 children with second branchial cleft anomalies, only 3 (3.8%) had otitis. Compared with children with second anomalies, children with first anomalies had a greater risk of requiring primary incision and drainage: 16 (59.3%) vs 2 (2.5%) (relative risk [RR], 3.5; 95% confidence interval [CI], 2.4-5; P<.0001). They were more likely to have persistent disease after primary excision: 7 (25.9%) vs 2 (2.5%) (RR, 3; 95% CI, 1.9-5; P=.0025). They were more likely to undergo additional surgery: 8 (29.6%) vs 3 (11.1%) (RR, 2.9; 95% CI, 1.8-4.7; P=.0025). Of 7 persistent first anomalies, 6 (85.7%) were medial to the facial nerve, and 4 (57.1%) required ear-specific surgery for management. Children with first branchial cleft anomalies often present with otologic complaints. They are at increased risk of persistent disease, particularly if anomalies lie medial to the facial nerve. They may require ear-specific surgery such as tympanoplasty. © American Academy of Otolaryngology—Head and Neck Surgery Foundation 2014.
NASA Technical Reports Server (NTRS)
Taylor, Patrick T.
2004-01-01
Bangui anomaly is the name given to one of the Earth s largest crustal magnetic anomalies and the largest over the African continent. It covers two-thirds of the Central African Republic and therefore the name derives from the capitol city-Bangui that is also near the center of this feature. From surface magnetic survey data Godivier and Le Donche (1962) were the first to describe this anomaly. Subsequently high-altitude world magnetic surveying by the U.S. Naval Oceanographic Office (Project Magnet) recorded a greater than 1000 nT dipolar, peak-to-trough anomaly with the major portion being negative (figure 1). Satellite observations (Cosmos 49) were first reported in 1964, these revealed a 40nT anomaly at 350 km altitude. Subsequently the higher altitude (417-499km) POGO (Polar Orbiting Geomagnetic Observatory) satellite data recorded peak-to-trough anomalies of 20 nT these data were added to Cosmos 49 measurements by Regan et al. (1975) for a regional satellite altitude map. In October 1979, with the launch of Magsat, a satellite designed to measure crustal magnetic anomalies, a more uniform satellite altitude magnetic map was obtained. These data, computed at 375 km altitude recorded a -22 nT anomaly (figure 2). This elliptically shaped anomaly is approximately 760 by 1000 km and is centered at 6%, 18%. The Bangui anomaly is composed of three segments; there are two positive anomalies lobes north and south of a large central negative field. This displays the classic pattern of a magnetic anomalous body being magnetized by induction in a zero inclination field. This is not surprising since the magnetic equator passes near the center of this body.
Congenital neurodevelopmental anomalies in pediatric and young adult cancer.
Wong-Siegel, Jeannette R; Johnson, Kimberly J; Gettinger, Katie; Cousins, Nicole; McAmis, Nicole; Zamarione, Ashley; Druley, Todd E
2017-10-01
Congenital anomalies that are diagnosed in at least 120,000 US infants every year are the leading cause of infant death and contribute to disability and pediatric hospitalizations. Several large-scale epidemiologic studies have provided substantial evidence of an association between congenital anomalies and cancer risk in children, suggesting potential underlying cancer-predisposing conditions and the involvement of developmental genetic pathways. Electronic medical records from 1,107 pediatric, adolescent, and young adult oncology patients were reviewed. The observed number (O) of congenital anomalies among children with a specific pediatric cancer subtype was compared to the expected number (E) of anomalies based on the frequency of congenital anomalies in the entire study population. The O/E ratios were tested for significance using Fisher's exact test. The Kaplan-Meier method was used to compare overall and neurological malignancy survival rates following tumor diagnosis. Thirteen percent of patients had a congenital anomaly diagnosis prior to their cancer diagnosis. When stratified by congenital anomaly subtype, there was an excess of neurological anomalies among children with central nervous system tumors (O/E = 1.56, 95%CI 1.13-2.09). Male pediatric cancer patients were more likely than females to have a congenital anomaly, particularly those <5 years of age (O/E 1.35, 95%CI 0.97-1.82). Our study provides additional insight into the association between specific congenital anomaly types and pediatric cancer development. Moreover, it may help to inform the development of new screening policies and support hypothesis-driven research investigating mechanisms underlying tumor predisposition in children with congenital anomalies. © 2017 The Authors. American Journal of Medical Genetics Part A Published by Wiley Periodicals, Inc.
Spectrum of Dental Phenotypes in Nonsyndromic Orofacial Clefting.
Howe, B J; Cooper, M E; Vieira, A R; Weinberg, S M; Resick, J M; Nidey, N L; Wehby, G L; Marazita, M L; Moreno Uribe, L M
2015-07-01
Children with oral clefts show a wide range of dental anomalies, adding complexity to understanding the phenotypic spectrum of orofacial clefting. The evidence is mixed, however, on whether the prevalence of dental anomalies is elevated in unaffected relatives and is mostly based on small samples. In the largest international cohort to date of children with nonsyndromic clefts, their relatives, and controls, this study characterizes the spectrum of cleft-related dental anomalies and evaluates whether families with clefting have a significantly higher risk for such anomalies compared with the general population. A total of 3,811 individuals were included: 660 cases with clefts, 1,922 unaffected relatives, and 1,229 controls. Dental anomalies were identified from in-person dental exams or intraoral photographs, and case-control differences were tested using χ(2) statistics. Cases had higher rates of dental anomalies in the maxillary arch than did controls for primary (21% vs. 4%, P = 3 × 10(-8)) and permanent dentitions (51% vs. 8%, P = 4 × 10(-62)) but not in the mandible. Dental anomalies were more prevalent in cleft lip with cleft palate than other cleft types. More anomalies were seen in the ipsilateral side of the cleft. Agenesis and tooth displacements were the most common dental anomalies found in case probands for primary and permanent dentitions. Compared with controls, unaffected siblings (10% vs. 2%, P = 0.003) and parents (13% vs. 7%, P = 0.001) showed a trend for increased anomalies of the maxillary permanent dentition. Yet, these differences were nonsignificant after multiple-testing correction, suggesting genetic heterogeneity in some families carrying susceptibility to both overt clefts and dental anomalies. Collectively, the findings suggest that most affected families do not have higher genetic risk for dental anomalies than the general population and that the higher prevalence of anomalies in cases is primarily a physical consequence of the cleft and surgical interventions. © International & American Associations for Dental Research 2015.
The association of spacecraft anomalies with electron/proton particle fluxes at different orbits
NASA Astrophysics Data System (ADS)
Yi, K.; Moon, Y. J.
2016-12-01
In this study, we investigate 195 satellite anomaly data from 1998 to 2010 from Satellite News Digest (SND) to understand the association between spacecraft anomaly and space weather condition. The spacecraft anomalies are classified into Attitude & Propulsion, Power, Control, Telemetry, Instrument and unknown. For the investigation we divide these data according to the spacecraft orbit and launched year. Spacecraft's orbits are classified into the following two groups : (1) high altitude and low inclination, and (2) low altitude and high inclination. Launched year of spacecraft are divided into two groups: 1991 1998 and 1999 2007. We examine the association between these anomaly data and daily peak particle (electron and proton) flux data from GOES as well as their occurrence rates. To determine the association, we use two criteria that electron criterion is >10,000 pfu and proton criterion is >100 pfu. Main results from this study are as follows. First, the number of days satisfying the criteria for electron flux has a peak near a week before the anomaly day and decreases from the peak day to the anomaly day, while that for proton flux has a peak near the anomaly day. Second, we found a similar pattern for the mean daily peak particle (electron and proton) flux as a function of day before the anomaly day. Third, an examination of multiple spacecraft anomaly events, which are likely to occur by severe space weather effects, shows that anomalies mostly occur either when electron fluxes are in the declining stage, or when daily proton peak fluxes are strongly enhanced. Fourth, the time delay between the anomaly day and the day having the highest daily peak electron flux for the recent launching period (1999-2007) is noticeably larger than those for the older periods, implying that the anomaly characteristics associated with electron flux change with time.
Anomaly Resolution in the International Space Station
NASA Technical Reports Server (NTRS)
Evans, William A.
2000-01-01
Topics include post flight 2A status, groundrules, anomaly resolution, Early Communications Subsystem anomaly and resolution, Logistics and Maintenance plan, case for obscuration, case for electrical short, and manual fault isolation, and post mission analysis. Photographs from flight 2A.1 are used to illustrate anomalies.
Conditional anomaly detection methods for patient–management alert systems
Valko, Michal; Cooper, Gregory; Seybert, Amy; Visweswaran, Shyam; Saul, Melissa; Hauskrecht, Milos
2010-01-01
Anomaly detection methods can be very useful in identifying unusual or interesting patterns in data. A recently proposed conditional anomaly detection framework extends anomaly detection to the problem of identifying anomalous patterns on a subset of attributes in the data. The anomaly always depends (is conditioned) on the value of remaining attributes. The work presented in this paper focuses on instance–based methods for detecting conditional anomalies. The methods rely on the distance metric to identify examples in the dataset that are most critical for detecting the anomaly. We investigate various metrics and metric learning methods to optimize the performance of the instance–based anomaly detection methods. We show the benefits of the instance–based methods on two real–world detection problems: detection of unusual admission decisions for patients with the community–acquired pneumonia and detection of unusual orders of an HPF4 test that is used to confirm Heparin induced thrombocytopenia — a life–threatening condition caused by the Heparin therapy. PMID:25392850
The prevalence of dental anomalies in a turkish population.
Aren, Gamze; Guven, Yeliz; Guney Tolgay, Ceren; Ozcan, Ilknur; Bayar, Ozlem Filiz; Kose, Taha Emre; Koyuncuoglu, Gulhan; Ak, Gulsum
2015-01-01
The aim of the present study was to investigate the prevalence of dental anomalies in a Turkish population according to the gender and age. A retrospective study was performed using panoramic radiographs of 2025 patients (885 males and 1140 females) ranging in age from 9 to 35 (mean age 25.61±10.04) years attending Department of Oral Radiology, University of Istanbul, Faculty of Dentistry. These patients were examined to determine the presence of developmental dental anomalies involving hypodontia, hyperdontia, microdontia, taurodontism and other root anomalies. The incidence of these anomalies were assessed according to the gender and age. Among the 2025 subjects, a total of 96 individuals (42 males and 54 females) showed at least one of the selected dental anomalies (4.74%). Tooth agenesis was the most common dental abnormality (1.77%) followed by taurodontism (1.18%), hyperdontia (0.79%), microdontia (0.54%) and root anomalies (0.44%), respectively. Tooth agenesis is the most common developmental dental anomaly in the studied Turkish population followed by taurodontism.
2017-01-01
The persistence of atmospheric circulation anomalies over East Asia shows a winter to winter recurrence (WTWR) phenomenon. Seasonal variations in sea level pressure anomalies and surface wind anomalies display significantly different characteristics between WTWR and non-WTWR years. The WTWR years are characterized by the recurrence of both a strong (weak) anomalous Siberian High and an East Asian winter monsoon over two successive winters without persistence through the intervening summer. However, anomalies during the non-WTWR years have the opposite sign between the current and ensuing winters. The WTWR of circulation anomalies contributes to that of surface air temperature anomalies (SATAs), which is useful information for improving seasonal and interannual climate predictions over East Asia and China. In the positive (negative) WTWR years, SATAs are cooler (warmer) over East Asia in two successive winters, but the signs of the SATAs are opposite in the preceding and subsequent winters during the non-WTWR years. PMID:28178351
Zhao, Xia; Yang, Guang
2017-01-01
The persistence of atmospheric circulation anomalies over East Asia shows a winter to winter recurrence (WTWR) phenomenon. Seasonal variations in sea level pressure anomalies and surface wind anomalies display significantly different characteristics between WTWR and non-WTWR years. The WTWR years are characterized by the recurrence of both a strong (weak) anomalous Siberian High and an East Asian winter monsoon over two successive winters without persistence through the intervening summer. However, anomalies during the non-WTWR years have the opposite sign between the current and ensuing winters. The WTWR of circulation anomalies contributes to that of surface air temperature anomalies (SATAs), which is useful information for improving seasonal and interannual climate predictions over East Asia and China. In the positive (negative) WTWR years, SATAs are cooler (warmer) over East Asia in two successive winters, but the signs of the SATAs are opposite in the preceding and subsequent winters during the non-WTWR years.
Barium and neodymium isotopic anomalies in the Allende meteorite
NASA Technical Reports Server (NTRS)
Mcculloch, M. T.; Wasserburg, G. J.
1978-01-01
The discovery of Ba and Nd isotopic anomalies in two inclusions from the Allende meteorite is reported. The inclusions are Ca-Al-rich objects typical of the type considered as high-temperature condensation products in the solar nebula and contain distinctive Mg and O isotopic anomalies of the FUN (mass Fractionation, Unknown Nuclear processes) type. Mass-spectrometry results are discussed which show that inclusion C1 has anomalies in Ba at masses 134 and 136, while inclusion EK1-4-1 exhibits large marked negative anomalies at 130, 132, 134, and 136, as well as a positive anomaly at 137. It is also found that inclusion EK1-4-1 shows marked negative anomalies in Nd at masses 142, 146, 148, and 150, in addition to a positive anomaly at 145. These isotopic shifts are attributed to addition of r-process nuclei rather than mass fractionation. It is suggested that an onion-shell supernova explosion followed by injection into the solar nebula is the most likely generic model that may explain the observations.
Congenital hand anomalies in Upper Egypt
Abulezz, Tarek; Talaat, Mohamed; Elsani, Asem; Allam, Karam
2016-01-01
Background: Congenital hand anomalies are numerous and markedly variant. Their significance is attributed to the frequent occurrence and their serious social, psychological and functional impacts on patient's life. Patients and Methods: This is a follow-up study of 64 patients with hand anomalies of variable severity. All patients were presented to Plastic Surgery Department of Sohag University Hospital in a period of 24 months. Results: This study revealed that failure of differentiation and duplication deformities were the most frequent, with polydactyly was the most common anomaly encountered. The mean age of presentation was 6 years and female to male ratio was 1.46:1. Hand anomalies were either isolated, associated with other anomalies or part of a syndrome. Conclusion: Incidence of congenital hand anomalies in Upper Egypt is difficult to be estimated due to social and cultural concepts, lack of education, poor registration and deficient medical survey. Management of hand anomalies should be individualised, carefully planned and started as early as possible to achieve the best outcome. PMID:27833283
Indo-Pacific sea level variability during recent decades
NASA Astrophysics Data System (ADS)
Yamanaka, G.; Tsujino, H.; Nakano, H.; Urakawa, S. L.; Sakamoto, K.
2016-12-01
Decadal variability of sea level in the Indo-Pacific region is investigated using a historical OGCM simulation. The OGCM driven by the atmospheric forcing removing long-term trends clearly exhibits decadal sea level variability in the Pacific Ocean, which is associated with eastern tropical Pacific thermal anomalies. During the period of 1977-1987, the sea level anomalies are positive in the eastern equatorial Pacific and show deviations from a north-south symmetric distribution, with strongly negative anomalies in the western tropical South Pacific. During the period of 1996-2006, in contrast, the sea level anomalies are negative in the eastern equatorial Pacific and show a nearly north-south symmetric pattern, with positive anomalies in both hemispheres. Concurrently, sea level anomalies in the south-eastern Indian Ocean vary with those in the western tropical Pacific. These sea level variations are closely related to large-scale wind fields. Indo-Pacific sea level distributions are basically determined by wind anomalies over the equatorial region as well as wind stress curl anomalies over the off-equatorial region.
Detailed gravity anomalies from Geos 3 satellite altimetry data
NASA Technical Reports Server (NTRS)
Gopalapillai, G. S.; Mourad, A. G.
1979-01-01
Detailed gravity anomalies are computed from a combination of Geos 3 satellite altimeter and terrestrial gravity data using least-squares principles. The mathematical model used is based on the Stokes' equation modified for a nonglobal solution. Using Geos 3 data in the calibration area, the effects of several anomaly parameter configurations and data densities/distributions on the anomalies and their accuracy estimates are studied. The accuracy estimates for 1 deg x 1 deg mean anomalies from low density altimetry data are of the order of 4 mgal. Comparison of these anomalies with the terrestrial data and also with Rapp's data derived using collocation techniques show rms differences of 7.2 and 4.9 mgal, respectively. Indications are that the anomaly accuracies can be improved to about 2 mgal with high density data. Estimation of 30 in. x 30 in. mean anomalies indicates accuracies of the order of 5 mgal. Proper verification of these results will be possible only when accurate ground truth data become available.
3D P-Wave Velocity Structure of the Crust and Relocation of Earthquakes in 21 the Lushan Source Area
NASA Astrophysics Data System (ADS)
Yu, X.; Wang, X.; Zhang, W.
2014-12-01
The double difference seismic tomography method is applied to the absolute first arrival P wave arrival times and high quality relative P arrival times of the Lushan seismic sequence to determine the detailed crustal 3D P wave velocity structure and the hypocenter parameters in the Lushan seismic area. The results show that the Lushan mainshock locates at 30.28 N, 103.98 E, with the depth of 16.38 km. The leading edge of aftershock in the northeast of mainshock present a spade with a steep dip angle, the aftershocks' extended length is about 12 km. In the southwest of the Lushan mainshock, the leading edge of aftershock in low velocity zone slope gently, the aftershocks' extended length is about 23 km. The P wave velocity structure of the Lushan seismic area shows obviously lateral heterogeneity. The P wave velocity anomalies represent close relationship with topographic relief and geological structure. In Baoxing area the complex rocks correspond obvious high-velocity anomalies extending down to 15 km depth,while the Cenozoic rocks are correlated with low-velocity anomalies. Our high-resolution tomographic model not only displays the general features contained in the previous models, but also reveals some new features. An obvious high-velocity anomaly is visible in Daxing area. The high-velocity anomalies beneath Baoxing and Daxing connect each other in 10 km depth, which makes the contrast between high and low velocity anomalies more sharp. Above 20 km depth the velocity structure in southwest and northeast segment of the mainshock shows a big difference: low-velocity anomalies are dominated the southwest segment, while high-velocity anomalies rule the northeast segment. The Lushan mainshock locates at the leading edge of a low-velocity anomaly surrounded by the Baoxing and Daxing high-velocity anomalies. The Lushan aftershocks in southwest are distributed in low-velocity anomalies or the transition belt: the footwall represents low-velocity anomalies, while the hanging wall shows high-velocity anomalies. The northeastern aftershocks are distributed at the boundary between high-velocity anomalies in Baoxing and Daxing area. The main seismogenic layer dips to northwest.
Global anomalies and effective field theory
DOE Office of Scientific and Technical Information (OSTI.GOV)
Golkar, Siavash; Sethi, Savdeep
2016-05-17
Here, we show that matching anomalies under large gauge transformations and large diffeomorphisms can explain the appearance and non-renormalization of couplings in effective field theory. We focus on thermal effective field theory, where we argue that the appearance of certain unusual Chern-Simons couplings is a consequence of global anomalies. As an example, we show that a mixed global anomaly in four dimensions fixes the chiral vortical effect coefficient (up to an overall additive factor). This is an experimentally measurable prediction from a global anomaly. For certain situations, we propose a simpler method for calculating global anomalies which uses correlation functionsmore » rather than eta invariants.« less
Neonate with VACTERL Association and a Branchial Arch Anomaly without Hydrocephalus
Velazquez, Danitza; Pereira, Elaine; Havranek, Thomas
2015-01-01
VACTERL (vertebral anomalies, anal atresia, cardiac defect, tracheoesophageal fistula, renal anomaly, limb anomalies) is an association of anomalies with a wide spectrum of phenotypic expression. While the majority of cases are sporadic, there is evidence of an inherited component in a small number of patients as well as the potential influence of nongenetic risk factors (maternal diabetes mellitus). Presence of hydrocephalus has been reported in VACTERL patients (VACTERL-H) in the past, with some displaying branchial arch anomalies. We report the unique case of an infant of diabetic mother with VACTERL association and a branchial arch anomaly—in the absence of hydrocephalus. PMID:26929876
NASA Technical Reports Server (NTRS)
Ruder, M. E.; Alexander, S. S.
1985-01-01
The MAGSAT equivalent-source anomaly field evaluated at 325 km altitude depicts a prominent anomaly centered over southeast Georgia, which is adjacent to the high-amplitude positive Kentucky anomaly. To overcome the satellite resolution constraint in studying this anomaly, conventional geophysical data were included in analysis: Bouguer gravity, seismic reflection and refraction, aeromagnetic, and in-situ stress-strain measurements. This integrated geophysical approach, infers more specifically the nature and extent of the crustal and/or lithospheric source of the Georgia MAGSAT anomaly. Physical properties and tectonic evolution of the area are all important in the interpretation.
Iron formations as the source of the West African magnetic crustal anomaly
NASA Astrophysics Data System (ADS)
Launay, Nicolas; Quesnel, Yoann; Rochette, Pierre; Demory, François
2018-04-01
The geological sources of major magnetic field anomalies are still poorly constrained, in terms of nature, geometry and vertical position. A common feature of several anomalies is their spatial correlation with cratonic shields and, for the largest anomalies, with Banded Iron Formations (BIF). This study first unveils the magnetic properties of some BIF samples from Mauritania, where the main part of the West African magnetic anomaly is observed. It shows how strong the magnetic susceptibility and natural remanent magnetization for such rocks are. High Koenigsberger ratios imply that the remanent magnetization should be taken into account to explain the anomaly. A numerical modeling of the crust beneath this anomaly is performed using these constraints and both gravity and magnetic field data. A forward approach is used, investigating the depth, thickness and magnetization intensity of all possible crustal lithologies. Our results show that BIF slices can be the only magnetized crustal sources needed to explain the anomaly, and that they could be buried several kilometers deep. The results of this study provide a new perspective to address the investigation of magnetic field anomaly sources in other cratonic regions with BIF outcrops.
Long-wavelength Magnetic and Gravity Anomaly Correlations of Africa and Europe
NASA Technical Reports Server (NTRS)
Vonfrese, R. R. B.; Hinze, W. J. (Principal Investigator); Olivier, R.
1984-01-01
Preliminary MAGSAT scalar magnetic anomaly data were compiled for comparison with long-wavelength-pass filtered free-air gravity anomalies and regional heat-flow and tectonic data. To facilitate the correlation analysis at satellite elevations over a spherical-Earth, equivalent point source inversion was used to differentially reduce the magnetic satellite anomalies to the radial pole at 350 km elevation, and to upward continue the first radial derivative of the free-air gravity anomalies. Correlation patterns between these regional geopotential anomaly fields are quantitatively established by moving window linear regression based on Poisson's theorem. Prominent correlations include direct correspondences for the Baltic Shield, where both anomalies are negative, and the central Mediterranean and Zaire Basin where both anomalies are positive. Inverse relationships are generally common over the Precambrian Shield in northwest Africa, the Basins and Shields in southern Africa, and the Alpine Orogenic Belt. Inverse correlations also presist over the North Sea Rifts, the Benue Rift, and more generally over the East African Rifts. The results of this quantitative correlation analysis support the general inverse relationships of gravity and magnetic anomalies observed for North American continental terrain which may be broadly related to magnetic crustal thickness variations.
Long-wavelength magnetic and gravity anomaly correlations on Africa and Europe
NASA Technical Reports Server (NTRS)
Vonfrese, R. R. B.; Olivier, R.; Hinze, W. J.
1985-01-01
Preliminary MAGSAT scalar magnetic anomaly data were compiled for comparison with long-wavelength-pass filtered free-air gravity anomalies and regional heat-flow and tectonic data. To facilitate the correlation analysis at satellite elevations over a spherical-Earth, equivalent point source inversion was used to differentially reduce the magnetic satellite anomalies to the radial pole at 350 km elevation, and to upward continue the first radial derivative of the free-air gravity anomalies. Correlation patterns between these regional geopotential anomaly fields are quantitatively established by moving window linear regression based on Poisson's theorem. Prominent correlations include direct correspondences for the Baltic shield, where both anomalies are negative, and the central Mediterranean and Zaire Basin where both anomalies are positive. Inverse relationships are generally common over the Precambrian Shield in northwest Africa, the Basins and Shields in southern Africa, and the Alpine Orogenic Belt. Inverse correlations also presist over the North Sea Rifts, the Benue Rift, and more generally over the East African Rifts. The results of this quantitative correlation analysis support the general inverse relationships of gravity and magnetic anomalies observed for North American continental terrain which may be broadly related to magnetic crustal thickness variations.
NASA Technical Reports Server (NTRS)
Kim, H.; Taylor, Patrick T.; vonFrese, R. R.; Kim, J. W.
2004-01-01
We compare crustal magnetic anomaly maps over the Kursk (Russia) and Bangui (Central African Republic) isolated anomalies and the Antarctic derived from the Magsat, \\Orsted and CHAMP satellite fields. We wish to demonstrate how progress in satellite magnetic missions has improved the recovery of the crustal magnetic field. The 6-month long Magsat mission of 25 years ago generated two major methods of processing satellite magnetic anomaly data for lithospheric studies. The first was a global perspective using spherical harmonics that emphasize the more regional and global lithospheric fields. However, these fields commonly do not resolve local anomaly features in any detail. Therefore a second procedure involved the use of the individual satellite orbit or track data to recover small-scale anomalies on a regional scale. We present results over prominent magnetic anomalies such as Kursk, Bangui and the large Antarctic continent that demonstrate how the various analysis methods affect the recovery of crustal anomalies. The more recent \\Orsted and CHAMP missions are successfully recording data with an improved accuracy and with full spatial and temporal coverage. We show and interpret the total magnetic intensity anomaly maps over these areas from all three satellite magnetometer data sets.
Competing Orders and Anomalies
Moon, Eun-Gook
2016-01-01
A conservation law is one of the most fundamental properties in nature, but a certain class of conservation “laws” could be spoiled by intrinsic quantum mechanical effects, so-called quantum anomalies. Profound properties of the anomalies have deepened our understanding in quantum many body systems. Here, we investigate quantum anomaly effects in quantum phase transitions between competing orders and striking consequences of their presence. We explicitly calculate topological nature of anomalies of non-linear sigma models (NLSMs) with the Wess-Zumino-Witten (WZW) terms. The non-perturbative nature is directly related with the ’t Hooft anomaly matching condition: anomalies are conserved in renormalization group flow. By applying the matching condition, we show massless excitations are enforced by the anomalies in a whole phase diagram in sharp contrast to the case of the Landau-Ginzburg-Wilson theory which only has massive excitations in symmetric phases. Furthermore, we find non-perturbative criteria to characterize quantum phase transitions between competing orders. For example, in 4D, we show the two competing order parameter theories, CP(1) and the NLSM with WZW, describe different universality class. Physical realizations and experimental implication of the anomalies are also discussed. PMID:27499184
Distribution of the Crustal Magnetic Field in Sichuan-Yunnan Region, Southwest China
Bai, Chunhua; Kang, Guofa; Gao, Guoming
2014-01-01
Based on the new and higher degree geomagnetic model NGDC-720-V3, we have investigated the spatial distribution, the altitude decay characteristics of the crustal magnetic anomaly, the contributions from different wavelength bands to the anomaly, and the relationship among the anomaly, the geological structure, and the geophysical field in Sichuan-Yunnan region of China. It is noted that the most outstanding feature in this area is the strong positive magnetic anomaly in Sichuan Basin, a geologically stable block. Contrasting with this feature, a strong negative anomaly can be seen nearby in Longmen Mountain block, an active block. This contradiction implies a possible relationship between the magnetic field and the geological activity. Completely different feature in magnetic field distribution is seen in the central Yunnan block, another active region, where positive and negative anomalies distribute alternatively, showing a complex magnetic anomaly map. Some fault belts, such as the Longmen Mountain fault, Lijiang-Xiaojinhe fault, and the Red River fault, are the transitional zones of strong and weak or negative and positive anomalies. The corresponding relationship between the magnetic anomaly and the geophysical fields was confirmed. PMID:25243232
Congenital anomalies of the limbs in mythology and antiquity.
Mavrogenis, Andreas F; Markatos, Konstantinos; Nikolaou, Vasilios; Gartziou-Tatti, Ariadne; Soucacos, Panayotis N
2018-04-01
Congenital anomalies of the limbs have been observed since ancient human civilizations, capturing the imagination of ancient physicians and people. The knowledge of the era could not possibly theorize on the biologic aspects of these anomalies; however, from the very beginning of civilization the spiritual status of people attempted to find a logical explanation for the existence of such cases. The next logical step of the spiritual and religious system of the ancients was to correlate these anomalies with the Gods and to attribute them to a different level of existence in order to rationalize their existence. In these settings, the mythology and religious beliefs of ancient civilizations comprised several creatures that were related to the observed congenital anomalies in humans. The purpose of this historic review is to summarize the depiction of congenital anomalies of the limbs in mythology and antiquity, to present several mythological creatures with resemblance to humans with congenital anomalies of the limbs, to present the atmosphere of the era concerning the congenital anomalies, and to theorize on the anomaly and medical explanation upon which such creatures were depicted. Our aim is to put historic information in one place, creating a comprehensive review that the curious reader would find interesting and enjoyable.
Fetal Alcohol Syndrome in Adolescents and Adults.
ERIC Educational Resources Information Center
Bert, Cynthia R. Greene; Bert, Minnie
Persons with fetal alcohol syndrome (FAS) may be diagnosed at birth based on specific symptoms and anomalies. These are history of prenatal alcohol exposure, mental retardation, central nervous system dysfunctions, growth deficiency, particular physical anomalies, and speech and language anomalies. With aging, cranial and skeletal anomalies become…
NASA Astrophysics Data System (ADS)
Sai Gowtam, V.; Tulasi Ram, S.
2017-10-01
Ionospheric winter and annual anomalies have been investigated during the ascending phase of solar cycle 24 using high-resolution global 3D - data of the FORMOSAT - 3/COSMIC (Formosa satellite - 3/Constellation Observing System for Meterology, Ionosphere and Climate) radio occultation observations. Our detailed analysis shows that the occurrence of winter anomaly at low-latitudes is confined only to the early morning to afternoon hours, whereas, the winter anomaly at mid-latitudes is almost absent at all local times during the ascending phase of solar cycle 24. Further, in the topside ionosphere (altitudes of 400 km and above), the winter anomaly is completely absent at all local times. In contrast, the ionospheric annual anomaly is consistently observed at all local times and altitudes during this ascending phase of solar cycle 24. The annual anomaly exhibits strong enhancements over southern EIA crest latitudes during day time and around Weddle Sea Anomaly (WSA) region during night times. The global mean annual asymmetry index is also computed to understand the altitudinal variation. The global mean AI maximizes around 300-500 km altitudes during the low solar active periods (2008-10), whereas it extends up to 600 km during moderate to high (2011) solar activity period. These findings from our study provide new insights to the current understanding of the annual anomaly.
Enabling NLDAS-2 Anomaly Analysis Using Giovanni
NASA Astrophysics Data System (ADS)
Loeser, C.; Rui, H.; Teng, W. L.; Vollmer, B.; Mocko, D. M.
2017-12-01
A newly implemented feature in Giovanni (GES DISC Interactive Online Visualization and Analysis Interface) allows users to explore and visualize anomaly data from the NLDAS-2 Primary Forcing and Noah model data sets. For a given measurement and location, an anomaly describes how conditions for a particular time period compare to normal conditions, based on long-term averages. Analyzing anomalies is important for monitoring droughts, determining weather trends, and studying land surface processes relevant for meteorology, hydrology, and climate. Using Giovanni to analyze anomalies for NLDAS-2 data allows for these studies to be efficiently conducted for the central North American region. Phase 2 of NLDAS (NLDAS-2) currently runs at an 1/8th degree resolution, in near-real time, with data sets extending back to January 1979. NLDAS-2 provides data for soil moisture, precipitation, temperature, and other hydrology measurements. Hourly, monthly, and 30-year (1980-2009) monthly climatology data are available for several land surface models and forcing data sets. The Giovanni anomaly tool calculates monthly anomalies, for a given user-defined variable, as the difference between the NLDAS-2 monthly climatology data and the monthly data. The resulting anomaly describes how a chosen month compares to the 30-year monthly average. The presentation will demonstrate the capabilities and usefulness of Giovanni's anomaly tool, detail the recently added NLDAS-2 variables for which anomalies are available, and show how users can access the data.
Enabling NLDAS-2 Anomaly Analysis Using Giovanni
NASA Technical Reports Server (NTRS)
Loeser, Carlee; Rui, Hualan; Teng, William; Vollmer, Bruce; Mocko, David
2017-01-01
A newly implemented feature in Giovanni (GES DISC Interactive Online Visualization and Analysis Interface) allows users to explore and visualize anomaly data from the NLDAS-2 Primary Forcing and Noah model data sets. For a given measurement and location, an anomaly describes how conditions for a particular time period compare to normal conditions, based on long-term averages. Analyzing anomalies is important for monitoring droughts, determining weather trends, and studying land surface processes relevant for meteorology, hydrology, and climate. Using Giovanni to analyze anomalies for NLDAS-2 data allows for these studies to be efficiently conducted for the central North American region. Phase 2 of NLDAS (NLDAS-2) currently runs at an 1/8th degree resolution, in near-real time, with data sets extending back to January 1979. NLDAS-2 provides data for soil moisture, precipitation, temperature, and other hydrology measurements. Hourly, monthly, and 30-year (1980-2009) monthly climatology data are available for several land surface models and forcing data sets. The Giovanni anomaly tool calculates monthly anomalies, for a given user-defined variable, as the difference between the NLDAS-2 monthly climatology data and the monthly data. The resulting anomaly describes how a chosen month compares to the 30-year monthly average. The presentation will demonstrate the capabilities and usefulness of Giovanni's anomaly tool, detail the recently added NLDAS-2 variables for which anomalies are available, and show how users can access the data.
Vertebral column anomalies in Indo-Pacific and Atlantic humpback dolphins Sousa spp.
Weir, Caroline R; Wang, John Y
2016-08-09
Conspicuous vertebral column abnormalities in humpback dolphins (genus Sousa) were documented for the first time during 3 photo-identification field studies of small populations in Taiwan, Senegal and Angola. Seven Taiwanese humpback dolphins S. chinensis taiwanensis with vertebral column anomalies (lordosis, kyphosis or scoliosis) were identified, along with 2 possible cases of vertebral osteomyelitis. There was evidence from several individuals photographed over consecutive years that the anomalies became more pronounced with age. Three Atlantic humpback dolphins S. teuszii were observed with axial deviations of the vertebral column (lordosis and kyphosis). Another possible case was identified in a calf, and 2 further animals were photographed with dorsal indents potentially indicative of anomalies. Vertebral column anomalies of humpback dolphins were predominantly evident in the lumbo-caudal region, but one Atlantic humpback dolphin had an anomaly in the cervico-thoracic region. Lordosis and kyphosis occurred simultaneously in several individuals. Apart from the described anomalies, all dolphins appeared in good health and were not obviously underweight or noticeably compromised in swim speed. This study presents the first descriptions of vertebral column anomalies in the genus Sousa. The causative factors for the anomalies were unknown in every case and are potentially diverse. Whether these anomalies result in reduced fitness of individuals or populations merits attention, as both the Taiwanese and Atlantic humpback dolphin are species of high conservation concern.
Examination of Martian sedimentary rocks to understand possible paleo-ocean and its age
NASA Technical Reports Server (NTRS)
Tanaka, T.
1988-01-01
It is well known that the terrestrial marine sediments have large cerium anomaly on their chondrite-normalized REE pattern. Siliceous shale and calcaleous sediments have negative Ce-anomaly. Ferromanganese nodule have positive or negative Ce-anomaly. The Ce-anomaly is considered to be a result of tetravalent state of cerium rather than common trivalent. Ferromanganese nodule which formed under reducing condition has negative Ce-anomaly. Then, combined study of Ce-anomaly with Ce isotopes is expected to play an important role in geochemistry. La-138 decays to Ce-138 and Ba-138 with a total half life of about 1 x 10 to the 11th years. Cerium anomalies (positive or negative) are expected in Martian paleo-ocean and in sediments as observed in the terrestrial environment. A list of things to be examined is given.
NASA Technical Reports Server (NTRS)
Susskind, Joel; Iredell, Lena; Lee, Jae N.
2014-01-01
In this presentation, we will show AIRS Version-6 area weighted anomaly time series over the time period September 2002 through August 2014 of atmospheric temperature and water vapor profiles as a function of height. These anomaly time series show very different behaviors in the stratosphere and in the troposphere. Tropical mean stratospheric temperature anomaly time series are very strongly influenced by the Quasi-Biennial Oscillation (QBO) with large anomalies that propagate downward from 1 mb to 100 mb with a period of about two years. AIRS stratospheric temperature anomalies are in good agreement with those obtained by MLS over a common period. Tropical mean tropospheric temperature profile anomalies appear to be totally disconnected from those of the stratosphere and closely follow El Nino La Nina activity.
NASA Technical Reports Server (NTRS)
Zhavoronkin, I. A.; Kopayev, V. V.
1985-01-01
The geological reasons for fluctuations in the anomalous field intensity along the polar axes were examined. The Kursk magnetic anomaly is used as the basis for the study. A geological-geophysical section was constructed which used the results of the interpretation of gravimagnetic anomalies.
Life cycles of persistent anomalies. I - Evolution of 500 mb height fields
NASA Technical Reports Server (NTRS)
Dole, Randall M.
1989-01-01
The life cycles of persistent anomalies of the extratropical Northern Hemisphere wintertime circulation are studied, focusing on the typical characteristics of the 500 mb height anomaly and flow patterns accompanying the development and breakdown of large-scale flow anomalies in the eastern North Atlantic and the northern Soviet Union. Following onset, anomaly centers develop and intensify in sequence downstream from the main center, forming a quasi-stationary wavetrain pattern. From development through decay, corresponding positive and negative patterns have similar evolutions.
1986-09-01
gravity anomalies for the study area were prepared by 15 Wa *~~~.. A *-S A J~ V Hildreth (1979) and are shown in Figure 8. Magnetic anomalies for...the gravity and the magnetic anomalies reflect the patterns of the folded strata and the associated faulting. The magnetic anomalies are in- dicative...BOUGUER GRAVITY ANOMALY 5 C- -- I5 CONTOUR INTERVAL 0 20 40 60 80 100 120 26 - -KM 2 AND 5 MILLIGALS BOUNDARY FOR EARTHQUAKE /: I SOURCE
NASA Technical Reports Server (NTRS)
Stoiber, R. E. (Principal Investigator); Rose, W. I., Jr.
1975-01-01
The author has identified the following significant results. Ground truth data collection proves that significant anomalies exist at 13 volcanoes within the test site of Central America. The dimensions and temperature contrast of these ten anomalies are large enough to be detected by the Skylab 192 instrument. The dimensions and intensity of thermal anomalies have changed at most of these volcanoes during the Skylab mission.
NASA Technical Reports Server (NTRS)
Hastings, D. A. (Principal Investigator)
1982-01-01
The problems associated with the use of an interactive magnetic modeling program are reported and a publication summarizing the MAGSAT anomaly results for Africa and the possible tectonic associations of these anomalies is provided. An overview of the MAGSAT scalar anomaly map for Africa suggested a correlation of MAGSAT anomalies with major crustal blocks of uplift or depression and different degrees of regional metamorphism. The strongest MAGSAT anomalies in Africa are closely correlated spatially with major tectonic features. Results indicate that the Bangui anomaly may be caused by a central old Precambrian shield, flanked to the north and south by two relatively young sedimentary basins.
Spherical earth gravity and magnetic anomaly analysis by equivalent point source inversion
NASA Technical Reports Server (NTRS)
Von Frese, R. R. B.; Hinze, W. J.; Braile, L. W.
1981-01-01
To facilitate geologic interpretation of satellite elevation potential field data, analysis techniques are developed and verified in the spherical domain that are commensurate with conventional flat earth methods of potential field interpretation. A powerful approach to the spherical earth problem relates potential field anomalies to a distribution of equivalent point sources by least squares matrix inversion. Linear transformations of the equivalent source field lead to corresponding geoidal anomalies, pseudo-anomalies, vector anomaly components, spatial derivatives, continuations, and differential magnetic pole reductions. A number of examples using 1 deg-averaged surface free-air gravity anomalies of POGO satellite magnetometer data for the United States, Mexico, and Central America illustrate the capabilities of the method.
NASA Technical Reports Server (NTRS)
Hinze, W. J.; Braile, L. W.; Vonfrese, R. R. B. (Principal Investigator); Keller, G. R.; Lidiak, E. G.
1984-01-01
Scalar magnetic anomaly data from MAGSAT, reduced to vertical polarization and long wavelength pass filtered free air gravity anomaly data of South America and the Caribbean are compared to major crustal features. The continental shields generally are more magnetic than adjacent basins, oceans and orogenic belts. In contrast, the major aulacogens are characterized by negative anomalies. Spherical earth magnetic modeling of the Amazon River and Takatu aulacogens in northeastern South America indicates a less magnetic crust associated with the aulacogens. Spherical earth modeling of both positive gravity and negative magnetic anomalies observed over the Mississippi Embayment indicate the presence of a nonmagnetic zone of high density material within the lower crust associated with the aulacogen. The MAGSAT scalar magnetic anomaly data and available free air gravity anomalies over Euro-Africa indicate several similar relationships.
Methods and Systems for Characterization of an Anomaly Using Infrared Flash Thermography
NASA Technical Reports Server (NTRS)
Koshti, Ajay M. (Inventor)
2013-01-01
A method for characterizing an anomaly in a material comprises (a) extracting contrast data; (b) measuring a contrast evolution; (c) filtering the contrast evolution; (d) measuring a peak amplitude of the contrast evolution; (d) determining a diameter and a depth of the anomaly, and (e) repeating the step of determining the diameter and the depth of the anomaly until a change in the estimate of the depth is less than a set value. The step of determining the diameter and the depth of the anomaly comprises estimating the depth using a diameter constant C.sub.D equal to one for the first iteration of determining the diameter and the depth; estimating the diameter; and comparing the estimate of the depth of the anomaly after each iteration of estimating to the prior estimate of the depth to calculate the change in the estimate of the depth of the anomaly.
The nature of subslab slow velocity anomalies beneath South America
NASA Astrophysics Data System (ADS)
Portner, Daniel Evan; Beck, Susan; Zandt, George; Scire, Alissa
2017-05-01
Slow seismic velocity anomalies are commonly imaged beneath subducting slabs in tomographic studies, yet a unifying explanation for their distribution has not been agreed upon. In South America two such anomalies have been imaged associated with subduction of the Nazca Ridge in Peru and the Juan Fernández Ridge in Chile. Here we present new seismic images of the subslab slow velocity anomaly beneath Chile, which give a unique view of the nature of such anomalies. Slow seismic velocities within a large hole in the subducted Nazca slab connect with a subslab slow anomaly that appears correlated with the extent of the subducted Juan Fernández Ridge. The hole in the slab may allow the subslab material to rise into the mantle wedge, revealing the positive buoyancy of the slow material. We propose a new model for subslab slow velocity anomalies beneath the Nazca slab related to the entrainment of hot spot material.
Continental and oceanic magnetic anomalies: Enhancement through GRM
NASA Technical Reports Server (NTRS)
Vonfrese, R. R. B.; Hinze, W. J.
1985-01-01
In contrast to the POGO and MAGSAT satellites, the Geopotential Research Mission (GRM) satellite system will orbit at a minimum elevation to provide significantly better resolved lithospheric magnetic anomalies for more detailed and improved geologic analysis. In addition, GRM will measure corresponding gravity anomalies to enhance our understanding of the gravity field for vast regions of the Earth which are largely inaccessible to more conventional surface mapping. Crustal studies will greatly benefit from the dual data sets as modeling has shown that lithospheric sources of long wavelength magnetic anomalies frequently involve density variations which may produce detectable gravity anomalies at satellite elevations. Furthermore, GRM will provide an important replication of lithospheric magnetic anomalies as an aid to identifying and extracting these anomalies from satellite magnetic measurements. The potential benefits to the study of the origin and characterization of the continents and oceans, that may result from the increased GRM resolution are examined.
Hamiltonian Anomalies from Extended Field Theories
NASA Astrophysics Data System (ADS)
Monnier, Samuel
2015-09-01
We develop a proposal by Freed to see anomalous field theories as relative field theories, namely field theories taking value in a field theory in one dimension higher, the anomaly field theory. We show that when the anomaly field theory is extended down to codimension 2, familiar facts about Hamiltonian anomalies can be naturally recovered, such as the fact that the anomalous symmetry group admits only a projective representation on the Hilbert space, or that the latter is really an abelian bundle gerbe over the moduli space. We include in the discussion the case of non-invertible anomaly field theories, which is relevant to six-dimensional (2, 0) superconformal theories. In this case, we show that the Hamiltonian anomaly is characterized by a degree 2 non-abelian group cohomology class, associated to the non-abelian gerbe playing the role of the state space of the anomalous theory. We construct Dai-Freed theories, governing the anomalies of chiral fermionic theories, and Wess-Zumino theories, governing the anomalies of Wess-Zumino terms and self-dual field theories, as extended field theories down to codimension 2.
Adams, Ashok; Mankad, Kshitij; Offiah, Curtis; Childs, Lucy
2016-02-01
The branchial arches are the embryological precursors of the face, neck and pharynx. Anomalies of the branchial arches are the second most common congenital lesions of the head and neck in children, with second branchial arch anomalies by far the most common. Clinically, these congenital anomalies may present as cysts, sinus tracts, fistulae or cartilaginous remnants with typical clinical and radiological findings. We review the normal embryological development of the branchial arches and the anatomical structures of the head and neck that derive from each arch. The typical clinical and radiological appearances of both common and uncommon branchial arch abnormalities are discussed with an emphasis on branchial cleft anomalies. • Anomalies of the branchial arches usually present as cysts, sinuses or fistulae. • Second branchial arch anomalies account for approximately 95 % of cases. • There are no pathognomonic imaging features so diagnosis depends on a high index of suspicion and knowledge of typical locations. • Persistent cysts, fistulae or recurrent localised infection may be due to branchial arch anomalies. • Surgical excision of the cyst or tract is the most common curative option.
Reliability of CHAMP Anomaly Continuations
NASA Technical Reports Server (NTRS)
vonFrese, Ralph R. B.; Kim, Hyung Rae; Taylor, Patrick T.; Asgharzadeh, Mohammad F.
2003-01-01
CHAMP is recording state-of-the-art magnetic and gravity field observations at altitudes ranging over roughly 300 - 550 km. However, anomaly continuation is severely limited by the non-uniqueness of the process and satellite anomaly errors. Indeed, our numerical anomaly simulations from satellite to airborne altitudes show that effective downward continuations of the CHAMP data are restricted to within approximately 50 km of the observation altitudes while upward continuations can be effective over a somewhat larger altitude range. The great unreliability of downward continuation requires that the satellite geopotential observations must be analyzed at satellite altitudes if the anomaly details are to be exploited most fully. Given current anomaly error levels, joint inversion of satellite and near- surface anomalies is the best approach for implementing satellite geopotential observations for subsurface studies. We demonstrate the power of this approach using a crustal model constrained by joint inversions of near-surface and satellite magnetic and gravity observations for Maude Rise, Antarctica, in the southwestern Indian Ocean. Our modeling suggests that the dominant satellite altitude magnetic anomalies are produced by crustal thickness variations and remanent magnetization of the normal polarity Cretaceous Quiet Zone.
NASA Astrophysics Data System (ADS)
Yusoh, R.; Saad, R.; Saidin, M.; Anda, S. T.; Muhammad, S. B.; Ashraf, M. I. M.; Hazreek, Z. A. M.
2018-04-01
Magnetic and resistivity method has become a reliable option in archeological exploration. The use of both method has become popular these day. However, both method gives different type of sensing in detecting anomalies and direct interpret from the anomalies will result large coverage area for excavation. Therefore, to overcome this issue, both anomalies can be extracted using ArcGIS software to reduce excavated coverage area. The case study located at Sungai Batu, Lembah Bujang near SB2ZZ lot expected buried clay brick monument which will be a perfect case to apply this technique. Magnetic and resistivity method was implemented at the study area where the anomalies coverage area for magnetic and resistivity is 531.5 m2 and 636 m2 respectively which total area of both anomalies was 764 m2. By applying combine technique, the anomalies area reduce to 403.7 m2 which reduce the suspected anomalies by 47.16 %. The unsuspected clay brick monument area was increase from 15.86% to 55.54% which improve the cost and labor work for excavation.
Congenital basis of posterior fossa anomalies
Cotes, Claudia; Bonfante, Eliana; Lazor, Jillian; Jadhav, Siddharth; Caldas, Maria; Swischuk, Leonard
2015-01-01
The classification of posterior fossa congenital anomalies has been a controversial topic. Advances in genetics and imaging have allowed a better understanding of the embryologic development of these abnormalities. A new classification schema correlates the embryologic, morphologic, and genetic bases of these anomalies in order to better distinguish and describe them. Although they provide a better understanding of the clinical aspects and genetics of these disorders, it is crucial for the radiologist to be able to diagnose the congenital posterior fossa anomalies based on their morphology, since neuroimaging is usually the initial step when these disorders are suspected. We divide the most common posterior fossa congenital anomalies into two groups: 1) hindbrain malformations, including diseases with cerebellar or vermian agenesis, aplasia or hypoplasia and cystic posterior fossa anomalies; and 2) cranial vault malformations. In addition, we will review the embryologic development of the posterior fossa and, from the perspective of embryonic development, will describe the imaging appearance of congenital posterior fossa anomalies. Knowledge of the developmental bases of these malformations facilitates detection of the morphological changes identified on imaging, allowing accurate differentiation and diagnosis of congenital posterior fossa anomalies. PMID:26246090
NASA Astrophysics Data System (ADS)
ELBAZ-POULICHET, F.; SEIDEL, J.
2001-05-01
Recent evidence of perturbation of REE signature marked by pronounced positive Gd anomalies have been found in surface waters of densely populated and industrialised regions, in Germany and Japan. This study presents REE data in water from a small Mediterranean basin (the Thau lagoon) located on the southwestern French Mediterranean coast, which is a densely populated region.. Positive Gd anomalies (up to 5) are observed in the major river feeding the lagoon and in the lagoon where the highest values are encountered in the close vicinity of the continental sources. The systematic and concomitant observation of similar anomalies, in sewage treatment plant effluents, suggests that they have an anthropogenic origin. The suspended load does not display any Gd anomaly indicating that the Gd input occurs mainly in the dissolved phase. In addition, the appearance of Gd anomaly is not accompanied by an overall increase of REE concentrations. The gadopentetic acid, Gd(DTPA)2- used as a contrasting agent in magnetic resonance imaging could account for such anomalies but remains to be confirmed. Finally positive Gd anomalies appear a common feature in waters of densely populated regions with high standard of living . These anomalies may have an application in water resource management as a tracer of anthropogenic impacts.
Urogenital anomalies in girls with sacrococcygeal teratoma: a commonly missed association.
Shalaby, Mohamed Sameh; O'Toole, Stuart; Driver, Chris; Bradnock, Tim; Lam, Jimmy; Carachi, Robert
2012-02-01
The association of urogenital (UG) anomalies and sacrococcygeal teratoma (SCT) has not been widely reported. Our aim was to look at the national incidence and presentation of this anomaly in patients with SCT and to provide the first report of a clear anatomical description of this commonly missed association. Sacrococcygeal teratoma cases in Scotland during the last 30 years were identified. Patients with associated UG anomalies were reviewed in detail to identify their presentation, anatomy, and management. Fifty-three patients with SCT were identified, including 41 girls. Five girls (12%) subsequently had a UG anomaly diagnosed, which was not apparent at the initial surgery. Two patients presented with retention, and their anomaly was diagnosed at 6 weeks and 7 months of age. The other 3 presented with incontinence, and despite thorough assessment, including cystoscopy, their UG anomalies were not recognized until the ages of 7, 9, and 13 years. Urogenital anomalies are surprisingly common in girls with SCT. The reason for this association is unclear. None of these cases were diagnosed initially, which means that it was either missed or acquired. Urogenital anomalies should be suspected in girls with SCT and actively excluded in those with voiding difficulties. Copyright © 2012 Elsevier Inc. All rights reserved.
NASA Astrophysics Data System (ADS)
Ding, Ruiqiang; Li, Jianping; Tseng, Yu-heng; Sun, Cheng; Xie, Fei
2017-01-01
Previous studies have indicated that boreal winter subtropical and extratropical sea surface pressure (SLP) anomalies over both the North and South Pacific are significantly related to the El Niño-Southern Oscillation (ENSO) state in the following boreal winter. Here we use observational data and model simulations to show that the ability of the boreal winter North Pacific SLP anomalies to initiate ENSO events a year later may strongly depend on the state of the simultaneous South Pacific SLP anomalies and vice versa. When the boreal winter North Pacific SLP anomalies are of the opposite sign to the simultaneous South Pacific anomalies, the correlation of the North or South Pacific anomalies with the following ENSO state becomes much weaker, and the strength of the ENSO events also tends to be weaker. One possible reason for this is that when the boreal winter North and South Pacific SLP anomalies have the opposite sign, the westerly anomalies over the western-central equatorial Pacific during the following boreal summer are greatly reduced by the interference between the antecedent North and South Pacific SLP anomalies, thereby not favoring the development of ENSO events. Further analysis indicates that a combination of North and South Pacific precursor signals may serve to enhance the ENSO prediction skill.
Prevalence of Dental Anomalies among School Going Children in India.
Kathariya, Mitesh D; Nikam, Atul Pralhad; Chopra, Kirti; Patil, Namrata N; Raheja, Hitesh; Kathariya, Renuka
2013-10-01
The purpose of the present study is to investigate the prevalence of dental anomalies according to gender among children. This cross-sectional study was conducted a group of 600 children, of them 293 (48.8%) were males and 275 (45.8%) females which were taken with proper sampling technique. Type III clinical examination was done to know the prevalence of dental anomalies. The Statistical software namely SPSS version 16.0 was used for data analysis. Chi-square test was used at p value of 0.05 or less. Impactions (39.2%) were the most common anomaly in this study and most of the impacted teeth were related to maxilla. A significant difference was seen in case of hypodontia, microdontia and talons cusp according to gender in which first two anomalies were more among females and last one among males. Children with one dental anomaly were 25.8%, and 13.4% were having more than one. The percentage of dental anomalies were high specially impaction and rotated teeth. So these anomalies should be treated earlier to avoid further complications. How to cite this article: Kathariya MD, Nikam AP, Chopra K, Patil NN, Raheja H, Kathariya R. Prevalence of Dental Anomalies among School Going Children in India. J Int Oral Health 2013; 5(5):10-4.
NASA Astrophysics Data System (ADS)
Li, Wang; Yue, Jianping; Guo, Jinyun; Yang, Yang; Zou, Bin; Shen, Yi; Zhang, Kefei
2018-03-01
The Circum-Pacific seismic belt is the region heavily affected by earthquakes in the world. The relationship between earthquake (e.g., the geographic location, occurrence time, magnitude, and focal depth) and ionospheric anomalies in the belt was investigated using 100 M7.0+ earthquakes during 2006-2015. The ground-based GPS measurements and global ionosphere map (GIM) data were used for the analyses of the ionospheric variations preceding the earthquakes. The results indicated that the occurrence rate of total electron content (TEC) anomalies was proportional to the magnitude and inversely proportional to the focal depth to a certain degree, and the occurrence frequency of anomalies had a rising trend with the days getting close to the main shock. The occurrence rate of TEC anomalies in the Southern hemisphere was larger than that in the Northern hemisphere. Besides, the spatial characteristics of TEC anomalies showed that the anomalies in low-middle latitudes did not coincide with the epicenter, sometimes the anomalies were also observed in the corresponding conjugated region. However, the TEC anomalies in the high latitude usually appeared around the epicenter and within the seismogenic zone while no TEC anomalies appeared in the conjugated area. These results may have potential applications to the earthquake prediction in the Circum-Pacific seismic belt.
Seismic data fusion anomaly detection
NASA Astrophysics Data System (ADS)
Harrity, Kyle; Blasch, Erik; Alford, Mark; Ezekiel, Soundararajan; Ferris, David
2014-06-01
Detecting anomalies in non-stationary signals has valuable applications in many fields including medicine and meteorology. These include uses such as identifying possible heart conditions from an Electrocardiography (ECG) signals or predicting earthquakes via seismographic data. Over the many choices of anomaly detection algorithms, it is important to compare possible methods. In this paper, we examine and compare two approaches to anomaly detection and see how data fusion methods may improve performance. The first approach involves using an artificial neural network (ANN) to detect anomalies in a wavelet de-noised signal. The other method uses a perspective neural network (PNN) to analyze an arbitrary number of "perspectives" or transformations of the observed signal for anomalies. Possible perspectives may include wavelet de-noising, Fourier transform, peak-filtering, etc.. In order to evaluate these techniques via signal fusion metrics, we must apply signal preprocessing techniques such as de-noising methods to the original signal and then use a neural network to find anomalies in the generated signal. From this secondary result it is possible to use data fusion techniques that can be evaluated via existing data fusion metrics for single and multiple perspectives. The result will show which anomaly detection method, according to the metrics, is better suited overall for anomaly detection applications. The method used in this study could be applied to compare other signal processing algorithms.
Oceanic Residual Depth Anomalies Maintained by a Shallow Asthenospheric Channel
NASA Astrophysics Data System (ADS)
Richards, F. D.; Hoggard, M.; White, N.
2016-12-01
Oceanic residual depth anomalies vary on wavelengths of 800-2,000 km and have amplitudesof ±1 km. There is also evidence from glacio-isostatic adjustment, plate motions and seismicanisotropy studies for the existence of a low-viscosity asthenospheric channel immediately beneaththe lithospheric plates. Here, we investigate whether global residual depth anomalies are consistentwith temperature variations within a sub-plate channel. For a given channel thickness, we convertresidual depth anomalies into temperature anomalies, assuming thermal isostasy alone (i.e. no mantle flow). Using aparameterisation that is calibrated against stacked oceanic shear wave velocity profiles, we convertthese temperature anomalies into velocity variations. We then compare the inferred velocity vari-ations with published seismic tomographic models. We find that thermal anomalies of ±100 °Cwithin a 150 ± 50 km thick channel yield a good match to > 95% of global residual depth anoma-lies. These temperature variations are consistent with geochemical evidence from mid-oceanic ridgebasalts and oceanic crustal thicknesses. The apparent success of this simple isostatic approach sup-ports the existence of a low-viscosity asthenospheric channel that plays a key role in controllingresidual depth anomalies. Far from subduction zones and from plume conduits, dynamic topog-raphy in the oceanic realm appears to be primarily controlled by temperature-induced buoyancyvariations within this channel.
The prevalence of specific dental anomalies in a group of Saudi cleft lip and palate patients.
Al-Kharboush, Ghada H; Al-Balkhi, Khalid M; Al-Moammar, Khalid
2015-04-01
The aims of this study were to investigate the prevalence and distribution of dental anomalies in a group of Saudi subjects with cleft lip and palate (CLP), to examine potential sex-based associations of these anomalies, and to compare dental anomalies in Saudi subjects with CLP with published data from other population groups. This retrospective study involved the examination of pre-treatment records obtained from three CLP centers in Riyadh, Saudi Arabia, in February and March 2010. The pre-treatment records of 184 subjects with cleft lip and palate were identified and included in this study. Pre-treatment maxillary occlusal radiographs of the cleft region, panoramic radiographs, and orthodontic study models of subjects with CLP were analyzed for dental anomalies. Orthopantomographs and occlusal radiographs may not be reliable for the accurate evaluation of root malformation anomalies. A total of 265 dental anomalies were observed in the 184 study subjects. Hypodontia was observed most commonly (66.8%), followed by microdontia (45.6%), intra-oral ectopic eruption (12.5%), supernumerary teeth (12.5%), intra-nasal ectopic eruption (3.2), and macrodontia (3.2%). No gender difference in the prevalence of these anomalies was observed. Dental anomalies were common in Saudi subjects with CLP type. This will complicate the health care required for the CL/P subjects. This study was conducted to epidemiologically explore the prevalence of dental anomalies among Saudi Arabian subjects with CLP.
Prevalence of dental anomalies in Indian population.
Patil, Santosh; Doni, Bharati; Kaswan, Sumita; Rahman, Farzan
2013-10-01
Developmental anomalies of the dentition are not infrequently observed by the dental practitioner. The aim of the present study was to determine the prevalence of dental anomalies in the Indian population. A retrospective study of 4133 panoramic radiographs of patients, who attended the Department of Oral Medicine and Radiology, Jodhpur Dental College General Hospital between September 2008 to December 2012 was done. The ages of the patients ranged from 13 to 38 years with a mean age of 21.8 years. The orthopantomographs (OPGs) and dental records were examined for any unusual finding such as congenitally missing teeth, impactions, ectopic eruption, supernumerary teeth, odontoma, dilacerations, taurodontism, dens in dente, germination and fusion, among others. 1519 (36.7%) patients had at least one dental anomaly. The congenitally missing teeth 673 (16.3%) had the highest prevalence, followed by impacted teeth 641 (15.5%), supernumerary teeth 51 (1.2%) and microdontia 41 (1.0%). Other anomalies were found at lower prevalence ranging from transposition 7 (0.1%) to ectopic eruption 30 (0.7%). The most prevalent anomaly in the Indian population was congenitally missing teeth (16.3%), and the second frequent anomaly was impacted teeth (15.5%), whereas, macrodontia, odontoma and transposition were the least frequent anomalies, with a prevalence of 0.2%, 0.2% and 0.1% respectively. While the overall prevalence of these anomalies may be low, the early diagnosis is imperative for the patient management and treatment planning. Key words:Dental anomaly, prevalence, panoramic radiography.
Aeromagnetic survey map of Sacramento Valley, California
Langenheim, Victoria E.
2015-01-01
Three aeromagnetic surveys were flown to improve understanding of the geology and structure in the Sacramento Valley. The resulting data serve as a basis for geophysical interpretations, and support geological mapping, water and mineral resource investigations, and other topical studies. Local spatial variations in the Earth's magnetic field (evident as anomalies on aeromagnetic maps) reflect the distribution of magnetic minerals, primarily magnetite, in the underlying rocks. In many cases the volume content of magnetic minerals can be related to rock type, and abrupt spatial changes in the amount of magnetic minerals commonly mark lithologic or structural boundaries. Bodies of serpentinite and other mafic and ultramafic rocks tend to produce the most intense positive magnetic anomalies (for example, in the northwest part of the map). These rock types are the inferred sources, concealed beneath weakly magnetic, valley-fill deposits, of the most prominent magnetic features in the map area, the magnetic highs that extend along the valley axis. Cenozoic volcanic rocks are also an important source of magnetic anomalies and coincide with short-wavelength anomalies that can be either positive (strong central positive anomaly flanked by lower-amplitude negative anomalies) or negative (strong central negative anomaly flanked by lower-amplitude positive anomalies), reflecting the contribution of remanent magnetization. Rocks with more felsic compositions or even some sedimentary units also can cause measurable magnetic anomalies. For example, the long, linear, narrow north-trending anomalies (with amplitudes of <50 nanoteslas [nT]) along the western margin of the valley coincide with exposures of the Mesozoic Great Valley sequence. Note that isolated, short-wavelength anomalies, such as those in the city of Sacramento and along some of the major roads, are caused by manmade features.
NASA Astrophysics Data System (ADS)
Fang, J.
2017-12-01
The structure and dynamics of decadal anomalies in the wintertime midlatitude North Pacific ocean- atmosphere system are examined in this study, using the NCEP/NCAR atmospheric reanalysis, HadISST SST and Simple Ocean Data Assimilation data for 1960-2010. The midlatitude decadal anomalies associated with the Pacific Decadal Oscillation are identified, being characterized by an equivalent barotropic atmospheric low (high) pressure over a cold (warm) oceanic surface. Such a unique configuration of decadal anomalies can be maintained by an unstable ocean-atmosphere interaction mechanism in the midlatitudes, which is hypothesized as follows. Associated with a warm PDO phase, an initial midlatitude surface westerly anomaly accompanied with intensified Aleutian low tends to force a negative SST anomaly by increasing upward surface heat fluxes and driving southward Ekman current anomaly. The SST cooling tends to increase the meridional SST gradient, thus enhancing the subtropical oceanic front. As an adjustment of the atmospheric boundary layer to the enhanced oceanic front, the low-level atmospheric meridional temperature gradient and thus the low-level atmospheric baroclinicity tend to be strengthened, inducing more active transient eddy activities that increase transient eddy vorticity forcing. The vorticity forcing that dominates the total atmospheric forcing tends to produce an equivalent barotropic atmospheric low pressure north of the initial westerly anomaly, intensifying the initial anomalies of the midlatitude surface westerly and Aleutian low. Therefore, it is suggested that the midlatitude ocean-atmosphere interaction can provide a positive feedback mechanism for the development of initial anomaly, in which the oceanic front and the atmospheric transient eddy are the indispensable ingredients. Such a positive ocean-atmosphere feedback mechanism is fundamentally responsible for the observed decadal anomalies in the midlatitude North Pacific ocean-atmosphere system.
Tectonic Interpretation of CHAMP Geopotential Data over the Northern Adriatic Sea.
NASA Astrophysics Data System (ADS)
Taylor, P. T.; Kim, H. R.; Mayer-Gürr, T.
2006-05-01
Recent aeromagnetic anomaly compilations (Chiappini et al., 2000 and Tontini et al., 2004) show a large positive (>700 nT) northwest-southeast trending magnetic anomaly off the Dalmatian coast. Unfortunately these aeromagnetic data cover only a part of this anomaly. We wanted to investigate if this large magnetic anomaly could be detected at satellite altitude and what is the extent and source of this feature. Therefore, magnetic and gravity anomaly maps were made from the CHAMP geopotential data, measured at the current low altitude of 345-350 km over the northern Adriatic Sea. We made the magnetic anomaly map over this relatively small region using 36 descending and 85 ascending orbits screened to be at the lowest altitude and the most magnetically quietest data. We removed the main field component (i.e., IGRF-10 up to degree and order 13) and then demeaned individual tracks and subtracted a second order polynomial to remove regional and/or un-modeled external field features. The resulting map from these well-correlated anomalies revealed a positive magnetic anomaly (>2 nT). Reduction-to-the pole brought these CHAMP anomaly features into coincidence with the aeromagnetic data. Previously Cantini et al. (1999) compared the surface magnetic data with MAGSAT by continuing upward the former and downwards the latter to 100 km and found a good correlation for wavelengths of 300-500 km. We also investigated the CHAMP gravity data. They were reduced using the kinematic short-arc integration method (Ilk et al., 2005 and Mayer Gürr et al., 2005). However, no corresponding short-wavelength gravity anomaly was observed in our study area. This tectonically complex region is under horizontal stress and the source of the large magnetic anomaly can be modelled by an associated ophiolite melange.
NASA Astrophysics Data System (ADS)
Heki, K.; He, L.
2017-12-01
We showed that positive and negative electron density anomalies emerge above the fault immediately before they rupture, 40/20/10 minutes before Mw9/8/7 earthquakes (Heki, 2011 GRL; Heki and Enomoto, 2013 JGR; He and Heki 2017 JGR). These signals are stronger for earthquake with larger Mw and under higher background vertical TEC (total electron conetent) (Heki and Enomoto, 2015 JGR). The epicenter, the positive and the negative anomalies align along the local geomagnetic field (He and Heki, 2016 GRL), suggesting electric fields within ionosphere are responsible for making the anomalies (Kuo et al., 2014 JGR; Kelley et al., 2017 JGR). Here we suppose the next Nankai Trough earthquake that may occur within a few tens of years in Southwest Japan, and will discuss if we can recognize its preseismic signatures in TEC by real-time observations with GNSS.During high geomagnetic activities, large-scale traveling ionospheric disturbances (LSTID) often propagate from auroral ovals toward mid-latitude regions, and leave similar signatures to preseismic anomalies. This is a main obstacle to use preseismic TEC changes for practical short-term earthquake prediction. In this presentation, we show that the same anomalies appeared 40 minutes before the mainshock above northern Australia, the geomagnetically conjugate point of the 2011 Tohoku-oki earthquake epicenter. This not only demonstrates that electric fields play a role in making the preseismic TEC anomalies, but also offers a possibility to discriminate preseismic anomalies from those caused by LSTID. By monitoring TEC in the conjugate areas in the two hemisphere, we can recognize anomalies with simultaneous onset as those caused by within-ionosphere electric fields (e.g. preseismic anomalies, night-time MSTID) and anomalies without simultaneous onset as gravity-wave origin disturbances (e.g. LSTID, daytime MSTID).
A robust background regression based score estimation algorithm for hyperspectral anomaly detection
NASA Astrophysics Data System (ADS)
Zhao, Rui; Du, Bo; Zhang, Liangpei; Zhang, Lefei
2016-12-01
Anomaly detection has become a hot topic in the hyperspectral image analysis and processing fields in recent years. The most important issue for hyperspectral anomaly detection is the background estimation and suppression. Unreasonable or non-robust background estimation usually leads to unsatisfactory anomaly detection results. Furthermore, the inherent nonlinearity of hyperspectral images may cover up the intrinsic data structure in the anomaly detection. In order to implement robust background estimation, as well as to explore the intrinsic data structure of the hyperspectral image, we propose a robust background regression based score estimation algorithm (RBRSE) for hyperspectral anomaly detection. The Robust Background Regression (RBR) is actually a label assignment procedure which segments the hyperspectral data into a robust background dataset and a potential anomaly dataset with an intersection boundary. In the RBR, a kernel expansion technique, which explores the nonlinear structure of the hyperspectral data in a reproducing kernel Hilbert space, is utilized to formulate the data as a density feature representation. A minimum squared loss relationship is constructed between the data density feature and the corresponding assigned labels of the hyperspectral data, to formulate the foundation of the regression. Furthermore, a manifold regularization term which explores the manifold smoothness of the hyperspectral data, and a maximization term of the robust background average density, which suppresses the bias caused by the potential anomalies, are jointly appended in the RBR procedure. After this, a paired-dataset based k-nn score estimation method is undertaken on the robust background and potential anomaly datasets, to implement the detection output. The experimental results show that RBRSE achieves superior ROC curves, AUC values, and background-anomaly separation than some of the other state-of-the-art anomaly detection methods, and is easy to implement in practice.
Grazuleviciene, Regina; Kapustinskiene, Violeta; Vencloviene, Jone; Buinauskiene, Jurate; Nieuwenhuijsen, Mark J
2013-01-01
Objectives Congenital anomalies have been inconsistently associated with maternal crude estimated exposure to drinking water trihalomethane (THM). We investigated the relationship between individual THM uptake during the first trimester of pregnancy and congenital anomalies. Methods We estimated maternal THM uptake for 3074 live births using residential tap water concentrations, drinking water ingestion, showering and bathing, and uptake factors of THM in the blood. Multiple logistic regression was used to investigate the association of THM exposure with congenital anomalies. Results We observed no statistically significant relationships between congenital anomalies and the total THM internal dose. We found little indication of a dose-response relationship for brominated THM and congenital heart anomalies. The relationship was statistically significant for bromodichloromethane (BDCM) (OR=2.16, 95% CI 1.05 to 4.46, highest vs lowest tertile) during the first month of pregnancy. During the first trimester of pregnancy, the probability of developing heart anomalies increased for every 0.1 μg/d increase in the BDCM and for every 0.01 μg/d increase in the internal dibromochloromethane (DBCM) dose (OR 1.70, 95% CI 1.09 to 2.66, and OR 1.25, 95% CI 1.01 to 1.54, respectively). A dose-response relationship was evident for musculoskeletal anomalies and DBCM exposure during the first and second months of pregnancy, while BDCM exposure tended to increase the risk of urogenital anomalies. Conclusions This study shows some evidence for an association between the internal dose of THM and the risk of congenital anomalies. In particular, increased prenatal exposure to brominated THM might increase the risk of congenital heart and musculoskeletal anomalies. PMID:23404756
NASA Astrophysics Data System (ADS)
Hood, Lon L.
2011-02-01
A re-examination of all available low-altitude LP magnetometer data confirms that magnetic anomalies are present in at least four Nectarian-aged lunar basins: Moscoviense, Mendel-Rydberg, Humboldtianum, and Crisium. In three of the four cases, a single main anomaly is present near the basin center while, in the case of Crisium, anomalies are distributed in a semi-circular arc about the basin center. These distributions, together with a lack of other anomalies near the basins, indicate that the sources of the anomalies are genetically associated with the respective basin-forming events. These central basin anomalies are difficult to attribute to shock remanent magnetization of a shocked central uplift and most probably imply thermoremanent magnetization of impact melt rocks in a steady magnetizing field. Iterative forward modeling of the single strongest and most isolated anomaly, the northern Crisium anomaly, yields a paleomagnetic pole position at 81° ± 19°N, 143° ± 31°E, not far from the present rotational pole. Assuming no significant true polar wander since the Crisium impact, this position is consistent with that expected for a core dynamo magnetizing field. Further iterative forward modeling demonstrates that the remaining Crisium anomalies can be approximately simulated assuming a multiple source model with a single magnetization direction equal to that inferred for the northernmost anomaly. This result is most consistent with a steady, large-scale magnetizing field. The inferred mean magnetization intensity within the strongest basin sources is ˜1 A/m assuming a 1-km thickness for the source layer. Future low-altitude orbital and surface magnetometer measurements will more strongly constrain the depth and/or thicknesses of the sources.
Study of 3D P-wave Velocity Structure in Lushan Area of Yunnan Province
NASA Astrophysics Data System (ADS)
Wang, X.
2017-12-01
The double difference seismic tomography method is applied to 50,711 absolute first arrival P wave arrival times and 7,294,691 high quality relative P arrival times of 5,285 events of Lushan seismic sequence to simultaneously determine the detailed crustal 3D P wave velocity structure and the hypocenter parameters in the Lushan seismic area. The results show that the front edge of aftershock in the northeast of mainshock present a spade with a steep dip angle. In the southwest of Lushan mainshock, the front edge of aftershock in low velocity zone slope gently. Our high-resolution tomographic model not only displays the general features contained in the previous models, but also reveals some new features. The Tianquan, Shuangshi and Daguan line lies in the transition zone between high velocity anomalies to the southeast and low velocity anomalies to the northwest at the ground surface. An obvious high-velocity anomaly is visible in Daxing area. With the depth increasing, Baoxing high velocity anomaly extends to Lingguan, while the southeast of the Tianquan, Shuangshi and Daguan line still shows low velocity. The high-velocity anomalies beneath Baoxing and Daxing connect each other in 10km depth, which makes the contrast between high and low velocity anomalies more sharp. Above all, the P wave velocity structure of Lushan seismic area shows obviously lateral heterogeneity. The P wave velocity anomalies represent close relationship with topographic relief and geological structure. In Baoxing area the complex rocks correspond obvious high-velocity anomalies extending down to 15km depth, while the Cenozoic rocks are correlated with low-velocity anomalies. Lushan mainshock locates at the leading edge of a low-velocity anomaly surrounded by the Baoxing and Daxing high-velocity anomalies. The main seismogenic layer dips to northwest. Meanwhile, a recoil seismic belt dips to southeast above the main seismogenic layer exists at the lower boundary of Baoxing high-velocity anomaly. A "y" distribution pattern is shown between two seismic belts.
Paranaiba, Lívia Máris Ribeiro; Coletta, Ricardo D; Swerts, Mário Sérgio Oliveira; Quintino, Rafaela Pacífico; de Barros, Letízia Monteiro; Martelli-Júnior, Hercílio
2013-07-01
Objective : Many studies have demonstrated a high frequency of dental anomalies in patients with cleft lip and/or palate. Because dental anomalies may complicate dental treatment, we investigated the prevalence of dental anomalies in a group of Brazilian patients with nonsyndromic cleft lip and/or palate. Design, Participants, Setting : Retrospective analysis was performed using clinical records of 296 patients aged between 12 and 30 years with repaired nonsyndromic cleft lip and/or palate without history of tooth extraction and orthodontic treatment. Associations between oral clefts and presence of dental anomalies outside the cleft area were investigated. Results : Dental anomalies were identified in 39.9% of the nonsyndromic cleft lip and/or palate patients, and tooth agenesis (47.5%), impacted tooth (13.1%), and microdontia (12.7%) were the most common anomalies. Cleft lip patients were less affected by dental anomalies compared with cleft palate or cleft lip and palate patients (p = .057). Specifically, patients with unilateral cleft lip and palate were significantly more affected by dental anomalies than those with bilateral cleft lip and palate (p = .00002), and individuals with unilateral complete cleft lip and palate (p = .002) and complete cleft palate (p = .01) were significantly more affected by tooth agenesis than other cleft types. Agenesis of the premolars (p = .043) and maxillary lateral incisors (p = .03) were significantly more frequent in patients with unilateral complete cleft lip and palate. Conclusions : The present study revealed a high frequency of dental anomalies in nonsyndromic cleft lip and/or palate patients and further demonstrated that patients with unilateral cleft lip and palate were frequently more affected by dental anomalies than those with bilateral cleft lip and palate. Moreover, our results demonstrate that dental anomalies should be considered during dental treatment planning for individuals affected by nonsyndromic cleft lip and/or palate.
How autumn Eurasian snow anomalies affect east asian winter monsoon: a numerical study
NASA Astrophysics Data System (ADS)
Luo, Xiao; Wang, Bin
2018-03-01
Previous studies have found that snow Eurasian anomalies in autumn can affect East Asian winter monsoon (EAWM), but the mechanisms remain controversial and not well understood. The possible mechanisms by which Eurasian autumn snow anomalies affect EAWM are investigated by numerical experiments with a coupled general circulation model and its atmospheric general circulation model component. The leading empirical orthogonal function mode of the October-November mean Eurasian snow cover is characterized by a uniform anomaly over a broad region of central Eurasia (40°N-65°N, 60°E-140°E). However, the results from a 150-ensemble mean simulation with snow depth anomaly specified in October and November reveal that the Mongolian Plateau and Vicinity (MPV, 40°-55°N, 80°-120°E) is the key region for autumn snow anomalies to affect EAWM. The excessive snow forcing can significantly enhance EAWM and the snowfall over the northwestern China and along the EAWM front zone stretching from the southeast China to Japan. The physical process involves a snow-monsoon feedback mechanism. The excessive autumn snow anomalies over the MPV region can persist into the following winter, and significantly enhance winter snow anomalies, which increase surface albedo, reduce incoming solar radiation and cool the boundary layer air, leading to an enhanced Mongolian High and a deepened East Asian trough. The latter, in turn, strengthen surface northwesterly winds, cooling East Asia and increasing snow accumulation over the MPV region and the southeastern China. The increased snow covers feedback to EAWM system through changing albedo, extending its influence southeastward. It is also found that the atmosphere-ocean coupling process can amplify the delayed influence of Eurasian snow mass anomaly on EAWM. The autumn surface albedo anomalies, however, do not have a lasting "memory" effect. Only if the albedo anomalies are artificially extended into December and January, will the EAWM be affected in a similar way as the impacts of autumn snow mass anomalies.
Chlorination Disinfection By-Products and Risk of Congenital Anomalies in England and Wales
Nieuwenhuijsen, Mark J.; Toledano, Mireille B.; Bennett, James; Best, Nicky; Hambly, Peter; de Hoogh, Cornelis; Wellesley, Diana; Boyd, Patricia A.; Abramsky, Lenore; Dattani, Nirupa; Fawell, John; Briggs, David; Jarup, Lars; Elliott, Paul
2008-01-01
Background Increased risk of various congenital anomalies has been reported to be associated with trihalomethane (THM) exposure in the water supply. Objectives We conducted a registry-based study to determine the relationship between THM concentrations and the risk of congenital anomalies in England and Wales. Methods We obtained congenital anomaly data from the National Congenital Anomalies System, regional registries, and the national terminations registry; THM data were obtained from water companies. Total THM (< 30, 30 to < 60, ≥60 μg/L), total brominated exposure (< 10, 10 to < 20, ≥20 μg/L), and bromoform exposure (< 2, 2 to < 4, ≥4 μg/L) were modeled at the place of residence for the first trimester of pregnancy. We included 2,605,226 live births, stillbirths, and terminations with 22,828 cases of congenital anomalies. Analyses using fixed- and random-effects models were performed for broadly defined groups of anomalies (cleft palate/lip, abdominal wall, major cardiac, neural tube, urinary and respiratory defects), a more restricted set of anomalies with better ascertainment, and for isolated and multiple anomalies. Data were adjusted for sex, maternal age, and socioeconomic status. Results We found no statistically significant trends across exposure categories for either the broadly defined or more restricted sets of anomalies. For the restricted set of anomalies with isolated defects, there were significant (p < 0.05) excess risks in the high-exposure categories of total THMs for ventricular septal defects [odds ratio (OR) = 1.43; 95% confidence interval (CI), 1.00–2.04] and of bromoform for major cardiovascular defects and gastroschisis (OR = 1.18; 95% CI, 1.00–1.39; and OR = 1.38; 95% CI, 1.00–1.92, respectively). Conclusion In this large national study we found little evidence for a relationship between THM concentrations in drinking water and risk of congenital anomalies. PMID:18288321
NASA Technical Reports Server (NTRS)
Hayling, Kjell Lennart
1988-01-01
Two aspects of the processing and interpretation of satellite measurements of the geomagnetic field are described. One deals with the extraction of the part of the geomagnetic field that originates from sources in the earth's atmosphere. The other investigates the possibility of using the thermal state of the oceanic lithosphere to further constrain modelling and interpretation of magnetic anomalies. It is shown that some of the magnetic signal in crustal anomaly maps can be an artifact of the mathematical algorithms that have been used to separate the crustal field from the observed data. Strong magnetic anomalies can be distorted but are probably real, but weak magnetic anomalies can arise from leakage of power from short wavelengths, and will also appear in anomaly maps as repetitions of the strong crustal anomaly. The distortion and the ghost anomalies follow the magnetic dip lines in a way that is similar to actual MAGSAT anomaly fields. This phenomenon will also affect the lower degree spherical harmonic terms in the power spectrum of the crustal field. A model of the magnetic properties of the oceanic crust that has been derived from direct measurements of the rock magnetic properties of oceanic rocks is presented. The average intensity of magnetization in the oceanic crust is not strong enough to explain magnetic anomalies observed over oceanic areas. This is the case for both near surface observations (ship and aeromagnetic data) and satellite altitude observations. It is shown that magnetic sources in the part of the upper mantle that is situated above the Curie isotherm, if sufficiently strong, can produce satellite magnetic anomalies that are comparable to MAGSAT data. The method developed for the study of depth to the Curie isotherm and magnetic anomalies can also be used in inverse modelling of satellite magnetic anomalies when the model is to be adjusted with an annihilator.
NASA Astrophysics Data System (ADS)
Frodsham, A. E.; Wen, L.
2006-12-01
A previous study [Wang and Wen, 2006] investigated the geometry and shear velocity structure of the "African Anomaly" along a great circle arc from the East Pacific Rise to the Japan Sea, and concluded the anomaly extends 1300 km above the core-mantle boundary, that the sides of the anomaly slope towards the apex and has velocity deviations of -5% in the base and -2% to -3% in the mid-lower mantle. Wang and Wen [2004] also reported on the very low velocity province that forms the base of the "African Anomaly" and its lateral extent, but the northern edge of the anomaly was poorly constrained because of the nature of the seismic data. In this presentation we focus on the nature of the anomaly in a cross-section of the mantle along a great arc, from New Zealand, to the Mid-Atlantic Ridge off the coast of Newfoundland, centered over the anomaly. In particular, we focus on the northern edge of the "African Anomaly" where a paucity of large, deep focus earthquakes makes seismic arrivals from the northwest difficult to analyze. We map the lateral extent, thickness, and shear velocity structures of the "African Anomaly" on the basis of forward travel time and waveform modeling of direct S, ScS, and SKS waves. Seismic data used in this study were collected from PASSCAL arrays: KAAPVAAL seismic array (operating years 1997-1999), Tanzania seismic array (1994- 1995), Ethiopia/Kenya seismic array (2000-2002), and the Global Seismographic Network (1994-2002). We minimize uncertainty from earthquake mislocation by relocation of the earthquakes using a global tomographic shear wave velocity model and also correct for heterogeneities outside the anomaly. We explore various methods of data processing, such as frequency filtration, low fold stacking, and cross correlation, to best interpret the arrival times of the various seismic phases and constrain the nature of the "African Anomaly" along a northwest to southeast cross-section.
Jacobson, Herbert Samuel; Tumer, Ural; Karahacioglu, Hamit
1972-01-01
This report reviews progress made during 1968 in the continuing Joint Haden Tetkik ve Arama Enstitusu (MSA)-U. S. Geological Survey (USGS) Mineral Exploration and Training Project, Subproject 2. Subproject 2 is concerned with aeromagnetic interpretation of MTA's aeromagnetic surveys, and ground investigations of selected aeromagnetic anomalies. This report includes new aeromagnetic maps for the Bolu, Canakkale-Karabiga, Demirkoy, and Orhaneli areas and reviews ground investigations in five areas. Activities for each area are sunmarized below: 1. Bolu area: The aeromagnetic map shows two belts of anomalies related to regional magnetite-bearing formations and a group of discrete anomalies, some of which may reflect significant concentrations of magnetite. To date three of these anomalies have been checked on the ground and at one a metamorphic rock containing 14 percent magnetite was observed. 2. Canakkale-Karabiga area: Ground checks were made of six aeromagnetic anomalies. At one locality (Cakirly-Koyu) 6 km south of Nazmara Sea a small magnetite deposit was found. The magnetic anomaly over the area is 150 meters long, and about 3 meters deep in the center of the anomaly exposed massive magnetite boulders. 3. Demirkoy area: The aeromagnetic map shows only one significant anomaly which was checked on the ground and found to be caused by minor magnetite at an intrusive contact. 4. Ezine area: A ground survey of 4.5 sq km area was made where magnetite boulders are locally present on the surface. No significant magnetic anomaly or iron mineralization were found. 5. Orhaneli area: The aeromagnetic map o# the area showed regional magnetic anomaly patterns related to magnetite in mafic intrusives, ultramafic rocks, and mafic flow rocks. In addition 16 localized anomalies were identified. Most of these anomalies were checked on the ground but no significant iron deposits were found. The largest deposit found was a one-meter wide magnetite vein. During the 1969 field season further investigation of anomalies in the Bolu and Orhaneli areas is planned.
Toward Continuous GPS Carrier-Phase Time Transfer: Eliminating the Time Discontinuity at an Anomaly
Yao, Jian; Levine, Judah; Weiss, Marc
2015-01-01
The wide application of Global Positioning System (GPS) carrier-phase (CP) time transfer is limited by the problem of boundary discontinuity (BD). The discontinuity has two categories. One is “day boundary discontinuity,” which has been studied extensively and can be solved by multiple methods [1–8]. The other category of discontinuity, called “anomaly boundary discontinuity (anomaly-BD),” comes from a GPS data anomaly. The anomaly can be a data gap (i.e., missing data), a GPS measurement error (i.e., bad data), or a cycle slip. Initial study of the anomaly-BD shows that we can fix the discontinuity if the anomaly lasts no more than 20 min, using the polynomial curve-fitting strategy to repair the anomaly [9]. However, sometimes, the data anomaly lasts longer than 20 min. Thus, a better curve-fitting strategy is in need. Besides, a cycle slip, as another type of data anomaly, can occur and lead to an anomaly-BD. To solve these problems, this paper proposes a new strategy, i.e., the satellite-clock-aided curve fitting strategy with the function of cycle slip detection. Basically, this new strategy applies the satellite clock correction to the GPS data. After that, we do the polynomial curve fitting for the code and phase data, as before. Our study shows that the phase-data residual is only ~3 mm for all GPS satellites. The new strategy also detects and finds the number of cycle slips by searching the minimum curve-fitting residual. Extensive examples show that this new strategy enables us to repair up to a 40-min GPS data anomaly, regardless of whether the anomaly is due to a data gap, a cycle slip, or a combination of the two. We also find that interference of the GPS signal, known as “jamming”, can possibly lead to a time-transfer error, and that this new strategy can compensate for jamming outages. Thus, the new strategy can eliminate the impact of jamming on time transfer. As a whole, we greatly improve the robustness of the GPS CP time transfer. PMID:26958451
DOE Office of Scientific and Technical Information (OSTI.GOV)
Chang, X; Liu, S; Kalet, A
Purpose: The purpose of this work was to investigate the ability of a machine-learning based probabilistic approach to detect radiotherapy treatment plan anomalies given initial disease classes information. Methods In total we obtained 1112 unique treatment plans with five plan parameters and disease information from a Mosaiq treatment management system database for use in the study. The plan parameters include prescription dose, fractions, fields, modality and techniques. The disease information includes disease site, and T, M and N disease stages. A Bayesian network method was employed to model the probabilistic relationships between tumor disease information, plan parameters and an anomalymore » flag. A Bayesian learning method with Dirichlet prior was useed to learn the joint probabilities between dependent variables in error-free plan data and data with artificially induced anomalies. In the study, we randomly sampled data with anomaly in a specified anomaly space.We tested the approach with three groups of plan anomalies – improper concurrence of values of all five plan parameters and values of any two out of five parameters, and all single plan parameter value anomalies. Totally, 16 types of plan anomalies were covered by the study. For each type, we trained an individual Bayesian network. Results: We found that the true positive rate (recall) and positive predictive value (precision) to detect concurrence anomalies of five plan parameters in new patient cases were 94.45±0.26% and 93.76±0.39% respectively. To detect other 15 types of plan anomalies, the average recall and precision were 93.61±2.57% and 93.78±3.54% respectively. The computation time to detect the plan anomaly of each type in a new plan is ∼0.08 seconds. Conclusion: The proposed method for treatment plan anomaly detection was found effective in the initial tests. The results suggest that this type of models could be applied to develop plan anomaly detection tools to assist manual and automated plan checks. The senior author received research grants from ViewRay Inc. and Varian Medical System.« less
NASA Astrophysics Data System (ADS)
Levine, P. A.; Xu, M.; Chen, Y.; Randerson, J. T.; Hoffman, F. M.
2017-12-01
Interannual variability of climatic conditions in the Amazon rainforest is associated with El Niño-Southern Oscillation (ENSO) and ocean-atmosphere interactions in the North Atlantic. Sea surface temperature (SST) anomalies in these remote ocean regions drive teleconnections with Amazonian surface air temperature (T), precipitation (P), and net ecosystem production (NEP). While SST-driven NEP anomalies have been primarily linked to T anomalies, it is unclear how much the T anomalies result directly from SST forcing of atmospheric circulation, and how much result indirectly from decreases in precipitation that, in turn, influence surface energy fluxes. Interannual variability of P associated with SST anomalies lead to variability in soil moisture (SM), which would indirectly affect T via partitioning of turbulent heat fluxes between the land surface and the atmosphere. To separate the direct and indirect influence of the SST signal on T and NEP, we performed a mechanism-denial experiment to decouple SST and SM anomalies. We used the Accelerated Climate Modeling for Energy (ACMEv0.3), with version 5 of the Community Atmosphere Model and version 4.5 of the Community Land Model. We forced the model with observed SSTs from 1982-2016. We found that SST and SM variability both contribute to T and NEP anomalies in the Amazon, with relative contributions depending on lag time and location within the Amazon basin. SST anomalies associated with ENSO drive most of the T variability at shorter lag times, while the ENSO-driven SM anomalies contribute more to T variability at longer lag times. SM variability and the resulting influence on T anomalies are much stronger in the eastern Amazon than in the west. Comparing modeled T with observations demonstrate that SST alone is sufficient for simulating the correct timing of T variability, but SM anomalies are necessary for simulating the correct magnitude of the T variability. Modeled NEP indicated that variability in carbon fluxes results from both SST and SM anomalies. As with T, SM anomalies affect NEP at a much longer lag time than SST anomalies. These results highlight the role of land-atmosphere coupling in driving climate variability within the Amazon, and suggest that land atmospheric coupling may amplify and delay carbon cycle responses to ocean-atmosphere teleconnections.
Marine magnetic anomalies in the NE Indian Ocean: the Wharton and Central Indian basins revisited
NASA Astrophysics Data System (ADS)
Jacob, J.; Dyment, J.; Yatheesh, V.; Bhattacharya, G. C.
2009-04-01
The North-eastern Indian Ocean has recently received a renewed interest. The disastrous earthquakes and tsunamis of Dec. 2004 off Sumatra have triggered a large international effort including several oceanographic cruises. The Ninetyeast Ridge, a long submarine ridge which extends NS on more than 4000 km, has been the focus of a recent cruise aiming to study the interaction of a hotspot with the oceanic lithosphere and spreading centres. Both the study of the seismogenic zone under Sumatra and the Ninetyeast Ridge formation require accurate determination of the age and structure of the oceanic lithosphere in the Wharton and Central Indian Basins. First we delineate tectonic elements such as the Sunda Trench, the Ninetyeast Ridge, and the fracture zones of the Wharton and Central Indian basins from a recent version of the free-air gravity anomaly deduced from satellite altimetry and available multibeam bathymetric data. We use all available magnetic data to identify magnetic anomalies and depict seafloor spreading isochrons in order to build a tectonic map of the Wharton Basin. To do so, we apply the analytic signal method to unambiguously determine the location of the magnetic picks. The new tectonic map shows more refinements than previous ones, as expected from a larger data set. The fossil ridge in the Wharton Basin is clearly defined; spreading ceased at anomaly 18 young (38.5 Ma), and, perhaps, as late as anomaly 15 (35 Ma). Symmetric anomalies are observed on both flanks of the fossil ridge up to anomaly 24 (54 Ma), preceded by a slight reorganization of the spreading compartments between anomalies 28 and 25 (64 - 56 Ma) and a more stable phase of spreading between anomalies 34 and 29 (83 - 64 Ma). Earlier, a major change of spreading direction is clearly seen in the bending fracture zones; interpolating in the Cretaceous Quiet Zone between anomaly 34 in the Wharton Basin and anomaly M0 off Australia leads to an age of ~100 Ma for this reorganization. Anomalies 20 to 34 are clearly identified in the western part of the Central Indian Basin. The interpretation is more difficult in the compartments located immediately west of the Ninetyeast Ridge, where multiple ridge jumps have been proposed to explain complex anomaly patterns. In a different way, we recognize a continuous sequence of anomalies 20 to 34, although the anomalies 25 to 29 seem to be wider and display complex boundaries.
Residual depth anomalies and the origin of the Australian-Antarctic discordance zone
NASA Astrophysics Data System (ADS)
Marks, Karen M.; Vogt, Peter R.; Hall, Stuart A.
1990-10-01
A new, high resolution depth anomaly map covering the anomalously deep and rough Australian-Antarctic Discordance (AAD) has been constructed using crustal ages derived from a detailed aeromagnetic survey. The map shows a large, arcuate-shaped, negative depth anomaly that is centered on the Southeast Indian Ridge and trends NNE across the Australian plate (SSE across the Antarctic plate). Within this broad scale feature, two prominent depth anomaly lows are observed at 45°S, 128°E (the northern flank) and 54°S, 125°E (the southern flank). Both lows are associated with 15 Ma oceanic crust. The observed depth anomaly patterns are compared with the distinctive patterns predicted by coldspot, downwelling limbs of convection cells, and thin crust models of the discordance source. The observed depth anomaly does not result from absolute plate motions over a fixed coldspot source because the predicted ENE trend on the Antarctic plate is not in agreement with the SSE trend observed. The symmetric arrangement of the large-scale depth anomaly and prominent lows about the ridge axis suggests instead a source that has varied in strength but remained located at the ridge axis as the ridge migrated northeastward in the absolute reference frame. The organized pattern of elongated depth anomaly highs and lows predicted for upper mantle convection (cells) is not evident in the observed depth anomaly map. Thus a convergence of downwelling limbs of convection cells beneath the discordance is not indicated. If the source of cooler upwelling that produces less magma and hence thin crust has not varied over time, nor migrated along the ridge, then the predicted depth anomaly would persist unchanged with distance from the ridge axis, and trend in the direction of relative plate motion (parallel to fracture zones). The observed depth anomaly trends obliquely across fracture zones and changes in both amplitude and location relative to the ridge axis, and is therefore not consistent with cool upwelling producing thin crust. To explain the features of the depth anomaly map, we propose that asthenospheric material flowing from the Amsterdam hotspot in the west, and the Balleny and Tasmantid hotspots in the east, collides within the discordance. Propagating rifts converging on the AAD provide evidence for such asthenospheric flow. Attenuated shear velocities beneath the George V fracture zone complex, and lavas geochemically identical to those from propagating rifts associated with hotspots, suggest a thermal anomaly producing additional asthenospheric flow east of the AAD. The increased flow and greater proximity of the discordance to the thermal anomaly and hotspots to the east produce a higher pressure gradient, and hence greater driving force, which results in a westward migration of the collision zone with time. Seafloor spreading over the westward moving collision zone has produced the observed arcuate-shaped anomaly with the accompanying oblique depth anomaly trends. We cannot decipher from depth anomalies alone whether the converging flows downwell within the AAD or simply mix with upwelling materials.
NASA Astrophysics Data System (ADS)
Yu, Xiangwei; Wang, Xiaona; Zhang, Wenbo
2016-04-01
Many researchers have investigated the Lushan source area with geological and geophysical approaches since the 2013 Lushan, China, earthquake happened. Compared with the previous tomographic studies, we have used a much large data set and an updated tomographic method to determine a small scale three-dimensional P wave velocity structure with spatial resolution less than 5km, which plays the important role for understanding the deep structure and the genetic mechanism beneath the Lushan area. The double difference seismic tomography method is applied to 50,711 absolute first arrival P wave arrival times and 7,294,691 high quality relative P arrival times of 5,285 events of Lushan seismic sequence to simultaneously determine the detailed crustal 3D P wave velocity structure and the hypocenter parameters in the Lushan seismic area. This method takes account of the path anomaly biases explicitly by making full use of valuable information of seismic wave propagation jointly with absolute and relative arrival time data. Our results show that the Lushan mainshock locates at 30.28N, 103.98E, with the depth of 16.38km. The front edge of aftershock in the northeast of mainshock present a spade with a steep dip angle, the aftershocks' extended length is about 12km. In the southwest of Lushan mainshock, the front edge of aftershock in low velocity zone slope gently, the aftershocks' extended length is about 23km. Our high-resolution tomographic model not only displays the general features contained in the previous models, but also reveals some new features. The Tianquan, Shuangshi and Daguan line lies in the transition zone between high velocity anomalies to the southeast and low velocity anomalies to the northwest at the ground surface. An obvious high-velocity anomaly is visible in Daxing area. With the depth increasing, Baoxing high velocity anomaly extends to Lingguan, while the southeast of the Tianquan, Shuangshi and Daguan line still shows low velocity. The high-velocity anomalies beneath Baoxing and Daxing connect each other in 10km depth, which makes the contrast between high and low velocity anomalies more sharp. Above 20km depth the velocity structure in southwest and northeast segment of mainshock shows a big difference: low-velocity anomalies are dominated the southwest segment, while high-velocity anomalies rule the northeast segment. Lushan aftershocks in southwest are distributed in low-velocity anomalies or the transition belt: the footwall represents low-velocity anomalies, while the hanging wall shows high-velocity anomalies. The northeastern aftershocks are distributed at the boundary between high-velocity anomalies in Baoxing and Daxing area. The P wave velocity structure of Lushan seismic area shows obviously lateral heterogeneity. The P wave velocity anomalies represent close relationship with topographic relief and geological structure. In Baoxingarea the complex rocks correspond obvious high-velocity anomalies extending down to 15km depth,while the Cenozoic rocks are correlated with low-velocity anomalies. Lushan mainshock locates at the leading edge of a low-velocity anomaly surrounded by the Baoxing and Daxing high-velocity anomalies. The main seismogenic layer dips to northwest. Meanwhile, a recoil seismic belt dips to southeast above the main seismogenic layer exists at the lower boundary of Baoxing high-velocity anomaly.
Identification of Biomarkers for Patients With Vascular Anomalies
2018-02-12
Vascular Anomaly; Generalized Lymphatic Anomaly; Kaposiform Hemangioendothelioma; Kaposiform Lymphangiomatosis; Gorham-Stout Disease; Klippel Trenaunay Syndrome; Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi
Nonrelativistic trace and diffeomorphism anomalies in particle number background
NASA Astrophysics Data System (ADS)
Auzzi, Roberto; Baiguera, Stefano; Nardelli, Giuseppe
2018-04-01
Using the heat kernel method, we compute nonrelativistic trace anomalies for Schrödinger theories in flat spacetime, with a generic background gauge field for the particle number symmetry, both for a free scalar and a free fermion. The result is genuinely nonrelativistic, and it has no counterpart in the relativistic case. Contrary to naive expectations, the anomaly is not gauge invariant; this is similar to the nongauge covariance of the non-Abelian relativistic anomaly. We also show that, in the same background, the gravitational anomaly for a nonrelativistic scalar vanishes.
Lorentz symmetry violation in the fermion number anomaly with the chiral overlap operator
NASA Astrophysics Data System (ADS)
Makino, Hiroki; Morikawa, Okuto
2016-12-01
Recently, Grabowska and Kaplan proposed a four-dimensional lattice formulation of chiral gauge theories on the basis of a chiral overlap operator. We compute the classical continuum limit of the fermion number anomaly in this formulation. Unexpectedly, we find that the continuum limit contains a term which is not Lorentz invariant. The term is, however, proportional to the gauge anomaly coefficient, and thus the fermion number anomaly in this lattice formulation automatically restores the Lorentz-invariant form when and only when the anomaly cancellation condition is met.
Do MAGSAT anomalies contain a record of past and present-day mantle convection under South America?
NASA Technical Reports Server (NTRS)
Hastings, D. A.
1985-01-01
Global anomaly maps from the National Aeronautics and Space Administration's Magnetic Field Satellite (MAGSAT) have been spatially filtered to reduce the prominence of long-wavelength east-west bands and to improve the discrimination of anomalies within structural provinces. Previous research suggested a correlation between total-field MAGSAT anomaly lows in equatorial regions with crustal bodies of relatively high average magnetic susceptibility (such as Archaean shields), and of anomaly highs with bodies of low susceptibility (such as deep parts of basins). These correlations reverse at higher latitudes.
Hanson, I M; Fletcher, J M; Jordan, T; Brown, A; Taylor, D; Adams, R J; Punnett, H H; van Heyningen, V
1994-02-01
Mutation or deletion of the PAX6 gene underlies many cases of aniridia. Three lines of evidence now converge to implicate PAX6 more widely in anterior segment malformations including Peters' anomaly. First, a child with Peters' anomaly is deleted for one copy of PAX6. Second, affected members of a family with dominantly inherited anterior segment malformations, including Peters' anomaly are heterozygous for an R26G mutation in the PAX6 paired box. Third, a proportion of Sey/+ Smalleye mice, heterozygous for a nonsense mutation in murine Pax-6, have an ocular phenotype resembling Peters' anomaly. We therefore propose that a variety of anterior segment anomalies may be associated with PAX6 mutations.
Adiabatic Quantum Anomaly Detection and Machine Learning
NASA Astrophysics Data System (ADS)
Pudenz, Kristen; Lidar, Daniel
2012-02-01
We present methods of anomaly detection and machine learning using adiabatic quantum computing. The machine learning algorithm is a boosting approach which seeks to optimally combine somewhat accurate classification functions to create a unified classifier which is much more accurate than its components. This algorithm then becomes the first part of the larger anomaly detection algorithm. In the anomaly detection routine, we first use adiabatic quantum computing to train two classifiers which detect two sets, the overlap of which forms the anomaly class. We call this the learning phase. Then, in the testing phase, the two learned classification functions are combined to form the final Hamiltonian for an adiabatic quantum computation, the low energy states of which represent the anomalies in a binary vector space.
Abnormal origins of the coronary arteries from the aortic root.
Hoffman, Julien I E
2014-10-01
Anomalous origin of a coronary artery from the aorta is a potentially serious anomaly that occurs in about 0.1-0.2% of the population. This percentage is small; however, it translates into about 4000 annual births with these anomalies. The clinical presentation of these anomalies is rare, and hence most are and will remain asymptomatic. The various anatomic anomalies are described, with anomalous origin of the left coronary artery that then passes between the aorta and pulmonary artery being the most serious of these anomalies. The pathophysiology resulting from these anomalies is described, as are methods for identifying those who require treatment; however, we still do not know the best methods of determining which patients need treatment.
The identification of factors contributing to self-reported anomalies in civil aviation.
Andrzejczak, Chris; Karwowski, Waldemar; Thompson, William
2014-01-01
The main objective of this study was to analyze anomalies voluntarily reported by pilots in civil aviation sector and identify factors leading to such anomalies. Experimental data were obtained from the NASA aviation safety reporting system (ASRS) database. These data contained a range of text records spanning 30 years of civilian aviation, both commercial (airline operations) and general aviation (private aircraft). Narrative data as well as categorical data were used. The associations between incident contributing factors and self-reported anomalies were investigated using data mining and correspondence analysis. The results revealed that a broadly defined human factors category and weather conditions were the main contributors to self-reported civil aviation anomalies. New associations between identified factors and reported anomaly conditions were also reported.
Lunar Bouguer gravity anomalies - Imbrian age craters
NASA Technical Reports Server (NTRS)
Dvorak, J.; Phillips, R. J.
1978-01-01
The Bouguer gravity of mass anomalies associated with four Imbrian age craters, analyzed in the present paper, are found to differ considerably from the values of the mass anomalies associated with some young lunar craters. Of the Imbrian age craters, only Piccolomini exhibits a negative gravity anomaly (i.e., a low density region) which is characteristic of the young craters studied. The Bouguer gravity anomalies are zero for each of the remaining Imbrian age craters. Since, Piccolomini is younger, or at least less modified, than the other Imbrian age craters, it is suggested that the processes responsible for the post-impact modification of the Imbrian age craters may also be responsible for removing the negative mass anomalies initially associated with these features.
NASA Technical Reports Server (NTRS)
Lyon-Caen, Helene; Molnar, Peter
1989-01-01
Gravity anomalies over the Alps and the Molasse Basin are examined, focusing on the relationship between the anomalies and the tectonic processes beneath the region. Bouguer gravity anomalies measured in France, Germany, Italy, and Switzerland are analyzed. No large isostatic anomalies are observed over the Alps and an elastic model is unable to account for gravity anomalies over the Molasse Basin. These results suggest that the dynamic processes that flexed the European plate down, forming the Molasse Basin and building the Alpine chain, have waned. It is proposed that the late Cenozoic uplift of the region may be due to a diminution or termination of downwelling of mantle material.
Analyzing and modeling gravity and magnetic anomalies using the SPHERE program and Magsat data
NASA Technical Reports Server (NTRS)
Braile, L. W.; Hinze, W. J.; Vonfrese, R. R. B. (Principal Investigator)
1981-01-01
Computer codes were completed, tested, and documented for analyzing magnetic anomaly vector components by equivalent point dipole inversion. The codes are intended for use in inverting the magnetic anomaly due to a spherical prism in a horizontal geomagnetic field and for recomputing the anomaly in a vertical geomagnetic field. Modeling of potential fields at satellite elevations that are derived from three dimensional sources by program SPHERE was made significantly more efficient by improving the input routines. A preliminary model of the Andean subduction zone was used to compute the anomaly at satellite elevations using both actual geomagnetic parameters and vertical polarization. Program SPHERE is also being used to calculate satellite level magnetic and gravity anomalies from the Amazon River Aulacogen.
Intracranial developmental venous anomaly: is it asymptomatic?
Puente, A Bolívar; de Asís Bravo Rodríguez, F; Bravo Rey, I; Romero, E Roldán
2018-03-16
Intracranial developmental venous anomalies are the most common vascular malformation. In the immense majority of cases, these anomalies are asymptomatic and discovered incidentally, and they are considered benign. Very exceptionally, however, they can cause neurological symptoms. In this article, we present three cases of patients with developmental venous anomalies that presented with different symptoms owing to complications derived from altered venous drainage. These anomalies were located in the left insula, right temporal lobe, and cerebellum. The exceptionality of the cases presented as well as of the images associated, which show the mechanism through which the symptoms developed, lies in the low incidence of symptomatic developmental venous anomalies reported in the literature. Copyright © 2018 SERAM. Publicado por Elsevier España, S.L.U. All rights reserved.
Environment induced anomalies on the TDRS and the role of spacecraft charging
NASA Technical Reports Server (NTRS)
Garrett, H. B.; Whittlesey, A.; Daughtridge, S.
1990-01-01
The NASA Tracking and Data Relay Satellites (TDRS) have experienced several classes of anomalies that appear to be related to the natural environment. The most serious of these have been anomalies in the Attitude Control System control processor electronics which resulted in check sum errors that were ultimately traced to high-energy, particle-induced single event upsets in the RAM memory. Three other types of anomalies on TDRS have also been correlated with environmental effects. This paper briefly documents the occurrences of these anomalies and describes the nature of each. These events are correlated with various environmental factors. For all cases, there appears to be a causal relationship between spacecraft charging events and the engineering anomalies.
Relational databases for rare disease study: application to vascular anomalies.
Perkins, Jonathan A; Coltrera, Marc D
2008-01-01
To design a relational database integrating clinical and basic science data needed for multidisciplinary treatment and research in the field of vascular anomalies. Based on data points agreed on by the American Society of Pediatric Otolaryngology (ASPO) Vascular Anomalies Task Force. The database design enables sharing of data subsets in a Health Insurance Portability and Accountability Act (HIPAA)-compliant manner for multisite collaborative trials. Vascular anomalies pose diagnostic and therapeutic challenges. Our understanding of these lesions and treatment improvement is limited by nonstandard terminology, severity assessment, and measures of treatment efficacy. The rarity of these lesions places a premium on coordinated studies among multiple participant sites. The relational database design is conceptually centered on subjects having 1 or more lesions. Each anomaly can be tracked individually along with their treatment outcomes. This design allows for differentiation between treatment responses and untreated lesions' natural course. The relational database design eliminates data entry redundancy and results in extremely flexible search and data export functionality. Vascular anomaly programs in the United States. A relational database correlating clinical findings and photographic, radiologic, histologic, and treatment data for vascular anomalies was created for stand-alone and multiuser networked systems. Proof of concept for independent site data gathering and HIPAA-compliant sharing of data subsets was demonstrated. The collaborative effort by the ASPO Vascular Anomalies Task Force to create the database helped define a common vascular anomaly data set. The resulting relational database software is a powerful tool to further the study of vascular anomalies and the development of evidence-based treatment innovation.
NASA Astrophysics Data System (ADS)
Huang, Wenyu; Chen, Ruyan; Yang, Zifan; Wang, Bin; Ma, Wenqian
2017-09-01
To examine the combined effects of the different spatial patterns of the Arctic Oscillation (AO)-related sea level pressure (SLP) anomalies and the El Niño-Southern Oscillation (ENSO)-related sea surface temperature (SST) anomalies on the wintertime surface temperature anomalies over East Asia, a nonlinear method based on self-organizing maps is employed. Investigation of identified regimes reveals that the AO can affect East Asian temperature anomalies when there are significant SLP anomalies over the Arctic Ocean and northern parts of Eurasian continent. Analogously, ENSO is found to affect East Asian temperature anomalies when significant SST anomalies are present over the tropical central Pacific. The regimes with the warmest and coldest temperature anomalies over East Asia are both associated with the negative phase of the AO. The ENSO-activated, Pacific-East Asian teleconnection pattern could affect the higher latitude continental regions when the impact of the AO is switched off. When the spatial patterns of the AO and ENSO have significant, but opposite, impacts on the coastal winds, no obvious temperature anomalies can be observed over south China. Further, the circulation state with nearly the same AO and Niño3 indices may drive rather different responses in surface temperature over East Asia. The well-known continuous weakening (recovery) of the East Asian winter monsoon that occurred around 1988 (2009) can be attributed to the transitions of the spatial patterns of the SLP anomalies over the Arctic Ocean and Eurasian continent, through their modulation on the occurrences of the Ural and central Siberian blocking events.
NASA Astrophysics Data System (ADS)
Ahmad, Nizam; Herdiwijaya, Dhani; Djamaluddin, Thomas; Usui, Hideyuki; Miyake, Yohei
2018-05-01
A satellite placed in space is constantly affected by the space environment, resulting in various impacts from temporary faults to permanent failures depending on factors such as satellite orbit, solar and geomagnetic activities, satellite local time, and satellite construction material. Anomaly events commonly occur during periods of high geomagnetic activity that also trigger plasma variation in the low Earth orbit (LEO) environment. In this study, we diagnosed anomalies in LEO satellites using electron data from the Medium Energy Proton and Electron Detector onboard the National Oceanic and Atmospheric Administration (NOAA)-15 satellite. In addition, we analyzed the fluctuation of electron flux in association with geomagnetic disturbances 3 days before and after the anomaly day. We selected 20 LEO anomaly cases registered in the Satellite News Digest database for the years 2000-2008. Satellite local time, an important parameter for anomaly diagnosis, was determined using propagated two-line element data in the SGP4 simplified general perturbation model to calculate the longitude of the ascending node of the satellite through the position and velocity vectors. The results showed that the majority of LEO satellite anomalies are linked to low-energy electron fluxes of 30-100 keV and magnetic perturbations that had a higher correlation coefficient ( 90%) on the day of the anomaly. The mean local time calculation for the anomaly day with respect to the nighttime migration of energetic electrons revealed that the majority of anomalies (65%) occurred on the night side of Earth during the dusk-to-dawn sector of magnetic local time.
NASA Astrophysics Data System (ADS)
Casey, J. F.; Gao, Y.; Benavidez, R.; Dragoi, C.
2010-12-01
The region between 12°N and 16°N along the Mid-Atlantic Ridge is known for its prolific development of oceanic core complexes and for a geochemical anomaly centered at ~14°N. We examine the correlation of the geochemical anomaly with a region characterized by low magma supply. Basalt glasses over the geochemical anomaly are unusual in exhibiting E-MORB to T-MORB HIMU-DMM isotopic gradients. The most enriched MORBs exhibit positive Ta and Nb anomalies and negative Th and Pb anomalies that are similar to some OIB basalts. Some more primitive basalts exhibit positive Ti, Sr and Eu anomalies. The center of the geochemical anomaly is characterized by elevated La/Sm ratios that are strongly correlated with Nb/La, Nb/Nb*, Ta/Ta* and Sr, Nd, Pb isotopic anomalies. In addition, we have recently documented a regional anomaly in δ7Li, with the lowest values ever recorded in MORB glasses near the center of the anomaly. We interpret this data to indicate that the mantle source in the 12-16°N region of the Mid-Atlantic Ridge involves subducted slab components including a refractory rutile-bearing eclogitic source that has suffered significant dehydration and a previously depleted mantle source that has undergone an ancient depletion event that results in little melt supply being contributed to the ridge axis. We examine melt supply implications in the context of core complex development and these unusual mantle source characteristics.
Celikoglu, M; Buyuk, S K; Sekerci, A E; Cantekin, K; Candirli, C
2015-01-01
To compare the frequency of maxillary dental anomalies in patients affected by unilateral (UCLP) and bilateral (BCLP) cleft lip with palate and to determine whether statistical differences were present or not between cleft and normal sides in UCLP group by using cone beam computed tomography (CBCT). In addition, the frequency of those dental anomalies was compared with previous studies presenting the same population without cleft Study Design: Fifty non-syndromic patients affected by UCLP (28 patients) and BCLP (22 patients) were selected for analysis of dental anomalies by means of CBCT. The frequency of maxillary dental anomalies including tooth agenesis, microdontia of lateral incisor, ectopic eruption and impaction of canine and supernumerary tooth were examined. Pearson chi-square and Fisher's exact tests were performed for statistical comparisons. All patients affected by UCLP and BCLP were found to have at least one maxillary dental anomaly. The most frequently observed dental anomaly was tooth agenesis (92.5% and 86.4%, respectively) in UCLP and BCLP groups. Tooth agenesis and canine impaction were observed more commonly in the cleft side (75.0% and 35.7%, respectively) than in the normal side (57.1% and 14.3%, respectively) in UCLP group (p≯0.05). All dental anomalies were found to be higher in both cleft groups than in general populations not affected by cleft. Since patients affected by UCLP and BCLP had at least one dental anomaly and higher dental anomaly frequency as compared to patients without cleft, those patients should be examined carefully prior to orthodontic treatment.
Analysis of renal anomalies in VACTERL association.
Cunningham, Bridget K; Khromykh, Alina; Martinez, Ariel F; Carney, Tyler; Hadley, Donald W; Solomon, Benjamin D
2014-10-01
VACTERL association refers to a combination of congenital anomalies that can include: vertebral anomalies, anal atresia, cardiac malformations, tracheo-esophageal fistula with esophageal atresia, renal anomalies (typically structural renal anomalies), and limb anomalies. We conducted a description of a case series to characterize renal findings in a cohort of patients with VACTERL association. Out of the overall cohort, 48 patients (with at least three component features of VACTERL and who had abdominal ultrasound performed) met criteria for analysis. Four other patients were additionally analyzed separately, with the hypothesis that subtle renal system anomalies may occur in patients who would not otherwise meet criteria for VACTERL association. Thirty-three (69%) of the 48 patients had a clinical manifestation affecting the renal system. The most common renal manifestation (RM) was vesicoureteral reflux (VUR) in addition to a structural defect (present in 27%), followed by unilateral renal agenesis (24%), and then dysplastic/multicystic kidneys or duplicated collected system (18% for each). Twenty-two (88%) of the 25 patients with a structural RM had an associated anorectal malformation. Individuals with either isolated lower anatomic anomalies, or both upper and lower anatomic anomalies were not statistically more likely to have a structural renal defect than those with isolated upper anatomic anomalies (p = 0.22, p = 0.284, respectively). Given the high prevalence of isolated VUR in our cohort, we recommend a screening VCUG or other imaging modality be obtained to evaluate for VUR if initial renal ultrasound shows evidence of obstruction or renal scarring, as well as ongoing evaluation of renal health. © 2014 Wiley Periodicals, Inc.
Causes of Upper-Ocean Temperature Anomalies in the Tropical North Atlantic
NASA Astrophysics Data System (ADS)
Rugg, A.; Foltz, G. R.; Perez, R. C.
2016-02-01
Hurricane activity and regional rainfall are strongly impacted by upper ocean conditions in the tropical North Atlantic, defined as the region between the equator and 20°N. A previous study analyzed a strong cold sea surface temperature (SST) anomaly that developed in this region during early 2009 and was recorded by the Pilot Research Array in the Tropical Atlantic (PIRATA) moored buoy at 4°N, 23°W (Foltz et al. 2012). The same mooring shows a similar cold anomaly in the spring of 2015 as well as a strong warm anomaly in 2010, offering the opportunity for a more comprehensive analysis of the causes of these events. In this study we examine the main causes of the observed temperature anomalies between 1998 and 2015. Basin-scale conditions during these events are analyzed using satellite SST, wind, and rain data, as well as temperature and salinity profiles from the NCEP Global Ocean Data Assimilation System. A more detailed analysis is conducted using ten years of direct measurements from the PIRATA mooring at 4°N, 23°W. Results show that the cooling and warming anomalies were caused primarily by wind-driven changes in surface evaporative cooling, mixed layer depth, and upper-ocean vertical velocity. Anomalies in surface solar radiation acted to damp the wind-driven SST anomalies in the latitude bands of the ITCZ (3°-8°N). Basin-scale analyses also suggest a strong connection between the observed SST anomalies and the Atlantic Meridional Mode, a well-known pattern of SST and surface wind anomalies spanning the tropical Atlantic.
NASA Astrophysics Data System (ADS)
Sunaryo
2018-03-01
The research with entitle response of gravity, magnetic, and geoelectrical resistivity methods on Ngeni Southern Blitar mineralization zone has been done. This study aims to find the response of several geophysical methods of gravity, magnetic, and geoelectrical resistivity in an integrated manner. Gravity data acquisition was acquired 224 data which covers the whole region of Blitar district by using Gravity Meter La Coste & Romberg Model “G”, and magnetic data acquisition were acquired 195 data which covers the southern Blitar district only by using Proton Precession Magnetometer G-856. Meanwhile geoelectrical resistivity data only done in Ngeni village which is the location of phyropilite mining with the composition content of Fe, Si, Ca, S, Cu, and Mn by using ABEM Terrameter SAS 300C. Gravity data processing was performed to obtain the Bouguer anomaly value, which included unit conversion, tidal correction, drift correction, correction of tie point, base station correction, free air correction, and Bouguer correction. Magnetic data processing has been done by some corrections i.e daily, drift, and IGRF(International Geomagnetic Refference Field) to obtain the total magnetic anomaly. From gravity data processing has been obtained the simple Bouguer anomaly value in range from -10mGal until 115mGal. From this data processing has been obtained the total magnetic anomaly value in range from -650nT until 800nT. Meanwhile from geoelectrical resistivity 3.03Ωm until 11249.91 Ωm. There is a correlation between gravity anomaly, magnetic anomaly, and geoelectrical resistivity anomaly that are associated with deep anomaly, middle anomaly, and shallow anomaly.
Distribution, Management Difficulty and Outcome of Branchial Anomalies.
Sattar, M A; Sultana, M T; Ahmed, S
2018-01-01
Branchial arch anomalies are one of the most common congenital anomalies of the neck. Developmental anomalies of the branchial apparatus account for 17% of all pediatric cervical masses. This study aimed to focus on proper diagnosis of branchial anomaly and describe occurrence, presentation, management and outcome of usual and unusual types. This ten-year prospective observational study was conducted from November 2005 to November 2015 including 2-year postoperative follow-up of the patients in Department of ENT, Bangabandhu Sheikh Mujib Medical University (BSMMU), Dhaka, Bangladesh. Total 89 patients were enrolled for this study. Information was recorded on Clinical examination, relevant investigation, Per-operative findings and Histo-pathological findings. After receiving Histo-pathological findings 61 cases were proved as branchial arch anomalies. Ultrasonography and Histopathology was done for every patient. Fistulogram and sinogram was done for patient of fistula and sinus respectively. CT scan was needed for 9 patients, MRI for 3 patients and 12 patient undergone FNAC. Outcomes of those patients were described in terms of Hospital stay, Complications and Follow up studies. Data analysis was done by Standard Statistical Method.Presentation of a number of participant's mimics Branchial arch anomalies; 4.91% was syndromal. Second branchial arch anomalies were the highest. Management was exclusively surgical. Recurrence rate was about 6.56%. Surgery is the tool for diagnosis, treatment, preventing complications, avoiding carcinoma for branchial arch anomalies.
Visualizing the chiral anomaly in Dirac and Weyl semimetals with photoemission spectroscopy
NASA Astrophysics Data System (ADS)
Behrends, Jan; Grushin, Adolfo G.; Ojanen, Teemu; Bardarson, Jens H.
2016-02-01
Quantum anomalies are the breaking of a classical symmetry by quantum fluctuations. They dictate how physical systems of diverse nature, ranging from fundamental particles to crystalline materials, respond topologically to external perturbations, insensitive to local details. The anomaly paradigm was triggered by the discovery of the chiral anomaly that contributes to the decay of pions into photons and influences the motion of superfluid vortices in 3He-A. In the solid state, it also fundamentally affects the properties of topological Weyl and Dirac semimetals, recently realized experimentally. In this work we propose that the most identifying consequence of the chiral anomaly, the charge density imbalance between fermions of different chirality induced by nonorthogonal electric and magnetic fields, can be directly observed in these materials with the existing technology of photoemission spectroscopy. With angle resolution, the chiral anomaly is identified by a characteristic note-shaped pattern of the emission spectra, originating from the imbalanced occupation of the bulk states and a previously unreported momentum dependent energy shift of the surface state Fermi arcs. We further demonstrate that the chiral anomaly likewise leaves an imprint in angle averaged emission spectra, facilitating its experimental detection. Thereby, our work provides essential theoretical input to foster the direct visualization of the chiral anomaly in condensed matter, in contrast to transport properties, such as negative magnetoresistance, which can also be obtained in the absence of a chiral anomaly.
Enhanced detection and visualization of anomalies in spectral imagery
NASA Astrophysics Data System (ADS)
Basener, William F.; Messinger, David W.
2009-05-01
Anomaly detection algorithms applied to hyperspectral imagery are able to reliably identify man-made objects from a natural environment based on statistical/geometric likelyhood. The process is more robust than target identification, which requires precise prior knowledge of the object of interest, but has an inherently higher false alarm rate. Standard anomaly detection algorithms measure deviation of pixel spectra from a parametric model (either statistical or linear mixing) estimating the image background. The topological anomaly detector (TAD) creates a fully non-parametric, graph theory-based, topological model of the image background and measures deviation from this background using codensity. In this paper we present a large-scale comparative test of TAD against 80+ targets in four full HYDICE images using the entire canonical target set for generation of ROC curves. TAD will be compared against several statistics-based detectors including local RX and subspace RX. Even a perfect anomaly detection algorithm would have a high practical false alarm rate in most scenes simply because the user/analyst is not interested in every anomalous object. To assist the analyst in identifying and sorting objects of interest, we investigate coloring of the anomalies with principle components projections using statistics computed from the anomalies. This gives a very useful colorization of anomalies in which objects of similar material tend to have the same color, enabling an analyst to quickly sort and identify anomalies of highest interest.
First branchial groove anomaly.
Kumar, M; Hickey, S; Joseph, G
2000-06-01
First branchial groove anomalies are very rare. We report a case of a first branchial groove anomaly presented as an infected cyst in an 11-month-old child. Management of such lesions is complicated because of their close association with the facial nerve. Surgical management must include identification and protection of the facial nerve. Embryology and facial nerve disposition in relation to the anomaly are reviewed.
Statistical Traffic Anomaly Detection in Time-Varying Communication Networks
2015-02-01
methods perform better than their vanilla counterparts, which assume that normal traffic is stationary. Statistical Traffic Anomaly Detection in Time...our methods perform better than their vanilla counterparts, which assume that normal traffic is stationary. Index Terms—Statistical anomaly detection...anomaly detection but also for understanding the normal traffic in time-varying networks. C. Comparison with vanilla stochastic methods For both types
Statistical Traffic Anomaly Detection in Time Varying Communication Networks
2015-02-01
methods perform better than their vanilla counterparts, which assume that normal traffic is stationary. Statistical Traffic Anomaly Detection in Time...our methods perform better than their vanilla counterparts, which assume that normal traffic is stationary. Index Terms—Statistical anomaly detection...anomaly detection but also for understanding the normal traffic in time-varying networks. C. Comparison with vanilla stochastic methods For both types
Cosmological Effects in Planetary Science
NASA Technical Reports Server (NTRS)
Blume, H. J.; Wilson, T. L.
2010-01-01
In an earlier discussion of the planetary flyby anomaly, a preliminary assessment of cosmological effects upon planetary orbits exhibiting the flyby anomaly was made. A more comprehensive investigation has since been published, although it was directed at the Pioneer anomaly and possible effects of universal rotation. The general subject of Solar System anomalies will be examined here from the point of view of planetary science.
Branchial anomalies in the pediatric population.
Schroeder, James W; Mohyuddin, Nadia; Maddalozzo, John
2007-08-01
We sought to review the presentation, evaluation, and treatment of branchial anomalies in the pediatric population and to relate these findings to recurrences and complications. We conducted a retrospective study at a tertiary care pediatric hospital. Ninety-seven pediatric patients who were treated for branchial anomalies over a 10-year period were reviewed. Patients were studied if they underwent surgical treatment for the branchial anomaly and had 1 year of postoperative follow-up; 67 children met criteria, and 74 anomalies were studied. Patients with cysts presented at a later age than did those with branchial anomaly fistulas or sinus branchial anomalies. 32% of branchial anomalies were previously infected. Of these, 71% had more than one preoperative infection. 18% of the BA were first arch derivatives, 69% were second arch derivatives and 7% were third arch derivatives. There were 22 branchial cysts, 31 branchial sinuses and 16 branchial fistulas. The preoperative and postoperative diagnoses differed in 17 cases. None of the excised specimens that contained a cystic lining recurred; all five recurrences had multiple preoperative infections. Recurrence rates are increased when there are multiple preoperative infections and when there is no epithelial lining identified in the specimen.
A Comparative Evaluation of Unsupervised Anomaly Detection Algorithms for Multivariate Data.
Goldstein, Markus; Uchida, Seiichi
2016-01-01
Anomaly detection is the process of identifying unexpected items or events in datasets, which differ from the norm. In contrast to standard classification tasks, anomaly detection is often applied on unlabeled data, taking only the internal structure of the dataset into account. This challenge is known as unsupervised anomaly detection and is addressed in many practical applications, for example in network intrusion detection, fraud detection as well as in the life science and medical domain. Dozens of algorithms have been proposed in this area, but unfortunately the research community still lacks a comparative universal evaluation as well as common publicly available datasets. These shortcomings are addressed in this study, where 19 different unsupervised anomaly detection algorithms are evaluated on 10 different datasets from multiple application domains. By publishing the source code and the datasets, this paper aims to be a new well-funded basis for unsupervised anomaly detection research. Additionally, this evaluation reveals the strengths and weaknesses of the different approaches for the first time. Besides the anomaly detection performance, computational effort, the impact of parameter settings as well as the global/local anomaly detection behavior is outlined. As a conclusion, we give an advise on algorithm selection for typical real-world tasks.
Thermal Infrared Anomalies of Several Strong Earthquakes
Wei, Congxin; Guo, Xiao; Qin, Manzhong
2013-01-01
In the history of earthquake thermal infrared research, it is undeniable that before and after strong earthquakes there are significant thermal infrared anomalies which have been interpreted as preseismic precursor in earthquake prediction and forecasting. In this paper, we studied the characteristics of thermal radiation observed before and after the 8 great earthquakes with magnitude up to Ms7.0 by using the satellite infrared remote sensing information. We used new types of data and method to extract the useful anomaly information. Based on the analyses of 8 earthquakes, we got the results as follows. (1) There are significant thermal radiation anomalies before and after earthquakes for all cases. The overall performance of anomalies includes two main stages: expanding first and narrowing later. We easily extracted and identified such seismic anomalies by method of “time-frequency relative power spectrum.” (2) There exist evident and different characteristic periods and magnitudes of thermal abnormal radiation for each case. (3) Thermal radiation anomalies are closely related to the geological structure. (4) Thermal radiation has obvious characteristics in abnormal duration, range, and morphology. In summary, we should be sure that earthquake thermal infrared anomalies as useful earthquake precursor can be used in earthquake prediction and forecasting. PMID:24222728
Thermal infrared anomalies of several strong earthquakes.
Wei, Congxin; Zhang, Yuansheng; Guo, Xiao; Hui, Shaoxing; Qin, Manzhong; Zhang, Ying
2013-01-01
In the history of earthquake thermal infrared research, it is undeniable that before and after strong earthquakes there are significant thermal infrared anomalies which have been interpreted as preseismic precursor in earthquake prediction and forecasting. In this paper, we studied the characteristics of thermal radiation observed before and after the 8 great earthquakes with magnitude up to Ms7.0 by using the satellite infrared remote sensing information. We used new types of data and method to extract the useful anomaly information. Based on the analyses of 8 earthquakes, we got the results as follows. (1) There are significant thermal radiation anomalies before and after earthquakes for all cases. The overall performance of anomalies includes two main stages: expanding first and narrowing later. We easily extracted and identified such seismic anomalies by method of "time-frequency relative power spectrum." (2) There exist evident and different characteristic periods and magnitudes of thermal abnormal radiation for each case. (3) Thermal radiation anomalies are closely related to the geological structure. (4) Thermal radiation has obvious characteristics in abnormal duration, range, and morphology. In summary, we should be sure that earthquake thermal infrared anomalies as useful earthquake precursor can be used in earthquake prediction and forecasting.
Prevalence of oro-dental anomalies among schoolchildren in Sana'a city, Yemen.
Basalamah, M; Baroudi, K
2016-04-19
Practitioners and policy-makers need information about the relative frequency of dental anomalies among children in their region. This study investigated the prevalence of different oral anomalies among schoolchildren in Sana'a city, Yemen. A sample of 1000 private and public schoolchildren aged 4-12 years were examined by the same examiner using disposable tongue blades. The total prevalence of oral anomalies was 15.1%, most commonly in boys (male:female ratio 3.2:1) aged 7-12 years. The most prevalent dental anomaly related to hard tissues was tooth hypoplasia (2.8%), followed by hypocalcification (2.6%), then microdontia (0.5%), macrodontia (0.4%), hypodontia (0.4%), supernumerary teeth (0.3%), tooth transposition (0.3%), dental fusion (0.2%) and gemination (0.2%). The most prevalent soft tissues anomaly was fissured tongue (4.0%), followed by ankyloglossia (1.8%), geographic tongue (0.9%), macroglossia (0.4%) and hairy tongue (0.3%). Appropriate measures need to be taken early to mitigate the negative impact and later costs of treatment of anomalies.
Frequency of developmental dental anomalies in the Indian population.
Guttal, Kruthika S; Naikmasur, Venkatesh G; Bhargava, Puneet; Bathi, Renuka J
2010-07-01
To evaluate the frequency of developmental dental anomalies in the Indian population. This prospective study was conducted over a period of 1 year and comprised both clinical and radiographic examinations in oral medicine and radiology outpatient department. Adult patients were screened for the presence of dental anomalies with appropriate radiographs. A comprehensive clinical examination was performed to detect hyperdontia, talon cusp, fused teeth, gemination, concrescence, hypodontia, dens invaginatus, dens evaginatus, macro- and microdontia and taurodontism. Patients with syndromes were not included in the study. Of the 20,182 patients screened, 350 had dental anomalies. Of these, 57.43% of anomalies occurred in male patients and 42.57% occurred in females. Hyperdontia, root dilaceration, peg-shaped laterals (microdontia), and hypodontia were more frequent compared to other dental anomalies of size and shape. Dental anomalies are clinically evident abnormalities. They may be the cause of various dental problems. Careful observation and appropriate investigations are required to diagnose the condition and institute treatment.
Lytle, R. Jeffrey; Lager, Darrel L.; Laine, Edwin F.; Davis, Donald T.
1979-01-01
Underground anomalies or discontinuities, such as holes, tunnels, and caverns, are located by lowering an electromagnetic signal transmitting antenna down one borehole and a receiving antenna down another, the ground to be surveyed for anomalies being situated between the boreholes. Electronic transmitting and receiving equipment associated with the antennas is activated and the antennas are lowered in unison at the same rate down their respective boreholes a plurality of times, each time with the receiving antenna at a different level with respect to the transmitting antenna. The transmitted electromagnetic waves diffract at each edge of an anomaly. This causes minimal signal reception at the receiving antenna. Triangulation of the straight lines between the antennas for the depths at which the signal minimums are detected precisely locates the anomaly. Alternatively, phase shifts of the transmitted waves may be detected to locate an anomaly, the phase shift being distinctive for the waves directed at the anomaly.
REE Partitioning in Lunar Minerals
NASA Technical Reports Server (NTRS)
Rapp, J. F.; Lapen, T. J.; Draper, D. S.
2015-01-01
Rare earth elements (REE) are an extremely useful tool in modeling lunar magmatic processes. Here we present the first experimentally derived plagioclase/melt partition coefficients in lunar compositions covering the entire suite of REE. Positive europium anomalies are ubiquitous in the plagioclase-rich rocks of the lunar highlands, and complementary negative Eu anomalies are found in most lunar basalts. These features are taken as evidence of a large-scale differentiation event, with crystallization of a global-scale lunar magma ocean (LMO) resulting in a plagioclase flotation crust and a mafic lunar interior from which mare basalts were subsequently derived. However, the extent of the Eu anomaly in lunar rocks is variable. Fagan and Neal [1] reported highly anorthitic plagioclase grains in lunar impact melt rock 60635,19 that displayed negative Eu anomalies as well as the more usual positive anomalies. Indeed some grains in the sample are reported to display both positive and negative anomalies. Judging from cathodoluminescence images, these anomalies do not appear to be associated with crystal overgrowths or zones.
Syntax does not necessarily precede semantics in sentence processing: ERP evidence from Chinese.
Zhang, Yaxu; Li, Ping; Piao, Qiuhong; Liu, Youyi; Huang, Yongjing; Shu, Hua
2013-07-01
Two event-related potential experiments were conducted to examine whether the processing of syntactic category or syntactic subcategorization frame always needs to temporally precede semantic processing during the reading of Chinese sentences of object-subject-verb construction. The sentences contained (a) no anomalies, (b) semantic only anomalies, (c) syntactic category plus semantic anomalies, or (d) transitivity plus semantic anomalies. In both experiments, all three types of anomalies elicited a broad negativity between 300 and 500 ms. This negativity included an N400 effect, given its distribution. Moreover, syntactic category plus semantic anomalies elicited a P600 response, whereas the other two types of anomalies did not. The finding of N400 effects suggests that semantic integration can be attempted even when the processing of syntactic category or syntactic subcategorization frame is unsuccessful. Thus, syntactic processing is not a necessary prerequisite for the initiation of semantic integration in Chinese. Copyright © 2013 Elsevier Inc. All rights reserved.
NASA Astrophysics Data System (ADS)
Sun, Hao; Zou, Huanxin; Zhou, Shilin
2016-03-01
Detection of anomalous targets of various sizes in hyperspectral data has received a lot of attention in reconnaissance and surveillance applications. Many anomaly detectors have been proposed in literature. However, current methods are susceptible to anomalies in the processing window range and often make critical assumptions about the distribution of the background data. Motivated by the fact that anomaly pixels are often distinctive from their local background, in this letter, we proposed a novel hyperspectral anomaly detection framework for real-time remote sensing applications. The proposed framework consists of four major components, sparse feature learning, pyramid grid window selection, joint spatial-spectral collaborative coding and multi-level divergence fusion. It exploits the collaborative representation difference in the feature space to locate potential anomalies and is totally unsupervised without any prior assumptions. Experimental results on airborne recorded hyperspectral data demonstrate that the proposed methods adaptive to anomalies in a large range of sizes and is well suited for parallel processing.
2018-01-23
Lymphatic Malformation; Generalized Lymphatic Anomaly (GLA); Central Conducting Lymphatic Anomaly; CLOVES Syndrome; Gorham-Stout Disease ("Disappearing Bone Disease"); Blue Rubber Bleb Nevus Syndrome; Kaposiform Lymphangiomatosis; Kaposiform Hemangioendothelioma/Tufted Angioma; Klippel-Trenaunay Syndrome; Lymphangiomatosis
Thermal surveillance of active volcanoes
NASA Technical Reports Server (NTRS)
Friedman, J. D. (Principal Investigator)
1973-01-01
The author has identified the following significant results. There are three significant scientific results of the discovery of 48 pinpoint anomalies on the upper flanks of Mt. Rainier: (1) Many of these points may actually be the location of fumarolic vapor emission or warm ground considerably below the summit crater. (2) Discovery of these small anomalies required specific V/H scanner settings for precise elevation on Mt. Rainier's flank, to avoid smearing the anomalies to the point of nonrecognition. Several past missions flown to map the thermal anomalies of the summit area did not/detect the flank anomalies. (3) This illustrates the value of the aerial IR scanner as a geophysical tool suited to specific problem-oriented missions, in contrast to its more general value in a regional or reconnaissance anomaly-mapping role.
An immunity-based anomaly detection system with sensor agents.
Okamoto, Takeshi; Ishida, Yoshiteru
2009-01-01
This paper proposes an immunity-based anomaly detection system with sensor agents based on the specificity and diversity of the immune system. Each agent is specialized to react to the behavior of a specific user. Multiple diverse agents decide whether the behavior is normal or abnormal. Conventional systems have used only a single sensor to detect anomalies, while the immunity-based system makes use of multiple sensors, which leads to improvements in detection accuracy. In addition, we propose an evaluation framework for the anomaly detection system, which is capable of evaluating the differences in detection accuracy between internal and external anomalies. This paper focuses on anomaly detection in user's command sequences on UNIX-like systems. In experiments, the immunity-based system outperformed some of the best conventional systems.
Modeling of self-potential anomalies near vertical dikes.
Fitterman, D.V.
1983-01-01
The self-potential (SP) Green's function for an outcropping vertical dike is derived from solutions for the dc resistivity problem for the same geometry. The Green's functions are numerically integrated over rectangular source regions on the contacts between the dike and the surrounding material to obtain the SP anomaly. The analysis is valid for thermoelectrical source mechanisms. Two types of anomalies can be produced by this geometry. When the two source planes are polarized in opposite directions, a monopolar anomaly is produced. This corresponds to the thermoelectrical properties of the dike being in contrast with the surrounding material. When the thermoelectric coefficients change monotonically across the dike, a dipolar anomaly is produced. In either case positive and negative anomalies are possible, and the greatest variation in potential will occur in the most resistive regions. -Author
NASA Technical Reports Server (NTRS)
Raychenko, L. V.
1974-01-01
Results are presented from a study of the region of anomalous cosmic radiation in the area of the Brazilian magnetic anomaly at the altitudes 250-500 km, using data measurements taken on the Kosmos-225 satellite (14-29 June 1968). The existence of a stable intensity anomaly discovered in the experiments on the second and third Soviet spacecraft-satellites is confirmed. The total vector of the geomagnetic field at different altitudes was compared with isoline maps. An altitude profile of the South Atlantic anomaly of radiation intensity was obtained, using data from the same instrument. The nature of the anomalies in cosmic radiation intensity over the regions of negative magnetic anomalies is discussed.
D'Antonio, F; Khalil, A; Garel, C; Pilu, G; Rizzo, G; Lerman-Sagie, T; Bhide, A; Thilaganathan, B; Manzoli, L; Papageorghiou, A T
2016-06-01
To explore the outcome in fetuses with prenatal diagnosis of posterior fossa anomalies apparently isolated on ultrasound imaging. MEDLINE and EMBASE were searched electronically utilizing combinations of relevant medical subject headings for 'posterior fossa' and 'outcome'. The posterior fossa anomalies analyzed were Dandy-Walker malformation (DWM), mega cisterna magna (MCM), Blake's pouch cyst (BPC) and vermian hypoplasia (VH). The outcomes observed were rate of chromosomal abnormalities, additional anomalies detected at prenatal magnetic resonance imaging (MRI), additional anomalies detected at postnatal imaging and concordance between prenatal and postnatal diagnoses. Only isolated cases of posterior fossa anomalies - defined as having no cerebral or extracerebral additional anomalies detected on ultrasound examination - were included in the analysis. Quality assessment of the included studies was performed using the Newcastle-Ottawa Scale for cohort studies. We used meta-analyses of proportions to combine data and fixed- or random-effects models according to the heterogeneity of the results. Twenty-two studies including 531 fetuses with posterior fossa anomalies were included in this systematic review. The prevalence of chromosomal abnormalities in fetuses with isolated DWM was 16.3% (95% CI, 8.7-25.7%). The prevalence of additional central nervous system (CNS) abnormalities that were missed at ultrasound examination and detected only at prenatal MRI was 13.7% (95% CI, 0.2-42.6%), and the prevalence of additional CNS anomalies that were missed at prenatal imaging and detected only after birth was 18.2% (95% CI, 6.2-34.6%). Prenatal diagnosis was not confirmed after birth in 28.2% (95% CI, 8.5-53.9%) of cases. MCM was not significantly associated with additional anomalies detected at prenatal MRI or detected after birth. Prenatal diagnosis was not confirmed postnatally in 7.1% (95% CI, 2.3-14.5%) of cases. The rate of chromosomal anomalies in fetuses with isolated BPC was 5.2% (95% CI, 0.9-12.7%) and there was no associated CNS anomaly detected at prenatal MRI or only after birth. Prenatal diagnosis of BPC was not confirmed after birth in 9.8% (95% CI, 2.9-20.1%) of cases. The rate of chromosomal anomalies in fetuses with isolated VH was 6.5% (95% CI, 0.8-17.1%) and there were no additional anomalies detected at prenatal MRI (0% (95% CI, 0.0-45.9%)). The proportions of cerebral anomalies detected only after birth was 14.2% (95% CI, 2.9-31.9%). Prenatal diagnosis was not confirmed after birth in 32.4% (95% CI, 18.3-48.4%) of cases. DWM apparently isolated on ultrasound imaging is a condition with a high risk for chromosomal and associated structural anomalies. Isolated MCM and BPC have a low risk for aneuploidy or associated structural anomalies. The small number of cases with isolated VH prevents robust conclusions regarding their management from being drawn. Copyright © 2015 ISUOG. Published by John Wiley & Sons Ltd. Copyright © 2015 ISUOG. Published by John Wiley & Sons Ltd.
The effect of scale on the interpretation of geochemical anomalies
Theobald, P.K.; Eppinger, R.G.; Turner, R.L.; Shiquan, S.
1991-01-01
The purpose of geochemical surveys changes with scale. Regional surveys identify areas where mineral deposits are most likely to occur, whereas intermediate surveys identify and prioritize specific targets. At detailed scales specific deposit models may be applied and deposits delineated. The interpretation of regional geochemical surveys must take into account scale-dependent difference in the nature and objectives of this type of survey. Overinterpretation of regional data should be resisted, as should recommendations to restrict intermediate or detailed follow-up surveys to the search for specific deposit types or to a too limited suite of elements. Regional surveys identify metallogenic provinces within which a variety of deposit types and metals are most likely to be found. At intermediate scale, these regional provinces often dissipate into discrete clusters of anomalous areas. At detailed scale, individual anomalous areas reflect local conditions of mineralization and may seem unrelated to each other. Four examples from arid environments illustrate the dramatic change in patterns of anomalies between regional and more detailed surveys. On the Arabian Shield, a broad regional anomaly reflects the distribution of highly differentiated anorogenic granites. A particularly prominent part of the regional anomaly includes, in addition to the usual elements related to the granites, the assemblage of Mo, W and Sn. Initial interpretation suggested potential for granite-related, stockwork Mo deposits. Detailed work identified three separate sources for the anomaly: a metal-rich granite, a silicified and stockwork-veined area with scheelite and molybdenite, and scheelite/powellite concentrations in skarn deposits adjacent to a ring-dike complex. Regional geochemical, geophysical and remote-sensing data in the Sonoran Desert, Mexico, define a series of linear features interpreted to reflect fundamental, northeast-trending fractures in the crust that served as the prime conduits for mineralizing fluids. At a larger scale, the linear, northeast-trending anomalies can be shown to result from a series of discrete mineralized systems with different ages and mineral assemblages. The linear pattern of anomalies disintegrates. A regional geochemical survey in the Sonoran Desert in southwestern Arizona displays a cluster of samples anomalous in Pb, Mo, Bi and W. In detail, the original regional anomaly separates into four discrete anomalous areas, each with its own distinctive suite of elements, geographic distribution and age of mineralization. A prominent regional gold anomaly in the Gobi Desert, Xinjiang, Peoples Republic of China, extends southeastward for 30 km from known lode gold deposits. Because the anomaly cuts both lithologic units and the structural grain, and because it parallels the prevailing direction of high-velocity winds, it was originally attributed to eolian dispersion. In detail, the regional anomaly consists of several east-west-trending anomalies, parallel to local lithology and structure that most likely reflect independent sources of lode gold. The regional anomaly results from smoothing of an en-echelon set of local anomalies. These examples emphasize that interpretation of regional anomalies must be tempered to consider regional-sized geologic features. Attempts to overinterpret anomalies by assigning deposit-scale attributes to regional anomalies can lead to confusion and incorrect interpretations. Potential targets that can be readily resolved only at intermediate or detailed scales of study may be overlooked. ?? 1991.
Creating a Team Archive During Fast-Paced Anomaly Response Activities in Space Missions
NASA Technical Reports Server (NTRS)
Malin, Jane T.; Hicks, LaDessa; Overland, David; Thronesbery, Carroll; Christofferesen, Klaus; Chow, Renee
2002-01-01
This paper describes a Web-based system to support the temporary Anomaly Response Team formed from distributed subteams in Space Shuttle and International Space Station missions. The system was designed for easy and flexible creation of small collections of files and links associated with work on a particular anomaly. The system supports privacy and levels of formality for the subteams. First we describe the supported groups and an anomaly response scenario. Then we describe the support system prototype, the Anomaly Response Tracking and Integration System (ARTIS). Finally, we describe our evaluation approach and the results of the evaluation.
NASA Technical Reports Server (NTRS)
Bentley, C. R.; Ritzwoller, M. H.
1983-01-01
Data selection and reduction procedures are described by which scalar and vector magnetic anomaly maps are constructed. The scalar and vertical magnetic anomalies are believed to be generated mainly in the Earth's crust. The horizontal anomalies are believed to be mainly due to short-period field-aligned currents. The correlation of scalar magnetic anomalies with known oceanic structure is remarkable -- magnetic highs are associated with oceanic ridges and magnetic lows with abyssal plains. The correlation between anomalies and continental geology is not so clear.
Nonaggressive obstetric management. An option for some fetal anomalies during the third trimester.
Chervenak, F A; McCullough, L B
1989-06-16
Nonaggressive obstetric management was used in 13 cases of anomalous fetuses during the third trimester. Criteria that define these anomalies are (1) a very high probability of a correct diagnosis and (2) either (a) a very high probability of death as an outcome of the anomaly diagnosed or (b) a very high probability of severe and irreversible deficit of cognitive developmental capacity as a result of the anomaly diagnosed. On the basis of two approaches to obstetric ethics, we defend the legitimacy of nonaggressive management of third-trimester pregnancies complicated by fetal anomalies that meet these criteria.
Behrendt, John C.; Blankenship, D.D.; Morse, D.L.; Bell, R.E.
2004-01-01
Aeromagnetic and radar ice sounding results from the 1991-1997 Central West Antarctica (CWA) aerogeophysical survey over part of the West Antarctic Ice Sheet (WAIS) and subglacial area of the volcanically active West Antarctic rift system have enabled detailed examination of specific anomaly sources. These anomalies, previously interpreted as caused by late Cenozoic subglacial volcanic centers, are compared to newly available glacial bed-elevation data from the radar ice sounding compilation of the entire area of the aeromagnetic survey to test this hypothesis in detail. We examined about 1000 shallow-source magnetic anomalies for bedrock topographic expression. Using very conservative criteria, we found over 400 specific anomalies which correlate with bed topography directly beneath each anomaly. We interpret these anomalies as indicative of the relative abundance of volcanic anomalies having shallow magnetic sources. Of course, deeper source magnetic anomalies are present, but these have longer wavelengths, lower gradients and mostly lower amplitudes from those caused by the highly magnetic late Cenozoic volcanic centers. The great bulk of these >400 (40-1200-nT) anomaly sources at the base of the ice have low bed relief (60-600 m, with about 80%10 million years ago. Eighteen of the anomalies examined, about half concentrated in the area of the WAIS divide, have high-topographic expression (as great as 400 m above sea level) and high bed relief (up to 1500 m). All of these high-topography anomaly sources at the base of the ice would isostatically rebound to elevations above sea level were the ice removed. We interpret these 18 anomaly sources as evidence of subaerial eruption of volcanoes whose topography was protected from erosion by competent volcanic flows similar to prominent volcanic peaks that are exposed above the surface of the WAIS. Further, we infer these volcanoes as possibly erupted at a time when the WAIS was absent. In contrast, at the other extreme, there are a number of shallow-source, volcanic appearing magnetic anomalies overlying the very smooth bed topography in the survey area beneath Ice Stream D (Bindshadler Ice Stream); the glacial bed probably comprises a very thin layer of unconsolidated sediments (till). Probably, the volcanic edifices here were removed at a more rapid rate because of fast glacial flow. A few of the very shallow-source "volcanic" anomalies overlie the ice shelf just downstream of the grounding line of Ice Stream D, suggesting a causal relationship, if the volcanism is recent. ?? 2004 Elsevier B.V. All rights reserved.
Comparison of liquid-state anomalies in Stillinger-Weber models of water, silicon, and germanium
NASA Astrophysics Data System (ADS)
Dhabal, Debdas; Chakravarty, Charusita; Molinero, Valeria; Kashyap, Hemant K.
2016-12-01
We use molecular dynamics simulations to compare and contrast the liquid-state anomalies in the Stillinger-Weber models of monatomic water (mW), silicon (Si), and germanium (Ge) over a fairly wide range of temperatures and densities. The relationships between structure, entropy, and mobility, as well as the extent of the regions of anomalous behavior, are discussed as a function of the degree of tetrahedrality. We map out the cascade of density, structural, pair entropy, excess entropy, viscosity, and diffusivity anomalies for these three liquids. Among the three liquids studied here, only mW displays anomalies in the thermal conductivity, and this anomaly is evident only at very low temperatures. Diffusivity and viscosity, on the other hand, show pronounced anomalous regions for the three liquids. The temperature of maximum density of the three liquids shows re-entrant behavior consistent with either singularity-free or liquid-liquid critical point scenarios proposed to explain thermodynamic anomalies. The order-map, which shows the evolution of translational versus tetrahedral order in liquids, is different for Ge than for Si and mW. We find that although the monatomic water reproduces several thermodynamic and dynamic properties of rigid-body water models (e.g., SPC/E, TIP4P/2005), its sequence of anomalies follows, the same as Si and Ge, the silica-like hierarchy: the region of dynamic (diffusivity and viscosity) anomalies encloses the region of structural anomalies, which in turn encloses the region of density anomaly. The hierarchy of the anomalies based on excess entropy and Rosenfeld scaling, on the other hand, reverses the order of the structural and dynamic anomalies, i.e., predicts that the three Stillinger-Weber liquids follow a water-like hierarchy of anomalies. We investigate the scaling of diffusivity, viscosity, and thermal conductivity with the excess entropy of the liquid and find that for dynamical properties that present anomalies there is no universal scaling of the reduced property with excess entropy for the whole range of temperatures and densities. Instead, Rosenfeld's scaling holds for all the three liquids at high densities and high temperatures, although deviations from simple exponential dependence are observed for diffusivity and viscosity at lower temperatures and intermediate densities. The slope of the scaling of transport properties obtained for Ge is comparable to that obtained for simple liquids, suggesting that this low tetrahedrality liquid, although it stabilizes a diamond crystal, is already close to simple liquid behavior for certain properties.
Comparison of liquid-state anomalies in Stillinger-Weber models of water, silicon, and germanium.
Dhabal, Debdas; Chakravarty, Charusita; Molinero, Valeria; Kashyap, Hemant K
2016-12-07
We use molecular dynamics simulations to compare and contrast the liquid-state anomalies in the Stillinger-Weber models of monatomic water (mW), silicon (Si), and germanium (Ge) over a fairly wide range of temperatures and densities. The relationships between structure, entropy, and mobility, as well as the extent of the regions of anomalous behavior, are discussed as a function of the degree of tetrahedrality. We map out the cascade of density, structural, pair entropy, excess entropy, viscosity, and diffusivity anomalies for these three liquids. Among the three liquids studied here, only mW displays anomalies in the thermal conductivity, and this anomaly is evident only at very low temperatures. Diffusivity and viscosity, on the other hand, show pronounced anomalous regions for the three liquids. The temperature of maximum density of the three liquids shows re-entrant behavior consistent with either singularity-free or liquid-liquid critical point scenarios proposed to explain thermodynamic anomalies. The order-map, which shows the evolution of translational versus tetrahedral order in liquids, is different for Ge than for Si and mW. We find that although the monatomic water reproduces several thermodynamic and dynamic properties of rigid-body water models (e.g., SPC/E, TIP4P/2005), its sequence of anomalies follows, the same as Si and Ge, the silica-like hierarchy: the region of dynamic (diffusivity and viscosity) anomalies encloses the region of structural anomalies, which in turn encloses the region of density anomaly. The hierarchy of the anomalies based on excess entropy and Rosenfeld scaling, on the other hand, reverses the order of the structural and dynamic anomalies, i.e., predicts that the three Stillinger-Weber liquids follow a water-like hierarchy of anomalies. We investigate the scaling of diffusivity, viscosity, and thermal conductivity with the excess entropy of the liquid and find that for dynamical properties that present anomalies there is no universal scaling of the reduced property with excess entropy for the whole range of temperatures and densities. Instead, Rosenfeld's scaling holds for all the three liquids at high densities and high temperatures, although deviations from simple exponential dependence are observed for diffusivity and viscosity at lower temperatures and intermediate densities. The slope of the scaling of transport properties obtained for Ge is comparable to that obtained for simple liquids, suggesting that this low tetrahedrality liquid, although it stabilizes a diamond crystal, is already close to simple liquid behavior for certain properties.
Prevalence of non-strabismic anomalies of binocular vision in Tamil Nadu: report 2 of BAND study.
Hussaindeen, Jameel Rizwana; Rakshit, Archayeeta; Singh, Neeraj Kumar; George, Ronnie; Swaminathan, Meenakshi; Kapur, Suman; Scheiman, Mitchell; Ramani, Krishna Kumar
2017-11-01
Population-based studies on the prevalence of non-strabismic anomalies of binocular vision in ethnic Indians are more than two decades old. Based on indigenous normative data, the BAND (Binocular Vision Anomalies and Normative Data) study aims to report the prevalence of non-strabismic anomalies of binocular vision among school children in rural and urban Tamil Nadu. This population-based, cross-sectional study was designed to estimate the prevalence of non-strabismic anomalies of binocular vision in the rural and urban population of Tamil Nadu. In four schools, two each in rural and urban arms, 920 children in the age range of seven to 17 years were included in the study. Comprehensive binocular vision assessment was done for all children including evaluation of vergence and accommodative systems. In the first phase of the study, normative data of parameters of binocular vision were assessed followed by prevalence estimates of non-strabismic anomalies of binocular vision. The mean and standard deviation of the age of the sample were 12.7 ± 2.7 years. The prevalence of non-strabismic anomalies of binocular vision in the urban and rural arms was found to be 31.5 and 29.6 per cent, respectively. Convergence insufficiency was the most prevalent (16.5 and 17.6 per cent in the urban and rural arms, respectively) among all the types of non-strabismic anomalies of binocular vision. There was no gender predilection and no statistically significant differences were observed between the rural and urban arms in the prevalence of non-strabismic anomalies of binocular vision (Z-test, p > 0.05). The prevalence of non-strabismic anomalies of binocular vision was found to be higher in the 13 to 17 years age group (36.2 per cent) compared to seven to 12 years (25.1 per cent) (Z-test, p < 0.05). Non-strabismic binocular vision anomalies are highly prevalent among school children and the prevalence increases with age. With increasing near visual demands in the higher grades, these anomalies could significantly impact the reading efficiency of children. Thus, it is recommended that screening for anomalies of binocular vision should be integrated into the conventional vision screening protocol. © 2016 Optometry Australia.
The South Asian Monsoon and the Tropospheric Biennial Oscillation.
NASA Astrophysics Data System (ADS)
Meehl, Gerald A.
1997-08-01
A mechanism is described that involves the south Asian monsoon as an active part of the tropospheric biennial oscillation (TBO) described in previous studies. This mechanism depends on coupled land-atmosphere-ocean interactions in the Indian sector, large-scale atmospheric east-west circulations in the Tropics, convective heating anomalies over Africa and the Pacific, and tropical-midlatitude interactions in the Northern Hemisphere. A key element for the monsoon role in the TBO is land-sea or meridional tropospheric temperature contrast, with area-averaged surface temperature anomalies over south Asia that are able to persist on a 1-yr timescale without the heat storage characteristics that contribute to this memory mechanism in the ocean. Results from a global coupled general circulation model show that soil moisture anomalies contribute to land-surface temperature anomalies (through latent heat flux anomalies) for only one season after the summer monsoon. A global atmospheric GCM in perpetual January mode is run with observed SSTs with specified convective heating anomalies to demonstrate that convective heating anomalies elsewhere in the Tropics associated with the coupled ocean-atmosphere biennial mechanism can contribute to altering seasonal midlatitude circulation. These changes in the midlatitude longwave pattern, forced by a combination of tropical convective heating anomalies over East Africa, Southeast Asia, and the western Pacific (in association with SST anomalies), are then able to maintain temperature anomalies over south Asia via advection through winter and spring to set up the land-sea meridional tropospheric temperature contrast for the subsequent monsoon. The role of the Indian Ocean, then, is to provide a moisture source and a low-amplitude coupled response component for meridional temperature contrast to help drive the south Asian monsoon. The role of the Pacific is to produce shifts in regionally coupled convection-SST anomalies. These regions are tied together and mutually interact via the large-scale east-west circulation in the atmosphere and contribute to altering midlatitude circulations as well. The coupled model results, and experiments with an atmospheric GCM that includes specified convective heating anomalies, suggest that the influence of south Asian snow cover in the monsoon is not a driving force by itself, but is symptomatic of the larger-scale shift in the midlatitude longwave pattern associated with tropical SST and convective heating anomalies.
Setup Instructions for the Applied Anomaly Detection Tool (AADT) Web Server
2016-09-01
ARL-TR-7798 ● SEP 2016 US Army Research Laboratory Setup Instructions for the Applied Anomaly Detection Tool (AADT) Web Server...for the Applied Anomaly Detection Tool (AADT) Web Server by Christian D Schlesiger Computational and Information Sciences Directorate, ARL...SUBTITLE Setup Instructions for the Applied Anomaly Detection Tool (AADT) Web Server 5a. CONTRACT NUMBER 5b. GRANT NUMBER 5c. PROGRAM ELEMENT
The fourth branchial complex anomaly: a rare clinical entity.
Patel, Alpen B; Hinni, Michael L
2011-01-01
Fourth branchial pouch anomalies are rare congenital disorders of the neck and are a consequence of abnormal development of the branchial apparatus during embryogenesis. Failure to appropriately recognize these anomalies may result in misdiagnosis, insufficient treatment, and continued recurrence. Here, we present an unique presentation of two cases, describe their diagnosis, clinical course, and management, and review the literature regarding these interesting anomalies.
The Fourth Branchial Complex Anomaly: A Rare Clinical Entity
Patel, Alpen B.; Hinni, Michael L.
2011-01-01
Fourth branchial pouch anomalies are rare congenital disorders of the neck and are a consequence of abnormal development of the branchial apparatus during embryogenesis. Failure to appropriately recognize these anomalies may result in misdiagnosis, insufficient treatment, and continued recurrence. Here, we present an unique presentation of two cases, describe their diagnosis, clinical course, and management, and review the literature regarding these interesting anomalies. PMID:22937376
Ground survey of active Central American volcanoes in November - December 1973
NASA Technical Reports Server (NTRS)
Stoiber, R. E. (Principal Investigator); Rose, W. I., Jr.
1974-01-01
The author has identified the following significant results. Thermal anomalies at two volcanoes, Santiaguito and Izalco, have grown in size in the past six months, based on repeated ground survey. Thermal anomalies at Pacaya volcano have became less intense in the same period. Large (500 m diameter) thermal anomalies exist at 3 volcanoes presently, and smaller scale anomalies are found at nine other volcanoes.
Laganà, G; Venza, N; Borzabadi-Farahani, A; Fabi, F; Danesi, C; Cozza, P
2017-03-11
To analyze the prevalence and associations between dental anomalies detectable on panoramic radiographs in a sample of non-orthodontic growing subjects. For this cross-sectional study, digital panoramic radiographs of 5005 subjects were initially screened from a single radiographic center in Rome. Inclusion criteria were: subjects who were aged 8-12 years, Caucasian, and had good diagnostic quality radiographs. Syndromic subjects, those with craniofacial malformation, or orthodontic patients were excluded and this led to a sample of 4706 subjects [mean (SD) age = 9.6 (1.2) years, 2366 males and 2340 females]. Sample was subsequently divided into four subgroups (8, 9, 10, and 11-12 year-old groups). Two operators examined panoramic radiographs to observe the presence of common dental anomalies. The prevalence and associations between dental anomalies were also investigated. The overall prevalence of dental anomalies was 20.9%. Approximately, 17.9% showed only one anomaly, 2.7% two anomalies, while only 0.3% had more than two anomalies. The most frequent anomalies were the displacement of maxillary canine (7.5%), hypodontia (7.1%), impacted teeth (3.9%), tooth ankylosis (2.8%), and tooth transposition (1.4%). The lower right second premolar was the most frequent missing teeth; 3.7% had only one tooth agenesis, and 0.08% had six or more missing tooth (Oligodontia). Mesiodens was the most common type of supernumerary tooth (0.66%). Two subjects had taurodontic tooth (0.04%). Tooth transpositions and displacement of maxillary canine were seen in 1.4 and 7.5%, retrospectively (approximately 69 and 58% were in the 8 and 9 year-old groups, retrospectively). Significant associations were detected between the different dental anomalies (P < .05). The results of our study revealed significant associations among different dental anomalies and provide further evidences to support common etiological factors.
Malformations associated with congenital diaphragmatic hernia: Impact on survival.
Bojanić, Katarina; Pritišanac, Ena; Luetić, Tomislav; Vuković, Jurica; Sprung, Juraj; Weingarten, Toby N; Schroeder, Darrell R; Grizelj, Ruža
2015-11-01
Congenital diaphragmatic hernia (CDH) is associated with high mortality. Survival is influenced by the extent of pulmonary hypoplasia and additional congenital defects. The purpose of this study was to assess the association of congenital anomalies and admission capillary carbon dioxide levels (PcCO2), as a measure of extent of pulmonary hypoplasia, on survival in neonates with CDH. This is a retrospective review of neonates with CDH admitted to a tertiary neonatal intensive care unit between 1990 and 2014. Logistic regression was used to assess whether hospital survival was associated with admission PcCO2 or associated anomalies (isolated CDH, CDH with cardiovascular anomalies, and CDH with noncardiac anomalies). The probabilities of survival (POS) score, based on birth weight and 5-min Apgar as defined by the Congenital Diaphragmatic Hernia Study Group were included as a covariate. Of 97 patients, 55 had additional malformations (cardiovascular n=12, noncardiac anomalies n=43). POS was lower in CDH with other anomalies compared to isolated CDH. Survival rate was 61.9%, 53.5% and 41.7% in isolated CDH, CDH with noncardiac anomalies and CDH with cardiovascular anomalies, respectively. After adjusting for POS score the likelihood of survival in CDH groups with additional anomalies was similar to isolated CDH (OR 0.95, 95% CI 0.22-4.15, and 1.10, 0.39-3.08, for CDH with and without cardiovascular anomalies, respectively). After adjusting for POS score, lower PcCO2 levels (OR=1.25 per 5mmHg decrease, P=0.003) were associated with better survival. Neonates with CDH have a high prevalence of congenital malformations. However, after adjusting for POS score the presence of additional anomalies was not associated with survival. The POS score and admission PcCO2 were important prognosticating factors for survival. Copyright © 2015 Elsevier Inc. All rights reserved.
NASA Astrophysics Data System (ADS)
Heki, K.; He, L.; Muafiry, I. N.
2016-12-01
We developed a simple program to perform three-dimensional (3-D) tomography of ionospheric anomalies observed using Global Navigation Satellite System (GNSS), and applied it for cases of ionospheric anomalies prior to two recent earthquakes, i.e. (1) positive and negative TEC anomalies starting 20 minutes before the 2015 September Illapel earthquake, Central Chile, and (2) stagnant MSTID that appeared 20-30 minutes before the 2016 April Kumamoto earthquake (mainshock), Kyushu, SW Japan, and stayed there until the earthquake occurred. Regarding (1), we analyzed GNSS data before and after three large earthquakes in Chile, and have reported that both positive and negative anomalies of ionospheric Total Electron Content (TEC) started 40 minutes (2010 Maule) and 20 minutes (2014 Iquique and 2015 Illapel) before earthquakes in He and Heki (2016 GRL). For the 2015 event, we further suggested that positive and negative anomalies occurred at altitudes of 200 and 400 km, respectively. This makes the epicenter, the positive anomaly, and the negative anomaly line up along the local geomagnetic field, consistent with the structure expected to occur in response to surface positive charges (e.g. Kuo et al., 2014 JGR). As for (2), we looked for ionospheric anomalies before the foreshock (Mw6.2) and the mainshock (Mw7.0) of the 2016 Kumamoto earthquakes, shallow inland earthquakes, using TEC derived from the Japanese dense GNSS network. Although we did not find anomalies as often seen before larger earthquakes (e.g. Heki and Enomoto, 2015 JGR), we found that a stationary linear positive TEC anomaly, with a shape similar to a night-time medium-scale traveling ionospheric disturbance (MSTID), emerged just above the epicenter 20 minutes before the mainshock. Unlike typical night-time MSTID, it did not propagate southwestward; instead, its positive crest stayed above the epicenter for 30 min. (see attached figure). This unusual behavior might be linked to crust-origin electric fields.
ENSO related SST anomalies and relation with surface heat fluxes over south Pacific and Atlantic
NASA Astrophysics Data System (ADS)
Chatterjee, S.; Nuncio, M.; Satheesan, K.
2017-07-01
The role of surface heat fluxes in Southern Pacific and Atlantic Ocean SST anomalies associated with El Nino Southern Oscillation (ENSO) is studied using observation and ocean reanalysis products. A prominent dipole structure in SST anomaly is found with a positive (negative) anomaly center over south Pacific (65S-45S, 120W-70W) and negative (positive) one over south Atlantic (50S-30S, 30W-0E) during austral summer (DJF) of El Nino (LaNina). During late austral spring-early summer (OND) of El Nino (LaNina), anomalous northerly (southerly) meridional moisture transport and a positive (negative) sea level pressure anomaly induces a suppressed (enhanced) latent heat flux from the ocean surface over south Pacific. This in turn results in a shallower than normal mixed layer depth which further helps in development of the SST anomaly. Mixed layer thins further due to anomalous shortwave radiation during summer and a well developed SST anomaly evolves. The south Atlantic pole exhibits exactly opposite characteristics at the same time. The contribution from the surface heat fluxes to mixed layer temperature change is found to be dominant over the advective processes over both the basins. Net surface heat fluxes anomaly is also found to be maximum during late austral spring-early summer period, with latent heat flux having a major contribution to it. The anomalous latent heat fluxes between atmosphere and ocean surface play important role in the growth of observed summertime SST anomaly. Sea-surface height also shows similar out-of-phase signatures over the two basins and are well correlated with the ENSO related SST anomalies. It is also observed that the magnitude of ENSO related anomalies over the southern ocean are weaker in LaNina years than in El Nino years, suggesting an intensified tropics-high latitude tele-connection during warm phases of ENSO.
Characteristics of chiral anomaly in view of various applications
NASA Astrophysics Data System (ADS)
Fujikawa, Kazuo
2018-01-01
In view of the recent applications of chiral anomaly to various fields beyond particle physics, we discuss some basic aspects of chiral anomaly which may help deepen our understanding of chiral anomaly in particle physics also. It is first shown that Berry's phase (and its generalization) for the Weyl model H =vFσ →.p →(t ) assumes a monopole form at the exact adiabatic limit but deviates from it off the adiabatic limit and vanishes in the high frequency limit of the Fourier transform of p →(t ) for bounded |p →(t )|. An effective action, which is consistent with the nonadiabatic limit of Berry's phase, combined with the Bjorken-Johnson-Low prescription, gives normal equal-time space-time commutators and no chiral anomaly. In contrast, an effective action with a monopole at the origin of the momentum space, which describes Berry's phase in the precise adiabatic limit but fails off the adiabatic limit, gives anomalous space-time commutators and a covariant anomaly to the gauge current. We regard this anomaly as an artifact of the postulated monopole and not a consequence of Berry's phase. As for the recent application of the chiral anomaly to the description of effective Weyl fermions in condensed matter and nuclear physics, which is closely related to the formulation of lattice chiral fermions, we point out that the chiral anomaly for each species doubler separately vanishes for a finite lattice spacing, contrary to the common assumption. Instead, a general form of pair creation associated with the spectral flow for the Dirac sea with finite depth takes place. This view is supported by the Ginsparg-Wilson fermion, which defines a single Weyl fermion without doublers on the lattice and gives a well-defined index (anomaly) even for a finite lattice spacing. A different use of anomaly in analogy to the partially conserved axial-vector current is also mentioned and could lead to an effect without fermion number nonconservation.
Goldfarb, Charles A; Shaw, Neil; Steffen, Jennifer A; Wall, Lindley B
2017-03-01
There have been few publications regarding the prevalence of congenital upper extremity anomalies and no recent reports from the United States. The purpose of this investigation was to examine the prevalence of congenital upper extremity anomalies in the total birth population of New York State over a 19-year period utilizing the New York Congenital Malformations Registry (NYCMR) database. The NYCMR includes children with at least 1 birth anomaly diagnosed by 2 years of age and listed by diagnosis code. We scrutinized these codes for specific upper extremity anomalies, including polydactyly, syndactyly, reduction defects, clubhand malformations, and syndromes with upper limb anomalies. We included children born between 1992 and 2010. There were a total of 4,883,072 live births in New York State during the study period. The overall prevalence of congenital upper extremity anomalies was 27.2 cases per 10,000 live births. Polydactyly was most common with 12,418 cases and a prevalence rate of 23.4 per 10,000 live births. The next most common anomalies included syndactyly with 627 cases affecting the hands (1498 total) and reduction defects (1111 cases). Specific syndromes were quite rare and were noted in a total of 215 live births. The prevalence of anomalies was higher in New York City compared with New York State populations at 33.0 and 21.9 per 10,000 live births, respectively. The NYCMR data demonstrate that congenital upper extremity anomalies are more common than previously reported. This is in large part due to the high prevalence of polydactyly. Although registries are imperfect, such data are helpful in monitoring prevalence rates over time, identifying potential causes or associations, and guiding health care planning and future research. Level I-diagnostic.
NASA Astrophysics Data System (ADS)
Mori, Taketoshi; Ishino, Takahito; Noguchi, Hiroshi; Shimosaka, Masamichi; Sato, Tomomasa
2011-06-01
We propose a life pattern estimation method and an anomaly detection method for elderly people living alone. In our observation system for such people, we deploy some pyroelectric sensors into the house and measure the person's activities all the time in order to grasp the person's life pattern. The data are transferred successively to the operation center and displayed to the nurses in the center in a precise way. Then, the nurses decide whether the data is the anomaly or not. In the system, the people whose features in their life resemble each other are categorized as the same group. Anomalies occurred in the past are shared in the group and utilized in the anomaly detection algorithm. This algorithm is based on "anomaly score." The "anomaly score" is figured out by utilizing the activeness of the person. This activeness is approximately proportional to the frequency of the sensor response in a minute. The "anomaly score" is calculated from the difference between the activeness in the present and the past one averaged in the long term. Thus, the score is positive if the activeness in the present is higher than the average in the past, and the score is negative if the value in the present is lower than the average. If the score exceeds a certain threshold, it means that an anomaly event occurs. Moreover, we developed an activity estimation algorithm. This algorithm estimates the residents' basic activities such as uprising, outing, and so on. The estimation is shown to the nurses with the "anomaly score" of the residents. The nurses can understand the residents' health conditions by combining these two information.
Midlatitude atmosphere-ocean interaction during El Nino. Part II. The northern hemisphere atmosphere
DOE Office of Scientific and Technical Information (OSTI.GOV)
Alexander, M.A.
The influence of midlatitude air-sea interaction on the atmospheric anomalies associated with El Nino is investigated by coupling the Community Climate Model to a mixed-layer ocean model in the North Pacific. Prescribed El Nino conditions, warm sea surface temperatures (SST) in the tropical Pacific, cause a southward displacement and strengthening of the Aleutian Low. This results in enhanced (reduced) advection of cold Asian air over the west-central (northwest) Pacific and northward advection of warm air over the eastern Pacific. Allowing air-sea feedback in the North Pacific slightly modified the El Nino-induced near-surface wind, air temperature, and precipitation anomalies. The anomalousmore » cyclonic circulation over the North Pacific is more concentric and shifted slightly to the east in the coupled simulations. Air-sea feedback also damped the air temperature anomalies over most of the North Pacific and reduced the precipitation rate above the cold SST anomaly that develops in the central Pacific. The simulated North Pacific SST anomalies and the resulting Northern Hemisphere atmospheric anomalies are roughly one-third as large as those related to the prescribed El Nino conditions in a composite of five cases. The composite geopotential height anomalies associated with changes in the North Pacific SSTs have an equivalent barotropic structure and range from -65 m to 50 m at the 200-mb level. Including air-sea feedback in the North Pacific tended to damp the atmospheric anomalies caused by the prescribed El Nino conditions in the tropical Pacific. As a result, the zonally elongated geopotential height anomalies over the West Pacific are reduced and shifted to the east. However, the atmospheric changes associated with the North Pacific SST anomalies vary widely among the five cases.« less
Slavikova, T; Zabojnikova, L; Babala, J; Varga, I
2015-01-01
The most common congenital gut motility disorder is the Hirschsprung disease (HSCR). This anomaly is characterized by absence of neural crest-derived enteric neuronal ganglia. The aim of our study was to analyze the relationship between HSCR and other congenital anomalies or malfunctions. We examined 130 patients with Hirschsprung disease from Slovakia for last 10 years. During patients examination we focused not only on morphological abnormalities, but also functional anomalies. The incidence of associated congenital anomalies in our patients with HSCR was 26.1 %. But if we add functional defects (hypothyroidism, malfunction in cellular immunity, neurological deficit) to the morphological congenital abnormalities, the rate of the patients with HSCR with additional defects achieves 50.1 %. Nine of our patients (6.9 %) had syndromic HSCR. The most frequent disorder (13.6 % of patients) was primary deficiency in cellular immunity. More than 12.3 % of patients with HSCR had genitourinary abnormalities, in 10.0 % of patients variable degree of psychomotor retardation was observed, and skeletal, muscle and limb anomalies involved 7.7 % of patients. In 7.6 % cases of patients we found congenital hypothyroidism (including 2 cases of agenesis of thyroid gland). More than 6.1 % of patients presented with an associated anomaly in gastrointestinal tract (mostly anorectal malformations). Up to 5.5 % patients had congenital anomaly of heart, 3.8 % had ophthalmic and 3.1 % had craniofacial anomalies. Down syndrome was the main diagnosis in 3.8 % patients. We discussed the relationship between HSCR and other anomalies, which are probably caused by abnormal migration, proliferation, or differentiation, of neural crest cells during embryogenesis (Tab. 1, Fig. 2, Ref. 75).
Hutchinson, Deborah R.; Klitgord, Kim D.; Tréhu, Anne M.; McBride, John H.; Nelson, K. D.
1990-01-01
Integration of magnetic anomaly analysis with COCORP deep reflection data from the southeastern United States provides three new constraints on the interpretation of the Brunswick and East Coast magnetic anomalies, as well as on the reflection data. These are as follows. (1) The source of the Brunswick anomaly lies within the deep crust. This anomaly is not caused by a Mesozoic rift basin, as proposed by some workers. (2) A simple, seaward-dipping, high- susceptibility slab model can explain both the Brunswick and East Coast magnetic anomalies. The along-strike change in character of the two anomalies results largely from a change in azimuth of the source body. (3) Beneath the southeastern United States, this source body dips south, lies immediately on the south flank of the prominent southward-dipping reflective zone revealed on COCORP surveys, and was previously associated with the Alleghanian suture between North America and Africa. These results imply that a dipping, highly magnetized zone in the upper plate of the Alleghanian suture is responsible for both the Brunswick and East Coast magnetic anomalies. The high- susceptibility material responsible for these anomalies might be mafic lower continental or oceanic crust thrust upward during Alleghanian continental collision, or mafic igneous material intruded into the upper plate of the suture zone during subsequent Mesozoic rifting, or both. The latter hypothesis implies that the Alleghanian suture acted, as a zone of weakness (a repository ?) which was reactivated to control the site of ultimate Atlantic rifting and possibly initial sea-floor spreading.
Randomized subspace-based robust principal component analysis for hyperspectral anomaly detection
NASA Astrophysics Data System (ADS)
Sun, Weiwei; Yang, Gang; Li, Jialin; Zhang, Dianfa
2018-01-01
A randomized subspace-based robust principal component analysis (RSRPCA) method for anomaly detection in hyperspectral imagery (HSI) is proposed. The RSRPCA combines advantages of randomized column subspace and robust principal component analysis (RPCA). It assumes that the background has low-rank properties, and the anomalies are sparse and do not lie in the column subspace of the background. First, RSRPCA implements random sampling to sketch the original HSI dataset from columns and to construct a randomized column subspace of the background. Structured random projections are also adopted to sketch the HSI dataset from rows. Sketching from columns and rows could greatly reduce the computational requirements of RSRPCA. Second, the RSRPCA adopts the columnwise RPCA (CWRPCA) to eliminate negative effects of sampled anomaly pixels and that purifies the previous randomized column subspace by removing sampled anomaly columns. The CWRPCA decomposes the submatrix of the HSI data into a low-rank matrix (i.e., background component), a noisy matrix (i.e., noise component), and a sparse anomaly matrix (i.e., anomaly component) with only a small proportion of nonzero columns. The algorithm of inexact augmented Lagrange multiplier is utilized to optimize the CWRPCA problem and estimate the sparse matrix. Nonzero columns of the sparse anomaly matrix point to sampled anomaly columns in the submatrix. Third, all the pixels are projected onto the complemental subspace of the purified randomized column subspace of the background and the anomaly pixels in the original HSI data are finally exactly located. Several experiments on three real hyperspectral images are carefully designed to investigate the detection performance of RSRPCA, and the results are compared with four state-of-the-art methods. Experimental results show that the proposed RSRPCA outperforms four comparison methods both in detection performance and in computational time.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Chen Yongqing, E-mail: ydonglai@mail.cgs.gov.cn; Zhao Pengda; Chen Jianguo
2001-03-15
A number of large and giant ore deposits have been discovered within the relatively small areas of lithospheric structure anomalies, including various boundary zones of tectonic plates. The regions have become the well-known intercontinental ore-forming belts, such as the circum-Pacific gold-copper, copper-molybdenum, and tungsten-tin metallogenic belts. These belts are typical geological anomalous areas. An investigation into the hydrothermal ore deposits in different regions in the former Soviet Union illustrated that the geologic structures of ore fields of almost all major commercial deposits have distinct features compared with the neighboring areas. These areas with distinct features are defined as geo-anomalies. Amore » geo-anomaly refers to such a geologic body or a combination of bodies that their composition, texture-structure, and genesis are significantly different from those of their surroundings. A geo-anomaly unit (GU) is an area containing distinct features that can be delineated with integrated ore-forming information using computer techniques on the basis of the geo-anomaly concept. Herein, the GU concept is illustrated by a case study of delineating the gold ore targets in the western Shandong uplift terrain, eastern China. It includes: (1) analyses of gold ore-forming factors; (2) compilation of normalized regional geochemical map and extraction of geochemical anomalies; (3) compilation of gravitational and aeromagnetic tectonic skeleton map and extraction of gravitational and aeromagnetic anomalies; (4) extraction of circular and linear anomalies from remote-sensing Landsat TM images; (5) establishment of a geo-anomaly conceptual model associated with known gold mineralization; (6) establishment of gold ore-forming favorability by computing techniques; and (7) delineation and assessment of ore-forming units. The units with high favorability are suggested as ore targets.« less
Prevalence of Congenital Anomalies in Infants with in Utero Exposure to Antiretrovirals
KNAPP, KATHERINE M.; BROGLY, SUSAN B.; MUENZ, DANIEL G.; SPIEGEL, HANS M.; CONWAY, DANIEL H.; SCOTT, GWENDOLYN B.; TALBOT, JEFFREY T.; SHAPIRO, DAVID E.; READ, JENNIFER S.
2011-01-01
Background While use of efficacious interventions, including antiretrovirals (ARVs), has reduced dramatically the rate of mother-to-child transmission (MTCT) of HIV, the safety of in utero ARV exposure remains of concern. Methods Data regarding 1112 infants enrolled in the International Maternal Pediatric Adolescent AIDS Clinical Trials Group (IMPAACT) protocol P1025 born between 2002 and 2007 were analyzed for this study. Congenital anomalies were classified based on the Metropolitan Atlanta Congenital Defects Program (MACDP) guidelines. Associations between congenital anomalies and timing of first in utero exposure to ARVs were evaluated by logistic regression analysis. Results 61 of the 1112 infants had congenital anomalies identified and confirmed, resulting in a prevalence of 5.49/100 live births (95%CI: 4.22–6.99). Among the 80 anomalies identified, the organ systems involved included: cardiovascular (n=33), musculoskeletal (n=15), renal (n=9), genitourinary (n=6), craniofacial (n=4), and central nervous system (n=2). First trimester exposure to efavirenz was associated with a significantly increased risk of congenital anomalies (OR 2.84, 95%CI: 1.13–7.16). No significant associations were observed between exposure to other individual ARVs or classes of ARVs started at any time during pregnancy and infant congenital anomalies. Conclusions The observed rate of congenital anomalies in this cohort is higher than previously reported for the general population, but is consistent with rates observed in other recent studies of children born to HIV-infected women. Cardiovascular anomalies occurred most frequently. With the exception of a known teratogen (efavirenz), no statistically significant associations between in utero exposure to ARVs and congenital anomalies were identified. PMID:21983213
Sadick, Maliha; Dally, Franz Josef; Schönberg, Stefan O; Stroszczynski, Christian; Wohlgemuth, Walter A
2017-10-01
Background Radiology is an interdisciplinary field dedicated to the diagnosis and treatment of numerous diseases and is involved in the development of multimodal treatment concepts. Method Interdisciplinary case management, a broad spectrum of diagnostic imaging facilities and dedicated endovascular radiological treatment options are valuable tools that allow radiology to set up an interdisciplinary center for vascular anomalies. Results Image-based diagnosis combined with endovascular treatment options is an essential tool for the treatment of patients with highly complex vascular diseases. These vascular anomalies can affect numerous parts of the body so that a multidisciplinary treatment approach is required for optimal patient care. Conclusion This paper discusses the possibilities and challenges regarding effective and efficient patient management in connection with the formation of an interdisciplinary center for vascular anomalies with strengthening of the clinical role of radiologists. Key points · Vascular anomalies, which include vascular tumors and malformations, are complex to diagnose and treat.. · There are far more patients with vascular anomalies requiring therapy than interdisciplinary centers for vascular anomalies - there is currently a shortage of dedicated interdisciplinary centers for vascular anomalies in Germany that can provide dedicated care for affected patients.. · Radiology includes a broad spectrum of diagnostic and minimally invasive therapeutic tools which allow the formation of an interdisciplinary center for vascular anomalies for effective, efficient and comprehensive patient management.. Citation Format · Sadick M, Dally FJ, Schönberg SO et al. Strategies in Interventional Radiology: Formation of an Interdisciplinary Center of Vascular Anomalies - Chances and Challenges for Effective and Efficient Patient Management. Fortschr Röntgenstr 2017; 189: 957 - 966. © Georg Thieme Verlag KG Stuttgart · New York.
The formation and analysis of a 5 deg equal area block terrestrial gravity field
NASA Technical Reports Server (NTRS)
Rapp, R. H.
1972-01-01
A set of 23,355 1 degree x 1 degree mean free air anomalies were used to predict a set of 5 degree equal area anomalies and their standard errors. Using the 1 degree data incorporating geophysically predicted values of ACIC, 1283 5 degree blocks were computed. Excluding the geophysically predicted anomalies 1249 blocks were computed. The 1 degree data were also used to compute covariance functions and the equatorial gravity and flattening implied by this data. The predicted anomalies were supplemented by model anomalies to form a complete 1654 global anomaly field. These data were used in a weighted least squares to determine potential coefficients to degree 15, and in a summation type formulation to determine potential coefficients to degree 25. These potential coefficients sets are compared to recent satellite determinations.
Geophysical interpretations of the Libby thrust belt, northwestern Montana
Kleinkopf, M. Dean; with sections by Harrison, Jack Edward; Stanley, W.D.
1997-01-01
Interpretations of gravity and aeromagnetic anomaly data, supplemented by results from two seismic reflection profiles and five magnetotelluric soundings, were used to study buried structure and lithology of the Libby thrust belt of northwestern Montana. The gravity anomaly data show a marked correlation with major structures. The Purcell anticlinorium and the Sylvanite anticline are very likely cored by stacks of thrust slices of dense crystalline basement rocks that account for the large gravity highs across these two structures. Gravity anomaly data for the Cabinet Mountains Wilderness show a string of four broad highs. The principal magnetic anomaly sources are igneous intrusive rocks, major fault zones, and magnetite-bearing sedimentary rocks of the Ravalli Group. The most important magnetic anomalies in the principal study area are five distinct positive anomalies associated with Cretaceous or younger cupolas and stocks.
[Coexistence of female sexual organ malformation and urinary tract anomalies].
Rzymski, P; Szpakowska-Rzymska, I; el Yubi, R; Wilczak, M; Sajdak, S; Opala, T
2001-02-01
The aim of the study was to estimate the correlation between sexual organs and urinary tract malformation. The retrospective analysis of clinical data obtained from 50 patients with sexual organs anomalies diagnosed in the Academic Gynaecological Centre between 1992-1999 was performed. Material included 24 patients with the Meyer-Rokitansky-Küster-Hauser syndrome and 26 with other sexual organs' malformations. Frequency of urinary tract anomalies was 42%, 11 patients with Meyer-Rokitansky-Küster-Hauser syndrome and 11 with other malformations. The gravity of urinary tract anomalies showed no statistical significant difference dependent on the type and symmetry of genital malformation. Urinary tract anomalies were more frequent in cases of asymmetric genital malformation and the difference was statistically significant. Intravenous urography proofed to be more sensitive than ultrasonography in diagnosing urinary tract anomalies.
Hussain, Afreen; De, Kalyan; Thomas, Liju; Nagesh, Rahul; Mote, Sambhaji; Ingole, Baban
2016-08-31
Skeletal tissue growth anomalies (STAs) of corals are capable of causing considerable degradation of reef health. This study is the first report of growth anomalies in Turbinaria corals and the first descriptive study of Indian corals. T. mesenterina colonies at 2 sites were affected by small, round to irregularly shaped growth anomalies. Prevalence of STAs was observed to be higher in T. mesenterina colonies with larger diameters. Prevalence of STAs on T. mesenterina was 71% at Site 1 and 40% at Site 2. Affected colonies were seen to be undergoing tissue damage and infiltration by filamentous algae. We describe the gross morphology of growth anomalies which can act as baseline data for growth anomalies from this region, but further investigation is needed to understand the form and etiology of this coral disease.
A model for anomaly classification in intrusion detection systems
NASA Astrophysics Data System (ADS)
Ferreira, V. O.; Galhardi, V. V.; Gonçalves, L. B. L.; Silva, R. C.; Cansian, A. M.
2015-09-01
Intrusion Detection Systems (IDS) are traditionally divided into two types according to the detection methods they employ, namely (i) misuse detection and (ii) anomaly detection. Anomaly detection has been widely used and its main advantage is the ability to detect new attacks. However, the analysis of anomalies generated can become expensive, since they often have no clear information about the malicious events they represent. In this context, this paper presents a model for automated classification of alerts generated by an anomaly based IDS. The main goal is either the classification of the detected anomalies in well-defined taxonomies of attacks or to identify whether it is a false positive misclassified by the IDS. Some common attacks to computer networks were considered and we achieved important results that can equip security analysts with best resources for their analyses.
Regional magnetic anomaly constraints on continental rifting
NASA Technical Reports Server (NTRS)
Vonfrese, R. R. B.; Hinze, W. J.; Olivier, R.; Bentley, C. R.
1985-01-01
Radially polarized MAGSAT anomalies of North and South America, Europe, Africa, India, Australia and Antarctica demonstrate remarkably detailed correlation of regional magnetic lithospheric sources across rifted margins when plotted on a reconstruction of Pangea. These major magnetic features apparently preserve their integrity until a superimposed metamorphoric event alters the magnitude and pattern of the anomalies. The longevity of continental scale magnetic anomalies contrasts markedly with that of regional gravity anomalies which tend to reflect predominantly isostatic adjustments associated with neo-tectonism. First observed as a result of NASA's magnetic satellite programs, these anomalies provide new and fundamental constraints on the geologic evolution and dynamics of the continents and oceans. Accordingly, satellite magnetic observations provide a further tool for investigating continental drift to compliment other lines of evidence in paleoclimatology, paleontology, paleomagnetism, and studies of the radiometric ages and geometric fit of the continents.
Prevalence of dental anomalies in a population of cleft lip and palate patients.
Al Jamal, Ghaida A; Hazza'a, Abdalla M; Rawashdeh, Ma'amon A
2010-07-01
The aim of our study was to investigate radiographically the prevalence of dental anomalies in a group of Jordanian cleft lip and/or palate subjects. This is a retrospective review of panoramic radiographs of 78 subjects with cleft lip and/or palate that were evaluated from their file records and investigated for possible dental anomalies. Dental anomalies were found frequently in cleft lip and/or palate subjects. Missing teeth were found in 66.7% of the patients; the tooth most commonly missing was the maxillary lateral incisor. Supernumerary teeth were found in 16.7% of patients; 37% had microdontia; 70.5% had taurodontism; 30.8% had transposition and/or ectopic teeth; 19.2% had dilacerations; and 30.8% had hypoplastic teeth. There was no statistically significant difference in the above anomalies' prevalence between males and females. However, it was found that subjects with bilateral cleft lip and/or palate had significantly more microdontia (p = .005), dilaceration (p = .002), and hypoplastic teeth (p = .0001) than subjects with unilateral cleft lip and/or palate. The prevalence of dental anomalies in cleft lip and/or palate patients was higher than what had been reported in the normal Jordanian population. This emphasizes the relation of cleft lip and/or palate to all dental anomalies studied. Although our study represents a thorough and complete description of dental anomalies present in a sample of cleft lip and/or palate subjects, larger samples are required to effectively determine the relationship of each dental anomaly with cleft type.
Sá, Jamile; Araújo, Luana; Guimarães, Laís; Maranhão, Samário; Lopes, Gabriela; Medrado, Alena; Coletta, Ricardo; Reis, Silvia
2016-01-01
Individuals with nonsyndromic cleft lip with or without cleft palate (NSCL±P) present high frequency of dental anomalies, which may represent complicating factors for dental treatment. The aim of this study was to investigate the prevalence of dental anomalies inside cleft area in a group of Brazilians with NSCL±P. Retrospective analysis of 178 panoramic radiographs of patients aged from 12 to 45 years old and without history of tooth extraction or orthodontic treatment was performed. Association between cleft type and the prevalence of dental anomalies was assessed by chi-square test with a significance level set at p≤ 0.05. Dental anomalies were found in 88.2% (n=157) of the patients. Tooth agenesis (47.1%), giroversion (20%) and microdontia (15.5%) were the most common anomalies. Individuals with unilateral complete cleft lip and palate (CLP, p<0.0001), bilateral complete CLP (p=0.0002) and bilateral incomplete CLP (p< 0.0001) were more affected by tooth agenesis than individuals with other cleft types. The maxillary lateral incisors were the most affected teeth (p<0.0001). The present study revealed a high frequency of dental anomalies inside cleft region in NSCL±P patients, and further demonstrated that patients with unilateral complete CLP and bilateral incomplete CLP were frequently more affected by dental anomalies. Moreover, our results demonstrate that dental anomalies should be considered during dental treatment planning of individuals affected by NSCL±P.
Garib, Daniela Gamba; Lancia, Melissa; Kato, Renata Mayumi; Oliveira, Thais Marchini; Neves, Lucimara Teixeira das
2016-01-01
To estimate the risk of PDC occurrence in children with dental anomalies identified early during mixed dentition. The sample comprised 730 longitudinal orthodontic records from children (448 females and 282 males) with an initial mean age of 8.3 years (SD=1.36). The dental anomaly group (DA) included 263 records of patients with at least one dental anomaly identified in the initial or middle mixed dentition. The non-dental anomaly group (NDA) was composed of 467 records of patients with no dental anomalies. The occurrence of PDC in both groups was diagnosed using panoramic and periapical radiographs taken in the late mixed dentition or early permanent dentition. The prevalence of PDC in patients with and without early diagnosed dental anomalies was compared using the chi-square test (p<0.01), relative risk assessments (RR), and positive and negative predictive values (PPV and NPV). PDC frequency was 16.35% and 6.2% in DA and NDA groups, respectively. A statistically significant difference was observed between groups (p<0.01), with greater risk of PDC development in the DA group (RR=2.63). The PPV and NPV was 16% and 93%, respectively. Small maxillary lateral incisors, deciduous molar infraocclusion, and mandibular second premolar distoangulation were associated with PDC. Children with dental anomalies diagnosed during early mixed dentition have an approximately two and a half fold increased risk of developing PDC during late mixed dentition compared with children without dental anomalies.
Turtle Carapace Anomalies: The Roles of Genetic Diversity and Environment
Velo-Antón, Guillermo; Becker, C. Guilherme; Cordero-Rivera, Adolfo
2011-01-01
Background Phenotypic anomalies are common in wild populations and multiple genetic, biotic and abiotic factors might contribute to their formation. Turtles are excellent models for the study of developmental instability because anomalies are easily detected in the form of malformations, additions, or reductions in the number of scutes or scales. Methodology/Principal Findings In this study, we integrated field observations, manipulative experiments, and climatic and genetic approaches to investigate the origin of carapace scute anomalies across Iberian populations of the European pond turtle, Emys orbicularis. The proportion of anomalous individuals varied from 3% to 69% in local populations, with increasing frequency of anomalies in northern regions. We found no significant effect of climatic and soil moisture, or climatic temperature on the occurrence of anomalies. However, lower genetic diversity and inbreeding were good predictors of the prevalence of scute anomalies among populations. Both decreasing genetic diversity and increasing proportion of anomalous individuals in northern parts of the Iberian distribution may be linked to recolonization events from the Southern Pleistocene refugium. Conclusions/Significance Overall, our results suggest that developmental instability in turtle carapace formation might be caused, at least in part, by genetic factors, although the influence of environmental factors affecting the developmental stability of turtle carapace cannot be ruled out. Further studies of the effects of environmental factors, pollutants and heritability of anomalies would be useful to better understand the complex origin of anomalies in natural populations. PMID:21533278
A Comparative Evaluation of Unsupervised Anomaly Detection Algorithms for Multivariate Data
Goldstein, Markus; Uchida, Seiichi
2016-01-01
Anomaly detection is the process of identifying unexpected items or events in datasets, which differ from the norm. In contrast to standard classification tasks, anomaly detection is often applied on unlabeled data, taking only the internal structure of the dataset into account. This challenge is known as unsupervised anomaly detection and is addressed in many practical applications, for example in network intrusion detection, fraud detection as well as in the life science and medical domain. Dozens of algorithms have been proposed in this area, but unfortunately the research community still lacks a comparative universal evaluation as well as common publicly available datasets. These shortcomings are addressed in this study, where 19 different unsupervised anomaly detection algorithms are evaluated on 10 different datasets from multiple application domains. By publishing the source code and the datasets, this paper aims to be a new well-funded basis for unsupervised anomaly detection research. Additionally, this evaluation reveals the strengths and weaknesses of the different approaches for the first time. Besides the anomaly detection performance, computational effort, the impact of parameter settings as well as the global/local anomaly detection behavior is outlined. As a conclusion, we give an advise on algorithm selection for typical real-world tasks. PMID:27093601
Practical method to identify orbital anomaly as spacecraft breakup in the geostationary region
NASA Astrophysics Data System (ADS)
Hanada, Toshiya; Uetsuhara, Masahiko; Nakaniwa, Yoshitaka
2012-07-01
Identifying a spacecraft breakup is an essential issue to define the current orbital debris environment. This paper proposes a practical method to identify an orbital anomaly, which appears as a significant discontinuity in the observation data, as a spacecraft breakup. The proposed method is applicable to orbital anomalies in the geostationary region. Long-term orbital evolutions of breakup fragments may conclude that their orbital planes will converge into several corresponding regions in inertial space even if the breakup epoch is not specified. This empirical method combines the aforementioned conclusion with the search strategy developed at Kyushu University, which can identify origins of observed objects as fragments released from a specified spacecraft. This practical method starts with selecting a spacecraft that experienced an orbital anomaly, and formulates a hypothesis to generate fragments from the anomaly. Then, the search strategy is applied to predict the behavior of groups of fragments hypothetically generated. Outcome of this predictive analysis specifies effectively when, where and how we should conduct optical measurements using ground-based telescopes. Objects detected based on the outcome are supposed to be from the anomaly, so that we can confirm the anomaly as a spacecraft breakup to release the detected objects. This paper also demonstrates observation planning for a spacecraft anomaly in the geostationary region.
The magnetic anomaly of the Ivreazone
NASA Technical Reports Server (NTRS)
Albert, G.
1979-01-01
A magnetic field survey was made in the Ivreazone in 1969/70. The results were: significant anomaly of the vertical intensity is found. It follows the basic main part of the Ivrea-Verbano zone and continues to the south. The width of the anomaly is about 10 km, the maximum measures about +800 gamma. The model interpretation shows that possibly the anomaly belongs to an amphibolitic body, which in connection with the Ivrea-body was found by deep seismic sounding. Therefore, the magnetic anomaly provides further evidence for the conception that the Ivrea-body has to be regarded as a chip of earthmantle material pushed upward by tectonic processes.
Paleo-Pole Positions from Martian Magnetic Anomaly Data
NASA Technical Reports Server (NTRS)
Taylor, Patrick T.; Frawley, James J.
2003-01-01
Magnetic component anomaly maps were made from five mapping cycles of the Mars Global Surveyor s magnetometer data. Our goal was to find and isolate positive and negative anomaly pairs which would indicate magnetization of a single source body. From these anomalies we could compute the direction of the magnetizing vector and subsequently the location of the magnetic pole existing at the time of magnetization. We found nine suitable anomaly pairs and from these we computed four North and 3 South poles with two at approximately 60 degrees north latitude. These results suggest that during the existence of the Martian main magnetic field it experienced several reversals.
Paleo-Pole Positions from Martian Magnetic Anomaly Data
NASA Technical Reports Server (NTRS)
Frawley, James J.; Taylor, Patrick T.
2004-01-01
Magnetic component anomaly maps were made from five mapping cycles of the Mars Global Surveyor's magnetometer data. Our goal was to find and isolate positive and negative anomaly pairs which would indicate magnetization of a single source body. From these anomalies we could compute the direction of the magnetizing vector and subsequently the location of the magnetic pole existing at the time of magnetization. We found nine suitable anomaly pairs and from these we computed paleo-poles that were nearly equally divided between north, south and mid-latitudes. These results suggest that during the existence of the martian main magnetic field it experienced several reversals and excursions.
GEOS 3 data processing for the recovery of geoid undulations and gravity anomalies
NASA Technical Reports Server (NTRS)
Rapp, R. H.
1979-01-01
The paper discusses the analysis of GEOS 3 altimeter data for the determination of geoid heights and point and mean gravity anomalies. Methods are presented for determining the mean anomalies and mean undulations from the GEOS 3 altimeter data available by the end of September 1977 without having a complete set of precise orbits. The editing of the data is extensive to remove questionable data, although no filtering of the data is carried out. An adjustment process is carried out to eliminate orbit error and altimeter bias. Representative point anomaly values are computed to investigate anomaly behavior across the Bonin Trench and over the Patton seamounts.
NASA Astrophysics Data System (ADS)
Tivey, M.; Tominaga, M.; Sager, W. W.
2012-12-01
The Jurassic sequence of marine magnetic anomalies i.e. older than M29 remain the last part of the marine magnetic anomaly sequence of the geomagnetic polarity timescale (GPTS) that can be gleaned from the ocean crustal record. While Jurassic crust is present in several areas of the world's ocean basins, the oldest and arguably best preserved sequence is in the western Pacific where three lineations sets (Japanese, Hawaiian and Phoenix) converge on the oldest remaining ocean crust on the planet (i.e. crust that has not been subducted). The magnetic anomalies in these 3 lineation sets are marked by low amplitude, relatively indistinct anomalies (tiny wiggles) that collectively have been called the Jurassic quiet Zone (JQZ). Over the past 20 years we have been working on resolving the character and origin of these anomalies with various technologies to improve our resolution of this period. Following an aeromagnetic survey that revealed the possible presence of lineated anomalies older than M29 in the Japanese lineations, we conducted a deeptow magnetometer survey of the Japanese sequence in 1992. In 2002/03 we extended and confirmed this deeptow record with a deeptowed sidescan and magnetometer survey of the Japanese lineation sequence by tying in ODP Hole 801C and extending the anomaly sequence between M29 and M44. These surveys reveal remarkably fast reversals that are lineated and decrease in intensity back in time until M38, prior to which the sequence becomes somewhat confused (the LAZ or low amplitude zone) before recovering in both amplitude and lineated character around Hole 801C (M42). These results are partially supported by recently reported terrestrial magnetostratigraphy records that show the existence of reversals back to M38. A Jurassic GPTS was constructed from this Japanese anomaly sequence, but the overall global significance of the reversal sequence and systematic field intensity changes require confirmation from crustal records created at different spreading centers. In 2011, we undertook the next generation of near-bottom magnetic studies utilizing new autonomous underwater vehicle (AUV) technology (Sentry) and concurrent deeptow and seismic profiling surveys of the Hawaiian anomaly sequence. Preliminary results show a similar anomaly record to the Japanese sequence: an overall decrease in anomaly amplitude from M19 to M38 and a period of low amplitude, which in turn is preceded by a return to stronger amplitude anomalies. The magnetic anomaly correlations between Hawaiian and Japanese sea-surface level profiles confirm the reversal record back in time, at least, to M38. At the mid-water and near-bottom AUV levels, the magnetic data clearly show the short-wavelength anomaly character of the M29-M38 sequence, indicating that the fast reversals observed in the Japanese lineations are also present in the Hawaiian lineation set. The strong similarity of overall anomaly patterns between Japanese and Hawaiian sequences supports the preliminary conclusion that geomagnetic field behavior during the Jurassic was dynamic, with fast reversals and changing intensity, and certainly not "quiet". Finally, AUV surveys provide measurements of the marine magnetic anomaly record whose resolution is limited only by the crustal recording process and crustal magnetic architecture rather than spatial resolution.
Gravity Anomaly Intersects Moon Basin
2012-12-05
A linear gravity anomaly intersecting the Crisium basin on the nearside of the moon has been revealed by NASA GRAIL mission. The GRAIL gravity gradient data are shown at left, with the location of the anomaly indicated.
NASA Astrophysics Data System (ADS)
Li, Changbo; Wang, Liangshu; Sun, Bin; Feng, Runhai; Wu, Yongjing
2015-09-01
In this paper, we introduce the method of Wavelet Multi-scale Decomposition (WMD) combined with Power Spectrum Analysis (PSA) for the separation of regional gravity and magnetic anomalies. The Songliao Basin is situated between the Siberian Plate and the North China Plate, and its main structural trend of gravity and magnetic anomaly fields is NNE. The study area shows a significant feature of deep collage-type construction. According to the feature of gravity field, the region was divided into five sub-regions. The gravity and magnetic fields of the Songliao Basin were separated using WMD with a 4th order separation. The apparent depth of anomalies in each order was determined by Logarithmic PSA. Then, the shallow high-frequency anomalies were removed and the 2nd-4th order wavelet detail anomalies were used to study the basin's major faults. Twenty-six faults within the basement were recognized. The 4th order wavelet approximate anomalies were used for the inversion of the Moho discontinuity and the Curie isothermal surface.
Reduced to pole long-wavelength magnetic anomalies of Africa and Europe
NASA Technical Reports Server (NTRS)
Olivier, R.; Hinze, W. J.; Vonfrese, R. R. B.
1985-01-01
To facilitate analysis of the tectonic framework for Africa, Europe and adjacent marine areas, MAGSAT scalar anomaly data are differentially reduced to the pole and compared to regional geologic information and geophysical data including surface free-air gravity anomaly data upward continued to satellite elevation (350 km) on a spherical Earth. Comparative analysis shows magnetic anomalies correspond with both ancient as well as more recent Cenozoic structural features. Anomalies associated with ancient structures are primarily caused by intra-crustal lithologic variations such as the crustal disturbance associated with the Bangui anomaly in west-central Africa. Anomalies correlative with Cenozoic tectonic elements appear to be related to Curie isotherm perturbations. A possible example of the latter is the well-defined trend of magnetic minima that characterize the Alphine orogenic belt from the Atlas mountains to Eurasia. In contrast, a well-defined magnetic satellite minimum extends across the stable craton from Finland to the Ural mountains. Prominent magnetic maxima characterize the Arabian plate, Iceland, the Kursk region of the central Russian uplift, and generally the Precambrian shields of Africa.
Reduced to Pole Long-wavelength Magnetic Anomalies of Africa and Europe
NASA Technical Reports Server (NTRS)
Hinze, W. J.; Vonfrese, R. R. B. (Principal Investigator); Olivier, R.
1984-01-01
To facilitate analysis of the tectonic framework for Africa, Europe and adjacent marine areas, MAGSAT scalar anomaly data are differentially reduced to the pole and compared to regional geologic information and geophysical data including surface free-air gravity anomaly data upward continued to satellite elevation (350 km) on a spherical Earth. Comparative analysis shows magnetic anomalies correspond with both ancient as well as more recent Cenozoic structural features. Anomalies associated with ancient structures are primarily caused by intra-crustal lithologic variations such as the crustal disturbance associated with the Bangui anomaly in west-central Africa. Anomalies correlative with Cenozoic tectonic elements appear to be related to Curie isotherm perturbations. A possible example of the latter is the well-defined trend of magnetic minima that characterize the Alpine orogenic belt from the Atlas mountains to Eurasia. In contrast, a well-defined magnetic satellite minimum extends across the stable craton from Finland to the Ural mountains. Prominent magnetic maxima characterize the Arabian plate, Iceland, the Kursk region of the central Russian uplift, and generally the Precambrian shields of Africa.
Prevalence of Dental Anomalies in Permanent Dentition of Brazilian Individuals with Down Syndrome
Cuoghi, Osmar Aparecido; Topolski, Francielle; Perciliano de Faria, Lorraine; Occhiena, Carla Machado; Ferreira, Nancy dos Santos Pinto; Ferlin, Camila Ribeiro; Rogério de Mendonça, Marcos
2016-01-01
Objective: The aim of this study was to evaluate the incidence of dental anomalies in the permanent dentition of individuals with Down Syndrome (DS) to increase the knowledge on the dental issues in this syndrome. Method: One hundred and five panoramic X-rays of patients with DS (61 males and 44 females), aged 7 to 42 years were used. The data were statistically analyzed using bivariate analyses test (p <0.05). Results: Dental anomalies were observed in 50.47% of the sample. More than one anomaly was observed in 9.52% of the individuals. The most frequent dental anomalies were hypodontia and microdontia (16.19%), followed by retained tooth (10.47%), taurodontism (9.52%), supernumerary teeth (5.71%), macrodontia (2.85%) and root dilaceration (0.95%). There was no statistically significant difference between genders for any of the anomalies. Conclusion: A high prevalence of dental anomalies was observed in individuals with DS. The results of the present study reinforce the importance of good dental care, offering a greater basis for professionals who provide dental service to these patients. PMID:27733874
Prevalence of Dental Anomalies in Permanent Dentition of Brazilian Individuals with Down Syndrome.
Cuoghi, Osmar Aparecido; Topolski, Francielle; Perciliano de Faria, Lorraine; Occhiena, Carla Machado; Ferreira, Nancy Dos Santos Pinto; Ferlin, Camila Ribeiro; Rogério de Mendonça, Marcos
2016-01-01
The aim of this study was to evaluate the incidence of dental anomalies in the permanent dentition of individuals with Down Syndrome (DS) to increase the knowledge on the dental issues in this syndrome. One hundred and five panoramic X-rays of patients with DS (61 males and 44 females), aged 7 to 42 years were used. The data were statistically analyzed using bivariate analyses test ( p <0.05). Dental anomalies were observed in 50.47% of the sample. More than one anomaly was observed in 9.52% of the individuals. The most frequent dental anomalies were hypodontia and microdontia (16.19%), followed by retained tooth (10.47%), taurodontism (9.52%), supernumerary teeth (5.71%), macrodontia (2.85%) and root dilaceration (0.95%). There was no statistically significant difference between genders for any of the anomalies. A high prevalence of dental anomalies was observed in individuals with DS. The results of the present study reinforce the importance of good dental care, offering a greater basis for professionals who provide dental service to these patients.
Dental anomalies associated with buccally- and palatally-impacted maxillary canines.
Sajnani, Anand K; King, Nigel M
2014-08-01
The aim of the present study was to determine the association of both buccally- and palatally-impacted canines with other dental anomalies. This retrospective study was conducted on a population of 533 southern Chinese children and adolescents who had impacted maxillary canines that had been treated in the Paediatric Dentistry and Orthodontics Clinic, Prince Philip Dental Hospital, The University of Hong Kong, Hong Kong. Descriptions of the impacted canine and other associated anomalies were obtained from the case notes and radiographs. Clinical photographs and study casts were used, where available. A total of 253 (47.5%) patients with impacted maxillary canines were diagnosed with other dental anomalies. Microdontia was the most frequently-occurring anomaly reported in these patients, with the maxillary lateral incisor the most commonly affected tooth. Other odontogenic anomalies that were associated with both buccally- and palatally-impacted canines included hypodontia, supernumerary teeth, transposition of other teeth, enamel hypoplasia, other impacted teeth, and dens invaginatus. Both buccally- and palatally-impacted canines were found to be associated with other odontogenic anomalies. © 2013 Wiley Publishing Asia Pty Ltd.
Road Anomalies Detection System Evaluation.
Silva, Nuno; Shah, Vaibhav; Soares, João; Rodrigues, Helena
2018-06-21
Anomalies on road pavement cause discomfort to drivers and passengers, and may cause mechanical failure or even accidents. Governments spend millions of Euros every year on road maintenance, often causing traffic jams and congestion on urban roads on a daily basis. This paper analyses the difference between the deployment of a road anomalies detection and identification system in a “conditioned” and a real world setup, where the system performed worse compared to the “conditioned” setup. It also presents a system performance analysis based on the analysis of the training data sets; on the analysis of the attributes complexity, through the application of PCA techniques; and on the analysis of the attributes in the context of each anomaly type, using acceleration standard deviation attributes to observe how different anomalies classes are distributed in the Cartesian coordinates system. Overall, in this paper, we describe the main insights on road anomalies detection challenges to support the design and deployment of a new iteration of our system towards the deployment of a road anomaly detection service to provide information about roads condition to drivers and government entities.
Anomalies, renormalization group flows, and the a-theorem in six-dimensional (1, 0) theories
Córdova, Clay; Dumitrescu, Thomas T.; Intriligator, Kenneth
2016-10-17
We establish a linear relation between the a-type Weyl anomaly and the ’t Hooft anomaly coeffcients for the R-symmetry and gravitational anomalies in sixdimensional (1,0) superconformal field theories. For RG flows onto the tensor branch, where conformal symmetry is spontaneously broken, supersymmetry relates the anomaly mismatch Δa to the square of a four-derivative interaction for the dilaton. This establishes the a-theorem for all such flows. The four-derivative dilaton interaction is in turn related to the Green-Schwarz-like terms that are needed to match the ’t Hooft anomalies on the tensor branch, thus fixing their relation to Δa. We use our formulamore » to obtain exact expressions for the a-anomaly of N small E 8 instantons, as well as N M 5-branes probing an orbifold singularity, and verify the a-theorem for RG flows onto their Higgs branches. We also discuss aspects of supersymmetric RG flows that terminate in scale but not conformally invariant theories with massless gauge fields.« less
Six-dimensional regularization of chiral gauge theories
NASA Astrophysics Data System (ADS)
Fukaya, Hidenori; Onogi, Tetsuya; Yamamoto, Shota; Yamamura, Ryo
2017-03-01
We propose a regularization of four-dimensional chiral gauge theories using six-dimensional Dirac fermions. In our formulation, we consider two different mass terms having domain-wall profiles in the fifth and the sixth directions, respectively. A Weyl fermion appears as a localized mode at the junction of two different domain walls. One domain wall naturally exhibits the Stora-Zumino chain of the anomaly descent equations, starting from the axial U(1) anomaly in six dimensions to the gauge anomaly in four dimensions. Another domain wall implies a similar inflow of the global anomalies. The anomaly-free condition is equivalent to requiring that the axial U(1) anomaly and the parity anomaly are canceled among the six-dimensional Dirac fermions. Since our formulation is based on a massive vector-like fermion determinant, a nonperturbative regularization will be possible on a lattice. Putting the gauge field at the four-dimensional junction and extending it to the bulk using the Yang-Mills gradient flow, as recently proposed by Grabowska and Kaplan, we define the four-dimensional path integral of the target chiral gauge theory.
Improved determination of vector lithospheric magnetic anomalies from MAGSAT data
NASA Technical Reports Server (NTRS)
Ravat, Dhananjay
1993-01-01
Scientific contributions made in developing new methods to isolate and map vector magnetic anomalies from measurements made by Magsat are described. In addition to the objective of the proposal, the isolation and mapping of equatorial vector lithospheric Magsat anomalies, isolation of polar ionospheric fields during the period were also studied. Significant progress was also made in isolation of polar delta(Z) component and scalar anomalies as well as integration and synthesis of various techniques of removing equatorial and polar ionospheric effects. The significant contributions of this research are: (1) development of empirical/analytical techniques in modeling ionospheric fields in Magsat data and their removal from uncorrected anomalies to obtain better estimates of lithospheric anomalies (this task was accomplished for equatorial delta(X), delta(Z), and delta(B) component and polar delta(Z) and delta(B) component measurements; (2) integration of important processing techniques developed during the last decade with the newly developed technologies of ionospheric field modeling into an optimum processing scheme; and (3) implementation of the above processing scheme to map the most robust magnetic anomalies of the lithosphere (components as well as scalar).
Marine Magnetic Anomalies and the Reconstruction of the World
NASA Technical Reports Server (NTRS)
Heirtzler, James R.; Smith, David E. (Technical Monitor)
2000-01-01
Until the middle of the 20th century little was known about magnetic anomalies in the oceans. Then it was discovered that there are relatively large anomalies in most of the oceans and they were unrelated to any geological structure known at that time. In the early 1950's large anomalies had been found over the Mid-Atlantic Ridge, and linear anomalies over the eastern continental shelf of North America and, shortly after that, off the west coast. A survey of the ridge south of Iceland showed that the anomalies were linear, parallel to the ridge axis, and symmetrical about the axis. Using the theory that the anomalies were caused by geomagnetic field reversals and seafloor spreading it was possible to greatly extend the time scale of geomagnetic reversals, to determine the velocity of seafloor spreading and estimate the time of opening of the North Atlantic. Lamont had a world-wide collection of marine magnetic profiles. These were used, systematically, to determine the positions of most of the land masses of the world since the beginnings of the world's present oceans.
Determinants of parental decisions to abort for chromosome abnormalities.
Drugan, A; Greb, A; Johnson, M P; Krivchenia, E L; Uhlmann, W R; Moghissi, K S; Evans, M I
1990-08-01
Parental decisions concerning the continuation of pregnancy following prenatal detection of abnormal chromosomes were evaluated for 80 patients whose diagnosis and prenatal counselling were performed in our centre. Twenty-two anomalies were diagnosed by chorionic villus sampling (CVS) and 58 by amniocentesis. The severity of the chromosome anomaly and associated ultrasound findings in the first vs. second trimester were correlated with patients' decisions. No difference was found in the likelihood of parental decisions to interrupt or continue a pregnancy between CVS and amniocentesis for either the 'severe' or the 'questionable' group of chromosome anomalies. Ninety-three per cent of patients with severe prognosis and 27 per cent with questionable prognosis opted for pregnancy termination (p less than 0.0001). The association of ultrasound anomalies and termination was highly significant (p less than 0.001). The severity of the chromosome anomaly, and, to a lesser extent, the visualization of anomalies on ultrasound were the major determinants of parental decisions to terminate the pregnancy. The diagnosis of an anomaly in the first trimester was no more likely ito lead to a termination of pregnancy than in the second trimester.
The possible physical mechanism for the EAP-SR co-action
NASA Astrophysics Data System (ADS)
Gong, Zhiqiang; Feng, Guolin; Dogar, Muhammad Mubashar; Huang, Gang
2017-11-01
The anomalous characteristics of summer precipitation and atmospheric circulation in the East Asia-West Pacific Region (EA-WP) associated with the co-action of East Asia/Pacific teleconnection-Silk Road teleconnection (EAP-SR) are investigated in this study. The compositions of EAP-SR phase anomalies can be expressed as pattern I (+ +), pattern II (+ -), pattern III (- -), and pattern IV (- +) using EAP and SR indices. It is found that the spatial distribution of summer precipitation anomalies in EA-WP corresponding to pattern I (III) shows a tripole structure in the meridional direction and a zonal dipole structure in the subtropical region, while pattern II (IV) presents a tripole pattern in meridional direction with compressed and continuous anomalies in the zonal direction over the subtropical region. The similar meridional and zonal structures are also found in the geopotential height anomalies at 500-hPa, as well as wind anomalies and moisture convergence at 850-hPa. Finally, a schematic mechanism for the EAP-SR co-action upon the summer precipitation in EA-WP is built: (1) Pattern I (III) exhibits that the negative (positive) sea surface temperature (SST) anomalies over tropical East Pacific may cause the enhanced (weakened) convective activity dominating the West Pacific, trigger the positive (negative) EAP teleconnection and produce more (less) precipitation. Besides, the negative (positive) SST anomalies over the Indonesia Maritime Continent (IMC) may further weaken (strengthen) anomalous downward (upward) motion over the South China Sea (SCS), cause negative (positive) geopotential height anomalies at the middle troposphere and surrounding regions through the function of the tropical Hadley circulation. Then the negative (positive) geopotential height anomalies could motivate the positive (negative) EAP teleconnection through the northward propagation of wave-activity perturbation. Meanwhile, a positive (negative) geopotential height anomalous pattern over Eastern Europe motivates a Rossby wave train propagation from Western Europe to west-central Asia. This circumstance can cause suppressed (enhanced) convection and less (more) precipitation over northwestern India and Pakistan, which could strengthen the negative (positive) geopotential height and positive (negative) vorticity anomalies over central East Asia, resulting in a negative (positive) SR teleconnection along the Asian jet stream. A positive (negative) lobe over the Korean Peninsula and Japan corresponding to SR overlaps with a positive (negative) lobe of EAP, which strengthens the anomalous phase contrast on both sides of 120°E. Accordingly, summer precipitation anomalies in EA-WP exhibit the meridional tripole pattern and the zonal dipole pattern. (2) Pattern II (IV) indicates that the normal SST anomalies over the tropical East Pacific cause the weak tele-impact on the tropical West Pacific, while the positive (negative) SST anomalies over the IMC will lead to a negative (positive) lobe of EAP over the subtropical region. This circumstance can weaken the positive (negative) lobe of SR over subtropical region, causing compressed and continuous negative (positive) anomalies of 500-hPa geopotential height and positive (negative) surface precipitation anomalies from central East China to Japan.
Hawking radiation and covariant anomalies
DOE Office of Scientific and Technical Information (OSTI.GOV)
Banerjee, Rabin; Kulkarni, Shailesh
2008-01-15
Generalizing the method of Wilczek and collaborators we provide a derivation of Hawking radiation from charged black holes using only covariant gauge and gravitational anomalies. The reliability and universality of the anomaly cancellation approach to Hawking radiation is also discussed.
Europium anomaly in plagioclase feldspar - Experimental results and semiquantitative model.
NASA Technical Reports Server (NTRS)
Weill, D. F.; Drake, M. J.
1973-01-01
The partition of europium between plagioclase feldspar and magmatic liquid is considered in terms of the distribution coefficients for divalent and trivalent europium. A model equation is derived giving the europium anomaly in plagioclase as a function of temperature and oxygen fugacity. The model explains europium anomalies in plagioclase synthesized under controlled laboratory conditions as well as the variations of the anomaly observed in natural terrestrial and extraterrestrial igneous rocks.
Europium anomaly in plagioclase feldspar: experimental results and semiquantitative model.
Weill, D F; Drake, M J
1973-06-08
The partition of europium between plagioclase feldspar and magmatic liquid is considered in terms of the distribution coefficients for divalent and trivalent europium. A model equation is derived giving the europium anomaly in plagioclase as a function of temperature and oxygen fugacity. The model explains europium anomalies in plagioclase synthesized under controlled laboratory conditions as well as the variations of the anomaly observed in natural terrestrial and extraterrestrial igneous rocks.
Estimation of subsurface thermal structure using sea surface height and sea surface temperature
NASA Technical Reports Server (NTRS)
Kang, Yong Q. (Inventor); Jo, Young-Heon (Inventor); Yan, Xiao-Hai (Inventor)
2012-01-01
A method of determining a subsurface temperature in a body of water is disclosed. The method includes obtaining surface temperature anomaly data and surface height anomaly data of the body of water for a region of interest, and also obtaining subsurface temperature anomaly data for the region of interest at a plurality of depths. The method further includes regressing the obtained surface temperature anomaly data and surface height anomaly data for the region of interest with the obtained subsurface temperature anomaly data for the plurality of depths to generate regression coefficients, estimating a subsurface temperature at one or more other depths for the region of interest based on the generated regression coefficients and outputting the estimated subsurface temperature at the one or more other depths. Using the estimated subsurface temperature, signal propagation times and trajectories of marine life in the body of water are determined.
Prevalence of Dental Anomalies in Odisha Population: A Panoramic Radiographic Study.
Goutham, Balasubramanya; Bhuyan, Lipsa; Chinnannavar, Sangamesh N; Kundu, Madhurima; Jha, Kunal; Behura, Shyam S
2017-07-01
The aim of this study was to evaluate the prevalence of dental anomalies (DAs) in Odisha population using panoramic radiographs. In this study, 1,080 panoramic radiographs were evaluated for DAs. Dental records were reviewed for diagnostic confirmation. Anomalies related to the shape, size, position of teeth, and number of roots (supernumerary roots) were evaluated. The study results showed the prevalence of DAs to be 35.27%. The most prevalent was dilaceration, which was seen in 46.71% cases followed by peg laterals in 20.99%. Dental anomalies were present in more than one-third of the study group, which was mostly related to shape of the teeth. Early diagnosis of these DAs helps in avoiding complications. Identification of DAs requires proper examination and thereby subsequent correct diagnosis. These anomalies can pose complications in normal functioning of orofacial complex. The knowledge of the prevalence of such anomalies aids dental practitioners for a proper treatment plan.
Common dental anomalies in cleft lip and palate patients.
Haque, Sanjida; Alam, Mohammad Khursheed
2015-01-01
Cleft lip and palate (CLP) is the most common orofacial congenital malformation in live births. CLP can occur individually or in combination with other congenital deformities. Affected patients experience a number of dental, aesthetic, speech, hearing, and psychological complications and have a higher incidence of severe dental conditions. The purpose of this study is to characterise the different types of dental anomalies that are frequently associated with CLP patients based on a literature survey. By literature survey, this study characterises the different types of dental anomalies that are frequently associated with cleft lip and palate patients. Common dental anomalies associated with CLP are supernumerary tooth, congenitally missing tooth, delayed tooth development, morphological anomalies in both deciduous and permanent dentition, delayed eruption of permanent maxillary incisors, microdontia, and abnormal tooth number. The incidence of certain dental anomalies is strongly correlated with Cleft lip and palate, a finding that is consistent with previous studies.
Congenital anomalies of the pulmonary arteries: spectrum of findings on computed tomography.
Bueno, J; Flors, L; Mejía, M
Congenital anomalies of the pulmonary arteries are uncommon. They can occur in isolation or in association with congenital heart defects. Isolated congenital anomalies remain undiscovered until they are reported as incidental findings on imaging tests, usually not until adolescence. We review the embryological development and normal anatomy of the pulmonary arteries as well as the spectrum of computed tomography findings for various congenital anomalies: unilateral interruption of the pulmonary artery, anomalous origin of the left pulmonary artery (pulmonary artery sling), idiopathic aneurysm of the pulmonary artery, and other anomalies associated with congenital heart defects. Congenital anomalies of the pulmonary arteries represent a diagnostic challenge for clinicians and radiologists. Computed tomography is useful for their diagnosis, and general radiologists need to be familiar with their imaging appearance because they are often discovered incidentally. Copyright © 2016 SERAM. Publicado por Elsevier España, S.L.U. All rights reserved.
Geophysical investigations of a geothermal anomaly at Wadi Ghadir, eastern Egypt
NASA Technical Reports Server (NTRS)
Morgan, P.; Boulos, F. K.; Hennin, S. F.; El-Sherif, A. A.; El-Sayed, A. A.; Basta, N. Z.; Melek, Y. S.
1984-01-01
During regional heat flow studies a geothermal anomaly was discovered approximately 2 km from the Red Sea coast at Wadi Ghadir, in the Red Sea Hills of Eastern Egypt. A temperature gradient of 55 C/km was measured in a 150 m drillhole at this location, indicating a heat flow of approximately 175 mw/sqm, approximately four times the regional background heat flow for Egypt. Gravity and magnetic data were collected along Wadi Ghadir, and combined with offshore gravity data, to investigate the source of the thermal anomaly. Magnetic anomalies in the profile do not coincide with the thermal anomaly, but were observed to correlate with outcrops of basic rocks. Other regional heat flow and gravity data indicate that the transition from continental to oceanic type lithosphere occurs close to the Red Sea margin, and that the regional thermal anomaly is possibly related to the formation of the Red Sea.
Real-time anomaly detection for very short-term load forecasting
DOE Office of Scientific and Technical Information (OSTI.GOV)
Luo, Jian; Hong, Tao; Yue, Meng
Although the recent load information is critical to very short-term load forecasting (VSTLF), power companies often have difficulties in collecting the most recent load values accurately and timely for VSTLF applications. This paper tackles the problem of real-time anomaly detection in most recent load information used by VSTLF. This paper proposes a model-based anomaly detection method that consists of two components, a dynamic regression model and an adaptive anomaly threshold. The case study is developed using the data from ISO New England. This paper demonstrates that the proposed method significantly outperforms three other anomaly detection methods including two methods commonlymore » used in the field and one state-of-the-art method used by a winning team of the Global Energy Forecasting Competition 2014. Lastly, a general anomaly detection framework is proposed for the future research.« less
NASA Astrophysics Data System (ADS)
Kostadinoff, José; Alfredo Bjerg, Ernesto; Gregori, Daniel; Delpino, Sergio; Dimieri, Luis; Raniolo, Ariel; Mogessie, Aberra; Hoinkes, Georg; Hauzenberger, Christoph; Felfernig, Anja
2001-07-01
This paper presents the results of a geophysical study of the southern portion of the Sierra Grande de San Luis, San Luis Province, Argentina. A 26 mGal amplitude Bouguer anomaly (Charlone anomaly), measuring 40 km long by 7 km wide, between Sierra de los Padres and Zanjitas reflects the presence of high-density rocks located at approximately 2000 m depth. Geophysical models based on more than 300 gravimetric, magnetometric, and geological field measurements and observations suggest that the mafic-ultramafic belt of Sierra Grande de San Luis continues south of San Luis. The low magnitude of the terrestrial magnetic field anomalies indicates that these mafic-ultramafic rocks do not carry a base metal sulfides (BMS) mineralization. The Charlone gravimetric anomaly is generated by a belt of mafic- ultramafic rocks whose amplitude is comparable with that responsible for the Virorco-Las Aguilas gravimetric anomaly.
Real-time anomaly detection for very short-term load forecasting
Luo, Jian; Hong, Tao; Yue, Meng
2018-01-06
Although the recent load information is critical to very short-term load forecasting (VSTLF), power companies often have difficulties in collecting the most recent load values accurately and timely for VSTLF applications. This paper tackles the problem of real-time anomaly detection in most recent load information used by VSTLF. This paper proposes a model-based anomaly detection method that consists of two components, a dynamic regression model and an adaptive anomaly threshold. The case study is developed using the data from ISO New England. This paper demonstrates that the proposed method significantly outperforms three other anomaly detection methods including two methods commonlymore » used in the field and one state-of-the-art method used by a winning team of the Global Energy Forecasting Competition 2014. Lastly, a general anomaly detection framework is proposed for the future research.« less
Global magnetic anomaly and aurora of Neptune
NASA Technical Reports Server (NTRS)
Cheng, Andrew F.
1990-01-01
The large offset and tilt of Neptune's dipole magnetic field combine to create a global magnetic anomaly, analogous to but much more important than earth's South Atlantic Anomaly. Energetic particle precipitation loss within the Neptune anomaly creates 'atmospheric drift shadows' within which particle fluxes are greatly reduced. The energetic particle dropout observed by Voyager near closest approach occurred near the predicted times when Voyager passed within the atmospheric drift shadow. Extremely soft, structured bursts of ions and electrons within the drift shadow may result from plasma wave-induced pitch angle scattering of trapped particles confined near the magnetic equator. The dropout does not necessarily imply that Voyager passed through an earth-like discrete auroral zone, as earlier reported. The ion and electron fluxes observed within the dropout period correspond to particles that must precipitate to Neptune's atmosphere within the anomaly region. This anomaly precipitation can account for a major portion of the ultraviolet emissions previously identified as Neptune aurora.
Spatial and Temporal scales of time-averaged 700 MB height anomalies
NASA Technical Reports Server (NTRS)
Gutzler, D.
1981-01-01
The monthly and seasonal forecasting technique is based to a large extent on the extrapolation of trends in the positions of the centers of time averaged geopotential height anomalies. The complete forecasted height pattern is subsequently drawn around the forecasted anomaly centers. The efficacy of this technique was tested and time series of observed monthly mean and 5 day mean 700 mb geopotential heights were examined. Autocorrelation statistics are generated to document the tendency for persistence of anomalies. These statistics are compared to a red noise hypothesis to check for evidence of possible preferred time scales of persistence. Space-time spectral analyses at middle latitudes are checked for evidence of periodicities which could be associated with predictable month-to-month trends. A local measure of the average spatial scale of anomalies is devised for guidance in the completion of the anomaly pattern around the forecasted centers.
Guerin, Andrea; So, Joyce; Mireskandari, Kamiar; Jougeh-Doust, Soghra; Chisholm, Caitlin; Klatt, Regan; Richer, Julie
2015-02-01
Ocular anomalies have been frequently reported in Noonan syndrome. Anterior segment anomalies have been described in 57% of PTPN11 positive patients, with the most common findings being corneal changes and in particular, prominent corneal nerves and cataracts. We report on a neonate with a confirmed PTPN11 mutation and ocular findings consistent with Axenfeld anomaly. The patient initially presented with non-immune hydrops and subsequently developed hypertrophic cardiomyopathy and dysmorphic features typical of Noonan syndrome. While a pathogenic mutation in PTPN11 was confirmed, prior testing for the two common genes associated with Axenfeld-Rieger syndrome, PITX2, and FOXC1 was negative. This finding expands the spectrum of anterior chamber anomalies seen in Noonan syndrome and perhaps suggests a common neural crest related mechanism that plays a critical role in the development of the eye and other organs. © 2014 Wiley Periodicals, Inc.
Seismic anisotropy in the lowermost mantle near the Perm Anomaly
NASA Astrophysics Data System (ADS)
Long, Maureen D.; Lynner, Colton
2015-09-01
The lower mantle is dominated by two large structures with anomalously low shear wave velocities, known as Large Low-Shear Velocity Provinces (LLSVPs). Several studies have documented evidence for strong seismic anisotropy at the base of the mantle near the edges of the African LLSVP. Recent work has identified a smaller structure with similar low-shear wave velocities beneath Eurasia, dubbed the Perm Anomaly. Here we probe lowermost mantle anisotropy near the Perm Anomaly using the differential splitting of SKS and SKKS phases measured at stations in Europe. We find evidence for lowermost mantle anisotropy in the vicinity of the Perm Anomaly, with geographic trends hinting at lateral variations in anisotropy across the boundaries of the Perm Anomaly as well as across a previously unsampled portion of the African LLSVP border. Our observations suggest that deformation is concentrated at the boundaries of both the Perm Anomaly and the African LLSVP.
Active Learning with Rationales for Identifying Operationally Significant Anomalies in Aviation
NASA Technical Reports Server (NTRS)
Sharma, Manali; Das, Kamalika; Bilgic, Mustafa; Matthews, Bryan; Nielsen, David Lynn; Oza, Nikunj C.
2016-01-01
A major focus of the commercial aviation community is discovery of unknown safety events in flight operations data. Data-driven unsupervised anomaly detection methods are better at capturing unknown safety events compared to rule-based methods which only look for known violations. However, not all statistical anomalies that are discovered by these unsupervised anomaly detection methods are operationally significant (e.g., represent a safety concern). Subject Matter Experts (SMEs) have to spend significant time reviewing these statistical anomalies individually to identify a few operationally significant ones. In this paper we propose an active learning algorithm that incorporates SME feedback in the form of rationales to build a classifier that can distinguish between uninteresting and operationally significant anomalies. Experimental evaluation on real aviation data shows that our approach improves detection of operationally significant events by as much as 75% compared to the state-of-the-art. The learnt classifier also generalizes well to additional validation data sets.
Congenital renal anomalies in cloacal exstrophy: Is there a difference?
Suson, K D; Inouye, B; Carl, A; Gearhart, J P
2016-08-01
Cloacal exstrophy (CE) is the most severe manifestation of the epispadias-exstrophy spectrum. Previous studies have indicated an increased rate of renal anomalies in children with classic bladder exstrophy (CBE). Given the increased severity of the CE defect, it was hypothesized that there would be an even greater incidence among these children. The primary objective was to characterize renal anatomy in CE patients. Two secondary objectives were to compare these renal anatomic findings in male and female patients, and female patients with and without Müllerian anomalies. An Institutional Review Board-approved retrospective review of 75 patients from an institutional exstrophy database. Data points included: age at analysis, sex, and renal and Müllerian anatomy. Abnormal renal anatomy was defined as a solitary kidney, malrotation, renal ectopia, congenital cysts, duplication, and/or proven obstruction. Abnormal Müllerian anatomy was defined as uterine or vaginal duplication, obstruction, and/or absence. The Summary Table presents demographic data and renal anomalies. Males were more likely to have renal anomalies. Müllerian anomalies were present in 65.7% of female patients. Girls with abnormal Müllerian anatomy were 10 times more likely to have renal anomalies than those with normal Müllerian anatomy (95% CI 1.1-91.4, P = 0.027). Patients with CE had a much higher rate of renal anomalies than that reported for CBE. Males and females with Müllerian anomalies were at greater risk than females with normal uterine structures. Mesonephric and Müllerian duct interaction is required for uterine structures to develop normally. It has been proposed that women with both Müllerian and renal anomalies be classified separately from other uterine malformations on an embryonic basis. In these patients, an absent or dysfunctional mesonephric duct has been implicated as potentially causal. This provided an embryonic explanation for uterine anomalies in female CE patients. There were also clinical implications. Women with renal agenesis and uterine anomalies were more likely to have endometriosis than those with isolated uterine anomalies, but were also more likely to have successful pregnancies. Males may have had an analogous condition with renal agenesis and seminal vesicle cysts. Future research into long-term kidney function in this population, uterine function, and possible male sexual duct malformation is warranted. Congenital renal anomalies occurred frequently in children with CE. They were more common in boys than in girls. Girls with abnormal Müllerian anatomy were more likely to have anomalous renal development. Mesonephric duct dysfunction may be embyologically responsible for both renal and Müllerian maldevelopment. Copyright © 2016 Journal of Pediatric Urology Company. Published by Elsevier Ltd. All rights reserved.
Precipitation Anomalies in Southern Brazil Associated with El Niño and La Niña Events.
NASA Astrophysics Data System (ADS)
Grimm, Alice M.; Ferraz, Simone E. T.; Gomes, Júlio
1998-11-01
The impact of El Niño and La Niña events (warm and cold phases of the Southern Oscillation) on rainfall over southern Brazil is investigated through the use of a large dataset of monthly precipitation from 250 stations. This region is partly dominated by rough orography and presents different climatic regimes of rainfall. As previous global studies on Southern Oscillation-precipitation relationships used data from only two stations in southern Brazil, this region was not included in the area of consistent Southern Oscillation-related precipitation in southeastern South America. The present analysis is based on the method by Ropelewski and Halpert, the sensitivity of which is assessed for this region. The spatial structure of the rainfall anomalies associated with warm (cold) events is analyzed and subregions with coherent anomalies are determined. Their distribution indicates the influence of relief, latitude, and proximity to the ocean. These areas are subjected to further analysis to determine the seasons of largest anomalies and assess their consistency during warm (cold) events.The whole of southern Brazil was found to have strong and consistent precipitation anomalies associated with those events. Their magnitude is even larger than in Argentina and Uruguay. All of the subregions have consistent wet anomalies during the austral spring of the warm event year, with a pronounced peak in November. The southeastern part also shows a consistent tendency to higher than average rainfall during the austral winter of the following year. There is also a consistent tendency to dryness in the year before a warm event. During the spring of cold event years strong consistent dry anomalies prevail over the whole region, also with maximum magnitude in November. They are even stronger and more consistent than the wet anomalies in warm event years. Consistent anomalies do not occur over large areas in the years before and after cold events. The wet anomalies during the austral spring of the warm event year weaken and even reverse during the following January. The same tendency, though not so clear, is observable in the dry anomalies of cold events. The seasons of largest anomalies disclosed by this study differ from those found by previous global studies for other regions in southeastern South America.This study expands the area of consistent warm (cold) event-related precipitation defined by previous studies in southeastern South America by including a region of larger anomalies, and provides a spatial and temporal refinement to the warm (cold) event-precipitation relationship.
Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data
Boyle, Breidge; Addor, Marie-Claude; Arriola, Larraitz; Barisic, Ingeborg; Bianchi, Fabrizio; Csáky-Szunyogh, Melinda; de Walle, Hermien E K; Dias, Carlos Matias; Draper, Elizabeth; Gatt, Miriam; Garne, Ester; Haeusler, Martin; Källén, Karin; Latos-Bielenska, Anna; McDonnell, Bob; Mullaney, Carmel; Nelen, Vera; Neville, Amanda J; O’Mahony, Mary; Queisser-Wahrendorf, Annette; Randrianaivo, Hanitra; Rankin, Judith; Rissmann, Anke; Ritvanen, Annukka; Rounding, Catherine; Tucker, David; Verellen-Dumoulin, Christine; Wellesley, Diana; Wreyford, Ben; Zymak-Zakutnia, Natalia; Dolk, Helen
2018-01-01
Objective To validate the estimates of Global Burden of Disease (GBD) due to congenital anomaly for Europe by comparing infant mortality data collected by EUROCAT registries with the WHO Mortality Database, and by assessing the significance of stillbirths and terminations of pregnancy for fetal anomaly (TOPFA) in the interpretation of infant mortality statistics. Design, setting and outcome measures EUROCAT is a network of congenital anomaly registries collecting data on live births, fetal deaths from 20 weeks’ gestation and TOPFA. Data from 29 registries in 19 countries were analysed for 2005–2009, and infant mortality (deaths of live births at age <1 year) compared with the WHO Mortality Database. Eight EUROCAT countries were excluded from further analysis on the basis that this comparison showed poor ascertainment of survival status. Results According to WHO, 17%–42% of infant mortality was attributed to congenital anomaly. In 11 EUROCAT countries, average infant mortality with congenital anomaly was 1.1 per 1000 births, with higher rates where TOPFA is illegal (Malta 3.0, Ireland 2.1). The rate of stillbirths with congenital anomaly was 0.6 per 1000. The average TOPFA prevalence was 4.6 per 1000, nearly three times more prevalent than stillbirths and infant deaths combined. TOPFA also impacted on the prevalence of postneonatal survivors with non-lethal congenital anomaly. Conclusions By excluding TOPFA and stillbirths from GBD years of life lost (YLL) estimates, GBD underestimates the burden of disease due to congenital anomaly, and thus declining YLL over time may obscure lack of progress in primary, secondary and tertiary prevention. PMID:28667189
Christiansen, Peter; Nielsen, Lars N; Steen, Kim A; Jørgensen, Rasmus N; Karstoft, Henrik
2016-11-11
Convolutional neural network (CNN)-based systems are increasingly used in autonomous vehicles for detecting obstacles. CNN-based object detection and per-pixel classification (semantic segmentation) algorithms are trained for detecting and classifying a predefined set of object types. These algorithms have difficulties in detecting distant and heavily occluded objects and are, by definition, not capable of detecting unknown object types or unusual scenarios. The visual characteristics of an agriculture field is homogeneous, and obstacles, like people, animals and other obstacles, occur rarely and are of distinct appearance compared to the field. This paper introduces DeepAnomaly, an algorithm combining deep learning and anomaly detection to exploit the homogenous characteristics of a field to perform anomaly detection. We demonstrate DeepAnomaly as a fast state-of-the-art detector for obstacles that are distant, heavily occluded and unknown. DeepAnomaly is compared to state-of-the-art obstacle detectors including "Faster R-CNN: Towards Real-Time Object Detection with Region Proposal Networks" (RCNN). In a human detector test case, we demonstrate that DeepAnomaly detects humans at longer ranges (45-90 m) than RCNN. RCNN has a similar performance at a short range (0-30 m). However, DeepAnomaly has much fewer model parameters and (182 ms/25 ms =) a 7.28-times faster processing time per image. Unlike most CNN-based methods, the high accuracy, the low computation time and the low memory footprint make it suitable for a real-time system running on a embedded GPU (Graphics Processing Unit).
NASA Astrophysics Data System (ADS)
Zhao, Mingkang; Wi, Hun; Lee, Eun Jung; Woo, Eung Je; In Oh, Tong
2014-10-01
Electrical impedance imaging has the potential to detect an early stage of breast cancer due to higher admittivity values compared with those of normal breast tissues. The tumor size and extent of axillary lymph node involvement are important parameters to evaluate the breast cancer survival rate. Additionally, the anomaly characterization is required to distinguish a malignant tumor from a benign tumor. In order to overcome the limitation of breast cancer detection using impedance measurement probes, we developed the high density trans-admittance mammography (TAM) system with 60 × 60 electrode array and produced trans-admittance maps obtained at several frequency pairs. We applied the anomaly detection algorithm to the high density TAM system for estimating the volume and position of breast tumor. We tested four different sizes of anomaly with three different conductivity contrasts at four different depths. From multifrequency trans-admittance maps, we can readily observe the transversal position and estimate its volume and depth. Specially, the depth estimated values were obtained accurately, which were independent to the size and conductivity contrast when applying the new formula using Laplacian of trans-admittance map. The volume estimation was dependent on the conductivity contrast between anomaly and background in the breast phantom. We characterized two testing anomalies using frequency difference trans-admittance data to eliminate the dependency of anomaly position and size. We confirmed the anomaly detection and characterization algorithm with the high density TAM system on bovine breast tissue. Both results showed the feasibility of detecting the size and position of anomaly and tissue characterization for screening the breast cancer.
Christiansen, Peter; Nielsen, Lars N.; Steen, Kim A.; Jørgensen, Rasmus N.; Karstoft, Henrik
2016-01-01
Convolutional neural network (CNN)-based systems are increasingly used in autonomous vehicles for detecting obstacles. CNN-based object detection and per-pixel classification (semantic segmentation) algorithms are trained for detecting and classifying a predefined set of object types. These algorithms have difficulties in detecting distant and heavily occluded objects and are, by definition, not capable of detecting unknown object types or unusual scenarios. The visual characteristics of an agriculture field is homogeneous, and obstacles, like people, animals and other obstacles, occur rarely and are of distinct appearance compared to the field. This paper introduces DeepAnomaly, an algorithm combining deep learning and anomaly detection to exploit the homogenous characteristics of a field to perform anomaly detection. We demonstrate DeepAnomaly as a fast state-of-the-art detector for obstacles that are distant, heavily occluded and unknown. DeepAnomaly is compared to state-of-the-art obstacle detectors including “Faster R-CNN: Towards Real-Time Object Detection with Region Proposal Networks” (RCNN). In a human detector test case, we demonstrate that DeepAnomaly detects humans at longer ranges (45–90 m) than RCNN. RCNN has a similar performance at a short range (0–30 m). However, DeepAnomaly has much fewer model parameters and (182 ms/25 ms =) a 7.28-times faster processing time per image. Unlike most CNN-based methods, the high accuracy, the low computation time and the low memory footprint make it suitable for a real-time system running on a embedded GPU (Graphics Processing Unit). PMID:27845717
Zhou, Guangwei; Schwartz, Lynn Thomas; Gopen, Quinton
2009-02-01
To identify the occurrence of inner ear structural anomalies and conductive hearing loss (CHL) in children with Apert syndrome. Retrospective review. Pediatric tertiary referral center. Twenty pediatric patients with Apert syndrome were found; all patients (38/40 ears) had inner ear anomalies. Computerized tomography of the head/temporal bone, pure-tone (including air and bone conduction) audiometry, and tympanometry. Imaging demonstrating inner ear anomalies, including malformations of the cochlea, dilated vestibule, and/or semicircular canal; audiologic findings of air-bone gap(s). Hearing loss was found in 90% of the patients with Apert syndrome, and 80% of them had CHL. Air-bone gaps were found at all frequencies, with larger gaps at low frequencies. Fifty percent (20/40) of the ears had better than 0 dB hearing level bone conduction thresholds at 250 and/or 500 Hz. Normal middle ear pressure and mobility were found in all ears with intact eardrum. Inner ear anomalies were found in all patients, and 90% of them had bilateral involvement. Most frequently observed inner ear anomalies were dilated vestibule, malformed lateral semicircular canal, and cochlear dysplasia. Children with Apert syndrome may present with significant CHL that cannot be explained by minor middle ear pathologies alone. This conductive loss may be, at least partially, attributed to the inner ear anomalies; however, these structural anomalies are usually not recognized in these patients. Failure to close air-bone gap after surgical intervention may raise the suspicion of inner ear anomalies, and computed tomographic scan of the temporal bone can provide definitive proof.
NASA Astrophysics Data System (ADS)
Khaki, M.; Forootan, E.; Sharifi, M. A.; Awange, J.; Kuhn, M.
2015-09-01
Satellite radar altimetry observations are used to derive short wavelength gravity anomaly fields over the Persian Gulf and the Caspian Sea, where in situ and ship-borne gravity measurements have limited spatial coverage. In this study the retracking algorithm `Extrema Retracking' (ExtR) was employed to improve sea surface height (SSH) measurements that are highly biased in the study regions due to land contaminations in the footprints of the satellite altimetry observations. ExtR was applied to the waveforms sampled by the five satellite radar altimetry missions: TOPEX/POSEIDON, JASON-1, JASON-2, GFO and ERS-1. Along-track slopes have been estimated from the improved SSH measurements and used in an iterative process to estimate deflections of the vertical, and subsequently, the desired gravity anomalies. The main steps of the gravity anomaly computations involve estimating improved SSH using the ExtR technique, computing deflections of the vertical from interpolated SSHs on a regular grid using a biharmonic spline interpolation and finally estimating gridded gravity anomalies. A remove-compute-restore algorithm, based on the fast Fourier transform, has been applied to convert deflections of the vertical into gravity anomalies. Finally, spline interpolation has been used to estimate regular gravity anomaly grids over the two study regions. Results were evaluated by comparing the estimated altimetry-derived gravity anomalies (with and without implementing the ExtR algorithm) with ship-borne free air gravity anomaly observations, and free air gravity anomalies from the Earth Gravitational Model 2008 (EGM2008). The comparison indicates a range of 3-5 mGal in the residuals, which were computed by taking the differences between the retracked altimetry-derived gravity anomaly and the ship-borne data. The comparison of retracked data with ship-borne data indicates a range in the root-mean-square-error (RMSE) between approximately 1.8 and 4.4 mGal and a bias between 0.4062 and 2.1413 mGal over different areas. Also a maximum RMSE of 4.4069 mGal, with a mean value of 0.7615 mGal was obtained in the residuals. An average improvement of 5.2746 mGal in the RMSE of the altimetry-derived gravity anomalies corresponding to 89.9 per cent was obtained after applying the ExtR post-processing.
Viscous remanent magnetization model for the Broken Ridge satellite magnetic anomaly
NASA Technical Reports Server (NTRS)
Johnson, B. D.
1985-01-01
An equivalent source model solution of the satellite magnetic field over Australia obtained by Mayhew et al. (1980) showed that the satellite anomalies could be related to geological features in Australia. When the processing and selection of the Magsat data over the Australian region had progressed to the point where interpretation procedures could be initiated, it was decided to start by attempting to model the Broken Ridge satellite anomaly, which represents one of the very few relatively isolated anomalies in the Magsat maps, with an unambiguous source region. Attention is given to details concerning the Broken Ridge satellite magnetic anomaly, the modeling method used, the Broken Ridge models, modeling results, and characteristics of magnetization.
Investigation of Surface Flux Feedbacks for Coupled Atmosphere-Ocean Anomalies
NASA Technical Reports Server (NTRS)
Roberts, J. Brent; Robertson, Pete
2010-01-01
The use of "dynamical coupling" rules allows for identifying coupled vs. uncoupled anomalies and one-way interaction. Results of this study are consistent with those of Pena et al. (2003,2004) although using a more recent reanalysis at higher resolution. Find more atmosphere-forcing coupled anomalies in the extratropics and ocean-forcing anomalies in the tropics. The LHF and SWR show the largest magnitude anomalies in the composite analysis. The turbulent flux responses are due to interactions between the differing responses in wind speed and near-surface gradients. The radiative fluxes responses are primarily tied to changes in cloud fraction, as expected, though longwave response can be tied more to changes in the upwelling component.
Gould, Sharon W; Epelman, Monica
2015-08-01
Developmental anomalies of the uterus and the vagina are associated with infertility and miscarriage and are most commonly detected in the postpubertal age-group. These conditions may also present in younger patients as a mass or pain owing to obstruction of the uterus or the vagina. Associated urinary tract anomalies are common, as well. Accurate diagnosis and thorough description of these anomalies is essential for appropriate management; however, evaluation may be difficult in an immature reproductive tract. Magnetic resonance imaging technique pertinent to imaging of the pediatric female reproductive tract is presented and illustrated along with the findings associated with various anomalies. Copyright © 2015 Elsevier Inc. All rights reserved.
Debendox does not cause the Poland anomaly.
David, T J
1982-01-01
The suggestion that Debendox may cause the Poland anomaly is refuted by a study of the antenatal drug exposure in 46 cases of the Poland anomaly and 32 cases of isolated absence of the pectoralis major. Debendox had been prescribed in one case of the Poland anomaly and in one case of isolated pectoralis absence, but in neither was the compound given during organogenesis. In none of the 78 cases could Debendox be causally implicated. PMID:7092316
Improving the geological interpretation of magnetic and gravity satellite anomalies
NASA Technical Reports Server (NTRS)
Hinze, W. J.; Braile, L. W. (Principal Investigator); Vonfrese, R. R. B.
1985-01-01
Current limitations in the quantitative interpretation of satellite-elevation geopotential field data and magnetic anomaly data were investigated along with techniques to overcome them. A major result was the preparation of an improved scalar magnetic anomaly map of South America and adjacent marine areas directly from the original MAGSAT data. In addition, comparisons of South American and Euro-African data show a strong correlation of anomalies along the Atlantic rifted margins of the continents.
Latent Space Tracking from Heterogeneous Data with an Application for Anomaly Detection
2015-11-01
specific, if the anomaly behaves as a sudden outlier after which the data stream goes back to normal state, then the anomalous data point should be...introduced three types of anomalies , all of them are sudden outliers . 438 J. Huang and X. Ning Table 2. Synthetic dataset: AUC and parameters method...Latent Space Tracking from Heterogeneous Data with an Application for Anomaly Detection Jiaji Huang1(B) and Xia Ning2 1 Department of Electrical
Overton, Jr., William C.; Steyert, Jr., William A.
1984-01-01
A superconducting quantum interference device (SQUID) magnetic detection apparatus detects magnetic fields, signals, and anomalies at remote locations. Two remotely rotatable SQUID gradiometers may be housed in a cryogenic environment to search for and locate unambiguously magnetic anomalies. The SQUID magnetic detection apparatus can be used to determine the azimuth of a hydrofracture by first flooding the hydrofracture with a ferrofluid to create an artificial magnetic anomaly therein.
Overton, W.C. Jr.; Steyert, W.A. Jr.
1981-05-22
A superconducting quantum interference device (SQUID) magnetic detection apparatus detects magnetic fields, signals, and anomalies at remote locations. Two remotely rotatable SQUID gradiometers may be housed in a cryogenic environment to search for and locate unambiguously magnetic anomalies. The SQUID magnetic detection apparatus can be used to determine the azimuth of a hydrofracture by first flooding the hydrofracture with a ferrofluid to create an artificial magnetic anomaly therein.
NASA Technical Reports Server (NTRS)
Liu, W.; Hu, H.; Xie, X.
1999-01-01
Liu et al.[1998] (hereafter referred as LTH), superimposed wind velocity anomalies observed by the NASA Scatterometer (NSCAT) on the map of sea surface temperature (SST) anomalies observed by the Advanced Very High Resolution Radiometer (AVHRR) in the Pacific at the end of May 1997, and illustrated that the three regions of anomalous warming in the North Pacific Ocean are related to wind anomalies through different mechanisms.
Prajapati, H J S; Martin, L G; Patel, T H
2014-01-01
The term vascular anomaly represents a broad spectrum of vascular pathology, including proliferating vascular tumours and vascular malformations. While the treatment of most vascular anomalies is multifactorial, interventional radiology procedures, including embolic therapy, sclerotherapy and laser coagulation among others, are playing an increasingly important role in vascular anomaly management. This review discusses the diagnosis and treatment of common vascular malformations, with emphasis on the technique, efficacy and complications of different interventional radiology procedures. PMID:24588666
Interannual Variations in Arctic Winter Temperature: The Role of Global Scale Teleconnections
2015-06-01
also advect warm air northward and eastward between Iceland and Scandinavia . Figure 7 shows the LTM patterns of global Z200 and shows the normal...with an extension of this warm anomaly into the subpolar regions of the North Atlantic (i.e., Baffin Bay- Scandinavia ). Weak positive anomalies in...positive anomalies over northern Siberia and Scandinavia . We speculate that these areas of positive and negative anomalies in Z850, and implied WAA, may
NASA Astrophysics Data System (ADS)
Allek, Karim; Boubaya, Djamel; Bouguern, Abderrahmane; Hamoudi, Mohamed
2016-12-01
The presence of near-surface magnetic anomalies over oil and gas accumulations and their contribution to exploration remain somewhat controversial despite encouraging results and an improved understanding of genetic links between hydrocarbon seepage-induced alterations and near-surface magnetic minerals. This controversy is likely to remain since the cause of shallow-sourced sedimentary magnetic anomalies may well be microseepage related, but could also result from other sources such as cultural features and detrital magnetite. The definite way of discriminating between them remains a challenge. In this paper we examine means to deal with this particular purpose using a Bayesian technique known as 'Weights-of-Evidence'. The technique is implemented in GIS to explore spatial associations between known hydrocarbon fields within the central Triassic province of Algeria and sedimentary residual magnetic anomalies. We use the results to show possible application of the method to the recognition of some characteristics (amplitude and width) of anomalies assumed to be induced by hydrocarbon microseepages. Our results reveal strong spatial association with certain typical class of anomalies, confirming therefore hypothesis that hydrocarbon microseepages may result in detectable magnetic anomalies. It is possible to use the anomalies occurring outside the known gas and oil fields to make informed decisions in the selection of new targets for more detailed hydrocarbon exploration.
EMPACT 3D: an advanced EMI discrimination sensor for CONUS and OCONUS applications
NASA Astrophysics Data System (ADS)
Keranen, Joe; Miller, Jonathan S.; Schultz, Gregory; Sander-Olhoeft, Morgan; Laudato, Stephen
2018-04-01
We recently developed a new, man-portable, electromagnetic induction (EMI) sensor designed to detect and classify small, unexploded sub-munitions and discriminate them from non-hazardous debris. The ability to distinguish innocuous metal clutter from potentially hazardous unexploded ordnance (UXO) and other explosive remnants of war (ERW) before excavation can significantly accelerate land reclamation efforts by eliminating time spent removing harmless scrap metal. The EMI sensor employs a multi-axis transmitter and receiver configuration to produce data sufficient for anomaly discrimination. A real-time data inversion routine produces intrinsic and extrinsic anomaly features describing the polarizability, location, and orientation of the anomaly under test. We discuss data acquisition and post-processing software development, and results from laboratory and field tests demonstrating the discrimination capability of the system. Data acquisition and real-time processing emphasize ease-of-use, quality control (QC), and display of discrimination results. Integration of the QC and discrimination methods into the data acquisition software reduces the time required between sensor data collection and the final anomaly discrimination result. The system supports multiple concepts of operations (CONOPs) including: 1) a non-GPS cued configuration in which detected anomalies are discriminated and excavated immediately following the anomaly survey; 2) GPS integration to survey multiple anomalies to produce a prioritized dig list with global anomaly locations; and 3) a dynamic mapping configuration supporting detection followed by discrimination and excavation of targets of interest.
Discovering System Health Anomalies Using Data Mining Techniques
NASA Technical Reports Server (NTRS)
Sriastava, Ashok, N.
2005-01-01
We present a data mining framework for the analysis and discovery of anomalies in high-dimensional time series of sensor measurements that would be found in an Integrated System Health Monitoring system. We specifically treat the problem of discovering anomalous features in the time series that may be indicative of a system anomaly, or in the case of a manned system, an anomaly due to the human. Identification of these anomalies is crucial to building stable, reusable, and cost-efficient systems. The framework consists of an analysis platform and new algorithms that can scale to thousands of sensor streams to discovers temporal anomalies. We discuss the mathematical framework that underlies the system and also describe in detail how this framework is general enough to encompass both discrete and continuous sensor measurements. We also describe a new set of data mining algorithms based on kernel methods and hidden Markov models that allow for the rapid assimilation, analysis, and discovery of system anomalies. We then describe the performance of the system on a real-world problem in the aircraft domain where we analyze the cockpit data from aircraft as well as data from the aircraft propulsion, control, and guidance systems. These data are discrete and continuous sensor measurements and are dealt with seamlessly in order to discover anomalous flights. We conclude with recommendations that describe the tradeoffs in building an integrated scalable platform for robust anomaly detection in ISHM applications.
Acharya, Sujeet S; Gundeti, Mohan S; Zagaja, Gregory P; Shalhav, Arieh L; Zorn, Kevin C
2009-04-01
Although malformations of the genitourinary tract are typically identified during childhood, they can remain silent until incidental detection in evaluation and treatment of other pathologies during adulthood. The advent of the minimally invasive era in urologic surgery has given rise to unique challenges in the surgical management of anomalies of the genitourinary tract. This article reviews the embryology of anomalies of Wolffian duct (WD) derivatives with specific attention to the seminal vesicles, vas deferens, ureter, and kidneys. This is followed by a discussion of the history of the laparoscopic approach to WD derivative anomalies. Finally, we present two cases to describe technical considerations when managing these anomalies when encountered during robotic-assisted radical prostatectomy. The University of Chicago Robotic Laparoscopic Radical Prostatectomy (RLRP) database was reviewed for cases where anomalies of WD derivatives were encountered. We describe how modifications in technique allowed for completion of the procedure without difficulty. None Of the 1230 RLRP procedures performed at our institution by three surgeons, only two cases (0.16%) have been noted to have a WD anomaly. These cases were able to be completed without difficulty by making simple modifications in technique. Although uncommon, it is important for the urologist to be familiar with the origin and surgical management of WD anomalies, particularly when detected incidentally during surgery. Simple modifications in technique allow for completion of RLRP without difficulty.
Deolia, Shravani Govind; Chhabra, Chaya; Chhabra, Kumar Gaurav; Kalghatgi, Shrivardhan; Khandelwal, Naresh
2015-01-01
Anomalies and enamel hypoplasia of deciduous dentition are routinely encountered by dental professionals and early detection and careful management of such conditions facilitates may help in customary occlusal development. The aim of this study was to determine the prevalence of hypodontia, microdontia, double teeth, and hyperdontia of deciduous teeth among Indian children. The study group comprised 1,398 children (735 boys, 633 girls). The children were examined in department of Pedodontics and Preventive Dentistry in Jodhpur Dental College General Hospital, Jodhpur, Rajasthan, India. Clinical data were collected by single dentist according to Kreiborg criteria, which includes double teeth, hypodontia, microdontia, and supernumerary teeth. Statistical analysis of the data was performed using the descriptive analysis and chi-square test. Dental anomalies were found in 4% of children. The distribution of dental anomalies were significantly more frequent (P = 0.001) in girls (5.8%, n = 38) than in boys (2.7%, n = 18). In relation to anomaly frequencies at different ages, significant difference was found between 2 and 3 years (P = 0.001). Double teeth were the most frequently (2.3%) observed anomaly. The other anomalies followed as 0.3% supernumerary teeth, 0.6% microdontia, 0.6% hypodontia. Identification of dental anomalies at an early age is of great importance as it prevents malocclusions, functional and certain psychological problems.
Using statistical anomaly detection models to find clinical decision support malfunctions.
Ray, Soumi; McEvoy, Dustin S; Aaron, Skye; Hickman, Thu-Trang; Wright, Adam
2018-05-11
Malfunctions in Clinical Decision Support (CDS) systems occur due to a multitude of reasons, and often go unnoticed, leading to potentially poor outcomes. Our goal was to identify malfunctions within CDS systems. We evaluated 6 anomaly detection models: (1) Poisson Changepoint Model, (2) Autoregressive Integrated Moving Average (ARIMA) Model, (3) Hierarchical Divisive Changepoint (HDC) Model, (4) Bayesian Changepoint Model, (5) Seasonal Hybrid Extreme Studentized Deviate (SHESD) Model, and (6) E-Divisive with Median (EDM) Model and characterized their ability to find known anomalies. We analyzed 4 CDS alerts with known malfunctions from the Longitudinal Medical Record (LMR) and Epic® (Epic Systems Corporation, Madison, WI, USA) at Brigham and Women's Hospital, Boston, MA. The 4 rules recommend lead testing in children, aspirin therapy in patients with coronary artery disease, pneumococcal vaccination in immunocompromised adults and thyroid testing in patients taking amiodarone. Poisson changepoint, ARIMA, HDC, Bayesian changepoint and the SHESD model were able to detect anomalies in an alert for lead screening in children and in an alert for pneumococcal conjugate vaccine in immunocompromised adults. EDM was able to detect anomalies in an alert for monitoring thyroid function in patients on amiodarone. Malfunctions/anomalies occur frequently in CDS alert systems. It is important to be able to detect such anomalies promptly. Anomaly detection models are useful tools to aid such detections.
Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype?
La Placa, Simona; Giuffrè, Mario; Gangemi, Antonella; Di Noto, Stefania; Matina, Federico; Nociforo, Federica; Antona, Vincenzo; Di Pace, Maria Rita; Piccione, Maria; Corsello, Giovanni
2013-07-10
VATER association was first described in 1972 by Quan and Smith as an acronym which identifies a non-random co-occurrence of Vertebral anomalies, Anal atresia, Tracheoesophageal fistula and/or Esophageal atresia, Radial dysplasia. It is even possible to find out Cardiovascular, Renal and Limb anomalies and the acronym VACTERL was adopted, also, embodying Vascular, as single umbilical artery, and external genitalia anomalies. Data on patients with esophageal atresia (EA) with or without tracheoesophageal fistula (TEF) admitted in the Neonatal Intensive Care Unit (NICU) between January 2003 and January 2013 were evaluated for the contingent occurrence of typical VACTERL anomalies (VACTERL-type) and non tipical VACTERL anomalies (non-VACTERL-type). The inclusion criterion was the presence of EA with or without TEF plus two or more of the following additional malformations: vertebral defects, anal atresia, cardiovascular defects, renal anomalies and lower limb deformities, like radial dysplasia. Among 52 patients with EA/TEF, 20 (38,4%) had isolated EA and 7 (21,8%) had a recognized etiology such a syndrome and therefore were excluded. Among 32 infants with EA and associated malformations, 15 (46,8%) had VACTERL association. The most common anomalies were congenital heart defects (73,3%), followed by vertebral anomalies (66,6%). Many patients also had additional non-VACTERL-type defects. Single umbilical artery was the most common one followed by nervous system abnormalities and anomalies of toes. Between the groups of infants with VACTERL type and non-VACTERL-type anomalies, there are several overlapping data regarding both the tipically described spectrum and the most frequently reported non-VACTERL-type malformations. Thus, it is possible to differentiate infants with a full phenotype (VACTERL full phenotype) and patients that do not meet all the criteria mentioned above, but with some homologies with the first group (VACTERL partial phenotype). The high frequency of non-VACTERL-type anomalies encountered in full and partial phenotype patients would suggest the need for an extension of the clinical criteria for the diagnosis of VACTERL association and also for pre- and post-operative management and follow-up in the short and long term.
Diagnosis and treatment of branchial cleft anomalies in UKMMC: a 10-year retrospective study.
Zaifullah, Syed; Yunus, Mohd Razif Mohamad; See, Goh Bee
2013-03-01
Branchial cleft anomalies result from abnormal persistence of branchial apparatus, which is located at the lateral part of the neck. These occur due to failure of obliteration of the branchial apparatus during embryonic development. Differential diagnoses of lateral neck mass are salivary gland or neurogenic neoplasms, paragangliomas, adenopathies, cystic hygroma or cystic metastasis from squamous cell carcinoma or thyroid papillary carcinoma. Clinically, a branchial cyst is smooth, round, fluctuant and non-tender, and usually occurs over the upper part of the neck, anterior to the sternocleidomastoid muscle. Sometimes, it may present as infected cyst (or abscess), a sinus or fistula. Surgical excision is the definitive treatment for branchial anomalies. The objective of the work was to study the demographic data, clinical presentation, definite diagnostic workup and treatment of patients diagnosed with branchial anomalies. This is a retrospective study of 26 patients who were diagnosed with branchial anomalies (branchial cyst and fistula), of which only 12 patients had data available between July 1999 and June 2009 at the Otorhinolaryngology, Head and Neck Surgery, Universiti Kebangsaan Malaysia Medical Centre. Twelve cases of branchial anomalies were seen, in which 10 patients had second branchial cyst anomalies, 1 had third branchial fistula and 1 had bilateral branchial lesion. There were seven females and five males. The age of the patients varied over a wide range (4-44 years), but the majority of the patients were in their second and third decade of life. All branchial anomalies occurred at the classical site; eight patients had left-sided neck lesion. Correct clinical diagnosis was made only in five patients (41.6 %). All patients underwent surgical excision with no reported recurrence. Branchial anomalies are frequently forgotten in the differential diagnosis of lateral neck swelling. Diagnosis is usually delayed, leading to improper treatment. The diagnosis of patients who present with lateral neck cystic swelling with or without episodes of recurrent neck abscess should be considered with a high suspicion for branchial anomalies. FNA cytology is a good investigative tool in reaching toward a diagnosis of branchial lesion, with the concurrent assistance of radiological modalities. Surgical excision is the gold standard treatment of lesions of branchial anomalies.
Webb, Michelle L; Rosen, Heather; Taghinia, Amir; McCarty, Erika R; Cerrato, Felecia; Upton, Joseph; Labow, Brian I
2011-06-01
Fanconi anemia (FA) is a rare genetic disorder of DNA repair that with near uniformity leads to bone marrow failure and resulting morbidity and mortality. Approximately 50% of FA patients are born with anomalies of the thumb or thumb and radius, and it has been recommended that all patients born with thumb anomalies undergo testing. However, the risk of FA in this population is unknown. We determined the incidence of FA in children with congenital thumb anomalies referred for FA testing and characterized those who tested positive. We queried our database for patients who presented with congenital thumb anomalies and who underwent diepoxybutane (DEB) testing for FA between 1999 and 2008 at Children's Hospital Boston and the Dana-Farber Cancer Institute. During this time period, 543 congenital thumb anomaly patients (235 with thumb hypoplasia) presented to our institution. A total of 81 patients with thumb abnormalities underwent DEB testing. Six patients (7% of those tested; 1% of the total; 3% of thumb hypoplasia patients) had a positive DEB test consistent with the diagnosis of FA; all had other non-upper-extremity anomalies associated with FA. Of 6 FA patients, 5 had bilateral involvement; all had some degree of thumb hypoplasia (3 also had radial dysplasia). Mean age at testing was 2.6 years (SD 4.3). Most of the patients tested had multiple physical anomalies (n = 66). The anomaly distribution was: thumb hypoplasia and radial dysplasia (n = 29), thumb hypoplasia (n = 26), radial polydactyly (n = 12), radial polydactyly and radial dysplasia (n = 1), and proximally placed thumb and radial dysplasia (n = 1). Twelve patients had other thumb anomalies. Although the incidence of FA in patients with thumb anomalies may be low, patients with thumb hypoplasia and other physical findings associated with FA, specifically café au lait spots and short stature, appear to have an increased risk of FA. Because hand surgeons see these patients early in life, they have the opportunity to refer these patients for FA testing to initiate early education, family genetic counseling, and treatment if warranted. Prognostic IV. Copyright © 2011 American Society for Surgery of the Hand. Published by Elsevier Inc. All rights reserved.
In-Situ Hydraulic Conductivities of Soils and Anomalies at a Future Biofuel Production Site
NASA Astrophysics Data System (ADS)
Williamson, M. F.; Jackson, C. R.; Hale, J. C.; Sletten, H. R.
2010-12-01
Forested hillslopes of the Upper Coastal Plain at the Savannah River Site, SC, feature a shallow clay loam argillic layer with low median saturated hydraulic conductivity. Observations from a grid of shallow, maximum-rise piezometers indicate that perching on this clay layer is common. However, flow measurements from an interflow-interception trench indicate that lateral flow is rare and most soil water percolates through the clay layer. We hypothesize that the lack of frequent lateral flow is due to penetration of the clay layer by roots of pine trees. We used ground penetrating radar (GPR) to map the soil structure and potential anomalies, such as root holes, down to two meters depth at three 10×10-m plots. At each plot, a 1×10-m trench was later back-hoe excavated along a transect that showed the most anomalies on the GPR maps. Each trench was excavated at 0.5-m intervals until the clay layer was reached (two plots were excavated to a final depth of 0.875 m and the third plot was excavated to a final depth of 1.0 m). At each interval, compact constant-head permeameters (CCHPs) were used to measure in-situ hydraulic conductivities in the clay-loam matrix and in any visually apparent anomalies. Conductivity was also estimated using a second 1×10-m transect of CCHP measurements taken within randomly placed augur holes. Additional holes targeted GPR anomalies. The second transect was created in case the back-hoe impacted conductivity readings. High-conductivity anomalies were also visually investigated by excavating with a shovel. Photographs of soil wetness were taken at visually apparent anomalies with a multispectral camera. We discovered that all visually apparent anomalies found are represented on the GPR maps, but that not all of the predicted anomalies on the GPR maps are visually apparent. We discovered that tree root holes create anomalies, but that there were also many conductivity anomalies that could not be visually distinguished from low-conductivity soil.
Calcium Isotopic Anomalies in the Allende CAIs and the Angrite Angra dos Reis
NASA Astrophysics Data System (ADS)
Chen, H. W.; Chen, J. C.; Lee, T.; Shen, J. J.
2010-03-01
Both negative 48Ca and 50Ti anomalies of the Angrite Angra dos Reis was identified in this study, and the result supported previous study of correlated negative 54Cr and 50Ti anomalies in achondrites.
de Almeida, J C; Reis, D F; Llerena Júnior, J; Barbosa Neto, J; Pontes, R L; Middleton, S; Telles, L F
1991-01-01
Two sibs with a phenotype characterised by short stature, brachydactyly, and ocular anomalies (Peters' anomaly) are reported (Peters'-plus syndrome). The consanguinity is in agreement with the proposed autosomal recessive inheritance. Images PMID:1856836
The North American upper mantle: density, composition, and evolution
Mooney, Walter D.; Kaban, Mikhail K.
2010-01-01
The upper mantle of North America has been well studied using various seismic methods. Here we investigate the density structure of the North American (NA) upper mantle based on the integrative use of the gravity field and seismic data. The basis of our study is the removal of the gravitational effect of the crust to determine the mantle gravity anomalies. The effect of the crust is removed in three steps by subtracting the gravitational contributions of (1) topography and bathymetry, (2) low-density sedimentary accumulations, and (3) the three-dimensional density structure of the crystalline crust as determined by seismic observations. Information regarding sedimentary accumulations, including thickness and density, are taken from published maps and summaries of borehole measurements of densities; the seismic structure of the crust is based on a recent compilation, with layer densities estimated from P-wave velocities. The resultant mantle gravity anomaly map shows a pronounced negative anomaly (−50 to −400 mGal) beneath western North America and the adjacent oceanic region and positive anomalies (+50 to +350 mGal) east of the NA Cordillera. This pattern reflects the well-known division of North America into the stable eastern region and the tectonically active western region. The close correlation of large-scale features of the mantle anomaly map with those of the topographic map indicates that a significant amount of the topographic uplift in western NA is due to buoyancy in the hot upper mantle, a conclusion supported by previous investigations. To separate the contributions of mantle temperature anomalies from mantle compositional anomalies, we apply an additional correction to the mantle anomaly map for the thermal structure of the uppermost mantle. The thermal model is based on the conversion of seismic shear-wave velocities to temperature and is consistent with mantle temperatures that are independently estimated from heat flow and heat production data. The thermally corrected mantle density map reveals density anomalies that are chiefly due to compositional variations. These compositional density anomalies cause gravitational anomalies that reach ~250 mGal. A pronounced negative anomaly (−50 to −200 mGal) is found over the Canadian shield, which is consistent with chemical depletion and a corresponding low density of the lithospheric mantle, also referred to as the mantle tectosphere. The strongest positive anomaly is coincident with the Gulf of Mexico and indicates a positive density anomaly in the upper mantle, possibly an eclogite layer that has caused subsidence in the Gulf. Two linear positive anomalies are also seen south of 40°N: one with a NE-SW trend in the eastern United States, roughly coincident with the Grenville-Appalachians, and a second with a NW-SE trend beneath the states of Texas, New Mexico, and Colorado. These anomalies are interpreted as being due to (1) the presence of remnants of an oceanic slab in the upper mantle beneath the Grenville-Appalachian suture and (2) mantle thickening caused by a period of shallow, flat subduction during the Laramie orogeny, respectively. Based on these geophysical results, the evolution of the NA upper mantle is depicted in a series of maps and cartoons that display the primary processes that have formed and modified the NA crust and lithospheric upper mantle.
Timonen-Soivio, Laura; Vanhala, Raija; Malm, Heli; Leivonen, Susanna; Jokiranta, Elina; Hinkka-Yli-Salomäki, Susanna; Gissler, Mika; Brown, Alan S; Sourander, Andre
2015-01-01
The first aim of this study was to evaluate the association between different subgroups of autism spectrum disorders (ASDs) (childhood autism, Asperger syndrome, and pervasive developmental disorder/pervasive developmental disorder - not otherwise specified [PDD/PDD-NOS]) and congenital anomalies. Second, we assessed the association among intellectually disabled children with ASDs in the subgroups of childhood autism and PDD/PDD-NOS. Nationwide population-based register data for children with a diagnosis of ASD (n=4449; 3548 males, 901 females) were collected during years 1987-2000 from the Finnish Hospital Discharge Register. Data on congenital anomalies were derived from the National Register of Congenital Malformations. Conditional logistic regression models were used as a statistical method. The association between ASD subgroups and congenital anomalies was stratified by the presence or absence of intellectual disability. Congenital anomalies occurred more frequently in all subgroups of ASD than in comparison participants (adjusted odds ratio [OR] for major congenital anomalies 1.8, 95% confidence interval [CI] 1.5-2.2, p<0.001). The association between congenital anomalies and childhood autism (OR 2.4, 95% CI 1.6-3.6, p<0.001) and between congenital anomalies and PDD/PDD-NOS (OR 3.7, 95% CI 2.4-5.7, p<0.001) among children with an intellectual disability was strong but remained significant also without intellectual disability (childhood autism: OR 1.7, 95% CI 1.3-2.3, p<0.001; PDD/PDD-NOS: OR 2.3, 95% CI 1.9-2.8, p<0.001). The results suggest a significant association between ASDs and congenital anomalies regardless of the ASD subgroup. The association between childhood autism and PDD/PDD-NOS and congenital anomalies is stronger among children with intellectual disability is stronger than among those without intellectual disability. These results may have relevance in examining early risk factors in autism during fetal neurodevelopment. © 2014 Mac Keith Press.
Saberi, Eshagh Ali; Ebrahimipour, Sediqe
2016-01-01
The objective of this study was to evaluate the prevalence of dental developmental anomalies in digital panoramic radiographs of the patients referred to the Zahedan medical imaging center and to evaluate the frequency of anomalies regarding the disorders in shape, position and number in the Southeast of Iran. A total of 1172 panoramic radiographs from 581 males and 586 females aged over 16 years were obtained from the files of the Zahedan medical imaging center between the years of 2014 and 2015. The selected radiographs were evaluated in terms of the anomalies such as dilacerations, taurodontism, supernumerary teeth, congenitally missing teeth, fusion, gemination, tooth impaction, tooth transposition, dens invagination, and peg lateral. Then, the anomalies were compared to each other regarding the frequency of the anomaly type (morphological, positional and numerical). Data were evaluated using descriptive statistics such as frequency and percent, and statistical tests such as X(2) at 0.05 significant level using the Statistical Package for the Social Sciences version 16.5. The prevalence of dental anomaly was 213 (18.17%), which was higher in females (9.90) than male, (8.28), however, this difference was not statistically significant (P > 0.05). The prevalence of dilacerated teeth was 62 (5.29%), taurodontism 63 (5.38%), supernumerary teeth 6 (0.51%), congenitally missing teeth 13 (1.11%), fusion 1 (0.09%), gemination 1 (0.09%), impaction 40 (3.41%), transposition 2 (0.18%), dens invagination 16 (1.37) and peg lateral was 9 (0.77%). The prevalence of morphological anomaly was 152 (71.36%), malposition 42 (19.72%) and numerous anomaly was 19 (8.92%). Dental anomalies are relatively common; although their occurrence is not symptomatic, they can lead to several clinical problems in patients. Detailed clinical and radiographic assessment and counseling during patient visits is a critical factor in assessing the patient's degree of difficulty to help the dentist for better preparedness for the treatment.
NASA Astrophysics Data System (ADS)
Baker, David M. H.; Head, James W.; Phillips, Roger J.; Neumann, Gregory A.; Bierson, Carver J.; Smith, David E.; Zuber, Maria T.
2017-08-01
High-resolution gravity data from the Gravity Recovery and Interior Laboratory (GRAIL) mission provide the opportunity to analyze the detailed gravity and crustal structure of impact features in the morphological transition from complex craters to peak-ring basins on the Moon. We calculate average radial profiles of free-air anomalies and Bouguer anomalies for peak-ring basins, protobasins, and the largest complex craters. Complex craters and protobasins have free-air anomalies that are positively correlated with surface topography, unlike the prominent lunar mascons (positive free-air anomalies in areas of low elevation) associated with large basins. The Bouguer gravity anomaly profiles of complex craters are highly irregular, with central positive anomalies that are generally absent or not clearly tied to interior morphology. In contrast, gravity profiles for peak-ring basins (∼200 km to 580 km) are much more regular and are highly correlated with surface morphology. A central positive Bouguer anomaly is confined within the peak ring and a negative Bouguer anomaly annulus extends from the edge of the positive anomaly outward to about the rim crest. A number of degraded basins lacking interior peak rings have diameters and gravity patterns similar to those of well-preserved peak-ring basins. If these structures represent degraded peak-ring basins, the number of peak-ring basins on the Moon would increase by more than a factor of two to 34. The gravity anomalies within basins are interpreted to be due to uplift of the mantle confined within the peak ring and an annulus of thickened crust between the peak ring and rim crest. We hypothesize that mantle uplift is influenced by interaction between the transient cavity and the mantle. Further, mascon formation is generally disconnected from the number of basin rings formed and occurs over a wide range of basin sizes. These observations have important implications for models of basin and mascon formation on the Moon and other planetary bodies.
NASA Astrophysics Data System (ADS)
Xu, Qi; Guan, Zhaoyong
2017-08-01
The Maritime Continent (MC) is under influences of both the tropical Pacific and the Indian Ocean. Anomalous convective activities over the MC have significant impacts on the East Asian summer monsoon (EASM) and climate in China. In the present study, the variation in convective activity over the MC in boreal summer and its relationship to EASM anomalies are investigated based on regression analysis of NCEP-NCAR reanalysis and CMAP [Climate Prediction Center (CPC) Merged Analysis of Precipitation] data, with a focus on the impacts of ENSO and the Indian Ocean Dipole (IOD). The most significant interannual variability of convective activity is found over 10°S-10°N, 95°-145°E, which can be roughly defined as the key area of the MC (hereafter, KMC). Outgoing longwave radiation anomaly (OLRA) exhibits 3- to 7-yr periodicities over the KMC, and around 70% of the OLRA variance can be explained by the ENSO signal. However, distinct convection and precipitation anomalies still exist over this region after the ENSO and IOD signals are removed. Abnormally low precipitation always corresponds to positive OLRA over the KMC when negative diabatic heating anomalies and anomalous cooling of the atmospheric column lead to abnormal descending motion over this region. Correspondingly, abnormal divergence occurs in the lower troposphere while convergence occurs in the upper troposphere, triggering an East Asia-Pacific/Pacific-Japan (EAP/PJ)-like anomalous wave train that propagates northeastward and leads to a significant positive precipitation anomaly from the Yangtze River valley in China to the islands of Japan. This EAP/PJ-like wave pattern becomes even clearer after the removal of the ENSO signal and the combined effects of ENSO and IOD, suggesting that convective anomalies over the KMC have an important impact on EASM anomalies. The above results provide important clues for the prediction of EASM anomalies and associated summer precipitation anomalies in China.
Response of Global Lightning Activity Observed by the TRMM/LIS During Warm and Cold ENSO Phases
NASA Technical Reports Server (NTRS)
Chronis, Themis G.; Cecil, Dan; Goodman, Steven J.; Buechler, Dennis
2007-01-01
This paper investigates the response of global lightning activity to the transition from the warm (January February March-JFM 1998) to the cold (JFM 1999) ENSO phase. The nine-year global lightning climatology for these months from the Tropical Rainfall Measuring Mission (TRMM) Lightning Imaging Sensor (LIS) provides the observational baseline. Flash rate density is computed on a 5.0x5.0 degree lat/lon grid within the LIS coverage area (between approx.37.5 N and S) for each three month period. The flash rate density anomalies from this climatology are examined for these months in 1998 and 1999. The observed lightning anomalies spatially match the documented general circulation features that accompany the warm and cold ENSO events. During the warm ENSO phase the dominant positive lightning anomalies are located mostly over the Western Hemisphere and more specifically over Gulf of Mexico, Caribbean and Northern Mid-Atlantic. We further investigate specifically the Northern Mid-Atlantic related anomaly features since these show strong relation to the North Atlantic Oscillation (NAO). Furthermore these observed anomaly patterns show strong spatial agreement with anomalous upper level (200 mb) cold core cyclonic circulations. Positive sea surface temperature anomalies during the warm ENSO phase also affect the lightning activity, but this is mostly observed near coastal environments. Over the open tropical oceans, there is climatologically less lightning and the anomalies are less pronounced. Warm ENSO related anomalies over the Eastern Hemisphere are most prominent over the South China coast. The transition to the cold ENSO phase illustrates the detected lightning anomalies to be more pronounced over East and West Pacific. A comparison of total global lightning between warm and cold ENSO phase reveals no significant difference, although prominent regional anomalies are located over mostly oceanic environments. All three tropical "chimneys" (Maritime Continent, Central Africa, and Amazon Basin) do not show any particular response to this transition.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Not Available
1979-06-01
Results of a high-sensitivity, aerial, gamma-ray spectrometer and magnetometer survey of the Lewistown Quadrangle, Montana, are presented. Instrumentation and methods are described in Volume 1 of this final report. Statistical and geological analysis of the radiometric data revealed 58 uranium anomalies worthy of field-checking as possible prospects. One anomaly may be associated with the Cambrian Flathead Quartzite that may contain deposits similar to the Blind River and Rand uranium deposits. Three anomalies may be indicative of sandstone-type deposits in Jurassic rocks, particularly the Morrison Formation, which hosts uranium mineralization elsewhere. One of the latter anomalies is also related to rocksmore » of the Mississippian Madison Group, and this suggests the possible presence of uranium in limestones of the Mission Canyon Formation. There are 45 anomalies related to the Cretaceous rocks. Lignite in the Hell Creek and Judith River formations and Eagle Sandstone may have caused the formation of 22 epigenetic uranium deposits. Many anomalies occur in the Bearpaw Shale and Claggett Formation. However, only five are considered significant of the remainder are expected to be caused by large amounts of radioactive bentonite or bentonitic shale. Two other Cretaceous units that may host sandstone-type deposits are the Colorado Shale and Kootenai Formation that register 16 and two anomalies respectively. Only one anomaly pertains to Tertiary rocks, and it may be indicative of vein-type deposits in the intrusives of the Judith Mountains. These rocks may also act as source rocks for deposits surrounding the Judith Mountains. Eight anomalies related only to Quaternary units may be demonstrative of uranium-rich source rocks that could host uranium mineralization.Several anomalies are located close to oil fields and may have been cause by radium-rich oil-field brines.« less
NASA Astrophysics Data System (ADS)
Chowdhury, Debanjan; Skinner, Brian; Lee, Patrick A.
2018-05-01
Electron tunneling into a system with strong interactions is known to exhibit an anomaly, in which the tunneling conductance vanishes continuously at low energy due to many-body interactions. Recent measurements have probed this anomaly in a quantum Hall bilayer of the half-filled Landau level, and shown that the anomaly apparently gets stronger as the half-filled Landau level is increasingly spin polarized. Motivated by this result, we construct a semiclassical hydrodynamic theory of the tunneling anomaly in terms of the charge-spreading action associated with tunneling between two copies of the Halperin-Lee-Read state with partial spin polarization. This theory is complementary to our recent work (D. Chowdhury, B. Skinner, and P. A. Lee, arXiv:1709.06091) where the electron spectral function was computed directly using an instanton-based approach. Our results show that the experimental observation cannot be understood within conventional theories of the tunneling anomaly, in which the spreading of the injected charge is driven by the mean-field Coulomb energy. However, we identify a qualitatively new regime, in which the mean-field Coulomb energy is effectively quenched and the tunneling anomaly is dominated by the finite compressibility of the composite Fermion liquid.
Li, Gang; He, Bin; Huang, Hongwei; Tang, Limin
2016-01-01
The spatial–temporal correlation is an important feature of sensor data in wireless sensor networks (WSNs). Most of the existing works based on the spatial–temporal correlation can be divided into two parts: redundancy reduction and anomaly detection. These two parts are pursued separately in existing works. In this work, the combination of temporal data-driven sleep scheduling (TDSS) and spatial data-driven anomaly detection is proposed, where TDSS can reduce data redundancy. The TDSS model is inspired by transmission control protocol (TCP) congestion control. Based on long and linear cluster structure in the tunnel monitoring system, cooperative TDSS and spatial data-driven anomaly detection are then proposed. To realize synchronous acquisition in the same ring for analyzing the situation of every ring, TDSS is implemented in a cooperative way in the cluster. To keep the precision of sensor data, spatial data-driven anomaly detection based on the spatial correlation and Kriging method is realized to generate an anomaly indicator. The experiment results show that cooperative TDSS can realize non-uniform sensing effectively to reduce the energy consumption. In addition, spatial data-driven anomaly detection is quite significant for maintaining and improving the precision of sensor data. PMID:27690035
Aeromagnetic anomalies over faulted strata
Grauch, V.J.S.; Hudson, Mark R.
2011-01-01
High-resolution aeromagnetic surveys are now an industry standard and they commonly detect anomalies that are attributed to faults within sedimentary basins. However, detailed studies identifying geologic sources of magnetic anomalies in sedimentary environments are rare in the literature. Opportunities to study these sources have come from well-exposed sedimentary basins of the Rio Grande rift in New Mexico and Colorado. High-resolution aeromagnetic data from these areas reveal numerous, curvilinear, low-amplitude (2–15 nT at 100-m terrain clearance) anomalies that consistently correspond to intrasedimentary normal faults (Figure 1). Detailed geophysical and rock-property studies provide evidence for the magnetic sources at several exposures of these faults in the central Rio Grande rift (summarized in Grauch and Hudson, 2007, and Hudson et al., 2008). A key result is that the aeromagnetic anomalies arise from the juxtaposition of magnetically differing strata at the faults as opposed to chemical processes acting at the fault zone. The studies also provide (1) guidelines for understanding and estimating the geophysical parameters controlling aeromagnetic anomalies at faulted strata (Grauch and Hudson), and (2) observations on key geologic factors that are favorable for developing similar sedimentary sources of aeromagnetic anomalies elsewhere (Hudson et al.).
Shaheen, Robina; Abaunza, Mariana M; Jackson, Teresa L; McCabe, Justin; Savarino, Joël; Thiemens, Mark H
2014-08-19
Sulfur-isotopic anomalies have been used to trace the evolution of oxygen in the Precambrian atmosphere and to document past volcanic eruptions. High-precision sulfur quadruple isotope measurements of sulfate aerosols extracted from a snow pit at the South Pole (1984-2001) showed the highest S-isotopic anomalies (Δ(33)S = +1.66‰ and Δ(36)S = +2‰) in a nonvolcanic (1998-1999) period, similar in magnitude to Pinatubo and Agung, the largest volcanic eruptions of the 20th century. The highest isotopic anomaly may be produced from a combination of different stratospheric sources (sulfur dioxide and carbonyl sulfide) via SOx photochemistry, including photoexcitation and photodissociation. The source of anomaly is linked to super El Niño Southern Oscillation (ENSO) (1997-1998)-induced changes in troposphere-stratosphere chemistry and dynamics. The data possess recurring negative S-isotope anomalies (Δ(36)S = -0.6 ± 0.2‰) in nonvolcanic and non-ENSO years, thus requiring a second source that may be tropospheric. The generation of nonvolcanic S-isotopic anomalies in an oxidizing atmosphere has implications for interpreting Archean sulfur deposits used to determine the redox state of the paleoatmosphere.
Hajnal, András; Csábi, Györgyi; Herold, Róbert; Jeges, Sára; Halmai, Tamás; Trixler, Dániel; Simon, Maria; Tóth, Ákos Levente; Tényi, Tamás
2016-03-30
Minor physical anomalies are external markers of abnormal brain development,so the more common appearance of these signs among the relatives of schizophrenia patients can confirm minor physical anomalies as intermediate phenotypes. The aim of the present study was to investigate the rate and topological profile of minor physical anomalies in the first-degree unaffected relatives of patients with schizophrenia compared to matched normal control subjects. Using a list of 57 minor physical anomalies (the Méhes Scale), 20 relatives of patients with the diagnosis of schizophrenia and as a comparison 20 matched normal control subjects were examined. Minor physical anomalies were more common in the head and mouth regions among the relatives of schizophrenia patients compared to normal controls. By the differentiation of minor malformations and phenogenetic variants, we have found that only phenogenetic variants were more common in the relatives of schizophrenia patients compared to the control group, however individual analyses showed, that one minor malformation (flat forehead) was more prevalent in the relative group. The results can promote the concept, that minor physical anomalies can be endophenotypic markers of the illness. Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.
Dental anomalies and dental age assessment in treated children with acute lymphoblastic leukemia.
Khojastepour, L; Zareifar, S; Ebrahimi, M
2014-01-01
This cross sectional study was performed to evaluate dental ages and incidence of dental anomalies in children treated for acute lymphoblastic leukemia (ALL). A total of 25 ALL patient who passed at least 2 years of chemotherapy and 25 healthy sex and age matched children were evaluated. Dental age as well as dental anomalies in shape, size, number, and structure was recorded based on their panoramic radiographies which were taken for dental purposes. The number of dental anomalies significantly increased in ALL treated children. Seven ALL cases (28%) in compression to only one (4%) in control group had at least one dental anomaly. However, there was neither statistically significant differences between the mean of dental (p=0.32) and chronologic age (p=0.12) in both groups, nor between dental age of cases and control group (p=0.62).The age at the onset of treatment as well as treatment durations has not affected dental age and the incidence of dental anomalies significantly (p<0.05). Chemotherapy in children results in emergence of dental anomaly. Dental age, maturity, and development process however seems to be independent from chemotherapy.
Dental Anomalies in Permanent Teeth after Trauma in Primary Dentition.
Bardellini, Elena; Amadori, Francesca; Pasini, Stefania; Majorana, Alessandra
This retrospective study aims to evaluate the prevalence of dental anomalies in permanent teeth as a result of a trauma concerning the predecessor primary teeth. A total of 241 records of children (118 males and 123 females, mean age 3.62 ± 1.40) affected by trauma on primary teeth were analyzed. All patients were recalled to evaluate the status of the permanent successor teeth by clinical and radiographic investigations. Out of 241 patients, 106 patients (for a total of 179 traumatized primary teeth) presented at the recall. Dental anomalies on successor permanent teeth were detected in 21 patients (19.8%), for a total of 26 teeth (14.5%) and 28 anomalies. Anomalies of the eruptive process were the most observed disturbances (60.7%), followed by enamel hypoplasia (25%) and white spots (14.3%). A higher percentage of anomalies on permanent teeth was observed when trauma occurred at an age less than 36 months (38.5% of cases). Intrusive and extrusive luxation were related with the most cases of clinical disturbances in the successor permanent teeth. The results of this study highlight the risk of dental anomalies after a trauma in primary dentition, especially in early-aged children and in case of intrusive luxation.
Pre-seismic anomalies from optical satellite observations: a review
NASA Astrophysics Data System (ADS)
Jiao, Zhong-Hu; Zhao, Jing; Shan, Xinjian
2018-04-01
Detecting various anomalies using optical satellite data prior to strong earthquakes is key to understanding and forecasting earthquake activities because of its recognition of thermal-radiation-related phenomena in seismic preparation phases. Data from satellite observations serve as a powerful tool in monitoring earthquake preparation areas at a global scale and in a nearly real-time manner. Over the past several decades, many new different data sources have been utilized in this field, and progressive anomaly detection approaches have been developed. This paper reviews the progress and development of pre-seismic anomaly detection technology in this decade. First, precursor parameters, including parameters from the top of the atmosphere, in the atmosphere, and on the Earth's surface, are stated and discussed. Second, different anomaly detection methods, which are used to extract anomalous signals that probably indicate future seismic events, are presented. Finally, certain critical problems with the current research are highlighted, and new developing trends and perspectives for future work are discussed. The development of Earth observation satellites and anomaly detection algorithms can enrich available information sources, provide advanced tools for multilevel earthquake monitoring, and improve short- and medium-term forecasting, which play a large and growing role in pre-seismic anomaly detection research.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Li, Renzhong; Sun, Gang; Xu, Limei, E-mail: limei.xu@pku.edu.cn
A group of materials including water and silicon exhibit many anomalous behaviors, e.g., density anomaly and diffusivity anomaly (increase upon compression). These materials are hypothesized to have a liquid-liquid phase transition (LLPT) and the critical fluctuation in the vicinity of the liquid-liquid critical point is considered as the origin of different anomalies. Liquid gallium was also reported to have a LLPT, yet whether it shows similar water-like anomalies is not yet studied. Using molecular dynamics simulations on a modified embedded-atom model, we study the thermodynamic, dynamic, and structural properties of liquid gallium as well as its LLPT. We find that,more » similar to water-like materials predicted to have the LLPT, gallium also shows different anomalous behaviors (e.g., density anomaly, diffusivity anomaly, and structural anomaly). We also find that its thermodynamic and structural response functions are continuous and show maxima in the supercritical region, the loci of which asymptotically approach to the other and merge to the Widom line. These phenomena are consistent with the supercritical phenomenon in a category of materials with a liquid-liquid critical point, which could be common features in most materials with a LLPT.« less
NASA Technical Reports Server (NTRS)
Phillips, R. J.
1986-01-01
Crustal anomaly detection with MAGSAT data is frustrated by the inherent resolving power of the data and by contamination from the external and core fields. The quality of the data might be tested by modeling specific tectonic features which produce anomalies that fall within the proposed resolution and crustal amplitude capabilities of the MAGSAT fields. To test this hypothesis, the north African hotspots associated with Ahaggar, Tibestia and Darfur have been modeled as magnetic induction anomalies due solely to shallower depth to the Curie isotherm surface beneath these features. The MAGSAT data were reduced by subtracting the external and core fields to isolate the scalar and vertical component crustal signals. The predicted model magnetic signal arising from the surface topography of the uplift and the Curie isotherm surface was calculated at MAGSAT altitudes by the Fourier transform technique modified to allow for variable magnetization. In summary it is suggested that the region beneath Ahaggar is associated with a strong thermal anomaly and the predicted anomaly best fits the associated MAGSAT anomaly if the African plate is moving in a northeasterly direction.
Spine and rib abnormalities and stature in spondylocostal dysostosis.
Takikawa, Kazuharu; Haga, Nobuhiko; Maruyama, Toru; Nakatomi, Akiko; Kondoh, Tatsuro; Makita, Yoshio; Hata, Akira; Kawabata, Hidehiko; Ikegawa, Shiro
2006-04-01
A retrospective study of radiographic and clinical findings of spondylocostal dysostosis. To determine the features of spondylocostal dysostosis diagnosed using consistent diagnostic criteria. To our knowledge, no clear definition of spondylocostal dysostosis exists, and little information is available regarding its clinical or radiographic features. We defined spondylocostal dysostosis as a congenital spinal disorder consisting of >or=2 vertebral anomalies associated with rib anomalies, without crab-like chest. For 30 patients, including 12 males and 18 females, who met these criteria, we evaluated vertebral and rib anomalies, birth and present body height, and associated anomalies. There were only 2 familial cases. Features of spondylocostal dysostosis were: (1) anomalies involved the thoracic region in all cases; many also involved the cervical spine; (2) most patients had >or=4 vertebral anomalies; (3) frequent vertebral anomalies were butterfly vertebra, hemivertebra, complete block, and unilateral bar, which were associated with both rib absence and fusion; (4) short stature was not always present at birth; and (5) complete block was 1 factor identified as being related to short stature after 12 years of age. Several features of sporadic spondylocostal dysostosis disorder were determined, including new findings related to body height.
Evaluation of Anomaly Detection Method Based on Pattern Recognition
NASA Astrophysics Data System (ADS)
Fontugne, Romain; Himura, Yosuke; Fukuda, Kensuke
The number of threats on the Internet is rapidly increasing, and anomaly detection has become of increasing importance. High-speed backbone traffic is particularly degraded, but their analysis is a complicated task due to the amount of data, the lack of payload data, the asymmetric routing and the use of sampling techniques. Most anomaly detection schemes focus on the statistical properties of network traffic and highlight anomalous traffic through their singularities. In this paper, we concentrate on unusual traffic distributions, which are easily identifiable in temporal-spatial space (e.g., time/address or port). We present an anomaly detection method that uses a pattern recognition technique to identify anomalies in pictures representing traffic. The main advantage of this method is its ability to detect attacks involving mice flows. We evaluate the parameter set and the effectiveness of this approach by analyzing six years of Internet traffic collected from a trans-Pacific link. We show several examples of detected anomalies and compare our results with those of two other methods. The comparison indicates that the only anomalies detected by the pattern-recognition-based method are mainly malicious traffic with a few packets.
A Hybrid Semi-Supervised Anomaly Detection Model for High-Dimensional Data.
Song, Hongchao; Jiang, Zhuqing; Men, Aidong; Yang, Bo
2017-01-01
Anomaly detection, which aims to identify observations that deviate from a nominal sample, is a challenging task for high-dimensional data. Traditional distance-based anomaly detection methods compute the neighborhood distance between each observation and suffer from the curse of dimensionality in high-dimensional space; for example, the distances between any pair of samples are similar and each sample may perform like an outlier. In this paper, we propose a hybrid semi-supervised anomaly detection model for high-dimensional data that consists of two parts: a deep autoencoder (DAE) and an ensemble k -nearest neighbor graphs- ( K -NNG-) based anomaly detector. Benefiting from the ability of nonlinear mapping, the DAE is first trained to learn the intrinsic features of a high-dimensional dataset to represent the high-dimensional data in a more compact subspace. Several nonparametric KNN-based anomaly detectors are then built from different subsets that are randomly sampled from the whole dataset. The final prediction is made by all the anomaly detectors. The performance of the proposed method is evaluated on several real-life datasets, and the results confirm that the proposed hybrid model improves the detection accuracy and reduces the computational complexity.
A Hybrid Semi-Supervised Anomaly Detection Model for High-Dimensional Data
Jiang, Zhuqing; Men, Aidong; Yang, Bo
2017-01-01
Anomaly detection, which aims to identify observations that deviate from a nominal sample, is a challenging task for high-dimensional data. Traditional distance-based anomaly detection methods compute the neighborhood distance between each observation and suffer from the curse of dimensionality in high-dimensional space; for example, the distances between any pair of samples are similar and each sample may perform like an outlier. In this paper, we propose a hybrid semi-supervised anomaly detection model for high-dimensional data that consists of two parts: a deep autoencoder (DAE) and an ensemble k-nearest neighbor graphs- (K-NNG-) based anomaly detector. Benefiting from the ability of nonlinear mapping, the DAE is first trained to learn the intrinsic features of a high-dimensional dataset to represent the high-dimensional data in a more compact subspace. Several nonparametric KNN-based anomaly detectors are then built from different subsets that are randomly sampled from the whole dataset. The final prediction is made by all the anomaly detectors. The performance of the proposed method is evaluated on several real-life datasets, and the results confirm that the proposed hybrid model improves the detection accuracy and reduces the computational complexity. PMID:29270197
The association between Mullerian anomalies and IUGR: a meta-analysis.
Karami, Manoochehr; Jenabi, Ensiyeh
2018-02-05
Published literature regarding the association between Mullerian anomalies and intrauterine growth restriction (IUGR) is controversial. To date, no meta-analysis has been performed for assessing the relationship between the Mullerian anomalies and IUGR. Therefore, the aim of this study was to perform a meta-analysis by combining data from relevant studies to assessing the association of between Mullerian anomalies and IUGR. A systematic search was conducted in PubMed, Scopus and Web of Science to identify of all studies prior to September 2017. Egger's and Begg's tests were carried out to quantitatively assess publication bias. To estimate the heterogeneity among studies the Q-statistic test and I-squared (I 2 ) test were used. The random-effects model was conducted to obtain pooled odds ratio (OR) as a measure of the association between Mullerian anomalies and IUGR. A total of seven studies were included in this meta-analysis with a sample of 605,005 participants. The pooled overall OR was 1.93 (95% CI: 1.52, 2.34). We reported that mullerian anomalies are a risk factor for IUGR. However, further evidence by larger prospective cohort studies is needed to make conclusive evidence regarding the association between mullerian anomalies and IUGR.
Observation of El Nino by the Nimbus-7 SMMR
NASA Technical Reports Server (NTRS)
Hwang, P. H.; Macmillan, D. S.; Fu, C. C.; Kim, S. T.; Han, Daesoo; Gloersen, P.
1986-01-01
The quality of Nimbus-7 Scanning Multichannel Microwave Radiometer (SMMR) derived SST, water vapor, and windspeed are assessed, and these parameters are used to study the El Nino event of 1982-1983 in the equatorial Pacific region from 120 deg to the South American coast. The features of the anomaly fields for these parameters, and the connections between these fields, are discussed. Anomaly fields are found to be qualitatively consistent with outgoing longwave radiation anomaly fields and wind vector anomaly fields.
Anteverted internal auditory canal as an inner ear anomaly in patients with craniofacial microsomia.
L'Heureux-Lebeau, Bénédicte; Saliba, Issam
2014-09-01
Craniofacial microsomia involves structure of the first and second branchial arches. A wide range of ear anomalies, affecting external, middle and inner ear, has been described in association with this condition. We report three cases of anteverted internal auditory canal in patients presenting craniofacial microsomia. This unique internal auditory canal orientation was found on high-resolution computed tomography of the temporal bones. This internal auditory canal anomaly is yet unreported in craniofacial anomalies. Copyright © 2014. Published by Elsevier Ireland Ltd.
Behavioral economics without anomalies.
Rachlin, H
1995-01-01
Behavioral economics is often conceived as the study of anomalies superimposed on a rational system. As research has progressed, anomalies have multiplied until little is left of rationality. Another conception of behavioral economics is based on the axiom that value is always maximized. It incorporates so-called anomalies either as conflicts between temporal patterns of behavior and the individual acts comprising those patterns or as outcomes of nonexponential time discounting. This second conception of behavioral economics is both empirically based and internally consistent. PMID:8551195
Magnetic and gravity anomalies in the Americas
NASA Technical Reports Server (NTRS)
Braile, L. W.; Hinze, W. J.; Vonfrese, R. R. B. (Principal Investigator)
1981-01-01
The cleaning and magnetic tape storage of spherical Earth processing programs are reported. These programs include: NVERTSM which inverts total or vector magnetic anomaly data on a distribution of point dipoles in spherical coordinates; SMFLD which utilizes output from NVERTSM to compute total or vector magnetic anomaly fields for a distribution of point dipoles in spherical coordinates; NVERTG; and GFLD. Abstracts are presented for papers dealing with the mapping and modeling of magnetic and gravity anomalies, and with the verification of crustal components in satellite data.
Abortive segmental perineal hemangioma.
Tlougan, Brook E; Gonzalez, Mercedes E; Orlow, Seth J
2011-10-15
A six-week-old girl presented with a segmental, focally atrophic, vascular patch in the diaper area, present since birth. It had undergone minimal proliferation, but had ulcerated. Evaluation to rule out LUMBAR (Lower body hemangioma/Lipoma or other cutaneous anomalies, Urogenital anomalies, Myelopathy, Bony deformities, Anorectal/Arterial anomalies, and Renal anomalies) syndrome, which included ultrasound and Doppler examination of the abdomen, spine, and pelvis, was negative. We report a unique case of an ulcerated, segmental abortive hemangioma of the anogenital area with excellent clinical response to topical timolol gel.
A global magnetic anomaly map. [obtained from POGO satellite data
NASA Technical Reports Server (NTRS)
Regan, R. D.; Davis, W. M.; Cain, J. C.
1974-01-01
A subset of POGO satellite magnetometer data has been formed that is suitable for analysis of crustal magnetic anomalies. Using a thirteenth order field model, fit to these data, magnetic residuals have been calculated over the world to latitude limits of plus 50 deg. These residuals averaged over one degree latitude-longitude blocks represent a detailed global magnetic anomaly map derived solely from satellite data. Preliminary analysis of the map indicates that the anomalies are real and of geological origin.
Identification and Evaluation of Submerged Anomalies, Mobile Harbor, Alabama.
1984-10-01
Bay Waters , 1864-1865 APPENDIX B: Description of Maps in National ill Archives Collection V LIST OF FIGURES Figure Page cover Torpedo Raft in Mobile Bay...Anomaly D-E 51 13 Magnetometer Chart, Anomaly F 53 14 Sketch of Steel Wreckage Found at Anomaly F 54 15 Approaches to Mobile City by Water (Merrill...Osage (1863-65) 84 30 CSS Albemarle, Prototype for the Huntsville 86 31 Magnolia, CSA-Utilized Vessel 109 32 Approaches to Mobile City by Water (1864
What drove the Pacific and North America climate anomalies in winter 2014/15?
NASA Astrophysics Data System (ADS)
Peng, Peitao; Kumar, Arun; Hu, Zeng-Zhen
2017-12-01
In late 2014 and early 2015, the canonical atmospheric response to the El Niño and Southern Oscillation (ENSO) event was not observed in the central and eastern equatorial Pacific, although Niño3.4 index exceeded the threshold for a weak El Niño. In an effort to understand why it was so, this study deconvoluted the observed 2014/15 December-January-February (DJF) mean sea surface temperature (SST), precipitation and 200 hPa stream function anomalies into the leading patterns related to the principal components of DJF SST variability. It is noted that the anomalies of these variables were primarily determined by the patterns related to two SST modes: one is the North Pacific mode (NPM), and the other the ENSO mode. The NPM was responsible for the apparent lack of coupled air-sea relationship in the central equatorial Pacific and the east-west structure of the circulation anomalies over North America, while the ENSO mode linked to SSTs in the central and eastern equatorial Pacific as well as the circulation in the central equatorial Pacific. Further, the ENSO signal in DJF 2014/15 likely evolved from the NPM pattern in winter 2013/14. Its full development, however, was impeded by the easterly anomalies in the central equatorial Pacific that was associated with negative SST anomalies in the southeastern subtropical Pacific. In addition, the analyses also indicates that the SST anomalies in the Niño3.4 region alone were not adequate for capturing the coupling of oceanic and atmospheric anomalies in the tropical Pacific, due to the fact that this index cannot distinguish whether the SST anomaly in the Niño3.4 region is associated with the ENSO mode or NPM, or both.
Qiu, Yaodong; Wang, Zhengtao; Jiang, Weiping; Zhang, Bingbing; Li, Fupeng; Guo, Fei
2017-01-26
CHAMP and Swarm satellite magnetic data are combined to establish the lithospheric magnetic field over the Tibetan Plateau at satellite altitude by using zonal revised spherical cap harmonic analysis (R-SCHA). These data are integrated with geological structures data to analyze the relationship between magnetic anomaly signals and large-scale geological tectonic over the Tibetan Plateau and to explore the active tectonic region based on the angle of the magnetic anomaly. Results show that the model fitting error is small for a layer 250-500 km high, and the RMSE of the horizontal and radial geomagnetic components is better than 0.3 nT. The proposed model can accurately describe medium- to long-scale lithospheric magnetic anomalies. Analysis indicates that a negative magnetic anomaly in the Tibetan Plateau significantly differs with a positive magnetic anomaly in the surrounding area, and the boundary of the positive and negative regions is generally consistent with the geological tectonic boundary in the plateau region. Significant differences exist between the basement structures of the hinterland of the plateau and the surrounding area. The magnetic anomaly in the Central and Western Tibetan Plateau shows an east-west trend, which is identical to the direction of the geological structures. The magnetic anomaly in the eastern part is arc-shaped and extends along the northeast direction. Its direction is significantly different from the trend of the geological structures. The strongest negative anomaly is located in the Himalaya block, with a central strength of up to -9 nT at a height of 300 km. The presence of a strong negative anomaly implies that the Curie isotherm in this area is relatively shallow and deep geological tectonic activity may exist.
Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data.
Boyle, Breidge; Addor, Marie-Claude; Arriola, Larraitz; Barisic, Ingeborg; Bianchi, Fabrizio; Csáky-Szunyogh, Melinda; de Walle, Hermien E K; Dias, Carlos Matias; Draper, Elizabeth; Gatt, Miriam; Garne, Ester; Haeusler, Martin; Källén, Karin; Latos-Bielenska, Anna; McDonnell, Bob; Mullaney, Carmel; Nelen, Vera; Neville, Amanda J; O'Mahony, Mary; Queisser-Wahrendorf, Annette; Randrianaivo, Hanitra; Rankin, Judith; Rissmann, Anke; Ritvanen, Annukka; Rounding, Catherine; Tucker, David; Verellen-Dumoulin, Christine; Wellesley, Diana; Wreyford, Ben; Zymak-Zakutnia, Natalia; Dolk, Helen
2018-01-01
To validate the estimates of Global Burden of Disease (GBD) due to congenital anomaly for Europe by comparing infant mortality data collected by EUROCAT registries with the WHO Mortality Database, and by assessing the significance of stillbirths and terminations of pregnancy for fetal anomaly (TOPFA) in the interpretation of infant mortality statistics. EUROCAT is a network of congenital anomaly registries collecting data on live births, fetal deaths from 20 weeks' gestation and TOPFA. Data from 29 registries in 19 countries were analysed for 2005-2009, and infant mortality (deaths of live births at age <1 year) compared with the WHO Mortality Database. Eight EUROCAT countries were excluded from further analysis on the basis that this comparison showed poor ascertainment of survival status. According to WHO, 17%-42% of infant mortality was attributed to congenital anomaly. In 11 EUROCAT countries, average infant mortality with congenital anomaly was 1.1 per 1000 births, with higher rates where TOPFA is illegal (Malta 3.0, Ireland 2.1). The rate of stillbirths with congenital anomaly was 0.6 per 1000. The average TOPFA prevalence was 4.6 per 1000, nearly three times more prevalent than stillbirths and infant deaths combined. TOPFA also impacted on the prevalence of postneonatal survivors with non-lethal congenital anomaly. By excluding TOPFA and stillbirths from GBD years of life lost (YLL) estimates, GBD underestimates the burden of disease due to congenital anomaly, and thus declining YLL over time may obscure lack of progress in primary, secondary and tertiary prevention. © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.
GARIB, Daniela Gamba; LANCIA, Melissa; KATO, Renata Mayumi; OLIVEIRA, Thais Marchini; NEVES, Lucimara Teixeira das
2016-01-01
ABSTRACT The early recognition of risk factors for the occurrence of palatally displaced canines (PDC) can increase the possibility of impaction prevention. Objective To estimate the risk of PDC occurrence in children with dental anomalies identified early during mixed dentition. Material and Methods The sample comprised 730 longitudinal orthodontic records from children (448 females and 282 males) with an initial mean age of 8.3 years (SD=1.36). The dental anomaly group (DA) included 263 records of patients with at least one dental anomaly identified in the initial or middle mixed dentition. The non-dental anomaly group (NDA) was composed of 467 records of patients with no dental anomalies. The occurrence of PDC in both groups was diagnosed using panoramic and periapical radiographs taken in the late mixed dentition or early permanent dentition. The prevalence of PDC in patients with and without early diagnosed dental anomalies was compared using the chi-square test (p<0.01), relative risk assessments (RR), and positive and negative predictive values (PPV and NPV). Results PDC frequency was 16.35% and 6.2% in DA and NDA groups, respectively. A statistically significant difference was observed between groups (p<0.01), with greater risk of PDC development in the DA group (RR=2.63). The PPV and NPV was 16% and 93%, respectively. Small maxillary lateral incisors, deciduous molar infraocclusion, and mandibular second premolar distoangulation were associated with PDC. Conclusion Children with dental anomalies diagnosed during early mixed dentition have an approximately two and a half fold increased risk of developing PDC during late mixed dentition compared with children without dental anomalies. PMID:28076458
Transient ice mass variations over Greenland detected by the combination of GPS and GRACE data
NASA Astrophysics Data System (ADS)
Zhang, B.; Liu, L.; Khan, S. A.; van Dam, T. M.; Zhang, E.
2017-12-01
Over the past decade, the Greenland Ice Sheet (GrIS) has been undergoing significant warming and ice mass loss. Such mass loss was not always a steady process but had substantial temporal and spatial variabilities. Here we apply multi-channel singular spectral analysis to crustal deformation time series measured at about 50 Global Positioning System (GPS) stations mounted on bedrock around the Greenland coast and mass changes inferred from Gravity Recovery and Climate Experiment (GRACE) to detect transient changes in ice mass balance over the GrIS. We detect two transient anomalies: one is a negative melting anomaly (Anomaly 1) that peaked around 2010; the other is a positive melting anomaly (Anomaly 2) that peaked between 2012 and 2013. The GRACE data show that both anomalies caused significant mass changes south of 74°N but negligible changes north of 74°N. Both anomalies caused the maximum mass change in southeast GrIS, followed by in west GrIS near Jakobshavn. Our results also show that the mass change caused by Anomaly 1 first reached the maximum in late 2009 in the southeast GrIS and then migrated to west GrIS. However, in Anomaly 2, the southeast GrIS was the last place that reached the maximum mass change in early 2013 and the west GrIS near Jakobshavn was the second latest place that reached the maximum mass change. Most of the GPS data show similar spatiotemporal patterns as those obtained from the GRACE data. However, some GPS time series show discrepancies in either space or time, because of data gaps and different sensitivities of mass loading change. Namely, loading deformation measured by GPS can be significantly affected by local dynamical mass changes, which, yet, has little impact on GRACE observations.
Flux-ratio anomalies from discs and other baryonic structures in the Illustris simulation
NASA Astrophysics Data System (ADS)
Hsueh, Jen-Wei; Despali, Giulia; Vegetti, Simona; Xu, Dandan; Fassnacht, Christopher D.; Metcalf, R. Benton
2018-04-01
The flux ratios in the multiple images of gravitationally lensed quasars can provide evidence for dark matter substructure in the halo of the lensing galaxy if the flux ratios differ from those predicted by a smooth model of the lensing galaxy mass distribution. However, it is also possible that baryonic structures in the lensing galaxy, such as edge-on discs, can produce flux-ratio anomalies. In this work, we present the first statistical analysis of flux-ratio anomalies due to baryons from a numerical simulation perspective. We select galaxies with various morphological types in the Illustris simulation and ray trace through the simulated haloes, which include baryons in the main lensing galaxies but exclude any substructures, in order to explore the pure baryonic effects. Our ray-tracing results show that the baryonic components can be a major contribution to the flux-ratio anomalies in lensed quasars and that edge-on disc lenses induce the strongest anomalies. We find that the baryonic components increase the probability of finding high flux-ratio anomalies in the early-type lenses by about 8 per cent and by about 10-20 per cent in the disc lenses. The baryonic effects also induce astrometric anomalies in 13 per cent of the mock lenses. Our results indicate that the morphology of the lens galaxy becomes important in the analysis of flux-ratio anomalies when considering the effect of baryons, and that the presence of baryons may also partially explain the discrepancy between the observed (high) anomaly frequency and what is expected due to the presence of subhaloes as predicted by the cold dark matter simulations.
Qiu, Yaodong; Wang, Zhengtao; Jiang, Weiping; Zhang, Bingbing; Li, Fupeng; Guo, Fei
2017-01-01
CHAMP and Swarm satellite magnetic data are combined to establish the lithospheric magnetic field over the Tibetan Plateau at satellite altitude by using zonal revised spherical cap harmonic analysis (R-SCHA). These data are integrated with geological structures data to analyze the relationship between magnetic anomaly signals and large-scale geological tectonic over the Tibetan Plateau and to explore the active tectonic region based on the angle of the magnetic anomaly. Results show that the model fitting error is small for a layer 250–500 km high, and the RMSE of the horizontal and radial geomagnetic components is better than 0.3 nT. The proposed model can accurately describe medium- to long-scale lithospheric magnetic anomalies. Analysis indicates that a negative magnetic anomaly in the Tibetan Plateau significantly differs with a positive magnetic anomaly in the surrounding area, and the boundary of the positive and negative regions is generally consistent with the geological tectonic boundary in the plateau region. Significant differences exist between the basement structures of the hinterland of the plateau and the surrounding area. The magnetic anomaly in the Central and Western Tibetan Plateau shows an east–west trend, which is identical to the direction of the geological structures. The magnetic anomaly in the eastern part is arc-shaped and extends along the northeast direction. Its direction is significantly different from the trend of the geological structures. The strongest negative anomaly is located in the Himalaya block, with a central strength of up to −9 nT at a height of 300 km. The presence of a strong negative anomaly implies that the Curie isotherm in this area is relatively shallow and deep geological tectonic activity may exist. PMID:28134755
NASA Astrophysics Data System (ADS)
Stanciu, A. C.; Humphreys, E.; Clayton, R. W.
2017-12-01
We construct a P-wave model of the upper mantle based on new and previously acquired data from the USArray-TA stations and regional deployments, including the HLP, ID-OR, and the currently recording Wallowa stations. Our teleseismic arrival times are corrected for crustal structure (based on surface wave, receiver function, and controlled-source models from the region). Our modeling incorporates 3-D ray tracing and several simple considerations of radial anisotropy on travel time. As imaged previously, we find high P-wave velocity anomalies located beneath the Wallowa Mountains and beneath the Idaho Batholith in central west Idaho. Our improved imaging finds that these two anomalies are located down to 350 km depth, and are clearly separated from one another and from a shallower fast anomaly in the uppermost mantle beneath the westernmost Snake River Plain. Our preferred interpretation includes a combination of delamination and slab fragments in this region. As fast (and presumably cool) structures, these upper-mantle anomalies are thought to have a lithospheric origin. The anomaly beneath central Idaho is interpreted as the leading edge of the Farallon slab associated with the accretion of Siletzia terrane to North America. This anomaly may include some North American lithosphere that delaminated from the Laramide-thickened lithospheric mantle, perhaps related to Challis magmatism. The Wallowa anomaly is likely to represent Farallon lithosphere that delaminated during the Columbia River flood basalt event. The small anomaly between the two deeper fast anomalies, occurring at depths above 150km, could represent an isolated lithospheric fragment or a structure created by the Columbia River flood basalt event.
Goldfarb, Charles A.; Wall, Lindley B.; Bohn, Deborah C.; Moen, Patrick; Van Heest, Ann E.
2014-01-01
Purpose To examine the relative presentation frequency of children with upper limb congenital anomalies at 3 Midwestern referral centers using the Oberg, Manske, and Tonkin (OMT) classification and to assess the utility of this new classification system. Methods 641 individuals with 653 congenital upper extremity anomalies were identified at 3 hospitals in 2 large metropolitan areas during a 1-year interval. Patients were identified prospectively and the specific upper extremity anomaly and any associated syndromes were confirmed using medical records and radiographs. We applied the OMT classification that categorizes anomalies using a dysmorphology outline as malformations, dysplasias, deformations, and syndromes, and assessed its utility and ease of use. Results There were 480 extremities (74%) with a limb malformation including 184 involving the entire limb. Arthrogryposis was the most common of these (53 extremities). Anomalies affecting only the hand plate accounted for 62% (296) of the malformations. Of these, radial polydactyly (15%) was the most common specific anomaly, followed by symbrachydactyly (13%) and cleft hand (11%). Dysplasias were noted in 86 extremities; 55 of these were multiple hereditary exostoses. There were 87 extremities with deformations and 58 of these were trigger digits. A total of 98 children had a syndrome or association. Constriction ring sequence was most common. The OMT was straightforward to use and most anomalies could be easily assigned. There were a few conditions, such as Madelung deformity and symbrachydactyly, that would benefit from clarification on how to best classify them. Conclusions Malformations were the most common congenital anomalies in the 653 upper extremities evaluated over a 1-year period at 3 institutions. We were able to classify all individuals using the OMT classification system. PMID:25534840
Goldfarb, Charles A; Wall, Lindley B; Bohn, Deborah C; Moen, Patrick; Van Heest, Ann E
2015-01-01
To examine the relative presentation frequency of children with upper limb congenital anomalies at 3 Midwestern referral centers using the Oberg, Manske, and Tonkin (OMT) classification and to assess the utility of this new classification system. 641 individuals with 653 congenital upper extremity anomalies were identified at 3 hospitals in 2 large metropolitan areas during a 1-year interval. Patients were identified prospectively and the specific upper extremity anomaly and any associated syndromes were confirmed using medical records and radiographs. We applied the OMT classification that categorizes anomalies using a dysmorphology outline as malformations, dysplasias, deformations, and syndromes, and assessed its utility and ease of use. There were 480 extremities (74%) with a limb malformation including 184 involving the entire limb. Arthrogryposis was the most common of these (53 extremities). Anomalies affecting only the hand plate accounted for 62% (296) of the malformations. Of these, radial polydactyly (15%) was the most common specific anomaly, followed by symbrachydactyly (13%) and cleft hand (11%). Dysplasias were noted in 86 extremities; 55 of these were multiple hereditary exostoses. There were 87 extremities with deformations and 58 of these were trigger digits. A total of 109 children had a syndrome or association. Constriction ring sequence was most common. The OMT was straightforward to use and most anomalies could be easily assigned. There were a few conditions, such as Madelung deformity and symbrachydactyly, that would benefit from clarification on how to best classify them. Malformations were the most common congenital anomalies in the 653 upper extremities evaluated over a 1-year period at 3 institutions. We were able to classify all individuals using the OMT classification system. Copyright © 2015 American Society for Surgery of the Hand. Published by Elsevier Inc. All rights reserved.
Pedersen, Marie; Garne, Ester; Hansen-Nord, Nete; Hjortebjerg, Dorrit; Ketzel, Matthias; Raaschou-Nielsen, Ole; Nybo Andersen, Anne-Marie; Sørensen, Mette
2017-11-01
Ambient air pollution has been associated with certain congenital anomalies, but few studies rely on assessment of fine-scale variation in air quality and associations with noise from road traffic are unexplored. Among 84,218 liveborn singletons (1997-2002) from the Danish National Birth Cohort with complete covariate data and residential address history from conception until birth, we identified major congenital anomalies in 4018 children. Nitrogen dioxide (NO 2 ) and noise from road traffic (L den ) burden during fetal life was modeled. Outcome and covariate data were derived from registries, hospital records and questionnaires. Odds ratios (ORs) for eleven major anomaly groups associated with road traffic pollution during first trimester were estimated using logistic regression with generalized estimating equation (GEE) approach. Most of the associations tested did not suggest increased risks. A 10-µg/m 3 increase in NO 2 exposure during first trimester was associated with an adjusted ORs of 1.22 (95% confidence interval: 0.98-1.52) for ear, face and neck anomalies; 1.14 0.98-1.33) for urinary anomalies. A 10-dB increase in road traffic noise was also associated with these subgroups of anomalies as well as with an increased OR for orofacial cleft anomalies (1.17, 0.94-1.47). Inverse associations for several both air pollution and noise were observed for atrial septal defects (0.85, 0.68-1.04 and 0.81, 0.65-0.99, respectively). Residential road traffic exposure to noise or air pollution during pregnancy did not seem to pose a risk for development of congenital anomalies. Copyright © 2017 Elsevier Inc. All rights reserved.
Impact of pre-pregnancy diabetes mellitus on congenital anomalies, Canada, 2002-2012.
Liu, S; Rouleau, J; León, J A; Sauve, R; Joseph, K S; Ray, J G
2015-07-01
To examine the impact of pre-pregnancy diabetes mellitus (DM) on the population birth prevalence of congenital anomalies in Canada. We carried out a population-based study of all women who delivered in Canadian hospitals (except those in the province of Quebec) between April 2002 and March 2013 and their live-born infants with a birth weight of 500 grams or more and/or a gestational age of 22 weeks or more. Pre-pregnancy type 1 or type 2 DM was identified using ICD-10 diagnostic codes. The association between DM and all congenital anomalies as well as specific congenital anomaly categories was estimated using adjusted odds ratios; the impact was calculated as a population attributable risk percent (PAR%). There were 118,892 infants with a congenital anomaly among 2,839,680 live births (41.9 per 1000). While the prevalence of any congenital anomaly declined from 50.7 per 1000 live births in 2002/03 to 41.5 per 1000 in 2012/13, the corresponding PAR% for a congenital anomaly related to pre-pregnancy DM rose from 0.6% (95% confidence interval [CI]: 0.4-0.8) to 1.2% (95% CI: 0.9-1.4). Specifically, the PAR% for congenital cardiovascular defects increased from 2.3% (95% CI: 1.7-2.9) to 4.2% (95% CI: 3.5-4.9) and for gastrointestinal defects from 0.8% (95% CI: 0.2-1.9) to 1.4% (95% CI: 0.7-2.6) over the study period. Although there has been a relative decline in the prevalence of congenital anomalies in Canada, the proportion of congenital anomalies due to maternal pre-pregnancy DM has increased. Enhancement of preconception care initiatives for women with DM is recommended.
Warm Anomaly Effects on California Current Phytoplankton
NASA Astrophysics Data System (ADS)
Gomez Ocampo, E.; Gaxiola-Castro, G.; Beier, E.; Durazo, R.
2016-02-01
Positive temperature anomalies were reported in the NE Pacific Ocean since the boreal winter of 2013-2014. Previous studies showed that these anomalies were caused by lower than normal rates of heat loss from the ocean to the atmosphere and by relatively weak cold water advection to the upper ocean. Anomalous Sea Surface Temperature (SST), Absolute Dynamic Topography (ADT), and Chlorophyll (CHL) obtained from monthly remote sensing data were registered in the California Current region during August 2014. Anomalies appeared around the coastal and oceanic zones, particularly in the onshore zone between Monterey Bay, California and Magdalena Bay, Baja California. High positive SST anomalous values up to 4ºC above the long-term mean, 20 cm in ADT, and less of 4.5 mg m-3 of CHL were registered. Changes of 20 cm in ADT above the average are equivalent to 50 m thermocline deepening considering typical values of stratification for the area, which in turn influenced the availability of nutrients and light for phytoplankton growth in the euphotic zone. To examine the influence of the warm anomaly on phytoplankton production, we fitted with Generalized Additive Models the relationship between monthly primary production satellite data and ADT. Primary production inferred from the model, showed during August 2014 high negative anomalies (up to 0.5 gC m-2 d1) in the coastal zone. The first empirical orthogonal function of ADT and PP revealed that the highest ADT anomalies and the lowest primary production occurred off the Baja California Peninsula, between Punta Eugenia and Cabo San Lucas. Preliminary conclusions showed that warm anomaly affected negatively to phytoplankton organisms during August 2014, being this evident by low biomass and negative primary production anomalies as result of pycnocline deepens.
Detecting Global Hydrological Cycle Intensification in Sea Surface Salinity
NASA Astrophysics Data System (ADS)
Poague, J.; Stine, A.
2016-12-01
Global warming is expected to intensify the global hydrological cycle, but significant regional differences exist in the predicted response. The proposed zonal mean thermodynamic response is enhanced horizontal moisture transport associated with increased saturation vapor pressure, which in turn drives additional net precipitation in the tropics and at high latitudes and additional net evaporation in the subtropics. Sea surface salinity (SSS) anomalies are forced from above by changes in evaporation minus precipitation (E-P) and thus will respond to changes in the global hydrological cycle, opening the possibility of using historical SSS anomalies to diagnose the response of the hydrological cycle to warming. We estimate zonal mean SSS trends in the Atlantic and Pacific ocean basins from 1955-2015 to test whether historical changes in the global hydrological cycle are consistent with a primarily thermodynamic response. Motivated by this observation, we calculate the sensitivity of basin zonal-mean SSS anomalies to sea surface temperature (SST) forcing as a function of timescale to diagnose and estimate the signal-to-noise ratio of the purely thermodynamic signal as a function of timescale. High-frequency variability in SSS anomalies is likely to be influenced by variability in atmospheric circulation, complicating the attribution of the link between basin zonal-mean SSS anomalies and global SST anomalies. We therefore estimate the basin zonal mean SSS anomaly response to the major modes of large-scale dynamic variability. We find a strong correlation between detrended zonal-mean SSS anomalies and the Pacific-North American index (R=0.71,P<0.01) in the Pacific Ocean. We interpret the relationship between zonal mean SSS anomalies and temperature in terms of the relative contribution of thermodynamic and dynamic processes.
NASA Astrophysics Data System (ADS)
Sharma, S. P.; Biswas, A.
2012-12-01
South Purulia Shear Zone (SPSZ) is an important region for prospecting of uranium mineralization. Geological studies and hydro-uranium anomaly suggest the presence of Uranium deposit around Raghunathpur village which lies about 8 km north of SPSZ. However, detailed geophysical investigations have not been carried out in this region for investigation of uranium mineralization. Since surface signature of uranium mineralization is not depicted near the location, a deeper subsurface source is expected for hydro uranium anomaly. To delineate the subsurface structure and to investigate the origin of hydro-uranium anomaly present in the area, Vertical Electrical Sounding (VES) using Schlumberger array and Gradient Resistivity Profiling (GRP) were performed at different locations along a profile perpendicular to the South Purulia Shear Zone. Apparent resistivity computed from the measured sounding data at various locations shows a continuously increasing trend. As a result, conventional apparent resistivity data is not able to detect the possible source of hydro uranium anomaly. An innovative approach is applied which depicts the apparent conductivity in the subsurface revealed a possible connection from SPSZ to Raghunathpur. On the other hand resistivity profiling data suggests a low resistive zone which is also characterized by low Self-Potential (SP) anomaly zone. Since SPSZ is characterized by the source of uranium mineralization; hydro-uranium anomaly at Raghunathpur is connected with the SPSZ. The conducting zone has been delineated from SPSZ to Raghunathpur at deeper depths which could be uranium bearing. Since the location is also characterized by a low gravity and high magnetic anomaly zone, this conducting zone is likely to be mineralized zone. Keywords: Apparent resistivity; apparent conductivity; Self Potential; Uranium mineralization; shear zone; hydro-uranium anomaly.
Arsenic in drinking water and congenital heart anomalies in Hungary.
Rudnai, Tamás; Sándor, János; Kádár, Mihály; Borsányi, Mátyás; Béres, Judit; Métneki, Júlia; Maráczi, Gabriella; Rudnai, Péter
2014-11-01
Inorganic arsenic can get easily through the placenta however there are very few human data on congenital anomalies related to arsenic exposure. Objective of our study was to explore the associations between arsenic content of drinking water and prevalence of some congenital anomalies. Four anomalies reported to the Hungarian Congenital Anomalies Registry between 1987 and 2003 were chosen to be analysed in relation to arsenic exposure: congenital anomalies of the circulatory system (n=9734) were considered as cases, while Down syndrome, club foot and multiple congenital malformations were used as controls (n=5880). Arsenic exposure of the mothers during pregnancy was estimated by using archive measurement data for each year and for each settlement where the mothers lived. Analysis of the associations between the prevalence of congenital heart anomalies and arsenic exposure during pregnancy was performed by logistic regression. The child's gender and age of the mother were adjusted for. The associations were evaluated by using the present EU health limit value of 10.0 μg/L arsenic concentration as a cut-off point. Regular consumption of drinking water with arsenic concentration above 10 μg/L during pregnancy was associated with an increased risk of congenital heart anomalies in general (adjusted OR=1.41; 95% C.I.: 1.28-1.56), and especially that of ductus Botalli persistens (adjusted OR=1.81, 95%C.I.: 1.54-2.11) and atrial septal defect (adjusted OR=1.79; 95%C.I.: 1.59-2.01). The presented results showed an increased risk of congenital heart anomalies among infants whose mothers were exposed to drinking water with arsenic content above 10 μg/L during pregnancy. Further studies of possible similar effects of concentrations below 10 μg/L are warranted. Copyright © 2014 Elsevier GmbH. All rights reserved.
Sheridan, Eamonn; Wright, John; Small, Neil; Corry, Peter C; Oddie, Sam; Whibley, Catherine; Petherick, Emily S; Malik, Teena; Pawson, Nicole; McKinney, Patricia A; Parslow, Roger C
2013-10-19
Congenital anomalies are a leading cause of infant death and disability and their incidence varies between ethnic groups in the UK. Rates of infant death are highest in children of Pakistani origin, and congenital anomalies are the most common cause of death in children younger than 12 in this ethnic group. We investigated the incidence of congenital anomalies in a large multiethnic birth cohort to identify the causes of the excess of congenital anomalies in this community. We obtained questionnaire data from the mothers of children with one or more anomalies from the Born in Bradford study, a prospective birth cohort study of 13,776 babies and their families in which recruitment was undertaken between 2007 and 2011. Details of anomalies were prospectively reported to the study and we cross checked these details against medical records. We linked data for anomalies to maternal questionnaire and clinical data gathered as part of the Born in Bradford study. We calculated univariate and multivariate risk ratios (RRs) with 95% CIs for various maternal risk factors. Of 11,396 babies for whom questionnaire data were available, 386 (3%) had a congenital anomaly. Rates for congenital anomaly were 305·74 per 10,000 livebirths, compared with a national rate of 165·90 per 10,000. The risk was greater for mothers of Pakistani origin than for those of white British origin (univariate RR 1·96, 95% CI 1·56-2·46). Overall, 2013 (18%) babies were the offspring of first-cousin unions. These babies were mainly of Pakistani origin--1922 (37%) of 5127 babies of Pakistani origin had parents in first-cousin unions. Consanguinity was associated with a doubling of risk for congenital anomaly (multivariate RR 2·19, 95% CI 1·67-2·85); we noted no association with increasing deprivation. 31% of all anomalies in children of Pakistani origin could be attributed to consanguinity. We noted a similar increase in risk for mothers of white British origin older than 34 years (multivariate RR 1·83, 95% CI 1·14-3·00). Maternal education to degree level was protective (0·53, 95% CI 0·38-0·75), irrespective of ethnic origin. Consanguinity is a major risk factor for congenital anomaly. The risk remains even after adjustment for deprivation, and accounts for almost a third of anomalies in babies of Pakistani origin. High levels of educational attainment are associated with reduced risk in all ethnic groups. Our findings will be valuable in health promotion and public health, and to those commissioning antenatal, paediatric, and clinical genetic services. Sensitive advice about the risks should be provided to communities at increased risk, and to couples in consanguineous unions, to assist in reproductive decision making. National Institute for Health Research Collaboration for Leadership in Applied Health Research and Care programme. Copyright © 2013 Elsevier Ltd. All rights reserved.
Precursory Anomaly in VLF/LF Recordings Prior to the July 30th, 2009
NASA Astrophysics Data System (ADS)
Buyuksarac, Aydin; Pınar, Ali; Kosaroglu, Sinan
2010-05-01
An international project network consisting of five receivers for sampling LF and VLF radio signals has been going on to record the data in Europe from different transmission stations around the World. One of them was established in Resadiye, Turkey, located just on the North Anatolian Fault Zone. The receiver works in VLF (16.4, 21.75, 37.5 and 45.9 kHz) and LF (153, 180, 183, 216 and 270 kHz) bands monitoring ten frequencies with one minute sampling interval. An earthquake of Mw = 4.9 took place 225 km away from the VLF/LF station at the eastern tip of the Erzincan basin at 4 km depth on July 30, 2009. We observed some anomalies on the radio signals (37.5 and 153 kHz) that initiated about 7 days before the earthquake and disappeared soon after the earthquake. We attribute this anomaly to the Mw=4.9 earthquake as a seismo-electromagnetic precursor. The radio anomaly that appeared 7 days before the occurrence of the 2009 Erzincan earthquake is in good agreement with other results indicating precursory anomalies in the project network mostly observed in seismically active countries such as Italy and Greece. Several data processing stages were applied to the data. Firstly, we processed the time series of the radio signals to understand how the frequency content of the anomaly differs from that of the normal trend. For this purpose we selected two time windows; one covering the anomaly period and the other spanning a normal period. The selected time window length was a 6 day. The sampling interval and the length of the time window limit the observed spectra from 120 seconds to six days. We identified a significant bias (drop) for the signal energy of the anomaly period at the whole frequency band. Secondly, in order to clearly depict the anomaly we estimated the daily Rayleigh Energy of the calculated spectra following the Parseval's theorem. We initiated the estimations well before the anomaly period. Such calculations gave an obvious sign for the impending event. Thirdly, we constructed a spectrogram including the whole frequency band of the data from fortnight before the earthquake to a week after the earthquake. The strongest anomaly in the spectrogram was identified for the periods larger than 60 hours. In earthquake prediction studies it is crucial to understand the source of the anomaly. Since the sources of the anomaly we are interested in are the earthquakes we tried to derive information on the properties of the earthquake that generated our anomaly in the radio signals. Within this frame, we analyzed the broadband data at several local seismic stations that recorded the event and estimated source parameters such as centroid moment tensor, source radius and stress drop. Our analysis shows that the event was a shallow one showing predominantly normal faulting mechanism and was associated with extremely high stress drop with an average value of about 250 bars.
Smith, D.B.; Theobald, P.K.; Shiquan, S.; Tianxiang, R.; Zhihui, H.
1993-01-01
In 1987, a cooperative project between the U.S. Geological Survey and the Institute of Geophysical and Geochemical Exploration was initiated to evaluate the origin of the Hatu gold anomaly. The anomaly is located in the Hatu mining district in the northwest corner of Xinjiang-Uygur Autonomous Region in northwest China. The climate is semiarid to arid and wind erosion predominates. A regional soil survey of the Hatu district, based on samples collected on a 200 by 500 m grid and composited prior to chemical analysis to a density of one sample per square km, delineated a series of south-southeast-trending Au anomalies. Anomalous Au values range from 5 ppb to more than 700 ppb. The Hatu anomaly, the most prominent of these anomalies, is more than 30 km long and about 5 km wide. The mining town of Hatu and the economic gold deposits of Qiqu 1 and Qiqu 2 are at the northern end of this anomaly. The axis of the Hatu anomaly cuts across mapped structure and stratigraphy in the district, but is parallel to the prevailing wind direction. This observation led to the hypothesis that the Hatu anomaly is the result of acolian dispersion of gold from the vicinity of Qiqu 1 and Qiqu 2. The alternative interpretation, that the anomalies reflected additional primary gold occurrences, was not consistent with existing information on the known occurrences and the geology. The investigation led to the identification of three types of gold in heavy-mineral concentrates derived from stream sediments that were collected along the axis of the Hatu anomaly: (1) free gold, (2) gold in pyrite, and (3) gold included in quartz. Gold in quartz was only observed within 2 km of Qiqu 1. The size of the gold particles and the number of gold particles in these samples did not decrease with distance from Qiqu 1 as would be expected from aeolian or fluvial dispersion from a point source. Instead, both the size and amount of gold increased significantly at a distance of 3.5 km from Qiqu 1 and this increase continued to approximately 5.5 km from Qiqu 1. The mean intermediate diameter of gold particles increased from 0.1 mm to approximately 0.25 mm and the gold particle content increased from approximately 0.3 particles per kg of sample to almost 8 particles per kg of sample. The morphology of the gold changed from a delicate filigree texture near Qiqu 1 to coarse, blocky particles in the southern part of the anomaly. The Hatu anomaly is caused primarily by alluvial dispersion of free gold from local point sources along the anomaly. Aeolian dispersion is restricted to very fine-grained (??2 ??m) gold included in sulfide minerals or quartz grains and is significant only within 1-2 km of the known deposits. ?? 1993.
NASA Astrophysics Data System (ADS)
Pampuch, L.; Ambrizzi, T.
2012-12-01
The Southeast region of Brazil comprises the states of Sao Paulo, Minas Gerais, Rio de Janeiro and Espirito Santo. It occupies 10.85% of Brazilian territory and is highly urbanized. The Southeast Brazil is the biggest geoeconomic region of the country having a strong and diverse economy. Agriculture dominates in all states of the region. The main agricultural products are sugar cane, coffee, cotton, maize, cassava, rice, beans and fruits. Livestock farming is also practiced in the region. The largest herd of cattle is found in the state of Minas Gerais. These activities are highly dependent on the amount and distribution of rainfall. Studies of extreme precipitation events over Brazil have been well emphasized in the literature over the years and their relationship with anomalies of sea surface temperature (SST) in both the Pacific and the Atlantic Ocean have been analyzed. This paper investigates the extreme events occurring in southeastern Brazil from 1982 to 2004 using the technique of quantiles. The composite technique was applied to precipitation, sea level pressure anomaly (SLP) and sea surface temperature anomaly (SST) data in order to investigate the characteristics of rainfall patterns, the position and intensity of South Atlantic subtropical high (SASH) and SST anomalies in the Southern Atlantic Ocean (SAO) in the occurrence of these events and to make a distinction between dry and wet extremes. Analyzing the precipitation patterns, it was noticed that the composition of dry events throughout the Southeast Brazil has negative precipitation anomalies. Particularly, in the southern part of the region there is a large precipitation deficit, having an average of 50mm in the winter months. The composition for the wet events shows that, on average, positive precipitation anomalies with the southern region containing the highest cumulative average, reaching a positive anomaly of 100mm. The composition of SLP in the case of dry events indicates a positive anomaly of pressure on SAO close to the South America continent and a negative anomaly far from the continent. This configuration might represent a southwest movement of the SASH. For the wet events composition is possible to note an opposite configuration: an negative anomaly is seen near the South American continent and a positive one is away of it. Such a configuration may represent a weakening of SASH and a shift to northeast part of the SAO. In the composition of the SST anomalies is possible to note a different pattern for both cases with regard to the tropical Pacific, indicating that in dry years an El Niño pattern is evident and during the wet years a La Niña pattern prevails. On the other hand, for the SAO, colder SST anomalies in the dry years was observed next to the coast of South America, and during the rainy years a positive anomaly was observed away from the continent.
Magnetosheath Flow Anomalies in 3-D
NASA Technical Reports Server (NTRS)
Vaisberg, O. L.; Burch, J. L.; Smirnov, V. N.; Avanov, L. A.; Moore, T. E.; Waite, J. H., Jr.; Skalsky, A. A.; Borodkova, N. L.; Coffey, V. N.; Gallagher, D. L.;
2000-01-01
Measurements of the plasma and magnetic field with high temporal resolution on the Interball Tail probe reveal many flow anomalies in the magnetosheath. They are usually seen as flow direction and number density variations, accompanied by magnetic field discontinuities. Large flow anomalies with number density variations of factor of 2 or more and velocity variations of 100 km/s or more are seen with periodicity of about I per hour. The cases of flow anomalies following in succession are also observed, and suggest their decay while propagating through the magnetosheath. Some magnetospheric disturbances observed in the outer magnetosphere after the satellite has crossed the magnetopause on the inbound orbit suggest their association with magnetosheath flow anomalies observed in the magnetosheath prior to magnetopause crossing.
NASA Technical Reports Server (NTRS)
Kis, K. I.; Taylor, Patrick T.; Wittmann, G.; Toronyi, B.; Puszta, S.
2012-01-01
In this study we interpret the magnetic anomalies at satellite altitude over a part of Europe and the Pannonian Basin. These anomalies are derived from the total magnetic measurements from the CHAMP satellite. The anomalies reduced to an elevation of 324 km. An inversion method is used to interpret the total magnetic anomalies over the Pannonian Basin. A three dimensional triangular model is used in the inversion. Two parameter distributions: Laplacian and Gaussian are investigated. The regularized inversion is numerically calculated with the Simplex and Simulated Annealing methods and the anomalous source is located in the upper crust. A probable source of the magnetization is due to the exsolution of the hematite-ilmenite minerals.
Detailed gravity anomalies from GEOS-3 satellite altimetry data
NASA Technical Reports Server (NTRS)
Gopalapillai, G. S.; Mourad, A. G.
1978-01-01
A technique for deriving mean gravity anomalies from dense altimetry data was developed. A combination of both deterministic and statistical techniques was used. The basic mathematical model was based on the Stokes' equation which describes the analytical relationship between mean gravity anomalies and geoid undulations at a point; this undulation is a linear function of the altimetry data at that point. The overdetermined problem resulting from the excessive altimetry data available was solved using Least-Squares principles. These principles enable the simultaneous estimation of the associated standard deviations reflecting the internal consistency based on the accuracy estimates provided for the altimetry data as well as for the terrestrial anomaly data. Several test computations were made of the anomalies and their accuracy estimates using GOES-3 data.
A Distance Measure for Attention Focusing and Anomaly Detection in Systems Monitoring
NASA Technical Reports Server (NTRS)
Doyle, R.
1994-01-01
Any attempt to introduce automation into the monitoring of complex physical systems must start from a robust anomaly detection capability. This task is far from straightforward, for a single definition of what constitutes an anomaly is difficult to come by. In addition, to make the monitoring process efficient, and to avoid the potential for information overload on human operators, attention focusing must also be addressed. When an anomaly occurs, more often than not several sensors are affected, and the partially redundant information they provide can be confusing, particularly in a crisis situation where a response is needed quickly. Previous results on extending traditional anomaly detection techniques are summarized. The focus of this paper is a new technique for attention focusing.
The south-central United States magnetic anomaly
NASA Technical Reports Server (NTRS)
Hinze, W. J.; Braile, L. W. (Principal Investigator); Starich, P. J.
1984-01-01
The South-Central United States Magnetic Anomaly is the most prominent positive feature in the MAGSAT scalar magnetic field over North America. The anomaly correlates with increased crustal thickness, above average crustal velocity, negative free air gravity anomalies and an extensive zone of Middle Proterozoic anorogenic felsic basement rocks. Spherical dipole source inversion of the MAGSAT scalar data and subsequent calculation of reduced to pole and derivative maps provide constraints for a crustal magnetic model which corresponds geographically to the extensive Middle Proterozoic felsic rocks trending northeasterly across the United States. These felsic rocks contain insufficient magnetization or volume to produce the anomaly, but are rather indicative of a crustal zone which was disturbed during a Middle Proterozoic thermal event which enriched magnetic material deep in the crust.
NASA Technical Reports Server (NTRS)
Lazarewicz, A. R.; Sailor, R. V. (Principal Investigator)
1982-01-01
A higher resolution anomaly map of the Broken Ridge area (2 degree dipole spacing) was produced and reduced to the pole using quiet time data for this area. The map was compared with equally scaled maps of gravity anomaly, geoid undulation, and bathymetry. The ESMAP results were compared with a NASA MAGSAT map derived by averaging data in two-degree bins. A survey simulation was developed to model the accuracy of MAGSAT anomaly maps as a function of satellite altitude, instrument noise level, external noise model, and crustal anomaly field model. A preliminary analysis of the geophysical structure of Broken Ridge is presented and unresolved questions are listed.
NASA Technical Reports Server (NTRS)
Rapp, R. H.
1974-01-01
The equations needed for the incorporation of gravity anomalies as unknown parameters in an orbit determination program are described. These equations were implemented in the Geodyn computer program which was used to process optical satellite observations. The arc dependent parameter unknowns, 184 unknown 15 deg and coordinates of 7 tracking stations were considered. Up to 39 arcs (5 to 7 days) involving 10 different satellites, were processed. An anomaly solution from the satellite data and a combination solution with 15 deg terrestrial anomalies were made. The limited data samples indicate that the method works. The 15 deg anomalies from various solutions and the potential coefficients implied by the different solutions are reported.
Subduction-zone magnetic anomalies and implications for hydrated forearc mantle
Blakely, R.J.; Brocher, T.M.; Wells, R.E.
2005-01-01
Continental mantle in subduction zones is hydrated by release of water from the underlying oceanic plate. Magnetite is a significant byproduct of mantle hydration, and forearc mantle, cooled by subduction, should contribute to long-wavelength magnetic anomalies above subduction zones. We test this hypothesis with a quantitative model of the Cascadia convergent margin, based on gravity and aeromagnetic anomalies and constrained by seismic velocities, and find that hydrated mantle explains an important disparity in potential-field anomalies of Cascadia. A comparison with aeromagnetic data, thermal models, and earthquakes of Cascadia, Japan, and southern Alaska suggests that magnetic mantle may be common in forearc settings and thus magnetic anomalies may be useful in mapping hydrated mantle in convergent margins worldwide. ?? 2005 Geological Society of America.
Miller, C.H.; Showail, A.A.; Kane, M.F.; Khoja, I.A.; Al Ghandi, S. A.
1989-01-01
The greatest complete Bouguer anomaly is associated with basaltic lava flows located in the northeastern part of the survey area. The thickness of the basalt in outcrop does not account for the anomalies with the highest amplitudes, but the latter may be due to the presence of a basalt-filled vent. Those anomalies that are present do not define the basalt flows well, but the largest free-air anomaly occurs over the southwestern margin of the Salma Caldera, located about 15 km from the basalt flows. The source of the free-air anomaly is unknown, but it may be related to another hidden basaltic vent.
Comment on "Chiral gauge field and axial anomaly in a Weyl semimetal"
NASA Astrophysics Data System (ADS)
Zhang, Kai; Zhang, Erhu; Zhang, Shengli
2017-12-01
In Liu et al. [Phys. Rev. B 87, 235306 (2013), 10.1103/PhysRevB.87.235306], the authors obtain that the cross coupling between vector gauge field and chiral gauge field can lead to the anomaly of vector current. We demonstrate that this anomaly is not a physical effect. On one hand, it can be regulated out by the proper regulation. On the other hand, it leads to unjustifiable results, the breaking of the vector gauge symmetry and the ambiguous boundary current. Moreover, the effects associated with anomaly of vector current are understood by random phase approximation (RPA) in the paper we comment on. We point out that the RPA cannot describe the effects resulting from the quantum anomaly.
Flavor non-universal gauge interactions and anomalies in B-meson decays
NASA Astrophysics Data System (ADS)
Tang, Yong; Wu, Yue-Liang
2018-02-01
Motivated by flavor non-universality and anomalies in semi-leptonic B-meson decays, we present a general and systematic discussion about how to construct anomaly-free U(1)‧ gauge theories based on an extended standard model with only three right-handed neutrinos. If all standard model fermions are vector-like under this new gauge symmetry, the most general family non-universal charge assignments, (a,b,c) for three-generation quarks and (d,e,f) for leptons, need satisfy just one condition to be anomaly-free, 3(a+b+c) = - (d+e+f). Any assignment can be linear combinations of five independent anomaly-free solutions. We also illustrate how such models can generally lead to flavor-changing interactions and easily resolve the anomalies in B-meson decays. Probes with {{B}}{s} - {{\\bar B}}{s} mixing, decay into τ ±, dilepton and dijet searches at colliders are also discussed. Supported by the Grant-in-Aid for Innovative Areas (16H06490)
NASA Technical Reports Server (NTRS)
Jozwiak, L. M.; Head, J. W., III; Neumann, G. A.; Wilson, L.
2016-01-01
Floor-fractured craters are a class of lunar crater hypothesized to form in response to the emplacement of a shallow magmatic intrusion beneath the crater floor. The emplacement of a shallow magmatic body should result in a positive Bouguer anomaly relative to unaltered complex craters, a signal which is observed for the average Bouguer anomaly interior to the crater walls. We observe the Bouguer anomaly of floor-fractured craters on an individual basis using the unfiltered Bouguer gravity solution from GRAIL and also a degree 100-600 band-filtered Bouguer gravity solution. The low-magnitude of anomalies arising from shallow magmatic intrusions makes identification using unfiltered Bouguer gravity solutions inconclusive. The observed anomalies in the degree 100-600 Bouguer gravity solution are spatially heterogeneous, although there is spatial correlation between volcanic surface morphologies and positive Bouguer anomalies. We interpret these observations to mean that the spatial heterogeneity observed in the Bouguer signal is the result of variable degrees of magmatic degassing within the intrusions.
Gravity anomaly and geoid undulation results in local areas from GEOS-3 altimeter data
NASA Technical Reports Server (NTRS)
Rapp, R. H.
1979-01-01
The adjusted GEOS-3 altimeter data, taken as averages within a data frame, have been used to construct free air anomaly and geoid undulation profiles and maps in areas of geophysical interest. Profiles were constructed across the Philippine Trench (at a latitude of 6 deg) and across the Bonin Trench (at a latitude of 28 deg). In the latter case an anomaly variation of 443 mgals in 143 km was derived from the altimeter data. These variations agreed reasonably with terrestrial estimates, considering the predicted point accuracy was about + or - 27 mgals. An area over the Patton Sea mounts was also investigated with the altimeter anomaly field agreeing well with the terrestrial data except for the point directly over the top of the sea mount. It is concluded that the GEOS-3 altimeter data is valuable not only for determining 5 deg and 1 deg x 1 deg mean anomalies, but also can be used to describe more local anomaly variations.
Delineation of The Sumatra Fault in The Central Part of West Sumatra based on Gravity Method
NASA Astrophysics Data System (ADS)
Saragih, R. D.; Brotopuspito, K. S.
2018-04-01
The Sumatra Fault System is elongated across the Sumatra Island, Indonesia, Southeast Asia including the central part of West Sumatra, Indonesia, Southeast Asia. The Sumatra Fault and subsurface structure on the Central Part of West Sumatra had been analyzed using gravity method. Bouguer anomaly data were obtained from GRDC (Geological Research and Development Centre) maps, Bandung, Indonesia (i.e. without terrain correction). In this study, terrain correction had been applied to these Bouguer data. Bouguer anomaly in a horizontal plane at 3000 meters high and equivalent depth of mass point 7000 meters were obtained using Dampney Method. Residual and regional anomalies were separated using upward continuation method at 8000 meters high. The result of the SVD on residual anomaly shows two negative anomalies on northwest – southeast. The zero miligal per meter square quantity coincides remarkably well with trace faults which is a part of the Sumatra Fault System. Two negative anomalies are located around the Sianok Segment and Sumani Segment.
The computation of 15 deg and 10 deg equal area block terrestrial free air gravity anomalies
NASA Technical Reports Server (NTRS)
Hajela, D. P.
1973-01-01
Starting with the set of 23,355 1 deg x 1 deg mean free air gravity anomalies used in Rapp (1972) to form a 5 deg equal area block terrestrial gravity field, the computation of 15 deg equal area block mean free air gravity anomalies is described along with estimates of their standard deviations. A new scheme of an integral division of a 15 deg block into 9 component 300 n. m. blocks, and each 300 n. m. block being subdivided into 25 60 n.mi. blocks, is used. This insures that there is no loss in accuracy, which would have resulted if proportional values according to area were taken of the 5 deg equal area anomalies to form the 15 deg block anomalies. A similar scheme is used for the computation of 10 deg equal area block mean free air gravity anomalies with estimates of their standard deviations. The scheme is general enough to be used for a 30 deg equal area block terrestrial gravity field.
Chahoud, I; Talsness, C E; Walter, A; Grote, K
2015-12-01
Classification of substances as teratogenic is based on the observation of external, visceral and skeletal anomalies. Characterization of anomalies as variation or malformation is contingent upon their postnatal persistence and adversity to health. Lack of information thereof may result in inconsistent or incorrect classification. The aim of this work is the examination of vertebral skeletal anomalies regarding their postnatal fate on PNDs 7 and 21. The anomalies unossified, asymmetric ossification, bipartite ossification, hemicentric, as well as misshapen, did not persist up to PND21 and should be classified as a variation. The finding, cervical vertebra centrum dumbbell-shaped, should be categorized as a malformation due to its continued presence on PND 21. Lumbar centrum supernumerary sinister/dexter/sinister+dexter should also be classified as a malformation. This study demonstrates that postnatal examination is useful and substantially improves the ability to perform a scientifically sound classification of an anomaly compared to investigations terminated on GD 21. Copyright © 2015 Elsevier Inc. All rights reserved.
A variant of the anomaly initialisation approach for global climate forecast models
NASA Astrophysics Data System (ADS)
Volpi, Danila; Guemas, Virginie; Doblas-Reyes, Francisco; Hawkins, Ed; Nichols, Nancy; Carrassi, Alberto
2014-05-01
This work presents a refined method of anomaly initialisation (AI) applied to the ocean and sea ice components of the global climate forecast model EC-Earth, with the following particularities: - the use of a weight to the anomalies, in order to avoid the risk of introducing too big anomalies recorded in the observed state, whose amplitude does not fit the range of the internal variability generated by the model. - the AI of the temperature and density ocean state variables instead of the temperature and salinity. Results show that the use of such refinements improve the skill over the Arctic region, part of the North and South Atlantic, part of the North and South Pacific and the Mediterranean Sea. In the Tropical Pacific the full field initialised experiment performs better. This is probably due to a displacement of the observed anomalies caused by the use of the AI technique. Furthermore, preliminary results of an anomaly nudging experiment are discussed.
NASA Astrophysics Data System (ADS)
Higuchi, Saki; Kato, Daiki; Awaji, Daisuke; Kim, Kang
2018-03-01
We present a study using molecular dynamics simulations based on the Fermi-Jagla potential model, which is the continuous version of the mono-atomic core-softened Jagla model [J. Y. Abraham, S. V. Buldyrev, and N. Giovambattista, J. Phys. Chem. B 115, 14229 (2011)]. This model shows the water-like liquid-liquid phase transition between high-density and low-density liquids at the liquid-liquid critical point. In particular, the slope of the coexistence line becomes weakly negative, which is expected to represent one of the anomalies of liquid polyamorphism. In this study, we examined the density, dynamic, and thermodynamic anomalies in the vicinity of the liquid-liquid critical point. The boundaries of density, self-diffusion, shear viscosity, and excess entropy anomalies were characterized. Furthermore, these anomalies are connected according to Rosenfeld's scaling relationship between the excess entropy and the transport coefficients such as diffusion and viscosity. The results demonstrate the hierarchical and nested structures regarding the thermodynamic and dynamic anomalies of the Fermi-Jagla model.
Contribution of Temperature and Precipitation Anomalies to the Ongoing California Drought
NASA Astrophysics Data System (ADS)
Luo, L.; Apps, D.; Arcand, S. E.
2015-12-01
The ongoing multiyear drought over California is a major concern for the residents of the golden state as it brings water restrictions in preparing for water shortages and wild fires due to dry and hot conditions. Both positive temperature and negative precipitation anomalies can contribute to drought developments, but how important are these anomalies for the ongoing California drought? Using the VIC hydrological model, this study investigated the relative contribution of temperature and precipitation anomalies to the ongoing 2011-2015 drought in comparison with another multiyear drought between 1987 and 1992 over the same region. By swapping the observed temperature and precipitation anomalies between two drought events, the study was able to show how temperature and precipitation anomalies and their spatial variability affect other elements of the hydrological cycle including evapotranspiration, soil moisture and streamflow, thus the severity of the drought. The comparison between these two events helps to reveal the unique characteristics of the current drought and provides useful insights for drought prediction and mitigation.
Yang, Yang; Wu, Fuyun; Zhou, Xiaolin
2015-01-01
The syntax-first model and the parallel/interactive models make different predictions regarding whether syntactic category processing has a temporal and functional primacy over semantic processing. To further resolve this issue, an event-related potential experiment was conducted on 24 Chinese speakers reading Chinese passive sentences with the passive marker BEI (NP1 + BEI + NP2 + Verb). This construction was selected because it is the most-commonly used Chinese passive and very much resembles German passives, upon which the syntax-first hypothesis was primarily based. We manipulated semantic consistency (consistent vs. inconsistent) and syntactic category (noun vs. verb) of the critical verb, yielding four conditions: CORRECT (correct sentences), SEMANTIC (semantic anomaly), SYNTACTIC (syntactic category anomaly), and COMBINED (combined anomalies). Results showed both N400 and P600 effects for sentences with semantic anomaly, with syntactic category anomaly, or with combined anomalies. Converging with recent findings of Chinese ERP studies on various constructions, our study provides further evidence that syntactic category processing does not precede semantic processing in reading Chinese.
A Survey on Anomaly Based Host Intrusion Detection System
NASA Astrophysics Data System (ADS)
Jose, Shijoe; Malathi, D.; Reddy, Bharath; Jayaseeli, Dorathi
2018-04-01
An intrusion detection system (IDS) is hardware, software or a combination of two, for monitoring network or system activities to detect malicious signs. In computer security, designing a robust intrusion detection system is one of the most fundamental and important problems. The primary function of system is detecting intrusion and gives alerts when user tries to intrusion on timely manner. In these techniques when IDS find out intrusion it will send alert massage to the system administrator. Anomaly detection is an important problem that has been researched within diverse research areas and application domains. This survey tries to provide a structured and comprehensive overview of the research on anomaly detection. From the existing anomaly detection techniques, each technique has relative strengths and weaknesses. The current state of the experiment practice in the field of anomaly-based intrusion detection is reviewed and survey recent studies in this. This survey provides a study of existing anomaly detection techniques, and how the techniques used in one area can be applied in another application domain.
Coronary artery anomalies overview: The normal and the abnormal
Villa, Adriana DM; Sammut, Eva; Nair, Arjun; Rajani, Ronak; Bonamini, Rodolfo; Chiribiri, Amedeo
2016-01-01
The aim of this review is to give a comprehensive and concise overview of coronary embryology and normal coronary anatomy, describe common variants of normal and summarize typical patterns of anomalous coronary artery anatomy. Extensive iconography supports the text, with particular attention to images obtained in vivo using non-invasive imaging. We have divided this article into three groups, according to their frequency in the general population: Normal, normal variant and anomaly. Although congenital coronary artery anomalies are relatively uncommon, they are the second most common cause of sudden cardiac death among young athletes and therefore warrant detailed review. Based on the functional relevance of each abnormality, coronary artery anomalies can be classified as anomalies with obligatory ischemia, without ischemia or with exceptional ischemia. The clinical symptoms may include chest pain, dyspnea, palpitations, syncope, cardiomyopathy, arrhythmia, myocardial infarction and sudden cardiac death. Moreover, it is important to also identify variants and anomalies without clinical relevance in their own right as complications during surgery or angioplasty can occur. PMID:27358682
NASA Astrophysics Data System (ADS)
Mansouri, E.; Feizi, F.; Karbalaei Ramezanali, A. A.
2015-10-01
Ground magnetic anomaly separation using the reduction-to-the-pole (RTP) technique and the fractal concentration-area (C-A) method has been applied to the Qoja-Kandi prospecting area in northwestern Iran. The geophysical survey resulting in the ground magnetic data was conducted for magnetic element exploration. Firstly, the RTP technique was applied to recognize underground magnetic anomalies. RTP anomalies were classified into different populations based on the current method. For this reason, drilling point area determination by the RTP technique was complicated for magnetic anomalies, which are in the center and north of the studied area. Next, the C-A method was applied to the RTP magnetic anomalies (RTP-MA) to demonstrate magnetic susceptibility concentrations. This identification was appropriate for increasing the resolution of the drilling point area determination and decreasing the drilling risk issue, due to the economic costs of underground prospecting. In this study, the results of C-A modelling on the RTP-MA are compared with 8 borehole data. The results show that there is a good correlation between anomalies derived via the C-A method and the log report of boreholes. Two boreholes were drilled in magnetic susceptibility concentrations, based on multifractal modelling data analyses, between 63 533.1 and 66 296 nT. Drilling results showed appropriate magnetite thickness with grades greater than 20 % Fe. The total associated with anomalies containing andesite units hosts iron mineralization.
New standards for reducing gravity data: The North American gravity database
Hinze, W. J.; Aiken, C.; Brozena, J.; Coakley, B.; Dater, D.; Flanagan, G.; Forsberg, R.; Hildenbrand, T.; Keller, Gordon R.; Kellogg, J.; Kucks, R.; Li, X.; Mainville, A.; Morin, R.; Pilkington, M.; Plouff, D.; Ravat, D.; Roman, D.; Urrutia-Fucugauchi, J.; Veronneau, M.; Webring, M.; Winester, D.
2005-01-01
The North American gravity database as well as databases from Canada, Mexico, and the United States are being revised to improve their coverage, versatility, and accuracy. An important part of this effort is revising procedures for calculating gravity anomalies, taking into account our enhanced computational power, improved terrain databases and datums, and increased interest in more accurately defining long-wavelength anomaly components. Users of the databases may note minor differences between previous and revised database values as a result of these procedures. Generally, the differences do not impact the interpretation of local anomalies but do improve regional anomaly studies. The most striking revision is the use of the internationally accepted terrestrial ellipsoid for the height datum of gravity stations rather than the conventionally used geoid or sea level. Principal facts of gravity observations and anomalies based on both revised and previous procedures together with germane metadata will be available on an interactive Web-based data system as well as from national agencies and data centers. The use of the revised procedures is encouraged for gravity data reduction because of the widespread use of the global positioning system in gravity fieldwork and the need for increased accuracy and precision of anomalies and consistency with North American and national databases. Anomalies based on the revised standards should be preceded by the adjective "ellipsoidal" to differentiate anomalies calculated using heights with respect to the ellipsoid from those based on conventional elevations referenced to the geoid. ?? 2005 Society of Exploration Geophysicists. All rights reserved.
Visual analytics of anomaly detection in large data streams
NASA Astrophysics Data System (ADS)
Hao, Ming C.; Dayal, Umeshwar; Keim, Daniel A.; Sharma, Ratnesh K.; Mehta, Abhay
2009-01-01
Most data streams usually are multi-dimensional, high-speed, and contain massive volumes of continuous information. They are seen in daily applications, such as telephone calls, retail sales, data center performance, and oil production operations. Many analysts want insight into the behavior of this data. They want to catch the exceptions in flight to reveal the causes of the anomalies and to take immediate action. To guide the user in finding the anomalies in the large data stream quickly, we derive a new automated neighborhood threshold marking technique, called AnomalyMarker. This technique is built on cell-based data streams and user-defined thresholds. We extend the scope of the data points around the threshold to include the surrounding areas. The idea is to define a focus area (marked area) which enables users to (1) visually group the interesting data points related to the anomalies (i.e., problems that occur persistently or occasionally) for observing their behavior; (2) discover the factors related to the anomaly by visualizing the correlations between the problem attribute with the attributes of the nearby data items from the entire multi-dimensional data stream. Mining results are quickly presented in graphical representations (i.e., tooltip) for the user to zoom into the problem regions. Different algorithms are introduced which try to optimize the size and extent of the anomaly markers. We have successfully applied this technique to detect data stream anomalies in large real-world enterprise server performance and data center energy management.
Coronary Artery Anomalies in Animals
Scansen, Brian A.
2017-01-01
Coronary artery anomalies represent a disease spectrum from incidental to life-threatening. Anomalies of coronary artery origin and course are well-recognized in human medicine, but have received limited attention in veterinary medicine. Coronary artery anomalies are best described in the dog, hamster, and cow though reports also exist in the horse and pig. The most well-known anomaly in veterinary medicine is anomalous coronary artery origin with a prepulmonary course in dogs, which limits treatment of pulmonary valve stenosis. A categorization scheme for coronary artery anomalies in animals is suggested, dividing these anomalies into those of major or minor clinical significance. A review of coronary artery development, anatomy, and reported anomalies in domesticated species is provided and four novel canine examples of anomalous coronary artery origin are described: an English bulldog with single left coronary ostium and a retroaortic right coronary artery; an English bulldog with single right coronary ostium and transseptal left coronary artery; an English bulldog with single right coronary ostium and absent left coronary artery with a prepulmonary paraconal interventricular branch and an interarterial circumflex branch; and a mixed-breed dog with tetralogy of Fallot and anomalous origin of all coronary branches from the brachiocephalic trunk. Coronary arterial fistulae are also described including a coronary cameral fistula in a llama cria and an English bulldog with coronary artery aneurysm and anomalous shunting vessels from the right coronary artery to the pulmonary trunk. These examples are provided with the intent to raise awareness and improve understanding of such defects. PMID:29056679
Effect of Varying Crustal Thickness on CHAMP Geopotential Data
NASA Technical Reports Server (NTRS)
Taylor, Patrick T.; Kis, Karoly I.; vonFrese, Ralph R. B.; Korhonen, Juha V.; Wittmann, Geza; Kim, Hyung Rae; Potts, Larmie V.
2003-01-01
Tn determine the effect of crustal thickness variation on satellite-altitude geopotential anomalies we compared two regions of Europe with vastly different values, South and Central Finland and the Pannonian Basin. In our study regions, crustal thickness exceeds 44 km in Finland and is less than 26 km in the Pannonian Basin. Heat-flow data indicate that the thinner and more active crust of the Pannonian Basin has a value nearly three times that of the Finnish Svecofennian Province. An ovoid positive CHAMP gravity anomaly (-4 mGal) is quasi-coincidental with the CHAMP magnetic anomaly traverses the Pannonian Basin while ground based gravity mapping in Hungary shows that the free-air gravity anomalies across the Pannonian Basin are near 0 to +20 mGal with shorter wavelength anomalies from +40 to less than +60 mGal and some 0 to greater than -20 mGal. Larger anomalies are detected in the mountainous areas. The minor value anomalies can indicate the isostatic equilibrium for Hungary (the central part of the Pannonian Basin). Gravity data over Finland bear overprint of de-glaciation. CHAMP gravity data indicates a west-east positive gradient of less than 4 mGal across South and Central Finland. CHAMP magnetic data (400 km) reveal elongated semi-circular negative anomalies for both regions with South-Central Finland having larger amplitude (less than -6 nT) than that over the Pannonian Basin, Hungary (less than -5 nT). In the latter subducted oceanic lithosphere has been proposed as the anomalous body.
Effect of Varying Crustal Thickness on CHAMP Geopotential Data
NASA Technical Reports Server (NTRS)
Taylor, P. T.; Kis, K. I.; vonFrese, R. R. B.; Korhonen, J. V.; Wittmann, G.; Kim, H. R.; Potts, L. V.
2003-01-01
To determine the effect of crustal thickness variation on satellite-altitude geopotential anomalies we compared two regions of Europe with vastly different values, Central/Southern Finland and the Pannonian Basin. Crustal thickness exceeds 62 km in Finland and is less than 26 km in the Pannonian Basin. Heat-flow maps indicate that the thinner and more active crust of the Pannonian Basin has a value nearly three times that of the Finnish Svecofennian Province. Ground based gravity mapping in Hungary shows that the free-air gravity anomalies across the Pannonian Basin are near 0 to +20 mGal with shorter wavelength anomalies from +40 to less than +60 mGal and some 0 to greater than -20 mGal. Larger anomalies are detected in the mountainous areas. The minor value anomalies can indicate the isostatic equilibrium for Hungary (the central part of the Pannonian Basin). Gravity data over Finland are complicated by de-glaciation. CHAMP gravity data (400 km) indicates a west-east positive gradient of greater than 4 mGal across Central/Southern Finland and an ovoid positive anomaly (approximately 4 mGal) quasi-coincidental with the magnetic anomaly traversing the Pannonian Basin. CHAMP magnetic data (425 km) reveal elongated semicircular negative anomalies for both regions with South-Central Finland having larger amplitude (less than -6 nT) than that over the Pannonian Basin, Hungary (less than -5 nT). In both regions subducted oceanic lithosphere has been proposed as the anomalous body.
Kouame, Bertin Dibi; N'guetta-Brou, Isabelle Ama; Kouame, Guy Serge Yapo; Sounkere, Moufidath; Koffi, Maxime; Yaokreh, Jean Baptiste; Odehouri-Koudou, Thierry; Tembely, Samba; Dieth, Gaudens Atafi; Ouattara, Ossenou; Dick, Ruffin
2015-01-01
Congenital abnormalities constitute one of the major causes of infant mortality, particularly in developing countries. The aim of this study was to describe the epidemiology of congenital anomalies in Cote d'Ivoire. It was a multicentric study of three academic hospitals and the Heart Institute of Abidjan over 10 years. The epidemiologic Data concerned the Parturients, the annual frequency of congenital abnormalities. Distribution of the congenital abnormalities according to the organs, overall mortality and lethality of congenital abnormalities were evaluated. Over 10 years, 1.632 newborns with 1.725 congenital anomalies were recorded. Frequency was 172.5 congenital anomalies per annum. Parturients were less than 35 years in 33% of cases, multigravida in 20%, multiparous in 18% and had a low socio economic status in 96% of cases. Prenatal diagnosis of congenital anomalies was performed in 1.5%. Congenital anomalies were orthopedic in 34%, neurological in 17%, gastrointestinal in 15%, facial in 11.5%, parietal in 13%, urogenital in 9% and cardiac in 0.5% of cases. The overall mortality rate of congenital anomalies was 52% and gastroschisis was the most lethal disease with 100% mortality. This descriptive study reveals the low socio economic status of Parturients with congenital anomalies and their poor prenatal diagnosis. These factors explain the very high mortality of congenital anomalies due to a delay management in our country in which medical expenses were borne by parents and where technical platforms remain obsoletes for good resuscitation and neonatal surgery.
Assessment of survey radiography as a method for diagnosis of congenital cardiac disease in dogs.
Lamb, C R; Boswood, A; Volkman, A; Connolly, D J
2001-11-01
In order to assess the diagnostic accuracy of survey radiography for canine congenital cardiac anomalies, thoracic radiographs of 57 dogs with congenital cardiac anomalies, 31 normal dogs and 27 dogs with acquired cardiac disease were mixed, and reviewed by two independent observers, who were blinded to any patient information. The congenital anomalies were aortic stenosis (n=25), pulmonic stenosis (n=10), patent ductus arteriosus (n=9), ventricular septal defect (n=8), tricuspid dysplasia (n=3) and mitral dysplasia (n=2). Both observers were moderately accurate at identifying dogs with cardiac disease. Their ability to distinguish dogs with congenital versus acquired cardiac disease was poorer and this assessment was probably influenced by the recognition of patients that were skeletally immature, which biased observers towards a diagnosis of congenital cardiac anomaly. The diagnosis rate for specific congenital anomalies was also poor (the differential list included a correct diagnosis in only 40 and 37 per cent of cases). Radiographic signs of specific cardiac chamber enlargement or pulmonary vascular abnormalities were recognised by both observers in only 20 per cent of instances in which they might be expected. They were, however, recognised more frequently in dogs with anomalies that imposed a volume load on the heart than in dogs with anomalies that induced a pressure load on the organ. It is concluded that survey radiography is an inaccurate method for diagnosis of canine congenital cardiac anomalies because of the difficulty of recognising radiographic signs, which are not present in many cases.
Maugans, Todd; Sheridan, Rachel M; Adams, Denise; Gupta, Anita
2011-07-01
Lumbosacral cutaneous vascular anomalies associated with neural tube defects are frequently described in the literature as "hemangiomas." The classification system for pediatric vascular anomalies developed by the International Society for the Study of Vascular Anomalies provides a framework to accurately diagnose these lesions. To apply this classification to vascular cutaneous anomalies overlying myelodysplasias. A retrospective analysis of patients with neural tube defects and lumbosacral cutaneous vascular lesions was performed. All eligible patients had detailed histopathologic analysis of skin and spinal cord/placode lesions. Clinical and radiologic features were analyzed. Conventional histology and GLUT-1 immunostaining were performed to differentiate infantile capillary hemangiomas from capillary vascular malformations. Ten cases with cutaneous lesions associated with neural tube defects were reviewed. Five lesions were diagnosed as infantile capillary hemangiomas based upon histology and positive GLUT-1 endothelial reactivity. These lesions had a strong association with dermal sinus tracts. No reoperations were required for residual intraspinal vascular lesions, and overlying cutaneous vascular anomalies involuted with time. The remaining 5 lesions were diagnosed as capillary malformations. These occurred with both open and closed neural tube defects, did not involute, and demonstrated enlargement and darkening due to vascular congestion. The International Society for the Study of Vascular Anomalies scheme should be used to describe the cutaneous vascular lesions associated with neural tube defects: infantile capillary hemangiomas and capillary malformations. We advocate that these lesions be described as "vascular anomalies" or "stains" pending accurate diagnosis by clinical, histological, and immunohistochemical evaluations.
Altered Orientation and Flight Paths of Pigeons Reared on Gravity Anomalies: A GPS Tracking Study
Blaser, Nicole; Guskov, Sergei I.; Meskenaite, Virginia; Kanevskyi, Valerii A.; Lipp, Hans-Peter
2013-01-01
The mechanisms of pigeon homing are still not understood, in particular how they determine their position at unfamiliar locations. The “gravity vector” theory holds that pigeons memorize the gravity vector at their home loft and deduct home direction and distance from the angular difference between memorized and actual gravity vector. However, the gravity vector is tilted by different densities in the earth crust leading to gravity anomalies. We predicted that pigeons reared on different gravity anomalies would show different initial orientation and also show changes in their flight path when crossing a gravity anomaly. We reared one group of pigeons in a strong gravity anomaly with a north-to-south gravity gradient, and the other group of pigeons in a normal area but on a spot with a strong local anomaly with a west-to-east gravity gradient. After training over shorter distances, pigeons were released from a gravitationally and geomagnetically normal site 50 km north in the same direction for both home lofts. As expected by the theory, the two groups of pigeons showed divergent initial orientation. In addition, some of the GPS-tracked pigeons also showed changes in their flight paths when crossing gravity anomalies. We conclude that even small local gravity anomalies at the birth place of pigeons may have the potential to bias the map sense of pigeons, while reactivity to gravity gradients during flight was variable and appeared to depend on individual navigational strategies and frequency of position updates. PMID:24194860
Anomaly detection in hyperspectral imagery: statistics vs. graph-based algorithms
NASA Astrophysics Data System (ADS)
Berkson, Emily E.; Messinger, David W.
2016-05-01
Anomaly detection (AD) algorithms are frequently applied to hyperspectral imagery, but different algorithms produce different outlier results depending on the image scene content and the assumed background model. This work provides the first comparison of anomaly score distributions between common statistics-based anomaly detection algorithms (RX and subspace-RX) and the graph-based Topological Anomaly Detector (TAD). Anomaly scores in statistical AD algorithms should theoretically approximate a chi-squared distribution; however, this is rarely the case with real hyperspectral imagery. The expected distribution of scores found with graph-based methods remains unclear. We also look for general trends in algorithm performance with varied scene content. Three separate scenes were extracted from the hyperspectral MegaScene image taken over downtown Rochester, NY with the VIS-NIR-SWIR ProSpecTIR instrument. In order of most to least cluttered, we study an urban, suburban, and rural scene. The three AD algorithms were applied to each scene, and the distributions of the most anomalous 5% of pixels were compared. We find that subspace-RX performs better than RX, because the data becomes more normal when the highest variance principal components are removed. We also see that compared to statistical detectors, anomalies detected by TAD are easier to separate from the background. Due to their different underlying assumptions, the statistical and graph-based algorithms highlighted different anomalies within the urban scene. These results will lead to a deeper understanding of these algorithms and their applicability across different types of imagery.
Role of Longwave Cloud-Radiation Feedback in the Simulation of the Madden-Julian Oscillation
NASA Technical Reports Server (NTRS)
Kim, Daehyun; Ahn, Min-Seop; Kang, In-Sik; Del Genio, Anthony D.
2015-01-01
The role of the cloud-radiation interaction in the simulation of the Madden-Julian oscillation (MJO) is investigated. A special focus is on the enhancement of column-integrated diabatic heating due to the greenhouse effects of clouds and moisture in the region of anomalous convection. The degree of this enhancement, the greenhouse enhancement factor (GEF), is measured at different precipitation anomaly regimes as the negative ratio of anomalous outgoing longwave radiation to anomalous precipitation. Observations show that the GEF varies significantly with precipitation anomaly and with the MJO cycle. The greenhouse enhancement is greater in weak precipitation anomaly regimes and its effectiveness decreases monotonically with increasing precipitation anomaly. The GEF also amplifies locally when convection is strengthened in association with the MJO, especially in the weak precipitation anomaly regime (less than 5 mm day(exp -1)). A robust statistical relationship is found among CMIP5 climate model simulations between the GEF and the MJO simulation fidelity. Models that simulate a stronger MJO also simulate a greater GEF, especially in the weak precipitation anomaly regime (less than 5 mm day(exp -1)). Models with a greater GEF in the strong precipitation anomaly regime (greater than 30 mm day(-1)) represent a slightly slower MJO propagation speed. Many models that lack the MJO underestimate the GEF in general and in particular in the weak precipitation anomaly regime. The results herein highlight that the cloud-radiation interaction is a crucial process for climate models to correctly represent the MJO.
Altered orientation and flight paths of pigeons reared on gravity anomalies: a GPS tracking study.
Blaser, Nicole; Guskov, Sergei I; Meskenaite, Virginia; Kanevskyi, Valerii A; Lipp, Hans-Peter
2013-01-01
The mechanisms of pigeon homing are still not understood, in particular how they determine their position at unfamiliar locations. The "gravity vector" theory holds that pigeons memorize the gravity vector at their home loft and deduct home direction and distance from the angular difference between memorized and actual gravity vector. However, the gravity vector is tilted by different densities in the earth crust leading to gravity anomalies. We predicted that pigeons reared on different gravity anomalies would show different initial orientation and also show changes in their flight path when crossing a gravity anomaly. We reared one group of pigeons in a strong gravity anomaly with a north-to-south gravity gradient, and the other group of pigeons in a normal area but on a spot with a strong local anomaly with a west-to-east gravity gradient. After training over shorter distances, pigeons were released from a gravitationally and geomagnetically normal site 50 km north in the same direction for both home lofts. As expected by the theory, the two groups of pigeons showed divergent initial orientation. In addition, some of the GPS-tracked pigeons also showed changes in their flight paths when crossing gravity anomalies. We conclude that even small local gravity anomalies at the birth place of pigeons may have the potential to bias the map sense of pigeons, while reactivity to gravity gradients during flight was variable and appeared to depend on individual navigational strategies and frequency of position updates.
Šípek, A; Gregor, V; Horáček, J; Šípek, A; Klaschka, J; Malý, M
2015-03-01
Analysis of the prevalence of selected congenital anomalies in the Czech Republic in 1994-2009. Retrospective epidemiological analysis of the postnatal and overall (including prenatally diagnosed cases) prevalence of congenital anomalies from the database of the National Registry of Congenital Anomalies of the Czech Republic. Data from the National Registry of Congenital Anomalies (NRCA) maintained by the Institute of Health Information and Statistics of the Czech Republic (IHIS CR) were used. The analysis was carried out for the entire Czech Republic, based on the data from 1994 to 2009. Additional data on prenatally diagnosed anomalies were obtained from medical genetics centres and laboratories in the Czech Republic. This study analyzed the postnatal and overall (including prenatally diagnosed cases) prevalence of congenital anomalies. More detailed analysis was carried out for the following diagnoses: anencephaly, spina bifida, encephalocoele, congenital hydrocephalus, omphalocoele, gastroschisis, oesophageal atresia and stenosis, anorectal anomalies, and diaphragmatic hernia. Prevalence trends were analysed using Poisson regression. In 2009, a total of 118 348 live births were recorded in the Czech Republic, 60 368 boys and 57 980 girls. Of this total, 4 653, i.e. 2 745 boys and 1 908 girls, were diagnosed with congenital anomalies. In 2007-2009, the total of life births with congenital anomalies ranged between 4.6 and 4.8 thousand per year. The respective ranges in this three-year period were in the order of 2.7 and 2.8 thousand per year for boys and 1.9 thousand per year for girls. The prevalence of postnatally diagnosed anencephaly was minimal, as most cases were diagnosed prenatally, and the data did not vary significantly. The prevalence of postnatally diagnosed cases remained at the same level. The effectiveness of the prenatal diagnosis of spina bifida increased and thus the prevalence of postnatally diagnosed cases decreased. The prevalence of prenatally diagnosed encephalocoele increased and that of postnatally diagnosed cases varied between years, with no clear trend. The prevalence of omphalocoele varied for both prenatally and postnatally diagnosed cases; nevertheless, the effectiveness of prenatal diagnosis of this defect increases. The prevalence of gastroschisis remained unchanged, but the number of live births with this diagnosis showed a non-significant upward trend. If the trend reflects the real situation, it could be a result of a changed approach to prenatal diagnosis due to advances in corrective surgery of this defect. The prevalence of live births with congenital hydrocephalus showed a downward trend in the second half of the period 1994-2009 thanks to the improved diagnosis. The prevalence rates of live births with congenital esophageal and anorectal anomalies were slightly increasing. The prevalence of congenital diaphragmatic hernia varied between years but the overall prevalence appeared to be slightly increasing. The prevalence of some congenital anomalies (spina bifida, omphalocoele, and congenital hydrocephalus) showed a downward trend over the study period 1994-2009, mainly as a result of effective prenatal diagnosis. The prevalence of other congenital anomalies such as anencephaly or encephalocoele remained unchanged in live births. As for anencephaly, postnatally diagnosed cases were rare as the prenatal diagnosis was close to 100 %. The trend in encephalocoele is explained by the low incidence of this diagnosis in the population. The third group of postnatally diagnosed congenital anomalies such as gastroschisis or esophageal and anorectal anomalies were on the rise. As for gastroschisis, the reason was the changed approach to prenatal diagnosis due to good prognosis of this operable defect. The prevalence of congenital esophageal and anorectal anomalies varied between years, with a slowly increasing trend, similarly to diaphragmatic hernia.
NASA Astrophysics Data System (ADS)
Buchbinder, I. L.; Mistchuk, B. R.; Pershin, V. D.
1995-02-01
A general BRST-BFV analysis of the anomaly in string theory coupled to background fields is carried out. An exact equation for the c-valued symbol of the anomaly operator is found and the structure of its solution is studied.
World Digital Magnetic Anomaly Map, development towards the Second Edition. (Invited)
NASA Astrophysics Data System (ADS)
Korhonen, J. V.
2009-12-01
Magnetic anomalies are small deviations in the Earth’s main magnetic field, caused by variation of magnetization in the uppermost lithosphere. Magnetic anomalies provide spatial key information for understanding the structure and evolution of the Earths crust. In practice these anomalies are used e.g. for assessment and prospecting of geological natural resources and planning of land use. A common way to calculate a magnetic anomaly value has been to subtract International Geomagnetic Reference Field (IGRF) from a total field measurement that is cleaned from short term variation of the Earth's magnetic field. World Digital Magnetic Anomaly Map (WDMAM) is a collaborative project between member organizations of International Association of Geomagnetism and Aeronomy (IAGA) and the Commission for Geological Map of the World (CGMW). The First Edition of the map was published in 2007. It consisted of a paper map 1:50 Million and a 3 minutes global grid of total field anomalies at an altitude of 5 km above the geoid. The First Edition was aimed to compile as much as possible available land and sea magnetic data, and homogenize it by comparing anomalies with a satellite magnetic lithospheric field model. This first version was prepared in a tight schedule, to show the usefulness of the map to the community and to form a basis for later development and future editions of the map. Hence, much was left to be improved for the second edition, including sparse coverage in two continents and all southern seas. The satellite models were understood to gain more detail in near future when the CHAMP-satellite would reach lower orbits, and hence higher resolution. The SWARM-satellite constellation was seen to produce even more suitable data in a few years thereafter. Ocean magnetic data sets required careful processing and leveling. The method of homogenization of anomalies included replacing long wavelength information by satellite model spectral data, and hence rejecting corresponding measurements. A challenge was left to include high quality anomaly levels of near ground measurements in global magnetic anomaly grid, where available. For these purposes WDMAM task force calls for both new and improved old data sets, advanced methods for data processing and compilation, and improved anomaly definition schemes. All these would be put together and submitted as candidate grids in 2010, and finally released as WDMAM 2011 (Second Edition) at IUGG 2011, in Australia. All contributions towards this purpose are solicited.
Taye, Molla; Afework, Mekbeb; Fantaye, Wondwossen; Diro, Ermias; Worku, Alemayehu
2018-04-25
The early stage of embryo development is extremely vulnerable to various teratogenic factors, leading to congenital anomalies. In Ethiopia, a significant number of babies are born with congenital anomalies, but the risk factors for the anomalies have never been studied. Understanding the specific risk factors for congenital anomalies is very essential to provide health education that aims at creating awareness and establishing preventive strategic plan/s. The main objective of this study was to assess the risk factors associated with congenital anomalies in Addis Ababa and the Amhara Region, Ethiopia. A case-control study was conducted from January 1- June 30, 2015. The participants were recruited at the purposively selected hospitals in Addis Ababa and the Amhara Region. A total of 207 cases and 207 controls were included in the study. Cases were neonates, infants, and children 0-11 months of age with external and internal major congenital anomalies diagnosed by pediatricians. Controls were neonates, infants, and children 0-11 months of age without external and internal anomalies. Data on sociodemographic characteristics, exposure to risk factors, and reproductive history were collected by face to face interviews with children's mothers/caregivers using a structured questionnaire. Binary logistic regression was employed to explore risk factors associated with the occurrence of the problems. About 87.4% of the children were below 6 months, and 12.6% were between 6 and 11 months. The majority (59.9%) of the children were male, with the M: F sex ratio of 1.49. The mean age of the mothers was 26 years (16-45 years). Unidentified medication use during early pregnancy (AOR = 4.595; 95% CI: 1.868-11.301, P-value = 0.001), maternal alcohol drinking (AOR = 2.394; 95% CI: 1.212-4.726, P-value = 0.012), and exposure to chemicals (AOR = 9.964; 95% CI = 1.238-80.193, P-value = 0.031) were significantly associated with the occurrence of congenital anomalies. Iron folate use (AOR = 0.051; 95% CI: 0.010-0.260, P-value = < 0.001) before and during early pregnancy had a protective effect on congenital anomaly. Unidentified medication use, alcohol drinking during early pregnancy, and exposure to chemicals had a significant association with the occurrence of congenital anomalies, whereas iron folate use before and during early pregnancy had a protective effect from congenital anomalies.
ERIC Educational Resources Information Center
Looney, Marilyn A.; Howell, Steven M.
2015-01-01
This article describes the "mathematical criteria" employed by the International Skating Union (ISU) to identify potential judging anomalies within competitive figure skating. The mathematical criteria have greater sensitivity to identify scoring anomalies for technical element scores than for the program component scores. This article…
Automated Network Anomaly Detection with Learning, Control and Mitigation
ERIC Educational Resources Information Center
Ippoliti, Dennis
2014-01-01
Anomaly detection is a challenging problem that has been researched within a variety of application domains. In network intrusion detection, anomaly based techniques are particularly attractive because of their ability to identify previously unknown attacks without the need to be programmed with the specific signatures of every possible attack.…
NASA Astrophysics Data System (ADS)
Girolami, C.; Barchi, M. R.; Heyde, I.; Pauselli, C.; Vetere, F.; Cannata, A.
2017-11-01
In this work, the gravity anomaly signal beneath Mount Amiata and its surroundings have been analysed to reconstruct the subsurface setting. In particular, the work focuses on the investigation of the geological bodies responsible for the Bouguer gravity minimum observed in this area.
A Bouguer Gravity Anomaly Map of Africa.
A Bouguer Gravity Anomaly Map of Africa has been compiled using only terrestrial data. The map is a contoured representation of one degree x one...The anomaly pattern shown on the map is discussed and evaluated with respect to regional and local tectonic and geologic patterns. The entire Bouguer
Systematic Screening for Subtelomeric Anomalies in a Clinical Sample of Autism
ERIC Educational Resources Information Center
Wassink, Thomas H.; Losh, Molly; Piven, Joseph; Sheffield, Val C.; Ashley, Elizabeth; Westin, Erik R.; Patil, Shivanand R.
2007-01-01
High-resolution karyotyping detects cytogenetic anomalies in 5-10% of cases of autism. Karyotyping, however, may fail to detect abnormalities of chromosome subtelomeres, which are gene rich regions prone to anomalies. We assessed whether panels of FISH probes targeted for subtelomeres could detect abnormalities beyond those identified by…
Mission Safety Evaluation Report for STS-43, Postflight Edition
NASA Technical Reports Server (NTRS)
Hill, William C.; Finkel, Seymour I.
1991-01-01
Some of the topics covered include: (1) an STS-43 mission summary; (2) safety risks factors/issues; (3) resolved STS-43 safety risk factors; (4) STS-40 inflight anomalies; (5) STS-37 inflight anomalies; and (6) STS-43 inflight anomalies. Background information and a list of acronyms are also presented.
Mission Safety Evaluation Report for STS-32, Postflight Edition
NASA Technical Reports Server (NTRS)
Hill, William C.; Finkel, Seymour I.
1990-01-01
The topics covered include: (1) an STS-32 mission summary; (2) safety risk factors/issues; (3) resolved STS-32 safety risk factors; (4) STS-32 inflight anomalies; (5) STS-28 inflight anomalies; and (6) STS-32 inflight anomalies. Background information and a list of acronyms are also presented.
Archean Isotope Anomalies as a Window into the Differentiation History of the Earth
NASA Astrophysics Data System (ADS)
Wainwright, A. N.; Debaille, V.; Zincone, S. A.
2018-05-01
No resolvable µ142Nd anomaly was detected in Paleo- Mesoarchean rocks of São Francisco and West African cratons. The lack of µ142Nd anomalies outside of North America and Greenland implies the Earth differentiated into at least two distinct domains.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Plyushchay, Mikhail S., E-mail: mikhail.plyushchay@usach.cl
A canonical quantization scheme applied to a classical supersymmetric system with quadratic in momentum supercharges gives rise to a quantum anomaly problem described by a specific term to be quadratic in Planck constant. We reveal a close relationship between the anomaly and the Schwarzian derivative, and specify a quantization prescription which generates the anomaly-free supersymmetric quantum system with second order supercharges. We also discuss the phenomenon of a coupling-constant metamorphosis that associates quantum systems with the first-order supersymmetry to the systems with the second-order supercharges.
The Compact Environmental Anomaly Sensor (CEASE) III
NASA Astrophysics Data System (ADS)
Roddy, P.; Hilmer, R. V.; Ballenthin, J.; Lindstrom, C. D.; Barton, D. A.; Ignazio, J. M.; Coombs, J. M.; Johnston, W. R.; Wheelock, A. T.; Quigley, S.
2016-12-01
The Air Force Research Laboratory's Energetic Charged Particle (ECP) sensor project is a comprehensive effort to measure the charged particle environment that causes satellite anomalies. The project includes the Compact Environmental Anomaly Sensor (CEASE) III, building on the flight heritage of prior CEASE designs. CEASE III consists of multiple sensor modules. High energy particles are observed using independent unique silicon detector stacks. In addition CEASE III includes an electrostatic analyzer (ESA) assembly which uses charge multiplication for particle detection. The sensors cover a wide range of proton and electron energies that contribute to satellite anomalies.
Hawking radiation from rotating black holes and gravitational anomalies
DOE Office of Scientific and Technical Information (OSTI.GOV)
Murata, Keiju; Soda, Jiro
2006-08-15
We study the Hawking radiation from Rotating black holes from the gravitational anomalies point of view. First, we show that the scalar field theory near the Kerr black hole horizon can be reduced to the 2-dimensional effective theory. Then, following Robinson and Wilczek, we derive the Hawking flux by requiring the cancellation of gravitational anomalies. We also apply this method to Hawking radiation from higher dimensional Myers-Perry black holes. In the appendix, we present the trace anomaly derivation of Hawking radiation to argue the validity of the boundary condition at the horizon.
Determination of mean gravity anomalies in the Taiwan Island
NASA Technical Reports Server (NTRS)
Chang, Ruey-Gang
1989-01-01
The fitting and proper regression coefficients were made of one hundred seventeen 10 x 10' blocks with observed gravity data and corresponding elevation in the Taiwan Island. To compare five different predicted models, and the proper one for the mean gravity anomalies were determined. The predicted gravity anomalies of the non-observed gravity blocks were decided when the coefficients obtained through the model with the weighted mean method. It was suggested that the mean gravity anomalies of 10 x 10' blocks should be made when comprehensive the observed and predicted data.