75 research outputs found

    Early Spring Feeding Habits of Bearded Seals (Erignathus Barbatus) in the Central Bering Sea, 1981

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    The diet of bearded seals, Erignathus barbatus, near St. Matthew Island, Bering Sea, was studied during the early spring of 1981. Eighty-six percent of the 78 seals' stomachs examined contained fish. Other prey taxon groups, in decreasing order of their percentages of occurrence, were crabs (73%), clams (55%), snails (47%), amphipods (32%), shrimp (18%), mysids (13%), marine worms (13%) and cephalopods (4%). The most frequently occurring prey species were capelin, Mallotus villosus, (82%); codfishes, Gadidae (64%); narrow snow crab, Chionoecetes opilio (63%); eelpouts, Lycodes spp. (56%); longsnout prickleback, Lumpenella longirostris (49%); nutshell clams, Nuculana sp. (42%); and moon snails, Polinices sp. (27%). Seventy-seven percent of the seals examined had consumed prey from three or more different taxon groups. We identified seven food items not previously reported as prey of the bearded seal in the Bering Sea. No differences were detected between the diets of males and females and between adults and juveniles, indicating no apparent segregation of foraging by sex or age. Bearded seals in the St. Matthew Island region of the Bering Sea forage in a manner similar to their conspecifics in other areas where fish constitute a major portion of their diet. Prey selection is probably dependent on availability, and diet may be highly diversified even within a relatively small area during a short period of time. Variety in prey consumption exemplified the ability of the bearded seal to forage in the seasonally changing habitat associated with the advance and retreat of the ice front.Key words: bearded seal, Erignathus barbatus, diet, demersal and pelagic fish, benthic invertebrates, prey species diversity On a étudié le régime alimentaire du phoque barbu, Erignathus barbatus, près de l'île Saint Matthew dans la mer de Béring, tôt au printemps de 1981. Quatre-vingt six p. cent des 78 estomacs de phoques examinés contenaient du poisson. Parmi les autres groupes de taxons servant de proies, on retrouvait, par pourcentages décroissants, les crabes (73 p. cent), les myes (55 p. cent), les gastéropodes (47 p. cent), les amphipodes (32 p. cent), les crevettes (18 p. cent), les mysis (13 p. cent), les vers marins (13 p. cent) et les céphalopodes (4 p. cent). Les espèces de proies les plus courantes étaient le capelan, Mallotus villosus (82 p. cent); la morue, Gadidae (64 p. cent); le crabe des neiges, Chionoecetes opilio (63 p. cent); la lotte, sp. Lycodes (56 p. cent); Lumpenella longirostris (49 p. cent); sp. Nuculana (42 p. cent); et la natice, sp. Polinices (27 p. cent). Soixante-dix-sept p. cent des phoques étudiés avaient ingéré des proies venant d'au moins trois différents groupes de taxons. On a identifié sept produits alimentaires qui n'avaient pas encore été reportés comme constituant une proie pour le phoque barbu dans la mer de Béring. On n'a détecté aucune différence entre les régimes alimentaires des mâles et ceux des femelles, ni entre ceux des adultes et ceux des petits, ce qui indique qu'il n'existe apparemment pas de ségrégation quant au sexe ou à l'âge lors du comportement visant la quête de nourriture. Les phoques barbus de la région de l'île Saint Matthew dans la mer de Béring recherchent leur nourriture comme leurs congénères dans d'autres régions où le poisson constitue une grande partie de leur régime. La sélection des proies dépend probablement de leur disponibilité et le régime peut être hautement diversifié, même dans une zone relativement petite et durant une courte période. La variété qui se manifeste dans la consommation des proies montre bien la capacité du phoque barbu à rechercher sa nourriture dans un habitat qui varie selon les saisons et est associé à l'avancée et au retrait du front glaciaire.Mots clés: phoque barbu, Erignathus barbatus, régime alimentaire, poissons démersaux et pélagiques, invertébres benthiques, variété des espèces servant de proi

    a report from the Children's Oncology Group and the Utah Population Database

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    Relatively little is known about the epidemiology and factors underlying susceptibility to childhood rhabdomyosarcoma (RMS). To better characterize genetic susceptibility to childhood RMS, we evaluated the role of family history of cancer using data from the largest case–control study of RMS and the Utah Population Database (UPDB). RMS cases (n = 322) were obtained from the Children's Oncology Group (COG). Population-based controls (n = 322) were pair-matched to cases on race, sex, and age. Conditional logistic regression was used to evaluate the association between family history of cancer and childhood RMS. The results were validated using the UPDB, from which 130 RMS cases were identified and matched to controls (n = 1300) on sex and year of birth. The results were combined to generate summary odds ratios (ORs) and 95% confidence intervals (CI). Having a first-degree relative with a cancer history was more common in RMS cases than controls (ORs = 1.39, 95% CI: 0.97–1.98). Notably, this association was stronger among those with embryonal RMS (ORs = 2.44, 95% CI: 1.54–3.86). Moreover, having a first-degree relative who was younger at diagnosis of cancer (<30 years) was associated with a greater risk of RMS (ORs = 2.37, 95% CI: 1.34–4.18). In the largest analysis of its kind, we found that most children diagnosed with RMS did not have a family history of cancer. However, our results indicate an increased risk of RMS (particularly embryonal RMS) in children who have a first-degree relative with cancer, and among those whose relatives were diagnosed with cancer at <30 years of age

    Short-term effects and long-term changes of FUEL—a digital sports nutrition intervention on REDs related symptoms in female athletes

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    Female endurance athletes are at high risk for developing Relative Energy Deficiency in Sport (REDs), resulting in symptoms such as menstrual dysfunction and gastrointestinal (GI) problems. The primary aim of this study was to investigate effects of the FUEL (Food and nUtrition for Endurance athletes—a Learning program) intervention consisting of weekly online lectures combined with individual athlete-centered nutrition counseling every other week for sixteen weeks on REDs related symptoms in female endurance athletes at risk of low energy availability [Low Energy Availability in Females Questionnaire (LEAF-Q) score ≥8]. Female endurance athletes from Norway (n = 60), Sweden (n = 84), Ireland (n = 17), and Germany (n = 47) were recruited. Fifty athletes with risk of REDs (LEAF-Q score ≥8) and with low risk of eating disorders [Eating Disorder Examination Questionnaire (EDE-Q) global score &lt;2.5], with no use of hormonal contraceptives and no chronic diseases, were allocated to either the FUEL intervention (n = 32) (FUEL) or a sixteen-week control period (n = 18) (CON). All but one completed FUEL and n = 15 completed CON. While no evidence for difference in change in LEAF-Q total or subscale scores between groups was detected post-intervention (BFincl &lt; 1), the 6- and 12-months follow-up revealed strong evidence for improved LEAF-Q total (BFincl = 123) and menstrual score (BFincl = 840) and weak evidence for improved GI-score (BFincl = 2.3) among FUEL athletes. In addition, differences in change between groups was found for EDE-Q global score post-intervention (BFincl = 1.9). The reduction in EDE-Q score remained at 6- and 12- months follow-up among FUEL athletes. Therefore, the FUEL intervention may improve REDs related symptoms in female endurance athletes.Clinical Trial Registrationwww.clinicaltrials.gov (NCT04959565)

    MODEL PENGELOLAAN PASCA TANGKAP SEBAGAI UPAYA PENGENTASAN KEMISKINAN MASYARAKAT KAMPUNG NELAYAN DI PULAU ENGGANO

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    Relatively little is known about the epidemiology and factors underlying susceptibility to childhood rhabdomyosarcoma (RMS). To better characterize genetic susceptibility to childhood RMS, we evaluated the role of family history of cancer using data from the largest case-control study of RMS and the Utah Population Database (UPDB). RMS cases (n=322) were obtained from the Children's Oncology Group (COG). Population-based controls (n=322) were pair-matched to cases on race, sex, and age. Conditional logistic regression was used to evaluate the association between family history of cancer and childhood RMS. The results were validated using the UPDB, from which 130 RMS cases were identified and matched to controls (n=1300) on sex and year of birth. The results were combined to generate summary odds ratios (ORs) and 95% confidence intervals (CI). Having a first-degree relative with a cancer history was more common in RMS cases than controls (ORs=1.39, 95% CI: 0.97-1.98). Notably, this association was stronger among those with embryonal RMS (ORs=2.44, 95% CI: 1.54-3.86). Moreover, having a first-degree relative who was younger at diagnosis of cancer (&lt;30years) was associated with a greater risk of RMS (ORs=2.37, 95% CI: 1.34-4.18). In the largest analysis of its kind, we found that most children diagnosed with RMS did not have a family history of cancer. However, our results indicate an increased risk of RMS (particularly embryonal RMS) in children who have a first-degree relative with cancer, and among those whose relatives were diagnosed with cancer at &lt;30years of age

    Targeted Sequencing in Chromosome 17q Linkage Region Identifies Familial Glioma Candidates in the Gliogene Consortium

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    Glioma is a rare, but highly fatal, cancer that accounts for the majority of malignant primary brain tumors. Inherited predisposition to glioma has been consistently observed within non-syndromic families. Our previous studies, which involved non-parametric and parametric linkage analyses, both yielded significant linkage peaks on chromosome 17q. Here, we use data from next generation and Sanger sequencing to identify familial glioma candidate genes and variants on chromosome 17q for further investigation. We applied a filtering schema to narrow the original list of 4830 annotated variants down to 21 very rare (,0.1% frequency), non-synonymous variants. Our findings implicate the MYO19 and KIF18B genes and rare variants in SPAG9 and RUNDC1 as candidates worthy of further investigation. Burden testing and functional studies are planned

    Cyclical changes in seroprevalence of leptospirosis in California sea lions: endemic and epidemic disease in one host species?

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    BackgroundLeptospirosis is a zoonotic disease infecting a broad range of mammalian hosts, and is re-emerging globally. California sea lions (Zalophus californianus) have experienced recurrent outbreaks of leptospirosis since 1970, but it is unknown whether the pathogen persists in the sea lion population or is introduced repeatedly from external reservoirs.MethodsWe analyzed serum samples collected over an 11-year period from 1344 California sea lions that stranded alive on the California coast, using the microscopic agglutination test (MAT) for antibodies to Leptospira interrogans serovar Pomona. We evaluated seroprevalence among yearlings as a measure of incidence in the population, and characterized antibody persistence times based on temporal changes in the distribution of titer scores. We conducted multinomial logistic regression to determine individual risk factors for seropositivity with high and low titers.ResultsThe serosurvey revealed cyclical patterns in seroprevalence to L. interrogans serovar Pomona, with 4-5 year periodicity and peak seroprevalence above 50%. Seroprevalence in yearling sea lions was an accurate index of exposure among all age classses, and indicated on-going exposure to leptospires in non-outbreak years. Analysis of titer decay rates showed that some individuals probably maintain high titers for more than a year following exposure.ConclusionThis study presents results of an unprecedented long-term serosurveillance program in marine mammals. Our results suggest that leptospirosis is endemic in California sea lions, but also causes periodic epidemics of acute disease. The findings call into question the classical dichotomy between maintenance hosts of leptospirosis, which experience chronic but largely asymptomatic infections, and accidental hosts, which suffer acute illness or death as a result of disease spillover from reservoir species

    Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

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    BRCA1-associated breast and ovarian cancer risks can be modified by common genetic variants. To identify further cancer risk-modifying loci, we performed a multi-stage GWAS of 11,705 BRCA1 carriers (of whom 5,920 were diagnosed with breast and 1,839 were diagnosed with ovarian cancer), with a further replication in an additional sample of 2,646 BRCA1 carriers. We identified a novel breast cancer risk modifier locus at 1q32 for BRCA1 carriers (rs2290854, P = 2.7×10-8, HR = 1.14, 95% CI: 1.09-1.20). In addition, we identified two novel ovarian cancer risk modifier loci: 17q21.31 (rs17631303, P = 1.4×10-8, HR = 1.27, 95% CI: 1.17-1.38) and 4q32.3 (rs4691139, P = 3.4×10-8, HR = 1.20, 95% CI: 1.17-1.38). The 4q32.3 locus was not associated with ovarian cancer risk in the general population or BRCA2 carriers, suggesting a BRCA1-specific associat
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