Grey seal (Halichoerus grypus) from the Northwest Atlantic: female reproductive rates, age at first birth, and age of maturity in males

1995 ◽  
Vol 52 (12) ◽  
pp. 2757-2761 ◽  
Author(s):  
M. O. Hammill ◽  
J. F. Gosselin

Mean age at first birth and reproductive rates were examined in a sample of 526 female grey seal (Halichoerus grypus) reproductive tracts collected between 1968 and 1992. Age of first birth determined from reproductive tracts with a fetus was 5.5 ± 0.12 yr (mean ± SD). No trend over time was observed in mean age at first birth or in pregnancy rates. Pregnancy rates determined from reproductive tracts containing a fetus were 0.18, 0.86, and 0.88 for animals aged 4+, 5+, and >6+ yr, respectively. Pregnancy rates calculated from the presence of a corpus luteum were 0.01, 0.45, 0.9, and 1 for ages 3+, 4+, 5+, and >6+, respectively. Mean age of sexual maturity of males was 5.6 yr as estimated from changes in testes mass in a sample of 89 seals collected during August–September 1992. A marked increase in testes mass was observed among animals aged 3+ yr. By age 7+ yr, virtually all males had attained sexual maturity.

1993 ◽  
Vol 50 (4) ◽  
pp. 858-864 ◽  
Author(s):  
Andrew W. Trites ◽  
Anne E. York

From 1956 to 1968, female northern fur seals (Callorhinus ursinus) were harvested on the Pribilof Islands, Alaska, in an effort to increase the productivity of the herd. In theory, pregnancy rates should have increased and the age at first birth should have declined as population density was reduced. Instead the opposite happened: pregnancy rates dropped and age of first birth increased. It is unlikely that these changes were caused by shortages of food or poor physical condition of the females, given that body size increased over this period. The most likely explanations for the changes observed between 1958 and 1974 are related to altered age and sex ratios of breeding animals caused by the depletion of females and/or the harvesting of young males. Changes in pregnancy rates and age at first birth are inconsistent with the density-dependence paradigm and suggest that relative densities of mature age and sex classes on the breeding beaches (a product of social interactions and territory size) may be more consequential than absolute population densities in affecting the reproductive biology of northern fur seals.


1988 ◽  
Vol 20 (2) ◽  
pp. 157-165 ◽  
Author(s):  
Howard Wineberg

SummaryThis paper enquires whether education and age at first birth, both strongly associated with completed fertility, are related to the timing of fertility, in particular the timing of the first three births, among once married white women. Analysis of data from the June 1985 United States Current Population Survey indicates that education is related to the timing of fertility; this relationship has remained relatively constant over time. Age at first birth is associated with the timing of fertility among older but not younger women.


2007 ◽  
Vol 6 ◽  
pp. 153 ◽  
Author(s):  
Erlingur Hauksson

Growth and reproduction in grey seals (Halichoerus grypus Fabricius, 1791) from Iceland were examined. The oldest Icelandic grey seals obtained were a 36 year old female and a 23 year old male. The longest animals were a 255 cm 13 year old male, and a 230 cm 20 year old female. The heaviest grey seal was an 11 year old male weighing 310 kg. The heaviest female was a 20 year old female that weighed 240 kg. Females reached an asymptotic standard length and weight of 200 (95% CI 196 - 204) cm and 164 (95% CI 157 - 171) kg. Males attained an asymptotic standard length of 243 (95% CI 232 - 254) cm and mass of 279 (95% CI 254 - 306) kg. Investigations of the ovaries and testes indicate that, by the time that females were seven years old, over 90% were pregnant. The average age of sexual maturity of females was 4.0 years (95% CI 3.59 - 4.41) and the average age of first pupping was 5.3 (95% CI 4.95 - 5.72). Average age of sexual maturity for males was 4.9 (95% CI 4.43 - 5.40). Seven out of 8 grey seal males had fully developed testes at the age of 7. All males, 8 years of age and older were mature. Adult (5+ years) females and males are fattest in the summer right before breeding in the autumn, but leanest in the winter after breeding and mating, and in the spring after moulting.


Author(s):  
Stephanie J. Ventura ◽  
William D. Mosher ◽  
Sally C. Curtin ◽  
Joyce C. Abma ◽  
Stanley Henshaw

2020 ◽  
Vol 655 ◽  
pp. 227-240
Author(s):  
KR Flanders ◽  
ZH Olson ◽  
KA Ono

Increasing grey seal Halichoerus grypus abundance in coastal New England is leading to social, political, economic, and ecological controversies. Central to these issues is the foraging ecology and diet composition of the seals. We studied grey seal feeding habits through next-generation sequencing of prey DNA using 16S amplicons from seal scat (n = 74) collected from a breeding colony on Monomoy Island in Massachusetts, USA, and report frequency of occurrence and relative read abundance. We also assigned seal sex to scat samples using a revised PCR assay. In contrast to current understanding of grey seal diet from hard parts and fatty acid analysis, we found no significant difference between male and female diet measured by alpha and beta diversity. Overall, we detected 24 prey groups, 18 of which resolved to species. Sand lance Ammodytes spp. were the most frequently consumed prey group, with a frequency of occurrence (FO) of 97.3%, consistent with previous studies, but Atlantic menhaden Brevoortia tyrannus, the second most frequently consumed species (FO = 60.8%), has not previously been documented in US grey seal diet. Our results suggest that a metabarcoding approach to seal food habits can yield important new ecological insights, but that traditional hard parts analysis does not underestimate consumption of Atlantic cod Gadus morhua (FO = 6.7%, Gadidae spp.) and salmon Salmo salar (FO = 0%), 2 particularly valuable species of concern.


2019 ◽  
Vol 34 (5) ◽  
pp. 881-893 ◽  
Author(s):  

Abstract STUDY QUESTION How has the timing of women’s reproductive events (including ages at menarche, first birth, and natural menopause, and the number of children) changed across birth years, racial/ethnic groups and educational levels? SUMMARY ANSWER Women who were born in recent generations (1970–84 vs before 1930) or those who with higher education levels had menarche a year earlier, experienced a higher prevalence of nulliparity and had their first child at a later age. WHAT IS KNOWN ALREADY The timing of key reproductive events, such as menarche and menopause, is not only indicative of current health status but is linked to the risk of adverse hormone-related health outcomes in later life. Variations of reproductive indices across different birth years, race/ethnicity and socioeconomic positions have not been described comprehensively. STUDY DESIGN, SIZE, DURATION Individual-level data from 23 observational studies that contributed to the International Collaboration for a Life Course Approach to Reproductive Health and Chronic Disease Events (InterLACE) consortium were included. PARTICIPANTS/MATERIALS, SETTING, METHODS Altogether 505 147 women were included. Overall estimates for reproductive indices were obtained using a two-stage process: individual-level data from each study were analysed separately using generalised linear models. These estimates were then combined using random-effects meta-analyses. MAIN RESULTS AND THE ROLE OF CHANCE Mean ages were 12.9 years at menarche, 25.7 years at first birth, and 50.5 years at natural menopause, with significant between-study heterogeneity (I2 > 99%). A linear trend was observed across birth year for mean age at menarche, with women born from 1970 to 1984 having menarche one year earlier (12.6 years) than women born before 1930 (13.5 years) (P for trend = 0.0014). The prevalence of nulliparity rose progressively from 14% of women born from 1940–49 to 22% of women born 1970–84 (P = 0.003); similarly, the mean age at first birth rose from 24.8 to 27.3 years (P = 0.0016). Women with higher education levels had fewer children, later first birth, and later menopause than women with lower education levels. After adjusting for birth year and education level, substantial variation was present for all reproductive events across racial/ethnic/regional groups (all P values < 0.005). LIMITATIONS, REASONS FOR CAUTION Variations of study design, data collection methods, and sample selection across studies, as well as retrospectively reported age at menarche, age at first birth may cause some bias. WIDER IMPLICATIONS OF THE FINDINGS This global consortium study found robust evidence on variations in reproductive indices for women born in the 20th century that appear to have both biological and social origins. STUDY FUNDING/COMPETING INTEREST(S) InterLACE project is funded by the Australian National Health and Medical Research Council project grant (APP1027196). GDM is supported by the Australian National Health and Medical Research Council Principal Research Fellowship (APP1121844).


1980 ◽  
Vol 40 (2) ◽  
pp. 331-350 ◽  
Author(s):  
Richard H. Steckel

This paper investigates the decline and regional differential in antebellum southern white fertility using published census materials and the 1860 population schedules. Demographic analysis is conducted with a synthetic total fertility rate that has four components: age at first birth, age at last surviving birth, surviving-child spacing, and the proportion of women who eventually have surviving children. The socioeconomic analysis employs regressions and focuses on causes of the underlying changes in the components. Family limitation appears to have been unimportant in this population. The distribution of wealth was.probably an important factor shaping the time trend and regional differential in fertility.


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