Biological Parameters of the Antarctic Minke Whale at the Virginal Population Level

1975 ◽  
Vol 32 (7) ◽  
pp. 995-1004 ◽  
Author(s):  
Seiji Ohsumi ◽  
Yasuaki Masaki
Keyword(s):  
Sex Ratio ◽  
Pregnancy Rate ◽  
Sexual Maturity ◽  
Population Level ◽  
Testis Weight ◽  
Natural Mortality ◽  
Biological Parameters ◽  
Antarctic Minke Whale ◽  
The Antarctic ◽  
Sexually Mature

New data from Japanese catches in Antarctic seasons 1971–72 and 1972–73 are used to calculate biological parameters. Determinations are: fetal sex ratio (52.0% females); sex ratio in catch (54.1% females); [Formula: see text], males (27.9 ft), females (29.5 ft); age at asymptotic body length, males (18–20 yr), females (20–22 yr); male sexual maturity at testis weight (0.4 kg); length at beginning of sexual maturity, males (21 ft), females (24 ft) and at 50% sexually mature, males (23.6 ft), females (26.2 ft); age at sexual maturity, females (6 yr); apparent pregnancy rate (89.5%); annual ovulation rate (0.866); litter size (1.007); natural mortality coefficient of sexually mature sample (0.127) and of sexually immature sample (0.213); age at recruitment (6 yr); and rate of recruitment in virgin population (0.119).

A new way to estimate the age of bowhead whales (Balaena mysticetus) using ovarian corpora counts

2011 ◽  
Vol 89 (9) ◽  
pp. 840-852 ◽  
Author(s):  
J.C. George ◽  
E. Follmann ◽  
J. Zeh ◽  
M. Sousa ◽  
R. Tarpley ◽  
...  
Keyword(s):  
Corpus Luteum ◽  
Pregnancy Rate ◽  
Sexual Maturity ◽  
Standard Errors ◽  
Reproductive Parameters ◽  
Balaena Mysticetus ◽  
Bowhead Whales ◽  
Aspartic Acid Racemization ◽  
Sexually Mature ◽  
Age Estimates

We used lengths and reproductive data for bowhead whales ( Balaena mysticetus L., 1758) harvested by Alaskan Eskimos to estimate female reproductive parameters and age. Data from 117 females determined that 75 were sexually mature and 42 were immature. Estimated length at sexual maturity was 13.35 m. Counts of ovarian corpora were obtained from 50 mature females. Corpora and baleen data were used with aspartic acid racemization (AAR) data to obtain estimated age at sexual maturity (ASM) at ≈26 years. The number of corpora counted in both ovaries (or estimated when only one ovary was counted) was used with ASM and estimated ovulation rate (OR) to obtain corpora age estimates ranging from 26 to 149 years. A stone harpoon tip recovered from whale 92B2 was consistent with her corpora age of 133 years. The correlation between corpora and AAR age estimates was 0.77. Estimated standard errors of corpora ages tended to be somewhat higher than those for comparable AAR ages. A sample of potentially mature females examined for maturity and presence of a corpus luteum and (or) fetus provided an OR value of 0.332·year–1 and an estimated pregnancy rate of 0.326·year–1, implying intervals between ovulations and pregnancies of 3.0 and 3.1 years.

Age-specific reproduction in female sea otters (Enhydra lutris) from south-central Alaska: analysis of reproductive tracts

1993 ◽  
Vol 71 (9) ◽  
pp. 1811-1815 ◽  
Author(s):  
James L. Bodkin ◽  
Dan Mulcahy ◽  
Calvin J. Lensink
Keyword(s):  
Sex Ratio ◽  
Sexual Maturity ◽  
Enhydra Lutris ◽  
Sea Otters ◽  
Older Mothers ◽  
South Central ◽  
In Situ Observations ◽  
Reproductive Rates ◽  
Sexually Mature

We estimated age at sexual maturity and age-specific reproductive rates by examining carcasses and reproductive tracts from 177 female sea otters (Enhydra lutris). Carcasses were recovered from south-central Alaska, primarily from western Prince William Sound, as a result of the T/V Exxon Valdez oil spill in 1989. We found 65% of our sample to be sexually mature. Sexual maturity was first attained at age 2. The proportion of sexually mature animals increased from 30% at age 2 to 100% at age 5. Annual reproductive rates increased from 22% at age 2 to 78% at age 5 and remained relatively stable (75–88%) through to age 15. The sex ratio (♀:♂) of 49 fetal sea otters was 18:37 and differed significantly from parity. Females younger than 8 tended to produce more female fetuses, while older mothers did not. Our estimates of the reproductive characteristics of female sea otters obtained by examination of reproductive tracts were similar to those reported in the literature based on in situ observations of marked individuals.

Akodon molinae (Rodentia Cricetidae), a new laboratory animal: breeding, management and reproductive performance

1980 ◽  
Vol 14 (2) ◽  
pp. 129-131 ◽  
Author(s):  
Maria Susana Merani ◽  
Marta Susana Lizarralde
Keyword(s):  
Sex Ratio ◽  
Reproductive Performance ◽  
Sexual Maturity ◽  
Laboratory Animal ◽  
Post Partum ◽  
Animal Breeding ◽  
Haemorrhagic Fever ◽  
Sex Ratio At Birth ◽  
Breeding Management ◽  
Laboratory Colony

Akodon molinae, a vole mouse widely distributed in central Argentina, shows remarkable chromosome polymorphisms. It is one of the natural reservoirs of the actiologic agent of haemorrhagic fever, and a laboratory colony could be of great help in investigating this disease. Pregnancy lasted 23 (range 21-25) days. Litters of 4-5 young were born to monogamous breeding pairs about every 30 days, with weaning at 26 days post partum. The sex ratio at birth was 505 males to 500 females: at weaning it was 460 to 440. Sexual maturity was attained at about 16 weeks of age in males and 12-20 weeks in females. Akodon molinae is easy to handle, but fighting and killing or neglect of young are problems.

Population parameters of ringed seals (Phoca hispida Schreber, 1775) in the Svalbard area

1987 ◽  
Vol 65 (4) ◽  
pp. 1021-1027 ◽  
Author(s):  
Christian Lydersen ◽  
Ian Gjertz
Keyword(s):  
Sex Ratio ◽  
Ringed Seal ◽  
Adult Males ◽  
Population Parameters ◽  
Phoca Hispida ◽  
Age Class ◽  
Ringed Seals ◽  
Males And Females ◽  
The Mean ◽  
Sexually Mature

Samples were taken from 284 ringed seals (Phoca hispida) in the Svalbard area during April–July 1981 and March–April 1982. The age of 283 seals was determined by reading annuli in the cementum of the canine teeth. The mean age of the males was 11.3 years, and of the females, 14.9 years. Females were found to be significantly older than males. The mean length of sexually mature ringed seals was 128.9 cm for both sexes. The mean weight of adult males and females was 53.5 and 61.4 kg, respectively. Females were found to be significantly heavier than males. The sex ratio was 47.8% males and 52.2% females. Studies of microscopic sections of testis and epididymis from ringed seal males showed that 63, 75, and 80% of 5-, 6-, and 7-year-old animals, respectively, were sexually mature. The weights of testis and epididymis, diameters of tubuli, and the size of testis all showed a marked increase in the 5-year age-class. Macroscopic sections of ovaries from ringed seal females showed that 20, 60, and 80% of 3-, 4-, and 5-year-old animals, respectively, were sexually mature. The size of the ovaries showed a marked increase in the 5-year age-class. The ovulation rate of ringed seals from Svalbard was calculated to be 0.91.

scholarly journals Decline in body condition in the Antarctic minke whale (Balaenoptera bonaerensis) in the Southern Ocean during the 1990s

Polar Biology ◽  
2021 ◽  
Vol 44 (2) ◽  
pp. 259-273
Author(s):  
Céline Cunen ◽  
Lars Walløe ◽  
Kenji Konishi ◽  
Nils Lid Hjort
Keyword(s):  
Model Selection ◽  
Body Condition ◽  
Model Building ◽  
Research Question ◽  
Information Criterion ◽  
The Body ◽  
Antarctic Minke Whale ◽  
Minke Whales ◽  
Balaenoptera Bonaerensis ◽  
The Antarctic

AbstractChanges in the body condition of Antarctic minke whales (Balaenoptera bonaerensis) have been investigated in a number of studies, but remain contested. Here we provide a new analysis of body condition measurements, with particularly careful attention to the statistical model building and to model selection issues. We analyse body condition data for a large number (4704) of minke whales caught between 1987 and 2005. The data consist of five different variables related to body condition (fat weight, blubber thickness and girth) and a number of temporal, spatial and biological covariates. The body condition variables are analysed using linear mixed-effects models, for which we provide sound biological motivation. Further, we conduct model selection with the focused information criterion (FIC), reflecting the fact that we have a clearly specified research question, which leads us to a clear focus parameter of particular interest. We find that there has been a substantial decline in body condition over the study period (the net declines are estimated to 10% for fat weight, 7% for blubber thickness and 3% for the girth). Interestingly, there seems to be some differences in body condition trends between males and females and in different regions of the Antarctic. The decline in body condition could indicate major changes in the Antarctic ecosystem, in particular, increased competition from some larger krill-eating whale species.

Reproductive Ecology of The Allied Rock-wallaby, Petrogale assimilis.

1996 ◽  
Vol 19 (2) ◽  
pp. 209
Author(s):  
R. Delaney
Keyword(s):  
Life History ◽  
Sex Ratio ◽  
Sexual Maturity ◽  
Post Partum ◽  
Reproductive Ecology ◽  
Oestrous Cycle ◽  
Embryonic Diapause ◽  
Minimum Age

Petrogale assimilis has a typical life history and reproductive ecology for a macropodid of its size. Both sexes are capable of reproducing continuously; gestation is about the same length as the oestrous cycle (approximately one month); a single young is born and, a post-partum oestrus and embryonic diapause probably occurs. The sex ratio of young is unbiased. Pouch young remain permanently attached to the teat until 110 - 143 days (n=11). Permanent exit from the pouch occurs at 180 - 231 days (mean=201 days, n=25), and weaning occurs between 267 - 387 days (n=5). Sexual maturity occurs at a minimum age of 17.5 months in females and 23 months in males.

scholarly journals Reproductive Biology of Round Sardinella (Sardinella Aurita) (Valenciennes, 1847) in Senegalese Coastal Waters

2018 ◽  
Vol 9 (1) ◽  
pp. 31
Author(s):  
Ismaïla NDIAYE ◽  
Alassane SARR ◽  
Alioune FAYE ◽  
Modou THIAW ◽  
Malick DIOUF ◽  
...  
Keyword(s):  
Sex Ratio ◽  
Reproductive Biology ◽  
Coastal Waters ◽  
Sexual Maturity ◽  
Reproductive Parameters ◽  
Monthly Variation ◽  
Relative Fecundity ◽  
The Mean ◽  
Sardinella Aurita ◽  
Somatic Index

In this study, a total of 1068 specimens Sardinella aurita of which 553 females and 515 males were examined. The objectif of this study was to determine the reproductive parameters of Sardinella aurita. The sex ratio was significantly in favor of females (55%). The size at first sexual maturity was estimated at 18.9 cm for females and 18.0 cm for males. The monthly variation of sexual maturity stages and gonado-somatic index (GSI) allowed to locate the reproduction periods from February to June and from September to December. The mean absolute fecundity was estimated at 110.794 ± 7582 oocytes whereas relative fecundity was about 422 ± 26 oocytes per gram of female.

scholarly journals Cetacean records along a coastal-offshore gradient in the Vitória-Trindade Chain, western South Atlantic Ocean

2014 ◽  
Vol 74 (1) ◽  
pp. 137-144 ◽  
Author(s):  
LL Wedekin ◽  
MR Rossi-Santos ◽  
C Baracho ◽  
AL Cypriano-Souza ◽  
PC Simões-Lopes
Keyword(s):  
Humpback Whale ◽  
South Atlantic ◽  
Breeding Habitat ◽  
Humpback Whales ◽  
Balaenoptera Physalus ◽  
Fin Whale ◽  
Antarctic Minke Whale ◽  
Trindade Island ◽  
The Antarctic ◽  
Species Being

Oceanic waters are difficult to assess, and there are many gaps in knowledge regarding cetacean occurrence. To fill some of these gaps, this article provides important cetacean records obtained in the winter of 2010 during a dedicated expedition to collect visual and acoustic information in the Vitória-Trindade seamounts. We observed 19 groups of cetaceans along a 1300-km search trajectory, with six species being identified: the humpback whale (Megaptera novaeangliae, N = 9 groups), the fin whale (Balaenoptera physalus, N = 1), the Antarctic minke whale (Balaenoptera bonaerensis, N = 1), the rough-toothed dolphin (Steno bredanensis, N = 1), the bottlenose dolphin (Tursiops truncatus, N = 2), and the killer whale (Orcinus orca, N = 1). Most humpback whale groups (N = 7; 78%) were observed in the Vitória-Trindade seamounts, especially the mounts close to the Abrolhos Bank. Only one lone humpback whale was observed near Trindade Island after a search effort encompassing more than 520 km. From a total of 28 acoustic stations, humpback whale songs were only detected near the seamounts close to the Abrolhos Bank, where most groups of this species were visually detected (including a competitive group and groups with calves). The presence of humpback whales at the Trindade Island and surroundings is most likely occasional, with few sightings and low density. Finally, we observed a significant number of humpback whales along the seamounts close to the Abrolhos Bank, which may function as a breeding habitat for this species. We also added important records regarding the occurrence of cetaceans in these mounts and in the Western South Atlantic, including the endangered fin whale.

Exteroceptive Factors, Sexual Maturation and Reproduction in the Female Rat

1979 ◽  
Vol 13 (3) ◽  
pp. 283-286 ◽  
Author(s):  
M. L. Norris ◽  
C. E. Adams
Keyword(s):  
Reproductive Performance ◽  
Sexual Maturation ◽  
Sexual Maturity ◽  
Mature Male ◽  
Female Rat ◽  
Vaginal Opening ◽  
Sexually Mature

Summary Keeping a sexually mature male with a weanling female rat advanced neither the time of vaginal opening nor that of 1st oestrus. In 2 of 3 experiments females kept singly after weaning reached sexual maturity significantly earlier than did grouped females. The reproductive performance of females mated at 1st oestrus was not significantly different from that of older primiparae. 26 rats gave birth to an average of 9·3 young at 59·5 days of age, and 22 of them reared 96% of the young to weaning.

scholarly journals Whales as Indicators of Historical and Current Changes in the Marine Ecosystem of the Indo-Pacific Sector of the Antarctic

2020 ◽  
Author(s):  
Yoshihiro Fujise ◽  
Luis A. Pastene
Keyword(s):  
Marine Ecosystem ◽  
Recruitment Rate ◽  
Minke Whale ◽  
Past Century ◽  
Baleen Whale ◽  
The Past ◽  
Antarctic Minke Whale ◽  
Minke Whales ◽  
Nutritional Conditions ◽  
The Antarctic

We review the scientific information on whales that could be indicative of historical and current changes in the ecosystem in the Indo-Pacific sector of the Antarctic. The increased krill availability in the middle of the past century as a result of the heavy harvesting of the larger baleen whale species could have been translated into better nutritional conditions for the Antarctic minke whale, resulting in a decreasing trend in the age at sexual maturity and an increasing trend in recruitment rate and hence total population size between approximately 1940 and 1970. This nutritional condition has deteriorated more recently, as revealed by a decrease in energy storage and stomach content weight since the 1980’s; these changes coincide with appreciable increases in the abundances of humpback and fin whales, which were heavily harvested in the first half of the past century. The historical demographic changes observed in the Antarctic minke whale are consistent with the pattern to be expected under the krill surplus hypothesis, with minke whales now again competing with other (recovering) baleen whale species for krill. However, these minke whales could also be using alternative feeding areas (e.g. polynias within the pack-ice) in response to the increase in abundance and geographical expansion of these other large whale species. This could provide an alternative explanation for indications from sighting surveys and population models of a decrease and then re-stabilisation of minke whale abundance in open water areas since the 1970s.

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