Literature DB >> 8457634

Growth in pinnipeds.

I A McLaren1.   

Abstract

This review presents summary figures of, and fits growth curves to, data on body lengths (as standard length, SL, whenever possible) of pinnipeds at ages estimated to O.I y. (1) Generalized von Bertalanffy (vB) growth curves are fitted to most data: Lx = L infinity (I - ea(x-x0)b, Lx is length at age x, x0 is the origin of the curve (here chosen a priori as time of initiation of embryonic growth), L infinity is asymptotic length, a (which is negative) determines rate of approach to the asymptote, and b influences the 'shape' of the approach. (2) No single monotonic growth equation suffices for growth in length, which is linear before birth and remains so during early life. The vB equation is only suitable to describe mean lengths of newborns, and animals one or more years old. (3) Also, for males of polygynous species, two functions are needed to account for accelerated growth at puberty. Generally a Gompertz equation is adequate for adult males of these species. (4) The fitted growth equations permit statistical comparisons of sizes and growth rates, as well as of individual variability (as growth-curve residuals), among populations and species. (5) For the following species (including different populations when available), the reliability of data is assessed and parameters of growth curves are presented (with sexes separated where significantly different): walrus, California and Steller sea lions, Antarctic, subantarctic and northern fur seals, Hawaiian monk seal, crabeater, Weddell and Leopard seals, southern and northern elephant seals, bearded, hooded, ringed, Baikal, Caspian, spotted, harbour, harp, ribbon and grey seals. (6) Some novel findings pertain to individual species as follows. Although the Pacific walrus is generally stated to be the larger subspecies, females from Hudson Bay and males from Foxe Basin, in the eastern Canadian Arctic, may be as long as those from the Bering Sea. Although female Weddell seals have been assumed to grow larger than males, there is no significant difference in growth curves fitted to the most complete data. Uniquely among populations examined, the relative variability (absolute growth curve residuals/predicted lengths) of male southern elephant seals is amplified with age. Among ringed seals from Svalbard, the eastern, western and high Canadian Arctic, and the Bering, Chukchi, Okhotsk, Barents and Baltic Seas, asymptotic sizes are larger among those that breed on land-fast ice rather than floes, and size may be more variable in more extreme Arctic environments. The Baikal seal is confirmed as the smallest species of pinniped.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1993        PMID: 8457634     DOI: 10.1111/j.1469-185x.1993.tb00731.x

Source DB:  PubMed          Journal:  Biol Rev Camb Philos Soc        ISSN: 0006-3231


  13 in total

1.  Links between muscle phenotype and life history: differentiation of myosin heavy chain composition and muscle biochemistry in precocial and altricial pinniped pups.

Authors:  Michelle R Shero; Peter J Reiser; Lauren Simonitis; Jennifer M Burns
Journal:  J Comp Physiol B       Date:  2019-10-15       Impact factor: 2.200

2.  Foraging fidelity as a recipe for a long life: foraging strategy and longevity in male Southern Elephant Seals.

Authors:  Matthieu Authier; Ilham Bentaleb; Aurore Ponchon; Céline Martin; Christophe Guinet
Journal:  PLoS One       Date:  2012-04-10       Impact factor: 3.240

3.  Climate change and seal survival: evidence for environmentally mediated changes in elephant seal, Mirounga leonina, pup survival.

Authors:  Clive R McMahon; Harry R Burton
Journal:  Proc Biol Sci       Date:  2005-05-07       Impact factor: 5.349

4.  Predicting climate change impacts on polar bear litter size.

Authors:  Péter K Molnár; Andrew E Derocher; Tin Klanjscek; Mark A Lewis
Journal:  Nat Commun       Date:  2011-02-08       Impact factor: 14.919

5.  Sizing ocean giants: patterns of intraspecific size variation in marine megafauna.

Authors:  Craig R McClain; Meghan A Balk; Mark C Benfield; Trevor A Branch; Catherine Chen; James Cosgrove; Alistair D M Dove; Leo Gaskins; Rebecca R Helm; Frederick G Hochberg; Frank B Lee; Andrea Marshall; Steven E McMurray; Caroline Schanche; Shane N Stone; Andrew D Thaler
Journal:  PeerJ       Date:  2015-01-13       Impact factor: 2.984

6.  The role of canine distemper virus and persistent organic pollutants in mortality patterns of Caspian seals (Pusa caspica).

Authors:  Susan C Wilson; Tariel M Eybatov; Masao Amano; Paul D Jepson; Simon J Goodman
Journal:  PLoS One       Date:  2014-07-02       Impact factor: 3.240

7.  Challenges and opportunities for comparative studies of survival rates: An example with male pinnipeds.

Authors:  Jamie L Brusa; Jay J Rotella; Katharine M Banner; Patrick R Hutchins
Journal:  Ecol Evol       Date:  2021-05-08       Impact factor: 2.912

8.  Animal-borne acoustic transceivers reveal patterns of at-sea associations in an upper-trophic level predator.

Authors:  Damian C Lidgard; W Don Bowen; Ian D Jonsen; Sara J Iverson
Journal:  PLoS One       Date:  2012-11-14       Impact factor: 3.240

9.  Haul-out behaviour of the world's northernmost population of harbour seals (Phoca vitulina) throughout the year.

Authors:  Charmain D Hamilton; Christian Lydersen; Rolf A Ims; Kit M Kovacs
Journal:  PLoS One       Date:  2014-01-22       Impact factor: 3.240

10.  Phocine distemper outbreak, The Netherlands, 2002.

Authors:  Jolianne M Rijks; Marco W G Van de Bildt; Trine Jensen; Joost D W Philippa; Albert D M E Osterhaus; Thijs Kuiken
Journal:  Emerg Infect Dis       Date:  2005-12       Impact factor: 6.883

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