The Influence of Growth Rate on Age and Body Size at Maturity in Female Snapping Turtles (Chelydra serpentina)

Copeia ◽  
1989 ◽  
Vol 1989 (4) ◽  
pp. 896 ◽  
Author(s):  
David A. Galbraith ◽  
Ronald J. Brooks ◽  
Martyn E. Obbard
Oecologia ◽  
1999 ◽  
Vol 121 (2) ◽  
pp. 224-235 ◽  
Author(s):  
Justin D. Congdon ◽  
Roy D. Nagle ◽  
Chirstopher W. Beck ◽  
Owen M. Kinney ◽  
S. Rebecca Yeomans ◽  
...  

2019 ◽  
Vol 10 (2) ◽  
pp. 458-467
Author(s):  
Tad M. Bartareau

Abstract Growth rate and body size at maturity are important life-history traits of interest because they represent a potential source of fitness variance within a species and provide information for understanding the nutritional condition, fecundity, and dynamics of populations. My objective here was to examine the growth rate and body size at maturity of Florida black bears Ursus americanus floridanus using body length, chest girth, and body weight measurements fitted to the nonlinear von Bertalanffy, Gompertz, and logistic size-at-age growth functions. The von Bertalanffy model had the largest Akaike weight, indicating the best fit for all measurements of both sexes. Growth models showed that females grew more slowly, with a younger age at maximum growth, faster rate at which maturity was reached, and attained significantly smaller asymptotic body length, chest girth, and weight than males. A more conservative growth strategy by females to invest available energy resources to costs of reproduction, together with intrasexual selection among males for larger body size to enhance intimidating and fighting ability to increase reproductive and survival success, are implicated as determinants of the male-biased direction and degree of sexual size dimorphism. In both sexes, the presence of human food in the diet increased the asymptotic body weight from the estimate for bears consuming a natural diet, but differences were insignificant. Females consuming human food had a slightly younger age at maximum growth and continued growth in body weight for a somewhat longer duration than did conspecifics that consumed a natural diet. In contrast, males that consumed human food had a slightly older age at maximum growth and decreased body weight growth somewhat earlier than did conspecifics consuming a natural diet. Florida black bears exhibited a larger asymptotic body size, faster growth rate, and younger age at maximum growth and maturity when compared with conspecifics in other mainland populations. Recognition of Florida black bear growth rate and adult body size provides wildlife managers a foundation for implementing measurable criteria to assess trends in population health.


1999 ◽  
Vol 77 (2) ◽  
pp. 278-289 ◽  
Author(s):  
Gary C Packard ◽  
Kirk Miller ◽  
Mary J Packard ◽  
Geoffrey F Birchard

We performed an experiment at a field site in north-central Nebraska, U.S.A., to assess the importance of the nest environment as a determinant of body size and condition in hatchling snapping turtles (Chelydra serpentina). The contents of newly constructed nests were manipulated by reciprocal transplant so that each of several nests received a complement of eggs from each of several females. The eggs were recovered from nests after 8 weeks and allowed to complete incubation under standard conditions in the laboratory. Live mass, dry mass and water content of carcasses, and dry mass of unused yolk varied significantly among hatchlings that incubated in different nests. This variation apparently resulted from variation in water exchange by eggs, because embryos in eggs that absorbed water during 8 weeks in the field consumed more of their yolk, grew to a larger size, and were better hydrated at hatching than embryos in eggs that lost water to the nest environment. Phenotypic variation of the magnitude observed in this investigation may affect survival of hatchlings, and therefore needs to be considered explicitly in theories for the evolution of life histories in these long-lived animals.


1998 ◽  
Vol 201 (3) ◽  
pp. 439-449
Author(s):  
S O'Steen

Snapping turtles (Chelydra serpentina) demonstrate temperature-dependent sex determination (TSD): intermediate egg incubation temperatures (23-27 degreesC) produce males, while extreme temperatures produce females. Snapping turtles are also sexually dimorphic: adult males are typically larger than females. Previous researchers hypothesized that male-producing egg temperatures enhanced the growth rate of juvenile turtles, resulting in the adult dimorphism and potentially providing an adaptive benefit for TSD. In reptiles, the choice of ambient temperature can also influence growth. I measured the effect of egg incubation temperature on juvenile growth rate and water temperature choice of C. serpentina. Eggs were incubated in the laboratory at 21.5, 24.5, 27.5 or 30.5 degreesC to produce both sexes, all males, both sexes or all females, respectively. Egg temperature was linearly and negatively correlated with growth rate of both male and female juveniles. Thus, growth was enhanced, but not maximized, by male-producing egg temperatures. Egg temperature was also negatively correlated with juvenile temperature choice such that, on average, turtles from 21.5 degreesC eggs selected 28 degreesC water, while turtles from 30.5 degreesC eggs chose 24.5 degreesC water. Additionally, these temperature choices were highly repeatable, even following a 6 month hibernation period at 7 degreesC. Thus, while male egg temperatures do not directly maximize growth, multiple effects of embryonic temperature may combine to create long-lasting differences in the behavioral physiology of male and female C. serpentina. Such differences could be important to the ecology and evolution of TSD.


Copeia ◽  
2002 ◽  
Vol 2002 (2) ◽  
pp. 504-510 ◽  
Author(s):  
Michael S. Finkler ◽  
Justin T. Bowen ◽  
Theresa M. Christman ◽  
Angela D. Renshaw

1999 ◽  
Vol 77 (2) ◽  
pp. 278-289 ◽  
Author(s):  
Gary C. Packard ◽  
Kirk Miller ◽  
Mary J. Packard ◽  
Geoffrey F. Birchard

Animals ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 2053
Author(s):  
Junsong Shi ◽  
Baohua Tan ◽  
Lvhua Luo ◽  
Zicong Li ◽  
Linjun Hong ◽  
...  

How to maximize the use of the genetic merits of the high-ranking boars (also called superior ones) is a considerable question in the pig breeding industry, considering the money and time spent on selection. Somatic cell nuclear transfer (SCNT) is one of the potential ways to answer the question, which can be applied to produce clones with genetic resources of superior boar for the production of commercial pigs. For practical application, it is essential to investigate whether the clones and their progeny keep behaving better than the “normal boars”, considering that in vitro culture and transfer manipulation would cause a series of harmful effects to the development of clones. In this study, 59,061 cloned embryos were transferred into 250 recipient sows to produce the clones of superior Pietrain boars. The growth performance of 12 clones and 36 non-clones and the semen quality of 19 clones and 28 non-clones were compared. The reproductive performance of 21 clones and 25 non-clones were also tested. Furthermore, we made a comparison in the growth performance between 466 progeny of the clones and 822 progeny of the non-clones. Our results showed that no significant difference in semen quality and reproductive performance was observed between the clones and the non-clones, although the clones grew slower and exhibited smaller body size than the non-clones. The F1 progeny of the clones showed a greater growth rate than the non-clones. Our results demonstrated through the large animal population showed that SCNT manipulation resulted in a low growth rate and small body size, but the clones could normally produce F1 progeny with excellent growth traits to bring more economic benefits. Therefore, SCNT could be effective in enlarging the merit genetics of the superior boars and increasing the economic benefits in pig reproduction and breeding.


2001 ◽  
Vol 35 (3) ◽  
pp. 514 ◽  
Author(s):  
Paul A. Sims ◽  
Gary C. Packard ◽  
Philip L. Chapman

2013 ◽  
Vol 142 (5) ◽  
pp. 1406-1414 ◽  
Author(s):  
Ian A. Tattam ◽  
James R. Ruzycki ◽  
Hiram W. Li ◽  
Guillermo R. Giannico
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