Some aspects of reproduction in a Lake Erie population of Blanding's turtle, Emydoidea blandingii

1988 ◽  
Vol 66 (10) ◽  
pp. 2317-2319 ◽  
Author(s):  
Ross D. MacCulloch ◽  
Wayne F. Weller
Keyword(s):  
Clutch Size ◽  
Lake Erie ◽  
Relative Mass ◽  
Egg Mass ◽  
Female Size ◽  
Regression Analyses ◽  
Emydoidea Blandingii ◽  
Blanding's Turtle ◽  
Clutch Mass ◽  
Blanding’S Turtle

A Lake Erie population of Emydoidea blandingii produced clutches of slightly greater relative mass than those of other emydids. Regression analyses showed that both clutch mass and relative clutch mass were significantly related to both female mass and female size, while clutch size was also related to female size. Mean egg mass was not related to either clutch size or female size.

scholarly journals The effects of climate on annual variation in reproductive output in Snapping Turtles (Chelydra serpentina)

2018 ◽  
Vol 96 (3) ◽  
pp. 221-228 ◽  
Author(s):  
A.R. Hedrick ◽  
H.M. Klondaris ◽  
L.C. Corichi ◽  
M.J. Dreslik ◽  
J.B. Iverson
Keyword(s):  
Climate Change ◽  
Clutch Size ◽  
Reproductive Output ◽  
Life History Traits ◽  
Annual Variation ◽  
Egg Mass ◽  
Female Size ◽  
Chelydra Serpentina ◽  
Snapping Turtles ◽  
Clutch Mass

Reptiles are highly dependent on climatic patterns to regulate their behavior and physiology, and studies of the effects of climate on the biology of organisms are increasingly important given expected climate change. Our study examined the effects of climate variation over 15 of the 26 years between 1990 and 2015 on the reproductive output of the Snapping Turtle (Chelydra serpentina (Linnaeus, 1758)). Egg mass, clutch size, and clutch mass (relative to body size) were significantly higher in years following warmer temperatures in September and October of the year before reproduction, but not related to temperatures in April and May just before reproduction. Of the above life-history traits, egg mass varied the least across years, and after warm autumns small turtles (225–285 mm carapace length) increased clutch mass by increasing clutch size but not egg mass. In contrast, under the same conditions, large turtles increased clutch mass by increasing egg mass but not clutch size. Our data suggest optimal egg mass may vary with female size. Climate change may already have impacted reproductive output in Snapping Turtles at the site because temperatures during September and October have increased about 0.5 °C each decade for the last 45 years.

Effects of a sudden increase in natural mortality of adults on a population of the common snapping turtle (Chelydra serpentina)

1991 ◽  
Vol 69 (5) ◽  
pp. 1314-1320 ◽  
Author(s):  
Ronald J. Brooks ◽  
Gregory P. Brown ◽  
David A. Galbraith
Keyword(s):  
Clutch Size ◽  
Research Area ◽  
Effective Density ◽  
Egg Mass ◽  
Sudden Increase ◽  
Chelydra Serpentina ◽  
Density Dependent ◽  
Snapping Turtles ◽  
The Mean ◽  
Clutch Mass

A northern population of snapping turtles (Chelydra serpentina) centred around Lake Sasajewun in the Wildlife Research Area in Algonquin Park, Ontario, has been studied and individually marked since 1972. From 1972 to 1985, annual mortality and survivorship of adult females had been estimated at 1 and 96.6%, respectively, and only six dead turtles were found. Lake Sasajewun's population of C. serpentina was estimated in 1978–1979 and 1984–1985 at 38 and 47 adults, respectively. From 1976 to 1987, total number of nests found in the study area remained fairly constant and there were no significant changes in mean clutch size, mean clutch mass, or mean egg mass. On the main nest site, recruitment from 1976 to 1987 was 1.15 (1.8%) new females per year. From 1987 to 1989, we found 34 dead adult snapping turtles in the Wildlife Research Area. Observations of freshly dead animals indicated that most were killed by otters (Lutra canadensis) during the turtles' winter hibernation. A few uninjured turtles also died of septicemia in early spring shortly after emerging from hibernation. The estimated number of adults in Lake Sasajewun was 31 in 1988–1989, and the minimum number of adult residents known to be alive in the lake dropped from 47 in 1986 to 16 in 1989. In 1986 and 1987, annual adult female survivorship was estimated at 80 and 55%, respectively, and estimated numbers of nesting females declined from 82 in 1986 to 71 and 55 in 1987 and 1988, respectively. The actual number of nests found declined by 38 and 20% over the same periods. Although no significant differences occurred in mean egg mass or mean clutch size between 1987 and 1989 and earlier years, the mean clutch mass in 1988 was larger than in 1977 or 1978. This difference appeared to be due to a gradual increase in the mean age and body size of breeding females rather than to density-dependent changes. Recruitment into the adult breeding female population in 1987–1989 remained less than two individuals per year. Hatchling survival and number of juveniles were low throughout the study. Our observations support the view that populations of species with high, stochastic juvenile mortality and long adult life spans may be decimated quickly by increased mortality of adult animals, particularly if numbers of juveniles and immigrants are low. Recovery of such populations should be very slow because of a lack of effective density-dependent response in reproduction and recruitment.

scholarly journals Emydoidea blandingii (Holbrook 1838) – Blanding’s Turtle

2008 ◽  
pp. 015.1-015.12 ◽  
Author(s):  
Justin Congdon ◽  
Terry Graham ◽  
Tom Herman ◽  
Jeffrey Lang
Keyword(s):  
Emydoidea Blandingii ◽  
Blanding's Turtle ◽  
Blanding’S Turtle

Clutch Mass, Offspring Mass, and Clutch Size: Body Mass Scaling and Taxonomic and Environmental Variation

2018 ◽  
pp. 68-97
Author(s):  
Douglas S. Glazier
Keyword(s):  
Life History ◽  
Body Size ◽  
Clutch Size ◽  
Body Mass ◽  
Life History Evolution ◽  
Offspring Size ◽  
Egg Mass ◽  
Mass Scaling ◽  
Scaling Relationships ◽  
Clutch Mass

In this chapter, I show how clutch mass, offspring (egg) mass, and clutch size relate to body mass among species of branchiopod, maxillipod, and malacostracan crustaceans, as well as how these important life history traits vary among major taxa and environments independently of body size. Clutch mass relates strongly and nearly isometrically to body mass, probably because of physical volumetric constraints. By contrast, egg mass and clutch size relate more weakly and curvilinearly to body mass and vary in inverse proportion to one another, thus indicating a fundamental trade-off, which occurs within many crustacean taxa as well. In general, offspring (egg) size and number and their relationships to body mass appear to be more ecologically sensitive and evolutionarily malleable than clutch mass. The body mass scaling relationships of egg mass and clutch size show much more taxonomic and ecological variation (log-log scaling slopes varying from near 0 to almost 1 among major taxa) than do those for clutch mass, a pattern also observed in other animal taxa. The curvilinear body mass scaling relationships of egg mass and number also suggest a significant, size-related shift in how natural selection affects offspring versus maternal fitness. As body size increases, selection apparently predominantly favors increases in offspring size and fitness up to an asymptote, beyond which increases in offspring number and thus maternal fitness are preferentially favored. Crustaceans not only offer excellent opportunities for furthering our general understanding of life history evolution, but also their ecological and economic importance warrants further study of the various factors affecting their reproductive success.

Annual variations in reproductive characteristics of painted turtles (Chrysemys picta)

1986 ◽  
Vol 64 (5) ◽  
pp. 1148-1151 ◽  
Author(s):  
Lin Schwarzkopf ◽  
Ronald J. Brooks
Keyword(s):  
Body Size ◽  
Clutch Size ◽  
Repeated Measures ◽  
Egg Size ◽  
Annual Variation ◽  
Egg Mass ◽  
Annual Variations ◽  
Painted Turtles ◽  
Sources Of Variation ◽  
Clutch Mass

In Algonquin Park, Ontario, body size and clutch characteristics were recorded for 51 female painted turtles (Chrysemyspicta) in 1983, 61 in 1984, and 24 in 1985. Clutch size, clutch mass, and egg width correlated significantly with body size (carapace length) in all 3 years. Egg length and egg mass were significantly related to body size in 1984 and 1985, but not in 1983. There were no significant correlations of egg width or egg mass to clutch size. For a group of the same individuals compared by repeated-measures ANOVA, mean clutch mass and mean egg size, but not mean clutch size, varied significantly among years. Correlation of egg size with body size, lack of correlation between egg size and clutch size, and annual variation in egg size, but not clutch size, all fail to support current versions of optimal egg size theory. Twenty-six females nested in both 1983 and 1984 and 11 females nested in both 1984 and 1985. Fourteen females nested twice in 1 year: six in 1983 and eight in 1984. Between 43 and 73% of adult females nested in a given year and 12–13% nested twice in a single season. These estimates are similar to those reported for other populations of this species. It appears that variations in both clutch size (frequency) and egg size are important sources of variation in reproductive output.

Body size, age distribution, and reproduction in a northern population of wood turtles (Clemmys insculpta)

1992 ◽  
Vol 70 (3) ◽  
pp. 462-469 ◽  
Author(s):  
Ronald J. Brooks ◽  
Cathy M. Shilton ◽  
Gregory P. Brown ◽  
Norman W. S. Quinn
Keyword(s):  
Body Size ◽  
Clutch Size ◽  
Partial Correlation ◽  
Age Distribution ◽  
Egg Mass ◽  
Female Size ◽  
After Effects ◽  
Mean Width ◽  
Wood Turtles ◽  
Provincial Park

A population of the wood turtle (Clemmys insculpta) was studied on the east side of Algonquin Provincial Park, Ontario, from 1987 to 1990. A total of 77 adults (56 females, 21 males) and 13 juveniles were captured, measured, and individually marked. Age at maturity was 17–18 years at a minimum carapace length of 185 mm for females and 199 mm for males. Our data supported the hypothesis that turtles in northern populations are larger and older at maturity than are those in southern populations. For 21 nests, mean clutch size was 8.8 eggs and egg mass was 96 g. Predators destroyed 15 of 17 nests in 1990, and had injured 60% of adult turtles observed. Therefore, our population had low recruitment, few juveniles, and high levels of predation on nests and adults. Comparisons among females refuted two predictions from optimal egg size theory. Mean width and mass, but not length, of eggs correlated positively with female size, and correlated positively with clutch size, even after effects of body size were removed by partial correlation. However, smaller females in the population had relatively longer eggs than did larger females, whereas the Algonquin females have absolutely smaller eggs than do much smaller females in a New Jersey population.

Population size and spatial ecology of Blanding’s Turtle (Emydoidea blandingii) in South March Highlands, Ottawa, Ontario, Canada

2015 ◽  
Vol 93 (7) ◽  
pp. 509-514 ◽  
Author(s):  
Caleb T. Hasler ◽  
Kevin Robinson ◽  
Nick Stow ◽  
Shawn R. Taylor
Keyword(s):  
Population Size ◽  
Spatial Ecology ◽  
Road Construction ◽  
Home Range Size ◽  
Adult Males ◽  
Emydoidea Blandingii ◽  
Blanding's Turtle ◽  
The Road ◽  
Gravid Females ◽  
Blanding’S Turtle

Between 2010 and 2011, an arterial road was constructed within provincially significant wetlands in the South March Highlands (SMH) located in Ottawa, Ontario, Canada. The wetlands and adjacent upland areas were determined to be sensitive habitat for Blanding’s Turtles (Emydoidea blandingii (Holbrook, 1838)) during the approval and permitting process, and a population study was required as part of the road construction project. The study consisted of a 4-year mark–recapture program and a movement study of radio-tagged adult turtles. General findings included the identification of 27 adult males and 55 females and a population estimate of 93 adults (95% Cl: 86–118). A 1:2.32 male to female sex bias was also found. Mean home-range size was 19.06 ha and tagged turtles moved, on average, more per observation in 2013 (191.40 m compared with 89.75 and 123.04 m in 2011 and 2012, respectively). Previously reported differences in movement patterns between males, females, and gravid females were not observed. The SMH Blanding’s Turtle population should be closely monitored because urban development continues in the area, which may further reduce the population size. Understanding the biology of imperiled populations across species’ ranges is necessary to promote conservation and adaptive wildlife management.

scholarly journals Reproductive traits of the gray ratsnake Ptyas korros from three geographically distinct populations

2012 ◽  
Vol 58 (6) ◽  
pp. 820-827 ◽  
Author(s):  
Long-Hui Lin ◽  
Fei Mao ◽  
Ce Chen ◽  
Xiang Ji
Keyword(s):  
Clutch Size ◽  
Egg Size ◽  
Reproductive Output ◽  
Reproductive Traits ◽  
Egg Laying ◽  
Laying Date ◽  
Egg Mass ◽  
Size Number ◽  
Female Reproductive Traits ◽  
Clutch Mass

Abstract We collected gravid gray rat snakes Ptyas korros from three geographically distinct populations in China, Chenzhou (CZ), Jiangshan (JS) and Dinghai (DH), to study geographical variation in female reproductive traits. Egg-laying dates differed among the three populations such that at the most northern latitude egg-laying was latest, and earliest at the most southern lati-tutde. Clutch size, clutch mass, egg mass, egg shape, within clutch variability in egg sizes and relative clutch mass differed among the three populations, whereas post-oviposition body mass did not. Except for egg-laying date, none of the traits examined varied in a geographically continuous trend. CZ and DH females, although separated by a distance of approximately 1100 km as the crow flies, were similar in nearly all traits examined. JS females were distinguished from CZ and DH females by their higher fecundity (clutch size), greater reproductive output (clutch mass) and more rounded eggs. Our data do not validate the prediction that larger offspring should be produced in colder localities. The absence of an egg size-number trade-off in each of the three populations presumably suggests that P. korros is among species where eggs are well optimized for size within a population.

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