scholarly journals Calcium isotopic patterns in enamel reflect different nursing behaviors among South African early hominins

2019 ◽  
Vol 5 (8) ◽  
pp. eaax3250 ◽  
Author(s):  
Théo Tacail ◽  
Jeremy E. Martin ◽  
Florent Arnaud-Godet ◽  
J. Francis Thackeray ◽  
Thure E. Cerling ◽  
...  
Keyword(s):  
Breast Milk ◽  
South African ◽  
Early Life ◽  
Tooth Enamel ◽  
Biological Evolution ◽  
Milk Consumption ◽  
Interbirth Interval ◽  
Australopithecus Africanus ◽  
The Social ◽  
Life Behavior

Nursing is pivotal in the social and biological evolution of hominins, but to date, early-life behavior among hominin lineages is a matter of debate. The calcium isotopic compositions (δ44/42Ca) of tooth enamel can provide dietary information on this period. Here, we measure the δ44/42Ca values in spatially located microsized regions in tooth enamel of 37 South African hominins to reconstruct early-life dietary-specific variability in Australopithecus africanus, Paranthropus robustus, and early Homo. Very low δ44/42Ca values (<−1.4‰), indicative of milk consumption, are measured in early Homo but not in A. africanus and P. robustus. In these latter taxa, transitional or adult nonmilk foods must have been provided in substantial quantities relative to breast milk rapidly after birth. The results suggest that early Homo have continued a predominantly breast milk–based nursing period for longer than A. africanus and P. robustus and have consequently more prolonged interbirth interval.

scholarly journals The energy allocation trade-offs underlying life history traits in hypometabolic strepsirhines and other primates

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Bruno Simmen ◽  
Luca Morino ◽  
Stéphane Blanc ◽  
Cécile Garcia
Keyword(s):  
Life History ◽  
Energy Expenditure ◽  
Body Mass ◽  
Life History Traits ◽  
Brain Size ◽  
Energy Allocation ◽  
Interbirth Interval ◽  
Energy Investment ◽  
Litter Mass ◽  
Trade Offs

AbstractLife history, brain size and energy expenditure scale with body mass in mammals but there is little conclusive evidence for a correlated evolution between life history and energy expenditure (either basal/resting or daily) independent of body mass. We addressed this question by examining the relationship between primate free-living daily energy expenditure (DEE) measured by doubly labeled water method (n = 18 species), life history variables (maximum lifespan, gestation and lactation duration, interbirth interval, litter mass, age at first reproduction), resting metabolic rate (RMR) and brain size. We also analyzed whether the hypometabolic primates of Madagascar (lemurs) make distinct energy allocation tradeoffs compared to other primates (monkeys and apes) with different life history traits and ecological constraints. None of the life-history traits correlated with DEE after controlling for body mass and phylogeny. In contrast, a regression model showed that DEE increased with increasing RMR and decreasing reproductive output (i.e., litter mass/interbirth interval) independent of body mass. Despite their low RMR and smaller brains, lemurs had an average DEE remarkably similar to that of haplorhines. The data suggest that lemurs have evolved energy strategies that maximize energy investment to survive in the unusually harsh and unpredictable environments of Madagascar at the expense of reproduction.

Weaning and Parent-offspring Conflict: Variation Relative to Interbirth Interval in Bison

Ethology ◽  
2010 ◽  
Vol 95 (2) ◽  
pp. 105-125 ◽  
Author(s):  
Wendy C. H. Green ◽  
Aron Rothstein ◽  
Joseph G. Griswold
Keyword(s):  
Interbirth Interval

Estimating hominid life history: the critical interbirth interval

2018 ◽  
Vol 60 (1-2) ◽  
pp. 127-142 ◽  
Author(s):  
Wataru Nakahashi ◽  
Shiro Horiuchi ◽  
Yasuo Ihara
Keyword(s):  
Life History ◽  
Interbirth Interval

Long-term data on the reproduction and maintenance of a colony of common marmosets (Callithrix jacchus jacchus) 1972-1983

1987 ◽  
Vol 21 (3) ◽  
pp. 249-260 ◽  
Author(s):  
H. O. Box ◽  
R. C. Hubrecht
Keyword(s):  
Perinatal Mortality ◽  
Callithrix Jacchus ◽  
Interbirth Interval ◽  
Common Marmosets ◽  
Interbirth Intervals ◽  
Additional Information ◽  
In Captivity ◽  
Term Data ◽  
Callithrix Jacchus Jacchus

We have used our laboratory records to compare data on the reproduction and maintenance of common marmosets in different colonies and to provide additional information on the species in captivity. Data are presented for a period of 12 years. This was long enough to allow information on longevity, mortality, aggression and incest. In addition 543 infants were born from a total of 202 births. No seasonality was found and the highest proportion of births overall was that of triplets. A significantly greater proportion of males was born, but perinatal mortality reduced this to a proportion of 52·2% surviving males. The interbirth interval for all normal births ranged from 145 to 382 days, with a median of 158 days. There was no evidence that interbirth intervals increased with age. The proportion of non-breeding pairs was small (4 out of 28) and progesterone assays showed that these females were ovulating.

Evaluation of Various IVC Systems According to Mouse Reproductive Performance and Husbandry and Environmental Parameters

2022 ◽  
Author(s):  
Mitchel G Stover ◽  
Jason S Villano
Keyword(s):  
Relative Humidity ◽  
Reproductive Performance ◽  
Environmental Parameters ◽  
Scoring Systems ◽  
Interbirth Interval ◽  
Noise Levels ◽  
Total Particulate Matter ◽  
Male And Female ◽  
Health Checks ◽  
Breeding Cycles

IVC systems are marketed for improving the health and management of mouse colonies. The current study compared mouse reproductive performance and husbandry and environmental parameters among 3 high-density (HD) IVC rack systems (RS1, RS2, and RS3), which were present in separate but comparable rooms. Three breeding trios each of Swiss Webster (CFW) and BALB/c mice were placed in each rack (n = 36 female, n = 18 male). Reproductive indices were measured for 3 breeding cycles over 2 generations; indices included time to parturition, litter size and pup weight, survivability, and interbirth interval. Over 18 wk, personnel used scoring systems to evaluate each RS daily to every other week according to cage dirtiness, need for spot changing, ease of cage changing, daily health checks, and cage wash processing. Macroenvironmental parameters (temperature, relative humidity, noise, total particulate matter) were measured weekly over 14 wks. Microenvironmental parameters (temperature, relative humidity, NH3, CO2, O2) of 2 cages each of male and female CFW mice (4 mice/cage) on each RS were measured at 6 time points over 2 wks. RS1 had significantly smaller mean litter sizes of CFW mice (mean ± 1 SD, 6.5 ± 2.9 pups) as compared with both RS2 (9.5 ± 1.7 pups) and RS3 (9.3 ± 3.8 pups). RS1 scored as beingsignificantly easier to process through the cage wash. RS2 had significantly lower room noise levels (46.0 ± 5.0 dBA) but higher humidity (58.6% ± 8.9%) as compared with both RS1 (43.7% ± 9.9%) and RS3 (46.0% ± 12.0%) over the 2-wk cycle, particularly at 8 and 12 d after cage change. In conclusion, in terms of mouse reproductive performance and husbandry and environmental parameters, each system had at least 1 advantage over the other 2. Therefore, various factors should be considered when choosing an IVC system for mice.

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