scholarly journals Sex-specific covariance between metabolic rate, behaviour and morphology in the ground beetle Carabus hortensis

PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e12455
Author(s):  
Elisabeth Yarwood ◽  
Claudia Drees ◽  
Jeremy E. Niven ◽  
Wiebke Schuett

Background Individuals within the same species often differ in their metabolic rates, which may covary with behavioural traits (such as exploration), that are consistent across time and/or contexts, and morphological traits. Yet, despite the frequent occurrence of sexual dimorphisms in morphology and behaviour, few studies have assessed whether and how sexes differ in metabolic trait covariances. Methods We investigated sex-specific relationships among resting or active metabolic rate (RMR and AMR, respectively) with exploratory behaviour, measured independently of metabolic rate in a novel environment, body size and body mass, in Carabus hortensis ground beetles. Results RMR, AMR and exploratory behaviour were repeatable among individuals across time, except for male RMR which was unrepeatable. Female RMR neither correlated with exploratory behaviour nor body size/body mass. In contrast, AMR was correlated with both body size and exploratory behaviour. Males with larger body sizes had higher AMR, whereas females with larger body sizes had lower AMR. Both male and female AMR were significantly related to exploratory behaviour, though the relationships between AMR and exploration were body mass-dependent in males and temperature-dependent in females. Discussion Differences between sexes exist in the covariances between metabolic rate, body size and exploratory behaviour. This suggests that selection acts differently on males and females to produce these trait covariances with potentially important consequences for individual fitness.

2019 ◽  
Vol 76 (2) ◽  
pp. 185-191 ◽  
Author(s):  
Emily Y. Campbell ◽  
Jason B. Dunham ◽  
Gordon H. Reeves ◽  
Steve M. Wondzell

Phenology can be linked to individual fitness, particularly in strongly seasonal environments where the timing of events has important consequences for growth, condition, and survival. We studied the phenology of coho salmon (Oncorhynchus kisutch) hatching and emergence in streams with contrasting thermal variability but in close geographic proximity. Following emergence, we tracked body sizes of cohorts of young-of-year fish until the end of the growing season. Hatch and emergence occurred at the same time among streams with marked variability in thermal regimes. We demonstrate that this can be explained in part by the thermal units accumulated during embryo development. At the end of the first growing season, there were some differences in body size, but overall fish size was similar among streams despite strong differences in thermal regimes. Collectively, these results provide novel insights into the interactions between environmental variability and the early life-history stages of coho salmon, furthering our understanding of the consequences of phenology on growth and survival for individuals within the critical first summer of life.


2019 ◽  
Vol 45 (4) ◽  
pp. 306-334 ◽  
Author(s):  
Pieternel Dijkstra ◽  
Odette Van Brummen-Girigori ◽  
Dick P. H. Barelds

Based on the assumptions of self-discrepancy theory, the present study examined the degree of overweight, weight-related body images, and the relation between these images and body mass index (BMI) among two samples of young people from Curaçao (secondary school students, n = 176; undergraduate students, n = 205). In addition to BMI, participants reported their current, ideal, and most feared body sizes, the thinnest and largest body sizes still acceptable to them, and the body size they considered the healthiest by means of the Contour Drawing Rating Scale. We expected females to show a larger discrepancy between current and ideal body size than males (Hypothesis 1) and that this discrepancy (as an indicator of body dissatisfaction) would be related more strongly to BMI among females than among males (Hypothesis 2). Results yielded support for Hypothesis 1 among secondary school students only. Only in the undergraduate sample, BMI and body dissatisfaction were related, but equally so for males and females. Possible explanations are discussed as well as implications for weight management interventions.


PLoS ONE ◽  
2021 ◽  
Vol 16 (11) ◽  
pp. e0260037
Author(s):  
Henrik H. Berntsen ◽  
Claus Bech

In birds, incubation temperature has received increased attention as an important source of phenotypic variability in offspring. A lower than optimal incubation temperature may negatively affect aspects of nestling physiology, such as body growth and energy metabolism. However, the long-term effects of sub-optimal incubation temperature on morphology and physiology are not well understood. In a previous study, we showed that zebra finches from eggs incubated at a low temperature (35.9°C) for 2/3 of the total incubation time suffered a lower post-fledging survival compared to individuals that had been incubated at higher temperatures (37.0 and 37.9°C). In the present study, we investigated whether these variations in incubation temperature could cause permanent long-lasting differences in body mass, body size, or basal metabolic rate. Furthermore, we tested whether the observed differences in survival between treatment groups would be reflected in the rate of physiological deterioration, assessed through oxidative damage and decreased metabolic rate with age (i.e. ‘metabolic aging’). Incubation temperature did not significantly affect embryonic or nestling body growth and did not influence final adult body mass or body size. Nor was there any long-term effect on basal metabolic rate. Birds from eggs incubated at the lowest temperature experienced an accumulation of oxidative damage with age, although this was not accompanied by an accelerated rate of metabolic aging. The present results suggest that the low survival in these birds was possibly mediated by increased oxidative stress, but independent of body growth and the basal metabolic rate.


2014 ◽  
Author(s):  
James F Gillooly

The tremendous variation in brain size among vertebrates has long been thought to be related to differences in species’ metabolic rates. Species with higher metabolic rates can supply more energy to support the relatively high cost of brain tissue. And yet, while body temperature is known to be a major determinant of metabolic rate, the possible effects of temperature on brain size have scarcely been explored. Thus, here I explore the effects of temperature on brain size among diverse vertebrates (fishes,amphibians, reptiles, birds and mammals). I find that, after controlling for body size,brain size increases exponentially with temperature in much the same way asmetabolic rate. These results suggest that temperature-dependent changes in aerobic capacity, which have long been known to affect physical performance, similarly affect brain size. The observed temperature-dependence of brain size may explain observed gradients in brain size among both ectotherms and endotherms across broad spatial and temporal scales.


2018 ◽  
Vol 92 (5) ◽  
pp. 896-910
Author(s):  
Craig S. Scott ◽  
Anne Weil ◽  
Jessica M. Theodor

AbstractMultituberculates were among the most taxonomically diverse mammals of the early Paleocene, having survived the catastrophic Cretaceous-Paleogene mass extinction and radiating soon thereafter. Although their evolution during the early Paleocene saw the advent of increasingly specialized dentitions, multituberculates generally remained small, rarely exceeding body sizes greater than those of extant rabbits. A conspicuous exception is the Taeniolabidoidea, a primarily North American clade whose members include the largest multituberculates yet discovered. Taeniolabidoidea includes several genera, with one of these,Catopsalis, being speciose and geographically wide ranging. Until recently, the chronological succession ofCatopsalisappeared to document a trend of increasing body size. We report here on a new species ofCatopsalisfrom the early Paleocene of Alberta that violates this trend and suggests that the evolutionary history ofCatopsalisis considerably more complex.Catopsalis kakwanew species is not only the smallest species ofCatopsalis, but is the smallest taeniolabidoid so far discovered, with an estimated body mass between 400 g and 660 g. In contrast to previous studies, we used recently proposed regressions based on lower cheek tooth row length to estimate body masses for North American taeniolabidoids. Our results propose more modest body mass estimates, particularly for the largest taeniolabidoids. The occurrence ofC.kakwan. sp. in the late early Paleocene implies either a significant ghost lineage, or reversal of several characters, including body size, during the latter part of the early Paleocene; the more likely of these scenarios must await a better understanding of the phylogenetic position ofC.kakwan. sp.UUID:http://zoobank.org/66d85345-49b8-4a46-ba6e-a4d4369cb3e0urn:lsid:zoobank.org:pub:AF7A5659-9068-4F2F-A6EC-5522A2BBA4CB


Paleobiology ◽  
1986 ◽  
Vol 12 (4) ◽  
pp. 355-369 ◽  
Author(s):  
Bruce J. MacFadden

The evolution of body size in fossil horses is frequently depicted as a gradual, progressive trend toward increased body size (Cope's Law). Body size (actually body mass) was estimated for 40 species of fossil horses using dental and skeletal characters and regression equations derived from the same characters in extant species of Equus with known body mass. After body sizes were estimated, rates of morphological evolution, in darwins (d), were calculated between known ancestral and descendant fossil horse species. For the first half of horse evolution (from ca. 57 to 25 ma) body mass remained relatively static between about 25 and 50 kg with very slow evolutionary rates of 0.003–0.04 d. During the early–middle Miocene (from ca. 25 to 10 ma) there was a major diversification of body mass to about 75–400 kg and consistently higher evolutionary rates between 0.04 and 0.24 d. Since the late Miocene, body mass has generally increased with a maximum seen (in natural populations) in Equus scotti (ca. 500 kg) during the middle Pleistocene. Therefore, for horses, the traditional interpretation of gradual increase in body size through time is oversimplified because: (1) although the exception to the rule, 5 of 24 species lineages studied are characterized by dwarfism; and (2) the general trend seems to have been a long period (32 ma) of relative stasis followed by 25 ma of diversification and progressive (although not necessarily gradual) change in body size.


Paleobiology ◽  
2008 ◽  
Vol 34 (4) ◽  
pp. 553-562 ◽  
Author(s):  
John A. Finarelli

Body mass is an important organism-level variable in mammalian biology, correlated with physiology, life history, and ecology. To analyze the dynamics of body size evolution, increases and decreases in body mass were tallied for ancestor-descendant (AD) species pairs for 519 terrestrial caniform taxa. To account for uncertainty phylogeny, a bootstrapping routine shuffled hypothesized AD pairs, and average proportions of increases were binned as a function of ancestral body mass. A set of models relating the rate of body size increase were evaluated with the Akaike Information Criterion (AIC). AIC selected three models of the candidate set as equivalent in support by the observed body mass data. These three models propose body size increase for small AD pairs and body size decrease for large AD pairs, although they differ in their treatment of taxa at intermediate sizes.These results demonstrate the presence of constraints bounding the caniform distribution at large and small body sizes, stabilizing the distribution through time, which stands in contrast to a broader mammalian pattern. At a finer phylogenetic scale, subclades within intermediate size classes display proportions that are significantly different from unbiased, with several clades previously cited as examples of “Cope's Rule” showing biased increases in size, and basal mustelids (badgers, and allied genera), Mephitidae (skunks), and Vulpini (“foxes”) exhibiting biased decreases. The caniform pattern is therefore the result of superimposed, clade-specific trajectories, demonstrating that the inferred dynamics of body size evolution and even the direction of trends in body size evolution within the Caniformia, and for mammals in general, depend on the hierarchical scale of the analysis.


2015 ◽  
Vol 22 (7) ◽  
pp. 878-883 ◽  
Author(s):  
AK Hedström ◽  
T Olsson ◽  
L Alfredsson

Objective: Obesity in childhood and during adolescence has repeatedly been associated with increased risk of developing multiple sclerosis (MS). We aimed to investigate whether the most critical period occurs during childhood or later, during adolescence. Methods: Using a population-based case-control study (1586 cases and 2800 controls), individuals with different body sizes at age 10 and different body mass indices at age 20 were compared regarding MS risk, by calculating odds ratios with 95% confidence intervals. Potential interactions between HLA-DRB1*15 and absence of HLA-A*02, respectively, and both childhood and adolescent obesity were evaluated by calculating the attributable proportion due to interaction. Results: Regardless of body size at age 10, individuals with adolescent obesity had a 90% increased risk of MS. Among participants who were not obese at age 20, no association was observed between body size at age 10 and subsequent MS risk. An interaction was observed between the HLA MS risk genes and adolescent, but not childhood, obesity. Conclusions: Our results suggest that BMI during adolescence, rather than childhood, is critical in determining MS risk.


2014 ◽  
Author(s):  
James F Gillooly

The tremendous variation in brain size among vertebrates has long been thought to be related to differences in species’ metabolic rates. Species with higher metabolic rates can supply more energy to support the relatively high cost of brain tissue. And yet, while body temperature is known to be a major determinant of metabolic rate, the possible effects of temperature on brain size have scarcely been explored. Thus, here I explore the effects of temperature on brain size among diverse vertebrates (fishes,amphibians, reptiles, birds and mammals). I find that, after controlling for body size,brain size increases exponentially with temperature in much the same way asmetabolic rate. These results suggest that temperature-dependent changes in aerobic capacity, which have long been known to affect physical performance, similarly affect brain size. The observed temperature-dependence of brain size may explain observed gradients in brain size among both ectotherms and endotherms across broad spatial and temporal scales.


1996 ◽  
Vol 82 (2) ◽  
pp. 651-656 ◽  
Author(s):  
Kim Rolland ◽  
Douglas Farnill ◽  
Rosalyn A. Griffiths

244 Australian schoolchildren aged between 8 and 12 years indicated their current and ideal body sizes by means of Collins' pictorial figures. Children's height and weight were also measured. Body-mass indices were calculated from these data, and percentile ranks estimated according to international reference data. Consistent with Collins' findings, 39% of girls and 26% of boys wanted to be thinner than they perceived themselves to be; however, this desire was strongly related to actual body size so the percentages were very different for weight categories established on the basis of Body Mass Index. In the overweight quartile, 76% of girls and 56% of boys wanted to be thinner, whereas in the underweight quartile only 10% of girls and no boys wanted to be thinner. The response of overweight children may be sensible, but the desire of some underweight girls to be even thinner is of concern. Some recent literature suggests that underweight individuals tend to overestimate their body sizes. About a half of our underweight children slightly overestimated their body sizes but only one child overestimated grossly.


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