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Body Sizes of Animal Predators and Animal Prey in Food Webs

Wiley
Journal of Animal Ecology
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Abstract

In c90% of the feeding links among the animal species with known sizes, a larger predator consumes a smaller prey. Larger predators eat prey with a wider range of body sizes than do smaller predators. The geometric mean predator size increases with the size of prey. The increase in geometric mean predator size is less than proportional to the increase in prey size (ie has a slope less than one on log-log coordinates). The geometric mean sizes of prey and predators increase as the habitat of webs changes from aquatic to terrestrial to coastal to marine. Within each type of habitat, mean prey sizes are always less than mean predator sizes, and prey and predator sizes are always positively correlated. Feeding relations order the metabolic types of organisms from invertebrate to vertebrate ectotherm to vertebrate endotherm. Organisms commonly eat other organisms with the same or lower metabolic type, but (with very rare exceptions) organisms do not eat other organisms with a higher metabolic type. Mean sizes of prey increase as the metabolic type of prey changes from the invertebrate to vertebrate ectotherm to vertebrate endotherm, but the same does not hold true for predators. Prey and predator sizes are positively correlated in links from invertebrate prey to invertebrate predators. In links with other combinations of prey and predator metabolic types, the correlation between prey and predator body sizes is rarely large when it is positive, and in some cases is even negative. Species sizes are roughly log-normally distributed. Body size offers a good interpretation of the ordering of animal species assumed in the cascade model, a stochastic model of food web structure. When body size is taken as the physical interpretation of the ordering assumed in the cascade model, and when the body sizes of different animal species are taken as log-normally distributed, many of the empirical findings can be explained in terms of the cascade model. -from Authors
... A simple reasoning explains that small animals can be predated by larger predators. Oppositely, the number of small predators with the capacity to attack bigger prey must necessarily be lower [118,[172][173][174][175][176][177][178][179][180]. ...
... Although predators tend to select smaller prey, smaller prey also occasionally dare to attack big predators. However" when the difference begins to increase, the prey starts to leave the range of optimal prey [178][179][180][181]. This may be the case of adult elephants weighing over 1000 kg-megaherbivores-in which the in the Zoo setting-with presumable low predatory risk (but also with minimal needs of time for foraging)-the sleeping time is 4.0-6.5 h per night. ...
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Simple Summary Many authors have stated that sleep detracts time used for foraging, defense, and anti-predatory activities. Therefore, sleep must provide some compensating advantage. Instead, we show that the sleep-related reductions in food intake and reproductive activities may be in fact benefits, both for the individual and the species. Furthermore, we show that the optimal prey are the immature, weak, sick, and senescent animals and rarely the sleeping individuals. Indeed, the reduced amounts of sleeping time observed in prey animals occurs not because of an antipredation evolutionary pressure, but mostly because of the need for time to eat and digest the high-cellulose contents of the herbivores’ diet, a set of tasks that leaves reduced time to sleep. In summary, no animal restrains their vital activities for sleeping, and this means that the need for sleep is low on the list of the vital activities. In fact, sleeping basically consists of doing nothing, and no live being can die from insomnia. Instead, what is important is maintaining efficient wakefulness, which can be achieved only after a sufficient amount of sleep.
... This result may suggest that S. semistriatus and S. planiusculus, the smallest species we studied, feed on smaller prey than M. brunneus or M. striola. Both species of Margarinotus may have a wider prey range-larger predators eat prey with a larger range of body sizes than smaller predators (Cohen et al. 1993). Differences in the body size of predators may reduce their competition for food and enable their co-occurrence. ...
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Clown beetles (Histeridae) are stable components of carrion communities, but their prey range is poorly recognised. An indirect way to deduce species' diet is to study the functional morphology of their mandibles. The use of a multimodal approach in the study of Margarinotus brunneus, Margarinotus striola succicola, Saprinus semistriatus, and Saprinus planiusculus revealed a hidden morphological diversity in their mandibles. Geometric morphometric analysis showed inter-and sex-specific differences in their shape. Synchrotron X-ray microtomography revealed variability in musculature between genera and the presence of a joint-like structure at the basal margins in the Saprinus species. Scanning electron microscopy showed variation in the surface of inner margins. Traditional morphometrics revealed differences in mandibular arc according to beetle species, sex, and left and right body sides. All species retained a roughly 17° asymmetry, with the right mandible always having the higher arc. We conclude that Saprinus species are adapted for cutting and puncturing soft-bodied prey, whereas Margarinotus beetles also feed on hard-bodied prey. Future studies should consider our findings for better planning of prey-choice experiments. Emphasis should be placed on recognising whether subtle differences in mandible shape involve differences in diets. This will be critical to determine the role of species in carrion ecosystems.
... Additionally, individuals from medium and high trophic levels of the Ariidae family presented greater consumption of microplastics than low levels. These results are in Fig. 4 Variations in the condition factor according to their microplastic intake in species of the Ariidae and Sciaenidae families from the Colombian Pacific accordance with what was found in the Liaohe estuary in China, where MP consumption was greater in individuals of higher trophic levels, such as fish, compared to mollusks, crustaceans, and worms (Wang et al. 2021), suggesting a greater presence of microplastics in individuals of higher trophic levels due to bioaccumulation and trophic transfer (Cohen et al. 1993;Jonsson et al. 2005;Bhutto et al. 2023). ...
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... Size-dependent predation is a well-established theory for aboveground animals. It states that the size of the predators has implications for the size of their prey (Cohen et al., 1993). Most of the smaller predators prefer smaller prey, because of their mouth opening size (Hambright, 1991). ...
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... Predator assemblages are often size-structured, with larger predators preferentially targeting larger prey and smaller predators being restricted to smaller prey (Cohen et al. 1993;Singer et al. 2017). This size structuring not only facilitates prey partitioning but also promotes sizedependent intraguild predation (e.g., Sinclair et al. 2003). ...
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... Stable isotope analysis offers a more integrated picture (Jackson et al. 2011;Newsome et al. 2007) but, can be uncertain for generalist or omnivorous consumers (Davis et al. 2012). Additionally, analysing morphological parts, such as mouth width (Cohen et al. 1993;Wilson 1975) and intestine FIGURE 2 | The sampling sites in the Middle Luhoho used in Kisekelwa et al. (2021). Striped area represents the Kahuzi-Biega National Park; and▐: Tchinganda Falls at Bulambika. ...
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Mouth morphology plays a crucial role in determining the trophic ecology of fish and sometimes underpins important lineage diversification. Freshwater teleost fish species belonging to the genus Labeobarbus, commonly found in Africa, exhibit intra‐ and interspecific variation and differences in the lower jaw occurring within and between species, respectively. Different phenotypes include a curved U‐shape (‘rubberlips’), a straight lower jaw (‘chiselmouth’) and an intermediate morphology known as the smiling phenotype. In some cases, smiling originates from hybridisation between chiselmouth and rubberlips. However, the trophic relationships of different mouth morphologies in the Labeobarbus taxa are still not well understood, particularly in the Congo Basin. Understanding the trophic ecology of Labeobarbus can enhance understanding of adaptive processes in morphologically diverse lineages. This study aims to investigate how differences in mouth morphology among multiple Labeobarbus species in the Luhoho River (Upper Congo Basin) link with different trophic niche uses. We combined information from gut morphometry, gut contents and stable isotope analyses on 202 fish specimens representing six species across four tributaries of the Middle Luhoho. All approaches consistently revealed trophic niche partitioning between chiselmouth and rubberlip species, respectively, more herbivorous/detritivorous and more insectivorous on the omnivory spectrum. In addition, trophic differences were also found between species within each mouth phenotype. Interestingly, the trophic niche of the smiling phenotype differed strongly from those of other phenotypes at all sites except for L. paucisquamatus, for which the trophic niches overlapped in Tchinganda. The pattern of trophic niche of Labeobarbus suggests subtle strategies to partition feeding resources when they occur across a narrow hydrographic scale.
... The trophodynamic theory indicates that community-level abundance or biomass decrease log-linearly with body size (Rice and Gislason, 1996), despite variable relative abundances or biomass of a single species (Cohen et al., 1993;Emmerson and Raffaelli, 2004). Based on this principle, several studies have used fish community's sizes to assess ecosystem conditions and functioning through fitting linear regressions with log-transformed abundance and size class datasets (e.g. ...
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... Taller individuals are more likely to win dyadic confrontations and display interpersonal dominance (Stulp et al., 2015), shorter men express intrasexual jealousy more intensely than taller men (Brewer & Riley, 2009;Buunk et al., 2008), shorter men may be more antagonistic (Kozłowska et al., 2023), and taller men are less sensitive to cues of dominance in other men compared to their shorter compatriots (Watkins et al., 2010). This association is not limited to humans; in many nonhuman species, height and size play critical roles in dominance and survival (Cohen et al., 1993;Preisser & Orrock, 2012) and play a role in reproductive fitness (Haley et al., 1994). ...
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... Ensuite, l'existence ou l'absence de certaines interactions dépend des traits morphologiques, phénologiques ou comportementaux des deux espèces considérées pour ces interactions potentielles. Un exemple est celui de la taille des individus : la plupart des prédateurs sélectionnent des proies plus petites, créant un rapport de force qui permet la réalisation d'une interaction trophique (Cohen et al., 1993;Brose et al., 2006). La variabilité inter-et intraspécifique des traits dans l'espace implique ainsi différentes probabilités d'interaction entre deux mêmes espèces dans des réseaux trophiques distants. ...
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