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158 results for “group size”
Data from: Effects of female group size on the number of males in blue monkey (Cercopithecus mitis) groups
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Fear effects and group size interact to shape herbivory on coral reefs
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Size-selective mortality induces evolutionary changes in group risk-taking behavior and the circadian system in a fish
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Data from: Group density, disease, and season shape territory size and overlap of social carnivores
<p>1. The spatial organization of a population can influence the spread of information, behaviour, and pathogens. Territory size and territory overlap, components of spatial organization, provide key information as these metrics may be indicators of habitat quality, resource dispersion, contact rates, and environmental risk (e.g., indirectly transmitted pathogens). Furthermore, sociality and behaviour can also shape space use, and subsequently, how space use and habitat quality together impact demography.</p> <p>2. Our study aims to identify factors shaping the spatial organization of wildlife populations and assess the impact of epizootics on space use. We also use network analysis to describe spatial organization and connectivity of social groups.</p> <p>3. Here, we assessed the seasonal spatial organization of Serengeti lions and Yellowstone wolves at the group level. We examine the factors predicting mean territory size and mean territory overlap for each population using generalized additive models. We further explore the mechanisms by which disease perturbations could cause changes in spatial organization.</p> <p>4. We demonstrate that lions and wolves were similar in that group-level factors, such as number of groups, shaped spatial organization more than population-level factors, such as population density. Factors shaping territory size were slightly different than factors shaping territory overlap; for example, wolf pack size was an important predictor of territory overlap, but not territory size. Lion spatial networks were more highly connected, while wolf spatial networks varied seasonally. We found that resource dispersion may be more important for driving territory size and overlap for wolves than for lions. Additionally, canine distemper epizootics may alter lion spatial organization, highlighting the importance of including behavioural and movement ecology in studies of pathogen transmission dynamics.</p> <p>5. We provide insight about when we might expect to observe the impacts of resource dispersion, disease perturbations, and other ecological factors on spatial organization. Our work highlights the importance of monitoring and managing social carnivore populations at the group level. Future research should elucidate the complex relationships between demographics, social and spatial structure, abiotic and biotic conditions, and pathogen infections. </p>
Data from: Policing effectiveness depends on relatedness and group size
Cohesion of social groups requires the suppression of individual selfishness. Indeed, worker egg laying in insect societies is usually suppressed or punished through aggression and egg removal. The effectiveness of such "policing" is expected to increase with decreasing relatedness, as inclusive fitness of group members is more strongly affected by selfish worker reproduction when group members are less closely related to each other. As inclusive fitness is also influenced by the costs and benefits of helping, the effectiveness of policing should decrease with increasing colony size, because the costs for the whole colony from selfish worker reproduction are proportionally reduced in large groups. Here, we show that policing effectiveness in colonies of the ant Temnothorax unifasciatus is low in large groups and high in small groups when relatedness is high. When we experimentally decreased the relatedness in groups, the policing effectiveness reached the same high level as in small highly related groups, irrespectively of group size. Therefore, our results indicate that policing effectiveness is simultaneously shaped by relatedness and group size, i.e. an ecological factor. This may have major implications for testing policing across species of animals.
Data from: The modulating role of group stability on fitness effects of group size is different in females and males of a communally rearing rodent
Group size may influence fitness benefits and costs that emerge from cooperative and competitive interactions in social species. However, evidence from plural breeding mammals indicates that group size is insufficient to explain variation in direct fitness, implying other attributes of social groups were overlooked. We studied the natural population of a social rodent during 5 years to test the hypothesis that social stability – in terms of group composition – modulates the effects of increasing number of breeding females (a proxy of communal rearing) and males on the number of offspring weaned (sired) and on the number of offspring weaned (sired) surviving to breeding age (two proxies of direct fitness). We quantified the effects of social stability (measured as changes in female or male group members between mating and the onset of lactation) on these fitness measures. We used live trapping, telemetry and DNA markers to determine social and fitness measures. Social stability in degus was variable in terms of the number of changes in group composition across groups. Low stability was mostly due to mortality and emigration of group members. Results supported a modulating role of social stability on the relationship between group size and the number of offspring weaned (sired). Stability in female and male group composition were both modulators of fitness to females and males. The modulatory role of stability was sex specific, where high social stability was often fitness beneficial to the females. Instead, low social stability was fitness enhancing to the males.
Data from: Group-size dependent punishment of idle subordinates in a cooperative breeder where helpers pay to stay
In cooperative breeding systems, dominant breeders sometimes tolerate unrelated individuals even if they inflict costs on the dominants. According to the 'pay-to-stay' hypothesis, (i) subordinates can outweigh these costs by providing help and (ii) dominants should be able to enforce help by punishing subordinates that provide insufficient help. This requires that dominants can monitor helping and can recognize group members individually. In a field experiment, we tested whether cooperatively breeding cichlid Neolamprologus pulcher subordinates increase their help after a forced 'idle' period, how other group members respond to a previously idle helper, and how helper behaviour and group responses depend on group size. Previously, idle helpers increased their submissiveness and received more aggression than control helpers, suggesting that punishment occurred to enforce help. Subordinates in small groups increased their help more than those in large groups, despite receiving less aggression. When subordinates were temporarily removed, dominants in small groups were more likely to evict returning subordinates. Our results suggest that only in small groups do helpers face a latent threat of punishment by breeders as predicted by the pay-to-stay hypothesis. In large groups, cognitive constraints may prevent breeders from tracking the behaviour of a large number of helpers.
Data from: Group size and social status affect scent marking in dispersing female meerkats
Many animal species use scent marks such as faeces, urine, and glandular secretions to find mates, advertise their reproductive status, and defend an exclusive territory. Scent marking may be particularly important during dispersal, when individuals emigrate from their natal territory searching for mates and a new territory to settle and reproduce. In this study, we investigated the scent marking behaviour of 30 dispersing female meerkats (Suricata suricatta) during the three consecutive stages of dispersal – emigration, transience, and settlement. We expected marking patterns to differ between dispersal stages and depending on social circumstances such as presence of unrelated mates and social status of the individuals within each dispersing coalition; but also to be influenced by water and food availability. We showed that defecation probability increased with group size during the settlement stage, when newly formed groups are expected to signal their presence to other resident groups. Urination probability was higher in subordinate than in dominant individuals during each of the three dispersal stages, and it overall decreased as the dispersal process progressed. Urine may thus be linked to advertisement of the social status within a coalition. Anal marking probability did not change across dispersal stages, but increased with the presence of unrelated males and was higher in dominants than in subordinates. We did not detect any effect of rain or foraging success on defecation and urination probability. Our results suggest that faeces, urine, and anal markings serve different communication purposes (e.g. within and between group communication) during the dispersal process.
Data from: Density and group size influence shoal cohesion, but not coordination in zebrafish (Danio rerio)
The formations made by gregarious animals can range from loose aggregates to highly synchronized and ordered structures. For very large, coordinated groups, both physical and social environments are important for determining the physical arrangement of individuals in the group. Here we tested whether physical and social factors are also important in determining the structure of small, loosely coordinated groups of zebrafish. We found that even though our fish were not crowded and did not use most of the available space, the distance between individual fish was explained primarily by the amount of available space (i.e., density). Zebrafish in a larger space spread out more and the total dimensions of the shoal were an additive function also of group size. We, however, did not find any impact of social or physical environment on the orientation of individual fish or shoal. Thus, both physical and social factors were important for shoal spatial arrangements, but not individual orientation and shoal alignment.
Data from: Personality composition is more important than group size in determining collective foraging behaviour in the wild
Describing the factors that shape collective behaviour is central to our understanding of animal societies. Countless studies have demonstrated an effect of group size in the emergence of collective behaviours, but comparatively few have accounted for the composition/diversity of behavioural phenotypes, which is often conflated with group size. Here, we simultaneously examine the effect of personality composition and group size on nest architecture and collective foraging aggressiveness in the social spider Stegodyphus dumicola. We created colonies of two different sizes (10 or 30 individuals) and four compositions of boldness (all bold, all shy, mixed bold and shy, or average individuals) in the field and then measured their collective behaviour. Larger colonies produced bigger capture webs, while colonies containing a higher proportion of bold individuals responded to and attacked prey more rapidly. The number of attackers during collective foraging was determined jointly by composition and size, although composition had an effect size more than twice that of colony size: our results suggest that colonies of just 10 bold spiders would attack prey with as many attackers as colonies of 110 'average' spiders. Thus, personality composition is a more potent (albeit more cryptic) determinant of collective foraging in these societies.
Data from: Cognitive performance is linked to group size and affects fitness in Australian magpies
The Social Intelligence Hypothesis argues that the demands of social life drive cognitive evolution. This idea receives support from comparative studies linking variation in group size or mating systems with cognitive and neuroanatomical differences across species, but findings are contradictory and contentious. To understand the cognitive consequences of sociality it is also important to investigate social variation within species. Here we show that in wild, cooperatively breeding Australian magpies, individuals living in larger groups show elevated cognitive performance, which in turn is linked to increased reproductive success. Individual performance was highly correlated across four cognitive tasks, hinting towards a "general intelligence factor" underlying cognitive performance. Repeated cognitive testing of juveniles at different ages showed that the group size – cognition correlation emerged in early life, suggesting that living in larger groups promotes cognitive development. Furthermore, we found a positive association between female task performance and three indicators of reproductive success, thus identifying a selective benefit of greater cognitive performance. Together, these results provide critical intraspecific evidence that sociality can shape cognitive development and evolution.
Data from: Influence of group size on the success of wolves hunting bison
An intriguing aspect of social foraging behaviour is that large groups are often no better at capturing prey than are small groups, a pattern that has been attributed to diminished cooperation (i.e., free riding) in large groups. Although this suggests the formation of large groups is unrelated to prey capture, little is known about cooperation in large groups that hunt hard-to-catch prey. Here, we used direct observations of Yellowstone wolves (Canis lupus) hunting their most formidable prey, bison (Bison bison), to test the hypothesis that large groups are more cooperative when hunting difficult prey. We quantified the relationship between capture success and wolf group size, and compared it to previously reported results for Yellowstone wolves hunting elk (Cervus elaphus), a prey that was, on average, 3 times easier to capture than bison. Whereas improvement in elk capture success levelled off at 2–6 wolves, bison capture success levelled off at 9–13 wolves with evidence that it continued to increase beyond 13 wolves. These results are consistent with the hypothesis that hunters in large groups are more cooperative when hunting more formidable prey. Improved ability to capture formidable prey could therefore promote the formation and maintenance of large predator groups, particularly among predators that specialize on such prey.
Data from: Seasonal variation in foraging group size of crab-eating foxes and hoary foxes in the Cerrado biome, Central Brazil
In regions with a pronounced dry season, such as the Cerrado Biome (Brazilian savannah), climate seasonality may affect food availability for canid species and, consequently, their foraging behavior. We investigated seasonal variation in foraging group size of crab-eating foxes (Cerdocyon thous) and hoary foxes (Pseudalopex vetulus) in the Cerrado region for three consecutive years. Data were obtained by direct observations of foraging foxes during spotlight surveys. Both species were sighted foraging individually or in pairs with or without their juvenile offspring. However, crab-eating foxes foraged in pairs more frequently in the wet season and individually more frequently in the dry season whereas hoary foxes foraged mostly individually throughout the year. The higher frequency of solitary foragers in the dry season is possibly a response to the seasonal shortages in the availability of clumped and locally abundant food resources such as fruit and insects, important items in the diet of the crab-eating fox during the wet season. The absence of seasonal variation in foraging group size of the hoary fox may be related to its specialized food habits, since termites predominate in the diet of this species in both seasons.
FIGURE 9 in Tarsal tetramery and extreme size reduction in Anillini (Coleoptera, Carabidae, Trechinae): the case of Typhlocharis Dieck, 1869; description of three new species and definition of a new intra-generic species group
FIGURE 9. Map of southwestern Iberian Peninsula. Black circles represent the distribution of quadridentata group: 1) T. quadridentata (Coiffait, 1969), 2) T. crespoi Serrano & Aguiar, 2008, 3) T. baeturica sp.n., 4) T. scrofa sp.n., 5) T. tetramera sp.n. Dotted lines indicate political frontiers.
FIGURE 8 in Tarsal tetramery and extreme size reduction in Anillini (Coleoptera, Carabidae, Trechinae): the case of Typhlocharis Dieck, 1869; description of three new species and definition of a new intra-generic species group
FIGURE 8. Comparison of pentamerous and tetramerous conditions in the tarsi of Typhlocharis. Light microscopy photographs and schematic diagrams of: A) Metatarsus with five tarsomeres in T. elenae Serrano & Aguiar, 2002. B) Metatarsus with four tarsomeres in T. baeturica sp.n. Note the fused aspect of the "fourth" tarsomere in T. baeturica sp.n. and the presence of remaining chaetotaxy in the middle region, equivalent to the distal setae of the fourth tarsomere in regular pentamerous tarsi.
FIGURE 6 in Tarsal tetramery and extreme size reduction in Anillini (Coleoptera, Carabidae, Trechinae): the case of Typhlocharis Dieck, 1869; description of three new species and definition of a new intra-generic species group
FIGURE 6. Typhlocharis tetramera sp.n. (A, B) Aedeagus: A) median lobe (dorsal view); B) median lobe and parameres (lateral view). C) Female genitalia (ventral view).
FIGURE 7 in Tarsal tetramery and extreme size reduction in Anillini (Coleoptera, Carabidae, Trechinae): the case of Typhlocharis Dieck, 1869; description of three new species and definition of a new intra-generic species group
FIGURE 7. Different types of gula in the genus Typhlocharis. Light microscopy photographs and schematic diagrams of: A) T. pacensis Zaballos & Jeanne, 1987; wide gula, approx. twice as long as wide, lateral sutures clearly visible. B) T. elenae Serrano & Aguiar, 2002; narrow gula, approx. four of five times as long as wide, lateral sutures clearly visible, subparallel. C) T. scrofa sp.n.; diffuse gula, same proportions as wide gula, but lateral sutures only visible in the proximal and distal ends, partially fused to the cephalic capsule.
FIGURE 5 in Tarsal tetramery and extreme size reduction in Anillini (Coleoptera, Carabidae, Trechinae): the case of Typhlocharis Dieck, 1869; description of three new species and definition of a new intra-generic species group
FIGURE 5. Typhlocharis tetramera sp.n. habitus: ventral (left half: male, right half: female) and dorsal (male) views. Abdomen not shown in dorsal view for a clearer view of elytral apex.
FIGURE 3 in Tarsal tetramery and extreme size reduction in Anillini (Coleoptera, Carabidae, Trechinae): the case of Typhlocharis Dieck, 1869; description of three new species and definition of a new intra-generic species group
FIGURE 3. Typhlocharis scrofa sp.n. habitus: ventral (left half: male, right half: female) and dorsal (male) views. Abdomen not shown in dorsal view for a clearer view of elytral apex.
FIGURE 4 in Tarsal tetramery and extreme size reduction in Anillini (Coleoptera, Carabidae, Trechinae): the case of Typhlocharis Dieck, 1869; description of three new species and definition of a new intra-generic species group
FIGURE 4. Typhlocharis scrofa sp. n. (A, B) Aedeagus: A) median lobe (dorsal view); B) median lobe and parameres (lateral view). C) Female genitalia (ventral view).
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.