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62 results for “social insects”
Data for: Crall et al., Spatial fidelity of workers predicts collective response to disturbance in a social insect
<p>Dataset for: Crall et al., Spatial fidelity of workers predicts collective response to disturbance in a social insect, in final revision for Nature Communications.</p> <p>Includes two files - one behavioral data from uniquely identified worker bumblebees, and the second containing metadata for the colonies from which these data were generated (including experimental treatments, locations, sizes, etc.).</p>
Datasets and R code for: Brood as booty: The effect of colony size and resource value in social insect contests
<p><strong>From the Manuscript: </strong>Animals engage in contests for access to resources like food, mates, and space. Intergroup contests between groups of organisms have received little attention, and it remains unresolved what information groups might use collectively to make contest decisions. We staged whole-colony contests using ant colonies (<em>Temnothorax rugatulus</em>), which perceive conspecific colonies as both a threat and resource from which to steal brood. We recorded individual behaviors and used demographic characteristics as proxies for resource value (number of brood items) and fighting ability (number of workers). We found that ants altered their fighting effort depending on the relative number of workers of their opponent. While the proximate mechanism for this ability remains uncertain, we found that colonies increased fighting when their opponent had relatively more brood, but not if opposing colonies had relatively many more workers. This suggests that ant colonies can use information about opposing colonies that shapes contest strategies. Further, the behavior of opposing colonies were strongly correlated with each other despite colony size differences ranging from 4-51%, consistent with the hypothesis that colonies can use opponent information. The behavior of a distributed, collective system of many individuals, like a eusocial insect colony, thus fits several predictions of contest models designed for individuals if we consider the gain and loss of worker ants analogous to energetic costs accrued during typical dyadic contests.</p>
(c) simulation on Repast: after queen adaptive development-MODELING SELF-ORGANIZING SYSTEMS WITH SOCIAL INSECTS ALGORITHMS
<p>On figures (b) and (c), simulations on RePast [11, 16, 18] are<br> provided at successive times. The last figure shows the adaptive mechanism<br> of the queen which grows with time according to the material density around<br> it, like in natural observations.</p>
Figure 7: Cultural equipment dynamics modeling-MODELING SELF-ORGANIZING SYSTEMS WITH SOCIAL INSECTS ALGORITHMS
<p>The multi-template modelling can be used to model cultural equipment<br> dynamics as described in figure 7. On this figure, we associate a queen to each<br> cultural center (cinema, theatre, ...). Each queen will emit many pheromon<br> templates, each template is associated to a specific criterium (according to age,<br> sex, ...). Initially, we put the material in the residential place. Each material<br> has some characteristics, corresponding to the people living in this residential<br> area. The simulation shows the self-organization processus as the result of the<br> set of the attractive effect of all the centers and all the templates.</p>
Figure 4: Complexity of geographical space with respect of emergent organizations-MODELING SELF-ORGANIZING SYSTEMS WITH SOCIAL INSECTS ALGORITHMS
<p>The applications we focus on in the models that we will propose in the<br> following, concerns specifically the multi-center (or multi-organizational) phenomona<br> inside urban development. As an artificial ecosystem, the city development<br> has to deal with many challenges, specifically for sustainable development,<br> mixing economical, social and environmental aspects. The decentralized<br> methodology proposed in the following allows to deal with multi-criteria problems,<br> leading to propose a decision making assistance, based on simulation<br> analysis.</p>
Figure 1: Complex spatial organizational model-MODELING SELF-ORGANIZING SYSTEMS WITH SOCIAL INSECTS ALGORITHMS
<p>On Figure 1, we describe a two-level model of spatial self-organizations with<br> interactions in both directions between these two levels: the emergence of organizations<br> from entities interactions but also the feed-back process describing<br> how organizations are regulating their own entities.</p>
Figure 2: Optimization in natural ants collective behavior: foraging and clustering (from [8])-Self-organization and social insects algorithms
<p>On figure 2, two examples of self-organization in natural ants are presented.<br> On the left side, the well-known Deneubourg experiment consists to highlight<br> with a very simple device the ant foraging problem. The ant objectives is<br> to find the optimal way from nest to food source, using pheromone trail deposition.<br> On the right side, cemetery clustering formation are shown at 4<br> successive times: ants form piles of corpses to clean their nests. Each of them<br> has elementary actions, unknowing the whole situation, but dealing only with<br> local information. There is no supervisor to lead the piles formation which<br> emerges from ant interactions.</p>
Data for: Intergenerational genotypic interactions drive collective behavioural cycles in a social insect
<p>Many social animals display collective activity cycles based on synchronous behavioural oscillations across group members. A classic example is the colony cycle of army ants, where thousands of individuals undergo stereotypical biphasic behavioural cycles of about one month. Cycle phases coincide with brood developmental stages, but the regulation of this cycle is otherwise poorly understood. Here, we probe the regulation of cycle duration through interactions between brood and workers in an experimentally amenable army ant relative, the clonal raider ant. We first establish that cycle length varies across clonal lineages using long-term monitoring data. We then investigate the putative sources and impacts of this variation in a cross-fostering experiment with four lineages combining developmental, morphological, and automated behavioural tracking analyses. We show that cycle length variation stems from variation in the duration of the larval developmental stage, and that this stage can be prolonged not only by the clonal lineage of brood (direct genetic effects), but also of the workers (indirect genetic effects). We find similar indirect effects of worker line on brood adult size and, conversely but more surprisingly, indirect genetic effects of the brood on worker behaviour (walking speed and time spent in the nest).</p>
Two simple movement mechanisms for spatial division of labour in social insects
<p>Many animal species divide space into a patchwork of home ranges, yet there is little consensus on the mechanisms individuals use to maintain fidelity to particular locations. Theory suggests that animal movement could be based upon simple behavioural rules that use local information such as olfactory deposits, or global strategies, such as long-range biases toward landmarks. However, empirical studies have rarely attempted to distinguish between these mechanisms. Here, we perform individual tracking experiments on four species of social insects, and find that colonies consist of different groups of workers that inhabit separate but partially-overlapping spatial zones. Our trajectory analysis and simulations suggest that worker movement is consistent with two local mechanisms: one in which workers increase movement diffusivity outside their primary zone, and another in which workers modulate turning behaviour when approaching zone boundaries. Parallels with other organisms suggest that local mechanisms might represent a universal method for spatial partitioning in animal populations.</p>
Social signal learning of referential communication in a social insect
<p>This is the dataset for a paper showing that honey bees can use social learning to improve their waggle dancing.</p>
Supplementary data for: Transcriptomics of mosaic brain differentiation underlying complex division of labor in a social insect
<p>Concerted developmental programming may constrain changes in component structures of the brain, thus limiting the ability of selection acting on individual brain compartments to form an adaptive mosaic independent of total brain size or body size. Measuring patterns of gene expression underpinning brain scaling in conjunction with anatomical brain atlases can aid in identifying influences of concerted and/or mosaic evolution. Species exhibiting exceptional size and behavioral polyphenisms provide excellent systems to test predictions of brain evolution models by quantifying brain gene expression. We examined patterns of brain gene expression in a remarkably polymorphic and behaviorally complex social insect, the leafcutter ant <em>Atta</em> <em>cephalotes</em>. Approximately ~50% of differential gene expression observed among three morphologically, behaviorally, and neuroanatomically differentiated worker size groups was attributable to body size, but we also found strong evidence of differential brain gene expression unexplained by worker morphological variation. Transcriptomic analysis identified patterns of gene expression not linearly correlated with worker size but rather, in some cases, mirroring neuropil scaling. Additionally, we observed enriched gene ontology terms associated with nucleic acid regulation, metabolism, neurotransmission, and sensory perception, further supporting a relationship between brain gene expression and worker social role. These findings demonstrate that differential brain gene expression among polymorphic workers is linked to behavioral and neuroanatomical differentiation underpinning complex agrarian division of labor in <em>A</em>. <em>cephalotes</em>.</p>
Supplementary data for: Transcriptomics of mosaic brain differentiation underlying complex division of labor in a social insect
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Datasets and R code for: Brood as booty: The effect of colony size and resource value in social insect contests
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Two simple movement mechanisms for spatial division of labour in social insects
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Data for: Intergenerational genotypic interactions drive collective behavioural cycles in a social insect
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Juvenile social experience and practice have a switch-like influence on adult mate preferences in an insect
<p>Social causes of variation in animal communication systems have important evolutionary consequences, including speciation. The relevance of these effects depends on how widespread they are among animals. There is evidence for such effects not only in birds and mammals, but also frogs and some insects and spiders. Here we analyse the social ontogeny of adult mate preferences in an insect, Enchenopa treehoppers. In these communal plant-feeding insects, individuals reared in isolation or in groups differ in their mate preferences, and the group-reared phenotype can be rescued by playbacks to isolation-reared individuals. We ask about the relative role of signalling experience and signalling practice during ontogeny on the development of adult mating preferences in Enchenopa females. Taking advantage of variation in the signal experience and signalling practice of isolation-reared individuals, we find switch-like effects for experience and practice on female mate preference phenotypes, with individuals having some experience and practice as juveniles best rescuing the group-reared preference phenotype. We discuss how understanding the nature and distribution of social-ontogenetic causes of variation in mate preferences and other sexual traits will bring new insights into how within- and between-population variation influences the evolution of communication systems.</p>
Diet composition and social environment determine food consumption, phenotype and fitness in an omnivorous insect
Nutrition is the single most important factor for individual's growth and reproduction. Consequently, the inability to reach the nutritional optimum imposes severe consequences for animal fitness. Yet, under natural conditions organisms may face a mixture of stressors that can modulate the effects of nutritional asymmetry. For instance, stressful environments caused by intense interaction with conspecifics. Here, we subjected the house-cricket Acheta domesticus to i) either of two types of diet that have proven to affect cricket performance and ii) simultaneously manipulated their social environment throughout their complete lifecycle. We aimed to track sex-specific consequences for multiple traits during insect development throughout all life stages. Both factors affected critical life-history traits with potential population-level consequences: Diet composition induced strong effects on insect development time, lifespan and fitness, whilst the social environment affected the number of nymphs that completed development, food consumption and whole-body lipid content. Additionally, both factors interactively determined female body mass. Our results highlight that insects may acquire and invest resources in a different manner when subjected to an intense interaction with conspecifics or when isolated. Furthermore, while only diet composition affected individual reproductive output, the social environment would determine the number of reproductive females, thus indirectly influencing population performance.
Dataset of ""Statistical atlases and automatic labelling strategies to accelerate the analysis of social insect brain evolution"
<p>Dataset of <em>Statistical atlases and automatic labelling strategies to accelerate the analysis of social insect brain evolution</em> by Sara Arganda, Ignacio Arganda-Carreras, Darcy G. Gordon, Andrew P. Hoadley, Alfonso Pérez-Escudero, Martin Giurfa and James F. A. Traniello.</p> <p>In this dataset, we are presenting:</p> <ul> <li>10 confocal brain images from <em>Pheidole spadonia </em>minors (in the original confocal TIFF format and in the open NRRD format), with manually segmented labels of 8 subregions (Optic Lobes, OL; Antennal Lobes, AL; Mushroom Body Medial Calyx, MB-MC; Mushroom Body Lateral Calyx, MB-LC; Mushroom Body Peduncle, MB-P; Central Complex, CX; Subesophageal zone, SEZ; and Rest of Central Brain, ROCB – in NRRD format) from one expert annotator.</li> <li>12 confocal brain images from <em>P. spadonia</em>, <em>P. rhea</em>, <em>P. tepicana</em> and <em>P. obtusospinosa</em> minors, with manually segmented labels of the same 8 subregions (OL; AL; MB-MC; MB-LC; MB-P; CX; SEZ; and ROCB) from one expert annotator.</li> <li>5 confocal brain images from <em>Pheidole spadonia </em>minors (“test brains”), with five sets of manually segmented labels of the same 8 subregions (OL; AL; MB-MC; MB-LC; MB-P; CX; SEZ; and ROCB) from three expert annotators (one set from annotator 1, one set from annotator 2 and three sets from annotator 3, to evaluate inter and intra person differences).</li> <li>1 group-wise template generated from the 10 confocal brain images from <em>Pheidole spadonia </em>minors, with three sets of manually segmented labels of the same 8 subregions (OL; AL; MB-MC; MB-LC; MB-P; CX; SEZ; and ROCB).</li> <li>5 group-wise templates generated from the 9 confocal brain images from <em>Pheidole spadonia </em>minors, with consensus labels of the same 8 subregions (OL; AL; MB-MC; MB-LC; MB-P; CX; SEZ; and ROCB).</li> <li>1 group-wise template generated from 12 confocal brain images from <em>P. spadonia</em>, <em>P. rhea</em>, <em>P. tepicana</em> and <em>P. obtusospinosa</em> minors, with consensus labels of the same 8 subregions (OL; AL; MB-MC; MB-LC; MB-P; CX; SEZ; and ROCB).</li> <li>7 sets of automatic labels for the 5 “test brains”: 3 sets of “Direct Labels”, 3 sets of “Consensus Labels”, 1 set of “Multispecies Template Labels”.</li> </ul> <p>Brain of minor workers were dissected from the ant head capsule in ice cold HEPES-buffered saline and were fixed and immunohistochemically stained using SYNORF1 (a monoclonal <em>Drosophila</em> synapsin I antibody obtained from the Developmental Studies Hybridoma Bank, catalog 3C11) and secondarily stained using Alexa Fluor 488 for visualization of neuropil (slightly modified from Ott, 2008). Later, brains were mounted in methyl salicylate and imaged on an Olympus Fluoview BX50 laser scanning confocal microscope with a ×20 objective at a resolution of ~0.7 × 0.7 × 5µm/voxel. All brain tissue manipulation, staining and recording was performed by Darcy G. Gordon. Brain images were obtained in TIFF format by the confocal microscope and then opened and saved as Amira Mesh (.am) stack images in Amira (version 6.0). Manual segmentation of each brain was done using Amira (version 6.0 or 2019.2). Labels were traced on eight compartments in only one brain hemisphere, except for the CX, SEZ and ROCB, which lack a clear subdivision between hemispheres. Brain grey image stacks and labels were transformed to NRRD format for template construction using the Fiji plugin SaveAsGzipNrrd<a href="#_ftn1">[1]</a>. Volume and volume similarity of labels were calculated using the Fiji toolbox MorphoLibJ<a href="#_ftn2">[2]</a>.</p> <p><strong>Acknowledgements: </strong>We thank Ming Huang (from Dr. Diana Wheeler’s laboratory) who kindly provided access to colonies from four species of the hyperdiverse ant genus <em>Pheidole</em> (<em>P. spadonia</em>, <em>P. rhea</em>, <em>P. tepicana </em>and <em>P. obtusospinosa</em>). This research was supported by National Science Foundation grants IOS 1354291 and IOS 1953393 to JT, a Marie Skłodowska-Curie Individual Fellowship BrainiAnts-660976 and Ayudas destinadas a la atracción de talento investigador a la Comunidad de Madrid en centros de I+D. This work is supported in part by the University of the <a href="https://www.sciencedirect.com/topics/engineering/basque-country">Basque Country</a> UPV/EHU grant GIU19/027.</p> <p> </p> <p><a href="#_ftnref1">[1]</a> https://github.com/iarganda/tefor</p> <p><a href="#_ftnref2">[2]</a> https://imagej.net/plugins/morpholibj</p>
Appendix II for: Social context modulates scale-free walks in a social insect
<p>Plots from the MLE (Maximum likelihood estimation) analysis for the step-lengths of the focal termite workers. Two competing models were tested: Truncated Pareto Lévy (TP - red line) vs exponential (EX - blue dashed line) for both (X and Y) axis. Data series are identified with "S" plus a number from 1 to 75). The Lévy exponent ($1 < \mu \leq 3.0$) and the Akaike weights (wAIC) for the competing models (1 for full support, 0 for not support) are shown in the plots. </p>
Data from: Comparative transcriptomic analysis of the mechanisms underpinning ageing and fecundity in social insects
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