Dataset Information

Ordering and topological defects in social wasps' nests.

ABSTRACT: Social insects have evolved a variety of architectural formations. Bees and wasps are well known for their ability to achieve compact structures by building hexagonal cells. Polistes wattii, an open nesting paper wasp species, builds planar hexagonal structures. Here, using the pair correlation function approach, we show that their nests exhibit short-range hexagonal order (no long-range order) akin to amorphous materials. Hexagonal orientational order was well preserved globally. We also show the presence of topological defects such as dislocations (pentagon-heptagon disclination pairs) and Stone-Wales quadrupoles, and discuss how these defects were organised in the nest, thereby restoring order. Furthermore, we suggest the possible role of such defects in shaping nesting architectures of other social insect species.

SUBMITTER: Krishna S

PROVIDER: S-EPMC9334299 | biostudies-literature | 2022 Jul

REPOSITORIES: biostudies-literature

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Ordering and topological defects in social wasps' nests.

Krishna Shivani S Gopinath Apoorva A Bhattacharjee Somendra M SM

Scientific reports 20220728 1

Social insects have evolved a variety of architectural formations. Bees and wasps are well known for their ability to achieve compact structures by building hexagonal cells. Polistes wattii, an open nesting paper wasp species, builds planar hexagonal structures. Here, using the pair correlation function approach, we show that their nests exhibit short-range hexagonal order (no long-range order) akin to amorphous materials. Hexagonal orientational order was well preserved globally. We also show t ...[more]

PMID: 35902614

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Project description:Spatial patterns in biodiversity are used to establish conservation priorities and ecosystem management plans. The environmental filtering of communities along urbanization gradients has been used to explain biodiversity patterns but demonstrating filtering requires precise statistical tests to link suboptimal environments at one end of a gradient to lower population sizes via ecological traits. Here, we employ a three-part framework on observational community data to test: (I) for trait clustering (i.e., phenotypic similarities among co-occurring species) by comparing trait diversity to null expectations, (II) if trait clustering is correlated with an urbanization graient, and (III) if species' traits relate to environmental conditions. If all criteria are met, then there is evidence that urbanization is filtering communities based on their traits. We use a community of 46 solitary cavity-nesting bee and wasp species sampled across Toronto, a large metropolitan city, over 3 years to test these hypotheses. None of the criteria were met, so we did not have evidence for environmental filtering. We do show that certain ecological traits influence which species perform well in urban environments. For example, cellophane bees (Hylaeus: Colletidae) secrete their own nesting material and were overrepresented in urban areas, while native leafcutting bees (Megachile: Megachilidae) were most common in greener areas. For wasps, prey preference was important, with aphid-collecting (Psenulus and Passaloecus: Crabronidae) and generalist spider-collecting (Trypoxylon: Crabronidae) wasps overrepresented in urban areas and caterpillar- and beetle-collecting wasps (Euodynerus and Symmorphus: Vespidae, respectively) overrepresented in greener areas. We emphasize that changes in the prevalence of different traits across urban gradients without corresponding changes in trait diversity with urbanization do not constitute environmental filtering. By applying this rigorous framework, future studies can test whether urbanization filters other nesting guilds (i.e., ground-nesting bees and wasps) or larger communities consisting of entire taxonomic groups.

Dataset Information

Ordering and topological defects in social wasps' nests.

Publications

Ordering and topological defects in social wasps' nests.

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