Dataset Information

Pair formation in insect swarms driven by adaptive long-range interactions.

ABSTRACT: In swarms of flying insects, the motions of individuals are largely uncoordinated with those of their neighbours, unlike the highly ordered motion of bird flocks. However, it has been observed that insects may transiently form pairs with synchronized relative motion while moving through the swarm. The origin of this phenomenon remains an open question. In particular, it is not known if pairing is a new behavioural process or whether it is a natural by-product of typical swarming behaviour. Here, using an 'adaptive-gravity' model that proposes that insects interact via long-range gravity-like acoustic attractions that are modulated by the total background sound (via 'adaptivity' or fold-change detection) and that reproduces measured features of real swarms, we show that pair formation can indeed occur without the introduction of additional behavioural rules. In the model, pairs form robustly whenever two insects happen to move together from the centre of the swarm (where the background sound is high) towards the swarm periphery (where the background sound is low). Due to adaptivity, the attraction between the pair increases as the background sound decreases, thereby forming a bound state since their relative kinetic energy is smaller than their pair-potential energy. When the pair moves into regions of high background sound, however, the process is reversed and the pair may break up. Our results suggest that pairing should appear generally in biological systems with long-range attraction and adaptive sensing, such as during chemotaxis-driven cellular swarming.

SUBMITTER: Gorbonos D

PROVIDER: S-EPMC7653370 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Similar Datasets

Project description:BackgroundEvolutionary processes can cause strong spatial genetic signatures, such as local loss of genetic diversity, or conflicting histories from mitochondrial versus nuclear markers. Investigating these genetic patterns is important, as they may reveal obscured processes and players. The maternally inherited bacterium Wolbachia is among the most widespread symbionts in insects. Wolbachia typically spreads within host species by conferring direct fitness benefits, and/or by manipulating its host reproduction to favour infected over uninfected females. Under sufficient selective advantage, the mitochondrial haplotype associated with the favoured maternally-inherited symbiotic strains will spread (i.e. hitchhike), resulting in low mitochondrial genetic variation across the host species range.MethodThe common bluetail damselfly (Ischnura elegans: van der Linden, 1820) has recently emerged as a model organism for genetics and genomic signatures of range expansion during climate change. Although there is accumulating data on the consequences of such expansion on the genetics of I. elegans, no study has screened for Wolbachia in the damselfly genus Ischnura. Here, we present the biogeographic variation in Wolbachia prevalence and penetrance across Europe and Japan (including samples from 17 populations), and from close relatives in the Mediterranean area (i.e. I. genei: Rambur, 1842; and I. saharensis: Aguesse, 1958).ResultsOur data reveal (a) multiple Wolbachia-strains, (b) potential transfer of the symbiont through hybridization, (c) higher infection rates at higher latitudes, and (d) reduced mitochondrial diversity in the north-west populations, indicative of hitchhiking associated with the selective sweep of the most common strain. We found low mitochondrial haplotype diversity in the Wolbachia-infected north-western European populations (Sweden, Scotland, the Netherlands, Belgium, France and Italy) of I. elegans, and, conversely, higher mitochondrial diversity in populations with low penetrance of Wolbachia (Ukraine, Greece, Montenegro and Cyprus). The timing of the selective sweep associated with infected lineages was estimated between 20,000 and 44,000 years before present, which is consistent with the end of the last glacial period about 20,000 years.ConclusionsOur findings provide an example of how endosymbiont infections can shape spatial variation in their host evolutionary genetics during postglacial expansion. These results also challenge population genetic studies that do not consider the prevalence of symbionts in many insects, which we show can impact geographic patterns of mitochondrial genetic diversity.

Dataset Information

Pair formation in insect swarms driven by adaptive long-range interactions.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets