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Monnin, T.

Publications and source records attributed to Monnin, T..

7 recordsLinked to original sources

Urbanisation and habitat fragmentation favour thermophilic and monogynous ant species

Environmental changes such as urbanisation and related habitat loss and fragmentation profoundly impact ecological communities by altering habitats, resources, and microclimates. Yet, the impacts of the resulting environmental conditions on metacommunity dynamics, ranging from species sorting to mass effects, remain a subject of debate. Ants, with diverse life histories and strong ecological effects, are ideal model species to study these pressures. We investigated the response of ant communities, including taxonomic and functional diversity, to urbanisation and habitat fragmentation in the Paris region, comparing wooded areas in 25 urban parks vs. 24 rural forests outside the city. We found a clear difference in species composition between urban and rural environments, with a higher prevalence of thermophilic species and a tendency for monogyny in the city. Forest communities were homogeneous across the size levels we studied, while park communities differed noticeably depending on park size, with larger parks harbouring more species. Our findings suggest that urbanisation selects specific ant traits and favours more thermophilic species, thereby increasing the mean thermal preference of urban communities. These selective effects influence which species can colonise and survive in different patches, shaping metacommunity structure and potentially affecting the resilience of ant communities under climate change.

ecology↗

Group or solitary dispersal: worker presence and number favour the success of colony foundation in ants

Dispersal strategies are highly variable. Any strategy is associated to costs and benefits, and understanding which factors favour or disfavour a strategy is a key issue in ecology and evolution. Ants exhibit different dispersal and colony foundation strategies. Some species have winged queens that disperse solitarily and far by flight, and that found new colonies alone. Others have apterous queens that disperse with workers over short walking distances, and found new colonies as a group (colony fission). The putative benefits conferred by workers have been little studied and quantified, because comparing the costs and benefits of solitary vs. group dispersal and foundation is difficult when comparing different species. We did this using the ant Myrmecina graminicola, one of the few species that use both strategies. Young queens were mated and allowed to found new colonies in the laboratory, with either zero, two or four workers. We monitored the survival and growth of foundations over one year. The presence of workers increased both survival and growth, with more workers yielding higher growth. These results show the benefit of dispersing and founding in a group. The presence of few workers (as little as two workers) was sufficient to provide benefits, suggesting group foundation does not require a dramatic decrease in the number of propagules produced in M. graminicola. Our results support the hypothesis that the two strategies coexist along a competition-colonization trade-off, where solitary foundation offers a colonization advantage while group foundation has a competitive advantage.

ecology↗

Habitat fragmentation selects for low dispersal in an ant species

Increased habitat fragmentation is one of the major global changes affecting biodiversity. It is characterised by a decrease in habitat availability and by an increase in the isolation of suitable habitat patches. The dispersal capacities of species may evolve in response to increased habitat fragmentation. Spatial heterogeneities and/or costs of dispersal, which are directly linked to habitat fragmentation, tend to select for lower dispersal abilities. We studied the effects of habitat fragmentation on dispersal using an ant species that exhibits a marked dispersal polymorphism. Myrmecina graminicola produces winged queens dispersing by flight over long distances, or apterous queens dispersing on foot over short distances. We sampled queens in 24 forests around Paris and 25 parks within Paris, representing varied levels of habitat fragmentation and habitat size. We identified the queen morphotypes in each environment and used it as a proxy of dispersal. Winged queens predominated in both environments. However, apterous queens were comparatively more common in parks than in forests, suggesting that high fragmentation counterselects dispersal in this species. We argue that this is because dispersing within urban environments is very costly and discuss the factors favouring each queen morph or resulting in their co-occurrence (maintenance of polymorphism).

evolutionary biology↗

To disperse or compete? Coevolution of traits leads to a limited number of reproductive strategies

Reproductive strategies are defined by a combination of behavioural, morphological, and life-history traits. Reproductive investment and offspring propagule size are two key traits defining reproductive strategies. While a substantial amount of work has been devoted to understanding the independent fitness effects of each of these traits, it remains unclear how coevolution between them ultimately affects the evolution of reproductive strategies, and how this might influence the relationship between dispersal and environmental factors. In this study we explore how the evolution of reproductive strategies defined by these two coevolving traits is influenced by resource availability and spatial structuring of the environment using a simulation model. We find three possible equilibrium strategies across all scenarios: a competitor strategy with high reproductive investment (producing large propagules which disperse short distances), and two coloniser strategies differing in reproductive investment (both producing small propagules which disperse long distances). The possible equilibrium strategies for each scenario depended on starting conditions, spatial structure and resource availability. Evolutionary transitions between these equilibrium strategies were more likely in heterogeneous than homogeneous landscapes and at higher resource levels. Transition from coloniser strategy to competitor strategy was usually a two-step process, with changes in propagule size following initial evolution in investment. This highlights how the interaction between the two trait axes affects the evolution of reproductive strategies, particularly where fitness valleys preclude the simultaneous evolution of traits. Our results highlight the need to incorporate trait coevolution into evolutionary models to help develop a more integrative understanding of the structure of natural populations and how the interaction between traits constrains or hinders evolutionary processes.

evolutionary biology↗

Evolution of dispersal and the maintenance of fragmented metapopulations

Because it affects dispersal risk and modifies competition levels, habitat fragmentation directly constrains dispersal evolution. When dispersal is traded-off against competitive ability, increased fragmentation is often expected to select higher dispersal. Such evolutionary effects could favor the maintenance of the metapopulation by fostering spatial rescue effects. Using an evolutionary model, we first investigate how dispersal evolves in a metapopulation when fragmentation and aggregation of this fragmentation are fixed. Our results suggest that high fragmentation indeed selects for dispersal increase, but this effect is largely reduced in aggregated landscapes, to the point of being nonexistent at the highest aggregation levels. Contrasted dispersal strategies coexist at high fragmentation levels and with no or low aggregation. We then simulate time-varying fragmentation scenarios to investigate the conditions under which evolutionary rescue of the metapopulation happens. Faster evolution of dispersal favors the persistence of the metapopulation, but this effect is very reduced in aggregated landscapes. Overall, our results highlight how the speed of evolution of dispersal and the structuration of the fragmentation will largely constrain metapopulation survival in changing environments.

evolutionary biology↗

Implications of the evolution of agriculture and resource foraging for the maintenance of species diversity and community structure

Agriculture is found in numerous taxa such as humans, ants, beetles, fishes and even bacteria. This type of niche construction has evolved independently from hunting, though many species remain primarily predators. When a consumer has a positive effect on its resource, we can expect an allocative cost of agriculture, as the agricultural care diverts time and energy from other activities. Defending the resource against predators may divert time from its consumption (exploitation cost). The cost may also occur on the foraging of alternative resources, for instance if the consumer spends more time nearby the farmed resource and underexploiting resources elsewhere (opportunity cost). We here investigate transitions from predation to agriculture in a simple three-species model of a farmer that consumes two resources and has a positive effect on one. We study the conditions for the (co)evolution of the investment into agriculture and specialization on the two resources, and its consequences on the ecological dynamics of the community. Eco-evolutionary dynamics generate a feedback between the evolution of agriculture and specialization on the helped resource, that can lead to varying selected intensity of agriculture, from generalist strategies with no agriculture, to specialist farmers, with possible coexistence between these two extreme strategies.

ecology↗

From apparent competition to facilitation, impacts of consumer niche construction on the coexistence and stability of consumer-resource communities.

O_LIIn addition to their direct trophic effects, some consumers have a positive indirect effect on their resource, due to niche construction. A predator can facilitate its prey resource acquisition, through prey transport, or through modifications of nutrient cycling. Other predators defend their prey against other predators, or actively manage it, as in agriculture, which is found in numerous taxa such as humans, but also ants, beetles, fishes and microbes.\nC_LIO_LIHere we investigate the ecological consequences of considering such positive effects in a simple two resource-one predator module, in which the consumer has a positive effect on one of the resources.\nC_LIO_LIWe consider several scenarios, in which the positive effect of the resource is either non costly, ie resulting from a by-product of the consumer phenotype such as nutrient cycling, or costly. The cost either decreases the exploitation of the helped resource or the opportunity to forage the alternative resource.\nC_LIO_LIWe show that by modifying the trophic interactions in the module, niche construction alters the apparent competition between the resources, thereby impacting their coexistence.\nC_LIO_LIWe investigate how the intensity of niche construction impacts species coexistence, the distribution of biomass among the three species, and the stability of the community. When niche construction has little or no cost, it leads to higher consumer and helped resource densities, while decreasing the alternative resource density. Alternatively, when niche construction has a strong cost, the alternative resource can increase in density, niche construction thereby leading to the emergence of facilitative interactions among resource species.\nC_LI

ecology↗