Biology subjects

Kellermann, V.

Publications and source records attributed to Kellermann, V..

8 recordsLinked to original sources

bioRxiv2025

Low temperature triggers sociality in a facultatively social bee

The evolutionary transition to eusociality in the solitary ancestors of social insects, like ants, termites, wasps, and bees, may have been initiated by an environmental induction of group living. Plasticity in social behaviour in response to the environment can be found in facultatively social insects. However, it is currently unknown which environmental cues trigger the individual decision of an insect to nest solitarily or socially. Such environmental cues could be identified by exposing individuals of a facultatively social insect to experimentally manipulated cues in a controlled environment. Here, we report such an experiment with the facultatively social allodapine bee Exoneura robusta, which we exposed to different temperature and predation treatments in climate chambers. We observed that low temperature triggered the bees to behave more socially. Furthermore, there was substantial variation in the tendency to be social among individual bees. Our study identifies a specific environmental cue that triggers a plastic response in sociality. Such plasticity could be crucial at the origin of group living and social breeding, facilitating the evolution of eusociality in insects.

evolutionary biology↗

bioRxiv2025

Nesting behaviour drives the evolution of heat tolerance and climate vulnerability in bees

Species vulnerability to climate change depends in part on their capacity to evolve in response to increasing heat1. Within terrestrial ectotherms, heat tolerance generally corresponds weakly to current climates, which has led many to conclude that this trait is evolutionarily constrained2-4. However, most studies have not accounted for the role of microclimates, potentially obscuring signals of local adaptation. We examined heat tolerance in 95 species of wild bees that varied in nesting behaviour across the latitudinal extent of Australia. Species nest (ground, wooden cavities, or plant stems) micro-climate temperatures predicted heat tolerance evolution, where stem nesters evolved the highest heat tolerances, and ground nesters evolved the lowest heat tolerances due to their ability to evade extreme heat. A moderate level of phylogenetic inertia in heat tolerance was explained by patterns of related species sharing nesting behaviours. This indicated repeated adaptive evolution of similar heat tolerances, rather than strong evolutionary constraints on heat tolerance. Finally, incorporating nesting behaviour into assessments of climate change vulnerability changed the rank order of which species were most at risk. This underscores the need to understand what drives the evolution of heat tolerance across species to better identify the taxa most at risk to climate change.

ecology↗

bioRxiv2025

Local adaptation in climate tolerance at a small geographic scale contrasts with broad latitudinal patterns

While climate adaptation is typically quantified across broad gradients, the potential for adaptation to the same environmental variables at small scales is rarely tested. If local-scale environmental heterogeneity can generate patterns of adaptation similar to broad gradients, then we currently underestimate adaptive capacity to global change. We quantified population variation in climate tolerance traits and their plasticity for five populations of Drosophila melanogaster from a 3000-km latitudinal gradient, which we contrasted with eight local populations from an environmentally heterogeneous 600x300km area. Population variation in stress tolerance at the local scale was comparable to that across latitude. Consistent with local adaptation, populations from warmer and drier environments showed greater heat and desiccation tolerance, and populations from more predictable environments showed greater plasticity. Climate adaptation at smaller geographic scales can therefore be comparable to adaptation across broad geographic scales. However, patterns of adaptation often changed across geography, which makes predicting responses to global change challenging.

evolutionary biology↗

bioRxiv2025

Variation in temperature but not diet determines the stability of latitudinal clines in tolerance traits and their plasticity

Latitudinal clines are routinely used as evidence of adaptation across broad climatic gradients. However, if environmental variation influences the strength of latitudinal clines, then clinal patterns will be unstable, and using patterns of adaptation to predict population responses to global change will be difficult. To test whether environmental variation influences latitudinal clines, we sampled five populations of Drosophila melanogaster spanning 3000-km of east coast Australia, and measured stress tolerance (heat, cold and desiccation) and body size on flies that developed in six combinations of temperature (13{degrees}C, 25{degrees}C and 29{degrees}C) and diet (standard and low-calorie) treatments. We found latitudinal clines where populations further from the equator had larger wings, higher cold tolerance and lower heat tolerance. For all traits, temperature determined the strength of latitudinal clines, whereas diet had little influence. Steeper clines often emerged in warmer treatments, created by latitudinal clines in plasticity. In the warmest temperature, higher latitude populations showed larger increases in heat tolerance, larger reductions in desiccation tolerance but smaller decreases in cold tolerance. Heat tolerance was the only trait that supported the climate variability hypothesis and a trade-off between plasticity and tolerance. Environment-dependent latitudinal clines are therefore likely to determine variation in population responses to global change.

evolutionary biology↗

bioRxiv2025

Variation in phenotypic plasticity in desiccation tolerance is driven by trade-offs, not climate, in Drosophila melanogaster

The capacity for species to respond to environmental variation via phenotypic plasticity has been proposed as a mechanism for buffering species against climate change. Two main theories are proposed to explain the evolution of phenotypic plasticity - the climate variability hypothesis and the trade-off hypothesis - but the evidence for these hypotheses remains mixed. In the current study, we examine phenotypic plasticity (hardening capacity) in desiccation resistance across populations of Drosophila melanogaster collected along a climatic gradient from eastern Australia. While climate was an important driver of innate desiccation tolerance, we found no evidence of climate shaping hardened desiccation tolerance or hardening capacity. Instead, we found that populations with high tolerance tended to have lower plasticity, indicative of a trade-off. Further analyses, accounting for statistical non-independence, showed a strong negative correlation between innate desiccation tolerance and hardening capacity, supporting the trade-off hypothesis. These results suggest that for species with high tolerance, phenotypic plasticity is unlikely to contribute to their response to climate change.

evolutionary biology↗

bioRxiv2024

Species richness patterns in Fijian bees are explained by constraints in physiological traits

Determining the ecological and evolutionary mechanisms that underpin patterns of species richness across elevational gradients is a key question in evolutionary ecology, and can help to understand species extinction risk under changing climates. In the tropical montane islands of Fiji, there are 28 species of endemic bee in the subgenus Lasioglossum (Homalictus), where species richness increases with elevation despite decreasing land surface (habitat) areas. We used a combination of spatially explicit phylogenetic diversity analyses and phylogenetic trait analyses to examine the factors shaping species distributions in these bees. We found that species at higher elevations had lower heat tolerance and desiccation resistance than those at lower elevations, consistent with these traits constraining species elevational ranges. We also found high species phylogenetic diversity within mountains, and high phylogenetic signal in species heat tolerance and minimum elevational ranges, consistent with these traits being evolutionarily conserved among mountain-top taxa following vicariant (allopatric) speciation. We found no evidence to suggest that interspecific competition is shaping species elevational ranges. In all, our findings indicate that phylogenetic conservatism in physiological traits related to climatic niche, such as heat tolerance, can explain why species richness is highest at mountain tops in this system, with species having tracked their climatic niches over time towards ever higher (cooler and wetter) elevations. Because high elevations in this archipelago are extremely limited ([~]2.3% of total land area), only miniscule elevational islands in the sky remain into which this diverse, but climate-restricted fauna, can retreat as climates warm.

evolutionary biology↗

bioRxiv2022

Physiological traits and their relationships vary along an aridity gradient within and among Fijian bee species

O_LITemperature and water availability are hypothesised to be important abiotic drivers of the evolution of metabolic rates and gas exchange patterns, respectively. Specifically, the metabolic cold adaptation hypothesis (MCA) predicts that cold environments select for faster metabolic rates to counter the thermodynamics of biochemical reactions while the hygric hypothesis predicts that dry environments select for discontinuous gas exchange to reduce water loss. C_LIO_LIAlthough these two hypotheses consider different physiological traits and how they vary along different abiotic gradients, metabolic rate drives frequency of gas exchange patterns in insects meaning these two traits are inherently linked. Despite this link, the MCA and hygric hypotheses are rarely considered together and the extent to which metabolic rates and frequency of gas exchange vary and co-vary across climatic gradients remains unclear. C_LIO_LIWe tested the MCA and hygric hypotheses within a species of endemic Fijian bee, Homalictus fijiensis, across an altitudinal gradient of 1100 m, and among four Fijian bee species, including H. fijiensis, that inhabit different altitudinal bands. In Fiji, environmental temperature is [~]5{degrees}C lower in the central highlands than in the coastal lowlands with the highlands receiving [~]100 mm of additional precipitation than the lowlands each month. C_LIO_LIWe found an MCA-like pattern within H. fijiensis and among Fijian bee species, where metabolic rate decreased with increasing temperature, but precipitation also explained variation in metabolic rate. However, we did not find support for the hygric hypothesis within H. fijiensis or among species (frequency of gas exchange was not negatively correlated with precipitation). C_LIO_LIThe relationship between metabolic rate and frequency of gas exchange was steeper for species that occupied lower elevations on average, suggesting it is possible that these two traits can evolve independently of each other despite being positively correlated. C_LI

evolutionary biology↗

bioRxiv2022

Linking physiology to ecosystem function: how vulnerable are different functional groups to climate change?

O_LIThe resilience of ecosystem function under global climate change is governed by individual species vulnerabilities and the functional groups they contribute to (e.g. decomposition, primary production, pollination, primary, secondary and tertiary consumption). Yet it remains unclear whether species that contribute to different functional groups, which underpin ecosystem function, differ in their vulnerability to climate change. C_LIO_LIIt is important to examine if functional group vulnerability differs across space (e.g. tropical vs temperate latitudes) to determine if some regions will be more vulnerable to loss of ecosystem function than others, and to examine whether localized effects of particular community compositions override global patterns of functional group vulnerability. C_LIO_LIWe used existing upper thermal limit data across a range of terrestrial species (N = 1,743) to calculate species warming margins (degrees distance between a species upper thermal limit and the maximum environmental temperature they inhabit), as a metric of climate change vulnerability, to determine whether species that comprise different functional groups exhibit differential vulnerability to climate change, and if vulnerability trends change across geographic space. C_LIO_LIWe found that primary producers had the broadest warming margins across the globe ( = 21.85 {degrees}C) and that tertiary consumers had the narrowest warming margins ( = 4.37 {degrees}C), where vulnerability tended to increase with trophic level. C_LIO_LISpecies that contribute towards primary production were more vulnerable in low-latitude than mid-latitude regions, but warming margins across all other functional groups did not differ across regions when evolutionary history was considered. However, when evolutionary history was excluded from the analyses (as closely related species often play similar functional roles within ecosystems demonstrating true variation in functional group warming margins) we found that pollinators are more vulnerable in mid-latitude regions and that primary producers are more vulnerable in low-latitude environments. C_LIO_LIThis study provides a critical first step in linking individual species vulnerabilities with whole ecosystem responses to climate change. C_LI

ecology↗