Search

Predicting whether microbial invaders will colonize an environment is critical for managing natural and engineered ecosystems, and controlling infectious disease. Invaders often face competition by resident microbes. But how invasions play out in communities dominated by facilitative interactions is less clear. We previously showed that growth medium toxicity can promote facilitation between four bacterial species, as species that cannot grow alone rely on others to survive. Following the same logic, here we allowed other bacterial species to invade the four-species community and found that invaders could more easily colonize a toxic medium when the community was present. In a more benign environment instead, invasive species that could survive alone colonized more successfully when the residents were absent. Next, we asked whether early colonists could exclude future ones through a priority effect, by inoculating the invaders into the resident community only after its members had co-evolved for 44 weeks. Compared to the ancestral community, the co-evolved resident community was more competitive toward invaders and less affected by them. Our experiments show how communities may assemble by facilitating one another in harsh, sterile environments, but that arriving after community members have co-evolved can limit invasion success., (© 2022. The Author(s).)

Adaptation to climate is expected to increase the performance of invasive species and their community-level impacts. However, while the fitness gains from adaptation should, in general, promote invader competitive ability, empirical demonstrations of this prediction are scarce. Furthermore, climate adaptation, in the form of altered timing of life cycle transitions, should affect the phenological overlap between nonnative and native competitors, with potentially large, but poorly tested, impacts on native species persistence. We evaluated these predictions by growing native California grassland plants in competition with nonnative Lactuca serriola , a species that flowers earlier in parts of its nonnative range that are drier than its putative European source region. In common garden experiments in southern California with L. serriola populations differing in phenology, plants originating from arid climates bolted up to 48 d earlier than plants from more mesic climates, and selection favored early flowering, supporting an adaptive basis for the phenology cline. The per capita competitive effects of L. serriola from early flowering populations on five early flowering native species were greater than the effects of L. serriola from later flowering populations. Consequently, the ability of the native species to increase when rare in competition with L. serriola , as inferred from field-parameterized competition models, declined with earlier L. serriola phenology. Indeed, changes to L. serriola phenology affected whether or not one native species was predicted to persist in competition with L. serriola Our results suggest that evolution in response to new climatic conditions can have important consequences for species interactions, and enhance the impacts of biological invasions on natural communities., Competing Interests: The authors declare no conflict of interest.

Invasive and endangered species reflect opposite ends of a spectrum of ecological success, yet they experience many similar eco-evolutionary challenges including demographic bottlenecks, hybridization and novel environments. Despite these similarities, important differences exist. Demographic bottlenecks are more transient in invasive species, which (i) maintains ecologically relevant genetic variation, (ii) reduces mutation load, and (iii) increases the efficiency of natural selection relative to genetic drift. Endangered species are less likely to benefit from admixture, which offsets mutation load but also reduces fitness when populations are locally adapted. Invading species generally experience more benign environments with fewer natural enemies, which increases fitness directly and also indirectly by masking inbreeding depression. Adaptive phenotypic plasticity can maintain fitness in novel environments but is more likely to evolve in invasive species encountering variable habitats and to be compromised by demographic factors in endangered species. Placed in an eco-evolutionary context, these differences affect the breadth of the ecological niche, which arises as an emergent property of antagonistic selection and genetic constraints. Comparative studies of invasions and extinctions that apply an eco-evolutionary perspective could provide new insights into the environmental and genetic basis of ecological success in novel environments and improve efforts to preserve global biodiversity.This article is part of the themed issue 'Human influences on evolution, and the ecological and societal consequences'., (© 2016 The Author(s).)

Biologists have recently devoted increasing attention to the role of rapid evolution in species' responses to environmental change. However, it is still unclear what evolutionary responses should be expected, at what rates, and whether evolution will save populations at risk of extinction. The potential of biological invasions to provide useful insights has barely been realised, despite the close analogies to species responding to global change, particularly climate change; in both cases, populations encounter novel climatic and biotic selection pressures, with expected evolutionary responses occurring over similar timescales. However, the analogy is not perfect, and invasive species are perhaps best used as an upper bound on expected change. In this article, we review what invasive species can and cannot teach us about likely evolutionary responses to global change and the constraints on those responses. We also discuss the limitations of invasive species as a model and outline directions for future research., (© 2014 John Wiley & Sons Ltd/CNRS.)

A topic of great current interest is the capacity of populations to adapt genetically to rapidly changing climates, for example by evolving the timing of life-history events, but this is challenging to address experimentally. I use a plant invasion as a model system to tackle this question by combining molecular markers, a common garden experiment and climatic niche modelling. This approach reveals that non-native Lactuca serriola originates primarily from Europe, a climatic subset of its native range, with low rates of admixture from Asia. It has rapidly refilled its climatic niche in the new range, associated with the evolution of flowering phenology to produce clines along climate gradients that mirror those across the native range. Consequently, some non-native plants have evolved development times and grow under climates more extreme than those found in Europe, but not among populations from the native range as a whole. This suggests that many plant populations can adapt rapidly to changed climatic conditions that are already within the climatic niche space occupied by the species elsewhere in its range, but that evolution to conditions outside of this range is more difficult. These findings can also help to explain the prevalence of niche conservatism among non-native species.

A non-native plant species spreading along an environmental gradient may need to adjust its growth to the prevailing conditions that it encounters by a combination of phenotypic plasticity and genetic adaptation. There have been several studies of how non-native species respond to changing environmental conditions along latitudinal gradients, but much less is known about elevational gradients. We conducted a climate chamber experiment to investigate plastic and genetically based growth responses of 13 herbaceous non-native plants along an elevational gradient from 100 to 2,000 m a.s.l. in Tenerife. Conditions in the field ranged from high anthropogenic disturbance but generally favourable temperatures for plant growth in the lower half of the gradient, to low disturbance but much cooler conditions in the upper half. We collected seed from low, mid and high elevations and grew them in climate chambers under the characteristic temperatures at these three elevations. Growth of all species was reduced under lower temperatures along both halves of the gradient. We found consistent genetically based differences in growth over the upper elevational gradient, with plants from high-elevation sites growing more slowly than those from mid-elevation ones, while the pattern in the lower part of the gradient was more mixed. Our data suggest that many non-native plants might respond to climate along elevational gradients by genetically based changes in key traits, especially at higher elevations where low temperatures probably impose a stronger selection pressure. At lower elevations, where anthropogenic influences are greater, higher gene flow and frequent disturbance might favour genotypes with broad ecological amplitudes. Thus the importance of evolutionary processes for invasion success is likely to be context-dependent.

Extreme abiotic conditions, geographic isolation, and low levels of disturbance have historically provided alpine, Arctic, and Antarctic regions with low input of and relative resistance to the introduction of new species. However, the climate is warming rapidly, concomitant with intense and diversified types of human influence in these cold environments. Consequently, many plant species, both native and nonnative, are now moving or expanding their ranges to higher elevations and latitudes, creating new species interactions and assemblages that challenge biodiversity conservation. Based on our synthesis, many of the same nonnative species invade multiple cold environments, and many more could move up or over from adjoining warmer areas. Transportation networks and the disturbances associated with burgeoning development are responsible for many movements. Prevention and monitoring for nonnative plant species is of paramount importance, and management should be directed toward species that negatively impact ecosystem function or human well-being. Management of native range shifters is more complicated; most movements will be desirable, but some may be locally undesirable. Overall, plant movements into alpine, arctic, and Antarctic areas are going to increase, and management will need to be adaptive because species movements and assemblages of the past will not reflect those of the future. [ABSTRACT FROM AUTHOR]

Aim: We investigated patterns of species richness and community dissimilarity along elevation gradients using globally replicated, standardized surveys of vascular plants. We asked how these patterns of diversity are influenced by anthropogenic pressures (road construction and non-native species). Location: Global. Time period: 2008-2015. Major taxa studied: Vascular plants. Methods: Native and non-native vascular plant species were recorded in 943 plots along 25 elevation gradients, in nine mountain regions, on four continents. Sampling took place in plots along and away from roads. We analysed the effects of elevation and distance from road on species richness patterns and community dissimilarity (beta-diversity), and assessed how non-native species modified such elevational diversity patterns. Results: Globally, native and total species richness showed a unimodal relationship with elevation that peaked at lower-mid elevations, but these patterns were altered along roads and due to non-native species. Differences in elevational species richness patterns between regions disappeared along roadsides, and non-native species changed the patterns' character in all study regions. Community dissimilarity was reduced along roadsides and through non-native species. We also found a significant elevational decay of beta-diversity, which however was not affected by roads or non-native species. Main conclusions: Idiosyncratic native species richness patterns in plots away from roads implicate region-specific mechanisms underlying these patterns. However, along roadsides a clearer elevational signal emerged and species richness mostly peaked at mid-elevations. We conclude that both roads and non-native species lead to a homogenization of species richness patterns and plant communities in mountains. [ABSTRACT FROM AUTHOR]

Background: In temperate mountains, most non-native plant species reach their distributional limit somewhere along the elevational gradient. However, it is unclear if growth limitations can explain upper range limits and whether phenotypic plasticity or genetic changes allow species to occupy a broad elevational gradient. Aims: We investigated how non-native plant individuals from different elevations responded to growing season temperatures, which represented conditions at the core and margin of the elevational distributions of the species. Methods: We recorded the occurrence of nine non-native species in the Swiss Alps and subsequently conducted a climate chamber experiment to assess growth rates of plants from different elevations under different temperature treatments. Results: The elevational limit observed in the field was not related to the species' temperature response in the climate chamber experiment. Almost all species showed a similar level of reduction in growth rates under lower temperatures independent of the upper elevational limit of the species' distribution. For two species we found indications for genetic differentiation among plants from different elevations. Conclusions: We conclude that factors other than growing season temperatures, such as extreme events or winter mortality, might shape the elevational limit of non-native species, and that ecological filtering might select for genotypes that are phenotypically plastic. [ABSTRACT FROM PUBLISHER]