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Urban Ecosystems · 2026 · Vol. 29 · Issue 4 · Springer
Urban environments exert selective pressures on the functional composition of plant communities. Green spaces associated with traffic are widespread in cities and could therefore support pollinator biodiversity. This emphasizes the need to characterize the diversity of pollination-related traits within plant communities occupying these habitats. Hence, we investigated how pollination-related functional traits are associated wi...
Molecular Ecology · 2026 · Vol. 35 · Issue 10 · Wiley
Marilia Souza Lucas; Christoph Rosche; Isabell Hensen; Stefan G. Michalski; Dávid U. Nagy; Diana Gamba; Renske E. Onstein; Karime Abidkulova; Mohammad Al‐Gharaibeh; Ali A. Al‐Namazi; Sirwan Babaei; Fernando Bastida; Caio Brunharo; Aurélien Caillon; Ragan M. Callaway; Sam St Clair; Darron A. Cullen; Ryan Donnelly; Alyson Ennis; David J. Ensing; Özkan Eren; Andrey Erst; Rita Filep; Luke Flory; Lauren J. Frazee; Yusufjon Gafforov; Fidji Gendron; Zigmantas Gudžinskas; Christopher Matt Guilliams; Avni Hajdari; Jian‐Hua Hao; Erin Haramoto; Anna A. Ivashchenko; Li Jun; Nolan Kane; Matthew A. Kaproth; Hesham Kassem; Abdelmajid Khabbach; Damase P. Khasa; Matthew Koski; Maria Kozhevnikova; Nikos Krigas; Denis Krivenko; Jesse R. Lasky; Ylva Lekberg; Mohamed Libiad; Vanessa Lozano; Wenbo Luo; Trobjon Makhkamov; Elizabete Marchante; Chandra Moffat; Abigail Moore; Albert Muldashev; Anush Nersesyan; Pål l Axel Olsson; Adrian Oprea; Robert Pal; Astghik Papikyan; Christopher Proctor; Vadim Prokhorov; Satu Ramula; Emily Rauschert; Bryan Reatini; Christian Rixen; Scott Rush; Gemma Rutten; Mariem Saadani; Ioulietta Samartza; Julian Selke; Stepan Senator; Manzoor A. Shah; Min Sheng; Jamal Sheriff; Baasanmunkh Shukherdorj; Peter Sikkema; Tatiana Silaeva; Satoshi N. Suzuki; Arpad E. Thoma; Baoliang Tian; Valeriy Tokhtar; Sabrina Träger; Tomonori Tsunoda; Orzimat Turginov; Kathryn G. Turner; Tatyana Vakhlamova; Yulia Vinogradova; Viktoria Wagner; Lydia Westberg; Sa Xiao; Christopher D. Barratt; Walter Durka
Invasive plant species present a growing ecological and economic challenge, and often adapt rapidly to their novel environments through complex demographic and evolutionary processes. Invasion genomics offers powerful tools to disentangle these processes, but most studies rely on geographically narrow sampling across native and non‐native ranges. Erigeron canadensis is a cosmopolitan weed native to North America that has succe...
Biological Invasions · 2025 · Vol. 27 · Issue 9 · Springer
Whilst temporal dynamics of the abundance of invasive alien species has gained interest, less is understood about complex interactions determining their impacts on, e.g., how coexistence mechanisms and the resulting ecological impact of alien species change with time. Using the invasive nitrogen-fixing Lupinus polyphyllus (lupine) and its native competitor Leucanthemum vulgaris (daisy), we investigated the effect of time since...
Plant and Soil · 2023 · Vol. 490 · Issue 1-2 · Springer
Background and aims For invasive plant species that associate with mutualistic symbionts, partner quality can be critical to their invasion success. This might be particularly true for legumes that host nitrogen-fixing bacteria (rhizobia). Here, we examined the relative effectiveness of rhizobial strains on the invasive legume Lupinus polyphyllus . Methods We isolated rhizobia from field populations of L. polyphyllus and condu...
Biological Invasions · 2022 · Vol. 24 · Issue 2 · Springer
The ecological impacts of invasive species may change or accumulate with time since local invasion, potentially inducing further changes in communities and the abiotic environment. Yet, time since invasion is rarely considered when investigating the ecological impacts of invasive non-native species. To examine the effect of time since invasion on the ecological impacts of Lupinus polyphyllus , a perennial nitrogen-fixing herb,...
Biological Invasions · 2022 · Vol. 24 · Issue 1 · Springer
Intraspecific variation in growth and defence among plant populations can be driven by differences in (a)biotic conditions, such as herbivory and resources. Introduction of species to novel environments affects simultaneously herbivory encountered by a plant and resource availability both directly and via altered competitive environment. Here, we address the question of how growth (leaf mass per area (LMA), plant size) and res...
Ecology Letters · 2021 · Vol. 24 · Issue 11 · Wiley
Genetic differentiation and phenotypic plasticity jointly shape intraspecific trait variation, but their roles differ among traits. In short‐lived plants, reproductive traits may be more genetically determined due to their impact on fitness, whereas vegetative traits may show higher plasticity to buffer short‐term perturbations. Combining a multi‐treatment greenhouse experiment with observational field data throughout the rang...
Biological Invasions · 2020 · Vol. 22 · Issue 10 · Springer
In order to manage invasive plant species efficiently, it is necessary to have a thorough understanding of different strategies of population control, including the underlying mechanisms of action and the consequences for target populations. Here, I explored the effectiveness of biomass removal as a method of control for the invasive perennial herb Lupinus polyphyllus . More specifically, using seed material from 11 population...
Ecology · 2019 · Vol. 100 · Issue 5 · Wiley
Biomass removal by herbivores usually incurs a fitness cost for the attacked plants, with the total cost per unit lost tissue depending on the value of the removed tissue (i.e., how costly it is to be replaced by regrowth). Optimal defense theory, first outlined in the 1960s and 1970s, predicted that these fitness costs result in an arms race between plants and herbivores, in which selection favors resistance strategies that e...
Ecology · 2018 · Vol. 99 · Issue 4 · Wiley
Temperature and precipitation determine the conditions where plant species can occur. Despite their significance, to date, surprisingly few demographic field studies have considered the effects of abiotic drivers. This is problematic because anticipating the effect of global climate change on plant population viability requires understanding how weather variables affect population dynamics. One possible reason for omitting the...
Ecology · 2018 · Vol. 99 · Issue 2 · Wiley
As a compensatory response to herbivory, plants may branch vigorously when the growth of dormant meristems is triggered by shoot damage. Undamaged plants, on the other hand, often restrain branching, and this limitation on growth can be considered a cost of tolerance to herbivory. Restrained branching is caused by apical dominance and may, alternatively, be associated with fitness benefits in competitive environments that favo...
Ecology Letters · 2010 · Vol. 13 · Issue 9 · Wiley
Ecology Letters (2010) 13: 1182–1197 Abstract Explaining variation in population growth rates is fundamental to predicting population dynamics and population responses to environmental change. In this study, we used matrix population models, which link birth, growth and survival to population growth rate, to examine how and why population growth rates vary within and among 50 terrestrial plant species. Population growth rates...