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A long‐standing question in ecology is how species interactions are structured within communities. Although evolutionary theory predicts close size matching between floral nectar tube depth and pollinator proboscis length of interacting species, such size matching has seldom been shown and explained in multispecies assemblages. Here, we investigated the degree of size matching among Asteraceae and their pollinators and its relationship with foraging efficiency. The majority of pollinators, especially Hymenoptera, choose plant species on which they had high foraging efficiencies. When proboscides were shorter than nectar tubes, foraging efficiency rapidly decreased because of increased handling time. When proboscides were longer than nectar tubes, a decreased nectar reward rather than an increased handling time made shallow flowers more inefficient to visit. Altogether, this led to close size matching. Overall, our results show the importance of nectar reward and handling time as drivers of plant–pollinator network structure.

[Aim] Intraspecific trait variation (ITV) within natural plant communities can be large, influencing local ecological processes and dynamics. Here, we shed light on how ITV in vegetative and floral traits responds to large‐scale abiotic and biotic gradients (i.e., climate and species richness). Specifically, we tested whether associations of ITV with temperature, precipitation and species richness were consistent with any of four hypotheses relating to stress tolerance and competition. Furthermore, we estimated the degree of correlation between ITV in vegetative and floral traits and how they vary along the gradients., [Location] Global., [Time period] 1975–2016., [Major taxa studied] Herbaceous and woody plants., [Methods] We compiled a dataset of 18,401 measurements of the absolute extent of ITV (measured as the coefficient of variation) in nine vegetative and seven floral traits from 2,822 herbaceous and woody species at 2,372 locations., [Results] Large‐scale associations between ITV and climate were trait specific and more prominent for vegetative traits, especially leaf morphology, than for floral traits. The ITV showed pronounced associations with climate, with lower ITV values in colder areas and higher values in drier areas. The associations of ITV with species richness were inconsistent across traits. Species‐specific associations across gradients were often idiosyncratic, and covariation in ITV was weaker between vegetative and floral traits than within the two trait groups. [Main conclusions] Our results show that, depending on the traits considered, ITV either increased or decreased with climate stress and species richness, suggesting that both factors can constrain or enhance ITV, which might foster plant‐population persistence in stressful conditions. Given the species‐specific responses and covariation in ITV, associations can be hard to predict for traits and species not yet studied. We conclude that consideration of ITV can improve our understanding of how plants cope with stressful conditions and environmental change across spatial and biological scales., Open Access funding was provided by Ulm University under the DEAL‐agreement.

Summary Biotic interactions do not occur in isolation but are imbedded in a network of species interactions. Network analysis facilitates the compilation and understanding of the complexity found in natural ecosystems and is a powerful tool to reveal information on the degree of specialization of the interacting partners and their niches. The indices measuring these properties are based on qualitative or quantitative observations of interactions between partners from different trophic levels, which informs about the structure of network patterns, but not about the underlying mechanisms. Functional traits may control the interaction strength between partners and also the (micro-) structure of networks. Here, we ask whether flower visitors specialize on certain plant traits and how this trait specialization contributes to niche partitioning and interaction partner diversity. We introduce two novel statistical approaches suited to evaluate the dimension of the realized niche and to analyse which traits determine niches. As basis for our analysis, we measured 10 quantitative flower traits and evaluated whether 31 arthropod taxa i visited flowers displaying only subsets of the available trait characteristics, indicating a specialization on these traits by narrow trait-widths 〈Si〉. The product of 10 trait- and species-specific trait-widths 〈Si〉 was defined as trait-volume Vi (expansion of a n-dimensional hypervolume) occupied by each taxon i. These indices are applicable beyond flower–visitor interactions to quantify realized niches based on various biotic and abiotic factors. Each flower visitor species showed some degree of specialization to a unique set of flower traits (realized niche). Overall, our data suggested a hierarchical sequence of flower traits influencing the flower visitors' behaviour and thus network structure: flowering phenology was found to have the strongest effect, followed by flower height, nectar-tube depth and floral reflectance. Less important were pollen-mass/flower, sugar/flower, anther position, phylogeny, display size and abundance. The species-specific specialization on traits suggests that plant communities with more diverse floral niches may sustain a larger number of flower visitors with non-redundant fundamental niches. Our study and statistical approach provide a basis for a better understanding of how plant traits shape interactions between flowers and their visitors and thus network structure.

The number of interactions with flower visitor species differs considerably among insect pollinated plants. Knowing the causes for this variation is central to the conservation of single species as well as whole plant � /flower visitor communities. Species specific constraints on flower visitor numbers are seldom investigated at the community level. In this study we tested whether flower size parameters set constraints on the morphology of the potential nectar feeding visitors and thus determine the number of visitor species. We studied three possible constraints: the depth and width of tubular structures hiding the nectar (nectar holder depth and width) and the size of flower parts that visitors can land on (size of the alighting place). In addition we assess the role of flower abundance on this relationship. We hypothesized that the stronger size constraints and the smaller flower abundance, the smaller the number of visitor species will be. Our study of a Mediterranean plant � /flower visitor community revealed that nectar holder depth, nectar holder width and number of flowers explained 71% of the variation in the number of visitor species. The size of the alighting place did not restrict the body length of the visitors and was not related to visitor species number. In a second step of the analyses we calculated for each plant species the potential number of visitors by determining for each insect species of the local visitor pool whether it passed the morphological limits set by the plant. These potential numbers were highly correlated with the observed numbers (r 2 � /0.5, p B /0.001). For each plant species we tested whether the observed visitors were a random selection out of these potential visitors by comparing the mean of the observed and expected proboscis length distributions. For most plant species the observed mean was not significantly different from the random means. Our findings shed light on the way plant � /flower visitor networks are structured. Knowing the constraints on interaction patterns will be an important prerequisite to formulate realistic null models and understand patterns of resource partitioning as well as coevolutionary processes.