Summary• It has long been believed that plant species from the tropics have higher levels of traits associated with resistance to herbivores than do species from higher latitudes. A meta-analysis recently showed that the published literature does not support this theory. However, the idea has never been tested using data gathered with consistent methods from a wide range of latitudes.• We quantified the relationship between latitude and a broad range of chemical and physical traits across 301 species from 75 sites world-wide.• Six putative resistance traits, including tannins, the concentration of lipids (an indicator of oils, waxes and resins), and leaf toughness were greater in highlatitude species. Six traits, including cyanide production and the presence of spines, were unrelated to latitude. Only ash content (an indicator of inorganic substances such as calcium oxalates and phytoliths) and the properties of species with delayed greening were higher in the tropics.• Our results do not support the hypothesis that tropical plants have higher levels of resistance traits than do plants from higher latitudes. If anything, plants have higher resistance toward the poles. The greater resistance traits of high-latitude species might be explained by the greater cost of losing a given amount of leaf tissue in low-productivity environments.

SummaryMost plant species have a range of traits that deter herbivores. However, understanding of how different defences are related to one another is surprisingly weak. Many authors argue that defence traits trade off against one another, while others argue that they form coordinated defence syndromes.We collected a dataset of unprecedented taxonomic and geographic scope (261 species spanning 80 families, from 75 sites across the globe) to investigate relationships among four chemical and six physical defences.Five of the 45 pairwise correlations between defence traits were significant and three of these were tradeoffs. The relationship between species' overall chemical and physical defence levels was marginally nonsignificant (P = 0.08), and remained nonsignificant after accounting for phylogeny, growth form and abundance. Neither categorical principal component analysis (PCA) nor hierarchical cluster analysis supported the idea that species displayed defence syndromes.Our results do not support arguments for tradeoffs or for coordinated defence syndromes. Rather, plants display a range of combinations of defence traits. We suggest this lack of consistent defence syndromes may be adaptive, resulting from selective pressure to deploy a different combination of defences to coexisting species.

Interactions between resource and consumer species are organized in ecological networks. Species interactions in these networks are influenced by the functional traits of the interacting partners, but the generality of trait-based interaction rules and the relationship between functional traits and a species' specialization on specific interaction partners are not yet understood. Here we combine data on eight interaction networks between fleshy-fruited plants and frugivorous birds sampled across the tropical and subtropical Andean range. We test which combinations of morphological plant and animal traits determine trait matching between resource and consumer species in these networks. In addition, we test which of the morphological traits influence functional specialization of plant and bird species. In a meta-analysis across network-specific fourth-corner analyses, we found that plant-animal trait pairs related to size matching (fruit size-beak size) and avian foraging behavior (plant height-wing shape and crop mass-body mass) were positively related in these networks. The degree of functional specialization on specific interaction partners was positively related to crop mass in plants and to the pointedness of the wing in birds. Our findings show that morphological trait matching between fleshy-fruited plants and frugivorous birds is a general phenomenon in plant-frugivore networks across the Andes and that specific plant and bird traits can be used to approximate the degree of functional specialization. These insights into the generality of interaction rules are the base for predictions of species interactions in ecological networks, for instance in novel communities in the future, and can be applied to identify plant and animal species that fulfill specialized functional roles in ecological communities.

We studied the efficiency (proportion of the crop removed) and quantitative effectiveness (number of fruits removed) of dispersal of Miconia fosteri and M. serrulata (Melastomataceae) seeds by birds in lowland tropical wet forest of Ecuador. Specifically, we examined variation in fruit removal in order to reveal the spatial scale at which crop size influences seed dispersal outcome of individual plants, and to evaluate how the effect of crop size on plant dispersal success may be affected by conspecific fruit abundance and by the spatial distribution of frugivore abundance. We established two 9-ha plots in undisturbed terra-firme understory, where six manakin species (Pipridae) disperse most seeds of these two plant species. Mean levels of fruit removal were low for both species, with high variability among plants. In general, plants with larger crop sizes experienced greater efficiency and effectiveness of fruit removal than plants with smaller crops. Fruit removal, however, was also influenced by microhabitat, such as local topography and local neighborhood. Fruit-rich and disperser-rich patches overlapped spatially for M. fosteri but not M. serrulata, nonetheless fruit removal of M. serrulata was still much greater in fruit-rich patches. Fruit removal from individual plants did not decrease in patches with many fruiting conspecifics and, in fact, removal effectiveness was enhanced for M. fosteri with small crop sizes when such plants were in patches with more conspecifics. These results suggest that benefits of attracting dispersers to a patch balanced or outweighed the costs of competition for dispersers. Spatial pattern of fruit removal, a measure of plant fitness, depended on a complex interaction among plant traits, spatial patterns of plant distribution, and disperser behavior.

Summary1. The fruit-tracking hypothesis predicts spatiotemporal links between changes in the abundance of fruit-eating birds and the abundance of their fleshy-fruit resources. 2. While the spatial scale of plant-frugivore interactions has been explored to understand mismatches between observed and expected fruit-frugivore patterns, methodological issues such as the consequences of measuring fruit and frugivore abundance rather than fruit availability and fruit consumption have not been evaluated. 3. Here, we explored whether predicted fruit-frugivore spatiotemporal links can be captured with higher accuracy by proximate measurements of interaction strength. We used a 6-ha grided plot in an Andean subtropical forest to study the link between (i) fruit and fruit-eating bird abundances; (ii) fruit availability and frequency of fruit consumption; and (iii) covariation between frugivore abundance and frequency of frugivory. We evaluated these links for the entire frugivore assemblage and for the four most important species using data gathered bimonthly along a 2-year period. 4. Fleshy-fruit availability and abundance varied sharply temporally and were patchily distributed in mosaics that differed in fruit quantity. Fruit availability and abundance also varied along spatial gradients extended over the whole study plot. We found a strong response of the entire frugivorous bird assemblage to fruit availability over time, and a weakly significant relationship over space at the local scale. The main frugivore species widely differed in their responses to changes in fruit abundance in such a way that response at the assemblage level cannot be seen as the sum of individual responses of each species. Our results suggest that fruit tracking in frugivorous-insectivorous birds may be largely explained by species-specific responses to changes in the availability of fruits and alternative resources. 5. In agreement with our prediction, more accurate measurements of interaction strength described fruit-frugivore relationships better than traditional measurements. Moreover, we show that covariation between frugivore abundance, frequency of fruit consumption and fruit availability must be included in the fruit-tracking hypothesis framework to demonstrate (or reject) spatiotemporal fruit tracking. We propose that estimation of nutrient and energy availability in fruits could be a new frontier to understanding the forces driving foraging decisions that lead to fruit tracking.

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Downsizing of animal communities due to defaunation is prevalent in many ecosystems. Yet, we know little about its consequences for ecosystem functions such as seed dispersal. Here, we use eight seed-dispersal networks sampled across the Andes and simulate how downsizing of avian frugivores impacts structural network robustness and seed dispersal. We use a trait-based modeling framework to quantify the consequences of downsizing—relative to random extinctions—for the number of interactions and secondary plant extinctions (as measures of structural robustness) and for long-distance seed dispersal (as a measure of ecosystem function). We find that downsizing leads to stronger functional than structural losses. For instance, 10% size-structured loss of bird species results in almost 40% decline of long-distance seed dispersal, but in less than 10% of structural loss. Our simulations reveal that measures of the structural robustness of ecological networks underestimate the consequences of animal extinction and downsizing for ecosystem functioning.

Habitat loss is the primary cause of local extinctions. Yet, there is considerable uncertainty regarding how fast species respond to habitat loss, and how time‐delayed responses vary in space. We focused on the Argentine Dry Chaco (c. 32 million ha), a global deforestation hotspot, and tested for time‐delayed response of bird and mammal communities to landscape transformation. We quantified the magnitude of extinction debt by modelling contemporary species richness as a function of either contemporary or past (2000 and 1985) landscape patterns. We then used these models to map communities' extinction debt. We found strong evidence for an extinction debt: landscape structure from 2000 explained contemporary species richness of birds and mammals better than contemporary and 1985 landscapes. This suggests time‐delayed responses between 10 and 25 years. Extinction debt was especially strong for forest specialists. Projecting our models across the Chaco highlighted areas where future local extinctions due to unpaid extinction debt are likely. Areas recently converted to agriculture had highest extinction debt, regardless of the post‐conversion land use. Few local extinctions were predicted in areas with remaining larger forest patches. Synthesis and applications. The evidence for an unpaid extinction debt in the Argentine Dry Chaco provides a substantial window of opportunity for averting local biodiversity losses. However, this window may close rapidly if conservation activities such as habitat restoration are not implemented swiftly. Our extinction debt maps highlight areas where such conservation activities should be implemented.