Conservation strategies often call for the utilization of corridors and/or stepping stones to promote dispersal among fragmented populations. However, the extent to which these strategies increase connectivity for an organism may depend not only on the corridors and stepping stones themselves, but also on the composition of the surrounding matrix. Using an herbivore–host‐plant system consisting of the planthopper Prokelisia crocea and its sole host plant, prairie cordgrass (Spartina pectinata), we show that the effectiveness of corridors and stepping stones for promoting planthopper dispersal among patches depended strongly on the intervening matrix habitat. In a low‐resistance matrix (one that facilitates high rates of interpatch dispersal), both stepping stones and corridors promoted high connectivity, increasing the number of colonists by threefold relative to patches separated by matrix habitat only. The effectiveness of stepping stones and corridors was significantly lower in a high‐resistance matrix (one that promotes low rates of interpatch dispersal), with stepping stones failing to improve connectivity for the planthoppers relative to controls. Thus, we conclude that the matrix is an integral component of landscapes and should be considered together with corridors and stepping stones in strategies designed to increase dispersal among fragmented populations.

The virulence–transmission trade‐off hypothesis proposed more than 30 years ago is the cornerstone in the study of host–parasite co‐evolution. This hypothesis rests on the premise that virulence is an unavoidable and increasing cost because the parasite uses host resources to replicate. This cost associated with replication ultimately results in a deceleration in transmission rate because increasing within‐host replication increases host mortality. Empirical tests of predictions of the hypothesis have found mixed support, which cast doubt about its overall generalizability. To quantitatively address this issue, we conducted a meta‐analysis of 29 empirical studies, after reviewing over 6000 published papers, addressing the four core relationships between (1) virulence and recovery rate, (2) within‐host replication rate and virulence, (3) within‐host replication and transmission rate, and (4) virulence and transmission rate. We found strong support for an increasing relationship between replication and virulence, and replication and transmission. Yet, it is still uncertain if these relationships generally decelerate due to high within‐study variability. There was insufficient data to quantitatively test the other two core relationships predicted by the theory. Overall, the results suggest that the current empirical evidence provides partial support for the trade‐off hypothesis, but more work remains to be done.

Nonlethal (trait‐mediated) effects of predators on prey populations, particularly with regard to prey dispersal, scarcely have been considered in spatial ecological studies. In this study, we report on the effects of spider predators on the mortality, dispersal, and spatial population dynamics of Prokelisia crocea planthoppers (Hemiptera: Delphacidae) in a prairie landscape. Based on a three‐generation survey of host‐plant patches (Spartina pectinata; Poaceae), the density of cursorial and web‐building spiders declined significantly with increasing patch size (a pattern the opposite of that for the planthopper). Independent of patch size effects, an increase in the density of web‐building and cursorial spiders had a negative effect on planthopper density in one of three generations each. Finally, the likelihood of extinction of local (patch) populations of planthoppers increased significantly with an increase in the density of web‐building spiders. Planthoppers in small host‐plant patches with high densities of web‐building spiders were especially at risk of extinction. To evaluate whether spider effects on planthopper spatial dynamics were mediated by predation and/or spider‐induced dispersal, we performed a field experiment in which host‐plant patches were either caged or left open and received one of three spider density treatments (removal, ambient levels, or high = triple ambient levels). For the caged patches, there was a nonsignificant decline in planthopper recaptures with increasing spider density, suggesting that mortality effects of spiders on planthoppers were weak. In contrast, planthopper recaptures in open patches declined by 85% between the removal and high spider treatments. This significant decline was mostly attributed to spider‐induced emigration. We conclude that, at high spider densities, spiders are likely to have a greater impact on planthopper densities through induced emigration than consumption. Because small cordgrass patches support high spider densities and favor high planthopper emigration rates, the nonlethal effects of spiders may play a very important role in determining critical patch size, source–sink properties of cordgrass patches, and the spatial distribution and spread of planthoppers.

Past studies with spatially structured herbivore populations have emphasized the primacy of intrinsic factors (e.g., patch quality), patch geometry (e.g., patch size and isolation), and more recently landscape context (e.g., matrix composition) in affecting local population abundance and dispersal rate. However, few studies have examined the relative importance of each factor, or how they might interact to affect herbivore abundance or dispersal. Here, we performed a factorial field experiment to examine the independent and interactive effects of patch quality (plant biomass, leaf protein, leaf phenolics) and matrix composition [mudflat or non-host grass (Bromus inermis)] on planthopper (Prokelisia crocea) emigration from host-plant patches (prairie cordgrass, Spartina pectinata). In addition, a field survey was conducted to examine the relative importance of patch quality, geography, and matrix composition on planthopper occupancy and density. In the experiment, we found that rates of emigration from low and intermediate quality patches were, on average, 21% percent higher for patches embedded in brome than mudflat. In contrast, the emigration rate was unaffected by matrix composition in nutrient-rich patches. Within matrix types, plant quality had little effect on emigration. In the survey, planthopper density and the patch occupancy rate of planthoppers increased nonadditively with increasing patch size and the percentage of the surrounding matrix composed of mudflat. This study suggests that landscape-level factors, such as the matrix, may be more important than factors intrinsic to the patches.

Cannibalism occurs in a majority of both carnivorous and noncarnivorous animal taxa from invertebrates to mammals. Similarly, infectious parasites are ubiquitous in nature. Thus, interactions between cannibalism and disease occur regularly. While some adaptive benefits of cannibalism are clear, the prevailing view is that the risk of parasite transmission due to cannibalism would increase disease spread and, thus, limit the evolutionary extent of cannibalism throughout the animal kingdom. In contrast, surprisingly little attention has been paid to the other half of the interaction between cannibalism and disease, that is, how cannibalism affects parasites. Here we examine the interaction between cannibalism and parasites and show how advances across independent lines of research suggest that cannibalism can also reduce the prevalence of parasites and, thus, infection risk for cannibals. Cannibalism does this by both directly killing parasites in infected victims and by reducing the number of susceptible hosts, often enhanced by the stage-structured nature of cannibalism and infection. While the well-established view that disease should limit cannibalism has held sway, we present theory and examples from a synthesis of the literature showing how cannibalism may also limit disease and highlight key areas where conceptual and empirical work is needed to resolve this debate.