Summary The ungulate–carnivore–vulture complex is a key trophic module of many terrestrial ecosystems, but one that is globally under threat. Few have explored cross‐species dependencies in this module, and the degree to which vultures rely on trophic facilitation by apex carnivores is rarely known and almost never quantified. We investigated the importance of puma Puma concolor predation on its native camelid prey, vicuñas Vicugna vicugna and guanacos Lama guanicoe, in food provisioning for Andean condors Vultur gryphus in the high Andes of north‐western Argentina. We evaluated the origin of wild food sources through carcass surveys. We quantified condor feeding habits via foraging observations and through the analysis of pellet contents and stable isotopes from moulted feathers. Of the 102 fresh camelid carcasses we monitored, nearly all (94%) resulted from puma predation, and the majority (85%) of camelid carcasses used by condors were killed by pumas. Camelids represented 88% of the prey items identified from 183 condor pellets, and isotopic analyses of moulted feathers from 86 individuals identified via multilocus genotyping revealed that camelids and Small livestock were the most important prey items, representing 45–58% and 28–38% of condor assimilated biomass, respectively. Synthesis and applications. Our results show that puma predation plays a key role in the foraging ecology of Andean condors, and highlight the importance of predatory processes that make carrion available to scavengers. We contend that targeting the conservation of ungulate–carnivore–vulture modules, rather than a species‐specific approach, will be a more effective strategy to ensure the long‐term persistence of Andean condors and other obligate scavengers.

Predator-prey games emerge when predators and prey dynamically respond to the behavior of one another, driving the outcomes of predator-prey interactions. Predation success is a function of the combined probabilities of encountering and capturing prey, which are influenced by both prey behavior and environmental features. While the relative importance of encounter and capture probabilities have been evaluated in a spatial framework, temporal variation in prey behavior and intrinsic catchability are likely to also affect the distribution of predation events. Using a single-predator-single-prey (puma-vicuña) system, we evaluated which factors predict predation events across both temporal and spatial dimensions of the components of predation by testing the prey-abundance hypothesis (predators select for high encounter probability) and the prey-catchability hypothesis (predators select for high relative capture probability) in time and space. We found that for both temporal and spatial analyses, neither the prey-abundance hypothesis nor the prey-catchability hypothesis alone predicted kill frequency or distribution; puma kill frequency was static throughout the diel cycle and pumas consistently selected a single habitat type when hunting, despite temporal and spatial variation in encounter rates and intrinsic catchability. Our integrated spatiotemporal analysis revealed that an interaction between time of day and habitat influences kill probability, suggesting that trade-offs in the temporal and spatial components of predation drive the probability of predation events. These findings reinforce the importance of examining both the temporal and spatial patterns of the components of predation, rather than unidimensional measures of predator or prey behavior, to comprehensively describe the feedbacks between predator and prey in the predator-prey game.

Disease outbreaks induced by humans increasingly threaten wildlife communities worldwide. Like predators, pathogens can be key top-down forces in ecosystems, initiating trophic cascades that may alter food webs. An outbreak of mange in a remote Andean protected area caused a dramatic population decline in a mammalian herbivore (the vicuña), creating conditions to test the cascading effects of disease on the ecological community. By comparing a suite of ecological measurements to pre-disease baseline records, we demonstrate that mange restructured tightly linked trophic interactions previously driven by a mammalian predator (the puma). Following the mange outbreak, scavenger (Andean condor) occurrence in the ecosystem declined sharply and plant biomass and cover increased dramatically in predation refuges where herbivory was historically concentrated. The evidence shows that a disease-induced trophic cascade, mediated by vicuña density, could supplant the predator-induced trophic cascade, mediated by vicuña behaviour, thereby transforming the Andean ecosystem.