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1. Video surveillance reveals a community of largely nocturnal Danaus plexippus (L.) egg predators

   https://doi.org/10.1007/s10841-020-00248-w  

   Myers, Andrew T.; Haan, Nathan L.; Landis, Douglas A. (May 2020, Journal of Insect Conservation)

   Monarch butterfly (Danaus plexippus L.) declines in eastern North America have prompted milkweed host plant restoration efforts in non-agricultural grasslands. However, grasslands harbor predator communities that exert high predation pressure on monarch eggs and larvae. While diurnal monarch predators are relatively well known, no studies have investigated the contribution of nocturnal monarch predators. We used video cameras to monitor sentinel monarch eggs and fourth instars on milkweed in southern Michigan to identify predators and determine if nocturnally-active species impose significant predation pressure. We observed ten arthropod taxa consuming monarch eggs and larvae, with 74% of egg predation events occurring nocturnally. Taxa observed attacking monarch eggs included European earwigs (Forficula auricularia L.), tree crickets (Oecanthus sp.), lacewing larvae (Neuroptera), plant bugs (Miridae), small milkweed bugs (Lygaeus kalmii Stal), ants (Formicidae), spiders (Araneae: Salticidae and other spp.), harvestmen (Opiliones), and velvet mites (Trombidiformes: Trombidiidae). Larvae were attacked by ground beetles (Calleida sp.), jumping spiders (Araneae: Salticidae), and spined soldier bugs (Podisus maculiventris Say). Our findings provide important information about monarch predator-prey interactions that could be used to develop strategies to conserve monarchs through reducing predation on early life stages. 

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2. Lack of neophobic responses to color in a jumping spider that uses color cues when foraging (Habronattus pyrrithrix)

   https://doi.org/10.1371/journal.pone.0254865  

   Vickers, Michael E.; Heisey, Madison L.; Taylor, Lisa A. (July 2021, PLOS ONE)

   Mettke-Hofmann, Claudia (Ed.)

   Chemically defended prey often advertise their toxins with bright and conspicuous colors. To understand why such colors are effective at reducing predation, we need to understand the psychology of key predators. In bird predators, there is evidence that individuals avoid novelty—including prey of novel colors (with which they have had no prior experience). Moreover, the effect of novelty is sometimes strongest for colors that are typically associated with aposematic prey (e.g., red, orange, yellow). Given these findings in the bird literature, color neophobia has been argued to be a driving force in the evolution of aposematism. However, no studies have yet asked whether invertebrate predators respond similarly to novel colors. Here, we tested whether naive lab-raised jumping spiders ( Habronattus pyrrithrix ) exhibit similar patterns of color neophobia to birds. Using color-manipulated living prey, we first color-exposed spiders to prey of two out of three colors (blue, green, or red), with the third color remaining novel. After this color exposure phase, we gave the spiders tests where they could choose between all three colors (two familiar, one novel). We found that H . pyrrithrix attacked novel and familiar-colored prey at equal rates with no evidence that the degree of neophobia varied by color. Moreover, we found no evidence that either prey novelty nor color (nor their interaction) had an effect on how quickly prey was attacked. We discuss these findings in the context of what is known about color neophobia in other animals and how this contributes to our understanding of aposematic signals. 

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3. Hemipteran defensive odors trigger predictable color biases in jumping spider predators

   https://doi.org/10.1038/s41598-020-78952-5  

   Vickers, Michael E.; Taylor, Lisa A. (December 2020, Scientific Reports)

   null (Ed.)

   Abstract Multimodal warning displays often pair one signal modality (odor) with a second modality (color) to avoid predation. Experiments with bird predators suggest these signal components interact synergistically, with aversive odors triggering otherwise hidden aversions to particular prey colors. In a recent study, this phenomenon was found in a jumping spider ( Habronattus trimaculatus ), with the defensive odor from a coreid bug ( Acanthocephala femorata ) triggering an aversion to red. Here, we explore how generalizable this phenomenon is by giving H. trimaculatus the choice between red or black prey in the presence or absence of defensive odors secreted from (1) eastern leaf-footed bugs ( Leptoglossus phyllopus , Hemiptera), (2) grass stinkbugs ( Mormidea pama , Hemiptera), (3) Asian ladybird beetles ( Harmonia axyridis , Coleoptera), and (4) eastern lubber grasshoppers ( Romalea microptera , Orthoptera). As expected, in the presence of the hemipteran odors, spiders were less likely to attack red prey (compared to no odor). Unexpectedly, the beetle and grasshopper odors did not bias spiders away from red. Our results with the hemipteran odors were unique to red; follow-up experiments indicated that these odors did not affect biases for/against green prey. We discuss our findings in the context of generalized predator foraging behavior and the functions of multimodal warning displays. 

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4. Changes in prey body size differentially reduces predation risk across predator and prey abundances

   https://doi.org/10.1111/oik.09933  

   Hammill, Edd; Hancey, Kayla; Cortez, Michael (April 2023, Oikos)

   Subject Editor: Gregor Kalinkat Editor-in-Chief: Dries Bonte (Ed.)

   Trophic interactions underpin the structure of ecological communities by describing the rates at which consumers exploit their resources. The rates at which predators consume their prey are influenced by prey traits, with many species inducing defensive modifications to prey traits following the threat of predation. Here we use different clonal lines of the protist Paramecium being consumed by Stenostomum predators to highlight how differences in prey traits impact rates of predation. Clonal lines differed in their body width traits, and in their ability to induce changes in body width. By using a factorial cross of predator and prey abundances for different clonal lines we demonstrate how evolutionary or induced alterations in prey traits can impact the relative threat of predation. Our experiments show how interference among predators impacts predation rate, and how increased body width increased predator handling times. Given that reductions in the strength of interspecific interactions are associated with increased levels of overall community stability, our results indicate how individual level changes may scale up to impact whole communities 

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5. Impacts of Selective Predation on Infection Prevalence and Host Susceptibility

   https://doi.org/10.1002/ece3.70778  

   Gutierrez, Stephanie O; Bernal, Ximena E; Searle, Catherine L (January 2025, Ecology and Evolution)

   ABSTRACT Predation can alter diverse ecological processes, including host–parasite interactions. Selective predation, whereby predators preferentially feed on certain prey types, can affect prey density and selective pressures. Studies on selective predation in infected populations have primarily focused on predators preferentially feeding on infected prey. However, there is substantial evidence that some predators preferentially consume uninfected individuals. Such different strategies of prey selectivity likely modulate host–parasite interactions, changing the fitness payoffs both for hosts and their parasites. Here we investigated the effects of different types of selective predation on infection dynamics and host evolution. We used a host–parasite system in the laboratory (Daphnia dentifera infected with the horizontally transmitted fungus,Metschnikowia bicuspidata) to artificially manipulate selective predation by removing infected, uninfected, or randomly selected prey over approximately 8–9 overlapping generations. We collected weekly data on population demographics and host infection and measured susceptibility from a subset of the remaining hosts in each population at the end of the experiment. After 6 weeks of selective predation pressure, we found no differences in host abundance or infection prevalence across predation treatments. Counterintuitively, populations with selective predation on infected individuals had a higher abundance of infected individuals than populations where either uninfected or randomly selected individuals were removed. Additionally, populations with selective predation for uninfected individuals had a higher proportion of individuals infected after a standardized exposure to the parasite than individuals from the two other predation treatments. These results suggest that selective predation can alter the abundance of infected hosts and host evolution. 

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