Studies of host-parasite relationships largely benefit from adopting a multifactorial approach, including the complexity of multi-host systems and habitat features in their analyses. Some host species concentrate most infection and contribute disproportionately to parasite and vector population maintenance, and habitat feature variation creates important heterogeneity in host composition, influencing infection risk and the fate of disease dynamics. Here, we examine how the availability of specific groups of hosts and habitat features relate to vector abundance and infection risk in 18 vector populations along the Mediterranean-type ecosystem of South America, where the kissing bug Mepraia spinolai is the main wild vector of the parasite Trypanosoma cruzi, the etiological agent of Chagas disease. For each population, data on vectors, vertebrate host availability, vegetation, precipitation, and temperature were collected and analyzed. Vector abundance was positively related to temperature, total vegetation, and European rabbit availability. Infection risk was positively related to temperature, bromeliad cover, and reptile availability; and negatively to the total domestic mammal availability. The invasive rabbit is suggested as a key species involved in the vector population maintenance. Interestingly, lizard species-a group completely neglected as a potential reservoir-, temperature, and bromeliads were relevant factors accounting for infection risk variation across populations.

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Trypanosoma cruzi, the cause agent of Chagas disease, is transmitted mainly by blood-feeding insects of the subfamily Triatominae. The T. cruzi life cycle alternates between triatomines and mammalian hosts, excluding birds and reptiles. Triatomines of Mepraia genus are wild vectors of T. cruzi in Chile. Mepraia specimens infected with T. cruzi have been detected in Pan de Azúcar and Santa María islands. The most common vertebrates that inhabit these islands are birds and reptiles, and it is unknown whether small mammals are present. Consequently, it is relevant to know whether there are any T. cruzi-infected small mammals on those islands to elucidate the T. cruzi cycle. To clarify this crossroads, islands of northern Chile were explored to determine if T. cruzi-infected triatomines and rodents co-occur in islands of northern Chile. T. cruzi DNA was detected by conventional and real-time PCR in three islands: on Santa María and Pan de Azúcar islands T. cruzi was detected in Mepraia sp samples, while on Pan de Azúcar (6.1%) and Damas islands (15%) was detected in the rodent Abrothrix olivacea. We show for the first time in Chile the occurrence of insular rodents infected with T. cruzi, and a complete T. cruzi life cycle in a coastal island. Our results provide new insights to understand the T. cruzi infection in the wild cycle.

Wind, a major source of environmental noise, forces invertebrates that communicate with plant-borne vibrations to adjust their signaling when communicating in windy conditions. However, the strategies that animals use to reduce the impact of wind noise on communication are not well studied. We investigated the effects of wind on the production of tremulatory signals in the neotropical katydid Copiphora brevirostris. First, we recorded katydid signaling activity and natural wind variation in the field. Additionally, we exposed katydid couples during their most active signaling time period to artificial wind of different levels, and we recorded the number of tremulations produced by the males. We found that wind levels are at their lowest between 2:00 and 5:00 in the morning, which coincides with peak signaling period for male katydids. Furthermore, we found that males produce significantly fewer tremulations when exposed to wind rather than acoustic noise or silence. Wind velocity significantly affected the number of tremulations produced during the wind treatment, with fewer tremulations produced with higher wind velocities. Our results show that katydids can time their vibratory signaling both in the short- and long-term to favorable sensory conditions, either through behavioral flexibility in response to short-term fluctuations in wind or as a result of an evolutionary process in response to predictable periods of low-wind conditions. Significance statement Animal communication can be hampered by noise across all sensory modalities. Most research on the effects of noise and the strategies to cope with it has focused on animals that use airborne sounds to communicate. However, although hundreds of thousands of invertebrates communicate with vibrational signals, we know very little about how noise affects this form of communication. For animals that rely on substrate-borne vibrations, wind represents the major source of environmental noise. Wind velocity levels can be predictable at a long-term scale (hours) but rather unpredictable at a short time scale (seconds). Both scales of variation are important for communication. Using a combination of field observations and lab experiments, we investigated the strategies used by a neotropical katydid Copiphora brevirostris to cope with vibrational noise induced by wind. Our results demonstrate that C. brevirostris times its signals at the long- and short-term range. Katydids signaled more at the times at night when wind velocity was lowest. Moreover, when exposed to wind gusts during their peak time of activity, katydids signaled more during the wind-free gaps.

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