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1.
Integr Zool ; 18(5): 876-890, 2023 Sep.
Article in English | MEDLINE | ID: mdl-36610047

ABSTRACT

Studies on functional performance are important to understand the processes responsible for the evolution of diversity. Morphological trait variation within species influences the energetic cost of locomotion and impacts life history traits, with ecological and evolutionary consequences. This study examined wing morphology correlates of flight performance measured by energetic expenditure in the Seba's short-tailed bat, Carollia perspicillata. In the flight experiments, nature caught bats (59 females, 57 males) were allowed to fly for 3 min in a room. After each flight, thermographic images were taken to measure body temperature, and biophysical models were used to calculate sensible heat loss as a measure of energetic expenditure. Wing morphological traits were measured for each individual and associated with heat loss and power required to fly on performance surfaces. Wing morphological traits explained 7-10% of flight energetic cost, and morphologies with the best performance would save the energy equivalent to 9-30% of total daily requirements. The optimal performance areas within the C. perspicillata morphospace were consistent with predicted selection trends from the literature. A trade-off between demands for flight speed and maneuverability was observed. Wing loading and camber presented sexual dimorphism. These morphological differences are likely associated with more economical but less maneuverable flight in females, leading them to fly more often in open areas along the forest edge. Our findings demonstrate how small scale changes in wing morphology can affect life history strategies and fitness.


Subject(s)
Chiroptera , Male , Female , Animals , Body Temperature , Body Temperature Regulation , Wings, Animal/anatomy & histology
2.
Article in English | MEDLINE | ID: mdl-31400499

ABSTRACT

Hematological measures are increasingly being used to analyse the impact of several stressors on the physiological condition of animals. Landscape degradation and habitat loss impacts terrestrial and volant mammals occurrence, however rarely the effects of these factors on physiological conditions and stress levels were analyzed. Here, we measured several hematological parameters to analyse the impacts of habitat amount on the physiological condition (body condition and health status) and stress level of four species of Neotropical fruit-eating bats. We measured hematocrit, hemoglobin concentration and calculated the hemoglobin-hematocrit residuals (HHR) and mean cell hemoglobin concentration (MCHC), as well as the neutrophil to lymphocyte ratio (N/L ratio) of four common frugivores bat species (Artibeus lituratus, Artibeus planirostris, Sturnira lilium and Carollia perspicilatta). The bats were captured in 20 landscapes within the Atlantic Forest biodiversity hotspot, in a gradient from 10 to 85% of habitat amount. We tested the influence of habitat amount, species, sex and reproductive condition on the physiological variables. We fit GLM to each of the response variables and performed a model selection to identify the most plausible to explain the patterns. N/L ratio was negatively influenced by habitat amount, while the other variables were not related to habitat amount. Overall, we found that habitat loss apparently did not jeopardize the physiological condition of fruit-eating bats and that stress level apparently is not high enough to have any deleterious effect. We suggest that the increase in glucocorticoids, indirectly assessed by the N/L ratio, is a predictive, beneficial response, that allow these bats to cope efficiently with the stressors associated with habitat loss.


Subject(s)
Biodiversity , Chiroptera/physiology , Conservation of Natural Resources , Animals , Chiroptera/blood , Ecosystem , Fruit/chemistry , Genitalia/physiology , Lymphocytes/physiology , Neutrophils/physiology
3.
Parasitology ; 146(8): 1013-1021, 2019 07.
Article in English | MEDLINE | ID: mdl-30915931

ABSTRACT

Fragmented habitats generally harbour small populations that are potentially more prone to local extinctions caused by biotic factors such as parasites. We evaluated the effects of botflies (Cuterebra apicalis) on naturally fragmented populations of the gracile mouse opossum (Gracilinanus agilis). We examined how sex, food supplementation experiment, season and daily climatic variables affected body condition and haemoglobin concentration in animals that were parasitized or not by botflies. Although parasitism did not affect body condition, haemoglobin concentrations were lower in parasitized animals. Among the non-parasitized individuals, haemoglobin concentration increased with the increase of maximum temperature and the decrease of relative humidity, a climatic pattern found at the peak of the dry season. However, among parasitized animals, the opposite relationship between haemoglobin concentration and relative humidity occurred, as a consequence of parasite-induced anaemia interacting with dehydration as an additional stressor. We conclude that it is critical to assess how climate affects animal health (through blood parameters) to understand the population consequences of parasitism on the survival of individuals and hence of small population viability.


Subject(s)
Diptera/physiology , Ecosystem , Host-Parasite Interactions , Myiasis/veterinary , Opossums , Animals , Brazil/epidemiology , Diptera/growth & development , Female , Larva/physiology , Male , Myiasis/epidemiology , Myiasis/parasitology , Seasons
4.
Infect Genet Evol ; 44: 510-513, 2016 10.
Article in English | MEDLINE | ID: mdl-27473780

ABSTRACT

Bats are notorious reservoirs of genetically-diverse and high-profile pathogens, and are playing crucial roles in the emergence and re-emergence of viruses, both in human and in animals. In this report, we identified and characterized previously unknown and diverse genetic clusters of bat coronaviruses in the Atlantic Forest Biome, Brazil. These results highlight the virus richness of bats and their possible roles in the public health.


Subject(s)
Chiroptera/virology , Coronavirus/classification , Coronavirus/genetics , Forests , Genetic Variation , Animals , Brazil , Female , Genome, Viral , Genotype , Male , Phylogeny , Phylogeography , RNA, Viral
5.
J Exp Zool A Ecol Genet Physiol ; 323(10): 731-744, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26349625

ABSTRACT

Physiological concepts and tools can help us to understand why organisms and populations respond to habitat fragmentation in the way they do, and allow us to determine the mechanisms or individual characteristics underlying this differential sensitivity. Here, we examine food intake, relative medullary thickness and distribution/expression of water channel aquaporin-1 in three species of South American rodents that have been reported to have different levels of tolerance to habitat fragmentation (Akodon montensis, Oligoryzomys nigripes, and Euryoryzomys russatus), using a classic water deprivation experiment to assess their abilities to cope with water shortage. We believe the mechanisms underlying this differential sensitivity are related to the organisms' capacities to maintain water balance, and therefore the species more tolerant to habitat fragmentation (A. montensis and O. nigripes) should have a higher capacity to maintain water balance. We found that A. montensis and O. nigripes were more tolerant to water deprivation than E. russatus, and this difference appears to be unrelated to differences in food ingestion rate. O. nigripes showed the highest values for RMT, followed by A. montensis and E. russatus. However all species showed RMT values that were 2.2% to 14.1% below the lower prediction limit when compared to other rodents through allometric relationships. Water deprivation seems to trigger changes in the distribution of aquaporin-1, mostly for O. nigripes and E. russatus, which may contribute to water balance maintenance. Our data suggest that these intrinsic physiological differences among these species could provide a mechanism for their differential tolerance of habitat fragmentation. J. Exp. Zool. 323A: 731-744, 2015. © 2015 Wiley Periodicals, Inc.

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