RESUMO

One of the most tangible outcomes of climate change is change in the frequency of El Niño/La Niña events. They have a large impact on rainfall in the Western hemisphere, but their impact on tropical fauna is largely unknown. A decade long capture-mark-recapture study of the widespread Ecuadorian butterfly Nessaea hewitsoni (Felder & Felder) from an intact forest allowed us to analyze patterns of monthly and seasonal population dynamics before, during, and after an El Niño event. El Niño events did not affect long-term population size, but a 5-month delayed El Niño led to temporary emigration of females, with their subsequent return. Increased rainfall correlated with reduced survival in both sexes, but this effect was twice as strong in females. This investigation is the longest, continuous population study on any Neotropical insect species. Though we sampled on a modest scale, the magnitude of El Niño events suggests that our findings likely reflect insect population responses across a much larger portion of Amazonian forests. This study underscores the importance of analyzing multiple, interacting population parameters beyond local abundance in order to understand the biotic responses to El Niño and climate change in tropical systems. Had our analyses not included temporary emigration, no effect would have been detected because El Niño did not affect local population abundance.

Assuntos

RESUMO

Local abundance results from the interaction between populational and environmental processes. The abundance of the species in a community is also one of the most basic descriptors of its structure. Despite its importance, information about species abundances is fragmentary, creating a knowledge gap about species abundances known as the Prestonian Shortfall. Here we present a comprehensive data set of small mammal abundance in the Atlantic Forest. Data were extracted from 114 published sources and from unpublished data collected by our research groups spanning from 1943 to 2017. The data set includes 1,902 records of at least 111 species in 155 localities, totaling 42,617 individuals represented. We selected studies that (1) were conducted in forested habitats of the Atlantic Forest, (2) had a minimum sampling effort of at least 500 trap-nights, and (3) contained species abundance data in detail. For each study, we recorded (1) latitude and longitude, (2) name of the locality, (3) employed sampling effort, (4) type of traps used, (5) study year, (6) country, and (7) species name with (8) its respective abundances. For every locality, we also obtained information regarding its (9) ecoregion, (10) predominant vegetation type, and (11) biogeographic subdivision. Whenever necessary, we also (12) updated the species names as new species were described and some genera suffered taxonomic revision since the publication. The localities are spread across the Atlantic Forest and most of the small mammal species known to occur in Atlantic Forest are present in the data set, making it representative of communities of the entire biome. This data set can be used to address various patterns in community ecology and geographical ecology, as the relation between local abundance and environmental suitability, hypothesis regarding local and regional factors on community structuring, species abundance distributions (SAD), functional and phylogenetic mechanisms on community assembling.

Assuntos

RESUMO

Estimates of local population abundances, which require carefully designed sampling procedures, can provide valuable information on population size and density. Even though small mammals are one of the most widely studied vertebrate groups, many surveys have not recorded basic information to estimate local abundances, for instance catching effort. Here we suggest a simple comparative trapping frequency index that can be used as an alternative to the relative abundance index in data sets that only contain the number of species and individuals collected, thus lacking information on sampling effort. To compare trapping frequency and relative abundances we used capture records from more than four years, from seven species of rodents and two marsupial species collected by the Brazilian Plague Service. We calculated the trapping frequency index of each species as the proportion of trapped individuals per total of all individuals caught. We found that this trapping index was significantly correlated with a relative abundance index (number of captured individuals divided by number of trap nights). Our findings suggest that the proposed index may be useful for comparisons in situations where data on catching effort is lacking. The index may also provide a simple, though approximate quantification of relative local abundances, with possible applications in comparative studies (e.g. meta-analysis). We suggest that this index is used in studies that do not focus on obtaining accurate population parameter estimates, but which nonetheless contain data that can still offer a representative measure to compare local population abundances.(AU)

Assuntos

RESUMO

Estimates of local population abundances, which require carefully designed sampling procedures, can provide valuable information on population size and density. Even though small mammals are one of the most widely studied vertebrate groups, many surveys have not recorded basic information to estimate local abundances, for instance catching effort. Here we suggest a simple comparative trapping frequency index that can be used as an alternative to the relative abundance index in data sets that only contain the number of species and individuals collected, thus lacking information on sampling effort. To compare trapping frequency and relative abundances we used capture records from more than four years, from seven species of rodents and two marsupial species collected by the Brazilian Plague Service. We calculated the trapping frequency index of each species as the proportion of trapped individuals per total of all individuals caught. We found that this trapping index was significantly correlated with a relative abundance index (number of captured individuals divided by number of trap nights). Our findings suggest that the proposed index may be useful for comparisons in situations where data on catching effort is lacking. The index may also provide a simple, though approximate quantification of relative local abundances, with possible applications in comparative studies (e.g. meta-analysis). We suggest that this index is used in studies that do not focus on obtaining accurate population parameter estimates, but which nonetheless contain data that can still offer a representative measure to compare local population abundances.

Assuntos

RESUMO

A major difficulty in the application of probabilistic models to estimations of mammal abundance is obtaining a data set that meets all of the assumptions of the model. In this paper, we evaluated the concordance correlation among three population size estimators, the minimum number alive (MNA), jackknife and the model suggested by the selection algorithm in CAPTURE (the best-fit model), using long-term data on three Brazilian small mammal species obtained from three different studies. The concordance correlation coefficients between the abundance estimates indicated that the probabilistic and enumeration estimators were highly correlated, giving concordant population estimates, except for one species in one of the studies. The results indicate the adequacy of using enumeration estimates as indexes for population size when scarce data do not allow for the use of probabilistic methods. Differences observed in the behavior of enumeration and probabilistic methods among species and studies can be related to the exclusive sampling design of each area, species-specific movement characteristics and whether a significant portion of the population could be sampled.(AU)

Assuntos

RESUMO

A major difficulty in the application of probabilistic models to estimations of mammal abundance is obtaining a data set that meets all of the assumptions of the model. In this paper, we evaluated the concordance correlation among three population size estimators, the minimum number alive (MNA), jackknife and the model suggested by the selection algorithm in CAPTURE (the best-fit model), using long-term data on three Brazilian small mammal species obtained from three different studies. The concordance correlation coefficients between the abundance estimates indicated that the probabilistic and enumeration estimators were highly correlated, giving concordant population estimates, except for one species in one of the studies. The results indicate the adequacy of using enumeration estimates as indexes for population size when scarce data do not allow for the use of probabilistic methods. Differences observed in the behavior of enumeration and probabilistic methods among species and studies can be related to the exclusive sampling design of each area, species-specific movement characteristics and whether a significant portion of the population could be sampled.

RESUMO

A major difficulty in the application of probabilistic models to estimations of mammal abundance is obtaining a data set that meets all of the assumptions of the model. In this paper, we evaluated the concordance correlation among three population size estimators, the minimum number alive (MNA), jackknife and the model suggested by the selection algorithm in CAPTURE (the best-fit model), using long-term data on three Brazilian small mammal species obtained from three different studies. The concordance correlation coefficients between the abundance estimates indicated that the probabilistic and enumeration estimators were highly correlated, giving concordant population estimates, except for one species in one of the studies. The results indicate the adequacy of using enumeration estimates as indexes for population size when scarce data do not allow for the use of probabilistic methods. Differences observed in the behavior of enumeration and probabilistic methods among species and studies can be related to the exclusive sampling design of each area, species-specific movement characteristics and whether a significant portion of the population could be sampled.

Assuntos

RESUMO

A fundamental step in the emerging Movement Theory is the description of movement paths, and the identification of its proximate and ultimate drivers. The most common characteristic used to describe and analyze movement paths is its tortuosity, and a variety of tortuosity indices have been proposed in different theoretical or empirical contexts. Here we review conceptual differences between five movement indices and their bias due to locations errors, sample sizes and scale-dependency: Intensity of Habitat use (IU), Fractal D, MSD (Mean Squared Distance), Straightness (ST), and Sinuosity (SI). Intensity of Habitat use and ST are straightforward to compute, but ST is actually an unbiased estimator of oriented search and ballistic movements. Fractal D is less straightforward to compute and represents an index of propensity to cover the plane, whereas IU is the only completely empirical of the three. These three indices could be used to identify different phases of path, and their path tortuosity is a dimensionless feature of the path, depending mostly on path shape, not on the unit of measurement. This concept of tortuosity differs from a concept implied in the sinuosity of BENHAMOU (2004), where a specific random walk movement model is assumed, and diffusion distance is a function of path length and turning angles, requiring their inclusion in a measure of sinuosity. MSD should be used as a diagnostic tool of random walk paths rather than an index of tortuosity. Bias due to location errors, sample size and scale, differs between the indices, as well as the concept of tortuosity implied. These differences must be considered when choosing the most appropriate index.

RESUMO

A fundamental step in the emerging Movement Theory is the description of movement paths, and the identification of its proximate and ultimate drivers. The most common characteristic used to describe and analyze movement paths is its tortuosity, and a variety of tortuosity indices have been proposed in different theoretical or empirical contexts. Here we review conceptual differences between five movement indices and their bias due to locations errors, sample sizes and scale-dependency: Intensity of Habitat use (IU), Fractal D, MSD (Mean Squared Distance), Straightness (ST), and Sinuosity (SI). Intensity of Habitat use and ST are straightforward to compute, but ST is actually an unbiased estimator of oriented search and ballistic movements. Fractal D is less straightforward to compute and represents an index of propensity to cover the plane, whereas IU is the only completely empirical of the three. These three indices could be used to identify different phases of path, and their path tortuosity is a dimensionless feature of the path, depending mostly on path shape, not on the unit of measurement. This concept of tortuosity differs from a concept implied in the sinuosity of BENHAMOU (2004), where a specific random walk movement model is assumed, and diffusion distance is a function of path length and turning angles, requiring their inclusion in a measure of sinuosity. MSD should be used as a diagnostic tool of random walk paths rather than an index of tortuosity. Bias due to location errors, sample size and scale, differs between the indices, as well as the concept of tortuosity implied. These differences must be considered when choosing the most appropriate index.

RESUMO

A fundamental step in the emerging Movement Theory is the description of movement paths, and the identification of its proximate and ultimate drivers. The most common characteristic used to describe and analyze movement paths is its tortuosity, and a variety of tortuosity indices have been proposed in different theoretical or empirical contexts. Here we review conceptual differences between five movement indices and their bias due to locations errors, sample sizes and scale-dependency: Intensity of Habitat use (IU), Fractal D, MSD (Mean Squared Distance), Straightness (ST), and Sinuosity (SI). Intensity of Habitat use and ST are straightforward to compute, but ST is actually an unbiased estimator of oriented search and ballistic movements. Fractal D is less straightforward to compute and represents an index of propensity to cover the plane, whereas IU is the only completely empirical of the three. These three indices could be used to identify different phases of path, and their path tortuosity is a dimensionless feature of the path, depending mostly on path shape, not on the unit of measurement. This concept of tortuosity differs from a concept implied in the sinuosity of BENHAMOU (2004), where a specific random walk movement model is assumed, and diffusion distance is a function of path length and turning angles, requiring their inclusion in a measure of sinuosity. MSD should be used as a diagnostic tool of random walk paths rather than an index of tortuosity. Bias due to location errors, sample size and scale, differs between the indices, as well as the concept of tortuosity implied. These differences must be considered when choosing the most appropriate index.