http://orcid.org/0000-0001-7087-1395
Figures
Abstract
Species co-existence depends on how organisms utilize their environment and resources. When two sympatric species are similar in some ecological requirements, their coexistence may arise from differences in resource use over time and/or space. Interactions among coexisting marsupials remain poorly understood, especially in the Neotropics. Here we combine spatial niche measurements, individual-resource networks, and isotopic niche approaches, to investigate the ecological strategies used by the Neotropical marsupials Didelphis aurita and Metachirus nudicaudatus to co-occur in an area of Serra do Mar State Park (southeast of Brazil). Both individual-resource networks and isotopic niche approaches indicate similar patterns of omnivory for both species. Isotopic analysis showed the species’ trophic niche to be similar, with 52% of overlap, and no differences between proportional contributions of each resource to their diets. Moreover, individual-resource network analysis found no evidence of diet nestedness or segregation. The trophic niche overlap observed was associated with spatial segregation between species. Despite using the same area over the year, D. aurita and M. nudicaudatus exhibited spatial segregation among seasons. These results illustrate that the detection of spatial segregation is scale-dependent and must be carefully considered. In conclusion, our findings provide a new perspective on the ecology of these two Neotropical marsupials by illustrating how the association of distinct but complementary methods can be applied to reach a more complete understanding of resource partitioning and species coexistence.
Citation: Kuhnen VV, Romero GQ, Linhares AX, Vizentin-Bugoni J, Porto EAC, Setz EZF (2017) Diet overlap and spatial segregation between two neotropical marsupials revealed by multiple analytical approaches. PLoS ONE 12(7): e0181188. https://doi.org/10.1371/journal.pone.0181188
Editor: Mathew S. Crowther, University of Sydney, AUSTRALIA
Received: February 21, 2017; Accepted: June 26, 2017; Published: July 12, 2017
Copyright: © 2017 Kuhnen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: Data are available from the Harvard Dataverse (https://dataverse.harvard.edu/dataset.xhtml?persistentId=doi:10.7910/DVN/V6XGW5).
Funding: V.V. Kuhnen PhD scholarship was funded by Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq, 142137/20120). J. Vizentin-Bugoni PhD scholarship was funded by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES). Isotopic analyses were funded by Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) project coordinated by GQ Romero. GQ Romero received a CNPq-Brazil research grant. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Species co-existence partly depends on how organisms utilize their resources and environment. All resources and conditions required by an organism to survive and reproduce are encompassed by the niche concept, which describes an n-dimensional hypervolume where dimensions represents distinct ecological requirement [1]. Hence, one way to analyze how species coexistence takes place is by measuring niche parameters and comparing them among species [2,3]. When two sympatric species have similar ecological requirements, there is niche overlap—which is the region of niche space shared by two or more species [4,5]. However, if niche dimensions of two species overlap completely, one species will probably supplant the other, leading to its local extinction (i.e. Gause’s competitive exclusion principle [6]). Therefore, coexistence may arise from niche shifts, for example, through partitioning resources along time and/or space [7,8].
The most tractable and frequently studied component of niche space is trophic niche width, often evaluated using dietary diversity [9]. Sympatric species can segregate trophic niches using different strategies, such as food type [10], foraging mode [11], spatial segregation [12], or circadian activity pattern [13]. A species’ diet can also respond to resource seasonality; thus, changes in food consumption across seasons can match fluctuations in food availability [14]. When resources are abundant, interspecific competition decreases and a higher trophic niche overlap is enabled [15]. However, diet overlap can also be observed when the demand for resources exceeds supply and species need to expand their trophic niche in order to make up for their nutritional demands [16]. A high degree of niche overlap may lead to competitive interactions [17, 18], leading to species displacement [19]. Therefore, other mechanisms of niche partitioning (e.g., spatial and/or time segregation) could allow co-existence among species with similar ecological requirements [20].
To investigate the structure of trophic relationships there are a variety of different approaches, such as individual-resource networks [21,22,23] and isotopic niche approaches [24,25]. Individual-resource networks are represented by two sets of nodes: one representing individuals of a population and one of food resource items or categories (ca. those found in fecal samples). The link between nodes represents the consumption of a given resource by an individual. Network structure can be investigated through metrics that characterize observed patterns of interactions [26]. There are some advantages associated with individual-resource networks based on fecal samples data, such as low costs and the possibility of collecting data from recaptured animals. Despite all the applicability, there are some inherent potential limitations associated to fecal samples data. For example, some items have different rates of digestion [27], thus, a sample may not contain traces from all items previously consumed. Besides that, the consumption of species without hard parts will probably not be tracked in the feces, biasing diet results. Food resource identification is not an accurate procedure as specific parts of the digested animals’ body are needed for reliable taxonomic identification. Those parts sometimes break down after digestion, leading to them being underrated in diet composition. Complementarily, some of these limitations can be remedied by using stable isotope signatures to provide a quantitative diet description [24,28].
Isotopic composition of animal tissues often contains a “signature” of the process that created it [29]. For example, stable carbon isotope ratios (δ13C) vary mostly according to the photosynthetic metabolism of plants and can be very effective tracers of different carbon sources [24]. The stable isotope commonly utilized to trace protein sources is nitrogen (δ15N). Therefore, the δ space (δ13C versus δ15N) is referred as the “isotopic niche” and has been comparable to the Hutchinson’s n-dimensional niche concept [1,29]. However, potential drawbacks in using this approach are: the unknown rate at which isotopic values from a given resource is assimilated by the tissues of the consumer, making it difficult to compare different tissues; the impossibility of using tissue samples for isotopic analyses from recaptured animals when bait is used; and, the challenge of accessing the isotopic signature of each consumed species. Therefore, using stable isotopes and fecal samples in conjunction provides a more complete representation of an individual or species’ dietary habit.
Here we combine spatial niche measurements, individual-resource networks analysis, and isotopic niche approaches to investigate the ecological strategies of two sympatric Neotropical marsupials (Didelphis aurita Wied-Neuwied, 1826 and Metachirus nudicaudatus (É. Geoffroy, 1803)) which co-occur in several Tropical Rainforest communities. Whereas M. nudicaudatus has a broad geographical range, D. aurita is restricted to Atlantic Rainforest biome [30]. Didelphis aurita is about three times larger than M. nudicaudatus [31], which makes the first a stronger competitor, as it is able to actively defend food resource [32,33]. Despite their morphological and behavioral differences, these two species are considered to be apparent competitors [34]. However, the processes underlying the coexistence of such species remain largely unknown.
As both, D. aurita and M. nudicaudatus, are mainly terrestrial, nocturnal, solitary, and feed on similar resources [35,36,37,38], strategies such as low trophic niche overlap or differential use of the space is expected, in order to promote their co-existence. Here, we investigated trophic niche overlap using both the isotopic approach [28] and analyzing the individual-resource network structure based on fecal samples. If, as suggested by literature [38], D. aurita is more generalist and M. nudicaudatus is predominantly insectivore, M. nudicaudatus’s diet would represent a subset of the broader diet of the generalist D. aurita. In this case, we would expect to find a nested structure for individual-resource network of both species [21,22] and overlapping isotopic niches. Alternatively, if individuals use distinct subsets of the available resources, we would expect a modular network structure, i.e. groups of individuals of the same species feeding on a subset of food items different than those exploited by the other species [39,22], with distinct isotopic niches.
Materials and methods
Study area
The study was conducted in Serra do Mar State Park, southeast Brazil (São Paulo State coast). Serra do Mar State Park comprises more than 300,000 ha of well-preserved rainforest—it is the largest protected Atlantic Rainforest remnant in Brazil [40]. The studied area is located 35 km northbound from the urban area of Ubatuba city, and 2 km from an isolated village (Sertão da Fazenda) (23°20’S and 44°50’W). The forest is characterized as lowland tropical evergreen, following Veloso et al. (1991) [41]. For a full description of the forest classification and structure, see Alves et al. (2010) [42] and Eisenlohr et al. (2013) [43]. The altitudes range from 43 to 89 m above sea level [43]. The regional climate is Tropical Humid, with hot summers and no dry season (Af/Cfa). Average annual precipitation is 2,500 mm, and monthly average temperature is 22°C [44].
Collection and preparation of samples
From May 2013 to April 2015, trapping sessions of four consecutive nights were conducted every month. Tomahawk traps (45×16×16 cm) were used to capture animals, baited with banana, peanut butter and bacon. Traps were placed 20 m apart from each other, compounding a rectangular grid of 3.4 ha (fifteen lines with seven traps each, 280 m x 120 m). Such spacing represents the average distance used in previous studies [36,45], and allows to caught individuals to be sampled and released readly early in the morning, at the day after the trapping. This is particularly important as frequent rain and temperature changes may lead to termoregulatory imbalances and death of individuals trapped for long time. In addition, a Sherman trap (10 x 11 x 38 cm) fixed on tree branch, and a Tomahawk trap (45 x 16 x 16 cm) were fixed with L-bracket method (according to Graipel et al. (2003) [46]) were place at each field station during the first six months of study. However, both methods presented low capture success (only 4 individuals caught in 6 months); therefore, we settled the traps in the forest understory in order to reduce the time between each sample station, and to arrive more readily at stations with captured animals. [47]. Five sample stations were excluded because of hard access. Thus, we worked with one hundred traps total, summing up 9600 trapping nights of sampling effort. Traps were placed on a hardboard platform to minimize the contamination of feces with litter contents. After the second night of trapping, all baits were replaced with new ones. Individuals captured were marked in each ear with a 1-g monel ear tag (National Band and Tag Co.®), weighed, identified as to sex and age (according to Tyndale-Biscoe and MacKenzie (1976) [48]); the sample station was also recorded.
Over two-years of capture-mark-recapture, we trapped 68 individuals of D. aurita (334 captures) and 34 individuals of M. nudicaudatus (127 captures). Samples for diet analysis were collected along the first year of the study and only from adults. For isotopic analysis we sampled 11 males and 8 females of D. aurita, and 6 females and 7 males of M. nudicaudatus. For fecal analysis we sampled 9 females and 9 males of D. aurita, and 5 females and 10 males of M. nudicaudatus. The first time an individual was captured, we would cut a nail sample off each finger from the left-hind foot for analysis of stable isotope ratios of C (δ13C) and N (δ15N). Only the free margin (distal edge) of the nail was cutted. As there are no nerve endings at this part, anaesthesia was not needed. Nails are keratin based and the turnover of elements in such tissues are slower, therefore being considered metabolically inert tissues [49]. As stable isotopes are allocated into the keratin structure during growth, the dietary information for the period during which the tissue was synthesized is preserved [50]. However, the rate with which animals incorporate the isotopic values of the resources they consume can vary between individuals and tissue types [51]. Since these rates are still unknown for Neotropical marsupials, we decided to not collect and analyze nails from recaptured individuals, thus preventing bias from bait consumption. Given that D. aurita and M. nudicaudatus are close relatives (i.e. same subfamily [52], we assumed that their nails integrate diet over similar amounts of time. Under a stereoscope, nail samples were gently cleaned in a petri dish with water, then with alcohol 70%, and again with water. After cleansing, samples were oven dried at 60°C for 48 hours, and weighed up to ~1 mg into tin capsules for isotopic analyses.
We also collected samples of available diet sources for isotopic analysis, based on the literature about the species’ diet. Source samples were divided into six categories: small vertebrates (reptiles and rodents), fruits, and four different guilds of arthropods (herbivores, predators, omnivores and detritivores). Although we might miss some diet items that can be eventually consumed, those six categories encompass the main food resources used by D. aurita and M. nudicaudatus [35,36,37,45,53,54,55,56,57]. Fruits were collected opportunistically, and to collect small vertebrates and arthropods we used three lines with eight pitfalls each (pitfall volume of 60 liters). The source samples were oven dried at 60°C for 48 hours, and weighed up to ~1 mg into tin capsules for isotopic analyses.
Fecal samples were collected from the bottom of the traps where the animal spent the night. In order to avoid potential influences of baits on the detection and identification of the feeding items (e.g. via differential digestive efficiency after bait ingestion) and also keep comparable sampling effort among all individuals caught, we did not consider feces from recaptured individuals during the same trapping season. A total of 70 fecal samples were collected from 9 females and 9 males of D. aurita, and 5 females and 10 males of M. nudicaudatus. Samples were frozen until analyzed. After thawing, they were dissolved in water, and then filtered through a 1 mm mesh screen sieve under running tap water. The material retained on the sieve was dried at environment temperature and analyzed with a stereoscope. The taxonomic identification of prey items was validated by specialists.
The spatial use of this grid, for each species, was analyzed by the percentage of spatial overlap, calculated through Morisita’s Index of Overlap [2]. For this analysis, we considered all captures during the two years of the study (334 captures of 68 individuals of D. aurita and 127 captures of 34 individuals of M. nudicaudatus). In order to avoid any odoriferous interference of a species in the probability of forthcoming captures, cages were cleaned after each capture with alcohol 50%.
Isotopic analyses
All isotopic analyses were conducted in the Stable Isotope Facility of the University of California, Davis, California, USA, using an online elemental analyzer (PDZ Europa ANCA-GSL, Sercon Ltd., Cheshire, UK) interfaced to a continuous-flow isotope ratio mass spectrometer (PDZ Europa 20–20).
For the statistical analyses, we used the convex hull (TA) approach to represent the overall dispersion within isotope niche space of D. aurita and M. nudicaudatus [25]. In order to analyze dietary similarity between the species, we compared the standard ellipse areas of the isotopic niches (SEA). SEA is estimated using Bayesian methods, which allow robust statistical comparisons between populations with unequal sample sizes, and contain the core mean of the population’s isotopic niche (40% of 10000 randomizations, [3]. Due to the small sample size, we employed a corrected sample size version of the SEA (SEAc, [3]). The overlap of SEAc was calculated as a measure of trophic niche overlap [28]. The relative contribution of each resource in D. aurita and M. nudicaudatus diets were estimated by the Bayesian mixing model SIAR [58].
Intra-population variation in diets was analyzed using two quantitative metrics originally developed by Layman et al. (2007) [25] and then adapted for a Bayesian inference by Jackson et al. [28]: a) mean distance to centroid (CDb) infers the population’s trophic diversity; b) standard deviation of nearest neighbor distance (SDNNDb) infers the population’s trophic evenness. All metrics were calculated using the software package SIAR v4.2.2 [59] in R programming environment [60].
Network analysis
We described the trophic interactions of D. aurita and M. nudicaudatus with their feeding items as a bipartite individual-resource network, consisting of two groups: captured individuals and the resources they consumed [22]. For such, we defined an incidence matrix where rows (i) correspond to individuals, and columns (j) correspond to each food resource found in fecal samples. For the network analysis, food resources were not divided into categories (as for isotopic analyses), but were considered all items found on feces, identified to the most accurate taxonomic level as possible. Each element (aij) of the matrix corresponds to whether the consumption of a resource was recorded (aij = 1) or not (aij = 0). In order to account for potential biases caused by recaptures of the same individuals, we grouped into the same line food items consumed by each individual within a season. To evaluate the potential bias arisen from this choice, we also recalculated the network metrics using the raw data, i.e. without grouping recaptures, and found the results to be consistent regardless of the choice (S4 Table).
We searched for nestedness and modularity into this network to test whether individuals of a species exploit a subset of resources used by individuals of another (nested network structure) or whether individuals of both species exploit distinct subset of resources (modules coincident with species should be detected). We used the NODF metric, based on overlap and decreasing fill for both lines and columns of the matrix [61], and the modularity index (Q) with the optimization algorithm QuanBiMo, which searches for subsets of individual–resource in the network, yielding the largest degree of modularity [62]. Despite that Q was developed to explore quantitative networks (see [62]), it is also suitable for binary networks. To access metric significances, we compared the observed NODF and Q values to those obtained by 1,000 and 100 null model randomizations, respectively. The null model used was shuffle.web, which rearranges interactions randomly inside the matrix but keeps the dimensions of the observed matrix [63]. Due to the large computational time required by the algorithm QuanBiMo, we used less randomizations for modularity. Due to the stochastic optimization technique associated to this algorithm (i.e. simulated annealing), Q values can be slightly different among runs. Thus, for each network we chose the higher values from five independent runs set to 107 swaps [63]. As the algorithm aims to find the highest modularity, getting the higher value among runs is a suitable procedure, as done by previous studies (e.g. [64]). The same was done for the null models in which we chose the higher Qs among five runs for each of the 100 randomizations. Metrics were considered significant when the observed value fell outside the 95% confidence interval expected by the null models (i.e. 1000 and 100 randomizations for NODF and Q, respectively). In order to evaluate temporal variation in the dietary structure, we split the network data into four seasons and repeated the analyses above to search for nestedness and modularity within a season. All analyses were run in R-package bipartite [65].
Results
Arthropods were the main diet items found in scats of both mammal species (Fig 1; Supporting Information, S1 Table). Coleoptera and Crustacea were the items most frequently found in D. aurita scats and Hymenoptera and Coleoptera for M. nudicaudatus. Vertebrates were found more frequently in D. aurita scats than in M. nudicaudatus, which presented only reptile traces. A wider diversity of seeds was found in D. aurita scats and in a higher frequency than in M. nudicaudatus. Despite these differences, isotopic analyses showed that D. aurita and M. nudicaudatus feed in the same proportions for each food resource category. Mean values of δ15N for D. aurita and M. nudicaudatus were 9.18 (±0.10 SE) and 9.32 (±0.16 SE), respectively; and, mean values of δ13C were -23.58 (±0.10 SE) and -23.64 (±0.08 SE) for D. aurita and M. nudicaudatus, respectively. Standard ellipse areas for isotopic niches of D. aurita (SEAc = 0.95) and M. nudicaudatus (SEAc = 0.56) were similar (p = 0.34), and both species showed high trophic niche overlap (Fig 2). Population-level metrics for trophic structures were also similar for both species (Table 1).
Each point represents an individual; solid lines represent the mean core of the population’s isotopic niche (SEAc), and; dotted lines represent the overall isotopic niche of the population (convex hull).
SIAR dietary mixing model did not detect any significant differences between the proportion that each resource group contributed to D. aurita and M. nudicaudatus diets (isotopic values for all resource samples are shown in S2 Table). For both species, diets seem split into three main resource groups (Fig 3, S3 Table). Top food web invertebrates (omnivores and predators) were crucial resources (~52.5%) while vertebrates and detritivores showed a smaller but also important proportional contribution (~38%), with vertebrates contributing more (~21.5%) than detritivores (~0.16%). Sources from the base of the food web (fruits and herbivores) were less important dietary components, with a proportional contribution of 0.02%.
Boxes illustrate the relative proportions of each food source with 50%, 75% and 95% confidence intervals from dark to light grey.
We found no evidence of diet nestedness or segregation between both species (Fig 4), as there were no differences from observed and expected results by the null model, neither for the nestedness index (NODF = 51.09, 95% IC = 50.00–54.61) nor modularity (Q = 0.30, 95% IC = 0.28–0.30) for bipartite matrices. Moreover, their diet remained consistently unstructured over time as both nestedness and modularity did not differ from the results expected by the null models for the seasons (S4 Table).
Links represent the consumption of a resource (right column) by each individual (left column). Black represents D. aurita and red M. nudicaudatus individuals.
When we merged 24 sampled months for spatial analysis, D. aurita and M. nudicaudatus overlapped 65% in the use of space. However, when thinner spatial scales were considered, i.e. seasons, spatial partitioning among the individuals became evident (Table 2). There was complete spatial segregation among individuals during the two springs and in the winter of 2013. Smaller spatial overlap was observed in the winter of 2014 and both autumns, staying between 14% and 24%. In the summer, individuals of both species had the highest grid use overlap (36%). There was no association between number of captures and spatial overlap. Higher capture rates for both species were recorded in the winter of 2013 and 2014, and there was no overlap of the grid area used (Table 2).
Discussion
Through a combination of isotopic and network analyses, we showed that D. aurita and M. nudicaudatus present omnivore diets, contradicting previous literature based on fecal samples data [37,66,67]. Whereas D. aurita has been classified in the literature as the most generalist marsupial in the Atlantic Rainforest, M. nudicaudatus has been claimed omnivore but predominantly insectivore [37,66,67]. On the other hand, our findings suggest that M. nudicaudatus is in fact generalist, but more than initially thought of, which provides a new perspective to its ecological role in the community.
Our results support the idea that the use of stable isotopes in conjunction to fecal samples provides a more complete representation of a species’ dietary habits, and the importance of considering different arrays of analytical approaches for diet analyses [68]. Both approaches used to analyze the species’ diet indicate the same pattern of omnivory. Isotopic results also revealed that D. aurita and M. nudicaudatus diets encompass similar proportions of prey categories. On the other hand, fecal samples allowed a proper taxonomic identification of some dietary items [69]. It is worth highlighting that isotopic analysis demonstrated that herbivore invertebrates (e.g. Coleoptera) and fruits had a small contribution to D. aurita and M. nudicaudatus diets; whereas, in fecal samples, those were the categories most frequently registered. This is probably because Coleoptera’s elytra and fruit seeds are more difficult to digest. It is possible that the proportions of D. aurita and M. nudicaudatus diets change from area to area, however, our results evidence that these two sympatric marsupials have high trophic niche overlap and might compete for food resources.
Remarkably, both methodologies used here were not able to distinguish subtle differences between D. aurita and M. nudicaudatus diets, such as species consumed. Differences in species consumed might exist due to differences on their climbing ability. Specifically, Didelphis aurita is a good climber and can be found in all forest strata despite preferring the ground [36,70,71], whereas M. nudicaudatus has morphological adaptations to a cursorial behavior and is rarely captured on other forest strata than ground [72,73]. Therefore, it is possible that D. aurita’s climbing ability allows the species to consume different prey species from canopy. Besides, M. nudicaudatus has a longer molar series [74], which can increase the crushing, cutting and grinding surface, potentially decreasing the probability of finding resource parts in feces that allow proper identification. Thus, likewise for some other mammals, it is still a challenge to determine the array of species consumed by M. nudicaudatus and D. aurita [75,76,77,78].
In the studied area, D. aurita and M. nudicaudatus trophic niche overlap was associated to spatial segregation within seasons. The same pattern has also been described to D. aurita and D. marsupialis [32] and in other systems, such as for Australian rodents [79] and African grazers [20]. Our findings reveal that the temporal scale is crucial for the detection of spatial partitioning among species. Over the two years, D. aurita and M. nudicaudatus were captured in almost all areas of the grid, indicating that there was no difference in habitat use by both species. On the other hand, there was a dynamic spatial exclusion between species among seasons. This is expected as during seasons with more resource availability, such as a regular summer, interspecific competition for food resources decreases, leading to species potentially tolerating a higher spatial overlap; and the opposite might be expected for seasons with low resource availability [7], such as winter. Indeed, our data indicates that in summers there is a higher spatial overlap while winter has a lower one.
Overall, interactions among marsupials remain poorly understood, especially in the Neotropics. For other mammal species, such as otters [80] and canids [81], feces and urine are used as visual and olfactory signals. Cougars, for instance, leave scrapes along travel routes as intraspecific signs [82]. Didelphis aurita and M. nudicaudatus have paracloacal scent glands that confer a peculiar smell to individuals [83,84] and are likely related to complex multifunctional behaviors [85,86]. The recognition of these olfactory signals in the environment could be a strategy of M. nudicaudatus to avoid encounters with D. aurita, that is three times bigger and very aggressive [87]. In this sense, further studies focusing on behavior may be valuable to better understand how interactions between these species result in the pattern of dietary overlap and space usage here described.
In conclusion, our findings provide evidence that both species are similarly omnivores but presenting preference for feeding on insects, and, despite using the same area over the year, exhibit spatial segregation among seasons. Therefore, spatial segregation is likely a major mechanism promoting coexistence by reducing competition for resources between these marsupials. Importantly, our results illustrate that the detection of spatial segregation is scale dependent and might be considered carefully. Finally, this paper provides a new perspective on the ecology of these two Neotropical marsupials, and also illustrates how the association of distinct but complementary methods can be applied to reach a more complete understanding of resource partitioning and species coexistence.
Supporting information
S1 Table. Frequencies of occurrence (%) of food items found in Didelphis aurita and Metachirus nudicaudatus fecal samples.
This is the S1 Table legend.
https://doi.org/10.1371/journal.pone.0181188.s001
(PDF)
S2 Table. δ13C and δ15N values for putative resources to the diet of Didelphis aurita and Metachirus nudicaudatus.
This is the S2 Table legend.
https://doi.org/10.1371/journal.pone.0181188.s002
(PDF)
S3 Table. Relative contribution of putative resources to the diet of Didelphis aurita and Metachirus nudicaudatus.
This is the S3 Table legend.
https://doi.org/10.1371/journal.pone.0181188.s003
(PDF)
S4 Table. Nestedness (NODF) and Modularity (Q) for Didelphis aurita and Metachirus nudicaudatus individual-resource networks.
This is the S4 Table legend.
https://doi.org/10.1371/journal.pone.0181188.s004
(PDF)
Acknowledgments
The authors thank Wesley Rodrigues Silva, Ana Paula Carmignotto and Emerson Monteiro Vieira for the valuable comments on the first draft of the manuscript. The authors are also thankful to Paulo R. Manzani and Jorge Tamashiro for the identification of vertebrates and seeds from fecal samples; José R. Trigo for lending the stereoscope; Marcos Almir Polettini for artwork; and Eber G. Cretton for English corrections. V.V.K. and J.V-B. PhD scholarships were funded by CNPq and CAPES, respectively. GQR received a CNPq-Brazil research grant. The isotopic analyses were funded by a FAPESP project coordinated by GQR.
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