Abstract

Frugivore bats are important seed dispersers in forests and their abundance are associated with the presence of zoochoric plants. In this context, the aim of our study was to investigate the association of the frugivore bat S. lilium with the diaspores of the zoochoric plant S. mauritianum, a common arboreal species present in forest fragments of southern Brazil. We also investigated the diet of the species based on seed content present in feces of individuals. Bats were mist-netted from November 2017 to April 2018 in a fragment of Atlantic Forest. The proportion of immature and mature diaspores of S. mauritianum was estimated in the same area where bats were sampled, and feces were sampled from captured individuals. In total, 61 individuals of S. lilium were captured, and 795 seeds were sampled from their feces. The abundance of S. lilium was significantly associated with the proportion of immature diaspores of S. mauritianum. We identified seeds of two botanical families: Solanaceae (89%) and Moraceae (11%) in the fecal samples. Our findings support the view that S. lilium is a legitimate disperser of S. mauritianum, and that its ecological function is probably a result of co-adaptation.

Key words
animal-plant interaction; diet; frugivory; seed dispersal

INTRODUCTION

Animal-plant interactions affect the population dynamics of species and thus are fundamental for the maintenance of communities’ structure and stability (Sette 2012SETTE IMS. 2012. Interação morcego-fruto: estado da arte no Brasil e um estudo da chuva de sementes por aves e morcegos em uma área do Cerrado em Brasília. Dissertação de Mestrado, Universidade de Brasília. (Unpublished)., Bascompte & Jordano 2014BASCOMPTE J & JORDANO P. 2014. Mutualistic networks. Princeton: Princeton University Press, 224 p.). More than 75% of tree species in tropical forests produce diaspores adapted to zoochoric dispersal. Among shrub and herbaceous vegetation this process also predominates (Howe & Smallwood 1982HOWE HF & SMALLWOOD J. 1982. Ecology of seed dispersal. Ann Rev Ecol Syst 13: 201-228., Morellato & Leitão-Filho 1990MORELLATO LPC & LEITÃO-FILHO HF. 1990. Estratégias fenológicas de espécies arbóreas em floresta mesófila na Serra do Japi, Jundiaí, SP. Rev Bras Bioc 50: 163-173.).

Between seed-dispersers mammals, Phyllostomidae bats are represented by high species diversity, and their abundance is associated with the presence of pioneer zoochoric plants (Molinari 1993MOLINARI J. 1993. El mutualismo entre frugívoros y plantas en las selvas tropicales: aspectos paleobiologicos, autoecologias, papel comunitário. Acta Biologica Venezuelica 14: 1-44., Muscarella & Fleming 2007MUSCARELLA R & FLEMING TH. 2007. The role of frugivorous bats in tropical forest succession. Biol Rev Camb Philos Soc 82: 573-590, Oliveira et al. 2017OLIVEIRA HFM, CAMARGO NF, GAGER Y & AGUIAR LMS. 2017. The response of bats (Mammalia: Chiroptera) to habitat modification in a neotropical savannah. Trop Conserv Sci 10: 1-14.). The ecological importance of bats is even greater due to their high movement ability, and because they defecate while flying, which allow seeds to be dispersed away from the parental plant and favors spatial heterogeneity of plant populations (Galetti & Morellato 1994GALETTI M & MORELLATO LPC. 1994. Diet of the large fruit-eating bat Artibeus lituratus in a forest fragment in Brazil. Mammalia 58: 661-665., Passos et al. 2003PASSOS FC, SILVA WR, PEDRO WA & BONIN MR. 2003. Frugivoria em morcegos (Mammalia, Chiroptera) no Parque Estadual Intervales, sudeste do Brasil. Rev Bras Zool 20: 511-517.).

Among phyllostomid bats, members of the subfamily Stenodermatinae feed almost exclusively on diaspores and are considered important dispersers of many trees and shrubs (Fleming & Sosa 1994FLEMING TH & SOSA VJ. 1994. Effects of nectarivorous and frugivorous mammals on reproductive success of plants. J Mammal 75: 845-851., Reis et al. 2017REIS NR, PERACCHI AL, BATISTAM CB, LIMA IP & PEREIRA AL. 2017. História Natural dos Morcegos Brazileiros: chave de identificação de espécies. Rio de Janeiro: Technical Books, 416 p.). The species Sturnira lilium (E. Geoffroy 1810) (Phyllostomidae, Stenodermatinae) is among the most widespread and locally abundant bats of the New World tropics, occurring in biomes associated with the Brazilian Shield: Atlantic Forest, Cerrado, Caatinga, and Chaco (Velazco & Patterson 2013VELAZCO PM & PATTERSON BD. 2013. Diversifcation of the yellow-shouldered bats, genus Sturnira (Chiroptera, Phyllostomidae), in the New World tropics. Mol Phylogenet Evol 68: 683-698.). The diet of the species is composed of plants represented by 28 families considering all its distribution area (Geiselman et al. 2002GEISELMAN CK, MORI SA & BLANCHARD F. 2002. Database of neotropical bat/plant interactions. [Internet]. Available from: http://www.nybg.org/botany/tlobova/mori/batsplants/database/dbase_frameset.htm/ accessed on February 02, 2019.
http://www.nybg.org/botany/tlobova/mori/... ). The preference of S. lilium for diaspores of plants of the genus Solanum (Solanaceae) is well described in the literature (Mello et al. 2008MELLO MAR, KALKO EKV & SILVA WR. 2008. Diet and abundance of the bat Sturnira lilium (Chiroptera) in a Brazilian Montane Atlantic Forest. J Mamm 89: 485-492., Marinho-Filho 1991MARINHO-FILHO JS. 1991. The coexistence of two frugivorous bat species and the phenology of their food plants in Brazil. J Trop Ecol 7: 59-67., Saldaña-Vázquez et al. 2013SALDAÑA-VÁZQUEZ RA, SOSA VJ, IÑIGUEZ-DÁVALOS LI & SCHONDUBE JE. 2013. The role of extrinsic and intrinsic factors in neotropical fruit bat-plant interactions. J Mammal 94: 632-639.). In addition, the maturation of the diaspores may also influence bats choice when feeding, and mature diaspores might be preferred in relation to immatures, since they provide higher energetic return (August 1981AUGUST PV. 1981. Fig fruit consumption and seed dispersal by Artibeus jamaicensis in the Llanos of Venezuela. Biotropica 13: 70-76., Carvalho 2010CARVALHO N. 2010. Germinação de sementes ingeridas por morcegos. Dissertação de Mestrado, Universidade Federal de Mato Grosso do Sul. (Unpublished).). Still, immature diaspores might also be consumed due to seasonal scarcity of resources and accentuated competition by mature diaspores (Carvalho 2010CARVALHO N. 2010. Germinação de sementes ingeridas por morcegos. Dissertação de Mestrado, Universidade Federal de Mato Grosso do Sul. (Unpublished).).

Besides diet, the relationship between S. lilium and the family Solanaceae seems to be very important ecologically. Bats defecate seeds after feeding, and Solanum plants are considered pioneer species, characterized by fast growth and seeds that develop under direct sunlight exposure (Charles-Dominique 1986CHARLES-DOMINIQUE P. 1986. Interrelations between frugivorous vertebrates and pioneer plants: Cecropia, birds and bats in French Guiana. In: Estrada A and Fleming TH (Eds), Frugivores and seed dispersal. Springer Netherlands, p. 119-135., Lobova et al. 2009LOBOVA TA, GEISELMAN CK & MORI SA. 2009. Seed dispersal by bats in the Neotropics. New York: New York Botanical Garden, 471 p.). Solanum mauritianum Scop. is a common species present in high densities in fragments of Atlantic Forest of southern Brazil (Gasper et al. 2013GASPER AL, UHLMANN A, SEVEGNANI L, LINGNER DV, RIGON-JUNIOR MJ, VERDI M, STIVAL-SANTOS A, DREVECK S, SOBRAL M & VIBRANS AC. 2013. Inventário Florístico Florestal de Santa Catarina: espécies da Floresta Estacional Decidual. Rodriguésia 64: 427-443.). The plant produces flowers and fruits at regular intervals throughout the year, enabling a single plant to produce excessive numbers of seeds (Denny 1999DENNY RP. 1999. Control of bugweed (Solanum mauritianum). Pamphlet of the Plant Protection Research Institute, Hilton, South Africa.). In south Brazil, flowering and fruiting of the species was documented throughout the year, occurring from January to December, except in frosty times (Lubke et al. 2021LUBKE M, LUBKE L, CORRÊA BJS, FILIPPI M & BECHARA FC. 2021. Phenodynamics of Solanum mauritianum Scop. in a plantation for subtropical forest restoration. Floresta 51: 439-446.). In this context, the aim of our study was to investigate the association of the frugivore bat S. lilium with the diaspores of S. mauritianum in different stages of maturation. We also investigated the diet of the species based on seed content present in feces of captured individuals. We expect that S. lilium abundance would be positively associated with the proportion of immature and mature diaspores of S. mauritianum. Likewise, we expect to find higher number of seeds of Solanaceae plants in bats feces in relation to other botanical families.

MATERIALS AND METHODS

Study area

The study was conducted in a fragment of mixed ombrophilous forest (MOF) of about 20 ha, located in Chapecó, Santa Catarina, southern Brazil (27º05’ S, 52º39’ W) (Figure 1). According to Köppen’s classification the climate of the region is of the Cfb type: subtropical, with a dominant influence of the territorial pattern, humid, with precipitation uniformly distributed through the year and mild summers (Alvares et al. 2013ALVARES CA, STAPE JL, SENTELHAS PC, GONÇALVES JLM & SPAROVEK G. 2013. Köppen’s climate classification map for Brazil. Meteorologische Zeitschrift 22: 711-728.). Natural vegetation is characteristic of the Atlantic Forest biome. The study area is situated in a transition between MOF and seasonal deciduous forest (SDF) (IBGE 2012IBGE - INSTITUTO BRASILEIRO DE GEOGRAFIA E ESTATÍSTICA. 2012. Manual técnico da vegetação Brasileira. 2. ed. Rio de Janeiro: IBGE.). MOF has complex structure and several types of plant communities within its distribution, with Araucaria angustifolia (Bertol.) Kuntze as dominant species (Longhi 1980LONGHI SJ. 1980. A estrutura de uma floresta natural de Araucaria angustifólia (Bert.) O. Ktze, no Sul do Brasil. Dissertação de Mestrado, Universidade Federal do Paraná. (Unpublished)., Leite & Klein 1990LEITE PF & KLEIN RM. 1990. Vegetação. In: Mesquita OV (Ed), Geografia do Brasil - Região Sul, Rio de Janeiro: IBGE 2: 113-150.). According to Siminski et al. (2011)SIMINSKI A, FANTINI AC, GURIES RP, RUSCHEL AR & REIS MS. 2011. Secondary forest succession in the Mata Atlantica, Brazil: floristic and phytosociological trends. Int Sch Res Not 11: 1-20., about 82% of arboreal species recorded in Santa Catarina occur in this kind of forest (Gasper et al. 2013GASPER AL, UHLMANN A, SEVEGNANI L, LINGNER DV, RIGON-JUNIOR MJ, VERDI M, STIVAL-SANTOS A, DREVECK S, SOBRAL M & VIBRANS AC. 2013. Inventário Florístico Florestal de Santa Catarina: espécies da Floresta Estacional Decidual. Rodriguésia 64: 427-443.). SDF comprises forests characterized by the predominance of deciduous trees, with more than 50% of plant species shedding all their leaves during unfavorable seasons (Reitz et al. 1978REITZ R, KLEIN RM & REIS A. 1978. Projeto Madeira de Santa Catarina. Sellowia 30: 1-320., IBGE 2012IBGE - INSTITUTO BRASILEIRO DE GEOGRAFIA E ESTATÍSTICA. 2012. Manual técnico da vegetação Brasileira. 2. ed. Rio de Janeiro: IBGE.). More than 400 species of plants occur in this forest formation in the region (Gasper et al. 2013GASPER AL, UHLMANN A, SEVEGNANI L, LINGNER DV, RIGON-JUNIOR MJ, VERDI M, STIVAL-SANTOS A, DREVECK S, SOBRAL M & VIBRANS AC. 2013. Inventário Florístico Florestal de Santa Catarina: espécies da Floresta Estacional Decidual. Rodriguésia 64: 427-443.). The species Solanum mauritianum (Solanaceae), commonly known as “cuvitinga” or “fumo-bravo”, is a native plant from southern Brazil and it is widely distributed across the country and commonly found in all forests of southern Brazil.

Figure 1
Location of the study area in southern Brazil. Circles represent points where bats were sampled and the proportion of diaspores of S. mauritianum were evaluated.

Data collection

Bats were mist-netted throughout 21 nights between the months of November of 2017 and April of 2018 in nine sampling campaigns (S1-S9). Each sampling consisted of two to four days, and interval between each sampling varied from 10 to 15 days. This period was chosen because it is the same period of fructification of the species S. mauritianum in the region. In each sample night, six different sampling points were sampled along the fragment. In each point, one mist-net of 12 × 3 m were set at 30 cm above ground level, opened at dusk and closed after 4 hours. Nets were placed close to food sources (S. mauritianum trees), trails and forest edges at a minimum distance of 50 m from each other. Total sampling effort was 18.144 m²/h. Captured animals were identified, measured and weighed, and individually placed in cotton bags for a period a one hour for feces collection. Feces defecated by each individual during retaining period were packed in identified and individualized paper envelopes for laboratory procedures. All individuals were released at their respective sampling locations by the end of each night. All procedures involving capture and handling the animals were approved by the Institutional Animal Care and Use Committee of the Universidade Comunitária da Região de Chapecó (protocol number 006/17). This study was conducted in accordance with the recommendations of the American Society of Mammalogists (Sikes and The Animal Care and use Committee of the American Society of Mammalogists 2016SIKES RS, The Animal Care and use Committee of the American Society of Mammalogists. 2016. Guidelines of the American Society of Mammalogists for the use of wild mammals in research and education. J Mammal 97: 663-688.).

Analysis of the proportion of S. mauritianum diaspores and fecal content of bats

The availability of diaspores of Solanum mauritianum present in the area was evaluated in the same sample periods that bats were being sampled (S1-S9). To do that, we established a 24 m line transect at each mist net point, five meters to the left or right from the mist net line, giving preference to the direction with higher vegetation density. All arboreal individuals of S. mauritianum whose treetops overlapped the line with a perimeter at breast height (PBH) equal or greater than 15 cm producing diaspores were evaluated. Botanical material sampled from each plant was herborized, identified (APG IV 2016AUGUST PV. 1981. Fig fruit consumption and seed dispersal by Artibeus jamaicensis in the Llanos of Venezuela. Biotropica 13: 70-76.) and registered as a specimen testimony in the Herbarium of the Universidade Comunitária da Região de Chapecó. We determined the proportion of immature and mature diaspores in each monitored plant by the FournierFOURNIER LA. 1974. Un método cuantitativo para la medición de características fenológicas en árboles. Turrialba 24: 422-423.’s Intensity Percentage (1974): class 1 (1 to 25 % of diaspores in relation to the plant crown); class 2 (26 to 50 %); class 3 (51 to 75 %); and class 4 (76 to 100 %). For the analysis of the proportion of S. mauritianum diaspores, the midpoint of each Fournier class was used, which correspond to the sum of the upper and lower limits of the class divided by two. This was done to obtain a continuous value representative of each sampled individual in each sample period. Subsequently, the calculation of immature and mature diaspores proportion consisted of summing the midpoints of each observation day separately, and the value obtained was divided by 100. We did not determine density of S. mauritianum plants.

Regarding bats fecal analysis, to assist in identification of fecal content of captured individuals, diaspores of zoochoric plants potentially consumed by bats of each line transect were sampled, and seeds were extracted to produce a spermatheca, which was used for comparison with seeds found in the feces. Feces from each captured individual were washed with distilled water and all seeds were individualized, quantified and identified to the taxonomic level of Family.

Data analysis

Species abundance were expressed as number of captured individuals. Captured animals of each sample night were maintained in cotton bags until the end of each sample to avoid recaptures. Proportion of immature and mature diaspores of S. mauritianum and seeds found in fecal samples were determined for each sample period. We used generalized linear models (GLMs) with Poisson distribution to verify the association of the proportion of immature and mature diaspores of S. mauritianum with the abundance of S. lilium. We separated the proportions of immature and mature diaspores in our model. A model was constructed with these two independent variables together without interactions. The sum of the captures of each sample period was used as a dependent variable. Statistical analyses were performed in the software R 3.0.0 (R Development Core Team 2017R DEVELOPMENT CORE TEAM. 2017. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. https://www.R-project.org/.
https://www.R-project.org/... ).

RESULTS

In total, 61 individuals of S. lilium were captured (38 males and 23 females). Two members of the family Phyllostomidae (Artibeus lituratus (Olfers 1818) (n = 1) and Sturnira tildae (de la Torre 1959) (n = 1)) and six members of the family Vespertilionidae (Histiotus velatus (E. Geoffroy 1824) (n = 4) and Myotis sp. (n = 2)) were also recorded. Results regarding the availability of diaspores of S. mauritianum and the proportion of immature and mature diaspores are summarized in Table I. We observed the presence of mature diaspores of S. mauritianum only between samples S4 to S6 (January and February of 2018). In relation to feces content, a total of 795 seeds were quantified in the feces of S. lilium bats. All sampled seeds belong from two botanical families: Solanaceae (709) and Moraceae (86). Seeds of the family Solanaceae represented 89% of seeds found. In one case, 160 seeds were quantified from a single fecal sample of an adult female (Table I).

The abundance of S. lilium was positively associated with the proportion of S. mauritianum immature diaspores (Coefficient= 0.345; z-value= 4.580; p= 0.0001). There was no significant association with the proportion of mature diaspores (Coefficient= -0.392; z-value= -1.327; p= 0.184) (Figures 2, 3).

DISCUSSION

Fluctuations in the abundance of frugivore bats are generally associated with food availability (Hodgkison et al. 2004HODGKISON R, BALDING ST, ZUBAID A & KUNZ TH. 2004. Temporal variation in the relative abundance of fruits bats (Megachiroptera: Pteropodidade) in relation to the availability of food in a lowland Malaysian rain forest. Biotropica 36: 522-533.), as we observed in the relationship between S. lilium and S. mauritianum. This fact corroborates our initial hypothesis of association among these species and reinforces the important interaction between S. lilium and the genus Solanum (Sette 2012SETTE IMS. 2012. Interação morcego-fruto: estado da arte no Brasil e um estudo da chuva de sementes por aves e morcegos em uma área do Cerrado em Brasília. Dissertação de Mestrado, Universidade de Brasília. (Unpublished).). Solanum mauritianum has characteristics that may facilitate the ecological interaction with frugivore bats, such as the exposure of diaspores above the foliage, coloring and the fermentation odor of the diaspores, and the permanence of diaspores in the peduncle even after maturation. These attributes increase the probability of this species to be dispersed by bats (Van der 1972VAN DER POL. 1972. Principles of dispersal in higher plants. New York: Springer, 154 p., Humphrey & Bonaccorso 1979HUMPHREY SR & BONACCORSO FJ. 1979. Population and community ecology: In: Baker RJ, Jones JK & Carter DC (Eds), Biology of bats of the New World family PhyIlostomatidae, Part III, Special Publication. The Museum Texas Tech University., Shanahan et al. 2001SHANAHAN MSS, COMPTON SG & CORLETT R. 2001. Fig-eating by vertebrate frugivores: a global review. Biol Rev Camb Philos Soc 76: 529-572.). The preference of S. lilium for S. mauritianum diaspores is confirmed by the prevalence of seeds of the family Solanaceae found in feces (89%).

In contrast, contrary to what was expected, we observed a positive relationship between S. lilium and the proportion of immature diaspores of S. mauritianum. Thus, it is possible that S. lilium might prefer to feed on immature diaspores of this species even when mature diaspores of other species are available, or alternatively, that the absence of S. mauritianum mature diaspores in the samples may indicate that they had already been consumed. In fact, with increasing production of S. mauritianum immature diaspores, a high amount of Solanum seeds was found in the feces. The preference of Sturnira bats for Solanum diaspores have already been demonstrated experimentally, even when diaspores of other plants present in the diet of the species were offered in higher quantities (Andrade et al. 2013ANDRADE TY, THIES W, ROGERI PK, KALKO EKV & MELLO MAR. 2013. Hierarchical fruit selection by Neotropical leaf-nosed bats (Chiroptera: Phyllostomidae). J Mammal 94: 1094-1101.). However, it might also be possible that the captured individuals could have fed in other areas of the region.

The predominance of Solanum seeds found in feces of Sturnira reinforces the importance of this bat in the maintenance of forest restoration, since Solanum plants are associated with initial stages of forest succession. Bats can consume several diaspores in a single night, and they defecate within 30 minutes after feeding (Laska 1990LASKA M. 1990. Olfactory sensitivity to food odor components in the short-tailed fruit bat, Carolia perspicillata (Phyllostomatidae, Chiroptera). J Comp Physiol 166: 395-399., Cockle 1997COCKLE A. 1997. Modalites de dissemination et d’etablissement de lianes de sous-bois (Cyclanthaceae et Philodendron) en foret guyanaise. Thèse de Doctorat, I’Université Paris., Neuweiler 2000NEUWEILER G. 2000. The biology of bats. New York: Oxford University Press, 310 p., Korine et al. 2000KORINE C, KALKO EKV & HERRE EA. 2000. Fruit characteristics and factors affecting fruit removal in a Panamanian community of strangler figs. Oecol 123: 560-568.). Thus, human disturbed areas such as pastures or abandoned crops can receive these seeds while bats are flying (Castaño 2009CASTAÑO J. 2009. Murcielagos frugívoros y plantas quiropterocoras: Descubriendo la estructura de sus interacciones mutualistas en una selva semi-caducifolia. Tesis de Maestria, Universidad de los Andes. (Unpublished).). Bats hardly damage small seeds when feeding (Humphrey & Bonaccorso 1979HUMPHREY SR & BONACCORSO FJ. 1979. Population and community ecology: In: Baker RJ, Jones JK & Carter DC (Eds), Biology of bats of the New World family PhyIlostomatidae, Part III, Special Publication. The Museum Texas Tech University., Carvalho 2010CARVALHO N. 2010. Germinação de sementes ingeridas por morcegos. Dissertação de Mestrado, Universidade Federal de Mato Grosso do Sul. (Unpublished).), and we observed that most of the seeds present in feces were in good physical condition. We also found seeds of the Moraceae family in the fecal samples, which is also important in the diet of frugivore bats, as it promotes food supply throughout the year asynchronously (Nason et al. 1998NASON JD, HERRE EA & HAMRICK JL. 1998. The breeding structure of a tropical keystone plant resource. Nature 39: 685-687., Bleher et al. 2003BLEHER B, POTGIETER CJ, JOHNSON DN & BÖHNING-GAESE K. 2003. The importance of figs for frugivores in a South African coastal forest. J Trop Ecol 19: 375-386.). It is important to mention that we cannot be sure if the seeds found in fecal samples of bats came from immature or mature diaspores. In addition, despite the overall dominance of S. mauritianum at the sample site and in the region, it is not possible to identify whether there are any seeds of other species of Solanum in the feces. However, the analysis of fecal content corroborates the data on food preference for the Solanaceae family by this bat (Mello et al. 2008MELLO MAR, KALKO EKV & SILVA WR. 2008. Diet and abundance of the bat Sturnira lilium (Chiroptera) in a Brazilian Montane Atlantic Forest. J Mamm 89: 485-492.). In spite of the overall variety of zoochoric diaspores that might be present in the area, the diet of S. lilium is generally dominated by fruits of the family Solanaceae.

Our results indicate that high consumption of Solanum diaspores, evidenced by the dominance of seeds in feces, reinforces the role of S. lilium as a disperser of this genus. Our findings support the view that S. lilium is a legitimate disperser of S. mauritianum, and that its ecological function is probably a result of co-adaptation (Andrade et al. 2013ANDRADE TY, THIES W, ROGERI PK, KALKO EKV & MELLO MAR. 2013. Hierarchical fruit selection by Neotropical leaf-nosed bats (Chiroptera: Phyllostomidae). J Mammal 94: 1094-1101.). We identified a strong relation with the proportion of S. mauritianum immature diaspores. In this context, we can affirm that the presence of Solanum plants in the area might influence the permanence of animals in the fragment, which may transport their seeds to other environments, contributing with ecological succession and regional vegetation dynamics, considering that S. lilium movement capacity can reach several kilometers in one night (Loayza & Loiselle 2008LOAYZA AP & LOISELLE BA. 2008. Preliminary information on the home range and movement patterns of Sturnira lilium (Phyllostomidae) in a naturally fragmented landscape in Bolivia. Biotropica 40: 630-635., Carvalho et al. 2017CARVALHO F, BÔLLA DAS, MIRANDA JMD & ZOCCHE JJ. 2017. Deslocamentos de morcegos frugívoros (Chiroptera: Phyllostomidae), entre diferentes fitofisionomias da Mata Atlântica, no Sul do Brazil. Rev Bras Bioc 15: 78-82.). This result reinforces the importance of conservation of frugivore bats, since they contribute to the recovery of degraded environments. We suggest that future studies explore the relationship between S. lilium and S. mauritianum immature diaspores and investigate whether seeds and nutrimental contents of ingested immature diaspores have potential for germination after they pass through the animal digestive tract.

ACKNOWLEDGMENTS

We are grateful to our colleagues C. Werlang, G.L.Teston, B. Dariva, R.B. Silva and M.M. Souza for support at various stages of this research; Professor Sérgio Althoff for helping in taxonomic identifications; G. Mergen for his support; Brazil Foods (Chapecó/SC) represented by Mr. Edevandro Invitti for the authorization to access the area; Herbarium and Laboratório de Ecologia e Química from Unochapecó for all the support at various stages of this research. This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) - Finance Code 001 and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq).

REFERENCES

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