Phylogeny of Thylamys (Didelphimorphia, Didelphidae) species, with special reference to Thylamys karimii

Filogenia das espécies de Thylamys (Didelphimorphia, Didelphidae), com ênfase a Thylamys karimii

Phylogeny of Thylamys (Didelphimorphia, Didelphidae) species, with special reference to Thylamys karimii

Filogenia das espécies de Thylamys (Didelphimorphia, Didelphidae), com ênfase a Thylamys karimii

Bianca de A. Carvalho^I; Luiz F. B. Oliveira^II; Margarete S. Mattevi^I

^IUniversidade Luterana do Brasil, Curso de Pós-Graduação em Genética e Toxicologia Aplicada, Av. Farroupilha, 800, 92420-280 Canoas, Rio Grande do Sul, Brazil. ([e-mail]; [e-mail])

^IIMuseu Nacional, Universidade Federal do Rio de Janeiro, Setor de Mastozoologia, 20940-040 Rio de Janeiro, Brazil. ([e-mail])

ABSTRACT

The genus Thylamys Gray, 1843 lives in the central and southern portions of South America inhabiting open and shrub-like vegetation, from prairies to dry forest habitats in contrast to the preference of other Didelphidae genera for more mesic environments. Thylamys is a speciose genus including T. elegans (Waterhouse, 1839), T. macrurus (Olfers, 1818), T. pallidior (Thomas, 1902), T. pusillus (Desmarest, 1804), T. venustus (Thomas, 1902), T. sponsorius (Thomas, 1921), T. cinderella (Thomas, 1902), T. tatei (Handley, 1957), T. karimii (Petter, 1968), and T. velutinus (Wagner, 1842) species. Previous phylogenetic analyses in this genus did not include the Brazilian species T. karimii, which is widely distributed in this country. In this study, phylogenetic analyses were performed to establish the relationships among the Brazilian T. karimii and all other previously analyzed species. We used 402-bp fragments of the mitochondrial cytochrome b gene, and the phylogeny estimates were conducted employing maximum parsimony (MP), maximum likelihood (ML), Bayesian (BY), and neighbor-joining (NJ). The topologies of the trees obtained in the different analyses were all similar and pointed out that T. karimii is the sister taxon of a group constituted of taxa from dry and arid environments named the dryland species. The dryland species consists of T. pusillus, T. pallidior, T. tatei, and T. elegans. The results of this work suggest five species groups in Thylamys. In one of them, T. velutinus and T. kariimi could constitute a sister group forming one Thylamys clade that colonized Brazil.

Keywords: Cytochrome b, Didelphidae, Didelphimorphia, South America, Thylamys phylogeny.

RESUMO

O gênero Thylamys Gray, 1843 ocorre na região central e ao sul da América do Sul, habitando vegetações abertas e arbustivas, desde pradarias até florestas de ambientes secos, em contraste à preferência por habitats mais úmidos dos outros gêneros de Didelphidae. O gênero inclui T. elegans (Waterhouse,1839), T. macrurus (Olfers, 1818), T. pallidior (Thomas, 1902), T. pusillus (Desmarest, 1804), T. venustus (Thomas, 1902), T. sponsorius (Thomas, 1921), T. cinderella (Thomas, 1902), T. tatei (Handley, 1957), T. karimii (Petter, 1968) e T. velutinus (Wagner, 1842). Análises filogenéticas anteriores não incluíram a espécie brasileira T. karimii, que apresenta uma ampla distribuição no país. Neste estudo foram feitas análises filogenéticas visando estabelecer a relação entre a espécie brasileira T. karimii e as demais espécies incluídas em outras análises. Foram utilizados fragmentos de 402pb do gene mitocondrial citocromo b. As filogenias foram estimadas pelos métodos de máxima parcimônia (MP), máxima verossimilhança (ML), Análise Bayesiana (BY) e Neighbor-Joining (NJ). As topologias das árvores obtidas nas diferentes análises mostraram-se semelhantes e evidenciaram que T. karimii agrupa-se com as espécies T. pusillus, T. pallidior, T. tatei, and T. elegans, de ambientes secos e áridos. Os resultados obtidos neste trabalho sugerem cinco grupos de espécies em Thylamys, dos quais um poderia ser composto pelo grupo-irmão T. velutinus e T. kariimi, o qual seria o clado que colonizou o Brasil.

Palavras-chave: Citocromo b, Didelphidae, Didelphimorphia, América do Sul, filogenia de Thylamys.

Considering mainly the morphology, TATE (1933) grouped the small American marsupials (mouse opossums) into five informally named units within the Marmosa genus: murina, cinerea, noctivaga, microtarsus, and elegans. Later, based on systematic revisions that included morphological and chromosomal characters and biochemical studies, the groups defined by TATE (1933) gained generic status and are currently recognized as the genera Chacodelphys (Voss, Gardner & Jansa, 2004), Cryptonanus (Voss, Lunde & Jansa, 2005), Marmosa (Gray, 1821), Micoureus (Lesson, 1842), Marmosops (Matschie, 1916), Gracilinanus (Gardner & Creighton, 1989) and Thylamys (Gray, 1843), respectively (CREIGHTON, 1985; REIG et al., 1985; GARDNER & CREIGHTON, 1989; VOSS et al., 2004; VOSS et al., 2005).

GARDNER & CREIGHTON (1989) recognized five valid species of Thylamys: T. elegans (Waterhouse, 1839), T. macrurus (Olfers, 1818), T. pallidior (Thomas, 1902), T. pusillus (Desmarest, 1804), and T. velutinus (Wagner, 1842). Additional species have been recognized as valid (JULIEN-LAFERRIÈRE, 1994; PALMA, 1995; FLORES et al., 2000; SOLARI, 2003): T. cinderella (Thomas, 1902), T. karimii (Petter, 1968), T. tatei (Handley, 1957), T. venustus (Thomas, 1902), and T. sponsorius (Thomas, 1921). This latter species, which was proposed previously by FLORES et al. (2000), was not supported as a valid species by the phylogenetic results of BRAUN et al. (2005).

Opossums of the genus Thylamys are small in size and have long, soft, hairy coats with a brown-gray threecolor pattern on the shoulders. They are pouchless, have exposed teats in the abdominal region, and a prehensile tail with storage capacity for a reserve substance at the base (GARDNER & CREIGHTON, 1989; HERSHKOVITZ, 1992; EISENBERG & REDFORD, 1999). Specimens of this genus are exclusive to South America and are found in Brazil, Peru, Bolivia, Chile, Paraguay, Uruguay, and Argentina in open, dry, semi-arid habitats mainly from sea level to heights of over 3,500 meters (CREIGHTON, 1985; PALMA, 1995).

GARDNER (2005) lists three Thylamys species in Brazil: T. karimii, found only in the states of Pernambuco and Mato Grosso; T. macrurus, found in the southern region; and T. velutinus, found in the southeastern region. However, ecological studies conducted in Central Brazil pointed to the presence of T. velutinus in the central portions of the Cerrado biome, therefore extending the geographic distribution of this species (PALMA & VIEIRA, 2006).

In the review of the genus conducted by CARMIGNOTTO & MONFORT (2006), the geographic distribution of T. karimii is considerably extended, including the glades in the ''Cerrado'' and ''Caatinga'' biomes in northeastern, southeastern, and central Brazil. The genus is currently known to live in the Brazilian states of Rondônia, Mato Grosso, Tocantins, Piauí, Pernambuco, Bahia, Goiás, and Minas Gerais. In central Brazil, T. karimii lives sympatrically with T. velutinus.

CARMIGNOTTO & MONFORT (2006) established that the three Brazilian species of Thylamys are different from one another and from the other members of the genus in terms of the combination of physical and craniodental characteristics. Thylamys karimii presents morphological traits adapted to terrestrial habits with an inconspicuous three-color dorsal pattern. The tail length is shorter than the sum of the head and the body length. The tail end is not prehensile and the paws and fingers are very small, with dermatoglyph-bearing plantar pads either too small or absent. The species that most resembles T. kariimi is T. velutinus, though in the former the dorsal region is brown and the sides are whitish, while the latter presents a reddish-brown dorsal region and grayish sides. Like the other species of the genus, T. karimii presents a chromosome diploid number of 2n = 14 with fundamental number variation: FN = 20 or 24 (CARMIGNOTTO & MONFORT, 2006; CARVALHO et al., 2002, respectively).

Molecular data published by PALMA & YATES (1998) and PALMA et al. (2002) suggest that there is a close relationship between T. macrurus and T. pusillus, which makes these species a separate group from the other species of the genus. These proposals led SOLARI (2003) to propose three species groups in Thylamys: the Andean group (T. elegans, T. pallidior, T. tatei, and T. venustus), the Paraguayan group (T. macrurus and T. pusillus), and the Brazilian group (T. karimii and T. velutinus). SOLARI (2003) and CARMIGNOTTO & MONFORT (2006) considered that the Brazilian group derived from the Paraguayan group, spreading across the Brazilian glades. Nevertheless, BRAUN et al. (2005) obtained arrangements that support four different groups: the Paraguayan (T. macrurus), Yungas (T. venustus and related taxa), Chacoan (T. pusillus), and Andean (T. elegans and related taxa and T. pallidior). In this proposal, the "forest species", represented by the Yungas and Paraguayan groups, are the most basal and the "dryland species", which are highly adapted to arid and semi-arid environments (Chacoan and Andean groups), are the most derived assemblage.

PALMA et al. (2002) and BRAUN et al. (2005) used cytochrome b sequences to estimate the phylogenetic relationships between the species of the Thylamys genus, but neither completely clarified the issue because in both investigations the Brazilian T. velutinus and T. karimii species (this one widely distributed in South American territories) were not included. The object of this study is, therefore, to re-analyze the relationships within the Thylamys genus using the same molecular markers, including T. karimii, to assess its position.

MATERIAL AND METHODS

Specimens. DNA samples were obtained from three Thylamys karimii specimens collected in two localities in Brazilian ''Cerrado'' (Goiás State - 55 km N Niquelândia city: 14º28'S; 48º27'W and 20 km NW Colinas do Sul city: 14º09'S; 48º04'W). Skins and skulls of these specimens are stored in the Mammals Collection at the Museu Nacional, Rio de Janeiro (MN36926, MN36285, and MN36405). The analysis also included 17 individuals of seven Thylamys species from five countries in South America (Tab. I) reported by PALMA et al. (2002) and BRAUN et al. (2005) (Fig. 1).

Since the localities coordinates of the exemplars collected by PALMA et al. (2002) and BRAUN et al. (2005) were not referred, they were estimated using the Global Gazetteer Software Version 2.1. (available at: http://www.fallingrain.com/world/).

The sequences of Gracilinanus agilis (Burmeister, 1854) and Marmosops impavidus (Tschudi, 1845) were chosen as outgroups because these genera were recovered in the same clade as Thylamys, in a phylogenetic analysis of didelphids employing the nuclear interphotoreceptor retinoid binding protein (IRBP) gene sequence (JANSA & VOSS, 2000).

Nucleotide acid sequence analysis. DNA was extracted from the kidney, liver, heart, or muscle (stored at -20ºC or in ethanol 70 % purity) using the standard protocol described in MEDRANO et al. (1990). The partial mitochondrial cytochrome b gene sequences were isolated via polymerase chain reaction (PCR) using the primers MVZ 05 (light-strand) - CGA AGC TTG ATA TGAAAAACC ATC GTT G with MVZ16 (heavy-strand) - TAG GAARTA TCAYTC TGG TTTRAT, as suggested by SMITH & PATTON (1993), and the following primers were used to amplify the complete cytochrome b sequence MVZ 05 (as mentioned above) with Mus 15398 (heavystrand) - GAA TAT CAG CTT TGG GTG TTG RTG in accordance with ANDERSON & YATES (2000). PCR products were purified with exonuclease I and shrimp alkaline phosphatase (Amersham Biosciences). The specimens were sequenced directly from purified PCR products using the primers cited above and the ABI Prism BigDye Terminator Cycle Sequencing Ready Reaction Kit (Applied Biosystems) according to the manufacturer's instructions. Sequencing of both strands was done using an ABI Prism 3100 Genetic Analyser (Applied Biosystems). The complete (MN36926) and partial (MN36405 and MN36285) cytochrome b sequences of the voucher specimens are available in GenBank as shown in table I.

Data analysis. The sequences obtained were read using the Chromas 1.45 program, and aligned using the Clustal X 1.81 program (THOMPSON et al., 1997) under the default setting costs, and were manually refined with the aid of the GeneDoc program (NICHOLAS & NICHOLAS, 1997). The composition of bases and Kimura 2-parameter distance (KIMURA, 1980) were obtained with the Molecular Evolution Genetics Analysis software, Version 4 (MEGA 4; TAMURA et al., 2007).

The phylogenetic analysis was performed using neighbor-joining (NJ), maximum likelihood (ML), and maximum parsimony (MP) algorithms using PAUP* v.4.0b10, (SWOFFORD, 2001). Prior to the analyses, the most appropriate model of DNA sequence evolution was evaluated using the ModelTest 3.7 (POSADA & CRANDALL, 1998). The ModelTest chose the HKY+I Ã model as the best fit for our data. For ML tree estimation, heuristic searches with as-is and tree bisection-reconnection (TBR) branch swapping were selected. The support estimates for the ML trees branches by bootstrap analysis were obtained as described in XIANG et al. (2002). MP analysis was performed using a heuristic search with TBR branch swapping with the MULPARS option in effect (this option requests the saving of all equally most parsimonious trees; without this option in effect, only one shortest tree is saved in each replicate) and 100 random-addition replicates. Bootstrap statistical support (FELSENSTEIN, 1985) was carried out with 10,000 replications of the heuristic search and simple taxon addition, with the "all trees saved" option.

Bayesian analyses of the data were performed using MrBayes 3.0b4 (HUELSENBECK & RONQUIST, 2001) to generate a posterior probability distribution using Markov Chain Monte Carlo (MCMC) methods. No a priori assumptions about the topology of the tree were made and all searches were provided with a uniform prior. The MCMC processes were set so that four chains were run simultaneously for one million generations, with trees being sampled every 100 generations for a total of 10,000 trees. We excluded the first 100,000 generations as the "burn-in" period.

For the distance analysis, trees were constructed using the NJ method (SAITOU & NEI, 1987) with Kimura two-parameter distances. Reliability of the trees was tested using 10.000 bootstrap replications (HEDGES, 1992).

RESULTS

Two partial (727bp and 758bp) and one complete cyt b gene sequences (1149bp) were obtained for the T. karimii specimens analyzed in this study. However, as the majority of the taxa was studied using a 402-bp cyt b gene sequence fragment (BRAUN et al., 2005), we performed the phylogenetic analyses using this fragment length to gather information about the majority of the Thylamys species.

In the analysis, 156 variable sites were observed, of which 30 (19.23 %) were in the first position, 13 (8.34 %) were in the second position, and 113 (72.43 %) were in the third codon position. The average transition/ transversion rate observed among the taxa analyzed was 2.6 and the CT transition occurred most frequently. Generally, the tree topologies obtained by these different methods of analysis were similar in that all bootstrap values of the nodes generated were higher than 50 %, the majority being higher than 90 %.

The tree generated by the ML analysis is shown in figure 2, where T. macrurus is recovered as the most basal taxon sister group of clades with high support (91 %). In the first clade (grouping the "dryland species"), T. karimii exemplars are positioned as the sister group of the clade T. pusillus + (T. pallidior + T. tatei + T. elegans) with a bootstrap value of approximately 70 %. The second clade, named Yungas group, includes T. cinderella and T. venustus recovered as reciprocally monophyletic sister groups with bootstrap support of 54.

The most parsimonious tree (not shown) presented 332 steps, a consistency index (CI) of 0.608, a retention index (RI) of 0.789, and the homoplasy index (HI) = 0.391. In the parsimony analysis, 130 sites were informative. The T. macrurus exemplar was recovered as basal to the other Thylamys taxa with a bootstrap value of 100. As seen in the ML tree, in this analysis (MP) the same two clades (dryland and Yungas) were observed, also with high support. In the clade that comprises the T. karimii specimens, it was also the most basal member but with a lower bootstrap value. The relationship among the other specimens of this clade (T. pusillus, T. pallidior, T. tatei, and T. elegans) was an unresolved politomy. The other clade comprised T. cinderella and T. venustus as sister groups.

In the NJ and BY analysis (not shown) the topologies generated in other analyses were in general maintained. In both analyses, T. karimii specimens positioned as the sister group of T. pusillus, T. pallidior, T. tatei, and T. elegans with 86% support (NJ) and 0.92 of probability (BY). T. venustus and T. cinderella, as observed in the ML tree, presented as the sister group of the other species of Thylamys with a bootstrap of 99 % (NJ) and a posterior probability of 1.0 (BY).

Percentage sequence divergences based on Kimura 2-parameters corrected distances were calculated among the specimens (Tab. II). An average genetic distance of 16.29 % was observed (ingroup only). With the exception of T. macrurus, which presented considerable genetic distances (the highest observed was 29.0 % when compared with T. pusillus from Argentina), the remaining species of the genus had smaller average distances between them (ranging from a minimum of 9.7 % between T. pallidior and T. pusillus to a maximum of 20.4 % between T. venustus and T. karimii). The identification of the T. macrurus specimen sequenced by PALMA et al. (2002) could not be verified by us, so we relied on the authors voucher identification. The three T. karimii specimens we sequenced presented intraspecific variations of 0.53 % and interspecific divergences from 15.8 % to 26.0 % when compared with the sequences of T. cinderella and T. macrurus, respectively.

DISCUSSION

Several hypotheses were suggested regarding the relationships of the three Brazilian Thylamys species with the other taxa of the genus. However, they were inconclusive because they did not include the species T. karimii, which is largely distributed in Brazilian territory. These relationships could be better clarified in this study with the inclusion, in a molecular analysis, of the Brazilian species T. karimii, which inhabits dry regions.

Previously, SOLARI (2003) and CARMIGNOTTO & MONFORT (2006), proposed three species groups in Thylamys as the first approach to natural groups: the Andean (T. elegans, T. pallidior, T. tatei, and T. venustus), the Paraguayan (T. macrurus and T. pusillus), and the Brazilian groups (T. karimii and T. velutinus). PALMA et al. (2002), and SOLARI (2003) suggested that T. karimii would present a basal position, possibly derived from T. macrurus and related to T. pusillus. BRAUN et al. (2005), through molecular data, obtained arrangements that were incongruent with those suggested by the authors mentioned earlier. The results obtained by BRAUN et al. (2005) supported four different groups: Paraguayan (T. macrurus), Yungas (T. venustus and related taxa), Chacoan (T. pusillus), and Andean (T. elegans and related taxa and T. pallidior). Our study showed that T. karimii is the sister taxon of the Andean species-group of BRAUN et al. (2005). In all topologies generated by the different analyses methods, we observed T. karimii positioned in the base of the Andean group (T. pusillus, T. pallidior, T. tatei, and T. elegans, sensu BRAUN et al., 2005), constituting a clade that lives in dry habitats (the dryland species). PALMA et al. (2002) suggest that this preference for dry environments may be the result of past dispersion events of T. macrurus (which we found occupying the most basal position in the genus) from a more humid environment to drier and more arid habitats, such as those found in the Brazilian Cerrado. This event would have promoted the differentiation of the Brazilian species of Thylamys, such as T. karimii. This is a small mouse opossum currently known to inhabit open vegetations, not living in fully semi-deciduous forests, from Paraguay to the southern Brazilian ''Cerrado'' (CÁCERES et al., 2007).

The Andean group is, in turn, formed by two sister groups: the T. pusillus specimens from Argentina and Paraguay (FLORES et al., 2000), and T. pallidior, T. tatei, and T. elegans. Thylamys tatei, an endemic species from Peru, positioned the sequenced specimens as the sister taxon of T. elegans, which inhabits Chile. These are in turn the sister groups of T. pallidior, a species widely distributed in western South America (west and south of Peru, north of Chile, and the south of Bolivia to the south of the Valdez peninsula in Argentina; GARDNER, 2005).

The second main clade is composed by T. cinderella and T. venustus, two taxa previously included in T. elegans, but in their revision FLORES et al. (2000) suggested that T. cinderella is a valid species. These authors also proposed that specimens from northern Argentina and Bolivia belonged to T. venustus, while those from southern Argentina were classified as T. cinderella. Afterwards, in a phylogenetic analysis BRAUN et al. (2005) examined the geographic relationships among these taxa by using molecular data and found that the specimens of the T. venustus (from Bolivia and Argentina) formed two well-defined clades, namely T. venustus and T. cinderella.

BAKER & BRADLEY (2006) suggest that the Kimura 2-parameter corrected distances to describe intraspecific variations for marsupials are on average 1.1 %, and the value to describe sister species variations are on average 10.4 %. Our low within-clade sequence divergence values are comparable with those reported by BAKER & BRADLEY (2006). The extensive sequence divergence within nonsister species observed in our study (more than 15 %) are also in the same level of the values described by these authors (18.1 % on average). As mentioned by PATTON & COSTA (2003), the high sequence divergence observed within other didelphidae genera (Philander, Marmosa, and Monodelphis, for example) suggests substantial depth to the ages of these taxa.

The relationship of T. velutinus to the other Thylamys species remains unknown at this time. We suggest five species groups in Thylamys: the four groups mentioned by BRAUN et al. (2005) and the Brazilian group observed in this work. It is possible that T. velutinus and T. karimii may constitute a sister group, forming one Thylamys clade that colonized Brazil.

Acknowledgments. Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Financiadora de Estudos e Projetos (FINEP), Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul (FAPERGS), and the Organization of the American States (OAS) provided support for this study. The authors are grateful to Luciano S. Silva, Jaqueline A. Miranda, Vanessa A. Mengue, Gustavo B. Miranda, Cristina C. Freygang, and Martin Montes for technical help; anonymous referees for critically reviewing the manuscript before publication.

Recebido em novembro de 2007.

Aceito em julho de 2009.

• ANDERSON, S. & YATES, T. L. 2000. A new genus and species of Phyllotine rodent from Bolivia. Journal of Mammalogy 81:18-36
• BAKER, R. J. & BRADLEY, R. D. 2006. Speciation in mammals and the genetic species concept. Journal of Mammalogy 87:643-662.
• BRAUN, J. K.; VAN DEN BUSSCHE, R. A.; MORTON, P. K. & MARES, M. A. 2005. Phylogenetic and biogeographic relationships of mouse opossums Thylamys (Didelphimorphia, Didelphidae) in southern South America. Journal of Mammalogy 86:147-159.
• CÁCERES, N. C.; NAPOLI, R. P.; LOPES, W. H.; CASELLA, J. & GAZETA G. S. 2007. Natural history of the marsupial Thylamys macrurus (Mammalia, Didelphidae) in fragments of savannah in southwestern Brazil. Journal of Natural History 41(2932):1979-1988.
• CARMIGNOTTO, A. P. & MONFORT, T. 2006. Taxonomy and distribution of the Brazilian species of Thylamys (Didelphimorphia: Didelphidae). Mammalia 70:126-144.
• CARVALHO, B. A.; OLIVEIRA, L. F. B.; NUNES, A. P. & MATTEVI, M. S. 2002. Karyotypes of nineteen marsupial species from Brazil. Journal of Mammalogy 83:58-70.
• CREIGHTON, G. K. 1985. Phylogenetic inference, biogeographic interpretations, and the pattern of speciation in Marmosa (Marsupialia: Didelphidae). Acta Zoologica Fenica 170:121-124.
• EISENBERG, J. F. & REDFORD, K. H. eds. 1999. Mammals of the Neotropics. The Northern Neotropics, The Central Neotropics: Ecuador, Peru, Bolivia, Brazil. Chicago, University of Chicago. 609p.
• FELSENSTEIN, J. 1985. Confidence limits on phylogenies: an approach using the bootstrap. Evolution 39:783-791.
• FLORES, D. A.; DIAZ, M. M. & BARQUEZ, R. M. 2000. Mouse opossums (Didelphimorphia, Didelphidae) of northwestern Argentina: systematics and distribution. Zeitschrift für Saugetierkunde 65:321-339.
• GARDNER, A. L. 2005. Didelphimorphia. In: WILSON, D. E. & REEDER, D. M. eds. Mammals species of the world Baltimore, Johns Hopkins University. p.3-18.
• GARDNER, A. L. & CREIGHTON, G. K. 1989. A new generic name for Tate's (1933) microtarsus group of South American mouse opossums (Marsupialia: Didelphidae). Proceedings of the Biological Society of Washington 102:3-7.
• HEDGES, S. B. 1992. The number of replications needed for accurate estimation of the bootstrap P value in phylogenetic studies. Molecular and Biological Evolution 9:366-369.
• HERSHKOVITZ, P. 1992. The South American Gracile Mouse Opossums, genus Gracilinanus Gardner and Creighton, 1989 (Marmosidae, Marsupialia): a taxonomic review with notes on general morphology and relationships. Fieldiana: Zoology 70:1-56.
• HUELSENBECK, J. P. & RONQUIST, F. 2001. Mr. Bayes: Bayesian inference of phylogeny. Bioinformatics 17:754,755.
• JANSA, S. A. & VOSS, R. S. 2000. Phylogenetic studies on Didelphid Marsupials I. Introduction and preliminary results from nuclear IRBP gene sequences. Journal of Mammalian Evolution 7:43-77.
• JULIEN-LAFERRIÈRE, D. 1994. Catalogue des types de marsupiaux (Marsupialia) du Muséum National d'Histoire Naturelle, Paris. Mammalia 58:1-39.
• KIMURA, M. 1980. A simple method for estimating evolutionary rate of base substitutions through comparative studies of nucleotide sequences. Journal of Molecular Evolution 16:111-120.
• MEDRANO, J. F.; AASEN, E. & SHARROW, L. 1990. DNA extraction from nucleated red-blood cells. Biotechniques 8:43.
• NICHOLAS, K. B. & NICHOLAS JR., H. B. 1997. GeneDoc: a tool for editing and annotating multiple sequence alignments Available at: <http://www.nrbsc.org/gfx/genedoc/gdsrc.htm>. Access on: 12.01.2008.
• PALMA, A. R. T. & VIEIRA, E. M. 2006. O gênero Thylamys no Brasil: história natural e distribuição geográfica. In: CÁCERES, N. C. & MONTEIRO-FILHO, E. L. A. eds. Os marsupiais do Brasil: biologia, ecologia e evolução Campo Grande, Universidade Federal de Mato Grosso do Sul. p.271-286.
• PALMA R. E. 1995. Range expansion of two South American mouse opossums (Thylamys, Didelphidae) and their biogeographic implications. Revista Chilena de Historia Natural 68(4):515-522.
• PALMA, R. E.; RIVERA-MILLA, E.; YATES, T. L.; MARQUET, P. A. & MEYNARD, A. 2002. Phylogenetic and biogeographic relationships of the mouse opossum Thylamys (Didelphimorphia, Didelphidae) in southern South America. Molecular Phylogenetics and Evolution 25:245-253.
• PALMA, R. E. & YATES, T. L. 1998. Phylogeny of southern South American mouse opossums (Thylamys, Didelphidae) based on allozyme and chromosomal data. Zeitschrift für Säugetierkunde 63:1-15.
• PATTON, J. L. & COSTA, L. P. 2003. Molecular phylogeography and species limits in rainforest didelphid marsupials of South America. In: JONES, M.; DICKMAN, C. & ARCHER, M. eds. Predators with pouches Collingwood, CSIRO Publishing. p.63-81.
• POSADA, D. & CRANDALL, K. A. 1998. Modeltest: testing the model of DNA substitution. Bioinformatics 14:817-818.
• REIG, O. A.; KIRSCH, J. A. W. & MARSHALL, L. G. 1985. New conclusions on the relationships of the opossum-like marsupials with an annotated classification of the Didelphimorphia. Ameghiniana 21:335-343.
• SAITOU, N. & NEI, M. 1987. The neighbor-joining method: a new method for reconstructing phylogenetic trees. Molecular and Biological Evolution 4:406-425.
• SMITH, M. F. & PATTON, J. L. 1993. The diversification of South American murid rodents: evidence from mitochondrial DNA sequence data for the akodontine tribe. Biological Journal of the Linnean Society 50:149-177.
• SOLARI, S. 2003. Diversity and distribution of Thylamys (Didelphidae) in South America, with emphasis on species from the western side of the Andes. In: JONES, M.; DICKMAN, C. & ARCHER, M. eds. Predators with pouches Collingwood, CSIRO Publishing. p.82-101.
• SWOFFORD, D. L. 2001. PAUP*: phylogenetic analysis using parsimony (*and other methods) Version 4.0 b10. Sunderland, MA. Sinauer Associates.
• TAMURA, K.; DUDLEY, J.; NEI, M. & KUMAR, S. 2007. MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0. Molecular Biology and Evolution 24:1596-1599.
• TATE, G. H. H. 1933. Systematic revision of the marsupial genus Marmosa, with a discussion of the adaptive radiation of the murine opossums (Marmosa). Bulletin of the American Museum of Natural History 66:1-250.
• THOMPSON, J. D.; GIBSON, T. J.; PLEWNIAK, F.; JEANMOUGIN, F. & HIGGINS, D. G. 1997. The Clustal X windows interface: flexible strategies for multiple alignments aided by quality analysis tools. Nucleic Acids Research 24:4876-4882.
• VOSS, R. S.; GARDNER, A. L. & JANSA, S. A. 2004. On the relationships of "Marmosa" formosa Shamel, 1930 (Marsupialia: Didelphidae), a phylogenetic puzzle from the Chaco of northern Argentina. American Museum Novitates 3442:1-18.
• VOSS, R. S.; LUNDE, D. P. & JANSA, S. A. 2005. On the contents of Gracilinanus Gardner and Creighton, 1989, with the descripition of a previously unrecognized clade of small didelphid marsupials. American Museum Novitates 3482:1-34.
• XIANG, Q-Y.; MOODY, M. L.; SOLTIS, D. E.; FAN C. & SOLTIS, P. S. 2002. Relationships within Cornales and circumscription of Cornaceae-matK and rbcL sequence data and effects of outgroups and long branches. Molecular Phylogenetics and Evolution 24:35-57.

Publication Dates

• Publication in this collection
  01 June 2010
• Date of issue
  Dec 2009

History

• Accepted
  July 2009
• Received
  Nov 2007