Check List 8(4): 617–619, 2012 © 2012 Check List and Authors Chec List ISSN 1809-127X (available at www.checklist.org.br) Journal of species lists and distribution An update on the myxomycete biota (Amoebozoa: Myxogastria) of Colombia Carlos Rojas 1*, Natalia Herrera 2 and Steven L. Stephenson 3 1 Universidad de Costa Rica, Instituto de Investigaciones en Ingeniería and Escuela de Biología. San Pedro de Montes de Oca 11501-2060, Costa Rica. 2 Universidad de Antioquia, Laboratorio de Química Orgánica de Productos Naturales, SIU. Medellín, Colombia. 3 University of Arkansas, Department of Biological Sciences. Fayetteville AR 72701-1201, United States of America. * Corresponding author. E-mail: crojas@fungica.com Abstract: Twelve new records of myxomycetes are reported for Colombia. These additions increase the number of myxomycetes known from this country to 108 species. Since the Colombian territory is part of a biodiversity-rich region in the heart of the Neotropics, the present effort may be considered as a minor contribution. However, due to scarcity of myxomycete research in this country and the importance of inventories involving microorganisms for such purposes as restoration ecology and ecosystem functioning projects, the data presented herein represent a necessary contribution to an understudied aspect of tropical ecology. Introduction significantly to the improvement and understanding of The myxomycetes, also known as myxogastrids or myxomycete occurrence and distribution at both local (e.g. plasmodial slime molds (Stephenson and Stempen 1994), Ko Ko et al. 2010) and regional (e.g. Ndiritu et al. 2009) comprise a monophyletic group of amoeboid protists (see levels. Pawlowski and Burki 2009) known to occur in most if not In Colombia, the most recent inventory of myxomycetes all terrestrial ecosystems (Stephenson 2003). Although was published by Uribe-Meléndez (1995) more than a myxomycetes are characterized by a complex life cycle decade ago. However, active research on myxomycetes that involves two different trophic (feeding) stages and has not been carried out in this country for at least two one reproductive (spore-producing) stage, studies of the decades (see Uribe-Meléndez 1995). In fact, for Colombia group invariably have been centered on the latter (see as a whole, only a handful of studies have been carried out Spiegel et al. 1995). In fact, the taxonomy of this group of on myxomycetes (see Lado and Wrigley de Basanta 2008). organisms is based almost exclusively on the morphology Fortunately, some additional research has taken place of the fruiting bodies in which the spores are produced recently (e.g. Herrera et al. 2011). However, a more active (e.g. Martin and Alexopoulos 1969). effort directed towards studying the myxomycete biota of The development of molecular techniques has resulted the country is still lacking. in a significant increase in our knowledge of phylogenetic In order to contribute to our knowledge of myxomycetes relationships among higher taxa within the myxomycetes in Colombia, the study described herein was carried out. (e.g. Fiore-Donno et al. 2008) and revealed the rather The main objective of this paper is to report species that artificial nature of the system of classification traditionally to our knowledge and according to information in the used within the group (see Fiore-Donno et al. 2010). available literature have not been recorded previously for These techniques also have been useful in developing an Colombia. The importance of these additions is related understanding that some morphospecies may consist of to the fact that updated distribution ranges for species of several biological entities (Winsett and Stephenson 2008). myxomycetes in the Neotropical region provide a more In spite of such advancements, a complete molecular- complete body of data on which to design more complex based phylogeny for the myxomycetes is still not available ecology-based projects in the future. (Stephenson 2011). In this context, the distribution of myxomycetes Materials and Methods around the world is still based on the occurrence of The results presented herein were generated from both distinct species that can be recognized on the basis of a series of rapid assessments of myxomycete biodiversity their morphological features. Using this approach, Lado carried out in Colombia during the period 2006-2008 and Wrigley de Basanta (2008) reported 431 species for as well as from an examination of records of specimens the entire Neotropics. However, more recent studies (e.g. deposited in the United States National Fungus Collection Rojas et al. 2010a, Rojas et al. 2010b) have resulted in a (BPI), as accessed through the Global Biodiversity moderate increase in that figure. In any case, it is likely that Information Facility portal. In all cases, the morphological additional records for the region will be generated as more concept of species has been used and the nomenclatural research is carried out in understudied areas. Recently, an treatment followed is that of Lado (2005-2012). All increasing number of efforts, focused on including such specimens obtained during the rapid assessments have areas in the global study of myxomycetes, has contributed been deposited in the mycological herbarium (UARKM) of 617 Li s t s o f sp e c i e s Rojas et al. | Update on the Myxomycete biota of Colombia the University of Arkansas. Comatricha laxa Rostaf. For records collected by the authors, the specimens K.P. Dumont, BPI 821467; January 11, 1976; road between representing the sources of the records were obtained Bogota and Villavincencio via Caqueza, SW of Bogotá; using a combination of both field and a laboratory-based elevation approximately 2700 m; 4°30’N, 74°7’W; methodology. In the first instance, fruiting bodies of Department of Cundinamarca. myxomycetes were searched for on dead plant material according to the opportunistic protocol described by Comatricha pulchella (C. Bab.) Rostaf. Cannon and Sutton (2004). For the laboratory-based K.P. Dumont, BPI 822076; January 24, 1976; road to methodology, the moist chamber culture technique Antonio Nariño airport from Pasto, SW Colombia; elevation outlined by Stephenson and Stempen (1994) was used. approximately 2400 m; 1°19’N, 77°16’W; Department of In both instances, when myxomycete fruiting bodies were Nariño. found, small portions of the substrate with the specimens present were glued onto pieces of paper placed in small * Comatricha tenerrima (M.A. Curtis) G. Lister pasteboard boxes and then allowed to dry out at room N. Herrera, UARKM 36137, 36138 and 36142; March 16, temperature. After this process, identification of particular 2008; University of Antioquia Campus, in a premontane specimens was carried out using standard monographs moist forest; elevation 1460 m; 6°16’6” N, 75°34’13” W; (e.g., Martin and Alexopoulos 1969), after which they were Department of Antioquia. placed in the herbarium. * Hemitrichia pardina (Minakata) Ing Results and Discussion C. Rojas, UARKM 30453, 30463 and 30476; June 8, In the list that follows, species are arranged 2006; Santa Elena de Medellin, in a Quercus humboldtii alphabetically by genus and then species. After the name dominated forest; elevation 2500 m; 6°13’7” N, 75°30’24” of the species, the name of the collector is included along W; Department of Antioquia. with the accession number for the herbarium where the specimen is deposited. The United States National Fungus Hemitrichia spinifera M.L. Farr Collections is abbreviated as BPI, whereas the mycological K.P. Dumont, BPI 838725; August 21, 1976; road between herbarium of the University of Arkansas as UARKM. Other Bucaramanga and Pamplona, NW Colombia; elevation relevant information such as collection date, location, approximately 2400 m; 7°30’N, 72°32’W; Department elevation and coordinates also have been included. of Norte de Santander. This collection represents an Finally, the administrative Colombian department in isotype of what is apparently a rare species as well as an which the collection was made is listed at the end. Those unreported record for the Neotropics according to Lado georeferences that include information in the form of and Wrigley de Basanta (2008). degrees, minutes and seconds represent measurements obtained directly in the field using a portable GPS unit, * Licea minima Fr. whereas those including only information in the form C. Rojas, UARKM 30484, 30473, 30478, 30480 and 30481; of degrees and seconds correspond to a centroid-based June 11, 2006; San Sebastián de Palmitas, in a premontane georeference derived by the authors using the information mixed forest in early stage of succession; 2700 m; 6°23’46” on the original herbarium label. N, 75°40’18” W; Department of Antioquia. Species with a synonym provided represent records of previously unpublished taxa for Colombia for which the * Licea pusilla Schrad. currently recognized name is different from the original C. Rojas, UARKM 30479; June 11, 2006; San Sebastián de name listed on the herbarium collection. Names marked Palmitas, in a premontane mixed forest in early stage of with one asterisk correspond to species collected as part succession; elevation 2700 m; 6°23’46” N, 75°40’18” W; of the rapid assessments carried out by the authors. Department of Antioquia. Names without an asterisk correspond to species for which records were found in the United States National Metatrichia floriformis (Schwein.) Nann.-Bremek. Fungus Collections but which have not been reported for K.P. Dumont, BPI 836500 as Trichia floriformis (Schwein.) Colombia previously. G. Lister; January 17, 1976; road between Florencia and A total of 12 new records of myxomycetes for Colombia El Doncello, SE Colombia; elevation approximately 250 m; are reported as a result of the combined methodology 1°21’N, 75°21’W; Department of Caquetá. used in the present study. Seven records are for specimens collected directly by the authors, whereas five were * Physarum echinosporum Lister located in the database of the United States National N. Herrera, UARKM 36157; April 9, 2008; Mompos, in a Fungus Collections. All of these records of myxomycetes lowland tropical rainforest; elevation 18 m; 9°14’24.14” for Colombia are provided below. N, 74°25’33.96” W; Department of Bolivar. Arcyria obvelata (Oeder) Onsberg * Physarum notabile T.Macbr. K.P. Dumont, BPI 833262 as Arcyria nutans (Bull.) Grev.; C. Rojas, UARKM 30458; June 8, 2006; Santa Elena de July 4, 1978; road to Medellin near Tenjo, NW of Bogotá; Medellín, in a Quercus humboldtii dominated forest; elevation approximately 2500 m; 4°37’N, 74°5’W; elevation 2500 m; 6°13’7” N, 75°30’24” W; Department Department of Cundinamarca. of Antioquia. 618 Rojas et al. | Update on the Myxomycete biota of Colombia * Stemonitis herbatica Peck Literature Cited N. Herrera, UARKM 36129 and 36130; November 20, Cannon, P. and B. Sutton. 2004. Microfungi on wood and plant debris; p. 217-239. In G. Mueller, G. Bills and M. Foster (ed.). Biodiversity 2007; University of Antioquia Campus, in a premontane of Fungi: Inventory and Monitoring Methods. Burlington: Elsevier moist forest; elevation 1460 m; 6°16’6” N, 75°34’13” W; Academic Press. Department of Antioquia. Fiore-Donno, A.M., M. Meyer, S. Baldauf and J. Pawlowski. 2008. Evolution of dark-spored Myxomycetes (slime-molds): molecules versus morphology. Molecular Phylogenetics and Evolution 46(3): 878-889. Uribe-Melendez (1995) reported a species listed as Fiore-Donno, A.M., S.I. Nikolaev, M. Nelson, J. Pawlowski, T. Cavalier-Smith Didymium cancellatum (Batsch) Macbr. According to Lado and S. Baldauf. 2010. Deep phylogeny and evolution of slimemolds. Protist 161(1): 55-70. (2005-2012), such a nomenclatural combination has never Franco, S., C.M. Suarez, C.B. Naranjo, L.C. Baez and P. Rozo. 2006. The existed. We consider it likely that the author misspelled the effects of the armed conflict on the life and health in Colombia. genus name and intended it to be Dictydium cancellatum Ciência & Saúde Coletiva 11(2):349-361.Herrera, N.A., C. Rojas, A.E. Franco-Molano, S.L. Stephenson and F. (Batsch) T. Macbr., which is now considered a synonym of Echeverri. 2011. Physarella oblonga-centered bioassays for testing Cribraria cancellata (Batsch) Nann.-Bremek. the biological activity of myxomycetes. Mycosphere 2(6): 637-644. The additions to the myxomycete biota of Colombia Ko Ko, T.W., T.T.H. Hanh, S.L. Stephenson, D.W. Mitchell, C. Rojas, K.D. Hyde, S. Lumyong and A.H. Bahkali. 2010. Myxomycetes of Thailand. presented herein are not surprising from a distributional Sydowia 62(2): 243-260. perspective. Most of the species are known to occur widely Lado, C 2005-2012. An online nomenclatural information system of throughout the Neotropical region (see Lado and Wrigley Eumycetozoa. Electronic database accessible at http://www.nomen.eumycetozoa.com. Captured on 22 March 2012. de Basanta 2008). However, for an underrepresented and Martin, G.W. and C.J. Alexopoulos. 1969. The myxomycetes. Iowa City: highly understudied area of the world, the effort presented University of Iowa Press. 561 p. in this study represents an important contribution to the Ndiritu, G.G., K.E. Winsett, F.W. Spiegel and S.L. Stephenson. 2009. A checklist of African myxomycetes. Mycotaxon 107: 353-356. distribution and ecology of tropical myxomycetes. Such an Pawlowski, J. and F. Burki. 2009. Untangling the phylogeny of amoeboid effort is remarkable if it is considered that myxomycete protists. Journal of Eukaryotic Microbiology 56(1): 16-25. research in Colombia has been practically absent during Rojas, C., S.L. Stephenson, A. Estrada-Torres, R. Valverde and O. Morales. 2010a. New records of myxomycetes from high-elevation areas of the last two decades. Mexico and Guatemala. Mycosphere 1(1): 73-82. Unfortunately, socio-political conflicts in forested Rojas, C., M. Schnittler and S.L. Stephenson. 2010b. A review of the Costa areas of Colombia have affected human activities in this Rican myxomycetes (Amebozoa). Brenesia 73-74: 39-57.Spiegel, F.W., S.B. Lee and S.A. Rusk. 1995. Eumycetozoans and molecular part of the world for almost 50 years already (Franco et systematics. Canadian Journal of Botany 73(S1): S738-S746. al. 2006). Among these activities, biological research has Stephenson, S.L. 2003. Fungi of New Zealand Vol. 3: Myxomycetes of New suffered a major impact due its field-based approach. It is Zealand. Hong Kong: Fungal Diversity Press. 238 p.Stephenson, S.L. and H. Stempen. 1994. Myxomycetes: a handbook of slime not surprising that a group such as the myxomycetes has molds. Oregon: Timber Press. 200 p. been practically forgotten in this part of the world. For Stephenson, S.L. 2011. From morphological to molecular: studies of this reason, any effort to activate additional studies of the myxomycetes since the publication of the Martin and Alexopoulos (1969) monograph. Fungal Diversity 50(1): 21-34. group in this country, even at the small scale presented in Uribe-Meléndez, J. 1995. Catálogo de los Myxomycetes registrados para this investigation, would seem worthwhile. Colombia. Caldasia 18(86): 23-36. Winsett, K.E. and S.L. Stephenson. 2008. Using ITS sequences to assess intraspecific genetic relationships among geographically separated Acknowledgments: We would like to thank the logistic contribution collections of the myxomycete Didymium squamulosum. Revista of Ana Esperanza Franco Molano and Aída Vasco at the University of Mexicana de Micología 27: 59-64. Antioquia. Appreciation is extended to the researchers of the Laboratory for Eumycetozoan Research of the University of Arkansas at the time of the study for their support during the laboratory process. Some of the Received: May 2012 rapid assessments that generated part of the information for this project Accepted: July 2012 were funded by the National Science Foundation through the grant DEB- Published online: August 2012 0316284. Editorial responsibility: Matias J. Cafaro 619