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New records of myxomycetes (Amoebozoa) from Colombia

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Colombia is located in one the megadiverse regions of the world. However, the number of known species of myxomycetes for this territory is low when compared to similar countries in the same region. The most important reason for such pattern is the systematic undersampling of ecosystems in that part of the world. For that reason, efforts to document the myxobiota of Colombia were set in place as part of collaborative initiatives among academic institutions in the region. Surveys focusing both on field collections and material for moist chamber cultures during the period between 2019-2021 as well as a search of vouchers in recognized herbaria yielded a total of 28 new records of myxomycetes for Colombia, most of which belong to the genera Arcyria, Physarum and Stemonitopsis. These results have increased the number of recognized myxomycetes in Colombian territories from 106 to 134, with an associated increment of about 26% directly related to the latest efforts. Similar surveys in different ecosystems in Colombia and more exploration of Colombian collections will likely increase the number of recognized species of myxomycetes even more, but the present study highlights the importance of establishing a baseline of research in one territory as a strategy to document its biota.
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New records of myxomycetes (Amoebozoa) from
Colombia
Carlos Rojas1, María Carolina García-Chaves2
1Department of Biosystems Engineering and Engineering Research Institute,
University of Costa Rica, San Pedro de Montes de Oca, 11501-Costa Rica
2School of Microbiology, University of Antioquia, Medellín, Colombia
*Corresponding author: carlos.rojasalvarado@ucr.acr.cr; mcarolina.garcia@udea.edu.co
| Received: 18 April 2022 | Accepted: 02 July 2022| Published Online: 04 July 2022|
How to cite: Rojas C, García-Chaves MC. 2022. New records of myxomycetes (Amoebozoa) from Colombia. J
New Biol Rep 11 (1): 10 15.
ABSTRACT
Colombia is located in one the megadiverse regions of the world. However, the number of known species of
myxomycetes for this territory is low when compared to similar countries in the same region. The most important
reason for such pattern is the systematic undersampling of ecosystems in that part of the world. For that reason,
efforts to document the myxobiota of Colombia were set in place as part of collaborative initiatives among
academic institutions in the region. Surveys focusing both on field collections and material for moist chamber
cultures during the period between 2019-2021 as well as a search of vouchers in recognized herbaria yielded a
total of 28 new records of myxomycetes for Colombia, most of which belong to the genera Arcyria, Physarum
and Stemonitopsis. These results have increased the number of recognized myxomycetes in Colombian territories
from 106 to 134, with an associated increment of about 26% directly related to the latest efforts. Similar surveys
in different ecosystems in Colombia and more exploration of Colombian collections will likely increase the
number of recognized species of myxomycetes even more, but the present study highlights the importance of
establishing a baseline of research in one territory as a strategy to document its biota.
Key words: myxogastrids, northern Andes, South America, slime molds.
INTRODUCTION
Colombia is a megadiverse country (Arbeláez-Cortés
2013). The variety of conditions for the establishment
of life in this part of the world allow for a wide diversity
of life strategies to coexist in this territory. High
biodiversity values have been commonly associated
with Colombian territories (Brummitt & Nic Lughadha
2003), even though most of these quantifications are
based on macroscopic forms that do not represent the
most species-rich groups. In this manner, microbial
diversity in Colombia, in a similar manner to other
countries (Wilson et al. 2007), has not been
documented with the same effort and intensity as more
popular groups of organisms.
In addition, the high load of paperwork and
general bureaucracy to conduct biodiversity research in
Colombia has been a recent impediment to generate
updated figures associated with many taxonomic
groups (Fernández 2011). In fact, it is acknowledged
that for the same contextual reasons the genomic
diversity associated with life forms in Colombia is
currently more incomplete than comparable data from
other Latin America countries (Noreña-P et al. 2018).
These limitations do not facilitate research on
microorganisms that do not have commercial or
applied value and have consequences on the
understanding of global microbial ecology (Gibbons &
Gilbert 2015).
Myxomycetes, a group of fruiting amoebae
found worldwide in association with decayed plant
parts (Keller et al. 2021) has been timidly studied in
Colombia. For instance, G.W. Martin mentioned only
34 species almost 90 years ago (Martin 1934), and M.
L. Farr (1976) updated such figure, 42 years later, to 57
species. In his review of Colombian myxomycetes,
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Rojas and García-Chaves JNBR 11(1) 10 15 (2022)
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11
Uribe-Meléndez (1995) increased the number up to 96
species and some years later Rojas et al. (2012)
provided a total value of 108 species. The last
publication, ten years ago, represents the most updated
reference to the biodiversity of myxomycetes in
Colombia. However, the value provided therein is still
today using the words of G W. Martin in the 1930s
“absurdly incomplete for so large a country with such
varied topography and climate”. For comparison, Costa
Rica, 22 times smaller than Colombia has 242 species
of myxomycetes reported (Lado & Rojas 2018).
Colombia must have a larger myxobiota and
even the most recent values of myxomycete
biodiversity are certainly the product of
undersampling. Similar to the case of other groups of
organisms, it has been difficult for both local and
foreign researchers to conduct biodiversity research in
Colombia in recent decades (Clerici et al. 2016). For
that reason, results from any efforts to do so should be
properly documented. The present study has been
carried out as part of explorations to document
ecological patterns of myxomycetes in urban areas
across the Neotropics and its objective is to
communicate a series of previously unrecorded species
of myxomycetes for Colombian territory. Such
information, in the context of similar regional data,
increases the robustness of analyses and interpretations
on microbial diversity, ecology and distribution.
MATERALS AND METHODS
To alleviate the disparity of available information on
myxomycetes between Mesoamerica and the Tropical
Andes biodiversity hotspot regions, a collaborative
effort was established in 2019. As part of this effort, a
series of surveys to document myxomycetes were
established in a) Cartagena, b) The Metropolitan Area
of the Aburrá Valley and c) the region West of the
Aburrá Valley within the Department of Antioquia.
Cartagena, in the northern Caribbean, is located
within a region of tropical dry forests, at just 2 m of
elevation, with an average yearly temperature of 27°C
and an annual precipitation of about 1100 liters per
square meter. In contrast, the other two studied areas
are located in the central Andes, between 500-1500 m
in elevation, and represent premontane moist forests
with an average yearly temperature of 21°C and an
annual precipitation of about 1700 liters per square
meter.
In all surveys, dead plant material was collected
and used to set up moist chamber cultures in the
manner described by Stephenson & Stempen (1994).
With this protocol, the collected material was placed in
petri dishes previously lined with filter paper and
abundant water was added in order to stimulate
myxomycete propagules. After 24 h, water was
discarded, pH was measured, and the culture was
examined during a period of approximately two
months.
When either plasmodia or fruiting bodies of
myxomycetes were observed, they were recorded and
in the case of the last ones, they were extracted with
fine forceps and glued to pasteboard boxes for
scientific storage. In the Metropolitan Area of the
Aburrá Valley, field collections were also obtained in
the Campus of the University of Antioquia. All
specimens were identified with appropriate
monographs (e.g., Martin & Alexopoulos 1969,
Poulain et al. 2011) using basic microscopical
techniques, and deposited in the Myxogastrid
Biorepository of the University of Costa Rica and the
HUA herbaria from the University of Antioquia. The
nomenclature used was that of Lado (2005-2022).
In addition to the surveys, deposited vouchers
and confirmed observations of myxomycetes from
Colombia in either recognized herbaria or repositories
in the United States were examined via the Mycology
Collections Portal (MyCoPortal 2022). When
myxomycetes from Colombia were found, collections
were checked for inconsistencies (e.g., doubtful
identifications, wrong geolocation) and only records
with fully valid information and confirmatory images
were used to complement the survey efforts.
The list of new records for Colombia provided
herein contains the month of collection, the
approximate locality and the substrate upon which the
specimen was found. The collection number assigned
to the deposited vouchers and institutional secondary
numbers in the case of unreported species in American
herbaria are provided as well. For all the latter, the Ro
acronym is from the Myxogastrid Biorepository at the
University of Costa Rica, BPI is from the US National
Fungus Collections, NYBG from the New York
Botanical Garden, ILLS from the Illinois Natural
History Survey Herbarium and MUOB from the
Mushroom Observer Repository (Wood 2008). In all
cases, the known distribution of the species in
neighboring countries was provided.
RESULTS
A total of 28 species of myxomycetes that had not been
previously communicated for Colombia were recorded
during the surveys. That result brought the total number
of myxomycetes in Colombian territories to 134. The
genus Ceratiomyxa, a sister group to the myxomycetes
and considered in all previous reports, was excluded in
these calculations. Those 28 new species for Colombia
represented an increment of 26.4% with respect to the
last published value of 106 (108 considering the two
Ceratiomyxa species).
In this manner, the ratio of species to genera
(known in the myxomycete literature as the taxonomic
diversity index) changed from 4.07 to 4.62 implying
that the currently documented intrageneric diversity
increased. Of the 134 species, 42 were associated with
the phylogenetically stable “bright-spored clade” and
92 species belonged to the “dark-spored clade” and the
number of new species within each group represented
Rojas and García-Chaves JNBR 11(1) 10 15 (2022)
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12
Fig. 1. Diderma acanthosporum Ro-9953, A. Spores under transmitted light scale bar=20 m, B. General
appearance scale bar = 1 mm. C. Sporocarp of Paradiacheopsis solitaria Ro-9611 under transmitted light
scale bar=100 m. D. Sporocarps of Physarum decipiens Ro- 9816 scale bar=1 mm. E. Sporocarps of
Badhamia melanospora Ro- 9748 scale bar=1 mm.
about 23% in the former and 19% in the latter implying
that species in the bright spore group were recorded at
a higher rate during the present effort.
From the newly communicated species for
Colombia, the most common genera were Physarum,
Arcyria and Stemonitopsis, with six, four and three
species, respectively. The genera Metatrichia and
Paradiacheopsis were communicated for the first time
in Colombia. Of the records observed in the surveys, 6
were associated exclusively with ground litter, 5 with
twigs and 4 with bark. Eight records were observed in
more than one substrate.
List of new records of myxomycetes for Colombia:
1. Arcyria afroalpina Rammeloo March 2022, from
the region West of the Aburrá Valley, Antioquia,
Colombia. On ground litter. Ro-9770, 9898, 9989,
10003 and 10033. Known from Panama and Costa
Rica.
2. Arcyria magna Rex March 2022, from the region
West of the Aburrá Valley, Antioquia, Colombia.
On twigs. Ro-9906. Known from Panama and
Costa Rica.
3. Arcyria minuta Buchet April 2019, from Campus
of the University of Antioquia, Medellín,
Antioquia, Colombia. On ground litter. Ro-10049
(Deposited in HUA). Known from Panama and
Costa Rica.
4. Arcyria occidentalis (T. Macbr.) G. Lister March
2022, from the region West of the Aburrá Valley,
Antioquia, Colombia. On twigs. Ro-10016. Known
from Mexico.
5. Badhamia melanospora Speg. March 2022, from
the region West of the Aburrá Valley, Antioquia,
Colombia. On both ground litter and twigs. Ro-
9748, 9754, 9877 and 9995. Fig 1E. Known from
Panama, Ecuador and Costa Rica.
6. Badhamia populina Lister & G. Lister July 1978,
from Sibundoy, between Pasto and Mocoa,
Putumayo, Colombia. On moss. KP Dumont 9581
(BPI 743914/NYBG 02678164). Known from
Chile.
7. Collaria arcyrionema (Rostaf.) Nann.-Bremek. ex
Lado March 2022, from the region West of the
Aburrá Valley, Antioquia, Colombia. On ground
litter. Ro-9720. Known from Panama, Ecuador and
Costa Rica.
8. Collaria rubens (Lister) Nann.-Bremek. March
2022, from Medellín. Antioquia, Colombia. On
bark of living trees. Ro-9612, 9630. Known from
Costa Rica.
9. Comatricha nigra (Pers. ex J.F. Gmel.) J. Schröt.
March 2022, from both the region West of the
Aburrá Valley and Medellín, Antioquia, Colombia.
On ground litter, twigs and bark of living trees. Ro-
9565, 9568, 9571, 9631, 9650, 9651, 9653, 9654,
9684, 9711, 9717, 9722, 9728, 9730, 9733, 9738,
9741, 9743, 9765, 9771, 9775, 9778, 9780, 9786,
9790, 9795, 9796, 9811, 9854, 9897, 9925, 9931,
9933, 9942, 10030 and 10044. Known from
Panama, Ecuador and Costa Rica.
10. Cribraria violacea Rex March 2022, from both
the region West of the Aburrá Valley and Medellín,
Antioquia, Colombia. On ground litter, twigs and
bark of living trees. Ro- 9575, 9657, 9660, 9667,
Rojas and García-Chaves JNBR 11(1) 10 15 (2022)
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9815, 9846, 9945, 9959, 9961, 9971 and 9998.
Known from Panama, Ecuador, Venezuela and
Costa Rica.
11. Diderma acanthosporum Estrada & Lado March
2022, from the region West of the Aburrá Valley,
Antioquia, Colombia. On ground litter. Ro-9953
and 9955. Figs. 1A and 1B. Known from Mexico.
12. Diderma deplanatum Fr. January 1976, from the
Bogotá-Villavicencio Road, via Cáqueza,
Cundinamarca, Colombia. On bamboo. K.P:
Dumont 2215 (ILLS 50343). Known from Costa
Rica.
13. Fuligo septica (L.) F.H. Wigg. July 2015, from
Valle del Cauca, Calí, Colombia. On decayed
wood. MUOB 170497, 208496, 210650, 218267
and 224909. Known from Known from Panama,
Ecuador, Venezuela and Costa Rica.
14. Macbrideola scintillans H.C. Gilbert March
2022, from the region West of the Aburrá Valley,
Antioquia, Colombia. On twigs. Ro-9912. Known
from Costa Rica.
15. Paradiacheopsis solitaria (Nann.-Bremek.) Nann.-
Bremek. March 2022, from Medellín. Antioquia,
Colombia. On bark of living trees. Ro-9611. Fig.
1C. Known from Costa Rica.
16. Perichaena corticalis (Batsch) Rostaf. March
2022, from the region West of the Aburrá Valley,
Antioquia, Colombia. On both ground litter and
twigs. Ro-9687, 9692, 9696, 9701, 9707, 9807,
9825, 9850, 9984, 9994, 10011, 10020, 10032 and
10042. Known from Panama, Ecuador and Costa
Rica.
17. Perichaena vermicularis (Schwein.) Rostaf.
March 2022, from the region West of the Aburrá
Valley, Antioquia, Colombia. On both ground litter
and twigs. Ro-9681, 9708, 9826 and 9966. Known
from Panama, Ecuador and Costa Rica.
18. Physarum decipiens M.A. Curtis March 2022,
from the region West of the Aburrá Valley,
Antioquia, Colombia. On twigs. Ro- 9816, 9821,
9828, 9835, 9838, 9841, 9845, 9851 and 9957.
Figure 1D. Known Costa Rica.
19. Physarum crateriforme Petch from both the
region West of the Aburrá Valley and Medellín,
Antioquia, Colombia. On both ground litter and
bark of living trees. Ro-9608. Known from Ecuador
and Costa Rica.
20. Physarum nudum T. Macbr. March 2022, from
the region West of the Aburrá Valley, Antioquia,
Colombia. On both ground litter and twigs. Ro-
9856 and 9874. Known from Belize.
21. Physarum polycephalum Schwein. March 2022,
from Medellín. Antioquia, Colombia. On bark of
living trees. Ro-9606. Known from Costa Rica.
22. Physarum serpula Morgan April 2019, from
Cartagena, Bolivar, Colombia. On ground litter.
Field observation. No voucher collected. Known
from Panama, Ecuador and Costa Rica.
23. Physarum virescens Ditmar March 2022, from
the region West of the Aburrá Valley, Antioquia,
Colombia. On ground litter. Ro-9891 and 10001.
Known from Venezuela and Costa Rica.
24. Stemonitopsis aequalis (Peck) Y. Yamam. March
2022, from both the region West of the Aburrá
Valley and Medellín, Antioquia, Colombia. On
ground litter, twigs and bark of living trees. Ro-
9578, 9581, 9585, 9607, 9626, 9633, 9669, 9833,
9844, 9852, 9921 and 9937. Known from Panama
and Costa Rica.
25. Stemonitopsis hyperopta (Meyl.) Nann.-Bremek.
March 2022, from both the region West of the
Aburrá Valley and Medellín, Antioquia, Colombia.
On both twigs and bark of living trees. Ro-9587,
9589, 9670, 9682, 9820 and 9911. Known from
Panama and Costa Rica.
26. Stemonitopsis subcaespitosa (Peck) Nann.-
Bremek. March 2022, from Medellín. Antioquia,
Colombia. On bark of living trees. Ro-9583.
Known from Costa Rica.
27. Tubifera corymbosa Leontyev, Schnittler, S.L.
Stephenson & L.M. Walker April 2019, from
Piedecuesta, Santander, Colombia. On decayed
wood. MUOB 365522. Known from Costa Rica.
28. Tubifera ferruginosa (Batsch) J.F. Gmel. October
2012, from Valle del Cauca, Calí, Colombia. On
decayed wood. MUOB 164907 and 184364.
Known from Ecuador, Panama and Costa Rica.
DISCUSSION
Most of the species documented herein are common in
the Neotropics. Eleven of them are known from more
than 10 countries in the region (Lado & Wrigley de
Basanta 2008, Rojas et al. 2018) and with the exception
of Arcyria occidentalis, Diderma acanthosporum,
Badhamia populina, and Physarum nudum, the rest of
the species have been documented in Costa Rica, a very
well-studied territory (Rojas et al. 2018). Of these
exceptions, the first two have been documented in
Mexico (Lado & Wrigley de Basanta 2008, Rojas et al.
2010), the third one is known from Chile and Bolivia
and the last one has been recorded in Belize (Lado &
Wrigley de Basanta 2008). These results simply point
out that all species have been previously
communicated in the Neotropics and that their presence
in Colombia is not extraordinary but expected.
To the best of our knowledge, the surveys where
these new records for Colombia were observed have
been the most intense recent assessments of
myxomycete diversity in that country. Interestingly,
more unrecorded species were expected from the
tropical dry forests of Cartagena based on previous
research in other neotropical areas (Estrada-Torres et
al. 2009). It is possible that a number of small forms in
such genera as Echinostelium, Licea or Macbrideola
were undetected due to the untrained eyes of the
students that examined the moist chamber cultures.
However, the presence of Physarum serpula in
Colombian dry forests highlights its occurrence in arid
Rojas and García-Chaves JNBR 11(1) 10 15 (2022)
__________________________________________________________________________________________
14
environments as observed in distributional data from
other parts of the Neotropics (Rojas et al. 2018).
The premontane forests of the general area
associated with the Aburrá Valley (within and
neighboring lands) provide adequate conditions for the
establishment and reproduction of myxomycetes. The
surveys that generated the information presented herein
only focused on such substrates as ground litter, twigs
and bark. However, previous investigations in similar
areas have demonstrated different assemblages of
myxomycetes in association with lianas, aerial litter
and inflorescences (Wrigley de Basanta et al. 2008,
Schnittler & Stephenson 2002). In this manner, it is
very likely that the number of species known to the
tropical Colombian Andes landscape will increase as
more specific surveys are implemented in the future. In
the work of Lado & Wrigley de Basanta (2008), they
showed very clearly that the number of known species
of myxomycetes for different territories in the
Neotropics is highly associated with the number of
publications for those jurisdictions, a proxy for survey
effort (r=0.88, r2=0.78).
Moreover, given the variety of conditions in
Colombia, a series of future surveys in unexplored
areas such as highlands, the coastal areas of the Pacific
Coast, the eastern plains and the Amazonian forests
will inevitably increase the number of known
myxomycetes in this part of the world. Such experience
has been the norm in other previously unexplored
regions in South America such as Chile and Peru (Lado
et al. 2013, Lado et al. 2016). However, given the
strategic geographical location of Colombia it is
possible that new species of myxomycetes for science
can be discovered in those campaigns. For instance, in
a high-intensity survey in specific locations in Brazil,
Costa Rica and Panama, Walker et al. (2019)
discovered that a form of stalked Perichaena common
to Neotropical forests did not quite correspond to the
known P. pedata and instead was a different species
with a similar morphology.
Finally, the presence of online platforms for
accessing information on historical biological
collections, not available few years ago, has increased
the potential of addressing issues related to biodiversity
in a different manner than ever before (Monfils et al.
2017). For instance, in the work of Rojas et al. (2012)
authors checked for myxomycete collections from
Colombia in the herbarium of the United States
National Fungus Collection (BPI) but were unaware at
that time of the records included herein and of the other
records at the New York Botanical Garden and the
Illinois Natural History Survey Herbarium. The
Mushroom Observer platform was in a very early stage
at that time. All these resources allow researchers to
synthesize information more properly, at the local or
regional levels, and promote higher quality feedback
for decision-makers in the fields of conservation and
natural resources management. Ultimately, studying
nature provides information that should be used for
humanity to determine a more responsible future path
and efforts to document biodiversity, like the one
presented herein, have been conceived with such goal
in mind.
ACKNOWLEDGMENTS
This study was partially financed by a research grant
from University of Costa Rica (Vicerrectoría de
Investigación 731-B7-721) and was finalized under the
scope of an international agreement between the two
institutions represented by the authors. The material
was legally obtained using the collecting license
granted by Resolución 0524 from the National
Authority of Environmental Licenses in Colombia
(ANLA). We would like to thank Esperanza Franco-
Molano and Pedro Rojas for their support during the
different activities that derived in the generation of the
information presented herein.
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... Some research has been directed toward niche modeling of myxomycetes in tropical forests, the assemblages of myxomycetes associated with urban landscapes, and assessing the influence of climate on the production of fruiting bodies. The latter is a three-year project carried out in Costa Rica that is designed to obtain data on phenology and the relationship between the dynamics of a forest community and the production of fruiting bodies [81][82][83][84][85][86][87]. ...
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Evidence from molecular studies indicates that myxomycetes (also called myxogastrids or plasmodial slime molds) have a long evolutionary history, and the oldest known fossil is from the mid-Cretaceous. However, they were not “discovered” until 1654, when a brief description and a woodcut depicting what is almost certainly the common species Lycogala epidendrum was published. First thought to be fungi, myxomycetes were not universally recognized as completely distinct until well into the twentieth century. Biodiversity surveys for the group being carried out over several years are relatively recent, with what is apparently the first example being carried out in the 1930s. Beginning in the 1980s, a series of such surveys yielded large bodies of data on the occurrence and distribution of myxomycetes in terrestrial ecosystems. The most notable of these were the All Taxa Biodiversity Inventory (ATBI) project carried out in the Great Smoky Mountains National Park, the Planetary Biodiversity Inventory Project (PBI) carried out in localities throughout the world, and the Myxotropic project being carried out throughout the Neotropics. The datasets available from both past and ongoing surveys now allow global and biogeographical patterns of myxomycetes to be assessed for the first time.
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Background Latin America harbors some of the most biodiverse countries in the world, including Colombia. Despite the increasing use of cutting-edge technologies in genomics and bioinformatics in several biological science fields around the world, the region has fallen behind in the inclusion of these approaches in biodiversity studies. In this study, we used data mining methods to search in four main public databases of genetic sequences such as: NCBI Nucleotide and BioProject, Pathosystems Resource Integration Center, and Barcode of Life Data Systems databases. We aimed to determine how much of the Colombian biodiversity is contained in genetic data stored in these public databases and how much of this information has been generated by national institutions. Additionally, we compared this data for Colombia with other countries of high biodiversity in Latin America, such as Brazil, Argentina, Costa Rica, Mexico, and Peru. Results In Nucleotide, we found that 66.84% of total records for Colombia have been published at the national level, and this data represents less than 5% of the total number of species reported for the country. In BioProject, 70.46% of records were generated by national institutions and the great majority of them is represented by microorganisms. In BOLD Systems, 26% of records have been submitted by national institutions, representing 258 species for Colombia. This number of species reported for Colombia span approximately 0.46% of the total biodiversity reported for the country (56,343 species). Finally, in PATRIC database, 13.25% of the reported sequences were contributed by national institutions. Colombia has a better biodiversity representation in public databases in comparison to other Latin American countries, like Costa Rica and Peru. Mexico and Argentina have the highest representation of species at the national level, despite Brazil and Colombia, which actually hold the first and second places in biodiversity worldwide. Conclusions Our findings show gaps in the representation of the Colombian biodiversity at the molecular and genetic levels in widely consulted public databases. National funding for high-throughput molecular research, NGS technologies costs, and access to genetic resources are limiting factors. This fact should be taken as an opportunity to foster the development of collaborative projects between research groups in the Latin American region to study the vast biodiversity of these countries using ‘omics’ technologies.
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The most active research period on myxomycetes in Costa Rica has taken place in the last three decades. During this time, most of the collections have been carried out and most of the scientific articles have been produced. However, the lack of standard protocols and systematic planning across the country generated a need to conduct an analysis of myxomycete records to define future lines of work. A compilation, cleaning, standardisation and analysis of information associated with a database of more than 7800 records that comprised 242 species of myxomycetes reported in Costa Rica during the last 110 years, was carried out. An interpretation of data with a conservation approach that integrated elements of data-mining and geographical information systems was conducted. Results showed that myxomycetes has been comparatively well studied in Costa Rica in relation to other regional or tropical countries. However, survey effort has been unequal within the territory, leaving some interesting areas or substrates understudied. The absence of long-term goals to study this country and Mesoamerica has limited the potential that the analysed data can have within the context of conservation. This could be the next logical step in the study of this group of microorganisms in that country.
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An updated analysis of myxomycete diversity in Costa Rica is provided herein as a product of an extensive data mining-based study intended to normalize the information on myxomycetes from that country. Within the context of the Mesoamerican Biodiversity Hotspot, the 242 species of myxomycetes are reported herein demonstrated the potential of this area for diversity-based studies. For the construction of the updated species list, a thorough analysis that included examination of vouchers and a literature review has been carried out, and some species previously included in other works have been rejected due to inconsistencies or misidentification. The present contribution is essential to address the Wallacean shortfall within Mesoamerica and important for providing updated data on microorganisms in the context of regional biodiversity monitoring.
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Colombia's decades-long Civil conflict, which resulted in more than 8 million victims (1), has never been so close to an end. The recently signed peace agreement (2) between the government and The Revolutionary Armed Forces of Colombia (FARC) covers a number of key areas, including government commitment to invest in rural small-landowner economy, land restitution, facilitation of the participation of new political movements, an arms amnesty for some guerrilla soldiers, and a program for soldier reintegration into society. Although a public vote rejected the agreement by a slim margin (3), there is still hope: The FARC rebels have reaffirmed their commitment to a ceasefire (4) while the agreement is revised. The Colombian government should take this opportunity to consider environmental implications as they work toward a final deal. When a definitive agreement is reached, national and international companies that avoided Colombia during the conflict will likely begin to exploit Colombia's natural resources under a fully legal framework, meaning that new natural areas and their resources will be at risk. To minimize environmental degradation, rural development should incentivize proper agroforestry and ecotourism practices. Resources should also be allocated to strengthen communal land tenure of indigenous and Afro-Colombian communities, key stakeholders for the sustainable management of large parts of the country's ecosystems. To protect biological resources, their ecological, social, and economic value needs to be understood and promoted by both policymakers and society. A multi-disciplinary approach is urgently needed. The natural and social sciences academic communities should partner with the government, the business sector, and the community at large to develop sustainable strategies that ensure benefits will be distributed among disparate social and ethnic groups, and natural capital protected. Colombia is at a crossroads in its history. The Colombian people have an opportunity to implement not only paradigms of sustainable economies but also a peaceful and dynamic society. The resulting equitable sharing of wealth will allow future generations to benefit from Colombia's immense biological richness. References 1. The Victim's Unit Counter (2016); http://rni.unidadvictimas.gov.co/RUV [in Spanish]. 2. Presidency of the Republic of Colombia (http://es.presidencia.gov.co/sitios/busqueda/noticia/160902-Presidente-Santos-anuncia-que-la-pazse-firmara-el-26-de-septiembre-en-Cartagena/Noticia) [in Spanish]. 3. Colombian Electoral Bureau, Registraduría General de la Nación (http://plebiscito.registraduria.gov.co/99PL/DPLZZZZZZZZZZZZZZZZZ_L1.htm) [in Spanish]. 4. FARC, Comunicado de las FARC-EP luego de los resultados del plebiscito (www.pazfarc-ep.org/comunicadosestadomayorfarc/item/3567-comunicadode-las-farc-ep-luego-de-los-resultados-del-plebiscito.html) [in Spanish].
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Results obtained from the first survey for myxomycetes in the hyperarid areas of Peru are reported. Sampling over three consecutive years was carried out at 96 localities between 0 and 1500 m elevation. A total of 78 species from 23 genera in all 6 myxomycete orders were determined from 723 collections of myxomycetes. One new species, Didymium peruvianum, is described, 2 species new to the Neotropics, 4 new records for South America and 41 additional new species for Peru are reported, increasing the country catalogue by over 50%. Results show that arid areas are rich in myxomycetes, and that each area has a unique species assemblage. Endemic plants had a particular relevance as myxomycete substrates. The predominance of the order Physarales in arid areas is reinforced, and the ecological importance of coastal fogs (garúas) is evident from the results. Comments are included on interesting or rare collections, as are SEM micrographs of several species and statistical evaluation of the results.
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The results of a biodiversity survey of a xeric Mexican Biosphere Reserve are presented. This survey represents the first intensive study of cacti and succulent plants ever carried out for myxomycetes. The results include 104 species and one variety, identified from 1200 records from field and moist chamber culture collections. Two new species (Didymium tehuacanense and Perichaena stipitata), found on decayed remains of Succulent plants, are described. Eleven species (Comatricha reticulosporo, Cribraria lepida, Didymium clavodecus, D. eremophilum, D. orthonemata, D. sturgisii, D. subreticulosporum, Licea belmontiana, Macbrideola oblonga, M. synsporos and Perichaena quadrata) are new records for the Neotropics, and seven others taxa have not been recorded previously from Mexico. Taxonomic comments, data on distribution and SM, LM and SEM micrographs of selected species are included. An analysis of the relationships that exist between myxomycetes and the substrates on which they develop confirms the presence of a distinct assemblage of myxomycetes associated with specific plants from and environments. Hypotheses are proposed for the patterns of species distribution and the ecological requirements of this specialised myxobiota.
Chapter
Definitions of myxomycete terminology used in species descriptions are provided and include those relating to the morphology of fruiting bodies, occurrences in habitats, and biology associated with life cycle stages. These definitions include illustrations of fruiting bodies and structural parts along with publications and page numbers to guide the user to information sources. In addition, a review, discussion, and illustrations are provided that highlight life cycle stages represented by spores, myxamoebae, swarm cells, plasmodia, sclerotia, as well as fruiting body development and ploidy levels. Genetics, reproduction, and mating systems are discussed.
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An assemblage of myxomycetes associated with inflorescences of large Neotropical herbs, a microhabitat not previously known to support these organisms, is described and characterized ecologically from a number of study sites in Costa Rica, Ecuador, and Puerto Rico. Thirty-one different taxa were found among 652 specimens of myxomycetes recorded in the field or obtained from 358 moist chamber cultures prepared with decaying floral parts. A comparison with the results of 696 moist chamber cultures prepared with various other litter substrates showed that thirteen myxomycete taxa occurred more often on inflorescences. Six taxa had a strong preference for this microhabitat, and three of those seem to be new for the Neotropics. Correspondence analysis of the data set compiled for inflorescences indicated that the assemblage of myxomycetes was relatively consistent across all of the various study sites. The actual myxomycete substrates were the rapidly decaying floral parts enclosed by the massive, still living bracts. Richest in myxomycetes were species of Heliconia and Costus. Here, nectar residuals probably promoted a rapidly developing community of yeasts and bacteria. A high density of these organisms was indicated by the frequent occurrence of myxobacteria in the moist chamber cultures prepared with floral parts. Results from canonical correspondence analysis suggested that a substrate pH between 8 and 9 and the presence of massive, compact inflorescences on plants occurring at lower elevations in localities with moderate annual rainfall provide optimal conditions for inflorescence-inhabiting myxomycetes. An incidental dispersal of myxomycete spores by birds that pollinate the flowers or feed upon the fruits seems possible and may have accounted for the high degree of preference exhibited by some of the inflorescence-inhabiting myxomycetes, for which the term “floricolous” is proposed.
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