| Records |
| Author |
Chaves, C.L.; Blanc-Jolivet, C.; Sebbenn, A.M.; Mader, M.; Meyer-Sand, B.R.V.; Paredes-Villanueva, K.; Honorio Coronado, E.N.; Garcia-Davila, C.; Tysklind, N.; Troispoux, V.; Massot, M.; Degen, B. |
| Title |
Nuclear and chloroplastic SNP markers for genetic studies of timber origin for Hymenaea trees |
Type |
Journal Article |
| Year |
2019 |
Publication |
Conservation Genetics Resources |
Abbreviated Journal |
Conserv. Gen. Res. |
| Volume |
11 |
Issue |
3 |
Pages |
329-331 |
| Keywords |
DNA fingerprints; Geographical origin; MiSeq; RADSeq |
| Abstract |
We developed nuclear and chloroplastic single nucleotide polymorphism (SNP) and INDEL (insertion/deletion) markers using restriction associated DNA sequencing (RADSeq) and low coverage MiSeq genome sequencing to set up a genetic tracking method of the geographical origin of Hymenaea sp. From two initial sets of 358 and 32 loci used to genotype at least 94 individuals, a final set of 75 nSNPs, 50 cpSNPs and 6 INDELs identifying significant population structure was developed. © 2018, Springer Nature B.V. |
Address  |
Departamento de Fitotecnia, Faculdade de Engenharia de Ilha Solteira, Universidade Estadual Paulista, Ilha Solteira, SP, Brazil |
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| Publisher |
Springer Netherlands |
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18777252 (Issn) |
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no |
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EcoFoG @ webmaster @ |
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908 |
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| Author |
Roy, M.; Schimann, H.; Braga-Neto, R.; Da Silva, R.A.E.; Duque, J.; Frame, D.; Wartchow, F.; Neves, M.A. |
| Title |
Diversity and Distribution of Ectomycorrhizal Fungi from Amazonian Lowland White-sand Forests in Brazil and French Guiana |
Type |
Journal Article |
| Year |
2016 |
Publication |
Biotropica |
Abbreviated Journal |
Biotropica |
| Volume |
48 |
Issue |
1 |
Pages |
90-100 |
| Keywords |
campina; campinarana; Amanitaceae; Amanitaceae; Boletaceae; Boletaceae; Campina; Campinarana; Herbarium; Herbário; Russulaceae; Russulaceae |
| Abstract |
White-sand forests are thought to host many ectomycorrhizal fungi, as demonstrated by the numerous fruiting body collections made by Rolf Singer in the lower Rio Negro in the late 1970s. Despite recognition of the importance of ectomycorrhizal fungi in white-sand forests, there has not yet been a systematic examination of diversity and taxonomic composition across white-sand forests, or more widely across lowland Amazonian forests. In an effort to broaden our view of ectomycorrhizal fungal diversity and distribution on white-sand forests, we collected ectomycorrhizal fruiting bodies in 10 plots of white-sand forests in Brazil and French Guiana between 2012 and 2014. We collected 221 specimens and 62 morphospecies, from the 10 plots, confirming that all studied white-sand forests host ectomycorrhizal fungi. Additionally, we searched for taxa associated with white sands among specimens deposited in Brazilian herbaria. We report 1006 unique ectomycorrhizal specimen records in 18 Brazilian herbaria, of which 137 specimens and 64 species are reported from white-sand forests, mainly in the state of Amazonas, Brazil. Russulaceae and Amanitaceae were frequent in all habitats, and Cortinarius were more frequent on white sands. Our results highlight the high diversity and heterogeneity of ectomycorrhizal communities on white-sand forests, and the wide distribution of ectomycorrhizal fungi throughout Brazil, irrespective of soil type. © 2016 The Association for Tropical Biology and Conservation. |
| Address |
Departamento de Sistemática e Ecologia, Universidade Federal da Paraíba, João Pessoa, PB, Brazil |
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Cited By :2; Export Date: 12 February 2016 |
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no |
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EcoFoG @ webmaster @ |
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658 |
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| Author |
Roy, M.; Vasco-Palacios, A.; Geml, J.; Buyck, B.; Delgat, L.; Giachini, A.; Grebenc, T.; Harrower, E.; Kuhar, F.; Magnago, A.; Rinaldi, A.C.; Schimann, H.; Selosse, M.-A.; Sulzbacher, M.A.; Wartchow, F.; Neves, M.-A. |
| Title |
The (re)discovery of ectomycorrhizal symbioses in Neotropical ecosystems sketched in Florianópolis |
Type |
Journal Article |
| Year |
2017 |
Publication |
New Phytologist |
Abbreviated Journal |
New Phytologist |
| Volume |
214 |
Issue |
3 |
Pages |
920-923 |
| Keywords |
barcoding; biodiversity; ectomycorrhizal fungi; ectomycorrhizal roots; ectomycorrhizal symbioses; fruitbodies; Neotropical ecosystems |
| Abstract |
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| Address |
Departamento de Sistemática e Ecologia/CCEN, Laboratório de Morfo-Taxonomia Fúngica, Universidade Federal da Paraíba, João Pessoa, Paraíba, Brazil |
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| Notes |
Cited By :1; Export Date: 23 April 2017 |
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no |
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EcoFoG @ webmaster @ |
Serial |
749 |
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| Author |
Zinger, L.; Donald, J.; Brosse, S.; Gonzalez, M.A.; Iribar, A.; Leroy, C.; Murienne, J.; Orivel, J.; Schimann, H.; Taberlet, P.; Lopes, C.M. |
| Title |
Advances and prospects of environmental DNA in neotropical rainforests |
Type |
Journal Article |
| Year |
2020 |
Publication |
Advances in Ecological Research |
Abbreviated Journal |
Adv. Ecol. Res. |
| Volume |
62 |
Issue |
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Pages |
331-373 |
| Keywords |
Biomonitoring; Conservation biology; DNA metabarcoding; eDNA; Environmental genomics; Neotropics; Rainforests |
| Abstract |
The rainforests of the Neotropics shelter a vast diversity of plant, animal and microscopic species that provide critical ecosystem goods and services for both local and worldwide populations. These environments face a major crisis due to increased deforestation, pollution, and climate change, emphasizing the need for more effective conservation efforts. The adequate monitoring of these ecosystems has proven a complex and time consuming endeavour, which depends on ever dwindling taxonomic expertise. To date, many species remain undiscovered, let alone described, with otherwise limited information regarding known species population distributions and densities. Overcoming these knowledge shortfalls and practical limitations is becoming increasingly possible through techniques based on environmental DNA (eDNA), i.e., DNA that can be obtained from environmental samples (e.g. tissues, soil, sediment, water, etc.). When coupled with high-throughput sequencing, these techniques now enable realistic, cost-effective, and standardisable biodiversity assessments. This opens up enormous opportunities for advancing our understanding of complex and species-rich tropical communities, but also in facilitating large-scale biomonitoring programs in the neotropics. In this review, we provide a brief introduction to eDNA methods, and an overview of their current and potential uses in both terrestrial and aquatic ecosystems of neotropical rainforests. We also discuss the limits and challenges of these methods for our understanding and monitoring of biodiversity, as well as future research and applied perspectives of these techniques in neotropical rainforests, and beyond. © 2020 Elsevier Ltd |
| Address |
Departamento de Zoologia, Instituto de Biociências, Universidade Estadual Paulista (UNESP), Rio Claro, SP, Brazil |
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| Publisher |
Academic Press Inc. |
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Editor |
Dumbrell A.J.; Turner E.C.; Fayle T.M. |
| Language |
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Summary Language |
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Original Title |
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| Series Editor |
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Series Title |
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Abbreviated Series Title |
Advances in Ecological Research |
| Series Volume |
62 |
Series Issue |
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Edition |
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| ISSN |
00652504 (Issn); 9780128211342 (Isbn) |
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no |
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EcoFoG @ webmaster @ |
Serial |
995 |
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| Author |
Farjalla, V.F.; González, A.L.; Céréghino, R.; Dezerald, O.; Marino, N.A.C.; Piccoli, G.C.O.; Richardson, B.A.; Richardson, M.J.; Romero, G.Q.; Srivastava, D.S. |
| Title |
Terrestrial support of aquatic food webs depends on light inputs: A geographically-replicated test using tank bromeliads |
Type |
Journal Article |
| Year |
2016 |
Publication |
Ecology |
Abbreviated Journal |
Ecology |
| Volume |
97 |
Issue |
8 |
Pages |
2147-2156 |
| Keywords |
Allochthonous carbon; Allochthony; Aquatic food webs; Autochthonous carbon; Autochthony; Natural microcosms; Stable isotopic analysis; Tank bromeliads; Tropics |
| Abstract |
Food webs of freshwater ecosystems can be subsidized by allochthonous resources. However, it is still unknown which environmental factors regulate the relative consumption of allochthonous resources in relation to autochthonous resources. Here, we evaluated the importance of allochthonous resources (litterfall) for the aquatic food webs in Neotropical tank bromeliads, a naturally replicated aquatic microcosm. Aquatic invertebrates were sampled in more than 100 bromeliads within either open or shaded habitats and within five geographically distinct sites located in four different countries. Using stable isotope analyses, we determined that allochthonous sources comprised 74% (±17%) of the food resources of aquatic invertebrates. However, the allochthonous contribution to aquatic invertebrates strongly decreased from shaded to open habitats, as light incidence increased in the tanks. The density of detritus in the tanks had no impact on the importance of allochthonous sources to aquatic invertebrates. This overall pattern held for all invertebrates, irrespective of the taxonomic or functional group to which they belonged. We concluded that, over a broad geographic range, aquatic food webs of tank bromeliads are mostly allochthonous-based, but the relative importance of allochthonous subsidies decreases when light incidence favors autochthonous primary production. These results suggest that, for other freshwater systems, some of the between-study variation in the importance of allochthonous subsidies may similarly be driven by the relative availability of autochthonous resources. © 2016 by the Ecological Society of America. |
| Address |
Department of Animal Biology, Institute of Biology, University of Campinas (UNICAMP), PO Box 6109, Campinas-SP, Brazil |
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| Notes |
Export Date: 1 September 2016 |
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no |
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EcoFoG @ webmaster @ |
Serial |
687 |
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| Author |
Gibson, J.C.; Larabee, F.J.; Touchard, A.; Orivel, J.; Suarez, A.V. |
| Title |
Mandible strike kinematics of the trap-jaw ant genus Anochetus Mayr (Hymenoptera: Formicidae) |
Type |
Journal Article |
| Year |
2018 |
Publication |
Journal of Zoology |
Abbreviated Journal |
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| Volume |
306 |
Issue |
2 |
Pages |
119-128 |
| Keywords |
catapult mechanism; comparative biomechanics; Formicidae; functional morphology; kinematics; mandible strike; power amplification |
| Abstract |
High-speed power-amplification mechanisms are common throughout the animal kingdom. In ants, power-amplified trap-jaw mandibles have evolved independently at least four times, including once in the subfamily Ponerinae which contains the sister genera Odontomachus and Anochetus. In Odontomachus, mandible strikes have been relatively well described and can occur in <0.15 ms and reach speeds of over 60 m s−1. In contrast, the kinematics of mandible strikes have not been examined in Anochetus, whose species are smaller and morphologically distinct from Odontomachus. In this study, we describe the mandible strike kinematics of four species of Anochetus representative of the morphological, phylogenetic, and size diversity present within the genus. We also compare their strikes to two representative species of Odontomachus. We found that two species, Anochetus targionii and Anochetus paripungens, have mandible strikes that overall closely resemble those found in Odontomachus, reaching a mean maximum rotational velocity and acceleration of around 3.7 × 104 rad s−1 and 8.5 × 108 rad s−2, respectively. This performance is consistent with predictions based on body size scaling relationships described for Odontomachus. In contrast, Anochetus horridus and Anochetus emarginatus have slower strikes relative to the other species of Anochetus and Odontomachus, reaching mean maximum rotational velocity and acceleration of around 1.3 × 104 rad s−1 and 2 × 108 rad s−2, respectively. This variation in strike performance among species of Anochetus likely reflects differences in evolutionary history, physiology, and natural history among species. © 2018 The Zoological Society of London |
| Address |
Department of Animal Biology, University of Illinois at Urbana-Champaign, Urbana, IL, United States |
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| Notes |
Export Date: 15 October 2018 |
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no |
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EcoFoG @ webmaster @ |
Serial |
826 |
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| Author |
Menzel, F.; Orivel, J.; Kaltenpoth, M.; Schmitt, T. |
| Title |
What makes you a potential partner? Insights from convergently evolved ant-ant symbioses |
Type |
Journal Article |
| Year |
2014 |
Publication |
Chemoecology |
Abbreviated Journal |
Chemoecology |
| Volume |
24 |
Issue |
3 |
Pages |
105-119 |
| Keywords |
Aggression; Coevolution; Cuticular hydrocarbons; Formicidae; Interspecific association; Parabiosis; Recognition cues |
| Abstract |
Mutualistic, commensalistic or parasitic interactions are unevenly distributed across the animals and plants: in certain taxa, such interspecific associations evolved more often than in others. Within the ants, associations between species of the genera Camponotus and Crematogaster evolved repeatedly and include trail-sharing associations, where two species share foraging trails, and parabioses, where two species share a nest without aggression. Camponotus and Crematogaster may possess life-history traits that favour the evolution of associations. To identify which traits are affected by the association, we investigated a neotropical parabiosis of Ca. femoratus and Cr. levior and compared it to a paleotropical parabiosis and a trail-sharing association. The two neotropical species showed altered cuticular hydrocarbon profiles compared to non-parabiotic species accompanied by low levels of interspecific aggression. Both species occurred in two chemically distinct types. Camponotus followed artificial trails of Crematogaster pheromones, but not vice versa. The above traits were also found in the paleotropical parabiosis, and the trail-following results match those of the trail-sharing association. In contrast to paleotropical parabioses, however, Camponotus was dominant, had a high foraging activity and often fought against Crematogaster over food resources. We suggest three potential preadaptations for parabiosis. First, Crematogaster uses molecules as trail pheromones, which can be perceived by Camponotus, too. Second, nests of Camponotus are an important benefit to Crematogaster and may create a selection pressure for the latter to tolerate Camponotus. Third, there are parallel, but unusual, shifts in cuticular hydrocarbon profiles between neotropics and paleotropics, and between Camponotus and Crematogaster. © 2014 Springer Basel. |
| Address |
Department of Animal Ecology and Tropical Biology Biocentre, University of Würzburg, Am Hubland, 97074 Würzburg, Germany |
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Birkhauser Verlag AG |
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09377409 (Issn) |
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Export Date: 10 June 2014; Coden: Chmoe; Correspondence Address: Menzel, F.; Department of Evolutionary Biology, Institute of Zoology, University of Mainz, Johannes-von-Müller-Weg 6, 55099 Mainz, Germany; email: menzelf@uni-mainz.de |
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no |
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EcoFoG @ webmaster @ |
Serial |
547 |
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Jaouen, G.; Sagne, A.; Buyck, B.; Decock, C.; Louisanna, E.; Manzi, S.; Baraloto, C.; Roy, M.; Schimann, H. |
| Title |
Fungi of French Guiana gathered in a taxonomic, environmental and molecular dataset |
Type |
Journal Article |
| Year |
2019 |
Publication |
Scientific data |
Abbreviated Journal |
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| Volume |
6 |
Issue |
206 |
Pages |
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| Abstract |
In Amazonia, the knowledge about Fungi remains patchy and biased towards accessible sites. This is particularly the case in French Guiana where the existing collections have been confined to few coastal localities. Here, we aimed at filling the gaps of knowledge in undersampled areas of this region, particularly focusing on the Basidiomycota. From 2011, we comprehensively collected fruiting-bodies with a stratified and reproducible sampling scheme in 126 plots. Sites of sampling reflected the main forest habitats of French Guiana in terms of soil fertility and topography. The dataset of 5219 specimens gathers 245 genera belonging to 75 families, 642 specimens are barcoded. The dataset is not a checklist as only 27% of the specimens are identified at the species level but 96% are identified at the genus level. We found an extraordinary diversity distributed across forest habitats. The dataset is an unprecedented and original collection of Basidiomycota for the region, making specimens available for taxonomists and ecologists. The database is publicly available in the GBIF repository ( https://doi.org/10.15468/ymvlrp ). |
| Address |
Department of Biological Science, Florida International University, FL, Miami, 33199, United States |
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| Notes |
Export Date: 28 October 2019 |
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no |
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EcoFoG @ webmaster @ |
Serial |
891 |
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| Author |
Fine, P.V.A.; Baraloto, C. |
| Title |
Habitat Endemism in White-sand Forests: Insights into the Mechanisms of Lineage Diversification and Community Assembly of the Neotropical Flora |
Type |
Journal Article |
| Year |
2016 |
Publication |
Biotropica |
Abbreviated Journal |
Biotropica |
| Volume |
48 |
Issue |
1 |
Pages |
24-33 |
| Keywords |
Amazon; Endemic; Functional traits; Habitat specialization; Niche conservatism; Speciation |
| Abstract |
White-sand forests represent natural laboratories of evolution over their long history throughout Amazonia and the Guiana Shield and pose significant physiological challenges to the plants and animals they host. The study of diversification in plant lineages comprising species endemic to white-sand forest can therefore give insights into processes of evolution and community assembly in tropical forests. In this article, we synthesize recent studies of white-sand forests to integrate patterns of plant species distribution with processes of lineage diversification and community assembly in the white-sand flora. We contrast lineages that have radiated uniquely in these habitats (e.g., Pagamea, Rubiaceae), with cosmopolitan lineages comprising specialists to white-sand forests and other habitats that may have arisen via ecological speciation across habitat gradients (e.g., Protium, Burseraceae). In both cases, similar suites of functional traits have evolved, including investment in dense, long-lived tissues that are well-defended structurally and chemically. White-sand endemics, therefore, play an important role in biodiversity conservation because they represent unique combinations of functional and phylogenetic diversity. Furthermore, white-sand endemics may respond differently than other tropical forest plant species to contemporary global changes because they comprise resilient functional types that may better withstand increased drought, temperature, and invasions of exotic pests in these regions. © 2016 The Association for Tropical Biology and Conservation. |
| Address |
Department of Biological Sciences and International Center for Tropical Botany, Florida International University, Miami, FL, United States |
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Cited By :3; Export Date: 12 February 2016 |
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no |
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EcoFoG @ webmaster @ |
Serial |
659 |
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| Author |
Henkel, T.W.; Wilson, A.W.; Aime, M.C.; Dierks, J.; Uehling, J.K.; Roy, M.; Schimann, H.; Wartchow, F.; Mueller, G.M. |
| Title |
Cantharellaceae of Guyana II: New species of Craterellus, new South American distribution records for Cantharellus guyanensis and Craterellus excelsus, and a key to the Neotropical taxa |
Type |
Journal Article |
| Year |
2014 |
Publication |
Mycologia |
Abbreviated Journal |
Mycologia |
| Volume |
106 |
Issue |
2 |
Pages |
307-324 |
| Keywords |
Cantharellales; Coccoloba; Dicymbe; Ectomycorrhizae; Guiana shield; Tropical fungi |
| Abstract |
Craterellus olivaceoluteus sp. nov. and Craterellus cinereofimbriatus sp. nov. are described as new to science. These fungi were collected from Guyana in association with ectomycorrhizal host trees in the genera Dicymbe (Fabaceae subfam. Caesalpinioideae) and Pakaraimaea (Dipterocarpaceae). Cantharellus guyanensis Mont., originally described from French Guiana, is redescribed from recent collections from Guyana, with additional range extensions for the species provided based on material examined from French Guiana, Venezuela, and north central, northeastern and southern Brazil, circumscribing nearly the entire Guiana Shield region and beyond. A new distribution record from French Guiana is provided for Craterellus excelsus T.W. Henkel & Aime. Macromorphological, micromorphological and habitat data are provided for the new species and C. guyanensis as well as DNA sequence data from the nuclear ribosomal regions of the internal transcribed spacer (ITS) and 28S large subunit (LSU); additional sequence data is provided for C. guyanensis and C. excelsus specimens collected outside Guyana. The relationships of these taxa within the Cantharellaceae were evaluated with phylogenetic analyses of ITS and LSU sequence data. This work brings the total number of Cantharellaceae species known from Guyana to eight. A key to the Cantharellus and Craterellus species known from the lowland Neotropics and extralimital montane Central and South America is provided. © 2014 by The Mycological Society of America. |
| Address |
Department of Biological Sciences, Boise State University, Boise, ID, 83725, United States |
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| Publisher |
Allen Press Inc. |
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15572536 (Issn) |
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Export Date: 10 June 2014; Coden: Mycoa; Correspondence Address: Henkel, T.W.; Department of Biological Sciences, Humboldt State University, Arcata, CA 95521, United States; email: twh5@humboldt.edu; Funding Details: DEB-0732968, NSF, National Science Foundation |
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no |
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EcoFoG @ webmaster @ |
Serial |
546 |
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