Mystery Migration

English

Whale Shark Logs
Longest-Recorded Migration

A whale shark named Anne swam all the way across the Pacific from Coiba National Park in Panama to the Marianas Trench.

Story location

Coiba, Panama

Marine Biology Fisheries and Marine Conservation Animal Behavior Sustaining a Biodiverse Planet Coibita Island blue Hector M. Guzman
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Mystery
Migration

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Declining reefs

English

What were Caribbean coral
reefs like before humans?

Fossil reefs from around the Caribbean show how biologically rich these ecosystems once were — and provide goalposts for conservationists hoping to restore them.

Story location

Panama and the Dominican Republic

Paleontology and Paleobiology Biodiversity Marine Biology Life in Deep Time Bocas del Toro The caribean's declining reefs blue Aaron O'Dea
Alternative Title: 

Declining
reefs

The caribean's declining reefs

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Kristin Saltonstall

English
Molecular Ecology Conservation Genetics

Invasive grasses pose a problem to the biological diversity of degraded tropical forests worldwide. They may increase the frequency and intensity of fire, inhibit tree regeneration, and outcompete native plants.

Kristin Saltonstall
STRI Coral Reef

My research focuses on the distribution of biodiversity across multiple spatial scales – globally, regionally, and locally. We use molecular tools to identify species, genetic lineages, and communities of organisms and describe how they are distributed across landscapes. Our genetic work on invasive species incorporates field and experimental studies to address fundamental issues related to invasion, impact, and restoration. Another focus is on soil and plant microbiomes. Despite their importance for global biogeochemical cycling, these microbial communities remain poorly described and our understanding of how these communities are linked to functional capabilities is limited. Our ongoing projects focus on describing soil communities across land use categories (such as land managed for agriculture, young secondary forest, and older forests) and how the structure of plant microbiomes changes across tissues and different management strategies.

How does genetic diversity influence biological invasions?

Many genetic traits make it possible for non-native plants to invade new environments. Knowledge of where invasive genotypes originate, how they are distributed, and how genetic diversity helps or hinders invasive species will lead to better understanding and management of biological invasions.

How do soil microbial communities influence the recovery of degraded tropical landscapes?

Soil microbes play critically important roles in ecosystem processes and the maintenance of forest diversity. Ongoing projects focus on variability in community structure of bacteria, archaea, and fungi across space and habitats using metagenomic and rRNA surveys. We work in natural forests, plantations, and agricultural landscapes to assess how land use change influences soil microbial communities and how these communities influence forest successional processes.

How can DNA inform biodiversity conservation?

Analysis of DNA provides genetic, geographic and sometimes historical answers to biological questions. We work with a variety of tissues and environmental samples to tell complex stories about the distribution of species, their spread, and evolutionary histories. Using a variety of genetic and genomic techniques we explore a wide range of topics, such as genetic diversity in endangered species, the geographic origins of invaders, the influence of climate on genetic diversity, and the evolution of disease spreading parasites.

2002 Ph.D. Yale University, Ecology and Evolutionary Biology

1996 M.F.S. Yale School of Forestry and Environmental Studies

1992 B.A. Wellesley College, Biological Sciences

Saltonstall, K., A.M. Lambert, and N. Rice.  2016.  What Happens in Vegas, Better Stay in Vegas: Phragmites australis Hybrids in the Las Vegas Wash.  Biological Invasions 2463-2474 DOI 10.1007/s10530-016-1167-5

Aiello, A, K. Saltonstall, and V. Young.  2016.  Brachyplatys vahlii, an introduced bug from Asia: first report in the Western Hemisphere (Hemiptera: Plataspidae: Brachyplatidinae).  BioInvasions Records 5: 7-12.  DOI: http://dx.doi.org/10.3391/bir.2016.5.1.02

Sellers,A,J. K. Saltonstall, and T.M. Davidson.  2015. The introduced alga Kappaphycus alvarezii in abandoned cultivation sites in Bocas del Toro, Panama.  Bioinvasions Records 4(1): 1-7. doi: http://dx.doi.org/10.3391/bir.2015.4.1.01

Kelehear,, C., K. Saltonstall, and M.E. Torchin. 2014. An introduced pentastomid parasite (Raillietiella frenata) infects native cane toads (Rhinella marina) in Panama.  Parasitology DOI: http://dx.doi.org/10.1017/S0031182014001759

Bonnett, G.D., J.N.S. Kushner, and K. Saltonstall.  2014.  The reproductive biology of Saccharum spontaneum L.: implications for management of this invasive weed in Panama.  NeoBiota 20: 61–79. doi: 10.3897/neobiota.20.6163

Saltonstall, K. H.E. Castilloand B. Blossey.  2014.  Confirmed field hybridization of native and introduced Phragmites australis (Poaceae) in North America. American Journal of Botany 101(1): 1–5.  doi:10.3732/ajb.1300298

Saltonstall, K. and Bonnett, G.D.  2012.  Fire promotes growth and reproduction of Saccharum spontaneum (L.) in Panama.  Biological Invasions 14: 2479-2488.  doi: 10.007/s10530-012-0245-6

Saltonstall, K., P.M. Peterson, and R. Soreng.  2004.  Recognition of Phragmites australis subsp. americanus (Poaceae: Arundinoideae) in North America: evidence from morphological and genetic analyses.  Sida 21(2): 683-692.

Saltonstall, K.  2002. Cryptic invasion of a non-native genotype of the common reed, Phragmites australis, into North America.  Proceedings of the National Academy of Sciences USA 99(4): 2445-2449.  www.pnas.org_cgi_doi_10.1073_pnas.032477999

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Noris Salazar

English
Plant Systematics

Of more than 18,000 bryophyte species thought to exist in the world, we’ve counted about 751 moss species, 457 liverwort species and 13 hornwort species in Panama, living in poorly characterized communities.

Noris Salazar Allen
STRI Coral Reef

Identification of volatile compounds from three species of Cyathodium (Marchantiophyta: Cyathodiaceae) and Leiosporoceros dussii (Anthocerotophyta: Leiosporocerotaceae) form Panama and C. foetidissimum from Costa Rica. N. Salazar Allen, A.I. Saldaña, N. Gómez, C. Chung C. & M.P. Gupta. Bol. Soc. Argent. Bot. 52(2): 357-370. 2017.

The enigmatic hornworts of the Cape Horn miniature forests, 2012

My lab works with bryophytes, which are a highly diverse group of non-vascular plants that includes mosses, hornworts and liverworts. We study the distribution of bryophytes in various regions throughout Panama, the type of habitat where they grow and compare their distribution and community composition in response to environmental and anthropogenic factors. We also study their morphology, genetics and chemistry to better understand their evolution, phylogenetic relationships, and the potential usefulness of their secondary metabolites in defending them against pathogens and in fighting disease or biologically controlling pests.

How does bryophyte evolution contribute to abundant tropical biodiversity?

Bryophytes (liverworts, mosses and hornworts) are the extant relatives of the earliest land colonizers and they hold clues of the eco-physiological and chemical adaptations to early life on land. In spite of recent advances, there is still a lack of information on many aspects of the life cycle, ecology and evolution of tropical bryophytes. The basic information on biodiversity and habitat dynamics in Neotropical species is still poorly known, despite the fact that the Neotropics is the richest hotspot of bryophyte diversity. Only through a collaborative and multidisciplinary approach we can address the daunting mysteries of bryophyte evolution and diversification. It remains a fascinating and challenging puzzle.

How does tropical forest composition and structure affect the composition of bryophyte communities? And what are the dynamics of bryophyte communities in different tropical forests?

The structure of the bark of some trees and the structure of the forest – whether it is open, closed, seasonal or wet all the time – are important in determining what bryophytes grow where, and why. Islands and tree species composition can also greatly influence bryophyte communities. This is due to the niches and microclimates that make the difference in what kind of bryophyte community can be developed.

Climate change, pollutants and forest disruption also play a big role in how bryophyte communities are shaped and structured. Some bryophytes prefer sun; others thrive in shade. As a result, a disturbed forest with light gaps may have a very different bryophyte community than a similar undisturbed forest. Some bryophytes have very specific niches and once the niches are gone, those particular bryophytes are gone.

What is the functional significance of endosymbiont associations in thalloid liverworts?

Symbiosis has been crucial in the origin of important evolutionary novelties that determined the successful conquest of land by early land plants.  Bryophytes like other plants have developed epiphytic and endophytic associations particularly with fungi and cyanobacteria. Both leafy and thalloid liverworts frequently develop endosymbiotic association with fungi and, hornworts and few liverworts (e.g., Blasia) with nitrogen-fixing cyanobacteria. Our studies focus on the relationships of fungal endosymbionts in two thalloid marchantialean liverworts, Dumortiera and Cyathodium. We are interested in the molecular diversity of fungi and their role in the successful adaptation of these plants to their environments. The information obtained could be useful for further studies on tropical microbiomes particularly in the Neotropics.

Do tropical liverworts produce compounds with biomedical or agricultural importance?

Chemically, liverworts have been one of the most studied bryophyte groups. Most liverworts have oil bodies, unique membrane bound organelles that synthesize many secondary metabolites (e.g., terpenoids and many aromatic compounds). These compounds have been useful as chemosystematic indicators and are also known to be bioactive against fungi, bacteria, some viruses, various food microorganisms, certain strains of cancer cells and some nematodes.

B.A., Trinity College, 1969.

M.A., State University of New York, 1973.

Ph.D., University of Alberta, 1986.

Identification of volatile compounds from three species of Cyathodium (Marchantiophyta: Cyathodiaceae) and Leiosporoceros dussii (Anthocerotophyta: Leiosporocerotaceae) form Panama and C. foetidissimum from Costa Rica. N. Salazar Allen, A.I. Saldaña, N. Gómez, C. Chung C. & M.P. Gupta. Bol. Soc. Argent. Bot. 52(2): 357-370. 2017.

Morfología y distribución de Dolotortula mniifolia y Trachyphyllum dusenii (Bryophyta) en Panamá. J.Gudiño L. & N. Salazar Allen. Bol. Soc. Argent. Bot. 52(2): 331-340. 2017.

Nuevas adiciones de especies de hepáticas (Marchantiophyta) para la flora de Panamá II. G. Dauphin, N. Salazar Allen, J.A. Gudiño, A. Sierra & D. Reyes. Brenesia 83-84: 16-21. 2015.

Forrest, L. L., Salazar Allen, N., Gudiño, J. A., Korpelainen, H., & Long, D. G. 2011. Molecular and morphological evidence for distinct species in Dumortiera (Dumortieraceae). The Bryologist 114(1): 102-115.

Salazar Allen, N., & Tan, B. C. 2010. Octoblepharum arthrocormoides (Calymperaceae) in N. Salazar Allen & B.C. Tan, sp. nov., a new species from Tropical Asia. Botany, 88(4), 439-442.

Bischler-Causse. H., Gradstein, S. R., Jovet-Ast, S., Long, D. G., & Salazar Allen, N. 2005. Marchantiidae. Flora Neotropica, 131-141. 

Salazar Allen, N., Lépiz, E., De Gracia, J.E. 2004. Cyathodium foetidissimum (Marchantiales) an Asiatic species new to Tropical America. The Bryologist 107: 41-46. 2004.

Gradstein, S. R., Churchill, S. P., & Salazar Allen, N. 2001. Guide to the Bryophytes of Tropical America. Memoirs of the New York Botanical Garden, 86, 1-577.

Korpelainen, H., Salazar Allen, N. 1999. Genetic variation in three species of epiphytic Octoblepharum(Leucobryaceae). Nova Hedwigia 68(3-4): 281-290.

Salazar Allen, N. 1993. A revision of the pantropical moss genus Leucophanes Brid. Bryophytorum Bibliotheca 46: 1-281. J. Cramer. Berlin.

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D. Ross Robertson

English
Biogeography Taxonomy

Much of what is supposed to be mimicry among tropical reef fishes could be a figment of overly enthusiastic imaginations.

D. Ross Robertson
STRI Coral Reef

Since I joined STRI’s scientific staff in 1975, I have conducted field research on a broad range of topics relating to the reproductive biology, demography, population biology, behavior, community ecology, evolution and biogeography of tropical reef fishes, with an emphasis on those species that live in the Neotropical seas on both sides of the Americas.

Biogeography of Neotropical marine fish faunas

Photographs and data for shorefishes on both sides of the Central American isthmus have led to the creation of comprehensive digital field guides and advanced understanding of fish species distribution. The research included the first quantitative analyses of the geographic limits and large-scale subdivisions of the distributions of the shorefishes of the two regions, and assessed how those patterns relate to environmental variation. This has provided a new appreciation of the regions’ biogeography, particularly in the Caribbean, where it revealed previously unsuspected patterns. We have also used that information to predict the actual size of the fauna of the tropical eastern Pacific and are working on a similar prediction for the Greater Caribbean. While the latter region has one of the most well studied shorefish faunas in the world, recent advances in genetic analyses have forced the realization that many presumed widespread species are in fact complexes of multiple, usually allopatric, species and that the biodiversity of this region is much higher than previously thought.

Deep reef fishes of the Caribbean

Due to their accessibility to scuba diving scientists, most of what we know about the Caribbean area reef-fish fauna relates to shallow water species. However, a substantial part of that fauna comprises deep-reef fishes that live well below the limits of scientific divers. While modern rebreather diving allows access to greater depths, it cannot extend to the lower depth limits of deeper living species.

Submarines provide access to the full range of fish species depths, and, most importantly, allow collecting of specimens. I am a participant in DROP (Deep Reef Observation Program), a joint effort by the Smithsonian’s Natural History Museum and STRI to study deep reef fishes using a manned submersible based at Curaçao.

This represents the first submarine-based collecting of deep-reef fishes, and of information on their depth distributions, in the southern Caribbean. It also represents a resumption of U.S. efforts to document tropical deep reef fish faunas along and near its Atlantic shores, a program that terminated decades ago. Our submarine-based collecting at Curaçao has shown how little we know: in an area of only several hectares of reef adjacent to the submarine base, one third of the deep reef fishes we have collected are new to science, and we have encountered new species at every new site around the shores of that small island that we have visited with the submersible. These discoveries provide the impetus for expanding the activities of this submarine to other parts of the Greater Caribbean.

Invasive marine fishes

Only a small handful of exotic marine fishes native to areas outside the Atlantic and eastern Pacific are known to have successfully invaded the Neotropics. My current research includes study of a new invasion by one such Indo-Pacific species, which was discovered in the southwest Gulf of Mexico in 2013. We are working to determine the site of origin of this species, the mode of its introduction, and the full extent of its current geographic range in the Gulf of Mexico. We are also working on estimating its success relative to its native area, the extent of any ecological impact on native reef fishes in the Caribbean area, and the likelihood of its further spread.

The Cobia, a large predatory fish that can be two meters long and weigh up to 78 kilograms, was recently released into the Eastern Pacific through the escape of many thousands of juveniles from a sea cage aquaculture facility in Ecuador. This entirely predictable event occurred a few months after the facility began operation. Cobia does not naturally occur in the Eastern Pacific or across the remaining eastern three quarters — or 13,000 km — of the Pacific. Some of those escaped juveniles travelled at least 1,000 km to Panama in less than three months after their release, indicating a potential for this highly migratory species to spread rapidly. Fish biologists at all Pacific American countries between Peru and the United States and at potential invasion sites in the central Pacific (the Marquesas and Hawaiian Islands) have been alerted to record data about any Cobia captures. This information will allow documentation of the rate and extent of its spread, and estimation of its success in establishing a resident population in the Eastern Pacific. It is not yet possible to determine if such a population will become established and what impact it will have if that occurs.

Mimicry in tropical reef fishes

Describing new cases of supposed mimicry among tropical reef fishes is a popular pastime among reef fish biologists. However, examples involving precise similarity and multifaceted interactions between a model and a true mimic are relatively rare among such fishes. In many (perhaps most) cases, pairs of species probably independently evolved shared similarities in their appearance. These similarities may have led to the development of behavioral associations between such pairs of species through one learning that there are rewards to be gained from doing so. Ongoing research on this topic includes examination of interactions between models and their supposed mimics, and of geographic variation in degrees of resemblance and associations among such pairs.

Feeding biology of parrotfishes

Parrotfishes are common and abundant members of tropical reef fish faunas. The prevailing wisdom concerning their feeding biology is that they are herbivores that consume benthic macroalgae, and, in doing so, help the establishment and growth of living corals. Recent research pioneered by my collaborators in Australia indicates that for some parrotfish species, this view is erroneous and that they actually consume and digest microorganisms that are either scraped from the surfaces of rocky reef substrata or are imbedded in and excavated from below those surfaces. We plan to test this revisionary idea on a complex of species found on Eastern Pacific reefs, which include not only scraping and excavating species, but also a common hybrid between scraper and excavator species. That test would include the first genetic assessment of what these fish are actually consuming and the first stable-isotope determination of what ingested species they are actually digesting.

Diffusion of information through electronic applications on Neotropical shorefish faunas

A long-standing interest in identification guides for tropical reef fishes led me to begin development of a guide book on Tropical Eastern Pacific shorefishes in 1990. Electronic media allow not only the presentation of large numbers of images and other graphical material very economically but also the inclusion and analyses of quantitative data on fish faunas. Shortly after that guide book was released, tools for adaptation of this material to an electronic format became available, which led to the production of a bilingual CD version of the guide, followed by website adaptation and expansion of that guide. This in turn was followed by an equivalent website for the shorefish fauna of the Greater Caribbean, the sister biogeographic region to the Tropical Eastern Pacific on the other side of the Central American isthmus, and most recently, to iOS mobile versions of the websites for both those faunas. The mobile apps are currently being redeveloped to provide both iOS and Android versions. With the completion of these the material in the websites will become available across all major platform types currently in use. Between them, these two app families, which are unique for tropical marine fishes, cover almost 3,000 species, or about 20% of all named tropical shorefishes.

Besides the updating of information in these to app-families to incorporate new taxonomic information and new data on the ranges and ecology of member fishes, ongoing work on these app families is aimed at two aspects: (1) The incorporation of an Image Identification API (one that has been trained using images from these websites), a small, independent program imbedded within the website that will allow users to identify fish in images taken in each region that are presented to the API in that region’s website; and (2) Expansion of the coverage in each fauna to include deepwater and oceanic species.

B.Sc. University of Queensland, Australia, 1966

Ph.D. University of Queensland, Australia, 1974

Robertson DR, Tornabene L, Lardizabal CC,  Baldwin CC 2022. Submersibles greatly enhance research on the diversity of deep-reef fishes in the Greater Caribbean. Frontiers in Marine Science. 8:800250. https://doi.org/10.3389/fmars.2021.800250

Carlon DB, Robertson DR, Barron RL, Choat JH, Anderson DJ, Schwartz SA, Sanchez-Ortiz CA 2021 The origin of the parrotfish species Scarus compressus in the Tropical Eastern Pacific: region-wide hybridization between ancient species pairs. BMC Ecology and Evolution 21, 7, 1-20. https://doi.org/10.1186/s12862-020-01731-3

Robertson DR, Dominguez-Dominguez O, Solís-Guzmán MG, Kingon KC 2021. Origins of isolated populations of an Indo-Pacific damselfish at opposite ends of the Greater Caribbean. Aquatic Invasions 16. https://doi.org/10.3391/ai.2021.16.2.04

Chollett I, Robertson DR. 2020 Comparing biodiversity databases: Greater Caribbean reef fishes as a case study. Fish and Fisheries 2020;00:1–18. https://doi.org/10.1111/faf.12497

Robertson DR, Van Tassell JVT (2019) Shorefishes of the Greater Caribbean: online information system. Version 2.0. Smithsonian Tropical Research Institute, Balboa, Panama https://biogeodb.stri.si.edu/caribbean/en/pages

Robertson, DR, Baldwin, CC, Bellwood, D, Pyle, R, Smith-Vaniz W., Tornabene, L, Van Tassell, James L. 2019. Aspiration or expiration: hypoxia and the interpretation of fish predation in the fossil record. Palaios, 34: 245-247. DOI: http://dx.doi.org/10.2110/palo.2019.027

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David Kenfack

English
Plant Taxonomy Plant Systematics

The main difficulty in identifying rare or completely unknown species lies in obtaining fertile specimens — the flowering and fruiting parts of trees.

David Kenfack
STRI Coral Reef

As the coordinator of the ForestGEO network’s forest monitoring plots in Africa —in Cameroon, Democratic Republic of Congo, Gabon, Kenya and Nigeria — I am part of the Smithsonian’s global effort to understand the mechanisms that underlie forest change both in tropical and temperate ecosystems. My personal research focuses on plant systematics and evolution. I use a combination of morphological, molecular, ecological and spatial data to explore plant groups with challenging taxonomy to understand their evolutionary history and biogeography.

My first question when I go into a forest is how many tree species are there?

Since the establishment of the forest dynamics plot in Cameroon’s Korup National Park in 1996, 24 new species of flowering plants have been described and ten more have been confirmed new to science. In addition, 65 other trees from the plot remain identified only to family or genus level, and we strongly believe that most of these will turn out to be new to science as well. The Korup plot has about 500 tree species.

Does ForestGEO help forest conservation efforts?

When ForestGEO is established in a forest it raises awareness — the place becomes famous because of the many researchers who work there. As soon as we put ForestGEO data on the website, the researchers receive two or three requests to use the data every week from all around the world. When something happens near or in a ForestGEO site, more people are concerned, and that can promote the conservation of that forest.

B.S in Botany, University of Yaoundé I, Cameroon 1987

MAITRISE ÈS SCIENCE, University of Yaoundé I, Cameroon 1988

DOCTORAT 3e CYCLE in Plant Systematics, University of Yaoundé I, Cameroon 1995

PH.D. (Ecology, Evolution and Systematics), University of Missouri-St. Louis, USA 2008

Baldeck C.A., Dalling J.W., Kembel S.W., Harms K.E., Yavitt J.B, John R., Valencia R., Navarrete H., Bunyavejchewin S., Kiratiprayoon S., Davies S., Chuyong G., Kenfack D., Thomas D., Vallejo M., Madawala S., Adzmi Y., Supardi Md.N.N. 2013. Phylogenetic signal in soil resource niches of tropical trees. Proceedings of the Royal Society B: Biological Sciences 280, 1753.

Parmentier I., Duminil J., Kuzmina M., Philippe M., Thomas D.W., Kenfack D., Chuyong G.B., Cruaud C. & Hardy O.J. 2013. How effective are DNA barcodes in the identification of african rainforest trees? PloS one 8, e54921

De Cáceres M., Legendre P., Valencia R., Cao M, Chang L-W, Chuyong G., Condit R., Hao Z., Hsieh C.-F., Hubbell S., Kenfack D., Ma K., Mi X., Noor M.N.S., Kassim A.R., Ren H., Su S.-H., Sun I.-F., Thomas D., Ye W., & He F. 2012. The variation of tree beta diversity across a global network of forest plots. Global Ecology and Biogeography 21: 1191–1202.

Kenfack D. 2011. Cassipourea atanganae sp. nov., a new species of Rhizophoraceae from Lower Guinea. Adansonia 33: 209 – 213.

Kenfack D. 2011. A synoptic revision of Carapa (Meliaceae). Harvard papers in Botany 16: 171 – 231.

Duminil J., Kenfack D., Viscosi V., Grumiau L. & Hardy O.J. 2011. Testing species delimitation in sympatric species complexes: the case of an African tropical tree, Carapa spp. (Meliaceae). Molecular Phylogenetics and Evolution 62: 275 – 285.

Parmentier I., Harrigan R.J., Buermann W., Mitchard E.T.A., Saatchi S., Malhi Y., Bongers F., Hawthorne W.D., Leal M.E., Lewis S.L., Nusbaumer L., Sheil D., Sosef M.S.M., Affum-Baffoe K., Bakayoko A., Chuyong G.B., Chatelain C., Comiskey J.A., Dauby G., Doucet J.-L., Faucet S., Gautier, Gillet J.-F., Kenfack D., Kouamé F.N., Kouassi E.K., Kouka L.A., Parren M.P. E., Peh L. K.S.-H., Reitsma J.M., Senterre B., Sonké B., Sunderland T.C.H., Swaine M.D., Tchouto M.G. P., Thomas D.W., Van Valkenburg J. L.C.H. & Hardy O.J. 2011. Predicting alpha diversity of African rain forests: models based on climate and satellite-derived data do not perform better than a purely spatial model. Journal of Biogeography 38: 1164 –1176.

Chuyong G.B., Kenfack D., Harms K.E., Thomas D.W., Condit R. & Comita L.S. 2011. Habitat specificity and diversity of tree species in an African wet tropical forest. Plant Ecology 212: 1363 – 1374.

Kenfack D. 2011. Carapa vasquezii (Meliaceae) a new species from western Amazonia. Brittonia: 63: 7 – 10.

Kenfack D. & Peréz A. 2011. Two new species of Carapa (Meliaceae) from Western Ecuador. Systematic Botany 36: 124 – 128.

Kenfack D. 2011. Resurrection in Carapa (Meliaceae): a reassessment of morphological variation and species boundaries using multivariate methods in a phylogenetic context. Botanical Journal of the Linnean Society 165: 186 – 221.

Weber N., Birnbaum P., Forget P.-M., Gueye M. & Kenfack D. 2010. L’huile de carapa (Carapa spp., Meliaceae) en Afrique de l’Ouest: utilisations et implications dans la conservation des peuplements naturels. Fruits 65: 343 – 354.

DeWalt S.J., Schnitzer S.A., Chave J., Bongers F., Burnham R.J., Cai Z., Chuyong G., Clark D.B., Ewango C.E.N., Gerwing J.J., Gortaire E., Hart T., Kenfack D., Macía M.J., Makana J.-R., Ibarra-Manríquez G., Martínez-Ramos M., Sainge M., Muller-Landau H.C., Parren M.P.E., Parthasarathy N., Pérez-Salicrup D.R., Putz F.E., Romero-Saltos H. & Thomas D. 2010. Annual rainfall and seasonality predict pan-tropical patterns of liana density and basal area. Biotropica 42: 309 – 317.

Forget P-M., Poncy O., Thomas R.S., Hammond D.S. & Kenfack D. 2009. A cryptic new species of Carapa Aublet (Meliaceae) from Central Guyana. Brittonia 64: 366 – 374.

Kenfack D. & Dick C.W. 2009. Isolation and characterization of 15 polymorphic microsatellite loci in Tetragastris panamensis (Burseraceae), a widespread neotropical forest tree. Conservation genetic resources. 1: 385 – 387.

Morlon H., Chuyong G.B., Condit R., Hubell S., Kenfack D., Thomas D.W., Valencia R., & Green J., 2008. A general framework for the distance-decay of similarity in ecological communities. Ecology Letters 11: 904 – 917.

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