Skip to main content

Advertisement

Log in

Do plant families with contrasting functional traits show similar patterns of endemism? A case study with Central African Orchidaceae and Rubiaceae

  • Original Paper
  • Published:
Biodiversity and Conservation Aims and scope Submit manuscript

Abstract

The influence of functional traits on floristic patterns remains poorly understood in tropical rain forests. This contribution explores whether patterns of endemism of plant species are influenced by their life form and mode of dispersal. We used a comprehensive dataset of 3650 georeferenced plant specimens collected in Cameroon belonging to 115 taxa of Orchidaceae and 207 Rubiaceae endemic to Atlantic Central Africa. Species diversity of each family was compared using raw species richness (SR) and an index of species diversity (S k ) using subsampling procedure to correct for sampling bias. Measures were compared at three scales (square grids of one half-degree and one-degree per side and ecoregions) and according to elevation and continentality gradients. Species similarity between grid cells was measured using the sample-size corrected NNESS index. For both families, SR and S k decreased along the continentality gradient. In forest habitats below 1500 m altitude, both Orchidaceae and Rubiaceae show similar endemism patterns, but they differ in intensity. At higher altitudes, S k is higher for orchids due to the presence of endemic terrestrial taxa in grasslands, where the endemic Rubiaceae flora is rather poor. Substantial endemism observed at the ecoregion level and turnover analysis supported the role of the Sanaga River as a phytogeographical boundary. Similar endemism patterns were observed in lowland forests for Orchidaceae and Rubiaceae, even though Orchidaceae are assumed to have better long distance dispersal capabilities. The dispersal ability of Orchidaceae could be limited by the need of specific mycorhizal fungi for seed germination or host specificity for epiphytic orchids.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  • Achoundong G (1994) Les Rinorea comme indicateurs des grands type forestiers du Cameroun. In: van der Maesen LJG, van der Burgt XM, de Rooy JM (eds) The biodiversity of African plants. Kluwer Academic Publishers, Netherlands, pp 534–544

    Google Scholar 

  • Anthony NM, Johnson-Bawe M, Jeffery K, Clifford SL, Abernethy KA, Tutin CE, Lahm SA, White LJT, Utley JF, Wickings EJ, Bruford MW (2007) The role of Pleistocene refugia and rivers in shaping gorilla genetic diversity in central Africa. Proc Natl Acad Sci USA 104:20432–20436

    Article  PubMed  CAS  Google Scholar 

  • Arditti J, Ghani AKA (2000) Numerical and physical properties of orchid seeds and their biological implications. New Phytol 145:367–421

    Article  Google Scholar 

  • Avise JC (2009) Phylogeography: retrospect and prospect. J Biogeogr 36:3–15

    Article  Google Scholar 

  • Bowie RCK, Fjeldsa J, Hackett SJ, Bates JM, Crowe TM (2006) Coalescent models reveal the relative roles of ancestral polymorphism, vicariance, and dispersal in shaping phylogeographical structure of an African montane forest robin. Mol Phylogenet Evol 38:171–188

    Article  PubMed  CAS  Google Scholar 

  • Brooks T, Balmford A, Burgess N, Fjeldsa J, Hansen LA, Moore J, Rahbek C, Williams P (2001) Toward a blueprint for conservation in Africa. Bioscience 51:613–624

    Article  Google Scholar 

  • Burgess N, Kuper W, Mutke J, Brown J, Westaway S, Turpie S, Meshack C, Taplin J, McClean C, Lovett JC (2005) Major gaps in the distribution of protected areas for threatened and narrow range Afrotropical plants. Biodivers Conserv 14:1877–1894

    Article  Google Scholar 

  • Cable S, Cheek M (1998) The plants of Mount Cameroon. In: Cable S, Cheek M (eds) A conservation checklist. Royal Botanic Gardens, Kew

  • Cheek M, Mackinder B, Gosline G, Onana JM, Achoundong G (2001) The phytogeography and flora of western Cameroon and the Cross River-Sanaga River interval. Syst Geogr Plants 71:1097–1100

    Article  Google Scholar 

  • Cheek M, Pollard BJ, Darbyshire I, Onana J-M, Wild C (2004) The Plants of Kupe, Mwanenguba and the Bakossi Mountains, Cameroon. In: Cheek M, Pollard BJ, Darbyshire I, Onana J-M, Wild C (eds) A conservation checklist. Royal Botanic Gardens, Kew

  • Chessel D, Dufour A-B, Thioulouse J (2004) The ade4 package-I: one-table methods. R News 4:5–10

    Google Scholar 

  • Colyn M, Gautierhion A, Verheyen W (1991) A reappraisal of paleoenvironmental history in central Africa—evidence for a major fluvial refuge in the Zaire Basin. J Biogeogr 18:403–407

    Article  Google Scholar 

  • Delisle F, Lavoie C, Jean M, Lachance D (2003) Reconstructing the spread of invasive plants: taking into account biases associated with herbarium specimens. J Biogeogr 30:1033–1042

    Article  Google Scholar 

  • Dennis RLH, Thomas CD (2000) Bias in butterfly distribution maps: the influence of hot spots and recorder’s home range. J Insect Conserv 4:73–77

    Article  Google Scholar 

  • Dressler RL (1981) The Orchids: natural history and classification. Harvard University Press, Cambridge, Mass

    Google Scholar 

  • Droissart V (2009) Etude taxonomique et biogéographique des plantes endémiques d’Afrique centrale atlantique : le cas des Orchidaceae. Ph.D. thesis, Université Libre de Bruxelles, Belgium

  • Droissart V, Sonké B, Stévart T (2006) Les Orchidaceae endémiques d’Afrique centrale atlantique présentes au Cameroun. Syst Geogr Plants 76:3–84

    Google Scholar 

  • Droissart V, Simo M, Sonké B, Cawoy V, Stévart T (2009) Le genre Stolzia (Orchidaceae) en Afrique centrale avec deux nouveaux taxons. Adansonia 31:25–40

    Article  Google Scholar 

  • Droissart V, Hardy O, Sonké B, Dahdouh-Guebas F, Stévart T (in press) Subsampling herbarium collections to assess geographic diversity gradients: a case-study with endemic Orchidaceae and Rubiaceae in Cameroon. Biotropica

  • Francis AP, Currie DJ (2003) A globally consistent richness-climate relationship for angiosperms. Am Nat 161:523–536

    Article  PubMed  Google Scholar 

  • Gallagher ED (1999) Documentation of COMPAH program

  • Gandawijaja D, Arditti J (1983) The orchids of Krakatau—evidence for a mode of transport. Ann Bot 52:127–130

    Google Scholar 

  • Gotelli NJ, Colwell RK (2001) Quantifying biodiversity: procedures and pitfalls in the measurement and comparison of species richness. Ecol Lett 4:379–391

    Article  Google Scholar 

  • Govaerts R, Campaccil MA, Baptista DH, Cribb PJ, George A, Kreuz K, Wood J (2010a) World checklist of Orchidaceae. http://www.kew.org/wcsp/. Accessed 5 Oct 2010

  • Govaerts R, Ruhsam M, Andersson L, Robbrecht E, Bridson D, Davis A, Schanzer I, Sonké B (2010b) World checklist of Rubiaceae. http://www.kew.org/wcsp/. Accessed 5 Oct 2010

  • Grassle JF, Smith W (1976) A similarity measure sensitive to the contribution of rare species and its use in investigation of variation in marine benthic communities. Oecologia 25:13–22

    Article  Google Scholar 

  • Haffer J (1997) Alternative models of vertebrate speciation in Amazonia: an overview. Biodivers Conserv 6:451–476

    Article  Google Scholar 

  • Hardy OJ (2010) BiodivR 1.2. A program to compute statistically unbiased indices of species diversity within sample and species similarity between samples using rarefaction principles. http://ebe.ulb.ac.be/ebe/Software.html. Accessed Oct 2010

  • Harris DJ, Poulsen AD, Frimodt M, Oslash, Ller C, Preston J, Cronk QCB (2000) Rapid radiation in Aframomum (Zingiberaceae): evidence from nuclear ribosomal DNA internal transcribed spacer (ITS) sequences. Edinb J Bot 57:377–395

    Article  Google Scholar 

  • Hill JL, Hill RA (2001) Why are tropical rain forests so species rich? Classifying, reviewing and evaluating theories. Prog Phys Geogr 25:326–354

    Google Scholar 

  • Hurlbert SH (1971) The nonconcept of species diversity: a critique and alternative parameters. Ecology 52:577–586

    Article  Google Scholar 

  • Johansson D (1974) Ecology of vascular epiphytes in West African rain forest. Acta Phytogeogr Suec 59:1–129

    Google Scholar 

  • Kier G, Mutke J, Dinerstein E, Ricketts TH, Kuper W, Kreft H, Barthlott W (2005) Global patterns of plant diversity and floristic knowledge. J Biogeogr 32:1107–1116

    Article  Google Scholar 

  • Kreft H, Jetz W (2007) Global patterns and determinants of vascular plant diversity. Proc Natl Acad Sci USA 104:5925–5930

    Article  PubMed  CAS  Google Scholar 

  • Kuper W, Sommer JH, Lovett JC, Mutke J, Linder HP, Beentje HJ, Van Rompaey R, Chatelain C, Sosef M, Barthlott W (2004) Africa’s hotspots of biodiversity redefined. Ann Mo Bot Gard 91:525–535

    Google Scholar 

  • Kuper W, Sommer JH, Lovett JC, Barthlott W (2006) Deficiency in African plant distribution data—missing pieces of the puzzle. Bot J Linn Soc 150:355–368

    Article  Google Scholar 

  • Leal ME (2004) The African rain forest during the last glacial maximum, an archipelago of forests in a sea of grass. Ph.D. thesis, Wageningen University, Wageningen, The Netherlands

  • Linder HP (2001) Plant diversity and endemism in sub-Saharan tropical Africa. J Biogeogr 28:169–182

    Article  Google Scholar 

  • Maley J (1987) Fragmentation de la forêt dense humide africaine et extension des biotopes montagnards au Quaternaire récent: nouvelles données polliniques et chronologiques. Implications paléoclimatiques et biogéographiques. Palaeoecol Africa 18:307–334

    Google Scholar 

  • Maley J (1996) The African rain forest—main characteristics of changes in vegetation and climate from the Upper Cretaceous to the Quaternary. Proc R Soc Edinb 104B:31–73

    Google Scholar 

  • Mayr E, O’Hara RJ (1986) The biogeographic evidence supporting the Pleistocene Forest Refuge Hypothesis. Evolution 40:55–66

    Article  Google Scholar 

  • Moritz C, Patton JL, Schneider CJ, Smith TB (2000) Diversification of rainforest faunas: an integrated molecular approach. Annu Rev Ecol Syst 31:533–563

    Article  Google Scholar 

  • Mutke J, Barthlott W (2005) Patterns of vascular plant diversity at continental to global scales. Plant diversity and complexity patterns: local, regional and global dimensions. In: Proceedings of an international symposium held at the royal Danish academy of sciences and letters in Copenhagen, Denmark, 25–28 May, 2003, pp 521–537

  • Myers N, Mittermeier RA, Mittermeier CG, da Fonseca GAB, Kent J (2000) Biodiversity hotspots for conservation priorities. Nature 403:853–858

    Article  PubMed  CAS  Google Scholar 

  • Nguembou KC (2006) Distribution des Rubiaceae endémiques du Cameroun. MSc thesis, Université Libre de Bruxelles, Belgium

  • Nichol JE (1999) Geomorphological evidence and Pleistocene refugia in Africa. The Geographical Journal 165:79–89

    Article  Google Scholar 

  • O’Brien EM (1998) Water-energy dynamics, climate, and prediction of woody plant species richness: an interim general model. J Biogeogr 25:379–398

    Article  Google Scholar 

  • Ochora J, Stock WD, Linder HP, Newton LE (2001) Symbiotic seed germination in twelve Kenyan orchid species. Syst Geogr Plants 71:585–596

    Article  Google Scholar 

  • Olson DM, Dinerstein E, Wikramanayake ED, Burgess ND, Powell GVN, Underwood EC, D’Amico JA, Itoua I, Strand HE, Morrison JC, Loucks CJ, Allnutt TF, Ricketts TH, Kura Y, Lamoreux JF, Wettengel WW, Hedao P, Kassem KR (2001) Terrestrial ecoregions of the world: a new map of life on earth. Bioscience 51:933–938

    Article  Google Scholar 

  • Plana V (2004) Mechanisms and tempo of evolution in the African Guineo-Congolian rainforest. Phil Trans R Soc Lond B Biol Sci 359:1585–1594

    Article  Google Scholar 

  • Plana V, Gascoigne A, Forrest LL, Harris D, Pennington RT (2004) Pleistocene and pre-pleistocene Begonia speciation in Africa. Mol Phylogenet Evol 31:449–461

    Article  PubMed  Google Scholar 

  • Prendergast JR, Wood SN, Lawton JH, Eversham BC (1993) Correcting for variation in recording effort in analyses of diversity hotspots. Biodiversity Letters 1:39–53

    Article  Google Scholar 

  • Querouil S, Verheyen E, Dillen M, Colyn M (2003) Patterns of diversification in two African forest shrews: Sylvisorex johnstoni and Sylvisorex ollula (Soricidae, Insectivora) in relation to paleo-environmental changes. Mol Phylogenet Evol 28:24–37

    Article  PubMed  Google Scholar 

  • Rietkerk M, Ketner P, de Wilde JJFE (1996) Caesalpinioideae and the study of forest refuges in central Africa. In: van der Maesen LJG, van der Burgt XM, de Rooy JM (eds) The biodiversity of African plants: Proceedings XIVth AETFAT congress. Kluwer Academic Publishers, Netherlands, pp 618–623

    Google Scholar 

  • Robbrecht E (1988) Tropical woody Rubiaceae. Characteristic features and progressions. Contributions to a new subfamilial classification. Opera Bot Belg 1:1–271

    Google Scholar 

  • Robbrecht E (1996) Geography of African Rubiaceae with reference to glacial rain forest refuges. In: van der Maesen LJG, van der Burgt XM, de Rooy JM (eds) The biodiversity of African plants. Proceedings XIVth AETFAT congress. Kluwer Academic Publishers, Netherlands, pp 564–581

    Google Scholar 

  • Rodrigues ASL, Andelman SJ, Bakarr MI, Boitani L, Brooks TM, Cowling RM, Fishpool LDC, da Fonseca GAB, Gaston KJ, Hoffmann M, Long JS, Marquet PA, Pilgrim JD, Pressey RL, Schipper J, Sechrest W, Stuart SN, Underhill LG, Waller RW, Watts MEJ, Yan X (2004) Effectiveness of the global protected area network in representing species diversity. Nature 428:640–643

    Article  PubMed  CAS  Google Scholar 

  • Sanders HL (1968) Marine benthic diversity: a comparative study. Am Nat 102:243–282

    Article  Google Scholar 

  • Sanford WW (1974) The ecology of orchids. In: Withner C (ed) The orchids, scientific studies. John Wiley & Sons, New York, NY, pp 1–101

    Google Scholar 

  • Simo M, Droissart V, Sonké B, Stévart T (2009) The orchid flora of the Mbam Minkom Hills (Yaoundé, Cameroon). Belg J Bot 142:111–123

    Google Scholar 

  • Sonké B, Nguembou KC, Neuba D (2006) Les Rubiaceae endémiques du Cameroun et leur statut de conservation. In: Ghazanfar SA, Beentje HJ (eds) Taxonomy and ecology of African plants, their conservation and uses. Proceedings du XVIIème Congrès de l’Aetfat. Royal Botanic Garden Kew, London, pp 97–109

    Google Scholar 

  • Soria-Auza RW, Kessler M (2008) The influence of sampling intensity on the perception of the spatial distribution of tropical diversity and endemism: a case study of ferns from Bolivia. Divers Distrib 14:123–130

    Article  Google Scholar 

  • Sosef MSM (1994) Refuge begonias: taxonomy, phylogeny and historical biogeography of Begonia sect. Loasibegonia and sect. Scutobegonia in relation to glacial rain forest refuges in Africa. Wageningen Agricultural University Papers 94:1–306

    Google Scholar 

  • Sosef MSM (1996) Begonias and African rain forest refuges: general aspects and recent progress. In: van der Maesen LJG, van der Burgt XM, de Rooy JM (eds) The biodiversity of African plants: Proceedings XIVth AETFAT congress. Kluwer Academic Publishers, Netherlands, pp 602–611

    Google Scholar 

  • Stévart T (2003) Etude taxonomique, écologique et phytogéographique des Orchidaceae en Afrique centrale atlantique. Ph.D. thesis, Université Libre de Bruxelles, Belgium

  • Stevens PF (2001 onwards) Angiosperm phylogeny website. Version 9, June 2008. http://www.mobot.org/MOBOT/research/APweb/. Accessed 22 September 2008

  • Taedoumg E (2007) Diversité et distribution des Rubiaceae endémiques du domaine bas-guinéen présentes au Cameroun. MSc thesis, University of Yaoundé I, Cameroon

  • Taylor DL, Bruns TD, Leake JR, Read DJ (2002) Mycorrhizal specificity and function in myco-heterotrophic plants. In: van der Heijden MGA, Sanders I (eds) Mycorrhizal ecology. Springer, Berlin, pp 375–414

    Google Scholar 

  • Tchouto MGP, Wilde JJFEd, Boer WFd, Maesen LJGvd, Cleef AM (2009) Bio-indicator species and Central African rain forest refuges in the Campo-Ma’an area, Cameroon. Syst Biodivers 7:21–31

    Article  Google Scholar 

  • Thiers B (2010) Index herbariorum: a global directory of public herbaria and associated staff. http://sweetgum.nybg.org/ih/. Accessed 01/10/2010

  • White F (1979) The Guineo-Congolian region and its relationships to other phytochoria. Bulletin du Jardin Botanique National de Belgique 49:11–55

    Article  Google Scholar 

  • White F (1981) The history of the Afromontane archipelago and the scientific need for its conservation. Afr J Ecol 19:33–54

    Article  Google Scholar 

  • White F (1983) The vegetation of Africa. A descriptive memoir to accompany the Unesco/AETFAT/UNSO vegetation map of Africa. Unesco/AETFAT/UNSO, Copedith, Paris

  • Zapfack L, Engwald S (2008) Biodiversity and spatial distribution of vascular epiphytes in two biotopes of the Cameroonian semi-deciduous rain forest. Plant Ecol 195:117–130

    Article  Google Scholar 

Download references

Acknowledgements

We express our sincere gratitude to Professor Jean Lejoly from the Université Libre de Bruxelles for his support in its laboratory, and to Dr Porter P. Lowry II, Dr Ingrid Parmentier and Dr Pierre Couteron for their helpful comments. Fieldwork was supported by the ECOFAC Program (EC-DG8), DIVEAC (CUD-ULB), the Fonds Leopold III, CARPE, the Wildlife Conservation Society (WCS), the Belgian Fund for Scientific Research (F.R.S.-FNRS) and “Sud Expert Plantes, projet#375” project under French Ministry of Foreign Affairs. Visits of V. Droissart in Wageningen, Paris and Kew Herbaria were funded by the European Commission’s Research Infrastructure action via the SYNTHESYS Project (applications FR-TAF-2418 & NL-TAF-1611) and by the F.R.S.-FNRS. The Keepers of the aforementioned herbaria are gratefully acknowledged. T. Stévart’s participation was supported by the U.S. National Science Foundation (1051547, TS as PI).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Vincent Droissart.

Appendix

Appendix

See Table 5.

Table 5 List of Orchidaceae and Rubiaceae taxa used in this study with their specimen count, life form and mode of dispersal

Rights and permissions

Reprints and permissions

About this article

Cite this article

Droissart, V., Sonké, B., Hardy, O.J. et al. Do plant families with contrasting functional traits show similar patterns of endemism? A case study with Central African Orchidaceae and Rubiaceae. Biodivers Conserv 20, 1507–1531 (2011). https://doi.org/10.1007/s10531-011-0042-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10531-011-0042-z

Keywords

Navigation