Second, the outcome of plant–plant interactions in plant communit

Second, the outcome of plant–plant interactions in plant communities – and especially the SGH – has been increasingly cited in recent years to be dependent on species-specific effects between facilitators LBH589 research buy and beneficiaries,

thus promoting niche differentiation (sensu Tilman, 1982) and resource use complementarity ( Liancourt et al., 2005, Callaway, 2007 and Gross et al., 2009; see Maestre et al., 2009 for a refined SGH taking into account these aspects). Accordingly, the fact that species architecture and species diversity may differ between TAE and extratropical environments also questions the global validity of plant–plant interaction models, which have been designed outside the alpine tropics. Herein, we review the ecological and environmental features of TAE in comparison with other alpine ecosystems. We then discuss the current state of knowledge on patterns and process of plant–plant interactions in TAE. We conclude by suggesting potential

avenues for future research on plant–plant interactions in TAE, including priority GKT137831 hypotheses to be tested, methodological approaches, and how current and future knowledge in this field may extend the conceptual framework of plant–plant interactions in alpine environments worldwide. Tropical alpine areas are defined as regions that are located above the natural high-altitude treeline, within 23°26′N and 23°26′S (Smith and Young, 1987, Körner, 2003 and Nagy and Grabherr, 2009). The lower altitudinal limit of TAE occurs between 3400 m and 3900 m a.s.l. although they may develop as low as 2000 m in various tropical buy Osimertinib islands, presumably because of a lack of tree species adapted to high altitude and/or a stronger aridity occurring in these types of TAE (Leuschner, 1996). The upper altitudinal limit commonly extends to between 4600 m and 5000 m a.s.l. (Smith and Young, 1987 and Luteyn, 1999). The term ‘tropical alpine’ encompasses a variety of regional terms

referring to such areas, including páramo, puna, afro-alpine, and zacatonal (see Smith and Young, 1987, for a detailed review on terms). The majority of TAE (probably more than 90% of the total area) are located in the Andes, between Venezuela and Chile–Argentina (Jacobsen, 2008). Further north, a relatively large area of dry TAE occurs in Mexico between 3000 m and 5000 m a.s.l. (Nagy and Grabherr, 2009). Residual páramo ecosystems also occur in Costa Rica (highest point: 3810 m) and Panama (3475 m; Luteyn, 1999). In Africa, most TAE are located in the eastern mountain ranges of the continent (White, 1983) but an isolated alpine zone has also been described on the volcanic Mount Cameroon (4095 m; Letouzey, 1985). New Guinea harbours the most extensive TAE in South-east Oceanic Asia (4884 m; Smith, 1994) with an area of approximately 700 km2 (Buytaert et al., 2011).

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