ECOGRAPHY 23: 349 – 359. Copenhagen 2000
A comparison of fine-scale distribution patterns of four plant
groups in an Amazonian rainforest
J. Vormisto, O. L. Phillips, K. Ruokolainen, H. Tuomisto and R. Va ´squez
Vormisto, J., Phillips, O. L., Ruokolainen, K., Tuomisto, H. and Va ´squez, R. 2000.
A comparison of fine-scale distribution patterns of four plant groups in an Amazo-
nian rainforest. – Ecography 23: 349 – 359.
We carried out a comparison among the floristic patterns of four different plant
groups (palms, trees, melastomes and pteridophytes) in a lowland rainforest site in
Peruvian Amazonia. The study site consisted of a mosaic of edaphic patches
reflecting the different geological formations that can be found on the surface. We
collected the data along a linear transect (500 m long, divided into 20 ×20 m or
5 ×20 m subplots), and recorded of the four plant groups all individuals that
exceeded a minimum size limit predefined for each plant group. We also recorded the
drainage conditions and soil type classes in each subplot of the transect. The results
indicated that different plant groups can produce similar floristic patterns in local
spatial scales, and that these patterns reflect similarities in edaphic conditions. All
matrix correlations calculated between pairs of the four plant groups were positive
and statistically significant. Floristic composition in all plant groups correlated with
soil class, and to a somewhat lesser degree with drainage. These results imply that
any one of the four plant groups could serve as a rough indicator of more general
floristic patterns, and that even the inventory of a limited part of the flora can shed
light on the floristic variation found in Amazonian forests.
J. Vormisto ( jaaor@utu.fi), K. Ruokolainen and H. Tuomisto, Dept of Biology, Uni.
of Turku, FIN-20014 Turku, Finland – O. L. Phillips, School of Geography, Uni. of
Leeds, Leeds U.K. LS29JT.– R. Va ´squez, Jardı ´n Bota ´nico de Missouri, Apartado
020, Jae ´n, Cajamarca, Peru.
Any study that aims at understanding the structure and
function of tropical forest plant communities can only
sample a part of the flora. The use of a limited set of
species is a practical necessity because the extreme
species richness, inadequate taxonomic knowledge and
logistic difficulties make it prohibitively laborious to
sample all plant species. Thus, floristic studies tradition-
ally deal only with trees (e.g. Ashton 1969, Lieberman
et al. 1985, Gentry 1988a, b, ter Steege et al. 1993,
Duivenvoorden 1995, Clinebell et al. 1995). More re-
cently, studies have also been done on ground herbs
(Poulsen and Balslev 1991, Poulsen 1996), palms (Kahn
and de Castro 1985, Kahn and de Granville 1992),
pteridophytes (Young and Leo ´n 1989, van der Werff
1990, Tuomisto and Ruokolainen 1994, Tuomisto et al.
1995, Tuomisto and Poulsen 1996, Ruokolainen et al.
1997), Lauraceae (van der Werff 1992), and Melastom-
ataceae (Tuomisto and Ruokolainen 1994, Tuomisto et
al. 1995, Ruokolainen et al. 1997). However, if the
results of studies on restricted components of the flora
are to be used as models for making generalisations
concerning the flora in general, and potentially for
developing conservation strategies, then it is important
to assess how well the studied part of the flora repre-
sents the unstudied part. In other words: are the studied
groups good ‘‘indicators’’ of floristic patterns in the rest
of the flora?
Although all plants need light, water and nutrients,
different plant groups may have different responses to
these resources (Cox and Larson 1993). An obvious
way to study the variation in ecological behaviour
among plant groups is to measure if the plant groups
Accepted 27 September 1999
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ISSN 0906-7590
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ECOGRAPHY 23:3 (2000) 349