Epiphytes and orchids are well suited to be indicators of the health
and biodiversity of the rainforest, not only because they are an important
source of nutrients for other flora and fauna, but because they are very
sensitive to shifts in microclimate and they have slow growth. The performance,
survival, and distribution of epiphytes is dependent on stand density,
microclimate, distance from seed source, tree size and species, type and
history of disturbance, population dynamics of epiphytes and trees, and
epiphyte physiology (Hietz 1999).
Epiphytes are far more vulnerable to deforestation than other
flora. For example, 26% of vacular plant species present in 1900
are now exinct, but 62% of epiphyte species are exinct. Epiphytes
are completely dependent on their host plants, so if a tree is cut down,
all of the epiphytes residing on that tree will die. In addition, they
have very specific zoning constraints, so secondary vegetation might not
have all of the nessassary microsites for different epiphyte species.
Table 1 (Hietz 1999) illustrates the loss of species and biodiversity in a plantation as compared with oldgrowth forest. While the number of species for the two groups is not very different, there is considerable loss of biodiversity, because only epiphytes residing in some of the locations on a tree are present.
TABLE 1. Epiphyte Richness and Occurrence of Ecological
Groups in an Oldgrowth Forest and an Alnus Plantation.
Figures in parentheses for the plantation are fertile
species, all species in the oldgrowth forest were found with fertile individuals.
Epiphytic Species Living on:
Oldgrowth
Plantation
stem base
9
0 (0)
stem and thick branches
14
7 (3)
thick and thin branches
11
11 (7)
preference unclear
5
3 (1)
total
39
21 (11)
In addition ot complete deforestation, epiphytes are hurt by fragmentation.
Their wellbeing depends on the distance from their fragment to closed forest,
and the shape of the fragment (these effect seed dispersal).
They are also affected more adversly by increased CO2 levels in the
atmosphere. Raised CO2 levels shift climate zones, forcing flora and fauna
to migrate. Although epiphytes could migrate more easily than trees, many
models of the effect of fluctuating CO2 levels predict increased seasonality
of precipitation, and thus a reduction of the perhumid area containing
the hightest epiphyte diversity (Hietz 1999).
Specific species or groups have been identified as good bioindicators.
Epiphyte N concentration:
Epiphytes obtain their Nitrogen either from canopy soil or from nutrients
in rainwater. Nitrogen-15 concentration is much higher in ground-rooted
plants than in epiphytes with access to canopy soil, pointing to a much
richer source of Nitrogen in terrestial soil versus canopy soil. In addition,
N-15 concentration is much higher for those epiphytes in canopy soil than
those on smaller branches, indicating that epiphytes on smaller branches
have to rely almost exclusively on rainwater as a source of Nitrogen. This
means that these epiphytes (on small branches) are much more susceptible
to drought and thus would be better bioindicators.
Sources:
Hietz, Peter. "Diversity and Conservation of Epiphytes in a Changing Environment." International Union of Pure and Applied Chemistry (IUPAC). 1998. Volume 70: Issue 11. Available at: http://www.iupac.org/symposia/proceedings/phuket97/hietz.html
Turner, T.H.; Tan, H.T. W.; Wee, Y.C.; Ibrahim, Ali Bin; Chew, P.T.; Corlett, R.T. "A Study of Plant Species Extinction in Singapore: Lessons for the Conservation of Tropical Biodiversity." Conservation Biology. September 1994. Volume 8: Issue3, pgs. 705-12.
Lambert, Frank R. and Marshall, Adrian G. "Keystone characteristics of Bird-dispersed Ficus in a Malaysian lowland Rain Forest." Journal of Ecology. 1991. Volume 79, pgs. 793-809.
Hietz, Peter; Wanck, Wolfgang; Wania, Rita; Nadkarni, Nalim M. "Nitrogen-15 natural abundance in a montane cloud forest canopy as an indicator of nitrogen cycling and epiphyte nutrition." Oecologia. 2002. Volume 131, pgs. 350-355.