ecology of phasmids - KLUEDO - Universität Kaiserslautern
ecology of phasmids - KLUEDO - Universität Kaiserslautern
ecology of phasmids - KLUEDO - Universität Kaiserslautern
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Community structure & host range 24<br />
2.4 Discussion<br />
This study is the first to demonstrate diversity and distributional patterns <strong>of</strong> the phasmid community <strong>of</strong> a<br />
tropical rainforest. The phasmid community <strong>of</strong> BCI was poor in species and in density. Spatially<br />
<strong>phasmids</strong> were largely restricted to forest edge habitats resulting in higher diversity and density<br />
compared to the forest understory. While phasmid abundances varied throughout the study period, no<br />
seasonal effect on phasmid abundance was detectable. The distribution pattern <strong>of</strong> phasmid species was<br />
clearly linked to restrictions in their host range that seemed to reflect the successional status <strong>of</strong> host<br />
plant species.<br />
2.4.1 Phasmid diversity, density, and distribution<br />
With a total <strong>of</strong> 12 species, the phasmid community <strong>of</strong> Barro Colorado Island was expectedly low in<br />
species richness. Worldwide, the order Phasmatodea contains about 3000 described species that occur<br />
mainly in tropical regions (Whiting et al. 2003) and is species poor compared to other insect orders that<br />
are highly diverse in herbivores like Lepidopterans, Coleopterans, and - to a lower extent –<br />
Orthopterans. For example, on BCI there are approximately 274 species <strong>of</strong> true butterfly (Lepidoptera,<br />
Papilionoidea; DeVries 1994) and 250 species <strong>of</strong> katydids (Orthoptera, Tettigoniidae; A. Lang,<br />
unpublished data). I found reports <strong>of</strong> 42 phasmid species occurring in Panamá (see Appendix 1 for<br />
species and references) where<strong>of</strong> BCI accommodates 26 %; plus one species not formerly reported from<br />
Panamá (Otocrania sp.). Analysis <strong>of</strong> collection records (Windsor, Aiello, Berger, unpublished data)<br />
indicates that Gamma-Diversity in Panamá is high with discrete regions giving shelter to different<br />
phasmid species. Together with the fact that I recorded all but one species previously reported from BCI<br />
(Trychopeplus laciniatus; Aiello, unpublished data) I am confident that I assessed the phasmid<br />
community adequately.<br />
I showed that forest edges and gaps represented important habitats to the majority <strong>of</strong> phasmid species on<br />
BCI. In contrast, the forest understory seemed to provide a suitable habitat for M. diocles only. Higher<br />
abundance <strong>of</strong> insect herbivores in gaps is <strong>of</strong>ten inferred from higher herbivore damage on gap-adapted<br />
versus understory plant species (Coley 1980, 1982, 1983; Coley & Barone 1996). Smiley (1978) found<br />
that Heliconius butterflies were more abundant in young successional than in understory habitats<br />
(Table 2-3). My results support this pattern on the phasmid community and species level. In forest edges<br />
phasmid density was 35 times, and M. diocles density three times higher than in the understory (cf.<br />
Table 2-1). Low densities <strong>of</strong> <strong>phasmids</strong> in the BCI forest understory correspond with Elton (1973) who<br />
found low total arthropod densities <strong>of</strong> 0.92 ind.*m -3 in the same habitat (18400 ind.*ha -1 , extrapolated<br />
on two meter height; Table 2-4).