Cockroache; Ecology, behavior & history - W.J. Bell
Cockroache; Ecology, behavior & history - W.J. Bell
Cockroache; Ecology, behavior & history - W.J. Bell
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Fig. 3.8 Periplaneta sp. in a sewer manhole in Houma, Louisiana.<br />
From Gary (1950).<br />
with each supporting a different community (Juberthie,<br />
2000b). The twilight zone near the entrance is closest to<br />
epigean conditions and has the largest and most diverse<br />
fauna. Next is a zone of complete darkness with variable<br />
temperature, and finally in the deep interior a zone of<br />
complete darkness, stable temperature, and stagnant air,<br />
where the obligate, troglomorphic fauna appear (Poulson<br />
and White, 1969). The degree of fidelity to a zone varies.<br />
While the Australian Para. rufa is found only from the entrance<br />
to 0.4 km into a cave, Trog. nullarborensis is found<br />
from the entrance to 4.8 km deep; it roams throughout<br />
the cave system and is one of the few troglomorphs<br />
recorded from the twilight zone (Richards, 1971). Eublaberus<br />
posticus and Eub. distanti may segregate in caves<br />
according to their particular moisture requirements. The<br />
former prefers the moist inner sections of caves, while the<br />
latter is more common in drier guano (Darlington, 1970).<br />
The habitable areas of caves, and consequently, populations<br />
of cave organisms, are dynamic—they move, expand,<br />
and contract, depending on climate and on pulses<br />
of organic matter (Humphreys, 1993). After an exceptionally<br />
cool night in Nasty Cave in Australia, for example,<br />
a common Nocticola cockroach could not be found<br />
and was thought to have retreated into cracks during the<br />
unfavorable conditions (Howarth, 1988). Initially a small<br />
species in the subfamily Anaplectinae was sporadically<br />
seen in a Trinidadian cave, subsequently formed a thriving<br />
colony, then was wiped out when the cave flooded. It<br />
did not reappear (Darlington, 1970).<br />
Caves with a source of vertebrate guano support very<br />
different cockroach communities than caves that lack<br />
such input. Guano caves typically contain very large<br />
numbers of few cockroach species able to maintain dense<br />
populations and exploit the abundant, rich, but rather<br />
monotonous food bonanza (Darlington, 1970). Examples<br />
include a population of more than 80,000 Gyna sp.<br />
in a South African cave (Braack, 1989), more than 43,000<br />
Eub. distanti in just one chamber of a cave in Trinidad<br />
(Darlington, 1970) (Fig. 3.9), and Pycnoscelus striatus<br />
found at approximately 2000–3000/m 2 in the Batu Caves<br />
of Malaysia (McClure, 1965). A similar scenario is that of<br />
approximately 3000 P. americana /m 2 in a sewer system<br />
more than 27 m beneath the University of Minnesota<br />
campus (Roth and Willis, 1957). In guano caves, the distribution<br />
of cockroaches usually coincides with that of<br />
bats and their excrement (Braack, 1989). Some species are<br />
consistently associated with bat guano, wherever it is<br />
found. One South African Gyna sp. was present in all batinhabited<br />
caves and cave-like habitats, including the roof<br />
of a post office (Braack, 1989).<br />
Highly troglomorphic cockroach species generally<br />
support themselves on less rich, less abundant food<br />
sources. Trogloblattella chapmani is typically found remote<br />
from guano beds in passages floored by damp sticky<br />
clay or silt (Roth, 1980). Metanocticola christmasensis is<br />
associated with the often luxuriant tree root systems that<br />
penetrate caves (Roth, 1999b), but their diet is unknown<br />
(Roth, 1999b). Troglomorphic cockroaches tend to move<br />
Fig 3.9 Habitat stratification in Eublaberus distanti in Guanapo<br />
Cave, Trinidad. (A) Adults on walls of cave; (B) nymphs<br />
on surface of fruit bat guano. Photos courtesy of J.P.E.C. Darlington.<br />
HABITATS 53