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Cockroache; Ecology, behavior & history - W.J. Bell

Cockroache; Ecology, behavior & history - W.J. Bell

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Fig. 1.9 Comparison of the relative size of the head and anterior<br />

nervous system in (A) Macropanesthia, and (B) Blattella.<br />

From Day (1950), with permission from CSIRO Publishing.<br />

tata, the greater adult weight of isolated animals results<br />

from a longer nymphal development. Males normally<br />

have three or four instars, but isolation results in a higher<br />

proportion of the four-instar type (Woodhead and Paulson,<br />

1983). A longer postembryonic development induced<br />

by suboptimal diet resulted in heavier adults in<br />

Blaptica dubia (Hintze-Podufal and Nierling, 1986). In<br />

three families of Cryptocercus clevelandi monitored under<br />

field conditions, some of each litter matured to adults a<br />

year before their siblings did. Those that matured in 6 yr<br />

had larger head widths than those that matured in 5<br />

(Nalepa et al., 1997).<br />

The dorsoventrally compressed morphotype typical of<br />

the “classic” cockroach has been taken to extremes in several<br />

distantly related taxa. These extraordinarily flattened<br />

insects resemble limpets and live in deep, narrow clefts<br />

such as those found under loose bark, at the log-soil interface,<br />

under stones, or in the cracks of boulders and<br />

rocks. In most species, the borders of the tergites are<br />

extended, flattened, and held flush with the substrate so<br />

that a close seal is formed (Fig. 1.10). The proximal parts<br />

of the femora may be distinctively flattened as part of<br />

the overall pancake syndrome (Mackerras, 1967b; Roth,<br />

1992). Included in this group are female West Indian<br />

Homalopteryx laminata (Epilamprinae) (Kevan, 1962)<br />

and several Australian taxa. A number of Leptozosteria<br />

and Platyzosteria spp. (Polyzosteriinae) live in deep, narrow<br />

clefts under rocks or bark (Mackerras, 1967b; Roach<br />

and Rentz, 1998). Members of the genus Laxta (Epilamprinae)<br />

live under eucalypt bark and are common under<br />

large slabs at the bases of trees (Roth, 1992; Rentz, 1996).<br />

Some Central and South American Zetoborinae (e.g.,<br />

Lanxoblatta emarginata, Capucina patula) and Blaberinae<br />

(e.g., Mon. biguttata nymphs) have a comparable<br />

body type and habitat (Roth, 1992; Grandcolas and Deleporte,<br />

1994; Pellens and Grandcolas, 2003; WJB, unpubl.<br />

obs.). Highly compressed morphotypes are associated<br />

THE ECOLOGY OF MORPHOTYPE<br />

The smooth, flattened body typical of many cockroaches<br />

is functionally related to their crevice-inhabiting lifestyle;<br />

it allows them to slip into narrow, horizontally extended<br />

spaces like those found in strata of matted, decayed leaves.<br />

There are, however, a number of variations on the basic<br />

body type that are exhibited by groups of often distantly<br />

related cockroaches occupying more or less the same<br />

ecological niche. These possess a complex of similar morphological<br />

characters reflecting the demands of their environment.<br />

Here we briefly profile seven distinct morphological<br />

groups. Two are defensive morphotypes, and<br />

two are forms specialized for penetrating solid substrates.<br />

Desert dwellers, those living in social insect nests, and<br />

cave cockroaches round out the gallery.<br />

The Pancake Syndrome<br />

Fig. 1.10 (A) Ventral view of head and expanded pronotum<br />

and metanotum of an unidentified, dorsoventrally flattened<br />

cockroach collected under bark in Brazil; most likely a female<br />

or nymph of Capucina patula or Phortioeca phoraspoides<br />

(LMR, pers. obs.). Note debris attached to the pronotal edges,<br />

which were closely applied to the wood surface. Photo courtesy<br />

of Edward S. Ross. (B) Female of Laxta friedmani (named after<br />

LMR’s urologist). Photo courtesy of David Rentz.<br />

10 COCKROACHES

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