21.03.2015 Views

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

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

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

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

Fig. 6.11 Examples of variation in male genitalia. (A) Genitalia (dorsal) of Allacta australiensis<br />

(Blattellidae: Pseudophyllodromiinae). Accessory median phallomere is broad, with an apical<br />

brush-like modification (arrow). From Roth (1991d). (B) Subgenital plate and genitalia (dorsal)<br />

of Hemithyrsocera nathani (Blattellidae: Blattellinae). A huge, sclerotized, densely setose brushlike<br />

structure is found on the left side (arrow). From Roth (1995a). (C) Subgenital plate and genitalia<br />

(dorsal) of Parasigmoidella atypicalis (Blattellidae: Blattellinae). Note distally curved median<br />

phallomere with a pick-axe-like apex (arrow) and three-fingered “claw” on right. From Roth<br />

(1999b). (D) Highly reduced phallomeres on the extruded aedeagal membrane of Panesthia<br />

cribrata (Blaberidae: Panesthiine). From Walker and Rose (1998). Phallomeres are labeled according<br />

to McKittrick’s (1964) classification. (E) Extraordinarily complex genitalia (dorsal) of<br />

Homopteroidea nigra (Polyphagidae). From Roth (1995d).<br />

blaberids, rivals disturb or attack courting or mating<br />

males. Copulations may be broken off because of interference<br />

in N. cinerea (Ewing, 1972). In B. craniifer males<br />

assault copulating pairs by jumping on their backs and attacking<br />

their point of juncture. The interference may<br />

cause separation of the pair, but only if it occurs during<br />

the first few seconds after they assume the opposed position.<br />

The copulating male “shows no reluctance in fighting<br />

with the intruder,” and “the trio may careen about the<br />

mating chamber” (Wendelken and Barth, 1985, 1987). A<br />

tight grasp of the female is also required because the pair<br />

may travel during copulation. Pairs are usually quiescent<br />

unless disturbed, in which case they move away. It is invariably<br />

the female that is responsible for the locomotion,<br />

dragging the passive male along in her wake (Roth and<br />

Barth, 1967). She can move with astonishing speed,<br />

pulling the “furiously backpedaling” male behind her (Simon<br />

and Barth, 1977a). Blattella germanica (Roth and<br />

Willis, 1952a), Byr. fumigata (Barth, 1964), Ell. humerale<br />

( affine) (Pope, 1953), Latiblattella spp. (Willis, 1970),<br />

Parcoblatta fulvescens (Wendelken and Barth, 1971), and<br />

P. americana (Simon and Barth, 1977a) are among the<br />

species in which this <strong>behavior</strong> has been reported. It also<br />

occurs in G. portentosa, even though the male is much<br />

heavier than the female (Barth, 1968c).<br />

Intromittent Organs<br />

The need for a secure connection, then, may account for<br />

some of the claspers, hooks, and spines in the male’s<br />

genitalic assemblage but cannot explain the bewildering<br />

complexity (Fig. 6.11E) of many components. The similarity<br />

of some cockroach structures to those of other,<br />

better-studied insects, however, allows us in some cases<br />

to make inferences from genitalic design. In particular,<br />

brushes and slender, elongate spines, rods, and flagellae,<br />

especially those with modified tips, may be sexually selected<br />

structures that increase a copulating male’s fertil-<br />

102 COCKROACHES

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!