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. 6.14 (A) Sagittal section of the female genitalia of Gromphadorhina portentosa (Blaberidae).<br />
(B) Diagrammatic sagittal section of blaberid female genitalia with ootheca in brood sac. From<br />
McKittrick (1964).<br />
2003). If multiple matings do increase female fitness, it<br />
follows that the control of female sexual receptivity is a<br />
source of conflict between the sexes, and females are expected<br />
to evolve resistance to the stimuli males use to induce<br />
receptivity loss (Arnqvist and Nilsson, 2000). That<br />
does not appear to be the case in N. cinerea. Copulation<br />
is known to confer numerous fitness benefits on female<br />
cockroaches (discussed below), but within the framework<br />
of cyclic receptivity typical of N. cinerea there is currently<br />
no evidence that more than one mate within the first<br />
reproductive cycle is advantageous. Moreover, morphological<br />
and experimental evidence suggests that spermatophore<br />
placement and therefore loss of receptivity in<br />
N. cinerea is likely under female control, suggesting that<br />
there is no conflict of reproductive interest between the<br />
sexes on this issue. Not only do females have morphological<br />
features specialized for proper spermatophore placement<br />
and retention, these features are regulated by her<br />
nervous system. Receptivity in N. cinerea is suppressed<br />
only if the spermatophore is firmly placed and properly<br />
positioned (Roth, 1964b). While in some blaberids a large<br />
amount of glue-like secretion cements the spermatophore<br />
into place, in Nauphoeta and several related genera<br />
the bursa is largely responsible for spermatophore retention<br />
(Graves, 1969). The bursa is deep, is extensively<br />
membranous, and almost completely wraps around the<br />
correspondingly elongated spermatophore. If the nerve<br />
cords are severed prior to mating in female R. maderae,<br />
another species with a deep, membranous bursa, 70% of<br />
males were not able to insert the spermatophore properly.<br />
They were placed elsewhere in the genital atrium or<br />
dropped by the male without being transferred. In many<br />
cases the male had pierced the wall of the brood sac and<br />
the spermatophore was in the female’s body cavity. “It<br />
seems the female takes an active role in the proper positioning<br />
of the spermatophore in the bursa copulatrix, and<br />
an intact nerve cord is needed for proper muscular movements<br />
of the female genitalia” (Roth and Stay, 1962a).<br />
Loss of Receptivity during Gestation<br />
Pregnant blaberid females typically do not respond to<br />
courting males. The physical presence of an ootheca in<br />
the brood sac inhibits mating <strong>behavior</strong>, and its removal<br />
leads to the return of receptivity (N. cinerea, Byr. fumigata)<br />
(Roth, 1962, 1964b; Grillou, 1973). The suppression<br />
of receptivity appears to be the direct result of sensory<br />
MATING STRATEGIES 109