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. 10.1 Decomposition of logs by Cryptocercus punctulatus,<br />
Mountain Lake Biological Station, Virginia. (A) Frass pile outside<br />
gallery entrance. (B) Small log hollowed and filled entirely<br />
with frass and fecal pellets. Photos by C.A. Nalepa.<br />
pushed to the outside of the logs, no doubt influencing<br />
local populations of bacteria, fungi, and microfauna (Fig.<br />
10.1). The typically substantial body size of these insects<br />
contributes to their impact; some species of Panesthia exceed<br />
5 cm in length (Roth, 1979c). Although these two<br />
taxa are the best known, many cockroach species potentially<br />
influence log decomposition (Table 3.2).<br />
Xeric Habitats<br />
<strong>Cockroache</strong>s are known to participate in the breakdown<br />
of plant organic matter in deserts and other arid and<br />
semiarid landscapes, and have a direct and substantial<br />
impact on nutrient flow. Anisogamia tamerlana is the<br />
main consumer of plant litter in Turkmenistan deserts<br />
(Kaplin, 1995), and cockroaches in the genus Heterogamia<br />
are the most abundant detritivore in the Mediterranean<br />
coastal desert of Egypt. The latter dominate the<br />
arthropod fauna living beneath the canopy of desert<br />
shrubs, with up to 116,000 cockroaches/ha, comprising<br />
82% of the arthropod biomass (Ghabbour et al., 1977;<br />
Ghabbour and Shakir, 1980). The daily food consumption<br />
of An. tamerlana is 17–18% of their dry body mass,<br />
with 57–69% assimilation. Females and juveniles consume<br />
840–1008 g/ha dry plant debris and produce 259–<br />
320 g/ha of excrement (Kaplin, 1995). These cockroaches<br />
improve the status of desert soils via their abundant fecal<br />
pellets, the nitrogen content of which is 10 times that of<br />
their leaf litter food source (El-Ayouty et al., 1978).<br />
Many of the ground-dwelling, wingless cockroaches of<br />
Australia are important in leaf litter breakdown. This is<br />
particularly true in stands of Eucalyptus, where litter production<br />
is high relative to other forest types, leaves decompose<br />
slowly, and more typical decomposers such as<br />
earthworms, isopods, and millipedes are uncommon<br />
(Matthews, 1976). The beautiful Striped Desert Cockroach<br />
Desmozosteria cincta, for example, lives among<br />
twigs and branches at the base of eucalypts (Rentz, 1996).<br />
In hummock grasslands and spinifex, genera such as<br />
Anamesia feed on the dead vegetation trapped between<br />
the densely packed stems (Park, 1990). The litter-feeding,<br />
soil-burrowing Geoscapheini are associated with a variety<br />
of Australian vegetation types ranging from dry sclerophyll<br />
to rainforest, and have perhaps the most potential<br />
ecological impact. First, they drag quantities of leaves,<br />
twigs, grass, and berries down into their burrows, thus<br />
moving surface litter to lower soil horizons. Second, they<br />
deposit excreta deep within the earth. Fecal pellets are<br />
abundant and large; those of Macropanesthia rhinoceros<br />
are roughly the size and shape of watermelon seeds.<br />
Third, burrowing by large-bodied insects such as these<br />
has profound physical and chemical effects on the soil.<br />
Burrows influence drainage and aeration, alter texture,<br />
structure, and porosity, mix soil horizons, and modify<br />
soil chemical profiles (Anderson, 1983; Wolters and<br />
Ekschmitt, 1997). The permanent underground lairs of<br />
M. rhinoceros have plastered walls and meander just beneath<br />
the soil surface before descending in a broad spiral<br />
(Fig. 10.2). The deepest burrows can be 6 m long, reach 1<br />
m below the surface, and have a cross section of 4–15 cm.<br />
Burrows may be locally concentrated; the maximum density<br />
found was two burrows/m 2 , with an average of 0.33/<br />
m 2 (Matsumoto, 1992; Rugg and Rose, 1991).<br />
<strong>Cockroache</strong>s in arid landscapes nicely illustrate two<br />
subtleties of the ecological role of decomposers: first, an<br />
often mutualistic relationship with individual plants, and<br />
second, the key role of gut microbiota. In sparsely vegetated<br />
xeric habitats, the density of cockroaches generally<br />
varies as a function of plant distribution. In deserts,<br />
Polyphagidae are frequently concentrated under shrubs<br />
(Ghabbour et al., 1977), and the burrows of Australian<br />
Geoscapheini are often associated with trees. Macropanesthia<br />
heppleorum tunnels amid roots in Callitris-<br />
Eucalyptus forest, and Geoscapheus woodwardi burrows<br />
are located under overhanging branches of Acacia spp. in<br />
mixed open forest (Roach and Rentz, 1998). Not only are<br />
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