The East African decapod crab Neosarmatium meinerti (de Man) sweeps mangrove floors clean of leaf litter.

Leaf litter removal by the abundant mangrove decapod crab Neosarmatium meinerti was studied in series of field and laboratory experiments in East Africa. In the high intertidal Avicennia marina zone crabs buried all leaves placed on the forest floor and consumed on average 67% of them within 2 hrs. High shore crabs in Kenya buried 4 g m(-2) leaf-litter in 1 hr, i.e. approx. twice the daily litter fall. In contrast, in the low shore Sonneratia alba zone, where typical leaf-eating crabs were absent, none of the offered leaves showed signs of herbivory. Leaf choice experiments in the laboratory showed that N. meinerti preferred some species to others. Leaf consumption per gram crab was higher in females than males. The laboratory studies also indicated that crabs could consume substantially more than the average daily litter fall. Video recordings documented frequent fights to gain or retain fallen leaves, suggesting strong competition for leaf litter. Earlier studies indicating that N. meinerti may sweep mangrove forest floors clean of leaf litter are confirmed. In high shore mangroves of East and South Africa where N. meinerti is common, energy flow appears unique: virtually all litter production is retained.

Does the wood-borer Sphaeroma terebrans (Crustacea) shape the distribution of the mangrove Rhizophora mucronata?

Field surveys were conducted to evaluate the occurrence of the isopod borer Sphaeroma terebrans (Crustacea) in aerial roots (prop roots) of the red mangrove Rhizophora mucronata on several different spatial scales (m to 100 km) in East Africa. In 6 out of 17 sites studied in Kenya and on Zanzibar Island, Tanzania, no signs of the isopods were found. When the isopods were present the frequency of infestation was high. Trees in muddy substrates in the lower intertidal, in particular at fringing channels or the open sea, showed high prevalence and intensity of infestation, with large part of their roots damaged or dead. Trees at the upper range of Rhizophora, in sandy and muddy areas, showed no signs of isopod infestation. This pattern recurred in mangrove forests on large spatial scales and there was no indication that island forests differed from the mainland forests. This indicates that sediment characteristics, vertical height in the tidal zone, and direct exposure to incoming water are the major factors controlling the abundance of S. terebrans. The isopod may play an important role in determining the lower intertidal limits of R. mucronata. Trees with numerous dead or nongrowing roots, as result of Sphaeroma attack, are likely to tumble due to a lack of root support and this is most likely to occur along channels at the lower, muddy intertidal. Tumbled trees were frequently observed along channels in the lower, muddy intertidal, but rarely in the mid or high intertidal. Implications for management of mangrove forests are discussed.

Effects of the deposit-feeding benthic bivalve Macoma balthica on meiobenthos.

To evaluate the effects of a deposit-feeding bivalve on meiobenthic assemblage structure in muddy habitats, a laboratory experiment was performed at the Askö Laboratory in the northwestern Baltic proper. Microcosms, surface area 104 cm2, containing a c. 7-cm thick layer of sieved (0.5 mm) sublittoral mud were established in June 1990. Two months later the tellinid bivalve Macoma balthica was added in quantities varying from 0 to 40 individuals per microcosm. After 5 months the effects of the bivalves on the meiofauna were surprisingly small. The density of harpacticoid copepods was lowest (P <0.05) in microcosms containing a high density of M. balthica. It is suggested that competition for food resources was responsible for this pattern. For all other meiofaunal groups, including nematodes which were the most abundant taxon (99%), no significant differences (P>0.05) were observed among treatments. The assemblage structure of the nematodes was similar between treatments. The vertical distribution of both major taxa and nematode species appeared to be unaffected by the presence of the bivalve.

Small-scale spatial distribution of marine meiobenthos: the effects of decaying macrofauna.

To evaluate the effects of decaying animals on small-scale horizontal distribution of meiobenthos in muddy habitats, a laboratory experiment was performed at the Askö Laboratory in the northwestern Baltic Sea. A microcosm (35×55×28 cm) containing a ca. 7-cm thick layer of sieved (0.5 mm) sublittoral mud was established in June 1990. Three months later specimens of the bivalve Macoma balthica were collected and killed in boiling water. The sediment inside the microcosm was implanted with empty shell, empty shell and dead animal or left alone. At the end of the experiment (17 days) visual examination of the microcosm revealed black spots at the sediment surface where dead animals had been implanted. The densities of nematodes, the most abundant group (98%), were not significantly different between areas. However total non-nematode fauna was found in much lower numbers (P<0.01) in the black spot areas. A multivariate analysis (detrended correspondence ordination) of nematode species abundance data separated samples from the black spot areas from the others. Of the 25 nematode species recorded in the microcosm, there was a significant difference between areas for four species. The decaying animals clearly attracted Monhystera disjuncta which was almost 6 times as abundant in the black spot areas compared to control and shell areas. Both the overall dominant species, Leptolaimus elegans and Calomicrolaimus honestus were found in lower numbers in the areas of dead Macoma than in control and shell areas. Sabatieria pulchra was found in lower numbers in the control areas compared to shell and dead animal areas. The overall structure of the nematode assemblage indicated a shift to lower dominance in the dead animal areas and it is speculated that decomposing animal tissue may be of primary importance regarding spatial distribution of meiobenthos.