Aphrodita

Abstract: Speciation by host shift is one of the explicit models of ecological speciation. A prerequisite of this model is the formation of host races (sympatric populations that show host-specific genetic structuring and phenotypes). Many members of the diverse marine bivalve superfamily Galeommatoidea have obligate commensal relationships with invertebrate hosts. Some species have the ability to occupy multiple host species, thereby providing potential opportunities to test for the formation of host races. The Northeast Pacific galeommatoidean Neaeromya rugifera attaches to two strikingly different hosts: the blue mud shrimp Upogebia pugettensis and the polychaete sea mouse Aphrodita spp. We tested if this host difference has resulted in the formation of host races using shell morphologies and genetic markers. We found that populations from different hosts differ significantly in shell morphology. However, based on mitochondrial makers, N. rugifera showed no distinct host-specific genetic structuring, indicating the existence of a panmictic population. We conclude that the host-specific morphologies these clams exhibit may reflect ecophenotypic plasticity rather than the existence of host races, but this needs to be corroborated with additional genetic data and larger sample sizes. The pronounced conchological variation within N. rugifera calls for further investigation of its taxonomic relationship with its poorly studied, but morphologically similar, sympatric congener Neaeromya compressa.

Abstract: A recent review of polychaete diets (Fauchald & Jumars, 1979) considered aphroditids to be slow-moving carnivores, taking microscopic prey if nothing else is available but specializing in slow-moving or sessile prey. This opinion was based on remarks by Day (1967) and on two documented gut analyses of Aphrodita aculeata (Blegvad, 1914; Hunt, 1925). Other reports in the literature were either derived from these few original statements or else gave unsubstantiated accounts of the type of food taken.In 1964 the late Gunnar Thorson told me that he had seen a specimen of A. aculeata swallowing a large Nereis virens and likened it to a hedgehog eating a snake. This vivid analogy puts Aphrodita in a rather different light, as an active predator capable of dealing with relatively large, powerful prey. In fact Hunt (1925) had recorded remains of ‘Pectinaria, Lumbriconereis, Polynoidae and Nereidae’ in 24 out of 26 specimens containing food. Very young crabs and hermit crabs were recorded in five guts and a nemertean in one. Blegvad (1914) recorded the chief food to be other worms, especially sabellids and terebellids, besides nemerteans, from examination of 50 specimens, 35 of which were empty.I have kept A. aculeata, obtained from Millport and from Plymouth, in bowls containing several centimetres depth of beach sand in a closed-circuit sea-water system. Worms without sand took no interest in items offered as food, neither did worms which had emerged from the sand and were wandering over the surface, but buried worms fed readily. A variety of living animals was given as potential food including Macoma balthica, Corophium volutator, Nephtys hombergi and Nereis diversicolor.

Abstract: Based on type material and additional specimens the review of the genera Aphrodita Linnaeus, 1758 and Aphroditella Roule, 1898 presented here comprises all species reported from the North East Atla...