Abstract

Although generally assumed to be filter feeders, branchiopod crustaceans of the laevicaudatan genus Lynceus O.F. Muller, 1776 possess no filters and do not collect food by filtration. Investigated species of these bivalved, multi-limbed animals have basically benthic habits and collect particulate food, mostly detritus, by scraping or sweeping it from surfaces with suitably armed trunk limbs. L. simiaefacies Harding, 1941, known only from a desert pool in Yemen, has trunk limbs that are armed with particularly robust scrapers and much of the complexity of these limbs and their armature is related to the collection and manipulation of detrital food by mechanical means. Material collected by scrapers borne distally on the more anterior limbs – although the anteriormost is very lightly armed – is swept posteriorly and dorsally, assisted by the armature of the more proximal endites, towards the posterior end of a deep food groove, whence it is passed anteriorly by the substantial gnathobases of the trunk limbs. The necessary movements of the trunk limbs are facilitated by a system of intrinsic muscles that enable individual endites to be moved independently – a remarkable specialized feature of a phyllopodial appendage. Before it enters the food groove, collected material is at all times confined to a narrow median chamber, or cage, between the two sets of opposed trunk limbs that extends over most of the anterior limbs – which are the largest. Each cage wall serves as a screen, covering the limbs of its side and is made up of long setose screening setae that superficially resemble coarse filter setae, and arise from the more proximal endites of most of the anterior trunk limbs. The screens prevent collected material from entering the inter-limb spaces into which water flows during each cycle of trunk limb movements, where its presence would be disastrous. They do not interfere with the spines of the proximal endites that can protrude between them. The screens do not extend to the extreme posterior end of the trunk limb series where a complex and dense array of specialized spines of the short posterior trunk limbs completes the task of sweeping food material into the food groove. Material is passed anteriorly along the food groove by the trunk limb gnathobases and the small but robustly armed maxillules to the mandibles. Although constructed on the basic, boat-like, branchiopod plan, in contrast to those of most particle-feeding branchiopods whose mandibles have a broad masticatory surface, those of Lynceus have a masticatory surface that is narrow and elongate in the antero-posterior plane. Interestingly, while the number of ‘teeth’ into which this surface is elaborated is few in most species of the genus, inviting comparison with a similar attribute in the Notostraca, L. simiaefacies has more numerous, smaller teeth. Although following the branchiopod plan, the mandibular musculature appears to have its own distinctive features but remains to be investigated in properly fixed material. At its distal extremity the oesophagus is differentiated into a small but complex gizzard, of which there appears to be no parallel in any other branchiopod order. This is described for the first time. Although provided with natatory antennae, species of Lynceus also employ their trunk limbs as organs of propulsion. In L. gracilicornis (Packard, 1871) the carapace valves can gape to more than 90°, which allows the trunk limbs to make a contribution to propulsion in a manner akin to that of the Anostraca. In this respect the Laevicaudata appears to stand in contrast to the Spinicaudata, in most species of which the trunk limbs contribute little or nothing to locomotion. More information is needed on representatives of both orders, which have received little study as living animals. Brief comments are made on the systematic position of the Laevicaudata, about which much remains to be resolved. © 2009 The Natural History Museum. Journal compilation © 2009 The Linnean Society of London, Zoological Journal of the Linnean Society, 2009, 155, 513–541.

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