Jensen, P.G., Moyse, J . , H~e g , J . & Af-Yahya, H. 1994. Comparative SEM studies of lattice organs: putative sensory structures on the carapace of larvae from Ascothoracida and Cirripedia (Crustacea Maxillopoda Thecostraca).-Acta Zoologica (Stockholm) 75: 125-142.Putative sensory structures, called lattice organs, were studied with scanning electron microscopy from ascothoracid or cypris larvae representing a wide range of families of the Ascothoracida and Cirripedia. These organs, situated dorsally on the carapace were, with few exceptions, always found in two anterior and three posterior pairs. The lattice organ morphology displayed by the Ascothoracida, a seta-like structure with a terminal pore, is believed to be the most plesiomorphic condition. Within the Cirripedia lattice organ morphology varied from types resembling the Ascothoracida in the Acrothoracica and the lepadomorph Capitulum mitella, to an elongate pore field with a larger terminal pore in most Thoracica and Rhizocephala. Akentrogonid Rhizocephala seem to display the most apomorphic condition. While lattice organ morphology was generally constant at the family level, cases were seen where closely related species such as Chthamalus stellatus and Chthamalus montagui showed minor, but clear cut differences.Lattice organs in 2 + 3 pairs are argued to represent a synapomorphy for the Ascothoracida and the Cirripedia. The results confirm that the cyprid morphology at the ultrastructural level will prove to be of high value in estimating phylogeny within the Cirripedia.
We present a cladistic analysis of the Cirripedia Thoracica using morphological characters and the Acrothoracica and Ascothoracida as outgroups. The list of characters comprised 32 shell and soft body features. The operational taxonomic units (OTUs) comprised 26 well‐studied fossil and extant taxa, principally genera, since uncertainty about monophyly exists for most higher ranking taxonomic units. Parsimony analyses using PAUP 3.1.1 and Hennig86 produced 189 trees of assured minimal length. We also examined character evolution in the consensus trees using MacClade and Clados. The monophyly of the Balanomorpha and the Verrucomorpha sensu stricto is confirmed, and all trees featured a sister group relationship between the ‘living fossil Neoverruca and me Brachylepadomorpha. In the consensus trees the sequential progression of ‘pedunculate‘sister groups up to a node containing Neolepas also conforms to current views, but certain well‐established taxa based solely on plesiomorphies stand out as paraphyletic, such as Pedunculata (= Lepadomorpha); Eolepadinae, Scalpellomorpha and Chthamaloidea. The 189 trees differed principally in the position of shell‐less pedunculates, Neoverruca, the scalpelloid Capitulum, and the interrelationships within the Balanomorpha, although the 50% majority rule consensus tree almost fully resolved the latter. A monophyletic Sessilia comprising both Verrucomorpha and Balanomorpha appeared among the shortest trees, but not in the consensus. A tree with a monophyletic Verrucomorpha including Neoverruca had a tree length two steps longer than the consensus trees. Deletion of all extinct OTUs produced a radically different tree, which highlights the importance of fossils in estimating cirripede phylogeny. Mapping of our character set onto a manually constructed cladogram reflecting die most recent scenario of cirripede evolution resulted in a tree length five steps longer than any of our shortest trees. Our analysis reveals that several key questions in cirripede phylogeny remain unsolved, notably the position of shell‐less forms and the transition from ‘pedunculate‘to ‘sessile‘barnacles. The inclusion of more fossil species at this point in our understanding of cirripede phylogeny will only result in even greater levels of uncertainty. When constructing the character list we also identified numerous uncertainties in the homology of traits commonly used in discussing cirripede evolution. Our study highlights larval ultrastructure, detailed studies of early ontogeny, and molecular data as the most promising areas for future research.
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