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ABSTRACT: We use sequences from the nuclear ribosomal genes, 18S and 28S to analyze the phylogeny of the Rhizocephala Akentrogonida including two species, Clistosaccus paguri and Chthamalophilus delagei, that are critical for understanding rhizocephalan evolution but have not previously been part of a molecularly based study. In addition we use light and scanning electron microscopy to compare the cypris larvae of C. paguri, Sylon hippolytes and two species of the family Thompsoniidae, since this larval stage offers a suite of characters for analyzing the evolution of these otherwise highly reduced parasites. The Rhizocephala Akentrogonida form a monophyletic group nested within a paraphyletic "Kentrogonida". C. paguri and S. hippolytes are sistergroups confirming the monophyly of the Clistosaccidae that was originally based on similarities in the cypris larvae. We find numerous LM and SEM level similarities between the two species, many of which appear to be correlated with their specialized sexual system, where male cyprids use an antennule to implant cells into the virgin female parasite. Some of these traits are also found in cyprids of the thompsoniid species. We conclude that the special cypris morphology and the implantation of males by antennular penetration was present in the stem species to the Thompsoniidae and the Clistosaccidae and emphasize the power of larval characters in rhizocephalan systematics. C. delagei is a sister group to Boschmaella balani and the two are nested deep within the Akentrogonida. This confirms the monophyly of the Chthamalophilidae and falsifies the theory that C. delagei should represent the most primitive extant rhizocephalan. Instead, chthamalophilid rhizocephalans represent some of the most highly advanced members of the parasitic barnacles.
Experimental Parasitology 09/2009; 125(1):3-12. · 2.12 Impact Factor
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ABSTRACT: Larval development of the parasitic barnacle Heterosaccus
papillosus (Cirripedia: Rhizocephala: Sacculinidae) is described from larvae reared in the laboratory. Lecithotrophic nauplii of H.
papillosus reached the cypris stage in 3·5 days, at 22–23°C. The development included five naupliar and the single cypris stage, thus following the typical pattern in the Rhizocephala Kentrogonida. Like the nauplii of all sacculinids, those of H.
papillosus had a single pigmented nauplius eye, unsegmented frontolateral horns each with two long spines and a tubercle between the furcal rami, but they lack a flotation collar and have no seta on the antennal basipod. The male larvae are larger than female ones, the mean lengths in the two sexes never overlap. The most interesting feature of this species are the morphological differences between the male and female larvae. In the male nauplii III to V the anterior body margin is noticeably convex, that is not characteristic for female larvae. The male cyprid also has a more acuited anterior region, whereas that of the female is rounded.
Journal of the Marine Biological Association of the UK 07/2005; 85(04):921 - 928. · 1.00 Impact Factor
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ABSTRACT: Lattice organs are peculiar chemoreceptors found only in the Crustacea Thecostraca (Facetotecta, Ascothoracida, Cirripedia). In these taxa, five pairs occur in the head shield (carapace) of the terminal larval instar (y-cyprid, ascothoracid larva, cyprid), which is the settlement stage. Lattice organs represent an autapomorphy for the Thecostraca but their evolutionary origin and possible homologues in other Crustacea remain obscure. We have used scanning electron microscopy to describe the setation pattern of the head shield in late nauplii of one species of Ascothoracida, one species of Facetotecta and several species of the Cirripedia Thoracica, Acrothoracica, and Rhizocephala. The naupliar head shield always carries two pairs setae situated anteriorly near the midline. Each of these setae carry a single pore, and positional, structural and ontogenetic evidence show that these setae are homologous in all the examined species and that they represent precursors of the two anterior pairs of lattice organs of the succeeding larval stage, viz., the ascothoracid larva (Ascothoracida), y-cyprid (Facetotecta), and cyprid (Cirripedia). This leads us to infer that lattice organs are among the most highly modified sensilla in all Crustacea and they have in most cases lost all external resemblance to a seta. The nauplii of the Rhizocephala carry an additional three pairs of setae situated more posteriorly on the head shield and they could be precursors of the three posterior pairs of lattice organs. All other species examined lack these posterior setae, except the Facetotecta which have one posteriorly situated pair.
Zoologischer Anzeiger - A Journal of Comparative Zoology.
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ABSTRACT: SEM and light microscopic studies on the larvae of the rhizocephalan barnacles Peltogasterella gracilis and P. sulcata reared in the laboratory revealed the presence of 5 naupliar instars, the newly found stage being instar 3. It resembles instar 2 but is larger and has a body slightly tapering towards the posterior end, a reduced subapical (preaxial) seta on the antennule, and both transverse grooves and a specific denticle ornamentation on the hind body of female larvae. In cultures, the larvae of both species develop into cyprids within 4–5 days after release. Peltogasterella nauplii have a size comparable to that seen in Sacculina and Peltogaster, but they are much smaller than the larvae of the cold-water Briarosaccus. The nauplii of Peltogasterella are lecitotrophic and have limb setation and other feeding structures highly reduced. Peltogasterella nauplii have a cuticular flotation collar encircling the body, but it is very small, delicate, and almost smooth. It therefore differs from the homologous, but much larger, and heavily ornamented flotation collars seen in nauplii of Peltogaster and Briarosaccus. A characteristic feature in Peltogasterella nauplii is the single subterminal seta at the distal end of each frontolateral horn, whereas nauplii of Briarosaccus and Peltogaster have two such setae. The antennulary basipod carries a short additional seta, which represents the only remaining rudiment of gnathobases. Nauplii of Briarosaccus and Peltogaster have a homologous, but significantly longer seta, whereas Sacculina nauplii lack this seta altogether. The nauplii of P. gracilis and P. sulcata are very similar in size and morphology, but those of P. sulcata differ by somewhat longer frontolateral horns and furcal spines. Another distinctive feature of P. gracilis nauplii is the ventral ornamentation of the hind body that shows different pattern at different stages of development and reflects an internal development of segments. This ornamentation is only weakly pronounced in P. sulcata nauplii. Comparison with larval development in Briarosaccus tenellus leads to the conclusion that the rhizocephalan ground pattern comprises six naupliar stages just as in other cirripedes (e.g., Thoracica). Comparison of lattice organ morphology indicates a sister group relationship between the families Peltogastridae and Lernaeodiscidae. Our study highlights the value of SEM revealed larval characters and of characters other than appendage setation as being important in rhizocephalan phylogeny.
Zoologischer Anzeiger - A Journal of Comparative Zoology.
