Radiolaria and Phaeodaria

Polycystina (~400–800 living species and several thousand extinct forms) and Phaeodaria (~400–500 living species) are exclusively marine, open-ocean planktonic protists, most of which possess elaborate siliceous skeletons. The cytoplasm is divided into an internal part (endoplasm) separated from the external, more vacuolated one (ectoplasm) by a perforated membrane – the central capsule. The Polycystina protrude long and slender cytoplasmic projections (axopodia) supported internally by a rigid central rod (axoneme); while the Phaeodria have anetwork ofperipheral finely interconnectedpseudopodia.Afew Polycystina are colonial, but most, as well as all Phaeodaria, are solitary, around 40 μm to almost 2 mm in size. Most polycystine species peak in abundance between 0 and 100 m, whereasphaeodarianstendtolivedeeper,oftenbelow300m.Polycystineshavea rich fossil record dating from the Cambrian and are important for stratigraphic, paleoecologic, and evolutionary studies. The world-wide biogeography and diversity of radiolarians is chiefly governed by water temperature. Radiolarian prey includes bacteria, algae, protozoa, and microinvertebrates. Many surfacedwelling species of Polycystina possess symbiotic algae and photosynthetic cyanobacteria that provide nourishment to the host. Some colonial radiolaria reproduce by binary fission of the central capsules. Sexual reproduction of polycystines or Phaeodaria has not been confirmed, but the release of motile swarmers, likely gametes, has been widely documented. In species with a radial symmetry (Spumellaria) shell-growth is centrifugal, whereas in the Nassellaria the internal cephalic elements and the cephalis appear first. Individual longevity is estimated to range between 2 and 3 weeks and 1–2 months

The Hidden Diversity of Zanclea Associated with Scleractinians Revealed by Molecular Data

Scleractinian reef corals have recently been acknowledged as the most numerous host group found in association with hydroids belonging to the Zanclea genus. However, knowledge of the molecular phylogenetic relationships among Zanclea species associated with scleractinians is just beginning. This study, using the nuclear 28S rDNA region and the fast-evolving mitochondrial 16S rRNA and COI genes, provides the most comprehensive phylogenetic reconstruction of the genus Zanclea with a particular focus on the genetic diversity among Zanclea specimens associated with 13 scleractinian genera. The monophyly of Zanclea associated with scleractinians was strongly supported in all nuclear and mitochondrial phylogenetic reconstructions. Furthermore, a combined mitochondrial 16S and COI phylogenetic tree revealed a multitude of hidden molecular lineages within this group (Clades I, II, III, V, VI, VII, and VIII), suggesting the existence of both host-generalist and genus-specific lineages of Zanclea associated with scleractinians. In addition to Z. gallii living in association with the genus Acropora, we discovered four well-supported lineages (Clades I, II, III, and VII), each one forming a strict association with a single scleractinian genus, including sequences of Zanclea associated with Montipora from two geographically separated areas (Maldives and Taiwan). Two host-generalist Zanclea lineages were also observed, and one of them was formed by Zanclea specimens symbiotic with seven scleractinian genera (Clade VIII). We also found that the COI gene allows the recognition of separated hidden lineages in agreement with the commonly recommended mitochondrial 16S as a DNA barcoding gene for Hydrozoa and shows reasonable potential for phylogenetic and evolutionary analyses in the genus Zanclea. Finally, as no DNA sequences are available for the majority of the nominal Zanclea species known, we note that they will be necessary to elucidate the diversity of the Zanclea-scleractinian association