Rimoportula Distribution, Heterovalvy and Heteropolarity in Hyalosira (Bacillariophyta: Rhabdonematales), with Revision of H. hesperia and Two New Species.

The genus Hyalosira Kützing was recently split and emended based on morphology and molecular phylogeny but many uniseriate taxa could not be resolved. All populations examined in that study had one rimoportula on each valve (i.e., 1 + 1 in the cell). Recent collections from Turkey, Australia, and Micronesia had uniseriate taxa with different numbers of rimoportulae and other new features distinguishing them from all other uniseriate taxa. Two species had two rimoportulae per valve (i.e., 2 + 2) and deep septa, of which one is shown to be Hyalosira hesperia Álvarez-Blanco & S.Blanco, for which we provide a revised description, and the other, from Melbourne and Yap, is proposed as H. pacifica, sp. nov. They are separated by stria density and copula areola density. A third species, from the Great Barrier Reef, H. flexa, sp. nov., is the first Hyalosira found with heterovalvy-including a rimoportula on only one valve (i.e., 1 + 0)-and heteropolarity, including three variously reduced pore fields and the fourth, with the rimoportula, always involved in attachment, essentially a basal pole. A corrected diagnosis of the genus is provided and implications for exploring the functions of rimoportulae are discussed.

Diatom Genus Hyalosira (Rhabdonematales emend.) and Resolution of its Polyphyly in Grammatophoraceae and Rhabdonemataceae with a New Genus, Placosira, and Five New Hyalosira Species.

Hyalosira gene sequences are divided into two clades within different families. We examined authentic material of Hyalosira (isotype material of H. obtusangula, synonymous with H. delicatula) and voucher specimens of published sequences, and pooled our observations of Hyalosira-like taxa from benthic and epizoic habitats in several parts of the globe. The two molecular clades corresponded to two morphological groups, with Hyalosira obtusangula associated with Grammatophoraceae. We emend the description and provide lectotypification for Hyalosira and propose Placosira to encompass the taxa in the other clade, associated with Rhabdonemataceae. We propose that Hyalosira has uniseriate to triseriate striae, sometimes different on valve face and mantle. Copulae in most species had shallow septa, though in one they were moderately deep. All species had girdle bands bearing two rows of areolae separated by a midrib. We name five new species of Hyalosira. Morphologies of taxa in the Placosira clade were superficially similar to Hyalosira but differed in having areolae with ricae, a single row of areolae on the girdle bands, and tubular rimoportulae on the valve-face-mantle junction. Hyalosira hustedtiana Patrick should revert to its original position in Striatella until the appropriate genus can be determined. We emend Rhabdonematales to encompass Rhabdonemataceae, Grammatophoraceae and Tabellariaceae.

Dispersal similarly shapes both population genetics and community patterns in the marine realm.

Dispersal plays a key role to connect populations and, if limited, is one of the main processes to maintain and generate regional biodiversity. According to neutral theories of molecular evolution and biodiversity, dispersal limitation of propagules and population stochasticity are integral to shaping both genetic and community structure. We conducted a parallel analysis of biological connectivity at genetic and community levels in marine groups with different dispersal traits. We compiled large data sets of population genetic structure (98 benthic macroinvertebrate and 35 planktonic species) and biogeographic data (2193 benthic macroinvertebrate and 734 planktonic species). We estimated dispersal distances from population genetic data (i.e., FST vs. geographic distance) and from ß-diversity at the community level. Dispersal distances ranked the biological groups in the same order at both genetic and community levels, as predicted by organism dispersal ability and seascape connectivity: macrozoobenthic species without dispersing larvae, followed by macrozoobenthic species with dispersing larvae and plankton (phyto- and zooplankton). This ranking order is associated with constraints to the movement of macrozoobenthos within the seabed compared with the pelagic habitat. We showed that dispersal limitation similarly determines the connectivity degree of communities and populations, supporting the predictions of neutral theories in marine biodiversity patterns.