The family Donacidae (Bivalvia: Tellinoidea) in Thai waters

The species belonging to the family Donacidae living in Thailand waters are herein revised. After an exhaustive bibliographical search, 29 nominal species were found from this area. Materials from several institutions and specimens collected during fieldwork in Phuket and the Gulf of Thailand were studied. All the type materials were illustrated and redescribed. Details of the type localities, repositories, habitats and biogeographical distribution are discussed. In addition, some collected specimens and the type materials of the valid species and synonyms are illustrated. Currently, eight valid species are confirmed as living in Thailand waters: Donax (Deltachion) spinosus Gmelin, 1791, Donax (Deltachion) semigranosus (Dunker, 1877), Donax (Dentilatona) incarnatus Gmelin, 1791, Donax (Hecuba) scortum (Linnaeus, 1758), Donax (Latona) cuneatus Linnaeus, 1758, Donax (Latona) faba Gmelin, 1791, Donax (Latona) solidus Spengler, 1798 and Donax (Paraserrula) introradiatus Reeve, 1855. The presence of Donax (Deltachion) semisulcatus Hanley, 1843, Donax brazieri Smith, 1892, Donax (Tentidonax) veruinus Hedely, 1913 and Donax victoris Fischer-Piette, 1942 in Thailand waters remains uncertain. These species have been reported in the study area in the literature, but they were not sampled during this study.Fil: Signorelli, Javier Hernan. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Centro Nacional Patagónico. Instituto de Biología de Organismos Marinos; ArgentinaFil: Printrakoon, Cheewarat. Kasetsart University; Tailandi

Phytochrome Signaling Mechanisms

Phytochromes are red (R)/far-red (FR) light photoreceptors that play fundamental roles in photoperception of the light environment and the subsequent adaptation of plant growth and development. There are five distinct phytochromes in Arabidopsis thaliana, designated phytochrome A (phyA) to phyE. phyA is light-labile and is the primary photoreceptor responsible for mediating photomorphogenic responses in FR light, whereas phyB-phyE are light stable, and phyB is the predominant phytochrome regulating de-etiolation responses in R light. Phytochromes are synthesized in the cytosol in their inactive Pr form. Upon light irradiation, phytochromes are converted to the biologically active Pfr form, and translocate into the nucleus. phyB can enter the nucleus by itself in response to R light, whereas phyA nuclear import depends on two small plant-specific proteins FAR-RED ELONGATED HYPOCOTYL 1 (FHY1) and FHY1-LIKE (FHL). Phytochromes may function as light-regulated serine/threonine kinases, and can phosphorylate several substrates, including themselves in vitro. Phytochromes are phosphoproteins, and can be dephosphorylated by a few protein phosphatases. Photoactivated phytochromes rapidly change the expression of light-responsive genes by repressing the activity of CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1), an E3 ubiquitin ligase targeting several photomorphogenesis-promoting transcription factors for degradation, and by inducing rapid phosphorylation and degradation of Phytochrome-Interacting Factors (PIFs), a group of bHLH transcription factors repressing photomorphogenesis. Phytochromes are targeted by COP1 for degradation via the ubiquitin/26S proteasome pathway