A new genus, Alanlewisia, of the family Caligidae is established to accommodate a sea louse species originally, but tentatively, placed in the genus Lepeophtheirus by Lewis (1967). The type species is Alanlewisia fallolunulus (Lewis, 1967) comb. n., which is redescribed in detail based on new material collected from bluespine unicornfish, Naso unicornis (Forsskål), caught off New Caledonia in the South Pacific. This species was originally described by Lewis (1967) under the binomen Lepeophtheirus? fallolunulus from the same host species collected in Hawaii. This species was subsequently transferred to the genus Anuretes by Ho and Lin (2000). Lewis was uncertain of the generic placement primarily because of the possession, in the females only, of paired lunule-like structures on the ventral surface of the modified frontal plates. In both sexes the first swimming leg is biramous, with a well-developed endopod bearing 2 long, sparsely-plumose setae, and the third leg has a 2-segmented exopod. This combination of characters serves to differentiate the new genus from existing genera. Preliminary phylogenetic analysis suggests that the new genus represents an early offshoot from the main caligid lineage, basal to the Paralebion-Tuxophorus-Caligus clade identified by Boxshall and Justine (2005).
Pseudorhabdosynochus seabassi sp. n. (Monogenea: Diplectanidae) from the gill filaments of Lates calcarifer Bloch, a marine teleost fish held in floating sea cages in Guangdong Province, China, is described based on morphological observations and molecular data. The shapes of the male copulatory organs (MCO) of Pseudorhabdosynochus spp. were the focus of this study. The typical proximal part of the MCO in most species of Pseudorhabdosynochus is reniform, heavily sclerotized, and divided into four chambers. However, the new species from L. calcarifer has a bulbous proximal region with four concentric layers of apparent muscular origin, instead of a reniform structure with four compartments. This organ is also different in Diplectanum grouperi Bu, Leong, Wong, Woo et Foo, 1999, being sclerotized, cup-shaped, wide proximally with four concentric muscular layers and tubular distally. The 3' terminal portion of the small subunit ribosomal RNA gene (ssrDNA) and the 5' terminal region (domains C1-D2) of the large subunit ribosomal RNA gene (lsrDNA) were used to reconstruct the phylogenetic relationships of P. seabassi and D. grouperi with related taxa utilizing maximum-parsimony and neighbour-joining methods. Phylogenetic analyses unequivocally placed D. grouperi amongst Pseudorhabdosynochus using either ssrDNA or lsrDNA data. All species of Pseudorhabdosynochus (including D. grouperi) used in this study clustered together, inferring monophyly. Based on molecular phylogenetic evidence, we propose that D. grouperi from Epinephelus coioides Hamilton be transferred to Pseudorhabdosynochus as P. grouperi comb. n.
We studied the survival adaptation strategy of Sophora alopecuroides L. to habitat conditions in an arid desert riparian ecosystem. We examined the responses of heliotropic leaf movement to light conditions and their effects on plant photochemical performance. S. alopecuroides leaves did not show any observable nyctinastic movement but they presented sensitive diaheliotropic and paraheliotropic leaf movement in the forenoon and at midday. Solar radiation was a major factor inducing leaf movement, in addition, air temperature and vapour pressure deficit could also influence the heliotropic leaf movement in the afternoon. Both diaheliotropic leaf movement in the forenoon and paraheliotropic leaf movement at midday could help maintain higher photochemical efficiency and capability of light utilisation than fixed leaves. Paraheliotropic leaf movement at midday helped plants maintain a potentially higher photosynthetic capability and relieve a risk of photoinhibition. Our findings indicated the effective adaptation strategy of S. alopecuroides to high light, high temperature, and dry conditions in arid regions. This strategy can optimise the leaf energy balance and photochemical performance and ensure photosystem II function., C. G. Zhu, Y. N. Chen, W. H. Li, X. L. Chen, G. Z. He., and Obsahuje bibliografii