Morphology and Phylogeny of Three New Loxophyllum Species (Ciliophora,Pleurostomatida) from Mangrove Wetlands of Southern China

Three new pleurostomatid ciliates, Loxophyllum meridionale sp. n., L. salinum sp. n., and L. planum sp. n., isolated from brackish waters of mangrove wetlands in southern China, were investigated using live observation and protargol impregnation. The main characteristic feature of L. meridionale sp. n. is the presence of three contractile vacuoles (CVs) along its dorsal margin. Loxophyllum salinum sp. n. can be identified by the presence of three closely spaced CVs along the ventral margin and 12–15 right and four to six left kineties. Loxophyllum planum sp. n. is characterized by the combination of two macronuclei, a single, subterminal CV, and the absence of cortical granules. Phylogenetic trees based on the small subunit rDNA sequence data recovered Loxophyllum as a monophyletic group within the pleurostomatids. Loxophyllum meridionale sp. n., L. salinum sp. n., and L. planum sp. n. were all nested within the Loxophyllum clade. Based on its ciliary pattern and general morphological features, Loxophyllum asetosum is transferred to the genus Amphileptus and a new combination is suggested: Amphileptus asetosus (Burkovsky 1970) comb. n. [basionym L. asetosum Burkovsky 1970].     

In-situ Tapering of Chalcogenide Fiber for Mid-infrared Supercontinuum Generation

Supercontinuum generation (SCG) in a tapered chalcogenide fiber is desirable for broadening mid-infrared (or mid-IR, roughly the 2-20 μm wavelength range) frequency combs^{1, 2} for applications such as molecular fingerprinting, ³ trace gas detection, ⁴ laser-driven particle acceleration, ⁵ and x-ray production via high harmonic generation. ⁶ Achieving efficient SCG in a tapered optical fiber requires precise control of the group velocity dispersion (GVD) and the temporal properties of the optical pulses at the beginning of the fiber, ⁷ which depend strongly on the geometry of the taper. ⁸ Due to variations in the tapering setup and procedure for successive SCG experiments-such as fiber length, tapering environment temperature, or power coupled into the fiber, in-situ spectral monitoring of the SCG is necessary to optimize the output spectrum for a single experiment.In-situ fiber tapering for SCG consists of coupling the pump source through the fiber to be tapered to a spectral measurement device. The fiber is then tapered while the spectral measurement signal is observed in real-time. When the signal reaches its peak, the tapering is stopped. The in-situ tapering procedure allows for generation of a stable, octave-spanning, mid-IR frequency comb from the sub harmonic of a commercially available near-IR frequency comb. ⁹ This method lowers cost due to the reduction in time and materials required to fabricate an optimal taper with a waist length of only 2 mm.The in-situ tapering technique can be extended to optimizing microstructured optical fiber (MOF) for SCG¹⁰ or tuning of the passband of MOFs, ¹¹ optimizing tapered fiber pairs for fused fiber couplers¹² and wavelength division multiplexers (WDMs), ¹³ or modifying dispersion compensation for compression or stretching of optical pulses.^14-16     

Two new species in the Pichia guilliermondii clade: Pichia caribbica sp. nov., the ascosporic state of Candida fermentati, and Candida carpophila comb. nov

Pichia caribbica sp. nov. (type strain DBVPG 4519, NRRL Y-27274, CBS 9966) is described as the ascosporic state of Candida fermentati, and Candida guilliermondii var. carpophila (type strain DBVPG 7739, NRRL Y-17905, CBS 5256) is elevated to species status as Candida carpophila comb. nov. These new taxa, which are indistinguishable on the basis of conventional taxonomic criteria, differ from one another and from Pichia guilliermondii by low DNA base sequence relatedness, different electrophoretic karyotypes, and nucleotide divergence in domains D1/D2 of 26S rDNA. Pichia caribbica produces one, rarely two, saturn-shaped ascospores in persistent asci. On the basis of molecular criteria, C. carpophila comb. nov., C. fukuyamaensis, and C. xestobii are conspecific, with the name C. carpophila having taxonomic priority.     

Research note: Amorphochlora amoebiformis gen. et comb. nov. (Chlorarachniophyceae)

A chlorarachniophycean alga, Lotharella amoebiformis, which has been classified in the genus Lotharella is placed into a new genus Amorphochlora gen. nov., based on its phylogenetic position, which has been clarified by the recently accumulated molecular phylogenetic information, and the morphological difference between the vegetative cells of the Lotharella species. Following this taxonomic treatment, a new combination Amorphochlora amoebiformis comb. nov., is proposed.     

白蚁菌圃真菌多样性研究进展

白蚁菌圃存在于白蚁巢中,具有硬而脆的多孔结构,是特殊的真菌生存环境。当有白蚁在白蚁巢内活动时,蚁巢伞Termitomyces是菌圃上的优势菌;当白蚁巢被废弃,炭角菌Xylaria成为菌圃上的优势真菌。菌圃中还存在其他微生物如无性型真菌（anamorphic fungi）和酵母等。菌圃中的真菌很多具有潜在药用价值或其他经济价值。从蚁巢伞、炭角菌等主要真菌类群出发,结合分子生态学研究菌圃真菌多样性的方法,综述了白蚁菌圃真菌多样性的研究进展,揭示了目前的研究热点及存在的问题,并针对这些问题提出可能的发展方向。     

A redescription of the marine hypotrichous ciliate, Nothoholosticha fasciola (Kahl, 1932) nov. gen., nov. comb. (Ciliophora: Urostylida) with brief notes on its cellular reorganization and SS rRNA gene sequence

The morphology and infraciliature of the marine hypotrichous ciliate Nothoholosticha fasciola (Kahl, 1932) nov. gen., nov. comb., isolated from mariculture waters near Qingdao, China, are redescribed based on live and protargol-impregnated specimens. Features reported for the first time include the possession of more than 50 macronuclear nodules and details of the infraciliature, i.e. 50–60 adoral membranelles, shortened paroral and endoral membranes, six frontal, one buccal and two to seven transverse cirri, ca. 40 pairs of midventral cirri, ca. 60–120 left and 70–120 right marginal cirri, three dorsal kineties, caudal and frontoterminal cirri absent. In addition, brief details of two stages of cellular reorganization in N. fasciola are supplied and comparisons with some related urostylids based on SS rRNA gene sequence data are reported. The new genus Nothoholosticha is established based primarily on the absence of frontoterminal cirri, which distinctly separates it from similar urostylid genera. Anteholosticha longissima is transferred to Nothoholosticha as N. longissima (Dragesco and Dragesco-Kernéis, 1986) nov. comb. and Holosticha antarctica is transferred to Pseudokeronopsis as P. antarctica (Wilbert and Song, 2008) nov. comb.     

Rediscovery and redescription of the marine peritrichous ciliate Epicarchesium abrae (Precht, 1935) nov. comb. (Protozoa, Ciliophora, Peritrichia)

The morphology, infraciliature and silverline system of the marine peritrichous ciliate, Epicarchesium abrae (Precht, 1935) nov. comb., isolated from an abalone-farming pond off the coast of Qingdao, China, are investigated. E. abrae is characterized by: size of zooid in vivo 68 μm×48 μm on average; macronucleus usually J-shaped; one dorsally-located contractile-vacuole; colony regularly dichotomously branched with 4–16 zooids; total number of transverse silverlines 62–72, from peristome to aboral ciliary wreath 41–47, from aboral ciliary wreath to scopula 21–25; outer kinety of peniculus 3 prolonged and converges with peniculus 1.     

Hierarchy of Attractants for Honey Bee Swarms

Chemical signals influence the selection of potential nest cavities by honey bee reproductive swarms. Attractants for swarms include the odors of old dark honey bee brood combs, odors from noncomb hive materials and propolis, and Nasonov pheromone, the odor released from the Nasonov glands of worker bees. Based on crossover and choice test experiments, swarms were shown to prefer, among otherwise identical cavities, those cavities containing Nasonov pheromone over cavities with only comb or other hive odors, cavities containing old comb over those with only noncomb odors or propolis, and cavities containing noncomb odors or propolis over those without bee or hive odor. Synergy between odors was not observed; that is, comb and/or noncomb hive odors did not enhance the attractiveness of Nasonov pheromone. The data support a model based on a hierarchy of olfactory attractants used by honey bee swarms, in order of highest to lowest: Nasonov pheromone, comb odor, noncomb and propolis odors, and, finally, absence of bee- or hive-produced odor.