Die-back of Phragmites australis: influence on the distribution and rate of sediment methanogenesis

Methanogenesis was measured during the summer of 1994, in sediment coresand bulk samples from a Phragmites australis wetland in northern Jutland,Denmark. We compared sediment from healthy reed and dying-back reed, andan open lagoon resulting from die-back. Cores revealed variability withdepth and between sites, with the highest rates coinciding with layers oforganic gyttja, and negligible methane production from the underlying sandbase. Methanogenesis rates in the lagoon and die back sites were higher(up to 100–150 nmol h^-1 g^-1dry wt. sediment) than in the healthy reed (50–80 nmolh^-1 g^-1), with the highest rates being recordedfrom May to July. At these times, methanogenesis was markedly temperature-limited; samples incubated at 30 °C anon-limiting temperature, gave rates as high as 200–400nmol h^-1 g^-1 for the lagoon and die-backareas and 150 nmol h^-1 g^-1 for the healthyarea. Addition of 8 mM acetate and H₂/CO₂headspace suggested that both acetate-fermenting andCO₂-reducing bacteria were present. Acetate additions suggested some co-limitation by substrate availability, with acetate limitation occurring in the healthy site during July and in the die-back site during August. Lower rates during August, especially in the healthy area, were associated with low water levels which resulted in more oxidized sediments. The data reveal highly variable methanogenesis in the sediment which, when considered with sediment depths, indicates that sites of Phragmites die-back have significantly greater rates of anaerobic mineralization than surrounding healthy wetland, and may be intense sources of methane.     

Catchment- and site-scale influences of forest cover and longitudinal forest position on the distribution of a diadromous fish

1. The hydrologic connectivity between landscape elements and streams means that fragmentation of terrestrial habitats could affect the distribution of stream faunas at multiple spatial scales. We investigated how catchment‐ and site‐scale influences, including proportion and position of forest cover within a catchment, and presence of riparian forest cover affected the distribution of a diadromous fish. 2. The occurrence of koaro (Galaxias brevipinnis) in 50‐m stream reaches with either forested or non‐forested riparian margins at 172 sites in 24 catchments on Banks Peninsula, South Island, New Zealand was analysed. Proportions of catchments forested and the dominant position (upland or lowland) of forest within catchments were determined using geographical information system spatial analysis tools. 3. Multivariate analysis of variance indicated forest position and proportion forested at the catchment accounted for the majority of the variation in the overall proportion of sites in a catchment with koaro. 4. Where forest was predominantly in the lower part of the catchments, the presence of riparian cover was important in explaining the proportion of sites with koaro. However, where forest was predominantly in the upper part of the catchment, the effect of riparian forest was not as strong. In the absence of riparian forest cover, no patterns of koaro distribution with respect to catchment forest cover or forest position were detected. 5. These results indicate that landscape elements, such as the proportion and position of catchment forest, operating at catchment‐scales, influence the distribution of diadromous fish but their influence depends on the presence of riparian vegetation, a site‐scale factor.     

Is Blepharisma hyalinum Truly Unpigmented?1

ABSTRACT. To answer whether Blepharisma hyalinum is truly unpigmented, the organism must be established in culture as pointed out by Giese in 1973. Accordingly, the present study deals with B. hyalinum kept in culture since its isolation in 1975. The organism still remains colorless after growth in the dark; however, it contains cortical granules resembling pigment granules in colored species. A comparative study was therefore undertaken of B. hyalinum and B. steini; both species have a compact macronucleus, though of different shape. Crude pigment was extracted with acetone from organisms grown in the dark for three weeks and the maxima were measured by absorption. Purified pigment was obtained from TLC-plate preparations and the absorption maxima were measured after removal of lipids with chloroform. No maxima characteristic of blepharismin were found in extracts of B. hyalinum, but these were present in extracts of B. steini. Electron microscopy of the cortical region revealed membrane-bound granules in both species; these granules differed in content but not in their capacity to extrude. In B. hyalinum all granules had a homogenous electron-dense substructure; in B. steini the granules had a net-like granulated substructure of varying electron density. This difference corresponds to that published on “pigment” granules in albino and pigmented strains of B. undulans. Our conclusions are that B. hyalinum is unpigmented (and a valid separate species) and that the cortical granules may serve other functions than that of storing blepharismin.     

Morphology and Morphogenesis of Fuscheria terricola n. sp. and Spathidium muscorum (Ciliophora: Kinetofragminophora)1

The morphology and morphogenesis of the kinetofragminophoran soil ciliates, Fuscheria terricola n. sp. and Spathidium muscorum Dragesco & Dragesco-Kerneis, 1979, are described. Stained specimens (protargol) are characterized biometrically. The new species differs from the other species of the genus in its body size, body shape, number of kineties, length of extrusomes, and habitat. Both species have telokinetal stomatogenesis, which commences with a proliferation of kinetosomes at those kineties which bear the brosse. Fuscheria terricola does not have a complex perioral ciliature; indeed, it might be that this species has only monokinetids. Thus only a proliferation of kinetosomes and the separation of the kineties takes place in the prospective division furrow. In contrast, S. muscorum differentiates short dikinetid kinetofragments in the region of the division furrow, which are arranged to form the perioral kinety of the opisthe in the intermediate and late stages of the stomatogenesis. The right part of the perioral kinety develops first. This and other studies show that telokinetal stomatogenesis proceeds very differently depending on the differentiation of the oral ciliature; however, detailed studies on the morphogenesis of kinetofragminophoran ciliates are still too few in number for subtypes to be defined.     

Effects of Some Chemicals on the Oxygen Evolution and Oxygen Uptake in Isolated Wheat Chloroplasts Irradiated without the Addition of an Oxidant

The oxygen exchange, obtained when isolated chloroplasts of Triticum aestivum, wheat, are irradiated without the addition of a Hill oxidant has been investigated using an oxygen electrode. Ascorbate, catalase, 2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone(DBMIB), diethyldithio-carbamate (DEDT), dichlorophenylmethylurea (DCMU), and potassium cyanide were added to the Chloroplasts in order to investigate the oxygen exchange. At least two oxygen uptake reactions, one sensitive to catalase and one catalase-insensitive, appeared upon irradiation. Hydrogen peroxide was the product of the oxygen uptake in the former process, and water was the reductant. The formation of hydrogen peroxide was probably associated with photosystem I. The other oxygen consuming reaction was found to be insensitive to both catalase and potassium cyanide. After the chloroplasts had been treated with DCMU, it was possible to show that the catalase-insensitive oxygen uptake was localized in photosystem I, and that a cyclic electron transport system or some endogenous reductant (-s) acted in the oxygen uptake. Addition of ascorbate or DEDT to the chloroplasts led to an enhanced oxygen uptake in 710 nm light. This was probably due to the effect of these compounds on the superoxide radical ion formed in photosystem I. The stimulated oxygen uptake was only weakly affected by catalase, indicating that hydrogen peroxide was not a product of this oxygen uptake. Addition of DEDT and potassium cyanide inhibited (strongly respectively weakly) the oxygen uptake when photosystem II was functioning. The effect of these compounds was probably due to an inhibition of the electron transport at the plastocyanin. DBMIB inhibited the oxygen uptake reactions and the cooperation between the two photosystems. The cooperation between the photosystems was also studied in DCMU-treated chloroplasts. The reactions in photosystem II, measured as oxygen evolution, were more inhibited than the coupling between the photosystems. The oxygen “gush” appearing upon irradiation in light of 650 nm was not affected by a DBMIB-treatment, showing that the oxygen evolution was due to the reduction of plastoquinone. The reoxidation in the dark of the plastoquinone pool was stimulated by DBMIB and potassium cyanide indicating that an oxygen uptake could be associated with plastoquinone. The sites of interaction of oxygen with the electron transport pathways in chloroplasts, and the different reductants for the oxygen consuming reactions are discussed.     

Initiation of Mammalian Viral Protein Synthesis

CULTURED human cells (KB) infected with human adenovirus type 2 (Ad 2) provide a model system for protein synthesis in mammalian cells. Adenovirus messenger RNA molecules are transcribed from nuclear viral DNA and transported to the cytoplasm for translation¹. Late after infection (18 h) 9–10 viral mRNA species with sedimentation values of 7S to 32S are present in polysomes (Parsons, Gardner and Green, in preparation) and specify eight viral structural proteins which account for 80–90% of the polypeptides synthesized in vivo^2–4. We now describe an in vitro cell-free system, derived from KB cells infected with Ad 2, which synthesizes 8–9 viral polypeptides and can initiate protein synthesis with a special class of yeast methionyl-tRNA. In vivo and in vitro experiments suggest that methionine is the initiator amino-acid for most, if not all, adenovirus structural proteins.