腹毛目纤毛虫皮膜演化的一种特殊形式--卵圆急纤虫无性二分裂期间的形态发生学

对海洋纤毛虫卵圆急纤虫无性分裂过程中的形态发生做了跟踪观察,结果表明,该种的皮膜演化表现了一系列在腹毛目种类中所罕见的特征:1)新老口围带有一临时性汇联为一的阶段;2)左右缘棘毛原基分步出现,即明显的不同步现象;3)大核的改组在细胞分裂开始前即已完成;4)本种后仔虫之棘毛原基的分化既非独立发生又非来自于老结构的反分化,而是紧靠口原基的一侧向外分衍并极可能是孤立地发展而成;5)老的波动膜在形态发生过程中亦无反分化现象,而呈独特的半原基模式.     

Free-living marine nematodes of shrimp culture ponds in Thailand. I. New species of the genera Diplolaimella and Thalassomonhystera (Monhysteridae) and Theristus (Xyalidae)

Three new species belonging to the genera Diplolaimella and Thalassomonhystera of the family Monhysteridae and Theristus of the family Xyalidae are described from shrimp culture ponds near mangrove zones of Khung Kraben Bay, Thailand. Diplolaimella thailandica sp. n. resembles D. dievengatensis but differs from it by features of the ratios b and V, and size of the spicules and tail of the male. Thalassomonhystera siamensis sp. n. resembles T. diplops but differs from it in features of the amphids, ocelli, cloaca and gubernaculum. Theristus (Penzancia) longisetifer sp. n. resembles T. flevensis, T. ambronensis, T. macroflevensis, and T. pratti but differs from them in features of the cervical setae, ventral supplement of the male and others. This revised version was published online in July 2006 with corrections to the Cover Date.     

Nitrogen mineralization by bacterial-feeding nematodes: verification and measurement

Bacterial feeding nematodes excrete N assimilated in excess of that required for growth. Because metabolic and developmental rates differ among nematode species, we hypothesized that their contribution to N mineralization in soil would differ. Sand-column microcosms amended with an organic substrate, bacteria, and with or without bacterial-feeding nematodes, were leached at 3-d intervals. Cumulative N, as NH ₄ ⁺ or NO ₃ ^- , leached from columns containing nematodes was consistently greater than from columns without nematodes. Maximum N-mineralization rates for populations of rhabditid nematodes, which predominated in field soils early in the summer were at lower temperatures than those for cephalobid nematodes, which predominated later in the summer. For an organic substrate with C-to-N ratio of 11:1, rates of N mineralization among species of different body size were similar, ranging between 0.0012 and 0.0058 g-N nematode^-1 d^-1, mainly as NH ₄ ⁺ . Smaller nematodes mineralized more N per unit of body weight than larger nematodes. We hypothesized that at low C-to-N ratios of the organic substrate, bacterial growth is C-limited and N-immobilization will be minimal; at high C-to-N ratios bacterial growth will be N-limited and there may be rapid immobilization of newly-mineralized N. Consequently, net N mineralization in the presence of nematodes will be lower when the organic substrate has a high C-to-N ratio. In experiments with different nematode species, net mineralization and the nematode contribution to mineralization generally decreased with increasing C-to-N ratio, consistent with the hypothesis; however, there were exceptions.     

The Potential of Thiarubrine C as a Nematicidal Agent against Plant- parasitic Nematodes

Thiarubrine C, a polyacetylenic 1,2-dithiin isolated from the roots of Rudbeckia hirta (Asteraceae), exhibited strong nematicidal activity in in vitro and growth chamber assays. Thiarubrine C was toxic, in the absence of light, to the plant-parasitic nematodes Meloidogyne incognita and Pratylenchus penetrans at LC₅₀s of 12.4 ppm and 23.5 ppm, respectively. A minimum exposure time between 12 and 24 hours was the critical period for nematode mortality due to thiarubrine C. Although thiarubrine C was not totally dependent on light for toxicity, activity was enhanced in the presence of light, especially with the microbivorous nematode, Teratorhabditis dentifera. Upon exposure of M. incognita juveniles to 20 ppm thiarubrine C for 1 hour, infection of tomato plants was greatly reduced compared to untreated checks. Thiarubrine C was also effective in reducing plant infection when mixed with soil 24 hours prior to or at planting, unlike other related compounds such as δ-terthienyl.     

Evidence for a Dosage Effect of the Mi gene on Partially Virulent Isolates of Meloidogyne javanica

The reproduction of single egg-mass isolates of Meloidogyne javanica from Crete that differed in virulence were compared on tomato (Lycopersicon esculentum) genotypes homozygous or heterozygous for the Mi gene. The reproduction of three isolates with partial virulence was much greater on tomato genotypes heterozygous for the Mi gene (cultivars Scala, Bermuda, and 7353) than on two homozygous genotypes (F8 inbred lines derived from Scala). The reproduction of a highly virulent isolate on the homozygous and heterozygous genotypes was similar to that on a susceptible cultivar. These results pose questions regarding the nature of partial virulence and indicate a quantitative effect of the Mi gene in relation to such virulence.     

Four acetylcholinesterase genes in the nematode Caenorhabditis elegans

Whereas a single gene encodes acetylcholinesterase (AChE) in vertebrates and most insect species, four distinct genes have been cloned and characterized in the nematode Caenorhabditis elegans. We found that ace-1 (mapped to chromosome X) is prominently expressed in muscle cells whereas ace-2 (located on chromosome I) is mainly expressed in neurons. Ace-x and ace-y genes are located in close proximity on chromosome II where they are separated by only a few hundred base pairs. The role of these two genes is still unknown.

Résumé

À l'inverse de la situation des vertébrés et de la majorité des insectes, chez qui un gène unique code pour l'acétylcholinestérase (AChE), quatre gènes d'AChE ont été clones et caractérisés chez Caenorhabditis elegans. Le gène ace-1 (localisé sur le chromosome X) et le gène ace-2 (chromosome I) assurent respectivement l'expression de l'AChE dans les tissus musculaire (ace-1) et nerveux (ace-2). Les gènes ace-x et ace-y ne sont séparés que de quelques centaines de paires de bases sur le chromosome II et leur rôle est pour l'instant inconnu.     

Control of Root-knot Nematode with Formulations of the Nematode-Trapping FungusArthrobotrys dactyloides

Arthrobotrys dactyloidesgrew readily in shaken flasks containing glucose corn steep powder and 8–10 g dry wt of fungal biomass/liter medium was usually produced in 5–6 days. However, it was difficult to convert this biomass into a viable, granulated product suitable for commercial use in biological control. Formulations prepared using kaolin and vermiculite as carriers and gum arabic as a binder showed poor viability when biomass was harvested from liquid culture, mixed with formulation ingredients, granulated, and then dried to a moisture content of less than 5%. Inclusion of a solid-phase incubation step following granulation and prior to drying (incubation of moist granules for 3 days at 25°C in a sterile plastic bag aerated with sterile air) markedly improved biological activity. When granules produced in this manner were placed on a glass slide in field soil, hyphae proliferated from granules and always produced traps. Seven experiments in soil microcosms showed that formulations which had been subjected to solid phase incubation prior to drying consistently reduced numbers ofMeloidogyne javanicajuveniles by more than 90%. In seven glasshouse experiments in which field soils were treated with granules (10 g/liter) and planted to tomatoes, the number of galls induced by the nematode was reduced by 57–96%.     

Functional analysis of plasma prophenoloxidase system in the marine mussel Perna viridis

The role of prophenoloxidase (proPO) system in recognition and phagocytosis of yeast cells by hemocytes was examined in vitro using whole plasma and proPO system isolated from the plasma of the marine mussel, Perna viridis. The proPO was isolated from the plasma by ammonium sulphate precipitation and gel filtration. The final proPO preparation was homogeneous in native PAGE, and could be activated by trypsin, α-chymotrypsin and pronase-E. Laminarin (a polymer of β-1, 3-glucan) and lipopolysaccharides (LPS) from diverse bacterial species effectively activated the isolated proPO, demonstrating the ability of this proenzyme to interact directly with microbial surface components. The susceptibility of proPO activation to inhibition by serine protease inhibitors such as soybean trypsin inhibitor (STI) or p-nitrophenyl-p′-guanidinobenzoate (p-NPGB), indicates that the isolated fraction may contain an integral serine protease domain in an inactive state. The presence of laminarin- or LPS-activated whole plasma of P. viridis facilitated adherence of yeast cells to hemocyte surface as well as eventually stimulated phagocytic uptake of the target cells by hemocytes, and no such hemocytic response was recorded with STI controls. This and other results strongly suggest that the intermediary factors generated during activation of plasma proPO system by non-self molecules play a key role in recognition and opsono-phagocytosis by hemocytes. However, the proPO system isolated from P. viridis plasma, after activation with microbial surface components, failed to show an opsonic effect.     

Sialic acid in hemolymph and affinity purified lectins from two marine bivalves

Sialic acids have been implicated in a variety of complex biological regulatory and signalling events and their functional importance is reflected by their presence in a wide variety of phyla. Potentially they may inhibit intermolecular and intercellular interactions. Lectins that exhibit specificity for sialic acid or sialoglycoconjugates are ubiquitous in the body fluids of invertebrates and this has supported the assumption that these lectins are involved in defense against microbes that express sialic acids on their surfaces. This biological function has also been inferred from the absence of sialic acids in lower invertebrates. However, most invertebrate lectins are heterogeneous and may also bind other ligands. The biological significance of the different carbohydrate specificities are not yet known. We have demonstrated the presence of sialic acids in hemolymph from two marine bivalves, the Pacific oyster Crassostrea gigas (≈15 μg ml⁻¹) and the horse mussel Modiolus modiolus (48–100 μg ml⁻¹) by several different assays. The sialic acid was mostly in free form. Affinity purified lectins from the horse mussel also contained bound sialic acids (2–5 μmol g⁻¹). Oyster hemolymph stimulated the in vitro phagocytosis of bacteria by oyster hemocytes. The stimulation by hemolymph is facilitated by a dialyzable component, that apparently is active irrespective of the binding to sialic acid (BSM). Addition of sialic acid had no significant effect on the in vitro phagocytosis of bacteria by oyster hemocytes.     

Changes in estuarine nematode communities following a decrease of organic pollution

The response of a nematode community to a decreasing organic matter loading was studied. Monthly observations were made at three stations at an intertidal brackish-water mudflat in the Ems estuary in 1980 (highly polluted), 1987 (moderately polluted) and 1993 (no significant pollution). Nematodes were identified and counted in the upper 1 cm of the sediment.The decrease of organic pollution was followed by an increase in species diversity, whereas numerical densities decreased. Diatom eating nematodes, being dominant under eutrophic conditions in 1980, decreased strongly, partly as a consequence of decreasing diatom standing stock. Eudiplogaster pararmatus, an indicator of organic enrichment, decreased strongly to disappear completely in 1993. Bonger's maturity index was used to describe the response of the nematode community. At 2 most polluted stations a strong response was observed from 1980 to 1987: a decrease of colonizer species. After 1987, although persister species increased, no further development towards a more natural succession type community occurred, probably due to the natural stress of the habitat (high mudflat, low salinities).