Structure of ovarioles in Adelges laricis, a representative of the primitive aphid family Adelgidae

The structure of ovaries has been analysed in advanced aphids only. In this paper we report the results of ultrastructural studies on the ovarioles of Adelges laricis, a representative of the primitive aphid family, Adelgidae. The ovaries of the studied species are composed of five telotrophic‐meroistic ovarioles that are subdivided into a terminal filament, tropharium (= trophic chamber) and vitellarium. The tropharium houses trophocytes (= nurse cells) and arrested oocytes. The vitellarium consists of one or two ovarian follicles. The total number of germ cells (trophocytes + oocytes) in the ovarioles analysed varies from 50 to 92 and is substantially higher than in previously studied aphids. The centre of the tropharium is occupied by a cell‐free region, termed a trophic core, which is connected both with trophocytes and oocytes. Trophocytes are connected to the core by means of cytoplasmic strands, whereas oocytes by nutritive cords. Both trophic core and nutritive cords are filled with parallel arranged microtubules. In the light of obtained results the anagenesis of hemipteran ovaries is discussed.     

Symbiosome-like intracellular colonization of cereals and other crop plants by nitrogen-fixing bacteria for reduced inputs of synthetic nitrogen fertilizers

It has been forecast that the challenge of meeting increased food demand and protecting environmental quality will be won or lost in maize, rice and wheat cropping systems,and that the problem of environmental nitrogen enrichment is most likely to be solved by substituting synthetic nitrogen fertilizers by the creation of cereal crops that are able to fix nitrogen symbiotically as legumes do. In legumes, rhizobia present intraceliularly in membrane-bound vesicular compartments in the cytoplasm of nodule cells fix nitrogen endosymbiotically. Within these symbiosomes, membrane-bound vesicular compartments, rhizobia are supplied with energy derived from plant photosynthates and in return supply the plant with biologically fixed nitrogen, usually as ammonia. This minimizes or eliminates the need for inputs of synthetic nitrogen fertilizers. Recently we have demonstrated, using novel inoculation conditions with very low numbers of bacteria, that cells of root meristems of maize, rice, wheat and other major non-legume crops, such as oilseed rape and tomato, can be intracellularly colonized by the non-rhizobial, non-nodulating, nitrogen fixing bacterium, Gluconacetobacter diazotrophicus that naturally occurs in sugarcane. G. diazotrophicus expressing nitrogen fixing (nifH) genes is present in symbiosome-like compartments in the cytoplasm of cells of the root meristems of the target cereals and non-legume crop species, somewhat similar to the intracellular symbiosome colonization of legume nodule cells by rhizobia. To obtain an indication of the likelihood of adequate growth and yield, of maize for example, with reduced inputs of synthetic nitrogen fertilizers,we are currently determining the extent to which nitrogen fixation, as assessed using various methods, is correlated with the extent of systemic intracellular colonization by G. diazotrophicus,with minimal or zero inputs.     

Influence of different storage methods on the predatory capacity of the fungi Arthrobotrys robusta and Monacrosporium thaumasium after passage through the bovine gastrointestinal tract

The biological control of helminth parasites of bovines by nematophagous fungi is an alternative to the use of drugs with the principal objective of reducing the source of infection available on pastureland. The maintenance of predatory activity of the fungal isolates is one of the basic prerequisites to ensure the success of this form of control. In this study behaviour of the isolates I31 of Arthrobotrys robusta and NF34a of Monacrosporium thaumasium was investigated following three storage methods: stored at 4 °C, cryopreserved with or without cryoprotectants or preserved in silica gel. All samples were subsequently passed through the gastrointestinal tract of calves. The latter involved the administration of 20 g of mycelia to the animals. This quantity was sufficient to recover fungal material from the faeces. The peak reduction in the number of infective larvae in the faeces occurred 24 h after administration of the samples (P < 0.05). The storage at 4 °C was the treatment that produced the greatest reduction in larvae for NF34a (81.3%) and I31 (65.1%) isolates. Nf34a isolate was responsible for the highest percentage reduction of larval helminth populations (P < 0.05). Cryopreservation appears to be an efficient method of preserving isolates, although diminished predatory capacity compared to storage at 4 °C was seen only for isolate NF34a (73.2%). Cryopreservation did not interfere in predatory activity of I31 isolate (P < 0.05). Maintenance of isolates in silica gel showed the lowest reduction throughout the experiment (P < 0.05).     

The role of natural environments in the evolution of resistance traits in pathogenic bacteria

Antibiotics are among the most valuable compounds used for fighting human diseases. Unfortunately, pathogenic bacteria have evolved towards resistance. One important and frequently forgotten aspect of antibiotics and their resistance genes is that they evolved in non-clinical (natural) environments before the use of antibiotics by humans. Given that the biosphere is mainly formed by micro-organisms, learning the functional role of antibiotics and their resistance elements in nature has relevant implications both for human health and from an ecological perspective. Recent works have suggested that some antibiotics may serve for signalling purposes at the low concentrations probably found in natural ecosystems, whereas some antibiotic resistance genes were originally selected in their hosts for metabolic purposes or for signal trafficking. However, the high concentrations of antibiotics released in specific habitats (for instance, clinical settings) as a consequence of human activity can shift those functional roles. The pollution of natural ecosystems by antibiotics and resistance genes might have consequences for the evolution of the microbiosphere. Whereas antibiotics produce transient and usually local challenges in microbial communities, antibiotic resistance genes present in gene-transfer units can spread in nature with consequences for human health and the evolution of environmental microbiota that are largely ignored.     

不同有机肥影响菠萝生长的生理生化机制

以菠萝品种'澳大利亚卡因'为材料,研究了施用不同有机肥对菠萝长叶期和抽蕾期植株生长量、生理生化指标以及土壤酶活性、微生物等的影响,以探讨不同有机肥对菠萝生长的影响机理.结果显示:(1)在花生麸处理中菠萝株高、青叶数、地上部和根鲜重较对照(施用化肥)提高,而在鸡粪和水肥处理中株高、青叶数、地上部鲜重较对照降低.(2)花生麸处理的菠萝叶片细胞膜透性较对照降低,而叶绿素含量、根系活力以及叶片和根系的可溶性糖、可溶性蛋白含量、SOD活性均较对照提高;鸡粪和水肥处理的叶片细胞膜透性和根系SOD酶活性较对照提高,而叶绿素含量、根系活力、长叶期叶片和根系的可溶性糖含量、长叶期和抽蕾期叶片的可溶性蛋白含量、叶片SOD酶活性均比对照降低.(3)花生麸能提高土壤脲酶、转化酶和过氧化氢酶的活性及土壤微生物数量;鸡粪和水肥能降低土壤脲酶、蛋白酶活性,却能增强土壤转化酶、过氧化氢酶活性,鸡粪使土壤微生物数量增加,水肥使长叶期土壤微生物数量增加,但使抽蕾期的减少.研究表明,施用花生麸能提高菠萝叶绿素含量、根系活力以及叶片和根系的可溶性糖、可溶性蛋白含量,并增强根和叶的SOD活性,同时增加了土壤相关酶活性和微生物数量,从而有效促进菠萝植株生长.     

温度对黑豆蚜体内共生菌胞数量及宿主体型大小的影响

为了明确饲养温度对黑豆蚜Aphis fabae 内共生菌和宿主蚜虫体型大小的影响,对在室内不同温度下饲养的黑豆蚜内共生菌胞数量和宿主蚜虫体型大小进行了观察和统计分析。结果表明,温度对同一发育时期蚜虫内共生菌胞数量的影响在不同温度范围内有所不同,1龄若蚜体内的菌胞数量除在25℃与35℃间有显著差异外,在其余各温度间没有显著差异; 其余时期的蚜虫内共生菌胞数量在高温（> 30℃）下显著低于较低温度下的菌胞数量,存在负直线相关性。温度对菌胞数量随宿主发育到产仔前的变化趋势有不同程度的影响,在较低温度（15℃、20℃和25℃）下,菌胞数量随虫体发育显著增加; 但在高温（30℃和35℃）下,蚜虫体内菌胞数逐渐增加直到3龄达到最高,然后略有下降（30℃）或显著下降（35℃）。除1龄若蚜外,蚜虫体型大小总体呈现随温度升高而降低的格局,但随其内共生菌数量增多而增大（35℃下除外）。据此认为,温度可能通过作用于蚜虫内共生菌胞数量而影响蚜虫体型的大小。     

The release of genetically engineered micro-organisms and viruses into the environment

This review considers the reasons for, and research governing, the regulation and monitoring of genetically engineered micro-organisms and viruses (GEMs) released into the environment. The hazards associated with releasing GEMs into the environment are the creation and evolution of new pests and diseases, and damage to the ecosystem and non target species. The similarities and differences between GEMs and conventional micro-organisms are discussed in relation to risk assessment. Other issues covered include the persistence of micro-organisms in the environment, transgene dispersal to non-engineered microbes and other organisms, the effects of transgenes and transformation on fitness, and the evolution of pests and pathogens that are given or acquire transgenes. Areas requiring further research are identified and recommendations for risk assessment made.