小青杨组织营养品质和舞毒蛾幼虫生长对大气CO2浓度升高的响应

利用开顶式气室研究了1年生小青杨绿叶、细根、粗根和树皮内营养成分对CO2浓度升高的响应,并检验了上树取食的舞毒蛾幼虫的生长反应.结果表明：CO2浓度升高环境下小青杨绿叶、细根、树皮和粗根中的氮含量显著降低,绿叶、树皮和粗根中的碳氮比显著增加,但细根中碳氮比增加未达到显著水平;CO2浓度升高对所有杨树组织的总碳含量均无影响;CO2浓度升高显著增加了绿叶中总可溶性糖和总非结构碳水化合物的浓度,而绿叶淀粉含量仅在部分采样日期发生显著增加,除细根可溶性糖含量在CO2浓度升高处理下降低外,根系和树皮中各碳水化合物指标的浓度均未发生显著变化;CO2浓度升高环境下2龄舞毒蛾幼虫上树取食13d后体重显著低于自然CO2浓度处理下幼虫的体重,但幼虫继续在各自的实验处理下取食11d后,体重未表现出显著性差异.大气CO2浓度升高对杨树各组织内的营养成分含量均有影响,绿叶营养品质变差可能是导致低龄舞毒蛾幼虫生长受抑制的主要原因.     

Impact of viral enhancin genes on potency of Lymantria dispar multiple nucleopolyhedrovirus in L. dispar following disruption of the peritrophic matrix

Enhancins are metalloproteases found in many betabaculoviruses and several alphabaculoviruses, which enhance alphabaculovirus potency by degrading a protein component of the peritrophic matrix (PM), facilitating passage of virions through this structure. Earlier studies on betabaculovirus enhancins within heterologous systems suggested that enhancins facilitate virion binding to midgut cells. We compared the potency of wild-type Lymantria dispar multiple nucleopolyhedrovirus (LdMNPV) with that of single and double enhancin deletion viruses in L. dispar in the presence and absence of an intact PM. Compared to wild-type virus, the double enhancin deletion virus was 6-fold and 14-fold less potent, respectively, indicating that within this homologous system the LdMNPV enhancin genes have a function beyond PM degradation.     

大气CO2浓度升高对不同施氮土壤酶活性的影响

利用中国唯一的无锡FACE（Free-air CO₂ enrichment,开放式空气CO₂浓度升高）平台,研究了大气CO₂浓度升高对土壤β-葡糖苷酶、转化酶、脲酶、酸性磷酸酶、β-氨基葡糖苷酶的影响。研究发现,不同氮肥处理下大气CO₂浓度升高对某些土壤酶活性的影响不同。在低氮施肥处理中,大气CO₂浓度升高显著降低β-葡糖苷酶活性,但是在高氮施肥处理下,大气CO₂浓度升高显著增加β-葡糖苷酶活性。在低氮和常氮施肥处理中大气CO₂浓度升高显著增加了土壤脲酶活性,但在高氮水平下影响不显著。在低氮、常氮施肥处理中,大气CO₂浓度升高对土壤酸性磷酸酶活性没有影响,而在高氮施肥处理中显著增强了土壤中磷酸酶活性。大气CO₂浓度升高对土壤转化酶活性和β-氨基葡糖苷酶的活性有增加趋势,但影响不显著。研究还发现,在不同的CO₂浓度下,土壤酶活性对不同氮肥处理的响应也不同。在正常CO₂浓度下,土壤中β-葡糖苷酶活性随着氮肥施用量的增加而降低,而在大气CO₂浓度升高条件下,却随着氮肥施用量的增加而增加。在大气CO₂浓度升高条件下,高氮施肥显著增加了转化酶和酸性磷酸酶活性,而在正常CO₂浓度下,影响不显著。在大气CO₂浓度升高条件下,氮肥处理对脲酶活性的影响不大,但在正常CO₂浓度下,脲酶活性随着氮肥施用量的增加而增加。氮肥对β-氨基葡糖苷酶活性的影响不明显。     

Plant respiration and elevated atmospheric CO2 concentration: cellular responses and global significance

BACKGROUND: Elevated levels of atmospheric [CO2] are likely to enhance photosynthesis and plant growth, which, in turn, should result in increased specific and whole-plant respiration rates. However, a large body of literature has shown that specific respiration rates of plant tissues are often reduced when plants are exposed to, or grown at, high [CO2] due to direct effects on enzymes and indirect effects derived from changes in the plant's chemical composition. SCOPE: Although measurement artefacts may have affected some of the previously reported effects of CO2 on respiration rates, the direction and magnitude for the effects of elevated [CO2] on plant respiration may largely depend on the vertical scale (from enzymes to ecosystems) at which measurements are taken. In this review, the effects of elevated [CO2] from cells to ecosystems are presented within the context of the enzymatic and physiological controls of plant respiration, the role(s) of non-phosphorylating pathways, and possible effects associated with plant size. CONCLUSIONS: Contrary to what was previously thought, specific respiration rates are generally not reduced when plants are grown at elevated [CO2]. However, whole ecosystem studies show that canopy respiration does not increase proportionally to increases in biomass in response to elevated [CO2], although a larger proportion of respiration takes place in the root system. Fundamental information is still lacking on how respiration and the processes supported by it are physiologically controlled, thereby preventing sound interpretations of what seem to be species-specific responses of respiration to elevated [CO2]. Therefore the role of plant respiration in augmenting the sink capacity of terrestrial ecosystems is still uncertain.     

Virulence and fitness of the fungal pathogen Entomophaga maimaiga in its host Lymantria dispar, for pathogen and host strains originating from Asia, Europe, and North America

In this study, we tested (1) whether non-North American gypsy moth strains are susceptible to North American isolates of Entomophaga maimaiga and (2) the potential for erosion in the efficacy of E. maimaiga in controlling gypsy moth. We used bioassays to assess the variability in virulence (measured as time to death) as well as fitness of the pathogen (measured as spore production) in four gypsy strains challenged with six E. maimaiga isolates, using host and pathogen strains originating from Asia, Europe, and North America. We found that all E. maimaiga isolates tested were pathogenic to all strains of Lymantria dispar, regardless of the geographical origin of the fungal isolate, with at least 86% mortality for all combinations of fungal isolate and gypsy moth strain. We therefore conclude that Asian gypsy moths are susceptible to North American strains of E. maimaiga. No significant interactions between fungal isolates and gypsy moth strains with regard to time to death were found, indicating that each fungal isolate had the same overall effect on all the gypsy moth strains tested. However, fungal isolates differed significantly with regard to virulence, with a Russian isolate being the slowest to kill gypsy moth (5.1+/-0.1 days) and a Japanese isolate being the overall fastest to kill its host (4.0+/-0.1 days). Fungal isolates also differed in fitness, with variability in types of spores produced. These differences in virulence and fitness were, however, not correlated with geographical origin of the fungal isolate. Gypsy moth strains had no or only little effect on fungal virulence and fitness. Based on our studies with laboratory-reared gypsy moth strains, erosion of successful control of gypsy moth by E. maimaiga seems unlikely.     

Horizontal and vertical transmission of a Nosema sp. (Microsporidia) from Lymantria dispar (L.) (Lepidoptera: Lymantriidae)

The gypsy moth, Lymantria dispar L. (Lepidoptera, Lymantriidae), a serious defoliator of deciduous trees, is an economically important pest when population densities are high. Outbreaking populations are, however, subject to some moderating influences in the form of entomopathogens, including several species of microsporidia. In this study, we conducted laboratory experiments to investigate the transmission of an unusual Nosema sp. isolated from L. dispar in Schweinfurt, Germany; this isolate infects only the silk glands and, to a lesser extent, Malpighian tubules of the larval host. The latent period ended between 8 and 15 days after oral inoculation and spores were continuously released in the feces of infected larvae until pupation. Exclusion of feces from the rearing cages resulted in a 58% decrease in horizontal transmission. The silk of only 2 of 25 infected larvae contained microsporidian spores. When larvae were exposed to silk that was artificially contaminated with Nosema sp., 5% became infected. No evidence was found for venereal or transovum (including transovarial) transmission of this parasite.     

Quantifying horizontal transmission of Nosema lymantriae, a microsporidian pathogen of the gypsy moth, Lymantria dispar (Lep., Lymantriidae) in field cage studies

Nosema lymantriae is a microsporidian pathogen of the gypsy moth, Lymantria dispar that has been documented to be at least partially responsible for the collapse of L. dispar outbreak populations in Europe. To quantify horizontal transmission of this pathogen under field conditions we performed caged-tree experiments that varied (1) the density of the pathogen through the introduction of laboratory-infected larvae, and (2) the total time that susceptible (test) larvae were exposed to these infected larvae. The time frame of the experiments extended from the early phase of colonization of the target tissues by the microsporidium to the onset of pathogen-induced mortality or pupation of test larvae. Upon termination of each experiment, the prevalence of infection in test larvae was evaluated. In the experiments performed over a range of pathogen densities, infection of test larvae increased with increasing density of inoculated larvae, from 14.2 ± 3.5% at density of 10 inoculated per 100 larvae to 36.7 ± 5.7% at 30 inoculated per 100 larvae. At higher densities, percent infection in test larvae appeared to level off (35.7 ± 5.5% at 50 inoculated per 100 larvae). When larval exposure to the pathogen was varied, transmission of N. lymantriae did not occur within the first 15 d post-inoculation (dpi) (11 d post-exposure of test larvae to inoculated larvae). We found the first infected test larvae in samples taken 20 dpi (16 d post-exposure). Transmission increased over time; in the cages sampled 25 dpi (21 d post-exposure), Nosema prevalence in test larvae ranged from 20.6% to 39.2%.     

Intrastadial developmental resistance of third instar gypsy moths (Lymantria dispar L.) to L. dispar nucleopolyhedrovirus

Gypsy moth larvae become increasingly resistant to lethal infection by the Lymantria dispar M nucleopolyhedrovirus (LdMNPV) as they age within the fourth instar. Newly molted larvae are most sensitive to infection, mid-instars are least sensitive, and late-instars display intermediate sensitivity. This resistance occurs whether the virus is delivered orally or intrahemocoelically. The present study reveals a nearly identical pattern of resistance in third instar larvae. An LD₄₈ dose of polyhedra for newly molted third instars produced 18%, 10%, 8%, 25%, and 24% mortalities in larvae to which virus was orally administered at 12, 24, 48, 72, and 96 hours post-molt (hpm), respectively, which is a 6-fold reduction in mortality between newly molted larvae and mid-instars. An LD₄₄ dose of budded virus for newly molted third instars produced 33%, 23%, 17%, 31%, and 31% mortalities when injected into larvae that were 12, 24, 48, 72, and 96 hpm, respectively, which is a 2.6-fold reduction in mortality between newly molted larvae and mid-instars, indicating that approximately half of this resistance is midgut-based and half is systemically based. Doubling the viral dose did not overcome developmental resistance whether the virus was delivered orally or intrahemocoelically. In addition, time to death was significantly affected by the time post-molt at which the insect was inoculated with the virus. We suggest that intrastadial developmental resistance may affect both the ecology and management of the gypsy moth.     

Microsporidian infections in Lymantria dispar larvae: interactions and effects of multiple species infections on pathogen horizontal transmission

The interactions in multiple species infections and effects on the horizontal transmission of three microsporidian species, Vairimorpha disparis, Nosema lymantriae and Endoreticulatus schubergi, infecting Lymantria dispar were evaluated in the laboratory. Simultaneous and sequential inoculations of host larvae were performed and the resulting infections were evaluated. Test larvae were exposed to the inoculated larvae to measure horizontal transmission. Dual species infections demonstrated interspecific competition between Nosema and Vairimorpha in the host larvae, but no observable competition occurred between Endoreticulatus and either of the other microsporidian species. Timing of inoculation was an important factor determining the outcome of competition between Nosema and Vairimorpha. The species inoculated first showed a higher rate of successful establishment; a time lag of 7 days between inoculations allowed the first species to essentially exclude the second. The microsporidia differed in efficiency of horizontal transmission. Nosema and Endoreticulatus were transmitted at very high rates, close to 100%. Horizontal transmission of Vairimorpha was less efficient, ranging from 25% to a maximum of 75%. The patterns of infection observed in inoculated larvae were reflected in the test larvae that acquired infections in the horizontal transmission experiments. Competition with Vairimorpha suppressed horizontal transmission of Nosema after simultaneous and sequential inoculation. In simultaneous inoculation experiments Endoreticulatus had no effect on transmission of Nosema and Vairimorpha.     

Acclimation of nitrogen uptake capacity of rice to elevated atmospheric CO2 concentration

Background and Aims: Nitrogen (N) is a major factor affecting yield gain of cropsunder elevated atmospheric carbon dioxide concentrations [CO₂].It is well established that elevated [CO₂] increases root mass,but there are inconsistent reports on the effects on N uptakecapacity per root mass. In the present study, it was hypothesizedthat the responses of N uptake capacity would change with theduration of exposure to elevated [CO₂]. Methods: The hypothesis was tested by measuring N uptake capacity inrice plants exposed to long-term and short-term [CO₂] treatmentsat different growth stages in plants grown under non-limitingN conditions in hydroponic culture. Seasonal changes in photosynthesisrate and transpiration rate were also measured. Key Results: In the long-term [CO₂] study, leaf photosynthetic responsesto intercellular CO₂ concentration (Ci) were not affected byelevated [CO₂] before the heading stage, but the initial slopein this response was decreased by elevated [CO₂] at the grain-fillingstage. Nitrate and ammonium uptake capacities per root dry weightwere not affected by elevated [CO₂] at panicle initiation, butthereafter they were reduced by elevated [CO₂] by 31–41% at the full heading and mid-ripening growth stages. In theshort-term study (24 h exposures), elevated [CO₂] enhanced nitrateand ammonium uptake capacities at the early vegetative growthstage, but elevated [CO₂] decreased the uptake capacities atthe mid-reproductive stage. Conclusions: This study showed that N uptake capacity was downregulated underlong-term exposure to elevated [CO₂] and its response to elevated[CO₂] varied greatly with growth stage.     

CO2浓度升高与氮沉降对南亚热带森林生态系统植物生物量积累及分配格局的影响

 CO₂浓度升高与氮沉降增加对陆地生态系统的耦合作用已成为全球变化的研究热点。应用大型开顶箱(OTC)人工控制手段研究了人工生态系统在1)高CO₂(700±20 μmol·mol^–1)+高氮沉降(100 kg N·hm^–2·a^–1)(CN); 2)高CO₂(700±20 μmol·mol^–1)+背景氮沉降(C＋); 3)高氮沉降(100 kg N· hm^–2·a^–1)＋背景CO₂(N＋); 4)背景CO₂＋背景氮沉降处理(CK) 4种处理条件下荷木 (Schima superba)、红锥(Castanopsis hystrix)、海南红豆(Ormosia pinnata)、肖蒲桃(Acmena acuminatissima)、红鳞蒲桃(Syzygium hancei)等主要南亚热带森林植物的生物量积累模式及其分配格局。连续近3年的实验结果表明: 不同处理条件下, 各参试植物生物量积累具有不同的响应特征, N＋处理显著促进荷木、肖蒲桃及红鳞蒲桃生物量的积累; C＋处理显著促进肖蒲桃、海南红豆生物量的积累; CN处理显著促进除红锥外其他物种生物量的积累, 并且具有两者单独处理的叠加效应。不同处理改变物种生物量的分配模式, N＋处理降低植物的根冠比, 促进地上部分生物量的积累; C＋处理增加红锥和红鳞蒲桃地下部分生物量的分配, 却促进荷木和海南红豆地上部分的积累; CN处理仅促进红磷蒲桃地下部分的积累。群落生物量的积累与分配格局取决于优势物种的生物量及其分配格局在群落中所占的权重。     

CO2浓度升高条件下内生真菌感染对宿主植物的生理生态影响

以内蒙古草原常见伴生种、感染内生真菌的天然禾草羽茅为研究对象,通过比较不同CO₂浓度和不同养分供应条件下,带内生真菌和不带菌植物在种子发芽和幼苗生长等方面的差异,探讨带内生真菌的天然禾草对CO₂浓度增加的响应。结果表明:CO₂浓度增加对带菌种子发芽率和发芽速度均无显著影响,但CO₂浓度增加显著降低了不带菌种子的发芽率和发芽速度,即CO₂浓度升高加大了带菌和不带菌种子发芽率之间的差异;内生真菌感染显著提高了宿主植物的最大净光合速率和水分利用效率;羽茅的营养生长受CO₂浓度和养分供应的交互影响,高CO₂浓度对生长的促进作用只出现在充足养分供应条件下;CO₂浓度升高和内生真菌感染对植物根系形态有显著的交互作用,在正常CO₂浓度下,带菌植株根径>1.05 mm的根系比例显著高于不带菌植株,随着CO₂浓度的升高,带菌植株上述根径根系所占比例无显著变化而不带菌植株所占比例显著升高,CO₂浓度升高导致带菌和不带菌不同根径根系分配之间的差异缩小。     

Deposition and germination of conidia of the entomopathogen Entomophaga maimaiga infecting larvae of gypsy moth,Lymantria dispar

Germination of conidia of Entomophaga maimaiga, an important fungal pathogen of gypsy moth, Lymantria dispar, was investigated on water agar and larval cuticle at varying densities. Percent germination was positively associated with conidial density on water agar but not on larval cuticle. When conidia were showered onto water agar, the rate of germination was much slower than on the cuticle of L. dispar larvae. From the same conidial showers, the resulting conidial densities on water agar were much higher than those on larval cuticle in part because many conidia adhered to setae and did not reach the cuticle. A second factor influencing conidial densities on larval cuticle was the location conidia occurred on larvae. Few conidia were found on the flexible intersegmental membranes in comparison with the areas of more rigid cuticle, presumably because conidia were physically dislodged from intersegmental membranes when larvae moved. Conidia were also exposed to heightened CO(2) to evaluate whether this might influence germination. When conidia on water agar were exposed to heightened CO(2) levels, germinating conidia primarily formed germ tubes while most conidia exposed to ambient CO(2) rapidly formed secondary conidia.     

大气CO２倍增对植物根内AMF群落的影响

采用环境控制生长室控制CO_２浓度的方法,研究了CO_２浓度（350～400μmol mol^－１和680～750μmol mol^－１对植物根内丛枝菌根真菌（arbuscular mycorrhizal fungi, AMF）群落的影响。12种宿主植物于CO_２浓度不同的生长室栽培180d后收获取样,通过CTAB法提取共生菌根内丛枝菌根真菌的DNA,由特异引物U1/U2扩增编码核糖体28S大亚基的rDNA部分序列,并进行DGGE电泳分析。结果表明,12种植物根内的AMF存在特异的AMF类群（unique species group, US）和共有类群(common species group, CS),而且CO_２浓度倍增使US减少而CS增加。与350μmol mol^－１对照相比,700μmol mol^－１处理的玉米、刺苋、大豆、陆稻、无芒稗、黑麦草6种植物的AMF群落多样性下降,下降幅度分别达27.12%、16.84%、10.12%、8.62%、8.58%和2.67%;白车轴、牛筋草、早熟禾、鼠曲草、野燕麦、北美车前6种植物的AMF群落多样性上升,分别达76.26%、28.50%、17.60%、15.08%、1.46%和0.96%。CO_２倍增处理后12种植物的AMF多样性平均指数略呈上升趋势。研究指出未来环境变化（如CO２增加）将影响AMF群落结构从而影响菌根共生体的形成。     

Interactions between Bacillus thuringiensis subsp. kurstaki HD-1 and midgut bacteria in larvae of gypsy moth and spruce budworm

We examined interaction between Bacillus thuringiensis subsp. kurstaki HD-1 (Foray 48B) and larval midgut bacteria in two lepidopteran hosts, Lymantria dispar and Choristoneura fumiferana. The pathogen multiplied in either moribund (C. fumiferana) or dead (L. dispar) larvae, regardless of the presence of midgut bacteria. Inoculation of L. dispar resulted in a pronounced proliferation of enteric bacteria, which did not contribute to larval death because B. thuringiensis was able to kill larvae in absence of midgut bacteria. Sterile, aureomycin- or ampicillin-treated larvae were killed in a dose-dependent manner but there was no mortality among larvae treated with the antibiotic cocktail used by [Broderick et al., 2006] and [Broderick et al., 2009]. These results do not support an obligate role of midgut bacteria in insecticidal activity of HD-1. The outcome of experiments on the role of midgut bacteria may be more dependent on which bacterial species are dominant at the time of experimentation than on host species per se. The L. dispar cohorts used in our study had a microflora, that was dominated by Enterococcus and Staphylococcus and lacked Enterobacter. Another factor that can confound experimental results is the disk-feeding method for inoculation, which biases mortality estimates towards the least susceptible portion of the test population.