基于高通量测序技术马肠道菌群研究进展

马肠道非常发达,其中定居着丰富又复杂的微生物菌群,这些微生物在宿主的生理、代谢、营养和免疫功能等方面有着重要作用.基于高通量测序的宏基因组学技术和分析手段的改进,对复杂环境中微生物的研究更加方便、透彻.本文就基于高通量测序的宏基因组技术在马肠道核心菌群、不同肠道段菌群结构、不同因素对肠道菌群结构的影响,以及马肠道微生物...     

Estimating the uncertainty in annual net ecosystem carbon exchange: spatial variation in turbulent fluxes and sampling errors in eddy-covariance measurements

Above forest canopies, eddy covariance (EC) measurements of mass (CO₂, H₂O vapor) and energy exchange, assumed to represent ecosystem fluxes, are commonly made at one point in the roughness sublayer (RSL). A spatial variability experiment, in which EC measurements were made from six towers within the RSL in a uniform pine plantation, quantified large and dynamic spatial variation in fluxes. The spatial coefficient of variation (CV) of the scalar fluxes decreased with increasing integration time, stabilizing at a minimum that was independent of further lengthening the averaging period (hereafter a ‘stable minimum’). For all three fluxes, the stable minimum (CV=9–11%) was reached at averaging times (τ_p) of 6–7 h during daytime, but higher stable minima (CV=46–158%) were reached at longer τ_p (>12 h) during nighttime. To the extent that decreasing CV of EC fluxes reflects reduction in micrometeorological sampling errors, half of the observed variability at τ_p=30 min is attributed to sampling errors. The remaining half (indicated by the stable minimum CV) is attributed to underlying variability in ecosystem structural properties, as determined by leaf area index, and perhaps associated ecosystem activity attributes. We further assessed the spatial variability estimates in the context of uncertainty in annual net ecosystem exchange (NEE). First, we adjusted annual NEE values obtained at our long‐term observation tower to account for the difference between this tower and the mean of all towers from this experiment; this increased NEE by up to 55 g C m^?2 yr^?1. Second, we combined uncertainty from gap filling and instrument error with uncertainty because of spatial variability, producing an estimate of variability in annual NEE ranging from 79 to 127 g C m^?2 yr^?1. This analysis demonstrated that even in such a uniform pine plantation, in some years spatial variability can contribute ～50% of the uncertainty in annual NEE estimates.     

Biotic and abiotic controls on the ecosystem significance of consumer excretion in two contrasting tropical streams

1. Excretion of nitrogen (N) and phosphorus (P) is a direct and potentially important role for aquatic consumers in nutrient cycling that has recently garnered increased attention. The ecosystem‐level significance of excreted nutrients depends on a suite of abiotic and biotic factors, however, and few studies have coupled measurements of excretion with consideration of its likely importance for whole‐system nutrient fluxes. 2. We measured rates and ratios of N and P excretion by shrimps (Xiphocaris elongata and Atya spp.) in two tropical streams that differed strongly in shrimp biomass because a waterfall excluded predatory fish from one site. We also made measurements of shrimp and basal resource carbon (C), N and P content and estimated shrimp densities and ecosystem‐level N and P excretion and uptake. Finally, we used a 3‐year record of discharge and NH₄‐N concentration in the high‐biomass stream to estimate temporal variation in the distance required for excretion to turn over the ambient NH₄‐N pool. 3. Per cent C, N, and P body content of Xiphocaris was significantly higher than that of Atya. Only per cent P body content showed significant negative relationships with body mass. C:N of Atya increased significantly with body mass and was higher than that of Xiphocaris. N : P of Xiphocaris was significantly higher than that of Atya. 4. Excretion rates ranged from 0.16–3.80 μmol NH₄‐N shrimp^?1 h^?1, 0.23–5.76 μmol total dissolved nitrogen (TDN) shrimp^?1 h^?1 and 0.002–0.186 μmol total dissolved phosphorus (TDP) shrimp^?1 h^?1. Body size was generally a strong predictor of excretion rates in both taxa, differing between Xiphocaris and Atya for TDP but not NH₄‐N and TDN. Excretion rates showed statistically significant but weak relationships with body content stoichiometry. 5. Large between‐stream differences in shrimp biomass drove differences in total excretion by the two shrimp communities (22.3 versus 0.20 μmol NH₄‐N m^?2 h^?1, 37.5 versus 0.26 μmol TDN m^?2 h^?1 and 1.1 versus 0.015 μmol TDP m^?2 h^?1), equivalent to 21% and 0.5% of NH₄‐N uptake and 5% and <0.1% of P uptake measured in the high‐ and low‐biomass stream, respectively. Distances required for excretion to turn over the ambient NH₄‐N pool varied more than a hundredfold over the 3‐year record in the high‐shrimp stream, driven by variability in discharge and NH₄‐N concentration. 6. Our results underscore the importance of both biotic and abiotic factors in controlling consumer excretion and its significance for nutrient cycling in aquatic ecosystems. Differences in community‐level excretion rates were related to spatial patterns in shrimp biomass dictated by geomorphology and the presence of predators. Abiotic factors also had important effects through temporal patterns in discharge and nutrient concentrations. Future excretion studies that focus on nutrient cycling should consider both biotic and abiotic factors in assessing the significance of consumer excretion in aquatic ecosystems.     

不同种植年限薰衣草根际土壤真菌群落结构的演变

土壤真菌群落结构和多样性对植物生长起着重要作用,了解种植年限对薰衣草根际土壤真菌群落结构的影响对薰衣草病害防治和增产的研究具有重要意义。探究不同种植年限薰衣草根际土壤真菌群落结构和多样性特征,及其随种植年限的演变规律。采集新疆伊犁霍城县种植年限1、3、5 a,以及未种植薰衣草土壤,对ITS 序列进行Illumina高通量测序。对测序结果进行分析,比较各样品组真菌多样性和群落分布规律及与种植年限的关联。结果表明,Alpha多样性分析显示随着种植年限的增加Shannon指数逐渐降低,而Chao1指数先降低后增高。在种植薰衣草土壤中共检测到12个门,28个纲,72个目,146个科,236个属。在门水平上,子囊菌门(Ascomycota)、担子菌门(Basidiomycota)、球囊菌门(Glomeromycota)为优势菌门。随着种植年限的增加,子囊菌门相对丰度逐渐降低,担子菌门逐渐增高,而球囊菌门先增加后降低。在属水平上优势菌属为Xylodon、锐孔菌属（Oxyporus)、镰刀菌属(Fusarium)、枝孢属(Cladosporium),均属于植物致病菌。随着种植年限的增加,Xylodon相对丰度增加,而锐孔菌属、镰刀菌属、枝孢属先增加后降低。丛枝菌根菌(AMF) 中第一优势属球囊霉属(Glomus)OTU数量随种植年限的增加逐渐减少。薰衣草连作种植造成根际土壤真菌群落结构和多样性改变,致病菌增加,AMF降低。本研究为薰衣草病虫害防治和增产提供理论依据,为薰衣草土壤科学管理提供参考。     

Biogeochemistry of a gypsum-encrusted microbial ecosystem

Gypsum crusts containing multicolored stratified microbial populations grow in the evaporation ponds of a commercial saltern in Eilat, Israel. These crusts contain two prominent cyanobacterial layers, a bright purple layer of anoxygenic phototrophs, and a lower black layer with active sulphate reduction. We explored the diel dynamics of oxygen and sulphide within the crust using specially constructed microelectrodes, and further explored the crust biogeochemistry by measuring rates of sulphate reduction, stable sulphur isotope composition, and oxygen exchange rates across the crust–brine interface. We explored crusts from ponds with two different salinities, and found that the crust in the highest salinity was the less active. Overall, these crusts exhibited much lower rates of oxygen production than typical organic‐rich microbial mats. However, this was mainly due to much lower cell densities within the crusts. Surprisingly, on a per cell‐volume basis, rates of photosynthesis were similar to organic‐rich microbial mats. Due to relatively low rates of oxygen production and deep photic zones extending from 1.5 to 3 cm depth, a large percentage of the oxygen produced during the day accumulated into the crusts. Indeed, only between 16% to 34% of the O₂ produced in the crust escaped, and the remainder was internally recycled, used mainly in O₂ respiration. We view these crusts as potential homologs to ancient salt‐encrusted microbial ecosystems, and we compared them to the 3.45 billion‐year‐old quartz barite deposits from North Pole, Australia, which originally precipitated gypsum.     

Growth and Development of the Banana Plant: 3. A. The Origin of the Inflorescence and the Development of the Flowers: B. The Structure and Development of the Fruit

In this paper, which is presented in two parts, the growth anddevelopment of the banana plant have been examined from thestandpoint of the origin of the inflorescence and the developmentof the flowers (Part A) and the structure and development ofthe fruit (Part B). First the main centres of growth in thesestructures are located and the manner of their development ispresented. Thereafter, attention is focused upon the salientevents which determine the alternative courses of developmentwith a view to designating the chemical and physiological stimulithat may be required.     

Occurrence of Endosperm Haustorium in Cannabis sativa L.: With thirteen Figures in the Text

The development and structure of the chalazal endosperm haustoriumin Cannabis sativa are described. The endosperm is nuclear anda haustorium is formed at the chalazal end. The latter remainsfree nuclear throughout. Enucleate vesicles appear in the upperpart of the endosperm but finally they merge with the cytoplasmof the haustorium. As the embryo reaches maturity it occupiesthe whole seed cavity, the haustorium collapses and the endospermpersists only as a thin layer.