Global airborne bacterial community-interactions with Earth's microbiomes and anthropogenic activities.

Airborne bacteria are an influential component of the Earth's microbiomes, but their community structure and biogeographic distribution patterns have yet to be understood. We analyzed the bacterial communities of 370 air particulate samples collected from 63 sites around the world and constructed an airborne bacterial reference catalog with more than 27 million nonredundant 16S ribosomal RNA (rRNA) gene sequences. We present their biogeographic pattern and decipher the interlacing of the microbiome co-occurrence network with surface environments of the Earth. While the total abundance of global airborne bacteria in the troposphere (1.72 × 1024 cells) is 1 to 3 orders of magnitude lower than that of other habitats, the number of bacterial taxa (i.e., richness) in the atmosphere (4.71 × 108 to 3.08 × 109) is comparable to that in the hydrosphere, and its maximum occurs in midlatitude regions, as is also observed in other ecosystems. The airborne bacterial community harbors a unique set of dominant taxa (24 species); however, its structure appears to be more easily perturbed, due to the more prominent role of stochastic processes in shaping community assembly. This is corroborated by the major contribution of surface microbiomes to airborne bacteria (averaging 46.3%), while atmospheric conditions such as meteorological factors and air quality also play a role. Particularly in urban areas, human impacts weaken the relative importance of plant sources of airborne bacteria and elevate the occurrence of potential pathogens from anthropogenic sources. These findings serve as a key reference for predicting planetary microbiome responses and the health impacts of inhalable microbiomes with future changes in the environment.

[Mercury Transport from Glacier to Runoff in Typical Inland Glacial Area in the Tibetan Plateau].

To investigate the transport of mercury from glacier to runoff in typical inland glacial area in the Tibetan Plateau, we selected Zhadang glacier and Qugaqie river Basin located in the Nyainqentanglha Range region and collected samples from snow pit, glacier melt-water and Qugaqie river water during 15th August to 9'h September 2011. Mercury speciation and concentrations were determined and their distribution and controlling factors in different environmental compartments were analyzed. The results showed that the average THg concentrations were (3.79 +/- 5.12) ng x L(-1), (1.06 +/- 0.77) ng x L(-1) and (1.02 +/- 0.24) ng x L(-1) for glacier snow, glacier melt-water and Qugaqie river water, respectively, all of which were at the global background levels. Particulate-bound mercury accounted for large proportion of mercury in all environmental matrices, while mercury in glacial melt-water was controlled by total suspended particle, and mercury in Qugaqie river water co-varied with runoff. With the increase of temperature, glacier melted and released water as well as mercury into glacier-fed river. Total mercury concentrations in glacier melt water, upstream and downstream peaked at 14:00, 16:00 and after 20:00, respectively, reflecting the process of mercury release from glacier and its subsequent transport in the glacier fed river. The transport of riverine mercury was controlled by multiple factors. Under the context of climate change, glacier ablation and the increasing runoff will play increasingly important roles in mercury release and transport.

[Composition and seasonal variations of carbon isotopes in aerosols of Lhasa, Tibet].

A total of 30 samples of total suspended particles were collected at an urban site in western of Lhasa city, Tibet from August 2006 to July 2007 for investigating carbonaceous aerosol features. 14C was taken as a reference to quantitatively distinguish the fossil and biogenic-derived origins along with the characteristics of seasonal variations of all carbonaceous materials in Lhasa are discussed. The results showed that the f(c) values in Lhasa ranged from 0.357 to 0.702, with an average of 0.493, which is higher than Beijing and Tokyo, but are far lower than that of remote/rural regions such as Launceston, indicating a major biogenic influence in Lhasa. Values of f(c) displayed clear seasonal variations with higher mean value in winter, a decreasing trend in spring, while relatively lower values in summer and autumn. Higher f(C) values in winter demonstrate that carbonaceous aerosol is mainly dominated by wood burning and incineration of agricultural wastes during the winter. The lower f(c) values in summer and autumn might be caused by increased diesel engines, motor vehicles emissions, which are related to the tourism in Lhasa. delta13C values ranged from -26.40% per hundred to approximately -25.10% per hundred, with an average of -25.8% per hundred, and showed no clear seasonal variation. The relative higher values in summer reflected the increment of fossil carbon emissions. 13C(TC) values are relatively homogeneous at -25.8% per hundred, considering the characteristics of seasonal variations of f(c) values, it can be concluded that carbonaceous aerosol of Lhasa was mainly influenced by a constant mixing of several pollution sources such as motor vehicles and wood burning emissions.

[Microparticle variations in snowpits from Mt. Geladaindong in the source region of Yangtze River and its environmental significance].

To study the variations of microparticles and their origins, microparticles concentrations, stable oxygen isotope (delta18 O) and major ion concentrations were analyzed in snow samples collected from Mt. Geladaindong in the source region of Yangtze River. The correlation coefficents of different size microparticles in three snowpits are above 0.9 (significant at the 99% level), respectively. Microparticle concentrations have distinct seasonal variations, about 2-4 times higher in non-monsoon season than those in monsoon season, and are consistent with variations of delta18 O, Ca2+, Mg2+ and SO4(2-). Microparticle fluxes in non-monsoon season in three snowpits are 73.6%, 92.3% & 97% of total annual fluxes, respectively. Air mass backward trajectories over Mt. Geladaindong region were analyzed using the HYSPLIT_4 model, and microparticles in Mt. Geladaindong snow were mostly influenced by dust aerosols from the northwestern Tibetan Plateau, South Asia. Coarse particles may come from the local rocks near glaciers. Research of seasonality of microparticle in snow could provide the information on modern environment processes, and is the base of further interpretation of ice core records.

Gradient distribution of persistent organic contaminants along northern slope of central-Himalayas, China.

High mountains may serve as condenser for persistent organic pollutants (POPs) and the vegetation in remote areas has been used as a means to characterized atmospheric concentrations of air pollutants. In this study, organochlorine pesticides (OCPs) and polycyclic aromatic hydrocarbons (PAHs) in Himalayan spruce needle samples from Zhangmu-Nyalam region (central-Himalayas) were analyzed and the altitudinal gradient of these pollutants was investigated. Total HCHs and DDTs concentration in needles were in the range of 1.3-2.9 ng g(-1) dry weight and 1.7-11 ng g(-1) dry weight, which were lower than concentrations reported in spruce needles from Alps, however higher than concentrations in conifer needles from mountain areas of Alberta. Total Himalayan spruce needle PAHs was below 600 ng g(-1) and fluorene, phenanthrene and acenaphthene were abundant individual compounds measured. The ratios of alpha-HCH/gamma-HCH in pine needles were similar with the usual values for technical HCH, implying technical HCHs might be used in this region. The high ratios of o-p'-DDT/p-p'-DDT and no p-p'-DDE measured in this study led to the suspicion that a new source of o-p'-DDT and/or p-p'-DDT existed in this region. In addition, higher ratios of low molecular weight-/high molecular weight-PAHs in this region indicated that petroleum combustion, vehicle emission and low-temperature combustion might be the major contributions of PAH source. To examine the POPs distillation, the analyte concentrations were correlated with altitude. The more volatile OCPs, alpha-HCH, gamma-HCH, aldrin and alpha-endosulfan positively correlated with altitude, however, less volatile OCPs (DDT and DDD) inversely related with elevation. Almost all PAHs detected in this area showed positive correlations with altitude. It is worthy to note that heavy PAHs (Benzo[k] fluoranthene and Benzo[a]anthracene) displayed positive correlation, which implied the sources of PAHs were near the sampling sites. The distillation of POPs was strongly affected by the proximity between sampling sites and contaminant sources. If the contaminant sources are close to the mountains, it may be the dominant factor that controls the concentration gradient.