Westerly drives long-distance transport of radionuclides from nuclear events to glaciers in the Third Pole.

Major nuclear bomb tests and nuclear power plant incidents release large amounts of radionuclides. This study investigates beta (ß) activities of radionuclides from four ice cores in the Third Pole (TP) to understand the transport routes and related atmospheric processes affecting the radionuclides deposition in glaciers of the region. All the ice cores show three major ß activity peaks in the ice layers corresponding to 1963, 1986, and 2011. The ß activity peak in the 1963 ice layer is referred to as the well-known 1962 Nuclear Bomb Test. Beta activity peaks in 1986 and 2011 ice layers from the Chernobyl and Fukushima Nuclear Incidents (CNI, FNI). Hysplit forward and backward trajectory analyses suggest that the radionuclides were transported by the westerly into the stratosphere and then to the high elevation TP glaciers. In the FNI case, the radionuclides traveled over Japan, the Pacific Ocean, Europe, and central Asia before being deposited in the TP glaciers. Investigations of the atmospheric circulation confirm that the stronger northern branch of westerly is responsible for high radionuclides during the FNI in the TP. Less precipitation with water vapor flux component divergence after the FNI also contributed to the enriched radionuclides.

Different patterns and origins between northwestern and southeastern Tibetan ice core glaciochemical records over the past century.

Atmospheric circulation systems differ between the northern and southern Tibetan Plateau (TP) and are characterized by prevailing westerly winds and the Indian monsoon, respectively. This leads to spatial differences between glaciochemical records in the northwestern and southeastern TP. We compared the spatial differences in major soluble ion concentrations (Ca2+, SO42-, NO3-, NH4+, Cl-, Na+, K+, and Mg2+) during the last century in the Aru (northwestern TP) and East Rongbuk (ER; southeastern TP) ice cores. Ca2+ exhibited the largest difference between the ice cores (2371 ppb in the Aru ice core and 65 ppb in the ER ice core), indicating that crustal processes were more dominant in the Aru ice core. NH4+ accounted for 17% of the total ion concentration in the ER ice core but only 3% in the Aru ice core, which may be related to the Indian monsoon traveling over NH3 emission zones in southern Asia. The major soluble ion concentrations exhibited decreasing trends in the Aru ice core but increasing trends in the ER ice core (P < 0.01). Empirical orthogonal function and backward trajectory analyses indicated that the major soluble ions in the Aru ice core originated from crustal sources in central Asia; those in the ER ice core had crustal, anthropogenic, and oceanic sources from southern Asia. The results from the Aru ice core suggest that dust events and enhanced prevailing westerly winds promoted the deposition of dust aerosols from the Taklamakan Desert and arid and semi-arid regions of central Asia. Contrastingly, the results from the ER ice core suggest that the Indian monsoon transported crustal and anthropogenic sources from southern Asia and oceanic sources from the Bay of Bengal and Arabian Sea. This study contributes to the comprehensive understanding of the differences in glaciochemical records and their causes between the northwestern and southeastern TP.

Demonstration of a memory calibration method in water isotope measurement by laser spectroscopy.

RATIONALE: Measuring δ18 O and δ2 H values in water using wavelength-scanned cavity ring down spectroscopy (WS-CRDS) requires multiple injections of up to six (and sometimes eight or more) of one sample to remove the memory effect, which decreases the sample throughput and increases the consumables cost. Thus, improved methods for removing the memory effect are required. METHODS: We calculated the memory coefficients by sequential WS-CRDS measurement of two lab standard waters with isotopic differences, and used them to establish calibration equations. We then used these equations to correct the measured δ18 O and δ2 H values by removing the memory effect, instead of using multiple injections in the routine daily measurements. RESULTS: By using this method, the number of injections per sample was reduced to one. The reproducibility (one standard deviation) of the δ18 O and δ2 H values obtained for quality control sample was less than 0.05‰ and 0.5‰ for an annual average, respectively. CONCLUSIONS: By measuring the memory coefficients and establishing the calibration equations, a highly effective method was developed for determining the δ18 O and δ2 H values of water, which could significantly improve sample throughput for liquid water dual isotope measurement without sacrificing the precision.

Comparative genomic analysis reveals the environmental impacts on two Arcticibacter strains including sixteen Sphingobacteriaceae species.

How the genomic diversity of species is driven by geographical isolation and environmental factors are not well understood for cold environments. Here, the environmental stress responses of two phylogenetically close Arcticibacter strains, A. eurypsychrophilus MJ9-5 and A. svalbardensis MN12-7, isolated from a Tibetan Plateau glacier and Svalbard soil, were analyzed. The comparative genomic analysis was performed with sixteen other related Sphingobacteriaceae species. Analyses of the relationships between growth temperature and genome composition, cold and heat shock genes showed that genomic adaption characteristics were more obvious when the strains were grouped by their upper limit in growth temperature, rather than by their minimal or optimal growth temperatures for Sphingobacteriaceae species. The very divergent genetic distance of genome fractions assigned to the functions of 'secondary metabolism', 'dormancy and sporulation' and 'metabolism of aromatic compounds' indicated the heterogeneous evolution of genes under different environmental pressures of the Sphingobacteriaceae species. The greatest differences between strains MJ9-5 and MN12-7 occurred in the genes devoted to the CRISPRs, osmotic adaption and metabolism of monosaccharides, nitrogen and aromatic compounds. These distinctions corresponded to two different environmental pressures, salinity and nutritional level, in the glacier ice and Svalbard soil environments.

Dramatic mass loss in extreme high-elevation areas of a western Himalayan glacier: observations and modeling.

Rapid climate change at high elevations has accelerated glacier retreat in the Himalayas and Tibetan Plateau. However, due to the lack of long-term glaciological measurements, there are still uncertainties regarding when the mass loss began and what the magnitude of mass loss is at such high elevations. Based on in situ glaciological observations during the past 9 years and a temperature-index mass balance model, this study investigates recent mass loss of the Naimona'nyi Glacier in the western Himalayas and reconstructs a 41-year (1973/74-2013/14) equilibrium line altitude (ELA) and glacier-wide mass loss. The result indicates that even at 6000 m above sea level (a.s.l.), the annual mass loss reaches ~0.73 m water equivalent (w.e.) during the past 9 years. Concordant with the abrupt climate shift in the end of 1980s, the ELA has dramatically risen from ~5969 ± 73 m a.s.l. during 1973/74-1988/89 to ~6193 ± 75 m a.s.l. during 1989/90-2013/14, suggesting that future ice cores containing uninterrupted climate records could only be recovered at least above 6200 m a.s.l. in the Naimona'nyi region. The glacier-wide mass balance over the past 41 years is averaged to be approximately -0.40 ± 0.17 m w.e., exhibiting a significant increase in the decadal average from -0.01 ± 0.15 to -0.69 ± 0.21 m w.e.

Levoglucosan evidence for biomass burning records over Tibetan glaciers.

Intense biomass burning (BB) events are widespread in tropical and subtropical Asia. However, the impact of BB aerosols on the Tibetan Plateau (TP), especially on Tibetan glaciers, is poorly understood. In this study, BB signals are revealed using the specific molecular tracer levoglucosan in snow and ice samples from different Tibetan glaciers. Tibetan glaciers mainly act as receptors of BB emissions from surrounding regions. Significant differences in levoglucosan concentrations in glacier samples collected from two slopes on the same mountain range indicate that high mountains can act as natural barriers to block the transport of smoke aerosols to the TP. Levoglucosan concentrations show a decreasing trend from west to east on glaciers impacted by the Indian summer monsoon on the southern edge of the TP, while the opposite pattern was observed on glaciers under the prevailing westerlies along the northern edge. The emission sources, the controlling climate system, as well as deposition and degradation during transport determined the spatial distribution regimes of levoglucosan concentration on Tibetan glaciers.

Black soot and the survival of Tibetan glaciers.

We find evidence that black soot aerosols deposited on Tibetan glaciers have been a significant contributing factor to observed rapid glacier retreat. Reduced black soot emissions, in addition to reduced greenhouse gases, may be required to avoid demise of Himalayan glaciers and retain the benefits of glaciers for seasonal fresh water supplies.

[Ionic chemistry in snowpits from Yamzhog Yumco Basion].

During August and September, 2006, a total of 50 samples had been collected from three different snowpits at the Yamzhog Yumco Basion in the south of the Tibetan Plateau. All samples were analyzed for major cations (Na+, NH4+, K+, Ca2+ and Mg2+), anions (Cl-, SO4(2-) and NO3-) and stable oxygen isotope ratio. The results of analyses show that the three snowpits represent accordant chemical characteristics, with NO3- (16.1-187.2 microg x L(-1), averaging at 93.7 microg x L(-1)) and Ca2+ (19.0-236.7 microg x L(-1), averaging at 81.0 microg x L(-1)) being the highest concentration of anions and cations respectively. Compared with data from other representative sites, major ion concentrations in the Yamzhog Yumco Basion accord with those in the south of the plateau, but they differ much from those in the north of th eplateau. Remarkable variabilities of major ion concentrations from monsoon period to non-monsoon period are demonstrated. Ion concentrations of NO3-, NH4+ increase 30%-40% in monsoon period due to the influences of vegetation, live-stock, anthropogenic activity and thunderstorm, whilst the concentrations of crustal source ions, such as Ca2+, Mg2+ reduce 80% due to decrease of dust and strong wind from the north of the plateau and crustal aerosols being washed out of the atmosphere by heavy precipitation during the monsoon period. Variation of ion concentrations are also impacted by elevation and post-deposition process, with Ca2+, Mg2+ increasing with a decrease in elevation and SO4(2-), NO3- decrease with an increase in elevation and the influence of post-deposition.