Mountaintop Site Research Articles

Traceable Calibration of Atmospheric Oxidized Mercury Measurements.

Most previous measurements of oxidized mercury were collected using a method now known to be biased low. In this study, a dual-channel system with an oxidized mercury detection limit of 6-12 pg m-3 was deployed alongside a permeation tube-based automated calibrator at a mountain top site in Steamboat Springs Colorado, USA, in 2021 and 2022. Permeation tubes containing elemental mercury and mercury halides were characterized via an International System of Units (SI)-traceable gravimetric method and gas chromatography/mass spectrometry before deployment in the calibrator. The dual-channel system recovered 97 ± 4 and 100 ± 8% (±standard deviation) of injected elemental mercury and HgBr2, respectively. Total Hg permeation rates and Hg speciation from the gravimetric method, the chromatography system, the dual-channel system, and an independent SI-traceable measurement method performed at the Jožef Stefan Institute laboratory were all comparable within the respective uncertainties of each method. These are the first measurements of oxidized mercury at low environmental concentrations that have been verified against an SI-traceable calibration system in field conditions while sampling ambient air, and they show that accurate, routinely calibrated oxidized mercury measurements are achievable.

Molecular characteristics and formation mechanisms of biogenic secondary organic aerosols in the mountainous background atmosphere of southern China

Biogenic secondary organic aerosols (BSOA) play a crucial role in atmospheric chemistry, with significant implications for air quality and human health. However, the mechanisms by which anthropogenic emissions influence the formation of BSOA in the real atmosphere have not been fully understood. In this study, fine aerosol (PM2.5) samples were collected during both the wet and dry seasons at a high-altitude (1690 m) background site in the Nanling Mountains. Eleven typical secondary organic aerosols (SOA) tracers derived from isoprene (SOAI), α/β-pinene (SOAM), β-caryophyllene (SOAS), and toluene (SOAA), as well as water-soluble inorganic ions and the ambient concentrations of isoprene and its two primary oxidation products, were measured. The results showed that the concentrations and composition of SOA tracers exhibited significant seasonal variations. The total concentration of SOA tracers in the wet season (159 ± 100 ng m−3) was almost three times higher than that in the dry season (61 ± 68 ng m−3). SOAI dominated in both seasons, followed by SOAM, SOAS, and SOAA. Compared with other studies, the concentrations of SOAI and SOAA in the wet season were relatively high, which was mainly attributed to the rapid oxidation of their precursors due to the higher atmospheric oxidative capacity. C5-alkene triols had a significantly higher proportion in SOAI species than in other mountaintop sites. Temperature was the main factor causing the seasonal difference in the concentration of SOAI. Anthropogenic pollutants significantly promoted the formation of SOAI in the wet season. The influence of anthropogenic pollutants on the reaction pathway of IEPOX was consistent in both seasons, favoring the formation of C5-alkene triols. Our study provides vital insights into the molecular characteristics and formation mechanisms of BSOA in a high-altitude background region. It also highlights that the complex air pollution not only affects BSOA concentrations but also the reaction pathways of biogenic volatile organic compounds (BVOCs) transforming into BSOA.

Measurements of Ice Crystal Fluxes from the Surface at a Mountain Top Site

New observations of anomalously high cloud ice crystal concentrations at the Jungfraujoch research station (Switzerland, 3.5 km a.s.l.) are presented. High-resolution measurements of these ice crystals using a high-speed 2D imaging cloud particle spectrometer confirm that the concentrations far exceed those expected from any known primary ice production mechanisms and are at temperatures well below those for known secondary ice production processes to contribute. The most likely explanation is due to a strong surface source generated by the interaction of turbulent deposition of supercooled droplets to fragile ice-covered snow surfaces. This process enhances the detachment of crystal fragments wherein the smaller size mode is turbulently re-suspended even at low wind speeds below expected blowing snow thresholds. These then continue to grow, adding significantly to the ice crystal number concentrations whose size and habit is determined by the transport time between the ice crystal source and measurement location and liquid water profile within the cloud. We confirm, using eddy covariance measurements of ice particle number fluxes, that the likely source is significantly far upwind to preclude flow distortion effects such that the source plume has homogenised by the time they are measured at the mountain top summit.

Comparison of vertical and horizontal atmospheric deposition of nitrate at Central European mountain-top sites during three consecutive winters

Nitrogen (N) deposition, a key process of atmospheric self-cleaning, represents an important pathway for nutrients and pollutants to ecosystems. Enhanced N deposition flux contributes to acidification, eutrophication and loss of biodiversity. N-NO3− concentrations in rime and snow were measured at 10 Czech plots situated in borderline mountains in 2009–2011 winters. The results were put in context with data-driven geostatistical modelling results of annual wet vertical and horizontal deposition. Our hypotheses were that: (i) rime and snow would be more polluted in the highly industrialized north than in the south, (ii) the N-NO3− concentrations would differ in the three winters studied, and (iii), that N-NO3− rime deposition is not negligible in Central European mountain ranges. Our results indicated that winter N-NO3− concentrations were significantly higher in rime than in snow and that there were much larger between-site differences in N-NO3− concentrations for rime than for snow. Relatively large differences were found between individual years. Atmospheric input of N-NO3− in winter was dominated by vertical deposition, i.e., snow. Modelled results showed that mean winter rime deposition corresponded to about 6–25 %, and mean winter snow deposition made up 25–72.5 % of mean annual N-NO3− wet-only deposition. Model N-NO3−occult deposition estimated from throughfall and total (wet and dry) deposition is highly uncertain, however: N throughfall is not a relevant proxy for estimation of realistic total N deposition due to N exchange between the tree canopy and atmosphere.

Unveiling atmospheric transport and mixing mechanisms of ice-nucleating particles over the Alps

Abstract. Precipitation over the mid-latitudes originates mostly from the ice phase within mixed-phase clouds, signifying the importance of initial ice crystal formation. Primary ice crystals are formed on ice-nucleating particles (INPs), which measurements suggest are sparsely populated in the troposphere. INPs are emitted by a large number of ground-based sources into the atmosphere, from where they can be lifted up to cloud heights. Therefore, it is vital to understand vertical INP transport mechanisms, which are particularly complex over orographic terrain. We investigate the vertical transport and mixing mechanisms of INPs over orographic terrain during cloudy conditions by simultaneous measurements of in situ INP concentration at a high valley and a mountaintop site in the Swiss Alps in late winter 2019. On the mountaintop, the INP concentrations were, on average, lower than in the high valley. However, a diurnal cycle in INP concentrations was observed at the mountaintop, which was absent in the high valley. The median mountaintop INP concentration equilibrated to the concentration found in the high valley towards the night. We found that, in nearly 70 % of the observed cases, INP-rich air masses were orographically lifted from low elevation upstream of the measurement site. In addition, we present evidence that, over the course of the day, air masses containing high INP concentrations were advected from the Swiss plateau towards the measurement sites, contributing to the diurnal cycle of INPs. Our results suggest a local INP concentration enhancement over the Alps during cloud events.

Accelerated toluene degradation over forests around megacities in southern China

Toluene is a typical anthropogenic pollutant that has profound impacts on air quality, climate change, and human health, but its sources and sinks over forests surrounding megacities remain unclear. The Nanling Mountains (NM) is a large subtropical forest and is adjacent to the Pearl River Delta (PRD) region, a well-known hotspot for toluene emissions in southern China. However, unexpectedly low toluene concentrations (0.16 ± 0.20 ppbv) were observed at a mountaintop site in NM during a typical photochemical period. A backward trajectory analysis categorized air masses received at the site into three groups, namely, air masses from the PRD, those from central China, and from clean areas. The results revealed more abundant toluene and its key oxidation products, for example, benzaldehyde in air masses mixed with urban plumes from the PRD. Furthermore, a more than three times faster degradation rate of toluene was found in this category of air masses, indicating more photochemical consumption in NM under PRD outflow disturbance. Compared to the categorized clean and central China plumes, the simulated OH peak level in the PRD plumes (15.8 ± 2.2 × 106 molecule cm−3) increased by approximately 30% and 55%, respectively, and was significantly higher than the reported values at other background sites worldwide. The degradation of toluene in the PRD plumes was most likely accelerated by increased atmospheric oxidative capacity, which was supported by isoprene ozonolysis reactions. Our results indicate that receptor forests around megacities are not only highly polluted by urban plumes, but also play key roles in environmental safety by accelerating the degradation rate of anthropogenic pollutants.

Contribution of rime to atmospheric sulphur deposition in Central Europe: A combined empirical and modelling approach

Rime is an under-researched pathway of atmospheric deposition of ecological and environmental relevance, in particular in mountain regions. We present data on sulphur (S) deposition via rime and snow collected at 10 mountaintop sites in the Czech Republic (CR) during three consecutive winters (2009–2011). The mean S concentrations in rime ranged between 3.35 mg L−1 [site Tetrevec (TET) in the north] and 0.78 mg L−1 [site Kamena Loucka (LOU) in the south]. The most S-polluted site thus had S concentrations in rime that were approximately four times higher than the least S-polluted site. Across the sites, S concentrations in rime were 5–10 times higher than in snow. TET, identified as the most S-polluted site, received as much as 60% S from rime and only 40% S from snow. Our results indicated a substantial decline in S rime deposition since the 1990s, following the introduction of desulphurisation measures in the CR. The results of direct measurements of winter-time S deposition via rime are discussed in the context of annual occult deposition, including both rime and fog, obtained from a data-driven geostatistical model. According to our model, occult S deposition ranged between 0 and 1.5 g m−2 year−1 over 99.7% of the forested area of the CR, and generally increased with altitude. At nine sites, the winter-time deposition of S via rime corresponded to 5–13% of annual wet-only S deposition, while it reached 25% at the most S-polluted TET site. In environmental studies, the S deposition pathway via rime should not be neglected, as it might substantially contribute to the total S deposition flux even in mountains of medium elevation.

Study on Full-scale Measurements of Wind Field Characteristics of Coastal Complex Mountainous Terrains

Based on full-scale wind field measurements of coastal complex mountainous terrains, data of fluctuating wind velocities at the height of 30m for four sites, including mountaintop and hillsides, are obtained. The wind load characteristics of mean wind velocities, wind directions, turbulence intensities and speed-up ratios of wind velocities are comprehensively examined. Results show that the maximum mean wind velocity at the mountaintop site is 12.4 m/s. The probability density distributions of mean wind velocities for the four measurement sites can be well represented by the Weibull probability model. The predominant wind directions are around the northeast and southwest. The longitudinal, lateral and vertical turbulence intensities decrease with the increase of mean wind velocities. The turbulence intensities for the mountaintop site are as many as 0.13,0.12 and 0.089 under maximum wind velocities, respectively for the previously mentioned three directions. The speed-up ratios of wind velocities between mountaintop and hillside sites are reduced, as the wind velocities increase. However, in cases of intensive wind with mean wind velocities larger than 8 m/s, the speed-up effects of wind velocities can also appear. The maximum speed-up ratio can reach 1.17.

On the drivers of droplet variability in alpine mixed-phase clouds

Abstract. Droplet formation provides a direct microphysical link between aerosols and clouds (liquid or mixed-phase), and its adequate description poses a major challenge for any atmospheric model. Observations are critical for evaluating and constraining the process. To this end, aerosol size distributions, cloud condensation nuclei (CCN), hygroscopicity, and lidar-derived vertical velocities were observed in alpine mixed-phase clouds during the Role of Aerosols and Clouds Enhanced by Topography on Snow (RACLETS) field campaign in the Davos, Switzerland, region during February and March 2019. Data from the mountain-top site of Weissfluhjoch (WFJ) and the valley site of Davos Wolfgang are studied. These observations are coupled with a state-of-the-art droplet activation parameterization to investigate the aerosol–cloud droplet link in mixed-phase clouds. The mean CCN-derived hygroscopicity parameter, κ, at WFJ ranges between 0.2–0.3, consistent with expectations for continental aerosols. κ tends to decrease with size, possibly from an enrichment in organic material associated with the vertical transport of fresh ultrafine particle emissions (likely from biomass burning) from the valley floor in Davos. The parameterization provides a droplet number that agrees with observations to within ∼ 25 %. We also find that the susceptibility of droplet formation to aerosol concentration and vertical velocity variations can be appropriately described as a function of the standard deviation of the distribution of updraft velocities, σw, as the droplet number never exceeds a characteristic limit, termed the “limiting droplet number”, of ∼ 150–550 cm−3, which depends solely on σw. We also show that high aerosol levels in the valley, most likely from anthropogenic activities, increase the cloud droplet number, reduce cloud supersaturation (< 0.1 %), and shift the clouds to a state that is less susceptible to changes in aerosol concentrations and very sensitive to vertical velocity variations. The transition from an aerosol to velocity-limited regime depends on the ratio of cloud droplet number to the limiting droplet number, as droplet formation becomes velocity limited when this ratio exceeds 0.65. Under such conditions, droplet size tends to be minimal, reducing the likelihood that large drops are present that would otherwise promote glaciation through rime splintering and droplet shattering. Identifying regimes where droplet number variability is dominated by dynamical – rather than aerosol – changes is key for interpreting and constraining when and which types of aerosol effects on clouds are active.

Aircraft-based observation of meteoric material in lower-stratospheric aerosol particles between 15 and 68° N

Abstract. We analyse aerosol particle composition measurements from five research missions between 2014 and 2018 to assess the meridional extent of particles containing meteoric material in the upper troposphere and lower stratosphere (UTLS). Measurements from the Jungfraujoch mountaintop site and a low-altitude aircraft mission show that meteoric material is also present within middle- and lower-tropospheric aerosol but within only a very small proportion of particles. For both the UTLS campaigns and the lower- and mid-troposphere observations, the measurements were conducted with single-particle laser ablation mass spectrometers with bipolar-ion detection, which enabled us to measure the chemical composition of particles in a diameter range of approximately 150 nm to 3 µm. The five UTLS aircraft missions cover a latitude range from 15 to 68∘ N, altitudes up to 21 km, and a potential temperature range from 280 to 480 K. In total, 338 363 single particles were analysed, of which 147 338 were measured in the stratosphere. Of these total particles, 50 688 were characterized by high abundances of magnesium and iron, together with sulfuric ions, the vast majority (48 610) in the stratosphere, and are interpreted as meteoric material immersed or dissolved within sulfuric acid. It must be noted that the relative abundance of such meteoric particles may be overestimated by about 10 % to 30 % due to the presence of pure sulfuric acid particles in the stratosphere which are not detected by the instruments used here. Below the tropopause, the observed fraction of the meteoric particle type decreased sharply with 0.2 %–1 % abundance at Jungfraujoch, and smaller abundances (0.025 %–0.05 %) were observed during the lower-altitude Canadian Arctic aircraft measurements. The size distribution of the meteoric sulfuric particles measured in the UTLS campaigns is consistent with earlier aircraft-based mass-spectrometric measurements, with only 5 %–10 % fractions in the smallest particles detected (200–300 nm diameter) but with substantial (> 40 %) abundance fractions for particles from 300–350 up to 900 nm in diameter, suggesting sedimentation is the primary loss mechanism. In the tropical lower stratosphere, only a small fraction (< 10 %) of the analysed particles contained meteoric material. In contrast, in the extratropics the observed fraction of meteoric particles reached 20 %–40 % directly above the tropopause. At potential temperature levels of more than 40 K above the thermal tropopause, particles containing meteoric material were observed in much higher relative abundances than near the tropopause, and, at these altitudes, they occurred at a similar abundance fraction across all latitudes and seasons measured. Above 440 K, the observed fraction of meteoric particles is above 60 % at latitudes between 20 and 42∘ N. Meteoric smoke particles are transported from the mesosphere into the stratosphere within the winter polar vortex and are subsequently distributed towards low latitudes by isentropic mixing, typically below a potential temperature of 440 K. By contrast, the findings from the UTLS measurements show that meteoric material is found in stratospheric aerosol particles at all latitudes and seasons, which suggests that either isentropic mixing is effective also above 440 K or that meteoric fragments may be the source of a substantial proportion of the observed meteoric material.

Towards parameterising atmospheric concentrations of ice-nucleating particles active at moderate supercooling

Abstract. A small fraction of freezing cloud droplets probably initiates much of the precipitation above continents. Only a minute fraction of aerosol particles, so-called ice-nucleating particles (INPs), can trigger initial ice formation at −15 ∘C, at which cloud-top temperatures are frequently associated with snowfall. At a mountaintop site in the Swiss Alps, we found that concentrations of INPs active at −15 ∘C can be parameterised by different functions of coarse (> 2 µm) aerosol particle concentrations, depending on whether an air mass is (a) precipitating, (b) non-precipitating, or (c) carrying a substantial fraction of dust particles while non-precipitating. Consequently, we suggest that a parameterisation at moderate supercooling should consider coarse particles in combination with air mass differentiation.

Cable-car measurements of vertical aerosol profiles impacted by mountain-valley breezes in Lushan Mountain, East China

In-situ field observations of vertical aerosol profiles for one month in complex terrain (Lushan Mountain, China) were carried out using a cable car, which resolved detailed vertical distributions of mountain aerosols with low-cost operation. Cable-car observations were conducted during the early morning and late afternoon, when mountain and valley winds dominated, respectively. The diurnal aerosol variations at the top and foot of Lushan Mountain were analyzed based on environmental and meteorological stations. The observations indicated that the mountain-valley breezes notably impacted the mountain-area aerosol distribution under weak weather conditions. More uniform aerosol profiles for the afternoon than the morning, with their decreasing rates of PM2.5 (particles with diameters less than 2.5 μm) were 1.64 and 2.28 μg m−3/100 m, respectively. The PM2.5/PM10 ratio at the mountain top increased from 0.69 to 0.81, and that at the mountain base decreased from 0.75 to 0.70 from morning to afternoon. The PM2.5 concentration decreased in and around Lushan Mountain from daytime to nighttime, with the impacted diameter of the 300-m topography line being smaller than ~5 km, while the concentration increased in Jiujiang City. The relative decreasing rate of PM2.5 was higher at the mountain top site (~20%) than at the base site (~2%) from daytime to nighttime. Moreover, uniform aerosol profiles could have been caused by regional transport through a relatively strong low-level synoptic flow (~5 m s−1) and the mountain's dynamic lifting effect.

Winter arsenic pollution in 10 forest ecosystems in the mountainous border regions of the Czech Republic.

Arsenic (As) concentrations and deposition fluxes were measured in snow and rime at 10 mountain-top sites near the borders between the Czech Republic and Austria, Germany, Poland, and Slovakia during three consecutive winter seasons (2009-2011). Our study was performed at a time following several decades of sharply decreasing regional atmospheric pollution and following the 2006 implementation of stricter air quality standards across Europe. Our objective was to compare vertical and horizontal depositions of soluble and insoluble As forms throughout the Czech Republic and define a recent Central European As pollution gradient. Arsenic soluble in weak nitric acid contributed 83 to 85% to the total As deposition, with the remaining 17-15% bound to stable particulate forms. The highest As deposition rates were recorded in the eastern Czech Republic near the borders with Poland and Slovakia. Complementary hydrochemical monitoring in four mountain-slope catchments situated near selected main study sites revealed a further decrease in open-area As deposition by the end of 2018 in the east of the country. In contrast, spruce canopy throughfall flux did not change significantly between 2009-2011 and 2016-2018. The site-specific relative roles of coal-burning-derived and ore-smelting-derived atmospheric As are discussed.

Overview of the CPOC Pilot Study at Whiteface Mountain, NY: Cloud Processing of Organics within Clouds (CPOC)

AbstractAqueous chemical processing within cloud and fog water is thought to be a key process in the production and transformation of secondary organic aerosol mass, found abundantly and ubiquitously throughout the troposphere. Yet, significant uncertainty remains regarding the organic chemical reactions taking place within clouds and the conditions under which those reactions occur, owing to the wide variety of organic compounds and their evolution under highly variable conditions when cycled through clouds. Continuous observations from a fixed remote site like Whiteface Mountain (WFM) in New York State and other mountaintop sites have been used to unravel complex multiphase interactions in the past, particularly the conversion of gas-phase emissions of SO2 to sulfuric acid within cloud droplets in the presence of sunlight. These scientific insights led to successful control strategies that reduced aerosol sulfate and cloud water acidity substantially over the following decades. This paper provides an overview of observations obtained during a pilot study that took place at WFM in August 2017 aimed at obtaining a better understanding of Chemical Processing of Organic Compounds within Clouds (CPOC). During the CPOC pilot study, aerosol cloud activation efficiency, particle size distribution, and chemical composition measurements were obtained below-cloud for comparison to routine observations at WFM, including cloud water composition and reactive trace gases. Additional instruments deployed for the CPOC pilot study included a Doppler lidar, sun photometer, and radiosondes to assist in evaluating the meteorological context for the below-cloud and summit observations.

Impacts of local versus long-range transported aerosols on PM10 concentrations in Seoul, Korea: An estimate based on 11-year PM10 and lidar observations

Extreme haze episodes have frequently occurred in Seoul since mid-2010s by the combined contributions of transboundary transported aerosols as well as locally emitted pollutants. In this study, we developed a novel method to estimate the contribution of long-range transport (LRT, aerosols are transported from any regions except local area near Seoul) and local pollution (LP, aerosols are originated from local area near Seoul) cases to the PM10 concentration in Seoul, Korea, using the PM10 concentration ratio between surface (PM10S) and mountaintop (PM10M) sites and the lidar-derived mixing layer height. The overall contributions of LRT and LP events to nighttime high-PM10 episodes (PM10 > 50 μg m−3) during the period of May 2008–April 2019 were estimated to be approximately 32% and 47%, respectively. The monthly contribution of LRT events to the PM10 concentration varied from approximately 18% (July) to 43% (January), whereas the contribution of LP events was estimated between 39% (March) and 69% (July); this pattern was associated with seasonal synoptic circulations. The similar PM10S values between the LRT (71 ± 22 μg m−3) and LP (73 ± 26 μg m−3) cases during the nighttime suggest that a reduction in local PM10 emissions is crucial to decrease the PM10 concentration during high-PM10 events. The high PM10S for daytime LRT cases can be explained by the combined effects of increased local emissions and LRT aerosols.

Winter damage is more important than summer temperature for maintaining the krummholz growth form above alpine treeline

Abstract Understanding the processes that control alpine treelines, the elevational limits of tree growth forms, has been a central question in ecology and is growing in importance with concern over climate change. Cool summer air temperatures are currently thought to be the ultimate limiter of upright tree growth at alpine treelines globally. However, winter damage has long been recognized as a shaping force near alpine treelines. Low‐growing krummholz growth forms provide an opportunity to test hypotheses about the controls of upright growth in environments above current treelines. To distinguish between effects of growing season temperature, winter damage and their interaction on preventing upright growth in krummholz, we conducted a field experiment on krummholz growth forms of Pinus albicaulis over the summer and winter of 2015–2016 at 10 mountain top sites in the Tobacco Root Mountains, Montana, USA. We experimentally manipulated four factors using a fully crossed design: shoot position (natural low position in the krummholz mat vs. propped up above the krummholz mat), summer warming (warming chamber vs. ambient), winter exposure (shelter cage vs. exposed), and elevation position (local high vs. low krummholz limits). We also conducted an observational study of the climatic conditions associated with recent natural emergent stem establishment from krummholz. Experimentally propped shoots that were exposed in winter experienced the highest mortality (10%–50%), while propped shoots in shelter cages and shoots located within the krummholz mat, whether caged or not, had low mortality (0%–10%). Summer warming had little influence on shoot mortality. Surviving mat shoots had marginally higher growth rates than surviving propped shoots during the early growing season after treatments were established. Natural emergent stem establishment was associated with warmer than average summer temperatures, but also warmer winter temperatures, lower winter wind speeds, and lower snowpack. Synthesis. Our results suggest winter damage plays a more important role than does growing season temperature in maintaining the krummholz growth form. While warming may increase opportunities for emergent shoot establishment above krummholz mats, establishment of upright trees in the krummholz zone will also require climatic change that reduces wind and snow transport which cause winter damage.

Model-measurement consistency and limits of bioaerosol abundance over the continental United States

Abstract. Due to low concentrations and chemical complexity, in situ observations of bioaerosol are geographically and temporally sparse, and this limits the accuracy of current emissions inventories. In this study, we apply a new methodology, including corrections for misidentification of mineral dust, to measurements of single particles over four airborne sampling campaigns to derive vertical profiles of bioaerosol over the continental United States. The new methodology is based on single-particle mass spectrometry (SPMS); it can extend historic datasets to include measurements of bioaerosol, it allows comparisons to other techniques, and it generally agrees with a global aerosol model. In the locations sampled, bioaerosols were at least a factor of 10 less abundant than mineral dust. Below 2 km, bioaerosol concentrations were measured between 6×103 and 2×104 m−3. Between 2 and 8 km, bioaerosol concentrations were between 0 and 2×104 m−3, and above 8 km, bioaerosol concentrations were between 0 and 1×103 m−3. Between 30 % and 80 % of single bioaerosol particles detected were internally mixed with dust. A direct comparison of the SPMS methodology with a co-located wideband integrated bioaerosol sensor (WIB) fluorescence sensor on a mountaintop site showed agreement to within a factor of 3 over the common size range.

A Koronivalu kei Bua: Hillforts in Bua Province (Fiji), their Chronology, Associations, and Potential Significance

Sixteen hillforts constructed and occupied perhaps several centuries before contact in the early nineteenth century are described from Bua district in northern Fiji. These hillforts represent inland settlements in fortifiable locations on high volcanic islands, plausibly established in response to the outbreak of sustained conflict. The chronology and functions of these hillforts were investigated through mapping, excavation, and collection of oral traditions. Four groups of hillforts are recognized. The Seseleka and Yadua (Island) groups represent single polities, comprising a mountaintop site surrounded with fortified narrow steep-sided basalt ridges with tributary sites at lower levels functioning as lookouts and/or food-processing sites. The Northwest Bua group comprises mountaintop sites occupied only when aggressors threatened, and are otherwise characterized by occupation around their bases. The Inland Bua group ranges along one of the highest ridges in the area and were all reportedly in conflict with each other. The Buan hillforts represent those found elsewhere in Fiji and on other high Pacific Islands. Insights from the study of these hillforts illuminate this period of Fiji history and help interrogate broader questions about drivers and proximate causes of the conflict that may have seen hillforts established near simultaneously on high Pacific Islands during the last millennium.

Elevated levels of glyoxal and methylglyoxal at a remote mountain site in southern China: Prompt in-situ formation combined with strong regional transport

The dicarbonyls glyoxal (Gly) and methylglyoxal (Mgly) are key tracers for the oxidation of volatile organic compounds (VOCs) in the atmosphere, but their atmospheric chemistry in remote forest environments is not well understood. A study was carried out during Jul. 31–Nov. 5 of 2016 at the summit of Mt. Tianjing (1690 m.a.s.l.), a remote mountaintop site in southern China, to measure the levels of Gly and Mgly and explore their sources and fate. During the study period, the average mixing ratios of Gly and Mgly were 509 ± 31 pptv and 340 ± 32 pptv, respectively, with the Gly/Mgly ratios averaging 1.8 ± 0.2. Both the dicarbonyl concentrations and the Gly/Mgly ratios were significantly higher than those observed in other background sites. Production yield calculations and meteorological data analysis indicate that high levels of Gly and Mgly observed at the study site were largely a combined result of rapid in-situ formation and regional transport by prevailing winds. On average, in-situ formation from precursors is estimated to account for 67% of the observed Mgly and about 9% of the observed Gly. There were significant changes in Gly and Mgly mixing ratios among different time periods when air masses from different source regions dominated, indicating contribution of regional transport to the observed dicarbonyl mixing ratios at the study site. Biogenic emissions in eastern China and anthropogenic emissions in the Pearl River Delta region were the two main sources responsible for the dicarbonyls observed at the site during most of the sampling period, but large-scale biomass burning in central China was also important in the late autumn, as supported by a backward trajectory analysis of fire spot data and the identification of biomass burning tracers. This study provides insights into the background atmospheric chemistry and the impact of biogenic and anthropogenic sources on the dicarbonyls speciation.

Observations of High Levels of Ozone-Depleting CFC-11 at a Remote Mountain-Top Site in Southern China

A field campaign was carried out in the autumn of 2017 to measure the CFC-11 concentrations at a remote mountain-top site in southern China. During the sampling period, the mixing ratios of CFC-11 ...