scholarly journals Wet and dry deposition of mineral dust particles in Japan: factors related to temporal variation and spatial distribution

2014 ◽  
Vol 14 (2) ◽  
pp. 1107-1121 ◽  
Author(s):  
K. Osada ◽  
S. Ura ◽  
M. Kagawa ◽  
M. Mikami ◽  
T. Y. Tanaka ◽  
...  
Keyword(s):  
Dry Deposition ◽  
Wet Deposition ◽  
Mineral Dust ◽  
Potential Temperature ◽  
Temporal Variations ◽  
Dust Particles ◽  
Spatial Distributions ◽  
Dust Deposition ◽  
Deposition Fluxes ◽  
Wet And Dry Deposition

Abstract. Recent ground networks and satellite remote-sensing observations have provided useful data related to spatial and vertical distributions of mineral dust particles in the atmosphere. However, measurements of temporal variations and spatial distributions of mineral dust deposition fluxes are limited in terms of their duration, location, and processes of deposition. To ascertain temporal variations and spatial distributions of mineral dust deposition using wet and dry processes, weekly deposition samples were obtained at Sapporo, Toyama, Nagoya, Tottori, Fukuoka, and Cape Hedo (Okinawa) in Japan during October 2008–December 2010 using automatic wet and dry separating samplers. Mineral dust weights in water-insoluble residue were estimated from Fe contents measured using an X-ray fluorescence analyser. Wet and dry deposition fluxes of mineral dusts were both high in spring and low in summer, showing similar seasonal variations to frequency of aeolian dust events (Kosa) in Japan. For wet deposition, highest and lowest annual dust fluxes were found at Toyama (9.6 g m−2 yr−1) and at Cape Hedo (1.7 g m−2 yr−1) as average values in 2009 and 2010. Higher wet deposition fluxes were observed at Toyama and Tottori, where frequent precipitation (> 60% days per month) was observed during dusty seasons. For dry deposition among Toyama, Tottori, Fukuoka, and Cape Hedo, the highest and lowest annual dust fluxes were found respectively at Fukuoka (5.2 g m−2 yr−1) and at Cape Hedo (2.0 g m−2 yr−1) as average values in 2009 and 2010. The average ratio of wet and dry deposition fluxes was the highest at Toyama (3.3) and the lowest at Hedo (0.82), showing a larger contribution of the dry process at western sites, probably because of the distance from desert source regions and because of the effectiveness of the wet process in the dusty season. Size distributions of refractory dust particles were obtained using four-stage filtration: > 20, > 10, > 5, and > 1 μm diameter. Weight fractions of the sum of > 20 μm and 10–20 μm (giant fraction) were higher than 50% for most of the event samples. Irrespective of the deposition type, the giant dust fractions generally decreased with increasing distance from the source area, suggesting the selective depletion of larger giant particles during atmospheric transport. Based on temporal variations of PMc (2.5 < D < 10 μm), ground-based lidar, backward air trajectories, and vertical profiles of potential temperatures, transport processes of dust particles are discussed for events with high-deposition and low-deposition flux with high PMc. Low dry dust depositions with high PMc concentrations were observed under stronger (5 K km−1) stratification of potential temperature with thinner and lower (< 2 km) dust distributions because the PMc fraction of dust particles only survived after depletion of giant dust particles by rapid gravitational settling at the time they reach Japan. In contrast, transport through a thicker (> 2 km) dust layer with weak vertical gradient of potential temperature carry more giant dust particles to Japan. Because giant dust particles are an important mass fraction of dust accumulation, especially in the North Pacific, which is known as a high-nutrient, low-chlorophyll (HNLC) region, the transport height and fraction of giant dust particles are important factors for studying dust budgets in the atmosphere and their role in biogeochemical cycles.

scholarly journals Wet and dry deposition of mineral dust particles in Japan: factors related to temporal variation and spatial distribution

2013 ◽  
Vol 13 (8) ◽  
pp. 21801-21835
Author(s):  
K. Osada ◽  
S. Ura ◽  
M. Kagawa ◽  
M. Mikami ◽  
T. Y. Tanaka ◽  
...  
Keyword(s):  
Dry Deposition ◽  
Wet Deposition ◽  
Mineral Dust ◽  
Temporal Variations ◽  
Dust Particles ◽  
Insoluble Residue ◽  
Spatial Distributions ◽  
Dust Deposition ◽  
Deposition Fluxes ◽  
Deposition Amount

Abstract. Data of temporal variations and spatial distributions of mineral dust deposition fluxes are very limited in terms of duration, location, and processes of deposition. To ascertain temporal variations and spatial distributions of mineral dust deposition by wet and dry processes, weekly deposition samples were obtained at Sapporo, Toyama, Nagoya, Tottori, Fukuoka, and Cape Hedo (Okinawa) in Japan during October 2008–December 2010 using automatic wet and dry separating samplers. Mineral dust weights in water-insoluble residue were estimated from Fe contents measured using an X-ray fluorescence analyzer. For wet deposition, highest and lowest annual dust fluxes were found at Toyama (9.6 g m−2 yr−1) and at Cape Hedo (1.7 g m−2 yr−1) as average values in 2009 and 2010. Higher wet deposition fluxes were observed at Toyama and Tottori, where frequent precipitation (>60% days per month) was observed during dusty seasons. For dry deposition among Toyama, Tottori, Fukuoka, and Cape Hedo, the highest and lowest annual dust fluxes were found respectively at Fukuoka (5.2 g m−2 yr−1) and at Cape Hedo (2.0 g m−2 yr−1) as average values in 2009 and 2010. Although the seasonal tendency of the monthly dry deposition amount roughly resembled that of monthly days of Kosa dust events, the monthly amount of dry deposition was not proportional to monthly days of the events. Comparison of dry deposition fluxes with vertical distribution of dust particles deduced from Lidar data and coarse particle concentrations suggested that the maximum dust layer height or thickness is an important factor for controlling the dry deposition amount after long-range transport of dust particles. Size distributions of refractory dust particles were obtained using four-stage filtration: >20, >10, >5, and >1 μm diameter. Weight fractions of the sum of >20 μm and 10–20 μm (giant fraction) were higher than 50% for most of the event samples. Irrespective of the deposition type, the giant dust fractions were decreasing generally with increasing distance from the source area, suggesting the selective depletion of larger giant particles during atmospheric transport. Because giant dust particles are an important mass fraction of dust accumulation, especially in the north Pacific where is known as a high-nutrient, low-chlorophyll (HNLC) region, the transport height of giant dust particles is an important factor for studying dust budgets in the atmosphere and their role in biogeochemical cycles.

scholarly journals Atmospheric total gaseous mercury (TGM) concentrations and wet and dry deposition of mercury at a high-altitude mountain peak in south China

2009 ◽  
Vol 9 (6) ◽  
pp. 23465-23504 ◽  
Author(s):  
X. W. Fu ◽  
X. Feng ◽  
Z. Q. Dong ◽  
R. S. Yin ◽  
J. X. Wang ◽  
...  
Keyword(s):  
South China ◽  
Dry Deposition ◽  
Urban Areas ◽  
Wet Deposition ◽  
Ambient Air ◽  
Total Gaseous Mercury ◽  
Deposition Fluxes ◽  
Wet And Dry Deposition ◽  
Gaseous Mercury ◽  
Seasonal And Diurnal Variations

Abstract. China is regarded as the largest contributor of mercury (Hg) to the global atmospheric Hg budget. However, concentration levels and depositions of atmospheric Hg in China are poorly known. Continuous measurements of atmospheric total gaseous mercury (TGM) were carried out from May 2008 to May 2009 at the summit of Mt. Leigong in south China. Wet and dry deposition fluxes of Hg were also calculated following collection of precipitation, throughfall and litterfall. Atmospheric TGM concentrations averaged 2.80±1.51 ng m−3, which was highly elevated compared to global background values but much lower than semi-rural and industrial/urban areas in China, indicating great emissions of Hg in central, south and southwest China. Seasonal and diurnal variations of TGM were observed, which reflected variations in source intensity, deposition processes and meteorological factors. Wet deposition of Hg was quite low, while its dry deposition of Hg (litterfall + throughfall-direct wet deposition) constituted a major portion of total deposition (~88% for total mercury (THg) and 84% for methyl mercury (MeHg)). This highlights the importance of vegetation to Hg atmospheric cycling. In a remote forest ecosystem of China, dry deposition of TGM, especially gaseous elemental mercury (GEM), was very important for the depletion of atmospheric Hg. Elevated TGM level in ambient air may accelerate the foliar uptake of Hg through air which may partly explain the elevated Hg dry deposition fluxes observed in Mt. Leigong.

scholarly journals Estimating chemical composition of atmospheric deposition fluxes from mineral insoluble particles deposition collected in the Western Mediterranean region

2017 ◽  
Author(s):  
Yinghe Fu ◽  
Karine Desboeufs ◽  
Julie Vincent ◽  
Elisabeth Bon Nguyen ◽  
Benoit Laurent ◽  
...  
Keyword(s):  
Trace Metals ◽  
Chemical Analysis ◽  
Atmospheric Deposition ◽  
Wet Deposition ◽  
Mediterranean Basin ◽  
Mineral Dust ◽  
Western Mediterranean ◽  
Dust Deposition ◽  
Deposition Fluxes ◽  
Western Mediterranean Basin

Abstract. In order to measure the mass flux of atmospheric insoluble deposition and to constrain regional models dust simulation, a network of automatic deposition collectors (CARAGA) has been installed throughout the western Mediterranean basin. Weekly samples of the insoluble fraction of total atmospheric deposition were collected concurrently on filters at 5 sites including 4 on western Mediterranean islands (Frioul and Corsica, France, Mallorca, Spain, and Lampedusa, Italy), and 1 in the southern French Alps (Le Casset), and a weighing and ignition protocol was applied in order to quantify their mineral fraction. Atmospheric deposition is both a strong source of nutrients and metals for marine ecosystems in this area. However, there is little data on trace metal deposition in the literature since their deposition measurement is difficult to perform. In order to obtain more information from CARAGA atmospheric deposition samples, this study aimed at testing their relevance to estimate elemental fluxes in addition to total fluxes. The elemental chemical analysis of ashed CARAGA filter samples was based on an acid digestion and an elemental analysis by inductively coupled plasma atomic emission spectroscopy (ICP-AES) and mass spectrometry (MS) in a clean room. The sampling and analytical protocols were tested to determine the elemental composition for mineral dust tracers (Al, Ca, K, Mg, and Ti), nutrients (P and Fe), and trace metals (Cd, Co, Cr, Cu, Mn, Ni, V and Zn) from simulated wet deposition of dust analogues and traffic soot. The relative mass loss by dissolution in wet deposition was lower than 1 % for Al and Fe, and reached 13 % for P due to its larger solubility in water. For trace metals, this loss represented less than 3 % of the total mass concentration, except for Zn, Cu and Mn for which it could reach 10 %, especially in traffic soot. The chemical contamination during analysis was negligible for all the elements except for Cd which is in very low concentration in dust. Tests allowed us to conclude that the CARAGA samples could be used to estimate contents of nutrients and trace metals in the limits of loss by dissolution. Chemical characterization of CARAGA deposition samples corresponding to the most intense dust deposition events recorded between 2011 and 2013 has been performed and showed elemental mass ratios consistent with the ones found in the literature for Saharan dust. However, the chemical analysis of CARAGA samples revealed the presence of some anthropogenic signatures, as for instance high Zn concentrations in some samples in Lampedusa, and also pointed out that mineral dust can be mixed with anthropogenic compounds in the deposition samples collected on the Frioul Island. Results showed that the chemical analysis of CARAGA ashed samples can be used to trace back origins of elemental deposition. The elemental atmospheric fluxes estimated from these chemical analyses of samples from the CARAGA network of weekly deposition monitoring constitute the first assessment of mass deposition fluxes of trace metals and P during intense dust deposition events at the scale of the western Mediterranean basin.

scholarly journals Atmospheric wet and dry deposition of trace elements at ten sites in Northern China

2014 ◽  
Vol 14 (14) ◽  
pp. 20647-20676 ◽  
Author(s):  
Y. P. Pan ◽  
Y. S. Wang
Keyword(s):  
Trace Elements ◽  
Atmospheric Deposition ◽  
Dry Deposition ◽  
Urban Areas ◽  
Wet Deposition ◽  
Northern China ◽  
Temporal Variations ◽  
Deposition Flux ◽  
Forest Site ◽  
Wet And Dry Deposition

Abstract. Atmospheric deposition is considered to be a major process that removes pollutants from the atmosphere and an important source of nutrients and contaminants for ecosystems. Trace elements (TEs), especially toxic metals deposited on plants and into soil and water, can cause substantial damage to the environment and human health due to their transfer and accumulation in food chains. Despite public concerns, quantitative knowledge of metal deposition from the atmosphere to ecosystems remains scarce. To advance our understanding of the spatio-temporal variations in the magnitudes, pathways, compositions and impacts of atmospherically deposited TEs, precipitation (rain and snow) and dry-deposited particles were collected simultaneously at ten sites in Northern China from December 2007 to November 2010. The measurements showed that the wet and dry depositions of TEs in the target areas were orders of magnitude higher than previous observations within and outside China, generating great concern over the potential risks. The spatial distribution of the total (wet plus dry) deposition flux was consistent with that of the dry deposition, with a significant decrease from industrial and urban areas to suburban, agricultural and rural sites. In contrast, the wet deposition exhibited less spatial variation. The seasonal variation of wet deposition was also different from that of dry deposition, although they were both governed by the precipitation and emission patterns. For the majority of TEs that exist as coarse particles, dry deposition dominated the total flux at each site. This was not the case for K, Ni, As, Pb, Zn, Cd, Se, Ag and Tl, for which the relative importance between wet and dry deposition fluxes varied by site. Whether wet deposition is the major atmospheric cleansing mechanism for the TEs depends on the size distribution and solubility of the particles. We found that atmospheric inputs of Cu, Pb, Zn, Cd, As and Se were of the same magnitude as their increases in the topsoil of agricultural systems. In addition, the total deposition flux of Pb observed at a forest site in this study was twice that of the critical load (7.0 mg m−2 yr−1) calculated for temperate forest ecosystems in Europe. These findings provide baseline data needed for future targeting policies to protect various ecosystems from long-term heavy metal input via atmospheric deposition.

scholarly journals Triple oxygen isotopes indicate urbanization affects sources of nitrate in wet and dry atmospheric deposition

2018 ◽  
Author(s):  
David M. Nelson ◽  
Urumu Tsunogai ◽  
Ding Dong ◽  
Takuya Ohyama ◽  
Daisuke D. Komatsu ◽  
...  
Keyword(s):  
Dry Deposition ◽  
Wet Deposition ◽  
Urban Environments ◽  
Rural Site ◽  
Urban Site ◽  
Peroxy Radicals ◽  
Long Distance ◽  
Wet And Dry Deposition ◽  
Atmospheric Nitrate ◽  
Nitrate Deposition

Abstract. Atmospheric nitrate deposition resulting from anthropogenic activities negatively affects human and environmental health. Identifying deposited nitrate that is produced locally vs. that originating from long-distance transport would help inform efforts to mitigate such impacts. However, distinguishing the relative transport distances of atmospheric nitrate in urban areas remains a major challenge since it may be produced locally and/or come from upwind regions. To address this uncertainty we assessed spatiotemporal variation in monthly weighted-average Δ17O and δ15N values of wet and dry nitrate deposition during one year at urban and rural sites along the western coast of the northern Japanese island of Hokkaido, downwind of the East Asian continent. Δ17O values of nitrate in wet deposition at the urban site mirrored those of wet and dry deposition at the rural site, ranging between ~ +22 and +30 ‰ with higher values during winter and lower values in summer, which suggests greater relative importance of oxidation of NO2 by O3 during winter and OH during summer. In contrast, Δ17O values of nitrate in dry deposition at the urban site were lower (+19–+25 ‰) and displayed less distinct seasonal variation. Furthermore, the difference between δ15N values of nitrate in wet and dry nitrate deposition was, on average, 3 ‰ greater at the urban than rural site, and Δ17O and δ15N values were correlated for both forms of deposition at both sites with the exception of dry deposition at the urban site. These results suggest that, relative to nitrate in wet deposition in urban environments and wet and dry deposition in rural environments, nitrate in dry deposition in urban environments forms from relatively greater oxidation of NO by peroxy radicals and/or oxidation of NO2 by OH. Given greater concentrations of peroxy radicals and OH in cities, these results imply that dry nitrate deposition results from local NOx emissions more so than wet deposition, which is transported longer distances. These results illustrate the value of stable isotope data for distinguishing the transport distances and reaction pathways of atmospheric nitrate pollution.

scholarly journals Introduction to project DUNE, a DUst experiment in a low Nutrient, low chlorophyll Ecosystem

2014 ◽  
Vol 11 (2) ◽  
pp. 425-442 ◽  
Author(s):  
C. Guieu ◽  
F. Dulac ◽  
C. Ridame ◽  
P. Pondaven
Keyword(s):  
Atmospheric Deposition ◽  
Surface Waters ◽  
Wet Deposition ◽  
Initial Conditions ◽  
Sediment Traps ◽  
Saharan Dust ◽  
Dust Particles ◽  
Dust Deposition ◽  
Mesocosm Experiments ◽  
Atmospheric Inputs

Abstract. The main goal of project DUNE was to estimate the impact of atmospheric deposition on an oligotrophic ecosystem based on mesocosm experiments simulating strong atmospheric inputs of eolian mineral dust. Our mesocosm experiments aimed at being representative of real atmospheric deposition events onto the surface of oligotrophic marine waters and were an original attempt to consider the vertical dimension after atmospheric deposition at the sea surface. This introductory paper describes the objectives of DUNE and the implementation plan of a series of mesocosm experiments conducted in the Mediterranean Sea in 2008 and 2010 during which either wet or dry and a succession of two wet deposition fluxes of 10 g m−2 of Saharan dust have been simulated based on the production of dust analogs from erodible soils of a source region. After the presentation of the main biogeochemical initial conditions of the site at the time of each experiment, a general overview of the papers published in this special issue is presented. From laboratory results on the solubility of trace elements in dust to biogeochemical results from the mesocosm experiments and associated modeling, these papers describe how the strong simulated dust deposition events impacted the marine biogeochemistry. Those multidisciplinary results are bringing new insights into the role of atmospheric deposition on oligotrophic ecosystems and its impact on the carbon budget. The dissolved trace metals with crustal origin – Mn, Al and Fe – showed different behaviors as a function of time after the seeding. The increase in dissolved Mn and Al concentrations was attributed to dissolution processes. The observed decrease in dissolved Fe was due to scavenging on sinking dust particles and aggregates. When a second dust seeding followed, a dissolution of Fe from the dust particles was then observed due to the excess Fe binding ligand concentrations present at that time. Calcium nitrate and sulfate were formed in the dust analog for wet deposition following evapocondensation with acids for simulating cloud processing by polluted air masses under anthropogenic influence. Using a number of particulate tracers that were followed in the water column and in the sediment traps, it was shown that the dust composition evolves after seeding by total dissolution of these salts. This provided a large source of new dissolved inorganic nitrogen (DIN) in the surface waters. In spite of this dissolution, the typical inter-elemental ratios in the particulate matter, such as Ti / Al or Ba / Al, are not affected during the dust settling, confirming their values as proxies of lithogenic fluxes or of productivity in sediment traps. DUNE experiments have clearly shown the potential for Saharan wet deposition to modify the in situ concentrations of dissolved elements of biogeochemical interest such as Fe and also P and N. Indeed, wet deposition yielded a transient increase in dissolved inorganic phosphorus (DIP) followed by a very rapid return to initial conditions or no return to initial conditions when a second dust seeding followed. By transiently increasing DIP and DIN concentrations in P- and N-starved surface waters of the Mediterranean Sea, wet deposition of Saharan dust can likely relieve the potential P and/or N limitation of biological activity; this has been directly quantified in terms of biological response. Wet deposition of dust strongly stimulated primary production and phytoplanktonic biomass during several days. Small phytoplankton (< 3 μm) was more stimulated after the first dust addition, whereas the larger size class (> 3 μm) significantly increased after the second one, indicating that larger-sized cells need further nutrient supply in order to be able to adjust their physiology and compete for resource acquisition and biomass increase. Among the microorganisms responding to the atmospheric inputs, diazotrophs were stimulated by both wet and dry atmospheric deposition, although N2 fixation was shown to be only responsible for a few percent of the induced new production. Dust deposition modified the bacterial community structure by selectively stimulating and inhibiting certain members of the bacterial community. The microbial food web dynamics were strongly impacted by dust deposition. The carbon budget indicates that the net heterotrophic character (i.e., ratio of net primary production to bacteria respiration < 1) of the tested waters remained (or was even increased) after simulated wet or dry deposition despite the significant stimulation of autotrophs after wet events. This indicates that the oligotrophic tested waters submitted to dust deposition are a net CO2 source. Nonetheless, the system was able to export organic material, half of it being associated with lithogenic particles through aggregation processes between lithogenic particles and organic matter. These observations support the "ballast" hypothesis and suggest that this "lithogenic carbon pump" could represent a major contribution of the global carbon export to deep waters in areas receiving high rates of atmospheric deposition. Furthermore, a theoretical microbial food web model showed that, all other things being equal, carbon, nitrogen and phosphorus stoichiometric mismatch along the food chain can have a substantial impact on the ecosystem response to nutrient inputs from dusts, with changes in the biomass of all biological compartments by a factor of ~ 2–4, and shifts from net autotrophy to net heterotrophy. Although the model was kept simple, it highlights the importance of stoichiometric constrains on the dynamics of microbial food webs.

Seasonal variations in black and organic carbon wet and dry deposition rates at SMEAR III station (60oN), Finland

2021 ◽  
Author(s):  
Outi Meinander ◽  
Enna Heikkinen ◽  
Jonas Svensson ◽  
Minna Aurela ◽  
Aki Virkkula ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Black Carbon ◽  
Dry Deposition ◽  
Wet Deposition ◽  
Total Carbon ◽  
Sampling Location ◽  
Atmospheric Measurements ◽  
Deposition Rates ◽  
Wet And Dry Deposition ◽  
Custom Made

&lt;p&gt;Black carbon (BC) and organic carbon (OC, including brown carbon BrC) aerosols in the atmosphere, and their wet and dry deposition, are important for their climatic and cryospheric effects. Seemingly small amounts of BC in snow, of the order of 10&amp;#8211;100 parts per billion by mass (ppb), have been shown to decrease its albedo by 1&amp;#8211;5 %. Due to the albedo-feedback mechanism, surface darkening accelerates snow and ice melt. In snow, the temporal variability of light absorbing aerosols, such as BC, depends both on atmospheric and cryospheric processes, mostly on sources and atmospheric transport, and dry and wet deposition processes, as well as post-depositional snow processes.&lt;/p&gt;&lt;p&gt;We started a new research activity on BC and OC wet and dry deposition at Helsinki Kumpula SMEAR III station (60&amp;#176;12 N, 24&amp;#176;57 E, Station for Measuring Ecosystem-Atmosphere Relations, https://www.atm.helsinki.fi/SMEAR/index.php/smear-iii). The work included winter, spring, summer and autumn deposition samples during January 2019 - June 2020 (sampling is currently on hold). In winter, wet deposition consisted of snowfall and rainwater samples. Dry deposition samples were separately collected in 2020. For sample collection, a custom-made device, including a heating-system, was applied. The samples were analyzed using the OCEC analyzer of the Finnish Meteorological Institute&amp;#8217;s aerosol laboratory, Helsinki, Finland. The special features in our deposition data are:&amp;#160;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;seasonal BC, OC, and TC (total carbon, the sum of BC and OC) deposition data for an urban background station at 60 &lt;sup&gt;o&lt;/sup&gt;N&lt;/li&gt; &lt;li&gt;precipitation received as either water or snow &amp;#160;&lt;/li&gt; &lt;li&gt;dry deposition samples included (only in 2020)&lt;/li&gt; &lt;li&gt;data as wet and dry deposition rates [concentration/time/area]&lt;/li&gt; &lt;li&gt;simultaneous atmospheric measurements of the SMEAR III station&lt;/li&gt; &lt;/ul&gt;&lt;p&gt;Since our deposition samples are collected manually, the data are non-continuous, yet they allow us to provide deposition rates. Such data can be utilized in various modeling approaches including, for example, climate and long-range transport and deposition modeling. According to our knowledge, these data are the first BC (determined as elemental carbon, EC), OC and TC wet and dry deposition data to represent Finland. Our sampling location, north of 60 deg. N, can be useful for other high-latitude studies and Arctic assessments, too.&lt;/p&gt;&lt;p&gt;&lt;em&gt;Acknowledgements. We gratefully acknowledge support from the Academy of Finland NABCEA-project of Novel Assessment of Black Carbon in the Eurasian Arctic (no. 296302) and the Academy of Finland Flagship funding (grant no. 337552).&lt;/em&gt;&lt;/p&gt;

scholarly journals Impact of dust deposition on carbon budget: a tentative assessment from a mesocosm approach

2014 ◽  
Vol 11 (19) ◽  
pp. 5621-5635 ◽  
Author(s):  
C. Guieu ◽  
C. Ridame ◽  
E. Pulido-Villena ◽  
M. Bressac ◽  
K. Desboeufs ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Atmospheric Deposition ◽  
Mediterranean Sea ◽  
Particulate Organic Carbon ◽  
Dry Deposition ◽  
Wet Deposition ◽  
Carbon Budget ◽  
Net Primary Production ◽  
Saharan Dust ◽  
Dust Deposition

Abstract. By bringing new nutrients and particles to the surface ocean, atmospheric deposition impacts biogeochemical cycles. The extent to which those changes are modifying the carbon balance in oligotrophic environments such as the Mediterranean Sea that receives important Saharan dust fluxes is unknown. The DUNE (DUst experiment in a low Nutrient, low chlorophyll Ecosystem) project provides the first attempt to evaluate the changes induced in the carbon budget of a large body of oligotrophic waters after simulated Saharan dust wet or dry deposition events, allowing us to measure (1) the metabolic fluxes while the particles are sinking and (2) the particulate organic carbon export. Here we report the results for the three distinct artificial dust seeding experiments simulating wet or dry atmospheric deposition onto large mesocosms (52 m3) that were conducted in the oligotrophic waters of the Mediterranean Sea in the summers of 2008 and 2010. Although heterotrophic bacteria were found to be the key players in the response to dust deposition, net primary production increased about twice in case of simulated wet deposition (that includes anthropogenic nitrogen). The dust deposition did not produce a shift in the metabolic balance as the tested waters remained net heterotrophic (i.e., net primary production to bacteria respiration ratio <1) and in some cases the net heterotrophy was even enhanced by the dust deposition. The change induced by the dust addition on the total organic carbon pool inside the mesocosm over the 7 days of the experiments, was a carbon loss dominated by bacteria respiration that was at least 5–10 times higher than any other term involved in the budget. This loss of organic carbon from the system in all the experiments was particularly marked after the simulation of wet deposition. Changes in biomass were mostly due to an increase in phytoplankton biomass but when considering the whole particulate organic carbon pool it was dominated by the organic carbon aggregated to the lithogenic particles still in suspension in the mesocosm at the end of the experiment. Assuming that the budget is balanced, the dissolved organic carbon (DOC) pool was estimated by the difference between the total organic carbon and the particulate organic carbon (POC) pool. The partitioning between dissolved and particulate organic carbon was dominated by the dissolved pool with a DOC consumption over 7 days of ∼1 μmol C L−1 d−1 (dry deposition) to ∼2–5 μmol C L−1 d−1 (wet deposition). This consumption in the absence of any allochthonous inputs in the closed mesocosms meant a small <10% decrease of the initial DOC stock after a dry deposition but a ∼30–40% decrease of the initial DOC stock after wet deposition. After wet deposition, the tested waters, although dominated by heterotrophy, were still maintaining a net export (corrected from controls) of particulate organic carbon (0.5 g in 7 days) even in the absence of allochthonous carbon inputs. This tentative assessment of the changes in carbon budget induced by a strong dust deposition indicates that wet deposition by bringing new nutrients has higher impact than dry deposition in oligotrophic environments. In the western Mediterranean Sea, the mineral dust deposition is dominated by wet deposition and one perspective of this work is to extrapolate our numbers to time series of deposition during similar oligotrophic conditions to evaluate the overall impact on the carbon budget at the event and seasonal scale in the surface waters of the northwestern Mediterranean Sea. These estimated carbon budgets are also highlighting the key processes (i.e., bacterial respiration) that need to be considered for an integration of atmospheric deposition in marine biogeochemical modeling.

scholarly journals Elemental carbon in snow at Changbai Mountain, northeastern China: concentrations, scavenging ratios, and dry deposition velocities

2014 ◽  
Vol 14 (2) ◽  
pp. 629-640 ◽  
Author(s):  
Z. W. Wang ◽  
J. C. Gallet ◽  
C. A. Pedersen ◽  
X. S. Zhang ◽  
J. Ström ◽  
...  
Keyword(s):  
Dry Deposition ◽  
Wet Deposition ◽  
Radiative Forcing ◽  
Elemental Carbon ◽  
Northeastern China ◽  
Snow Surface ◽  
Deposition Fluxes ◽  
The Mean ◽  
Deposition Processes ◽  
Scavenging Ratio

Abstract. Light-absorbing aerosol – particularly elemental carbon (EC) – while mixed with snow and ice is an important climate driver from the enhanced absorption of solar radiation. Currently, considerable efforts are being made to estimate its radiative forcing on a global scale, but several uncertainties remain, particularly those regarding its deposition processes. In this study, concurrent measurements of EC in air and snow are performed for three years (2009–2012) at Changbai station, northeastern China. The scavenging ratio and the wet- and dry-deposition fluxes of EC over the snow surface are estimated. The mean EC concentration in the surface snow is 1000 ± 1500 ng g−1, ranging from 7 to 7640 ng g−1. The mean value of the scavenging ratio of EC by snow is 140 ± 100, with a median value of 150, which is smaller than that reported in Arctic areas. A non-rimed snow process is a significant factor in interpreting differences with Arctic areas. Wet-deposition fluxes of EC are estimated to be 0.47 ± 0.37 μg cm−2 month−1 on average over the three snow seasons studied. Dry deposition is more than five times higher, with an average of 2.65 ± 1.93 μg cm−2 month−1; however, only winter period estimation is possible (December–February). During winter in Changbai, 87% of EC in snow is estimated to be due to dry deposition, with a mean dry deposition velocity of 6.44 × 10−3 m s−1 and median of 8.14 × 10−3 m s−1. Finally, the calculation of the radiative effect shows that 500 ng g−1 of dry-deposited EC to a snow surface absorbs three times more incoming solar energy than the same mass mixed in the snow through wet deposition. Deposition processes of an EC-containing snow surface are, therefore, crucial to estimate its radiative forcing better, particularly in northeastern China, where local emission strongly influences the level and gradient of EC in the snowpack, and snow-covered areas are cold and dry due to the atmospheric general circulation. Furthermore, this study builds on the knowledge to characterize the conditions in the snow-laden Chinese rural areas better as well as to constrain transport of EC to the Arctic better.

Environmental Significance of Holocene Dust Accumulation in Archaeological Hilltop Ruins in the Southern Levant

2020 ◽  
Author(s):  
Joel Roskin ◽  
Bernhard Lucke ◽  
Kim André Vanselow ◽  
Hendrik J. Bruins ◽  
Nizar Abu-Jaber ◽  
...  
Keyword(s):  
Dry Deposition ◽  
Wet Deposition ◽  
Sediment Sources ◽  
Dust Deposition ◽  
Southern Levant ◽  
Environmental Significance ◽  
Crust Formation ◽  
Loess Deposition ◽  
End Members ◽  
Sedimentation Processes

&lt;p&gt;Pleistocene primary and secondary loess remains cover large parts of the landscape in the Negev in Israel and have been postulated in southern Jordan, but Holocene deposits are absent. We hypothesized that archaeological structures might represent effective dust traps which preserve Holocene dust, and investigated soils developed on archaeological hilltop ruins. These were compared them with local soils, paleosols, geological outcrops, and current dust. Statistically modeled grain size end-members were identified and demonstrate that the ruin soils in both regions consist of mixtures of local and remote sediment sources that differ from dust compositions deposited during current storms. This discrepancy is attributed to fixation processes connected with sediment-fixing agents such as vegetation, biocrusts, and/or clast pavements associated with vesicular layers (similar to desert pavements). It suggests that dust deposition depends not only on supply, but that sedimentation processes play a major role. Precipitation may have contributed to dust accretion, as a snowstorm in the Petra region delivered a significantly higher amount of sediment than rain or dry deposition. Snowfall dust had a unique particle size distribution relatively similar to the ruin soils. Wet deposition and snow might catalyze dust deposition and enhance fixation by fostering vegetation and crust formation, which suggests that more frequent snowfall during the Pleistocene may have been an important mechanism of primary loess deposition in the southern Levant.&lt;/p&gt;

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