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2.
ISME J ; 16(6): 1479-1490, 2022 06.
Article in English | MEDLINE | ID: mdl-35082431

ABSTRACT

Hydrothermal plumes transport reduced chemical species and metals into the open ocean. Despite their considerable spatial scale and impact on biogeochemical cycles, niche differentiation of abundant microbial clades is poorly understood. Here, we analyzed the microbial ecology of two bathy- (Brothers volcano; BrV-cone and northwest caldera; NWC) and a mesopelagic (Macauley volcano; McV) plumes on the Kermadec intra-oceanic arc in the South Pacific Ocean. The microbial community structure, determined by a combination of 16S rRNA gene, fluorescence in situ hybridization and metagenome analysis, was similar to the communities observed in other sulfur-rich plumes. This includes a dominance of the vent characteristic SUP05 clade (up to 22% in McV and 51% in BrV). In each of the three plumes analyzed, the community was dominated by a different yet uncultivated chemoautotrophic SUP05 species, here, provisionally named, Candidatus Thioglobus vadi (McV), Candidatus Thioglobus vulcanius (BrV-cone) and Candidatus Thioglobus plumae (BrV-NWC). Statistical analyses, genomic potential and mRNA expression profiles suggested a SUP05 niche partitioning based on sulfide and iron concentration as well as water depth. A fourth SUP05 species was present at low frequency throughout investigated plume samples and may be capable of heterotrophic or mixotrophic growth. Taken together, we propose that small variations in environmental parameters and depth drive SUP05 niche partitioning in hydrothermal plumes.


Subject(s)
Hydrothermal Vents , Bacteria , Hydrothermal Vents/microbiology , In Situ Hybridization, Fluorescence , Oxidation-Reduction , Phylogeny , RNA, Ribosomal, 16S/genetics , RNA, Ribosomal, 16S/metabolism , Seawater/microbiology , Sulfur/metabolism
3.
Sci Adv ; 7(25)2021 Jun.
Article in English | MEDLINE | ID: mdl-34134989

ABSTRACT

Today's oceans store as much dissolved organic carbon (DOC) in the water column as there is CO2 in the atmosphere, and as such dissolved organic matter (DOM) is an important component of the global carbon cycle. It was shown that in anoxic marine sediments, reduced sulfur species (e.g., H2S) abiotically react with organic matter, contributing to carbon preservation. It is not known whether such processes also contribute to preserving DOM in ocean waters. Here, we show DOM sulfurization within the sulfidic waters of the Black Sea, by combining elemental, isotopic, and molecular analyses. Dissolved organic sulfur (DOS) is formed largely in the water column and not derived from sediments or allochthonous nonmarine sources. Our findings suggest that during large-scale anoxic events, DOM may accumulate through abiotic reactions with reduced sulfur species, having long-lasting effects on global climate by enhancing organic carbon sequestration.

4.
Environ Sci Technol ; 54(7): 4528-4535, 2020 04 07.
Article in English | MEDLINE | ID: mdl-32167291

ABSTRACT

Reducing CO2 emissions is a key task of modern society to attenuate climate change and its environmental effects. Accelerated weathering of limestone (AWL) has been proposed as a tool to capture CO2 from effluent gas streams and store it primarily as bicarbonate in the marine environment. We evaluated the performance of the biggest AWL-reactor to date that was installed at a coal-fired power plant in Germany. Depending on the gas flow rate, approximately 55% of the CO2 could be removed from the flue gas. The generated product water was characterized by an up to 5-fold increase in alkalinity, which indicates the successful weathering of limestone and the long-term storage of the captured CO2. A rise of potentially harmful substances in the product water (NO2-, NOx-, NH4+, SO42-, and heavy metals) or in unreacted limestone particles (heavy metals) to levels of environmental concern could not be observed, most likely as a result of a desulfurization of the flue gas before it entered the AWL reactor. At locations where limestone and water availability is high, AWL could be used for a safe and long-term storage of CO2.


Subject(s)
Air Pollutants , Carbon Dioxide , Calcium Carbonate , Carbon , Coal , Germany , Power Plants
5.
Ecol Evol ; 8(13): 6699-6713, 2018 Jul.
Article in English | MEDLINE | ID: mdl-30038768

ABSTRACT

Plant performance is correlated with element concentrations in plant tissue, which may be impacted by adverse chemical soil conditions. Antibiotics of veterinary origin can adversely affect plant performance. They are released to agricultural fields via grazing animals or manure, taken up by plants and may be stored, transformed or sequestered by plant metabolic processes. We studied the potential effects of three antibiotics (penicillin, sulfadiazine, and tetracycline) on plant element contents (macro- and microelements). Plant species included two herb species (Brassica napus and Capsella bursa-pastoris) and two grass species (Triticum aestivum and Apera spica-venti), representing two crop species and two noncrop species commonly found in field margins, respectively. Antibiotic concentrations were chosen as to reflect in vivo situations, that is, relatively low concentrations similar to those detected in soils. In a greenhouse experiment, plants were raised in soil spiked with antibiotics. After harvest, macro- and microelements in plant leaves, stems, and roots were determined (mg/g). Results indicate that antibiotics can affect element contents in plants. Penicillin exerted the greatest effect both on element contents and on scaling relationships of elements between plant organs. Roots responded strongest to antibiotics compared to stems and leaves. We conclude that antibiotics in the soil, even in low concentrations, lead to low-element homeostasis, altering the scaling relationships between roots and other plant organs, which may affect metabolic processes and ultimately the performance of a plant.

6.
Nat Commun ; 8: 14914, 2017 04 11.
Article in English | MEDLINE | ID: mdl-28398353

ABSTRACT

Changes in penguin populations on the Antarctic Peninsula have been linked to several environmental factors, but the potentially devastating impact of volcanic activity has not been considered. Here we use detailed biogeochemical analyses to track past penguin colony change over the last 8,500 years on Ardley Island, home to one of the Antarctic Peninsula's largest breeding populations of gentoo penguins. The first sustained penguin colony was established on Ardley Island c. 6,700 years ago, pre-dating sub-fossil evidence of Peninsula-wide occupation by c. 1,000 years. The colony experienced five population maxima during the Holocene. Overall, we find no consistent relationships with local-regional atmospheric and ocean temperatures or sea-ice conditions, although the colony population maximum, c. 4,000-3,000 years ago, corresponds with regionally elevated temperatures. Instead, at least three of the five phases of penguin colony expansion were abruptly ended by large eruptions from the Deception Island volcano, resulting in near-complete local extinction of the colony, with, on average, 400-800 years required for sustainable recovery.


Subject(s)
Fossils , Ice Cover , Spheniscidae/physiology , Volcanic Eruptions , Algorithms , Animals , Antarctic Regions , Geography , Islands , Models, Theoretical , Population Dynamics , Temperature
7.
Front Microbiol ; 8: 2550, 2017.
Article in English | MEDLINE | ID: mdl-29326679

ABSTRACT

By now, only limited information on the Roseobacter group thriving at the seafloor is available. Hence, the current study was conducted to determine their abundance and diversity within Pacific sediments along the 180° meridian. We hypothesize a distinct biogeographical distribution of benthic members of the Roseobacter group linked to nutrient availability within the sediments and productivity of the water column. Lowest cell numbers were counted at the edge of the south Pacific gyre and within the north Pacific gyre followed by an increase to the north with maximum values in the highly productive Bering Sea. Specific quantification of the Roseobacter group revealed on average a relative abundance of 1.7 and 6.3% as determined by catalyzed reported deposition-fluorescence in situ hybridization (CARD-FISH) and quantitative PCR (qPCR), respectively. Corresponding Illumina tag sequencing of 16S rRNA genes and 16S rRNA transcripts showed different compositions containing on average 0.7 and 0.9% Roseobacter-affiliated OTUs of the DNA- and RNA-based communities. These OTUs were mainly assigned to uncultured members of the Roseobacter group. Among those with cultured representatives, Sedimentitalea and Sulfitobacter made up the largest proportions. The different oceanic provinces with low nutrient content such as both ocean gyres were characterized by specific communities of the Roseobacter group, distinct from those of the more productive Pacific subarctic region and the Bering Sea. However, linking the community structure to specific metabolic processes at the seafloor is hampered by the dominance of so-far uncultured members of the Roseobacter group, indicating a diversity that has yet to be explored.

8.
Environ Monit Assess ; 187(7): 401, 2015 Jul.
Article in English | MEDLINE | ID: mdl-26041061

ABSTRACT

Heavy metal contamination of clay waste through the phosphate beneficiation process is a serious problem faced by scientists and regulators worldwide. Through the beneficiation process, heavy metals naturally present in the phosphate rocks became concentrated in the clay waste. This study evaluated the concentration of heavy metals and their fractions in the clay waste in order to assess the risk of environmental contamination. A five-step sequential extraction method, the risk assessment code (RAC), effects range low (ERL), effects range medium (ERM), the lowest effect level (LEL), the severe effect level (SEL), the redistribution index (U tf), the reduced partition index (I), residual partition index (I R), and the Nemerow multi-factor index (PC) were used to assess for clay waste contamination. Heavy metals were analyzed using high-resolution inductively coupled plasma mass spectrometry (HR-ICP-MS) and inductively coupled plasma optical emission spectroscopy (ICP-OES). Correlation analyses were carried out to better understand the relationships between the chemical characteristics and the contents of the different phase fractions. Concentrations of Cd and Cu confirmed that both were bound to the exchangeable fraction (F1) and the carbonate fraction (F2), presenting higher mobility, whereas Pb was most abundant in the Fe-Mn oxide fraction (F3) and organic matter fraction (F4). The residual fraction (F5) contained the highest concentrations (>60%) of As, Cr, Mo, V, and Zn, with lower mobility. Application of the RAC index showed that Cd and Cu should be considered a moderate risk, whereas As, Cr, Mo, Pb, and Zn presented a low risk. Cadmium and Cu contents in mobile fractions F1 and F2 were higher than ERL but lower than ERM. On the other hand, As, Pb, and Zn contents of mobile fractions F1 and F2 were lower than ERL and ERM guideline values. Moreover, total Pb concentrations in the clay waste were below the lowest effect level (LEL) threshold value period, Cr and Zn values in the clay waste were determined to have exceeded the severe effect level (SEL) limit values, whereas Cd and Cu level ranges between LEL and SEL indicate moderate contamination. I R values of heavy metals in the clay waste confirmed that Cd and Cu were bound to the exchangeable and carbonate fractions and presented higher mobility, whereas As, Cr, Mo, Pb, V, and Zn were bound to organic or residual fractions and consequently exhibit lower mobility. A Nemerow multi-factor index revealed that the mine site contains high levels of Cd, Cu, V, and Zn pollution. As and Cr were found at a moderate level of contamination, whereas Pb was present at a safe level of contamination. The order of the comprehensive contamination indices was Cd > Cu > Mo > Zn > V > Cr > As > Pb, indicating that the assessment of clay waste, especially with Cd and Cu, should be undertaken to control heavy metal contamination in adjacent urban and mine areas at the Eshidiya mines.


Subject(s)
Aluminum Silicates/analysis , Arsenic/analysis , Industrial Waste/analysis , Metals, Heavy/analysis , Clay , Environmental Monitoring , Jordan , Mining , Phosphates , Risk Assessment
9.
PLoS One ; 9(7): e101139, 2014.
Article in English | MEDLINE | ID: mdl-24988389

ABSTRACT

Phosphorus (P) is a key nutrient for marine organisms. The only long-term removal pathway for P in the marine realm is burial in sediments. Iron (Fe) bound P accounts for a significant proportion of this burial at the global scale. In sediments underlying anoxic bottom waters, burial of Fe-bound P is generally assumed to be negligible because of reductive dissolution of Fe(III) (oxyhydr)oxides and release of the associated P. However, recent work suggests that Fe-bound P is an important burial phase in euxinic (i.e. anoxic and sulfidic) basin sediments in the Baltic Sea. In this study, we investigate the role of Fe-bound P as a potential sink for P in Black Sea sediments overlain by oxic and euxinic bottom waters. Sequential P extractions performed on sediments from six multicores along two shelf-to-basin transects provide evidence for the burial of Fe-bound P at all sites, including those in the euxinic deep basin. In the latter sediments, Fe-bound P accounts for more than 20% of the total sedimentary P pool. We suggest that this P is present in the form of reduced Fe-P minerals. We hypothesize that these minerals may be formed as inclusions in sulfur-disproportionating Deltaproteobacteria. Further research is required to elucidate the exact mineral form and formation mechanism of this P burial phase, as well as its role as a sink for P in sulfide-rich marine sediments.


Subject(s)
Deltaproteobacteria/physiology , Iron Compounds/chemistry , Minerals/chemistry , Phosphates/chemistry , Water Microbiology , Black Sea , Iron Compounds/metabolism , Minerals/metabolism , Phosphates/metabolism , Sulfides/chemistry , Sulfides/metabolism
10.
Mar Pollut Bull ; 70(1-2): 100-11, 2013 May 15.
Article in English | MEDLINE | ID: mdl-23490348

ABSTRACT

Recently, within the framework of European directives, the importance of marine monitoring programs has increased. In this study, a dense sampling grid was applied for a detailed assessment of the metal contents of surface sediments and suspended particulate matter from the Jade Bay, one of the tidal basins in the southern North Sea. The local lithogenic background was defined and compared with average shale, a common reference material. Based on the calculated non-lithogenic fraction and a cluster analysis, the metals are distributed in two groups: (i) elements of mainly natural origin (Co, Cr, and a major portion of Cd) and (ii) elements associated with anthropogenic activity (As, Cd, Cu, Ni, Pb, Sn, and Zn). However, even the metals of the second group are enriched by at most a factor of two relative to the local background, suggesting minimal anthropogenic impact. Spatial distribution maps show that the harbor area of Wilhelmshaven may be a particularly important source of metal.


Subject(s)
Environmental Monitoring , Geologic Sediments/chemistry , Metals/analysis , Water Pollutants, Chemical/analysis , Bays/chemistry , Germany , Particulate Matter/analysis , Particulate Matter/chemistry , Seawater/chemistry , Water Pollution, Chemical/statistics & numerical data
11.
ISME J ; 7(4): 850-67, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23254516

ABSTRACT

Ancient mariners knew that dust whipped up from deserts by strong winds travelled long distances, including over oceans. Satellite remote sensing revealed major dust sources across the Sahara. Indeed, the Bodélé Depression in the Republic of Chad has been called the dustiest place on earth. We analysed desert sand from various locations in Chad and dust that had blown to the Cape Verde Islands. High throughput sequencing techniques combined with classical microbiological methods showed that the samples contained a large variety of microbes well adapted to the harsh desert conditions. The most abundant bacterial groupings in four different phyla included: (a) Firmicutes-Bacillaceae, (b) Actinobacteria-Geodermatophilaceae, Nocardiodaceae and Solirubrobacteraceae, (c) Proteobacteria-Oxalobacteraceae, Rhizobiales and Sphingomonadaceae, and (d) Bacteroidetes-Cytophagaceae. Ascomycota was the overwhelmingly dominant fungal group followed by Basidiomycota and traces of Chytridiomycota, Microsporidia and Glomeromycota. Two freshwater algae (Trebouxiophyceae) were isolated. Most predominant taxa are widely distributed land inhabitants that are common in soil and on the surfaces of plants. Examples include Bradyrhizobium spp. that nodulate and fix nitrogen in Acacia species, the predominant trees of the Sahara as well as Herbaspirillum (Oxalobacteraceae), a group of chemoorganotrophic free-living soil inhabitants that fix nitrogen in association with Gramineae roots. Few pathogenic strains were found, suggesting that African dust is not a large threat to public health.


Subject(s)
Air Microbiology , Bacteria/classification , Bacteria/isolation & purification , Dust , Fungi/classification , Wind , Africa, Northern , Cabo Verde , Chad , Desert Climate , Dust/analysis , Fungi/isolation & purification , Soil/analysis
12.
Talanta ; 85(3): 1695-7, 2011 Sep 15.
Article in English | MEDLINE | ID: mdl-21807241

ABSTRACT

We present a method for the rapid and direct determination of dissolved Thallium (Tl) using high resolution sector field inductively coupled mass spectrometry (SF-ICP-MS) suitable for the measurement of large time series (e.g. during monitoring). Thallium data are presented for a series of natural sea water samples, which were validated with sea water standards CASS-4 and NASS-5. The sea water samples and standards were diluted 10 times prior to measurement with SF-ICP-MS in low resolution mode (R=300, LR). For both CASS-4 and NASS-5 (salinity of 30.5) we calculated a concentration of about 11 ng L(-1) when using Tl values of 14±2 ng L(-1) (at salinity of 35±1) published by Flegal and Patterson for Atlantic and Pacific sea water. For CASS-4 we report a Tl value of 10.6±0.7 ng L(-1) (n=70), for NASS-5 a Tl value of 10.3±0.8 ng L(-1) (n=11). For Tl in both CASS-4 and NASS-5, the overall error in accuracy and precision is less than 4% and 8% (2s), respectively. Further, values of 7.7±0.3 and 6.7±0.2 ng L(-1) Tl were found for the estuarine standard SLEW-3 (salinity of 15) and the river water standard SLRS-4, respectively, for which no certified value exists so far. The detection and quantification limits of our method are 0.1 and 0.3 ng L(-1), respectively. Slight differences in the accuracy of our method and other published methods for the determination of Tl in sea water are discussed. Time-series of natural coastal water samples gave Tl values (6-12 ng L(-1)), which correspond to determined salinities, and hence, appear realistic and oceanographically consistent.


Subject(s)
Mass Spectrometry/methods , Seawater/analysis , Thallium/analysis , Fresh Water/analysis , Fresh Water/chemistry , Geography , Germany , Reproducibility of Results , Rivers/chemistry , Seawater/chemistry , Time Factors
13.
FEMS Microbiol Ecol ; 71(2): 226-36, 2010 Feb.
Article in English | MEDLINE | ID: mdl-19925634

ABSTRACT

Oxic-anoxic interfaces harbor significant numbers and activity of chemolithoautotrophic microorganisms, known to oxidize reduced sulfur or nitrogen species. However, measurements of in situ distribution of bulk carbon dioxide (CO(2)) assimilation rates and active autotrophic microorganisms have challenged the common concept that aerobic and denitrifying sulfur oxidizers are the predominant autotrophs in pelagic oxic-anoxic interfaces. Here, we provide a comparative investigation of nutrient, sulfur, and manganese chemistry, microbial biomass distribution, as well as CO(2) fixation at the pelagic redoxcline of the eastern Gotland Basin, Baltic Sea. Opposing gradients of oxygen, nitrate, and sulfide approached the detection limits at the chemocline at 204 m water depth. No overlap of oxygen or nitrate with sulfide was observed, whereas particulate manganese was detected down to 220 m. More than 70% of the bulk dark CO(2) assimilation, totaling 9.3 mmol C m(-2) day(-1), was found in the absence of oxygen, nitrite, and nitrate and could not be stimulated by their addition. Maximum fixation rates of up to 1.1 mumol C L(-1) day(-1) were surprisingly susceptible to altered redox potential or sulfide concentration. These results suggest that novel redox-sensitive pathways of microbial sulfide oxidation could account for a significant fraction of chemolithoautotrophic growth beneath pelagic chemoclines. A mechanism of coupled activity of sulfur-oxidizing and sulfur-reducing microorganisms is proposed.


Subject(s)
Carbon Dioxide/metabolism , Epsilonproteobacteria/metabolism , Gammaproteobacteria/metabolism , Sulfur/metabolism , Water Microbiology , Anaerobiosis , Biomass , Nitrates/analysis , Nitrites/analysis , Oxidation-Reduction , Oxygen/analysis , Seawater/chemistry , Seawater/microbiology
14.
Environ Microbiol ; 9(12): 2911-22, 2007 Dec.
Article in English | MEDLINE | ID: mdl-17956563

ABSTRACT

Charles Darwin, like others before him, collected aeolian dust over the Atlantic Ocean and sent it to Christian Gottfried Ehrenberg in Berlin. Ehrenberg's collection is now housed in the Museum of Natural History and contains specimens that were gathered at the onset of the Industrial Revolution. Geochemical analyses of this resource indicated that dust collected over the Atlantic in 1838 originated from the Western Sahara, while molecular-microbiological methods demonstrated the presence of many viable microbes. Older samples sent to Ehrenberg from Barbados almost two centuries ago also contained numbers of cultivable bacteria and fungi. Many diverse ascomycetes, and eubacteria were found. Scanning electron microscopy and cultivation suggested that Bacillus megaterium, a common soil bacterium, was attached to historic sand grains, and it was inoculated onto dry sand along with a non-spore-forming control, the Gram-negative soil bacterium Rhizobium sp. NGR234. On sand B. megaterium quickly developed spores, which survived for extended periods and even though the numbers of NGR234 steadily declined, they were still considerable after months of incubation. Thus, microbes that adhere to Saharan dust can live for centuries and easily survive transport across the Atlantic.


Subject(s)
Bacteria , Dust , Fungi , Microbiology/history , Wind , Africa, Western , Atlantic Ocean , Bacillus megaterium/growth & development , Bacteria/classification , Bacteria/genetics , Bacteria/growth & development , Barbados , Fungi/classification , Fungi/genetics , Fungi/growth & development , History, 19th Century , Microbial Viability , Minerals/analysis , Minerals/chemistry , Rhizobium/growth & development , Silicon Dioxide
15.
Anal Chem ; 75(14): 3396-3403, 2003 Jul 15.
Article in English | MEDLINE | ID: mdl-14570189

ABSTRACT

A simple method of simultaneous preconcentration and matrix reduction was developed for the analysis of rare earth elements (REEs) in seawater and groundwater by ID ICPMS. The method utilizes partitioning of the REEs with solid hydroxides to separate them from soluble matrix species (e.g., Ba2+, NOM, seawater salts). Acidified samples were spiked and equilibrated with an enriched isotope cocktail (142Ce, 145Nd, 161Dy, 171Yb). Aqueous NH3 was then added to the spiked samples to induce the coprecipitation of the REEs with a small fraction of the natural Mg2+ as Mg(OH)2. The samples were centrifuged and the precipitate was rinsed to remove more than 99.8% of the Ba2+ along with the matrix salts. The precipitate was dissolved in 400 microL of 10% HNO3 for ICPMS analysis. The four spiked elements, determined by isotope dilution, served as internal standards for the remaining REEs. Analysis of NASS-4 and NASS-5 seawater reference materials showed good agreement with published values. Calculated limits of detection for a 1.65-g sample ranged from 0.1 pg/g for the light REEs to 0.02 pg/g for the heavy REEs. The reagent blanks ranged from a high of 0.28 pg/sample for Ce to a low of 0.0036 pg/sample for Tb.


Subject(s)
Fresh Water/analysis , Metals, Rare Earth/analysis , Seawater/analysis , Indicators and Reagents , Mass Spectrometry
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