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| 2. |
- Cheung, Henry Lok Shan, et al.
(author)
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Denitrification, anammox, and DNRA in oligotrophic continental shelf sediments
- 2024
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In: Limnology and Oceanography. - 1939-5590 .- 0024-3590.
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Journal article (peer-reviewed)abstract
- Continental shelf sediments are considered hotspots for nitrogen (N) removal. While most investigations have quantified denitrification in shelves receiving large amounts of anthropogenic nutrient supply, we lack insight into the key drivers of N removal on oligotrophic shelves. Here, we measured rates of N removal through denitrification and anammox by the revised-isotope pairing technique (r-IPT) along the Northeastern New Zealand shelf. Denitrification dominated total N2 production at depths between 30 and 128 m with average rates (± SE) ranging from 65 ± 28 to 284 ± 72 μmol N m−2 d−1. N2 production by anammox ranged from 3 ± 1 to 28 ± 11 μmol N m−2 d−1 and accounted for 2–19% of total N2 production. DNRA was negligible in these oligotrophic settings. Parallel microbial community analysis showed that both Proteobacteria and Planctomycetota were key taxa driving denitrification. Denitrification displayed a negative correlation with oxygen penetration depth, and a positive correlation with macrofauna abundance. Our denitrification rates were comparable to oligotrophic shelves from the Arctic, but were lower than those from nutrient-rich Pacific and Atlantic shelves. Based on our results and existing IPT measurements, the global shelf denitrification rate was reassessed to be 53.5 ± 8.1 Tg N yr−1, equivalent to 20 ± 2% of marine N removal. We suggest that previous estimates of global shelf N loss might have been overestimated due to sampling bias toward areas with high N loads in the Northern Hemisphere.
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| 3. |
- Roth, Florian, et al.
(author)
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High spatiotemporal variability of methane concentrations challenges estimates of emissions across vegetated coastal ecosystems.
- 2022
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In: Global change biology. - : Wiley. - 1365-2486 .- 1354-1013. ; 28:14, s. 4308-4322
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Journal article (peer-reviewed)abstract
- Coastal methane (CH4 ) emissions dominate the global ocean CH4 budget and can offset the "blue carbon" storage capacity of vegetated coastal ecosystems. However, current estimates lack systematic, high-resolution, and long-term data from these intrinsically heterogeneous environments, making coastal budgets sensitive to statistical assumptions and uncertainties. Using continuous CH4 concentrations, δ13 C-CH4 values, and CH4 sea-air fluxes across four seasons in three globally pervasive coastal habitats, we show that the CH4 distribution is spatially patchy over meter-scales and highly variable in time. Areas with mixed vegetation, macroalgae, and their surrounding sediments exhibited a spatiotemporal variability of surface water CH4 concentrations ranging two orders of magnitude (i.e., 6-460 nM CH4 ) with habitat-specific seasonal and diurnal patterns. We observed (1) δ13 C-CH4 signatures that revealed habitat-specific CH4 production and consumption pathways, (2) daily peak concentration events that could change >100% within hours across all habitats, and (3) a high thermal sensitivity of the CH4 distribution signified by apparent activation energies of ~1 eV that drove seasonal changes. Bootstrapping simulations show that scaling the CH4 distribution from few samples involves large errors, and that ~50 concentration samples per day are needed to resolve the scale and drivers of the natural variability and improve the certainty of flux calculations by up to 70%. Finally, we identify northern temperate coastal habitats with mixed vegetation and macroalgae as understudied but seasonally relevant atmospheric CH4 sources (i.e., releasing ≥ 100 μmol CH4 m-2 day-1 in summer). Due to the large spatial and temporal heterogeneity of coastal environments, high-resolution measurements will improve the reliability of CH4 estimates and confine the habitat-specific contribution to regional and global CH4 budgets.
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| 4. |
- Wurzbacher, Christian, 1980, et al.
(author)
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Poorly known microbial taxa dominate the microbiome of permafrost thaw ponds.
- 2017
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In: The ISME journal. - : Springer Science and Business Media LLC. - 1751-7370 .- 1751-7362. ; 11:8, s. 1938-1941
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Journal article (peer-reviewed)abstract
- In the transition zone of the shifting permafrost border, thaw ponds emerge as hotspots of microbial activity, processing the ancient carbon freed from the permafrost. We analyzed the microbial succession across a gradient of recently emerged to older ponds using three molecular markers: one universal, one bacterial and one fungal. Age was a major modulator of the microbial community of the thaw ponds. Surprisingly, typical freshwater taxa comprised only a small fraction of the community. Instead, thaw ponds of all age classes were dominated by enigmatic bacterial and fungal phyla. Our results on permafrost thaw ponds lead to a revised perception of the thaw pond ecosystem and their microbes, with potential implications for carbon and nutrient cycling in this increasingly important class of freshwaters.
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| 5. |
- Wang, Y. J., et al.
(author)
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The formation of nitro-aromatic compounds under high NOx and anthropogenic VOC conditions in urban Beijing, China
- 2019
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In: Atmospheric Chemistry and Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 19:11, s. 7649-7665
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Journal article (peer-reviewed)abstract
- Nitro-aromatic compounds (NACs), as important contributors to the light absorption by brown carbon, have been widely observed in various ambient atmospheres; however, their formation in the urban atmosphere was little studied. In this work, we report an intensive field study of NACs in summer 2016 at an urban Beijing site, characterized by both high-NO(x)and anthropogenic VOC dominated conditions. We investigated the factors that influence NAC formation (e.g., NO2, VOC precursors, RH and photolysis) through quantification of eight NACs, along with major components in fine particulate matter, selected volatile organic compounds, and gases. The average total concentration of the quantified NACs was 6.63 ng m(-3), higher than those reported in other summertime studies (0.14-6.44 ng m(-3)). 4-Nitrophenol (4NP, 32.4 %) and 4-nitrocatechol (4NC, 28.5 %) were the top two most abundant NACs, followed by methyl-nitrocatechol (MNC), methyl-nitrophenol (MNP), and dimethyl-nitrophenol (DMNP). The oxidation of toluene and benzene in the presence of NOx was found to be a more dominant source of NACs than primary biomass burning emissions. The NO2 concentration level was found to be an important factor influencing the secondary formation of NACs. A transition from low- to high-NOx regimes coincided with a shift from organic- to inorganic-dominated oxidation products. The transition thresholds were NO2 similar to 20 ppb for daytime and NO2 similar to 25 ppb for nighttime conditions. Under low-NOx conditions, NACs increased with NO2, while the NO3 concentrations and (NO3-)/NACs ratios were lower, implying organic-dominated products. Under high-NOx conditions, NAC concentrations did not further increase with NO2, while the NO3- concentrations and (NO3-)/NACs ratios showed increasing trends, signaling a shift from organic- to inorganic-dominated products. Nighttime enhancements were observed for 3M4NC and 4M5NC, while daytime enhancements were noted for 4NP, 2M4NP, and DMNP, indicating different formation pathways for these two groups of NACs. Our analysis suggested that the aqueous-phase oxidation was likely the major formation pathway of 4M5NC and 3M5NC, while photo-oxidation of toluene and benzene in the presence of NO2 could be more important for the formation of nitrophenol and its derivatives. Using the (3M4NC+4M5NC) / 4NP ratios as an indicator of the relative contribution of aqueous-phase and gas-phase oxidation pathways to NAC formation, we observed that the relative contribution of aqueous-phase pathways increased at elevated ambient RH and remained constant at RH > 30 %. We also found that the concentrations of VOC precursors (e.g., toluene and benzene) and aerosol surface area acted as important factors in promoting NAC formation, and photolysis as an important loss pathway for nitrophenols.
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| 7. |
- Le Breton, Michael, 1986, et al.
(author)
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Chlorine oxidation of VOCs at a semi-rural site in Beijing: significant chlorine liberation from ClNO2 and subsequent gas- and particle-phase Cl-VOC production
- 2018
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In: Atmospheric Chemistry and Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 18:17, s. 13013-13030:18, s. 13013-13030
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Journal article (peer-reviewed)abstract
- Nitryl chloride (ClNO2) accumulation at night acts as a significant reservoir for active chlorine and impacts the following day's photochemistry when the chlorine atom is liberated at sunrise. Here, we report simultaneous measurements of N2O5 and a suite of inorganic halogens including ClNO2 and reactions of chloride with volatile organic compounds (Cl-VOCs) in the gas and particle phases utilising the Filter Inlet for Gas and AEROsols time-of-flight chemical ionisation mass spectrometer (FIGAERO-ToF-CIMS) during an intensive measurement campaign 40 km northwest of Beijing in May and June 2016. A maximum mixing ratio of 2900 ppt of ClNO2 was observed with a mean campaign nighttime mixing ratio of 487 ppt, appearing to have an anthropogenic source supported by correlation with SO2, CO and benzene, which often persisted at high levels after sunrise until midday. This was attributed to such high mixing ratios persisting after numerous e-folding times of the photolytic lifetime enabling the chlorine atom production to reach 2.3 x 10(5) molecules cm(-3) from ClNO2 alone, peaking at 09:30 LT and up to 8.4 x 10(5) molecules cm(-3) when including the supporting inorganic halogen measurements. Cl-VOCs were observed in the particle and gas phases for the first time at high time resolution and illustrate how the iodide ToF-CIMS can detect unique markers of chlorine atom chemistry in ambient air from both biogenic and anthropogenic sources. Their presence and abundance can be explained via time series of their measured and steady-state calculated precursors, enabling the assessment of competing OH and chlorine atom oxidation via measurements of products from both of these mechanisms and their relative contribution to secondary organic aerosol (SOA) formation.
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| 8. |
- Sonesten, Lars
(author)
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Miljöövervakningen av Sveriges sjöar och vattendrag : Representativiteten av den kontrollerande miljöövervakningen
- 2013
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Reports (other academic/artistic)abstract
- Samtliga ytvattenkategorier inom ett vattendistrikt ska omfattas av övervakningsprogram inklusive övervakningsnät för kontrollerande övervakning som upprättas enligt kap. 7 VFF. En översyn av hur representativt Sveriges kontrollerade övervakningsnät är har tidigare inte kunnat utföras på grund av omfattande kvalitetsbrister i länsstyrelserna och vattenmyndigheternas datasystem VISS (VattenInformationsSystem Sverige). Kvaliteten på informationen i VISS har under senare år genomgått en omfattande kvalitetssäkring, vilket har gett förutsättningarna för att nu kunna genomföra den sammanställning och översyn över den svenska miljöövervakningen av sjöar och vattendrag. Denna översyn har varit starkt önskad under flera år, då det finns ett stort behov av att se över och analysera hur ett representativt samordnat kontrollerande övervakningsprogram skulle kunna se ut. Översynen sker mot bakgrund av den samlade vatten övervakning som bedrivs i Sverige, bland annat för att optimera befintlig övervakning och att kunna förstärka den där brister har identifierats. Arbetet är också viktigt för att säkerställa att kommande rapporteringar såväl internationellt som nationellt blir så bra som möjligt.Uppdraget för projektet Representativ kontrollerande miljöövervakning (RepKöp) syftar till att ta fram ett förslag på hur ett representativt kontrollerande övervakningsprogram med avseende på (vattentyper), kvalitetsfaktorer och statusklasser bör se ut på nationell och distriktsnivå i Sverige. Förslaget tas fram mot bakgrund av den samlade vattenövervakningen som bedrivs i Sverige idag och mot bakgrund av vad behövs för att uppfylla vattendirektivets krav på kontrollerande övervakning av vattenförekomster.Resultaten från översynen är tänkta att dels fungera som underlag för att underlätta Havs och vattenmyndighetens och Vattenmyndigheternas arbete inför rapporteringen 2012, men framför allt ska projektet ge underlag för att ta fram optimerade övervakningsprogram för sjöar och vattendrag till en långsiktig plan med en första anhalt 2016. För att RepKÖP ska få praktisk betydelse i övervakningsSverige skall projektet resultera i ett underlag för framtida revision av befintliga övervakningsprogram för respektive distrikt.Arbetet inom RepKöp är uppdelat i flera delar, vilka tillsammans ska fungera som vägledning till:• Vattenförvaltningens arbete med kontrollerande övervakning• Upplägg av nationell och regional miljöövervakningMålgruppen för arbetet är i första hand:• Vattenmyndigheter• Länsstyrelserna• Naturvårdsverket• Havs och vattenmyndigheten• Datavärdar och utförare av miljöövervakningFöreliggande rapport är en sammanställning och analys av miljöövervakningen av svenska sjöar och vattendrag så som de beskrevs i VISS vid datauttaget för sjöar i oktober 2011 och vattendrag i maj 2012. Sammanställningen av informationen från VISS har initierat en hel del korrigeringar i systemet, men tyvärr har det inte av praktiska skäl varit möjligt att ta hänsyn till dessa i arbetet. Man skall vara medveten om att VISS är en levande databas som ständigt uppdateras och korrigeras, vilket gör att endast en ”ögonblicksbild” kan analyseras. Detta gör att när analysen är färdig har verkligheten med stor sannolikhet redan till viss del hunnit förändrats.
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| 9. |
- Drake, Henrik, 1979-, et al.
(author)
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Ancient microbial activity in deep hydraulically conductive fracture zones within the Forsmark target area for deep geological nuclear waste disposal, Sweden
- 2018
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In: Geosciences. - : MDPI AG. - 2076-3263. ; 8
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Journal article (peer-reviewed)abstract
- Recent studies reveal that organisms from all three domains of life—Archaea, Bacteria, and even Eukarya—can thrive under energy-poor, dark, and anoxic conditions at large depths in the fractured crystalline continental crust. There is a need for an increased understanding of the processes and lifeforms in this vast realm, for example, regarding the spatiotemporal extent and variability of the different processes in the crust. Here, we present a study that set out to detect signs of ancient microbial life in the Forsmark area—the target area for deep geological nuclear waste disposal in Sweden. Stable isotope compositions were determined with high spatial resolution analyses within mineral coatings, and mineralized remains of putative microorganisms were studied in several deep water-conducting fracture zones (down to 663 m depth), from which hydrochemical and gas data exist. Large isotopic variabilities of 13Ccalcite (?36.2 to +20.2‰V-PDB) and 34Spyrite (?11.7 to +37.8‰V-CDT) disclose discrete periods of methanogenesis, and potentially, anaerobic oxidation of methane and related microbial sulfate reduction at several depth intervals. Dominant calcite–water disequilibrium of 18O and 87Sr/86Sr precludes abundant recent precipitation. Instead, the mineral coatings largely reflect an ancient archive of episodic microbial processes in the fracture system, which, according to our microscale Rb–Sr dating of co-genetic adularia and calcite, date back to the mid-Paleozoic. Potential Quaternary precipitation exists mainly at ~400 m depth in one of the boreholes, where mineral–water compositions corresponded.
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