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  • 1
    Publication Date: 2021-07-05
    Description: In a widely‐held conception, the biological carbon pump (BCP) is equal to the export of organic matter out of the euphotic zone. Using global ocean‐atmosphere model experiments we show that the change in export production is a poor measure of the biological pump's feedback to the atmosphere. The change in global true oxygen utilization (TOU), an integrative measure of the imprint of the BCP on marine oxygen, however, is in good agreement with the net change in the biogenic air‐sea flux of oxygen. Since TOU correlates very well with apparent oxygen utilization (AOU) in our experiments, we propose to measure the change of AOU from data of global float programs to monitor the feedback of the BCP to the atmosphere. For the current ocean we estimate that BCP changes effect a CO2 uptake by the ocean in the range of 0.07 to 0.14 GtC/yr.
    Description: Plain Language Summary: The biological carbon pump is an important element of marine carbon cycling and climate control on millennium timescales. In a widely‐held conception the export of organic carbon from the productive surface layer of the ocean is used as the essential measure of this carbon pump. Using numerical ocean modeling, we show here that the change in export production is, however, a poor measure of the biological carbon pump's feedback to the atmosphere on centennial timescales. In the contrary, we find that an oxygen‐based measure, the apparent oxygen utilization can be used to quantify the impact of biological pump changes on the atmosphere. Since the apparent oxygen utilization is easily accessible from an existing network of marine floats, our study suggests that the atmospheric impact of any future changes of the biological carbon pump can be monitored and quantified. For past decades our study proposes a negligible CO2 feedback to climate from biological carbon processing.
    Description: Key Points: Apparent oxygen utilization is proposed to quantify the feedback of the biological carbon pump to the atmosphere in a warming ocean. Changes in export production are unrelated to changes in biotic oxygen air‐sea gas exchange. The CO2‐flux due to changes of the biological carbon pump over the recent decades is negligible compared to the total marine CO2 uptake.
    Description: Deutsche Forschungsgemeinschat
    Description: Bundesministerium für Bildung und Forschung http://dx.doi.org/10.13039/501100002347
    Keywords: 551.9 ; biological carbon pump ; export production ; climate change ; AOU
    Type: article
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  • 2
    Publication Date: 2021-07-05
    Description: To monitor the success of carbon dioxide removal (CDR) or solar radiation management (SRM) that offset anthropogenic climate change, the forced response to any external forcing is required to be detectable against internal variability. Thus far, only the detectability of SRM has been examined using both a stationary and nonstationary detection and attribution method. Here, the spatiotemporal detectability of the forced response to artificial ocean alkalinization (AOA) and stratospheric aerosol injection (SAI) as exemplary methods for CDR and SRM, respectively, is compared in Max Planck Institute Earth System Model (MPI‐ESM) experiments using regularized optimal fingerprinting and single‐model estimates of internal variability, while working under a stationary or nonstationary null hypothesis. Although both experiments are forced by emissions according to the Representative Concentration Pathway 8.5 (RCP8.5) and target the climate of the RCP4.5 scenario using AOA or SAI, detection timescales reflect the fundamentally different forcing agents. Moreover, detectability timescales are sensitive to the choice of null hypothesis. Globally, changes in the CO2 system in seawater are detected earlier than the response in temperature to AOA but later in the case of SAI. Locally, the detection time scales depend on the physical, chemical, and radiative impacts of CDR and SRM forcing on the climate system, as well as patterns of internal variability, which is highlighted for oceanic heat and carbon storage.
    Description: Key Points: Detectability is robust using regularized optimal fingerprinting and single‐model estimates of internal variability. Changes in the CO2 system in seawater are detected earlier than the thermodynamic response to AOA but later in the case of SAI. Local detectability depends on patterns of internal variability and physical, chemical, and radiative impacts of external forcing.
    Description: Deutsche Forschungsgemeinschaft (DFG) http://dx.doi.org/10.13039/501100001659
    Description: Open access funding enabled and organized by Projekt DEAL.
    Keywords: 551.9 ; detection and attribution ; ocean alkalinization ; stratospheric aerosol injection ; Earth system modeling
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  • 3
    Publication Date: 2021-07-05
    Description: In soils and sediments, large amounts of total organic carbon (TOC) mark reducing conditions. As dark sediment colors are good predictors for high‐TOC zones, they indicate hot spots of biogeochemical turnover and microbial activity. Traditionally, obtaining the sediment color or TOC at depth requires costly core sampling, resulting in poor horizontal resolution and related uncertainty caused by interpolation. We suggest using a direct‐push tool for optical screening of the sediment color to acquire multiple high‐resolution vertical color profiles and demonstrate its applicability to a biogeochemical transition zone in floodplain sediments, dominated by tufa. We use Gaussian mixture models for a cluster analysis of 35 color logs in the International Commission on Illumination (CIE) L*a*b* color space to identify three colorfacies that differ in lithology and TOC content: a dark colorfacies that agrees well with peat layers, a gray colorfacies associated with clay, and a creamy‐brown facies made of autochthonous carbonate precipitates. We test different approaches either to infer the TOC content from color metrics, namely, the lightness and chroma, across all facies, or to identify TOC ranges for each colorfacies. Given the high variability in TOC due to organic carbon specks in the tufa, the latter approach appears more realistic. In our application we map the 3‐D distribution of organic matter in a floodplain in distinct facies over 20,000 m2 down to 12 m depth. While we relate the sediment color only to the TOC content, direct‐push color logging may also be used for in situ mapping of other biogeochemically relevant properties, such as the ferric‐iron content or sedimentary structure.
    Description: Plain Language Summary: Geologists can say a lot about soils and loose materials in the ground by looking at their color. Dark materials normally contain dead plants, called organic carbon, which are food for bacteria and cause chemical reactions. To get the color of the soil, geologists normally need soil samples, but getting them from depth takes time and money. We test a method of pushing a camera into the ground and recording the color therein. From the recorded color we can say which type of geological material is at which depth and how much organic carbon is there without taking samples everywhere. This can be done very quickly, so that we can do it over a large area and down to the depth of the loose material in the ground, where most of the groundwater flows.
    Description: Key Points: Direct‐push methods allow vertical in situ profiling of sediment color at high resolution. Cluster analysis reproducibly delineates colorfacies indicative of sedimentary units. Site‐specific relationships between color and TOC in sediments permit identifying biogeochemical hot spots.
    Description: German Research Foundation (Deutsche Forschungsgemeinschaft, DFG)
    Keywords: 551.9 ; direct‐push ; color logging ; colorfacies ; peat ; total organic carbon (TOC)
    Type: article
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  • 4
    Publication Date: 2021-07-05
    Description: Organic micropollutants of anthropogenic origin in river waters may impair aquatic ecosystem health and drinking water quality. To evaluate micropollutant fate and turnover on a catchment scale, information on input source characteristics as well as spatial and temporal variability is required. The influence of tributaries from agricultural and urban areas and the input of wastewater were investigated by grab and Lagrangian sampling under base flow conditions within a 7.7‐km‐long stretch of the Ammer River (southwest Germany) using target screening for 83 organic micropollutants and 4 in vitro bioassays with environmentally relevant modes of action. In total, 9 pesticides and transformation products, 13 pharmaceuticals, and 6 industrial and household chemicals were detected. Further, aryl hydrocarbon receptor induction, peroxisome proliferator–activated receptor activity, estrogenicity, and oxidative stress response were measured in the river. The vast majority of the compounds and mixture effects were introduced by the effluent of a wastewater‐treatment plant, which contributed 50% of the total flow rate of the river on the sampling day. The tributaries contributed little to the overall load of organic micropollutants and mixture effects because of their relatively low discharge but showed a different chemical and toxicological pattern from the Ammer River, though a comparison to effect‐based trigger values pointed toward unacceptable surface water quality in the main stem and in some of the tributaries. Chemical analysis and in vitro bioassays covered different windows of analyte properties but reflected the same picture. Environ Toxicol Chem 2020;39:1382–1391. © 2020 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.
    Description: Deutsche Forschungsgemeinschaft http://dx.doi.org/10.13039/501100001659
    Keywords: 551.9 ; Chemical analysis ; Bioassays ; Catchment scale ; Micropollutant mixtures ; Lagrangian sampling
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  • 5
    Publication Date: 2021-07-05
    Description: The combined algae test is a 96‐well plate‐based algal toxicity assay with the green algae Raphidocelis subcapitata that combines inhibition of 24‐h population growth rate with inhibition of photosynthesis detected after 2 and 24 h with pulse‐amplitude modulated (PAM) fluorometry using a Maxi‐Imaging PAM. The combined algae test has been in use for more than a decade but has had limitations due to incompatibilities of the measurements of the 2 biological endpoints on the same microtiter plates. These limitations could be overcome by increasing growth rates and doubling times on black, clear‐bottom 96‐well plates by application of dichromatic red/blue light‐emitting diode illumination. Different robotic dosing approaches and additional data evaluation methods helped to further expand the applicability domain of the assay. The combined algae test differentiates between nonspecifically acting compounds and photosynthesis inhibitors, such as photosystem II (PSII) herbicides. The PSII herbicides acted immediately on photosynthesis and showed growth rate inhibition at higher concentrations. If growth was a similar or more sensitive endpoint than photosynthesis inhibition, this was an indication that the tested chemical acted nonspecifically or that a mixture or a water sample was dominated by chemicals other than PSII herbicides acting on algal growth. We fingerprinted the effects of 45 chemicals on photosynthesis inhibition and growth rate and related the effects of the single compounds to designed mixtures of these chemicals detected in water samples and to the effects directly measured in water samples. Most of the observed effects in the water samples could be explained by known photosystem II inhibitors such as triazines and phenylurea herbicides. The improved setup of the combined algae test gave results consistent with those of the previous method but has lower costs, higher throughput, and higher precision. Environ Toxicol Chem 2020;39:2496–2508. © 2020 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.
    Description: The combined algae test (CAT) allows cost‐efficient high‐throughput monitoring of chemicals and water samples for their algae toxicity with a diagnostic component to differentiate between the mixture effects of photosynthesis inhibitors and other chemicals.
    Description: Deutsche Forschungsgemeinschaft http://dx.doi.org/10.13039/501100001659
    Keywords: 551.9 ; Algae ; Aquatic toxicology ; Effects‐based monitoring ; Herbicide ; Mixture toxicology ; Photosynthesis inhibition
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  • 6
    Publication Date: 2021-07-05
    Description: A Jurassic negative carbon isotope excursion (CIE), co‐evolved with Toarcian Oceanic Anoxic Event (OAE) at ~183 Ma, is suggested to be linked to a global carbon‐cycle perturbation and is well documented for Toarcian terrestrial fossil woods and marine sediments around the globe. A theoretically coupled δ13Ccarb‐δ13Corg pattern due to such dubbed global carbon‐cycle event from the negative CIE in Dotternhausen Toarcian stratigraphic profile (southwest Germany) is unexpectedly disturbed by two‐step δ13Ccarb‐δ13Corg decoupling in which the last step, upper in the stratigraphic order, is of higher magnitude. However, the trigger(s) for these sudden decoupling disturbances are still poorly constrained. Here, connecting new carbon and oxygen isotope data with documentary lipid biomarkers shows that the global carbon cycle during the Toarcian OAE was disturbed by enhanced green sulfur bacteria (GSB) metabolisms and early diagenesis at local scales. The first step δ13Ccarb‐δ13Corg decoupling was induced in the initial stage of the GSB bloom. The second step of much larger δ13Ccarb‐δ13Corg decoupling arising from a GSB prosperity was, however, exaggerated by early diagenesis through the respiration of sulfate‐reducing bacteria (SRB). Paleo‐geographically distinct localities of the Tethys region show contrasting decoupled δ13Ccarb‐δ13Corg patterns, which implies that the second‐order carbon‐cycle perturbations have pervasively and independently impacted the global carbon event during the Toarcian OAE.
    Description: China Scholarship Council http://dx.doi.org/10.13039/501100004543
    Keywords: 551.9 ; carbon isotope excursion ; green sulfur bacteria ; local carbon cycling ; Toarcian ; δ13Ccarb‐δ13Corg decoupling
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  • 7
    Publication Date: 2021-07-05
    Description: Early marine diagenetic dolomite is a rather thermodynamically‐stable carbonate phase and has potential to act as an archive of marine porewater properties. However, the variety of early to late diagenetic dolomite phases that can coexist within a single sample can result in extensive complexity. Here, the archive potential of early marine dolomites exposed to extreme post‐depositional processes is tested using various types of analyses, including: petrography, fluid inclusion data, stable δ13C and δ18O isotopes, 87Sr/86Sr ratios, and U‐Pb age dating of various dolomite phases. In this example, a Triassic carbonate platform was dissected and overprinted (diagenetic temperatures of 50 to 430°C) in a strike‐slip zone in Southern Spain. Eight episodes of dolomitization, a dolostone cataclasite and late stage meteoric/vadose cementation were recognized. The following processes were found to be diagenetically relevant: (i) protolith deposition and fabric‐preservation, and marine dolomitization of precursor aragonite and calcite during the Middle–Late Triassic; (ii) intermediate burial and formation of zebra saddle dolomite and precipitation of various dolomite cements in a Proto‐Atlantic opening stress regime (T ca 250°C) during the Early–Middle Jurassic; (iii) dolomite cement precipitation during early Alpine tectonism, rapid burial to ca 15 km, and high‐grade anchizone overprint during Alpine tectonic evolution in the Early Eocene to Early Miocene; (iv) brecciation of dolostones to cataclasite during the onset of the Carboneras Fault Zone activity during the Middle Miocene; and (v) late‐stage regression and subsequent meteoric overprint. Data shown here document that, under favourable conditions, early diagenetic marine dolomites and their archive data may resist petrographic and geochemical resetting over time intervals of 108 or more years. Evidence for this preservation includes preserved Late Triassic seawater δ13CDIC values and primary fluid inclusion data. Data also indicate that oversimplified statements based on bulk data from other petrographically‐complex dolomite archives must be considered with caution.
    Description: DFG http://dx.doi.org/10.13039/501100001659
    Keywords: 551.9 ; Diagenesis ; dolomite ; dolomitization ; fluid inclusions ; geochemistry ; petrography ; tectonic overprint ; U‐Pb dating
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  • 8
    Publication Date: 2021-07-21
    Description: Amphistegina are common larger benthic foraminifer in coral reefs, with a nearly circumtropical distribution, and are major contributors to the CaCO3 budget of shallow marine environments. The family Amphisteginidae is dominant in Cenozoic carbonates. However, its potential as a proxy for paleoclimate reconstruction has not been completely explored. The intratest variability in trace elements of Amphistegina lessonii has been investigated using femtosecond‐laser ablation‐inductively coupled plasma‐mass spectrometry (fs‐LA‐ICP‐MS). We collected and analyzed adult specimens of A. lessonii in September 2003, November 2003, January 2004, and March 2004, from ∼2 m water depth in the coral reefs of Akajima, Okinawa, Japan. Tests of A. lessonii from these four collections were analyzed for Mg/Ca of the septa to observe Test Size‐Lifespan relationships. The lifespan of a specimen of A. lessonii of 1,200 µm in diameter is estimated at ∼3 and ∼2 months for specimens 900 µm in size. Over the estimated lifespans, Mg/Ca of individual specimens of A. lessonii is highly variable and displays co‐variation with temperature and tidal heights. Future projects may apply and further test this approach for the reconstruction of the tropical shallow marine paleoenvironments.
    Description: Plain Language Summary: Larger Benthic Foraminifera (LBF) have slow growth rates and can be used as a proxy to reconstruct seasonal variations in temperature. Amphistegina, a common genus of LBF found within the Cenozoic era including the past 55 million years, was sampled across four seasons from a modern coral reef of Okinawa, Japan. The trace element concentrations in nine specimens of A. lessonii were measured using femtosecond LA‐ICP‐MS. The intratest variation in Mg/Ca covaried with tidal heights and seawater temperature, assuming the ages of the specimens to be 2–3 months. We provide a temperature calibration equation for A. lessonii for reconstructing paleotemperatures of shallow marine environments of the Cenozoic.
    Description: Key Points: Specimens of Amphistegina lessonii sampled across 4 months from Akajima are used for calibration for Mg/Ca temperature using femtosecond‐laser ablation‐inductively coupled plasma‐mass spectrometry. The Mg/Ca along the septa of A. lessonii covaries with seawater temperature and tidal heights while Na/Ca and Sr/Ca show no correlation. Intratest variations in Mg/Ca of A. lessonii are affected by light intensity attenuation by sediment re‐suspension caused by tidal currents.
    Keywords: 551.9 ; Amphistegina lessonii ; fs‐LA‐ICP‐MS ; sea‐surface temperature ; tidal heights ; trace elements
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  • 9
    Publication Date: 2021-07-05
    Description: The magnitude of future emissions of greenhouse gases from the northern permafrost region depends crucially on the mineralization of soil organic carbon (SOC) that has accumulated over millennia in these perennially frozen soils. Many recent studies have used radiocarbon (14C) to quantify the release of this “old” SOC as CO2 or CH4 to the atmosphere or as dissolved and particulate organic carbon (DOC and POC) to surface waters. We compiled ~1,900 14C measurements from 51 sites in the northern permafrost region to assess the vulnerability of thawing SOC in tundra, forest, peatland, lake, and river ecosystems. We found that growing season soil 14C‐CO2 emissions generally had a modern (post‐1950s) signature, but that well‐drained, oxic soils had increased CO2 emissions derived from older sources following recent thaw. The age of CO2 and CH4 emitted from lakes depended primarily on the age and quantity of SOC in sediments and on the mode of emission, and indicated substantial losses of previously frozen SOC from actively expanding thermokarst lakes. Increased fluvial export of aged DOC and POC occurred from sites where permafrost thaw caused soil thermal erosion. There was limited evidence supporting release of previously frozen SOC as CO2, CH4, and DOC from thawing peatlands with anoxic soils. This synthesis thus suggests widespread but not universal release of permafrost SOC following thaw. We show that different definitions of “old” sources among studies hamper the comparison of vulnerability of permafrost SOC across ecosystems and disturbances. We also highlight opportunities for future 14C studies in the permafrost region.
    Description: Key Points: We compiled ~1,900 14C measurements of CO2, CH4, DOC, and POC from the northern permafrost region. Old carbon release increases in thawed oxic soils (CO2), thermokarst lakes (CH4 and CO2), and headwaters with thermal erosion (DOC and POC). Simultaneous and year‐long 14C analyses of CO2, CH4, DOC, and POC are needed to assess the vulnerability of permafrost carbon across ecosystems.
    Description: EC | H2020 | H2020 Priority Excellent Science | H2020 European Research Council (ERC) http://dx.doi.org/10.13039/100010663
    Description: Gouvernement du Canada | Natural Sciences and Engineering Research Council of Canada (NSERC) http://dx.doi.org/10.13039/501100000038
    Description: National Science Foundation (NSF) http://dx.doi.org/10.13039/100000001
    Keywords: 551.9 ; permafrost thaw ; radiocarbon ; carbon dioxide ; methane ; dissolved organic carbon ; particulate organic carbon
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  • 10
    Publication Date: 2021-07-05
    Description: We compared stable isotopes of water in plant stem (xylem) water and soil collected over a complete growing season from five well‐known long‐term study sites in northern/cold regions. These spanned a decreasing temperature gradient from Bruntland Burn (Scotland), Dorset (Canadian Shield), Dry Creek (USA), Krycklan (Sweden), to Wolf Creek (northern Canada). Xylem water was isotopically depleted compared to soil waters, most notably for deuterium. The degree to which potential soil water sources could explain the isotopic composition of xylem water was assessed quantitatively using overlapping polygons to enclose respective data sets when plotted in dual isotope space. At most sites isotopes in xylem water from angiosperms showed a strong overlap with soil water; this was not the case for gymnosperms. In most cases, xylem water composition on a given sampling day could be better explained if soil water composition was considered over longer antecedent periods spanning many months. Xylem water at most sites was usually most dissimilar to soil water in drier summer months, although sites differed in the sequence of change. Open questions remain on why a significant proportion of isotopically depleted water in plant xylem cannot be explained by soil water sources, particularly for gymnosperms. It is recommended that future research focuses on the potential for fractionation to affect water uptake at the soil‐root interface, both through effects of exchange between the vapour and liquid phases of soil water and the effects of mycorrhizal interactions. Additionally, in cold regions, evaporation and diffusion of xylem water in winter may be an important process.
    Description: We compared stable isotopes of water in plant stem (xylem) water and soil collected over a complete growing season from five well‐known long‐term study sites in northern/cold regions. Xylem water was isotopically depleted compared to soil waters, most notably for deuterium. At all sites except one, water sources of angiosperms could be associated with soil water, while the sources of water uptake by gymnosperms were much less easily explained.
    Description: FP7 Ideas: European Research Council http://dx.doi.org/10.13039/100011199
    Description: KAW Branch‐Point project
    Description: SITES (VR)
    Description: Boise State University http://dx.doi.org/10.13039/100007233
    Description: US National Science Foundation
    Description: Leverhulme Trust through the ISO‐LAND project
    Keywords: 551.9 ; cold regions ; critical zone ; northern environments ; stable isotopes ; soil isotopes ; xylem isotopes
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