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  • PANGAEA  (46)
  • BioMed Central  (40)
  • National Academy of Sciences  (36)
  • 2015-2019  (122)
  • 1990-1994
  • 2015  (122)
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  • 2015-2019  (122)
  • 1990-1994
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  • 1
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    PANGAEA
    In:  Supplement to: Hoff, Ulrike; Biskaborn, Boris K; Dirksen, Veronika G; Dirksen, Oleg V; Kuhn, Gerhard; Meyer, Hanno; Nazarova, Larisa B; Roth, Alexandra; Diekmann, Bernhard (2015): Holocene environment of Central Kamchatka, Russia: Implications from a multi-proxy record of Two-Yurts Lake. Global and Planetary Change, 134, 101-117, https://doi.org/10.1016/j.gloplacha.2015.07.011
    Publication Date: 2023-03-07
    Description: Within the scope of Russian-German palaeoenvironmental research, Two-Yurts Lake (TYL, Dvuh-Yurtochnoe in Russian) was chosen as the main scientific target area to decipher Holocene climate variability on Kamchatka. The 5x2 km large and 26 m deep lake is of proglacial origin and situated on the eastern flank of Sredinny Ridge at the northwestern end of the Central Kamchatka Valley, outside the direct influence of active volcanism. Here, we present results of a multi-proxy study on sediment cores, spanning about the last 7000 years. The general tenor of the TYL record is an increase in continentality and winter snow cover in conjunction with a decrease in temperature, humidity, and biological productivity after 5000-4500 cal yrs BP, inferred from pollen and diatom data and the isotopic composition of organic carbon. The TYL proxy data also show that the late Holocene was punctuated by two colder spells, roughly between 4500 and 3500 cal yrs BP and between 1000 and 200 cal yrs BP, as local expressions of the Neoglacial and Little Ice Age, respectively. These environmental changes can be regarded as direct and indirect responses to climate change, as also demonstrated by other records in the regional terrestrial and marine realm. Long-term climate deterioration was driven by decreasing insolation, while the short-term climate excursions are best explained by local climatic processes. The latter affect the configuration of atmospheric pressure systems that control the sources as well as the temperature and moisture of air masses reaching Kamchatka.
    Keywords: AWI_PerDyn; Permafrost Research (Periglacial Dynamics) @ AWI
    Type: Dataset
    Format: application/zip, 12 datasets
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  • 2
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    PANGAEA
    In:  Supplement to: Abelmann, Andrea; Gersonde, Rainer; Knorr, Gregor; Zhang, Xu; Chapligin, Bernhard; Maier, Edith; Esper, Oliver; Friedrichsen, Hans; Lohmann, Gerrit; Meyer, Hanno; Tiedemann, Ralf (2015): The seasonal sea-ice zone in the glacial Southern Ocean as a carbon sink. Nature Communications, 6, 8136, https://doi.org/10.1038/ncomms9136
    Publication Date: 2023-03-30
    Description: Reduced surface-deep ocean exchange and enhanced nutrient consumption by phytoplankton in the Southern Ocean have been linked to lower glacial atmospheric CO2. However, identification of the biological and physical conditions involved and the related processes remains incomplete. Here we specify Southern Ocean surface-subsurface contrasts using a new tool, the combined oxygen and silicon isotope measurement of diatom and radiolarian opal, in combination with numerical simulations. Our data do not indicate a permanent glacial halocline related to melt water from icebergs. Corroborated by numerical simulations, we find that glacial surface stratification was variable and linked to seasonal sea-ice changes. During glacial spring-summer, the mixed layer was relatively shallow, while deeper mixing occurred during fall-winter, allowing for surface-ocean refueling with nutrients from the deep reservoir, which was potentially richer in nutrients than today. This generated specific carbon and opal export regimes turning the glacial seasonal sea-ice zone into a carbon sink.
    Keywords: AWI_Paleo; Paleoenvironmental Reconstructions from Marine Sediments @ AWI
    Type: Dataset
    Format: application/zip, 12 datasets
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  • 3
    Publication Date: 2023-03-30
    Keywords: Actinomma antarctica; ANT-IX/4; Atlantic Ridge; AWI_Paleo; Depth, bottom/max; Depth, top/min; DEPTH, water; Discovery Seamount; Event label; MSN; Multiple opening/closing net; Paleoenvironmental Reconstructions from Marine Sediments @ AWI; Polarstern; PS18; PS18/259; PS18/261; PS18/263; PS18/265; PS2101-2; PS2103-3; PS2105-4; PS2107-2; Spongotrochus glacialis
    Type: Dataset
    Format: text/tab-separated-values, 59 data points
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  • 4
    Publication Date: 2023-05-13
    Description: This data set contains four time series of particulate and dissolved soil nitrogen measurements from the main experiment plots of a large grassland biodiversity experiment (the Jena Experiment; see further details below). In the main experiment, 82 grassland plots of 20 x 20 m were established from a pool of 60 species belonging to four functional groups (grasses, legumes, tall and small herbs). In May 2002, varying numbers of plant species from this species pool were sown into the plots to create a gradient of plant species richness (1, 2, 4, 8, 16 and 60 species) and functional richness (1, 2, 3, 4 functional groups). Plots were maintained by bi-annual weeding and mowing. 1. Total nitrogen from solid phase: Stratified soil sampling was performed every two years since before sowing in April 2002 and was repeated in April 2004, 2006 and 2008 to a depth of 30 cm segmented to a depth resolution of 5 cm giving six depth subsamples per core. In 2002 five samples per plot were taken and analyzed independently. Averaged values per depth layer are reported. In later years, three samples per plot were taken, pooled in the field, and measured as a combined sample. Sampling locations were less than 30 cm apart from sampling locations in other years. All soil samples were passed through a sieve with a mesh size of 2 mm in 2002. In later years samples were further sieved to 1 mm. No additional mineral particles were removed by this procedure. Total nitrogen concentration was analyzed on ball-milled subsamples (time 4 min, frequency 30 s-1) by an elemental analyzer at 1150°C (Elementaranalysator vario Max CN; Elementar Analysensysteme GmbH, Hanau, Germany). 2. Total nitrogen from solid phase (high intensity sampling): In block 2 of the Jena Experiment, soil samples were taken to a depth of 1m (segmented to a depth resolution of 5 cm giving 20 depth subsamples per core) with three replicates per block ever 5 years starting before sowing in April 2002. Samples were processed as for the more frequent sampling but were always analyzed independently and never pooled. 3. Mineral nitrogen from KCl extractions: Five soil cores (diameter 0.01 m) were taken at a depth of 0 to 0.15 m (and between 2002 and 2004 also at a depth of 0.15 to 0.3 m) of the mineral soil from each of the experimental plots at various times over the years. In addition also plots of the management experiment, that altered mowing frequency and fertilized subplots (see further details below) were sampled in some later years. Samples of the soil cores per plot (subplots in case of the management experiment) were pooled during each sampling campaign. NO3‐N and NH4‐N concentrations were determined by extraction of soil samples with 1 M KCl solution and were measured in the soil extract with a Continuous Flow Analyzer (CFA, 2003–2005: Skalar, Breda, Netherlands; 2006–2007: AutoAnalyzer, Seal, Burgess Hill, United Kingdom). 4. Dissolved nitrogen in soil solution: Glass suction plates with a diameter of 12 cm, 1 cm thickness and a pore size of 1–1.6 µm (UMS GmbH, Munich, Germany) were installed in April 2002 in depths of 10, 20, 30 and 60 cm to collect soil solution. The sampling bottles were continuously evacuated to a negative pressure between 50 and 350 mbar, such that the suction pressure was about 50 mbar above the actual soil water tension. Thus, only the soil leachate was collected. Cumulative soil solution was sampled biweekly and analyzed for nitrate (NO3-), ammonium (NH4+) and total dissolved nitrogen concentrations with a continuous flow analyzer (CFA, Skalar, Breda, The Netherlands). Nitrate was analyzed photometrically after reduction to NO2- and reaction with sulfanilamide and naphthylethylenediamine-dihydrochloride to an azo-dye. Our NO3- concentrations contained an unknown contribution of NO2- that is expected to be small. Simultaneously to the NO3- analysis, NH4+ was determined photometrically as 5-aminosalicylate after a modified Berthelot reaction. The detection limits of NO3- and NH4+ were 0.02 and 0.03 mg N L-1, respectively. Total dissolved N in soil solution was analyzed by oxidation with K2S2O8 followed by reduction to NO2- as described above for NO3-. Dissolved organic N (DON) concentrations in soil solution were calculated as the difference between TDN and the sum of mineral N (NO3- + NH4+).
    Keywords: JenExp; The Jena Experiment
    Type: Dataset
    Format: application/zip, 16 datasets
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  • 5
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    PANGAEA
    In:  Alfred Wegener Institute, Helmholtz Centre for Polar and Marine Research, Bremerhaven
    Publication Date: 2023-05-31
    Keywords: ANT-XXIX/7; AWI_PhyOce; CT; Physical Oceanography @ AWI; Polarstern; PS81; PS81/7-track; Underway cruise track measurements; Weddell Sea
    Type: Dataset
    Format: application/zip, 84.7 MBytes
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  • 6
    Publication Date: 2023-06-24
    Description: This data set contains two time series of measurements of dissolved phosphorus (organic, inorganic and total with a biweekly resolution) and dissolved inorganic phosphorus with a seasonal resolution. In addition, data on phosphorus from soil samples measured in 2007 and fractionated by different acid-extrations (Hedley fractions) are provided. All data measured at the main experiment plots of a large grassland biodiversity experiment (the Jena Experiment; see further details below). In the main experiment, 82 grassland plots of 20 x 20 m were established from a pool of 60 species belonging to four functional groups (grasses, legumes, tall and small herbs). In May 2002, varying numbers of plant species from this species pool were sown into the plots to create a gradient of plant species richness (1, 2, 4, 8, 16 and 60 species) and functional richness (1, 2, 3, 4 functional groups). Plots were maintained by bi-annual weeding and mowing. 1. Dissolved phosphorus in soil solution: Suction plates installed on the field site in 10, 20, 30 and 60 cm depth were used to sample soil pore water. Cumulatively extracted soil solution was collected every two weeks from October 2002 to May 2006. The biweekly samples from 2002, 2003 and 2004 were analyzed for dissolved organic phosphorus (DOP), dissolved inorganic phosphorus (PO4P) and dissolved total phosphorus (TDP) by Continuous Flow Analyzer (CFA SAN ++, SKALAR [Breda, The Netherlands]). 2. Seasonal values of dissolved inorganic phosphorus in soil solution were calculated as volume-weighted mean values of the biweekly measurements (spring = March to May, summer = June to August, fall = September to November, winter = December to February). 3. Phosphorus fractions in soil: Five independent soil samples per plot were taken in a depth of 0-15 cm using a soil corer with an inner diameter of 1 cm. The five samples per plot were combined to one composite sample per plot. A four-step sequential P fractionation (Hedley fractions) was applied and concentrations of P fractions in soil were measured photometrically (molybdenum blue-reactive P) with a Continuous Flow Analyzer (Bran&Luebbe, Germany).
    Keywords: JenExp; The Jena Experiment
    Type: Dataset
    Format: application/zip, 8 datasets
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  • 7
    Publication Date: 2023-06-24
    Description: This data set contains three time series of measurements of soil carbon (particular and dissolved) from the main experiment plots of a large grassland biodiversity experiment (the Jena Experiment; see further details below). In the main experiment, 82 grassland plots of 20 x 20 m were established from a pool of 60 species belonging to four functional groups (grasses, legumes, tall and small herbs). In May 2002, varying numbers of plant species from this species pool were sown into the plots to create a gradient of plant species richness (1, 2, 4, 8, 16 and 60 species) and functional richness (1, 2, 3, 4 functional groups). Plots were maintained by bi-annual weeding and mowing. 1. Particulate soil carbon: Stratified soil sampling was performed every two years since before sowing in April 2002 and was repeated in April 2004, 2006 and 2008 to a depth of 30 cm segmented to a depth resolution of 5 cm giving six depth subsamples per core. Total carbon concentration was analyzed on ball-milled subsamples by an elemental analyzer at 1150°C. Inorganic carbon concentration was measured by elemental analysis at 1150°C after removal of organic carbon for 16 h at 450°C in a muffle furnace. Organic carbon concentration was calculated as the difference between both measurements of total and inorganic carbon. 2. Particulate soil carbon (high intensity sampling): In one block of the Jena Experiment soil samples were taken to a depth of 1 m (segmented to a depth resolution of 5 cm giving 20 depth subsamples per core) with three replicates per block ever 5 years starting before sowing in April 2002. Samples were processed as for the more frequent sampling. 3. Dissolved organic carbon: Suction plates installed on the field site in 10, 20, 30 and 60 cm depth were used to sample soil pore water. Cumulative soil solution was sampled biweekly and analyzed for dissolved organic carbon concentration by a high TOC elemental analyzer. Annual mean values of DOC are provided.
    Keywords: JenExp; The Jena Experiment
    Type: Dataset
    Format: application/zip, 13 datasets
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  • 8
    Publication Date: 2023-06-24
    Description: This data set contains a time series of plant height measurements (vegetative and reproductive) from the main experiment plots of a large grassland biodiversity experiment (the Jena Experiment; see further details below). In addition, data on species specific plant heights for the main experiment are available from 2002. In the main experiment, 82 grassland plots of 20 x 20 m were established from a pool of 60 species belonging to four functional groups (grasses, legumes, tall and small herbs). In May 2002, varying numbers of plant species from this species pool were sown into the plots to create a gradient of plant species richness (1, 2, 4, 8, 16 and 60 species) and functional richness (1, 2, 3, 4 functional groups). Plots were maintained by bi-annual weeding and mowing. 1. Plant height was recorded, generally, twice a year just before biomass harvest (during peak standing biomass in late May and in late August). Methodologies of measuring height have varied somewhat over the years. In earlier year the streched plant height was measured, while in later years the standing height without streching the plant was measured. Vegetative height was measured either as the height of the highest leaf or as the length of the main axis of non-flowering plants. Regenerating height was measured either as the height of the highest flower on a plant or as the height of the main axis of flowering. Sampled plants were either randomly selected in the core area of plots or along transects in defined distances. For details refer to the description of individual years. Starting in 2006, also the plots of the management experiment, that altered mowing frequency and fertilized subplots (see further details in the general description of the Jena Experiment) were sampled. 2. Species specific plant height was recorded two times in 2002: in late July (vegetative height) and just before biomass harvest during peak standing biomass in late August (vegetative and regenerative height). For each plot and each sown species in the species pool, 3 plant individuals (if present) from the central area of the plots were randomly selected and used to measure vegetative height (non-flowering indviduals) and regenerative height (flowering individuals) as stretched height. Provided are the means over the three measuremnts per plant species per plot.
    Keywords: JenExp; The Jena Experiment
    Type: Dataset
    Format: application/zip, 7 datasets
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  • 9
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    PANGAEA
    In:  Supplement to: Lehrmann, Daniel; Stepchinski, Leanne; Altiner, Demir; Orchard, Michael J; Montgomery, Paul; Enos, Paul; Ellwood, Brooks B; Bowring, Samuel A; Ramezani, Jahandar; Wang, Hongmei; Wei, Jiayong; Yu, Meiyi; Griffiths, James D; Minzoni, Marcello; Schaal, Ellen K; Li, Xiaowei; Meyer, Katja M; Payne, Jonathan L (2015): An integrated biostratigraphy (conodonts and foraminifers) and chronostratigraphy (paleomagnetic reversals, magnetic susceptibility, elemental chemistry, carbon isotopes and geochronology) for the Permian–Upper Triassic strata of Guandao section, Nanpanjiang Basin, south China. Journal of Asian Earth Sciences, 108, 117-135, https://doi.org/10.1016/j.jseaes.2015.04.030
    Publication Date: 2023-07-10
    Description: The chronostratigraphy of Guandao section has served as the foundation for numerous studies of the end-Permian extinction and biotic recovery in south China. Guandao section is continuous from the Permian-Triassic boundary to the Upper Triassic. Conodonts enable broad delineation of stage and substage boundaries and calibration of foraminifer biostratigraphy as follows. Changhsingian-Griesbachian: first Hindeodus parvus, and first appearance of foraminifers Postcladella kalhori and Earlandia sp. Griesbachian-Dienerian: first Neospathodus dieneri, and last appearance of foraminifer P. grandis. Dienerian-Smithian: first Novispathodus waageni and late Dienerian first appearance of foraminifer Hoyenella ex gr. sinensis. Smithian-Spathian: first Nv? crassatus and last appearance of foraminifers Arenovidalina n. sp. and Glomospirella cf. vulgaris. Spathian-Aegean: first Chiosella timorensis and first appearance of foraminifer Meandrospira dinarica. Aegean-Bithynian: first Nicoraella germanica and first appearance of foraminifer Pilammina densa. Bithynian-Pelsonian: after last Neogondolella regalis, prior to first Paragondolella bulgarica and first appearance of foraminifer Aulotortus eotriasicus. Pelsonian-Illyrian: first Pg. excelsa and last appearance of foraminifers Meandrospira? deformata and Pilamminella grandis. Illyrian-Fassanian: first Budurovignathus truempyi, and first appearance of foraminifers Abriolina mediterranea and Paleolituonella meridionalis. Fassanian-Longobardian: first Bv. mungoensis and last appearance of foraminifer A. mediterranea. Longobardian-Cordevolian: first Quadralella polygnathiformis and last appearance of foraminifers Turriglomina mesotriasica and Endotriadella wirzi. The section contains primary magnetic signature with frequent reversals occurring around the Permian-Triassic, Olenekian-Anisian, and Anisian-Ladinian boundaries. Predominantly normal polarity occurs in the lower Smithian, Bithynian, and Longobardian-Cordevolian. Predominantly reversed polarity occurs in the upper Griesbachian, Induan-Olenekian, Pelsonian and lower Illyrian. Reversals match well with the GPTS. Large amplitude carbon isotope excursions, attaining values as low as -2.9 per mil d13C and high as +5.7 per mil d13C, characterize the Lower Triassic and basal Anisian. Values stabilize around +2 per mil d13C through the Anisian to Carnian. Similar signatures have been reported globally. Magnetic susceptibility and synthetic gamma ray logs show large fluctuations in the Lower Triassic and an overall decline in magnitude of fluctuation through the Middle and Upper Triassic. The largest spikes in magnetic susceptibility and gamma ray, indicating greater terrestrial lithogenic flux, correspond to positive d13C excursions. High precision U-Pb analysis of zircons from volcanic ash beds provide a robust age of 247.28 ± 0.12 Ma for the Olenekian-Anisian boundary at Guandao and an age of 251.985 ± 0.097 Ma for the Permian-Triassic boundary at Taiping. Together, the new U-Pb geochronology from the Guandao and Taiping sections suggest an estimated duration of 4.71 ± 0.15 Ma for the Early Triassic Epoch.
    Keywords: Abriolina mediterranea; Agathammina sp.; Age, dated; Age, dated standard error; Age, Uranium-Lead; Arenovidalina sp.; Aulotortus eotriasicus; Austrocolomia marschalli; Bianyang, Guizhou, China; Budurovignathus hungaricus; Budurovignathus mungoensis; Budurovignathus truempyi; Chemical Gamma Ray; Chiosella gondolelloides; Chiosella timorensis; Clarkina changxingensis; Conservatella conservativa; Cornudina sp.; Cratognathus spp; Discretella discreta; Endoteba bithynica; Endoteba controversa; Endotebanella kocaeliensis; Endotebanella sp.; Endoteba obturata; Endotriada thyrrhenica; Endotriadella wirzi; Eurygnathodus sp.; Foraminifera, benthic indeterminata; Galeanella sp.; Gladigondolella carinata; Gladigondolella tethydis; Glomospirella cf. vulgaris; Guandao_Section; Guangxidella bransoni; HAND; Hindeodus anterodentatus; Hindeodus parvus; Hindeodus typicalis; Hoyenella ex gr. sinensis; Inductively coupled plasma - mass spectrometry (ICP-MS); Krikoumbilica pileiformis; Light microscope; Magnetic susceptibility; Magnetometer, cryogenic, 2G-755R, thermal demagnetization; Malayspirina sp.; Mass spectrometer Finnigan MAT 252; Meandrospira cheni; Meandrospira deformata; Meandrospira dinarica; Meandrospira pusilla; Meandrospira sp.; Meandrospirillina irregularis; Mosherella newpassensis; Neogondolella bifurcata; Neogondolella constricta; Neogondolellaregalis; Neogondolella trammeri; Neogondolella transita; Neospathodus crassatus; Neospathodus cristagalli; Neospathodus dieneri; Neospathodus pakistanensis; Neospathodus peculiaris; Neospathodus triangularis; Neostrachanognathus spp.; Nicoraella germanica; Nicoraella kockeli; Nicoraella sp.; Novispathodus abruptus; Novispathodus waageni; Ophthalmidium exiguum; Ophthalmidium spp.; Paleolituonella meridionalis; Paleolituonella reclinata; Paragondolella alpina; Paragondolella bifurcata; Paragondolella bulgarica; Paragondolella excelsa; Paragondolella foliata; Paragondolella fuelopi; Paragondolella inclinata; Piallina bronnimanni; Pilammina densa; Pilamminella grandi; Planiinvoluta mesotriasica; Quadralella polygnathiformis; Quadralella tadpole; Sample code/label; Sampling by hand; SECTION, height; Spathicuspus spathi; Susceptibility bridge; Tolypammina gregaria; Triadodiscus sp.; Triassospathodus brochus; Triassospathodus homeri; Triassospathodus symmetricus; Trochammina almtalensis; Turriglomina carnica; Turriglomina cf. magna; Turriglomina mesotriasica; Turrispirillina sp.; Virtual geomagnetic pole latitude; δ13C, carbonate
    Type: Dataset
    Format: text/tab-separated-values, 93579 data points
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  • 10
    Publication Date: 2023-07-09
    Keywords: Achnanthes bioretti; Achnanthes calcar; Achnanthes clevei; Achnanthes clevei var. bottnica; Achnanthes daonensis; Achnanthes exigua; Achnanthes helvetica; Achnanthes laevis var. laevis; Achnanthes lanceolata; Achnanthes lanceolata ssp. frequentissima; Achnanthes lanceolata ssp. lanceolata var. haynaldii; Achnanthes lanceolata ssp. lanceolatoides; Achnanthes lanceolata var. dubia; Achnanthes lanceolata var. rostrata; Achnanthes laterostrata; Achnanthes minutissima; Achnanthes obliqua; Achnanthes oestrupii; Achnanthes oestrupii var. pungens; Achnanthes peragalli; Achnanthes rossii; Achnanthes spp.; Achnanthes ssp. lanceolata var. lanceolata var. elliptica; Achnanthidium lauenburgianum; AGE; Amphora fogediana; Amphora inariensis; Amphora libyca; Amphora ovalis; Amphora pediculus; Amphora spp.; Asterionella formosa; Asterionella ralfsii; Aulacoseira auxospore; Aulacoseira crenulata; Aulacoseira granulata; Aulacoseira islandica; Aulacoseira spp.; Aulacoseira subarctica; Aulacoseira subarctica forma recta; AWI_PerDyn; AWI Arctic Land Expedition; Caloneis bacillaris; Caloneis silicula; Cocconeis neodiminuta; Cocconeis placentula var. klinoraphis; Cocconeis placentula var. lineata; Cocconeis placentula var. tenuistriata; Counting, diatoms; Cyclotella comensis; Cyclotella distinguenda var. unipunctata; Cyclotella meneghiniana; Cyclotella ocellata; Cyclotella pseudostelligera; Cyclotella rossii; Cyclotella spp.; Cyclotella tripartita; Cymbella cistula; Cymbella schimanskii; Cymbella silesiaca; Cymbella spp.; Depth, bottom/max; Depth, composite; Depth, top/min; Diatoma hyemalis; Diatoma mesodon; Diatoma tenuis; Diatoms; Diatoms indeterminata; Didymosphenia geminata; Diploneis elliptica; Encyonema minutum; Eolimna subminuscula; Epithemia sorex; Epithemia spp.; Eunotia arcus; Eunotia bilunaris; Eunotia praerupta; Eunotia spp.; Fragilaria acus; Fragilaria arcus var. arcus; Fragilaria arcus var. recta; Fragilaria brevistriata; Fragilaria capucina; Fragilaria capucina var. capucina; Fragilaria capucina var. vaucheriae; Fragilaria construens forma binodis; Fragilaria construens forma venter; Fragilaria construens var. construens; Fragilaria fasciculata; Fragilaria flexura; Fragilaria lapponica; Fragilaria leptostauron; Fragilaria leptostauron var. martyi; Fragilaria mazamaensis; Fragilaria nanana; Fragilaria parasitica; Fragilaria parasitica var. parasitica; Fragilaria parasitica var. subconstricta; Fragilaria pinnata; Fragilaria spp.; Fragilaria ulna; Fragilaria virescens; Fragiliaria capucina var. mesolepta; Frustulia rhomboides var. crassinervia; Geissleria schoenfeldii; Gomphonema angustatum; Gomphonema angustum; Gomphonema clevei; Gomphonema olivaceum; Gomphonema olivaceum var. minutissimum; Gomphonema parvulum; Gomphonema spp.; Gomphonema truncatum; Gyrosigma acuminatum; Hantzschia amphioxys; Hantzschia spp.; Kamchatka2007; KOL; Luticola goeppertiana; Melosira lineata; Melosira spp.; Melosira undulata; Meridion circulare; Navicula bryophila; Navicula capitata; Navicula clementis; Navicula constans var. symmetrica; Navicula costulata; Navicula cryptocephala; Navicula cryptotenella; Navicula laterostrata; Navicula modica; Navicula placentula; Navicula porifera; Navicula pseudolanceolata; Navicula pseudolanceolata var. denselineolata; Navicula pseudoscutiformis; Navicula pupula var. aqueductae; Navicula reinhardtii; Navicula rhynchocephala; Navicula schoenfeldii; Navicula spp.; Navicula trivialis; Neidium ampliatum; Neidium iridis; Neidium spp.; Nitzschia acicularis; Nitzschia angustata; Nitzschia capitellata; Nitzschia dissipata; Nitzschia frustulum var. frustulum; Nitzschia heufleriana; Nitzschia inconspicua; Nitzschia lanceolata; Nitzschia microcephala; Nitzschia palea; Nitzschia perminuta; Nitzschia recta; Nitzschia spp.; Nitzschia tubicola; Orthoseira roseana; Permafrost Research (Periglacial Dynamics) @ AWI; PG1857-5; Pinnularia borealis; Pinnularia similis; Pinnularia spp.; Piston corer (Kiel type); Planothidium joursacense; Pseudostaurosira elliptica; Rhoicosphenia abbreviata; Rhopaloidia gibba; Rhopaloidia operculata; RU-Land_2007_Kamchatka; see reference(s); Sellaphora pupula; Stauroneis anceps var. siberica; Stauroneis phoenicenteron; Stauroneis spp.; Stephanodiscus alpinus; Stephanodiscus hantzschii; Stephanodiscus medius; Stephanodiscus minutulus; Surirella amphioxys; Surirella angusta; Surirella brebissonii; Surirella linearis; Surirella robusta; Surirella spp.; Tabellaria fenestrata; Taxa; Two-Yurts Lake
    Type: Dataset
    Format: text/tab-separated-values, 2730 data points
    Location Call Number Expected Availability
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