This dataset comprises environmental parameters for biological soil crusts in coastal sand dunes in northern Germany. Biological soil crusts (biocrusts) are autonomous ecosystems consisting of prokaryotic and eukaryotic microorganisms growing on the topsoil. They colonize global climatic zones, including temperate dunes. This study examined changes in the community structure of biocrust phototrophic organisms along a dune chronosequence at the Baltic Sea compared to an inland dune in Northern Germany. The community composition and their shift between different successional stages of dune development were related to physico-chemical sediment properties. A vegetation survey followed by species determination and sediment analyses were conducted. The sampling took place on the 25th of April and on the 5th of May 2020. The samples were collected at a costal dune area, namely the Schaabe spit on the island Rügen, Mecklenburg Wester-Pomerania, Germany, and in an inland dune area at Verden (Aller), Lower Saxony, Germany. Biocrust samples were taken along one transect per study site. Each transect followed a natural succession gradient in the dune area. Along each transect, the different successional dune stages were visually identified and further named as dune subsites. At each subsite, a sampling plot of 1 m2 was established and used for further vegetation analyses, biocrust and sediment sampling. Along the Schaabe spit transect four subsites with one sampling plot each were established and three subsites were established in the inland dune in Verden. For the vegetation survey seven different functional groups were defined describing the overall surface coverage: Thin (1-3 mm) green algae-dominated biocrusts were defined as early successional stages. Later successional stages, in which the green algae biocrusts became slightly thicker (3-8 mm) and moss-covered, were defined as the intermediate successional biocrust stage. Moss-dominated biocrusts and those who additionally lichenized characterized the mature successional stages of biocrusts. Vascular plants, and litter (dead material, i.e., pine needles, leaves, and branches) were two of the non-cryptogamic but still biotic functional groups. Bare sediment was the only abiotic functional group. The predefined functional groups were recorded within each plot according to the point intercept method by Levy and Madden (1933). Each of the seven sampling plots was divided into 16 equal subplots (0.0625 m2). A 25 cm x 25 cm (0.0625 m2) grid of 25 intersections was placed randomly into 4 of these subplots. Within each sub-plot, the functional groups were recorded by 25 point measurements according to the approach of Williams et al. (2017). That allowed 100 point measurements per sampling plot (1 m2).
This data collection comprises environmental data and taxonomic parameters of the investigated biocrusts of sampling sites in coastal and inland sand dunes in northern Germany. Sampling took place in spring 2020 and winter 2021. Biocrusts and uppermost sediment samples were collected along dune successional gradients and sequenced by LGC Genomics Ltd. Corresponding sequence data of biocrust organisms are archived at the European Nucleotide Archive.
This dataset comprises the microbial community composition of biological soil crusts in north-German sand dunes. For this we obtained enrichment cultures of phototrophic microorganisms, by placing fragments of biocrusts of the same Petri dishes as used for sequencing, in Petri dishes with Bold Basal (1N BBM) agarized medium (Bischoff and Bold 1963). Cultures were grown under standard laboratory conditions: with a 12-hour alteration of light and dark phases and irradiation of 25 μmol photons m-2 s-1 at a temperature 20 ± 5 ºС. Microscopic study of these raw cultures began in the third week of cultivation. Morphological examinations were performed using Olympus BX53 light microscope with Nomarski DIC optics (Olympus Ltd, Hamburg, Germany). Micrographs were taken with a digital camera (Olympus LC30) attached to the microscope, and processed by the Olympus software cellSens Entry. Direct microscopy of rewetted samples was performed in parallel with cultivation for evaluation of dominating species of algae and cyanobacteria in the original samples. Morphological identification of the biocrust organisms was based mainly on Ettl and Gärtner (2014) for green microalgae, and on Komárek (2013) for cyanobacteria, as well as on some monographs and papers devoted to taxonomic revisions of the taxa of interest (Darienko and Pröschold 2019). Moss and lichens samples were air-dried after collection. For determination, a microscope with a maximum magnification of 400x was used. Morphological identification of mosses followed Frahm and Frey (2004) with taxonomical reference to (Hodgetts et al. 2020). Lichens were determined according to Wirth et al. (2013). Morphologically critical species of the genus Cladonia where additionally analyzed by thin-layer chromatography according to (Culberson and Ammann 1979) in solvent system A.
The dataset compiles total organic carbon (TOC), total inorganic carbon (TIC), total nitrogen (TN) and total sulfur (TS) contents and stable isotope signatures (δ13C of TOC, δ15N, δ34S) of fine-grained deposits (clay, loam) over sandy subsoils of the saltmarsh of the barrier island Spiekeroog at the southern North Sea coast. Sampling was performed in September 2016 along three transects spanning from the high saltmarsh to the pioneer zone. At each sample point, soil samples were taken from the first 5 cm of the upper part (top samples) and from the deepest 5 cm of the lower part (bottom samples) of the fine-grained deposit. If the fine-grained deposit layer had a thickness < 10 cm, only one bulk soil sample (single samples) was taken for the depth range equal to the deposit thickness. Samples were ground to fine powder. TIC was measured on oven-dried samples coulometrically with an Analytik Jena multi EA 4000 analyzer. The total carbon (TC), TN, and TS were analyzed using a Thermo Scientific Flash EA Isolink Elemental Analyzer. The TOC contents were calculated as the difference between TC and TIC. TOC, TN, and TS contents are reported based on the original dry mass. For isotope analysis, dried and homogenized samples were weighed in tin cups and combusted in a Thermo Scientific Flash EA Isolink Elemental Analyzer, connected to a Thermo Finnigan MAT 253 gas mass spectrometer via a Thermo Conflo IV split interface. The δ13C values of TOC were measured after decalcification of the ground powders with p. a. grade HCl. The TN and δ34S analysis were carried out on a separate aliquot of sample powder. The isotope results are given in the conventional δ-notation.
A shallow subtidal area in the northern Wadden Sea was monitored for sediment parameters and macrobenthic fauna using stratified random sampling of a grid of 33 sampling positions. Samples were collected with a Reineck-type box-corer of 0.02 m² surface area. Granulometric sediment composition was analysed from a sub-sample of each box-core using a diffraction laser particle-size analyser. Macrobenthos (sieved through 1 mm square meshes and fixed in buffered formalin solution) was counted, identified to species level, and the size of hard-shelled individuals measured. The amount of shell detritus was quantified as wet-weight in the benthos samples. This dataset contains the results from the sampling events in 2019.
A shallow subtidal area in the northern Wadden Sea was monitored over 17 years for sediment parameters and macrobenthic fauna using stratified random sampling of a grid of 50 sampling positions. Samples were collected with a Reineck-type box-corer of 0.02 m² surface area, always during preceeded high tide. Granulometric sediment composition was analysed from a sub-sample of each box-core using a diffraction laser particle-size analyser. Macrobenthos (sieved through 1 mm square meshes and fixed in buffered formalin solution) was counted, identified to species level, and the size of hard-shelled individuals measured. The amount of shell detritus was quantified as wet-weight in the benthos samples. From 2003 to 2007 sampling was approximatively monthly and from 2008 to 2013 seasonally. When a new ship with larger drought was put into operation, the number of sampling sites needed to be reduced to 33 from 2014 onwards and sampling frequency was only once per year in autumn.
The dataset compiles total organic carbon (TOC), total inorganic carbon (TIC), total nitrogen (TN) and total sulfur (TS) contents and stable isotope signatures (δ13C of TOC, δ15N, δ34S) of fine-grained deposits (clay, loam) over sandy subsoils of the saltmarsh of the barrier island Spiekeroog at the southern North Sea coast. Sampling was performed in September 2016 along three transects spanning from the high saltmarsh to the pioneer zone. At each sample point, soil samples were taken from the first 5 cm of the upper part (top samples) and from the deepest 5 cm of the lower part (bottom samples) of the fine-grained deposit. If the fine-grained deposit layer had a thickness < 10 cm, only one bulk soil sample (single samples) was taken for the depth range equal to the deposit thickness. Samples were ground to fine powder. TIC was measured on oven-dried samples coulometrically with an Analytik Jena multi EA 4000 analyzer. The total carbon (TC), TN, and TS were analyzed using a Thermo Scientific Flash EA Isolink Elemental Analyzer. The TOC contents were calculated as the difference between TC and TIC. TOC, TN, and TS contents are reported based on the original dry mass. For isotope analysis, dried and homogenized samples were weighed in tin cups and combusted in a Thermo Scientific Flash EA Isolink Elemental Analyzer, connected to a Thermo Finnigan MAT 253 gas mass spectrometer via a Thermo Conflo IV split interface. The δ13C values of TOC were measured after decalcification of the ground powders with p. a. grade HCl. The TN and δ34S analysis were carried out on a separate aliquot of sample powder. The isotope results are given in the conventional δ-notation.
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