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Grundwassermessstelle APP_GWMN_637

Dieser Datensatz beschreibt die Grundwassermessstelle APP_GWMN_637 in Schleswig-Holstein. Die Messstelle liegt im Grundwasserkörper N8 : Südholstein. Es liegen insgesamt 23316 Messwerte vor. Es liegen außerdem 6 Probenentnahmen vor (siehe Resourcen).

INSPIRE SN - InVeKoS LPIS, GSA

Im Rahmen des Integrierten Verwaltungs- und Kontrollsystems (InVeKoS) werden in Sachsen die Feldblöcke und Landschaftselemente als Referenzflächen zur Identifizierung landwirtschaftlicher Parzellen (LPIS) gepflegt und bereitgestellt. Die punktförmig bereitgestellten GSA-Daten werden nach Einreichung aus den Antragsparzellen (= Schläge/GSA-Daten) im Rahmen der Antragstellung abgeleitet.

Lichtsignalanlagen Hamburg

Der Datensatz enthält Lage, Namen und Knotennummer aller Lichtsignalanlagen im Hamburger Stadtgebiet (ohne Hamburg Port Authority [HPA]). Signalisierte Übergänge/Einmündung etc., die als Teilknoten der LSA festgelegt sind, werden nicht als gesonderter Punkt dargestellt.

Historische Amtliche Basiskarte NW 1:5 000 Schwarz-Weiß

Die Historische Amtliche Basiskarte (Historische ABK) deckt den Kartenmaßstab 1 : 5 000 als topographisches Basiskartenwerk ab. Die Historische ABK stellt die Schnittstelle zwischen der eigentumsorientierten Liegenschaftskarte und den topographischen Landeskartenwerken dar und wird ausschließlich aus den Informationen des Liegenschaftskatasters (ALKIS) abgeleitet. Am Ende eines Jahres werden die Datenbestände der ABK als Zeitschnitte historisiert und bereitgestellt. Die Jahresschnitte sind ab 2016 verfügbar. Ab 2020 ist die Historische ABK in einer farbigen Signaturierung und einer schwarz-weißen Präsentation als Strichkarte verfügbar. Bis 2019 wurde eine vorläufige schwarz-weiße Präsentation abgleitet, welche als Historische ABK* bezeichnet wird. Das „*“ steht für eine Übergangslösung, bis die ABK komplett und flächendeckend in NRW vorlag. Die ABK* gibt den jeweiligen ABK-Erfassungsstand der Katasterbehörden in der Signaturierung der ABK wieder. Die Signaturierung zwischen der Historischen ABK und Historischen ABK* unterscheiden sich geringfügig.

Amtliche Basiskarte NW 1:5 000 Schwarz-Weiß

Die Amtliche Basiskarte (ABK) deckt den Kartenmaßstab 1 : 5 000 als topographisches Basiskartenwerk ab. Die ABK stellt die Schnittstelle zwischen der eigentumsorientierten Liegenschaftskarte und den topographischen Landeskartenwerken dar und wird ausschließlich aus den Informationen des Liegenschaftskatasters (ALKIS) abgeleitet. Die ABK ist in einer schwarz-weißen Präsentation als Strichkarte abgeleitet. Stand der verwendeten Daten: 01.01.2026.

Grundwassermessstelle DEGM_SH_1290: SÜDERLÜGUMFELD

Stammdaten und Analysedaten zu den Grundwassermessstellen im EUA-Messnetz: Messtelle DEGM_SH_1290 (SÜDERLÜGUMFELD)

WFS ST ALKIS Vereinfacht

Das Liegenschaftskataster wird in elektronischer Form im Amtlichen Liegenschaftskatasterinformationssystem (ALKIS) geführt. Der vorliegende Web Feature Service ermöglicht das gezielte Herunterladen von in ALKIS geführten GeoObjekten auf Basis einer Suchanfrage (Direktzugriffs-Downloaddienst). Der Dienst stellt ausschließlich folgende GeoObjekte beschränkt auf die wesentlichen Eigenschaften im Format eines vereinfachten Datenaustauschschemas bereit, das in dieser Produktspezifikation festgelegt ist: Flurstücke, Gebäude, Tatsächliche Nutzungen, Verwaltungseinheiten, Katasterbezirke. Der Dienst ist konzipiert zur Nutzung in einfachen praxisgängigen GIS-Clients ohne komplexe Funktionalitäten. Maßstab: 1:1000; Bodenauflösung: nullm; Scanauflösung (DPI): null

Geochemical parameters in peat depth profiles from ombrotrophic bogs in North and Central Europe. Pichlmaier Moor, Austria

This dataset contains geochemical variables measured in six depth profiles from ombrotrophic peatlands in North and Central Europe. Peat cores were taken during the spring and summer of 2022 from Amtsvenn (AV1), Germany; Drebbersches Moor (DM1), Germany; Fochteloër Veen (FV1), the Netherlands; Bagno Kusowo (KR1), Poland; Pichlmaier Moor (PI1), Austria and Pürgschachen Moor (PM1), Austria. The cores AV1, DM1 and KR1 were taken using a Wardenaar sampler (Royal Eijkelkamp, Giesbeek, the Netherlands) and had diameter of 10 cm. The cores FV1, PM1 and PI1 had an 8 cm diameter and were obtained using an Instorf sampler (Royal Eijkelkamp, Giesbeek, the Netherlands). The cores FV1, DM1 and KR1 were 100 cm, core AV1 was 95 cm, core PI1 was 85 cm and core PM1 was 200 cm. The cores were subsampeled in 1 cm (AV1, DM1, KR1, FV1) and 2 cm (PI1, PM1) sections. The subsamples were milled after freeze drying in a ballmill using tungen carbide accesoires. X-Ray Fluorescence (WD-XRF; ZSX Primus II, Rigaku, Tokyo, Japan) was used to determine Al (μg g-1), As (μg g-1), Ba (μg g-1), Br (μg g-1), Ca (g g-1), Cl (μg g-1), Cr (μg g-1), Cu (μg g-1), Fe (g g-1), K (g g-1), Mg (μg g-1), Mn (μg g-1), Na (μg g-1), P (μg g-1), Pb (μg g-1), Rb (μg g-1), S (μg g-1), Si (μg g-1), Sr (μg g-1), Ti (μg g-1) and Zn (μg g-1). These data were processed and calibrated using the iloekxrf package (Teickner & Knorr, 2024) in R. C, N and their stable isotopes were determined using an elemental analyser linked to an isotope ratio mass spectrometer (EA-3000, Eurovector, Pavia, Italy & Nu Horizon, Nu Instruments, Wrexham, UK). C and N were given in units g g-1 and stable isotopes were given as δ13C and δ15N for stable isotopes of C and N, respectively. Raw data C, N and stable isotope data were calibrated with certified standard and blank effects were corrected with the ilokeirms package (Teickner & Knorr, 2024). Using Fourier Transform Mid-Infrared Spectroscopy (FT-MIR) (Agilent Cary 670 FTIR spectromter, Agilent Technologies, Santa Clara, Ca, USA) humification indices (HI) were determined. Spectra were recorded from 600 cm-1 to 4000 cm-1 with a resolution of 2 cm-1 and baselines corrected with the ir package (Teickner, 2025) to estimate relative peack heights. The HI (no unit) for each sample was calculated by taking the ratio of intensities at 1630 cm-1 to the intensities at 1090 cm-1. Bulk densities (g cm-3) were estimated from FT-MIR data (Teickner et al., in preparation).

Geochemical parameters in peat depth profiles from ombrotrophic bogs in North and Central Europe. Fochteloër Veen, the Netherlands

This dataset contains geochemical variables measured in six depth profiles from ombrotrophic peatlands in North and Central Europe. Peat cores were taken during the spring and summer of 2022 from Amtsvenn (AV1), Germany; Drebbersches Moor (DM1), Germany; Fochteloër Veen (FV1), the Netherlands; Bagno Kusowo (KR1), Poland; Pichlmaier Moor (PI1), Austria and Pürgschachen Moor (PM1), Austria. The cores AV1, DM1 and KR1 were taken using a Wardenaar sampler (Royal Eijkelkamp, Giesbeek, the Netherlands) and had diameter of 10 cm. The cores FV1, PM1 and PI1 had an 8 cm diameter and were obtained using an Instorf sampler (Royal Eijkelkamp, Giesbeek, the Netherlands). The cores FV1, DM1 and KR1 were 100 cm, core AV1 was 95 cm, core PI1 was 85 cm and core PM1 was 200 cm. The cores were subsampeled in 1 cm (AV1, DM1, KR1, FV1) and 2 cm (PI1, PM1) sections. The subsamples were milled after freeze drying in a ballmill using tungen carbide accesoires. X-Ray Fluorescence (WD-XRF; ZSX Primus II, Rigaku, Tokyo, Japan) was used to determine Al (μg g-1), As (μg g-1), Ba (μg g-1), Br (μg g-1), Ca (g g-1), Cl (μg g-1), Cr (μg g-1), Cu (μg g-1), Fe (g g-1), K (g g-1), Mg (μg g-1), Mn (μg g-1), Na (μg g-1), P (μg g-1), Pb (μg g-1), Rb (μg g-1), S (μg g-1), Si (μg g-1), Sr (μg g-1), Ti (μg g-1) and Zn (μg g-1). These data were processed and calibrated using the iloekxrf package (Teickner & Knorr, 2024) in R. C, N and their stable isotopes were determined using an elemental analyser linked to an isotope ratio mass spectrometer (EA-3000, Eurovector, Pavia, Italy & Nu Horizon, Nu Instruments, Wrexham, UK). C and N were given in units g g-1 and stable isotopes were given as δ13C and δ15N for stable isotopes of C and N, respectively. Raw data C, N and stable isotope data were calibrated with certified standard and blank effects were corrected with the ilokeirms package (Teickner & Knorr, 2024). Using Fourier Transform Mid-Infrared Spectroscopy (FT-MIR) (Agilent Cary 670 FTIR spectromter, Agilent Technologies, Santa Clara, Ca, USA) humification indices (HI) were determined. Spectra were recorded from 600 cm-1 to 4000 cm-1 with a resolution of 2 cm-1 and baselines corrected with the ir package (Teickner, 2025) to estimate relative peack heights. The HI (no unit) for each sample was calculated by taking the ratio of intensities at 1630 cm-1 to the intensities at 1090 cm-1. Bulk densities (g cm-3) were estimated from FT-MIR data (Teickner et al., in preparation).

Geochemical parameters in peat depth profiles from ombrotrophic bogs in North and Central Europe. Pürgschachen Moor, Austria

This dataset contains geochemical variables measured in six depth profiles from ombrotrophic peatlands in North and Central Europe. Peat cores were taken during the spring and summer of 2022 from Amtsvenn (AV1), Germany; Drebbersches Moor (DM1), Germany; Fochteloër Veen (FV1), the Netherlands; Bagno Kusowo (KR1), Poland; Pichlmaier Moor (PI1), Austria and Pürgschachen Moor (PM1), Austria. The cores AV1, DM1 and KR1 were taken using a Wardenaar sampler (Royal Eijkelkamp, Giesbeek, the Netherlands) and had diameter of 10 cm. The cores FV1, PM1 and PI1 had an 8 cm diameter and were obtained using an Instorf sampler (Royal Eijkelkamp, Giesbeek, the Netherlands). The cores FV1, DM1 and KR1 were 100 cm, core AV1 was 95 cm, core PI1 was 85 cm and core PM1 was 200 cm. The cores were subsampeled in 1 cm (AV1, DM1, KR1, FV1) and 2 cm (PI1, PM1) sections. The subsamples were milled after freeze drying in a ballmill using tungen carbide accesoires. X-Ray Fluorescence (WD-XRF; ZSX Primus II, Rigaku, Tokyo, Japan) was used to determine Al (μg g-1), As (μg g-1), Ba (μg g-1), Br (μg g-1), Ca (g g-1), Cl (μg g-1), Cr (μg g-1), Cu (μg g-1), Fe (g g-1), K (g g-1), Mg (μg g-1), Mn (μg g-1), Na (μg g-1), P (μg g-1), Pb (μg g-1), Rb (μg g-1), S (μg g-1), Si (μg g-1), Sr (μg g-1), Ti (μg g-1) and Zn (μg g-1). These data were processed and calibrated using the iloekxrf package (Teickner & Knorr, 2024) in R. C, N and their stable isotopes were determined using an elemental analyser linked to an isotope ratio mass spectrometer (EA-3000, Eurovector, Pavia, Italy & Nu Horizon, Nu Instruments, Wrexham, UK). C and N were given in units g g-1 and stable isotopes were given as δ13C and δ15N for stable isotopes of C and N, respectively. Raw data C, N and stable isotope data were calibrated with certified standard and blank effects were corrected with the ilokeirms package (Teickner & Knorr, 2024). Using Fourier Transform Mid-Infrared Spectroscopy (FT-MIR) (Agilent Cary 670 FTIR spectromter, Agilent Technologies, Santa Clara, Ca, USA) humification indices (HI) were determined. Spectra were recorded from 600 cm-1 to 4000 cm-1 with a resolution of 2 cm-1 and baselines corrected with the ir package (Teickner, 2025) to estimate relative peack heights. The HI (no unit) for each sample was calculated by taking the ratio of intensities at 1630 cm-1 to the intensities at 1090 cm-1. Bulk densities (g cm-3) were estimated from FT-MIR data (Teickner et al., in preparation).

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