46 citations as recorded by crossref.

1. Nitrogen isotope compositions of the Upper Triassic Chang 7 Shale, Ordos Basin, North China: Implications for depositional redox conditions R. Chen et al. https://doi.org/10.1016/j.marpetgeo.2019.06.027
2. Salinity as a key control on the diazotrophic community composition in the southern Baltic Sea C. Reeder et al. https://doi.org/10.5194/os-18-401-2022
3. Nitrogen attenuation, dilution and recycling in the intertidal hyporheic zone of a subtropical estuary S. Lamontagne et al. https://doi.org/10.5194/hess-22-4083-2018
4. Nitrogen cycling during the Mesoproterozoic as informed by the 1400 million year old Xiamaling Formation X. Wang et al. https://doi.org/10.1016/j.earscirev.2023.104499
5. Isotopic fingerprints of benthic nitrogen cycling in the Peruvian oxygen minimum zone A. Dale et al. https://doi.org/10.1016/j.gca.2018.10.025
6. Linking nitrogen sources utilised by seagrass in a temperate marine embayment to patterns of seagrass change during drought A. Hirst et al. https://doi.org/10.3354/meps11708
7. Earthworms as plug flow reactors: a first-order kinetic study on the gut of the vermicomposting earthworm Eudrilus eugeniae K. Kiyasudeen et al. https://doi.org/10.1007/s11356-018-3074-z
8. Isotope fractionation and isotope decoupling during anammox and denitrification in marine sediments K. Dähnke & B. Thamdrup https://doi.org/10.1002/lno.10237
9. Quantification of nitrate fate in a karst conduit using stable isotopes and numerical modeling A. Husic et al. https://doi.org/10.1016/j.watres.2019.115348
10. No nitrogen fixation in the Bay of Bengal? C. Löscher et al. https://doi.org/10.5194/bg-17-851-2020
11. An in-situ analyzer based on CCD spectral integration for enhanced dynamic range fluorometric detection of ammonium in seawater H. Li et al. https://doi.org/10.1016/j.aca.2026.346328
12. Nitrogen cycling in sediments on the NW African margin inferred from N and O isotopes in benthic chambers A. Dale et al. https://doi.org/10.3389/fmars.2022.902062
13. Deciphering long-term seasonal and tidal water quality trends in the Mahanadi estuary T. Acharyya et al. https://doi.org/10.1007/s11852-021-00843-2
14. Anthropogenic and climatic impacts on a coastal environment in the Baltic Sea over the last 1000 years W. Ning et al. https://doi.org/10.1016/j.ancene.2018.02.003
15. Interactive Effects of Ocean Acidification, Elevated Temperature, and Reduced Salinity on Early-Life Stages of the Pacific Oyster G. Ko et al. https://doi.org/10.1021/es501611u
16. Nitrite isotope characteristics and associated soil N transformations D. Lewicka-Szczebak et al. https://doi.org/10.1038/s41598-021-83786-w
17. Using N and O isotope fractionation for evaluating denitrification in aquatic systems R. Margalef-Marti et al. https://doi.org/10.1016/j.trac.2025.118527
18. Nitrate removal rates, isotopic fractionation, and denitrifying bacteria in a woodchip-based permeable reactive barrier system: a long-term column experiment A. Buyanjargal et al. https://doi.org/10.1007/s11356-022-24826-4
19. Spatially and temporally variable production pathways support the Lake Erie central basin food web J. Tellier et al. https://doi.org/10.1016/j.jglr.2023.07.006
20. Isotopic composition of nitrate and particulate organic matter in a pristine dam reservoir of western India: implications for biogeochemical processes P. Bardhan et al. https://doi.org/10.5194/bg-14-767-2017
21. N‐loss isotope effects in the Peru oxygen minimum zone studied using a mesoscale eddy as a natural tracer experiment A. Bourbonnais et al. https://doi.org/10.1002/2014GB005001
22. Differences in Diet of Green (Haliotis fulgens) and Pink (Haliotis corrugata) Wild Abalone along the Pacific Coast of the Baja California Peninsula, Using Stable Isotope Analyses P. Vega-García et al. https://doi.org/10.2983/035.034.0317
23. Multi-species measurements of nitrogen isotopic composition reveal the spatial constraints and biological drivers of ammonium attenuation across a highly contaminated groundwater system N. Wells et al. https://doi.org/10.1016/j.watres.2016.04.025
24. Simplified bacterial denitrification method using Stenotrophomonas nitritireducens for nitrite dual isotope analysis in low-concentration environmental samples S. Deb & D. Lewicka-Szczebak https://doi.org/10.3389/fenvs.2025.1536882
25. Benthic nitrogen fluxes and fractionation of nitrate in the Mauritanian oxygen minimum zone (Eastern Tropical North Atlantic) A. Dale et al. https://doi.org/10.1016/j.gca.2014.02.026
26. Reviews and syntheses: Trends in primary production in the Bay of Bengal – is it at a tipping point? C. Löscher https://doi.org/10.5194/bg-18-4953-2021
27. Bladder wrack (Fucus vesiculosus) as a multi-isotope bio-monitor in an urbanized fjord of the western Baltic Sea V. Winde et al. https://doi.org/10.1080/10256016.2017.1316980
28. An N isotopic mass balance of the Eastern Tropical North Pacific oxygen deficient zone C. Fuchsman et al. https://doi.org/10.1016/j.dsr2.2017.12.013
29. Chemodenitrification by Fe(II) and nitrite: Effects of temperature and dual N O isotope fractionation G. Chen et al. https://doi.org/10.1016/j.chemgeo.2021.120258
30. Benthic-pelagic coupling and isotopic fractionation of barium in Kiel Bight, SW Baltic Sea F. Scholz et al. https://doi.org/10.3389/fmars.2023.1101095
31. Summer upwelling at the Boknis Eck time-series station (1982 to 2012) – a combined glider and wind data analysis J. Karstensen et al. https://doi.org/10.5194/bg-11-3603-2014
32. The effect of redox conditions and bioirrigation on nitrogen isotope fractionation in marine sediments J. Rooze & C. Meile https://doi.org/10.1016/j.gca.2016.04.040
33. Close coupling of N‐cycling processes expressed in stable isotope data at the redoxcline of the Baltic Sea C. Frey et al. https://doi.org/10.1002/2013GB004642
34. Vertical migration of multi-source nitrates driven by multiple water inputs in groundwater based on combined nitrogen-oxygen and hydrogen-oxygen stable isotopes T. Zhang et al. https://doi.org/10.1016/j.jhazmat.2026.141181
35. Porewater nitrate isotope dynamics in selected benthic habitats: Modulation by sediment reactivity and process coupling via nitrite A. Mazzoli et al. https://doi.org/10.1016/j.gca.2026.09.035
36. The isotope effect of denitrification in permeable sediments A. Kessler et al. https://doi.org/10.1016/j.gca.2014.02.029
37. Benzene degradation in contaminated aquifers: Enhancing natural attenuation by injecting nitrate C. Müller et al. https://doi.org/10.1016/j.jconhyd.2020.103759
38. Nitrate and Carbon Availability as Drivers of Isotopic Fractionation of Nitrate in Estuarine Sediments A. Laverman et al. https://doi.org/10.1021/acsestwater.5c00310
39. Fate of nitrogen in floating-raft aquaponic systems using natural abundance nitrogen isotopic compositions S. Wongkiew et al. https://doi.org/10.1016/j.ibiod.2017.08.006
40. Wastewater nitrogen budgets can be resolved by complementary functional gene and physicochemical methods A. Rose et al. https://doi.org/10.1016/j.jwpe.2019.100802
41. Nitrogen fixation in Arctic coastal waters (Qeqertarsuaq, West Greenland): influence of glacial melt on diazotrophs, nutrient availability, and seasonal blooms I. Schlangen et al. https://doi.org/10.5194/bg-23-1-2026
42. Source Versus Recycling Influences on the Isotopic Composition of Nitrate and Nitrite in the East China Sea S. Liu et al. https://doi.org/10.1029/2020JC016061
43. Phytoplankton Community Response to Environmental Changes in Mahanadi Estuary and Its Adjoining Coastal Waters of Bay of Bengal: a Multivariate and Remote Sensing Approach S. Naik et al. https://doi.org/10.1007/s41976-020-00036-9
44. Isotopically resolved fate and processes of nitrogen in a constructed wetland treating domestic effluent D. Allen et al. https://doi.org/10.1016/j.scitotenv.2025.178816
45. Microbial nitrogen transformations tracked by natural abundance isotope studies and microbiological methods: A review S. Deb et al. https://doi.org/10.1016/j.scitotenv.2024.172073
46. Nitrate isotope investigations reveal future impacts of climate change on nitrogen inputs and cycling in Arctic fjords: Kongsfjorden and Rijpfjorden (Svalbard) M. Santos-Garcia et al. https://doi.org/10.5194/bg-19-5973-2022