68 citations as recorded by crossref.

1. Gradually Cooling of the Yellow Sea Warm Current Driven by Tropical Pacific Subsurface Water Temperature Changes Over the Past 5 kyr D. Li et al. https://doi.org/10.1029/2021GL093534
2. Processes and Microorganisms Involved in the Marine Nitrogen Cycle: Knowledge and Gaps S. Pajares & R. Ramos https://doi.org/10.3389/fmars.2019.00739
3. Nitrogen removal processes coupled with nitrification in coastal sediments off the north East China Sea Y. Chang et al. https://doi.org/10.1007/s11368-021-02964-5
4. Genome-Resolved Metagenomic Insights into Massive Seasonal Ammonia-Oxidizing Archaea Blooms in San Francisco Bay A. Rasmussen et al. https://doi.org/10.1128/msystems.01270-21
5. Distribution and Activity of Ammonia-Oxidizers on the Size-Fractionated Particles in the Pearl River Estuary L. Ma et al. https://doi.org/10.3389/fmars.2021.685955
6. Influence of organic particle addition on nitrification rates and ammonium oxidiser abundances in Baltic seawater S. Kache et al. https://doi.org/10.3354/meps13797
7. Nitrification and denitrification in recirculating aquaculture systems: the processes and players P. Preena et al. https://doi.org/10.1111/raq.12558
8. Diversity, Abundance, and Niche Differentiation of Ammonia-Oxidizing Prokaryotes in Mud Deposits of the Eastern China Marginal Seas S. Yu et al. https://doi.org/10.3389/fmicb.2016.00137
9. Distinct Features of Sedimentary Archaeal Communities in Hypoxia and Non-Hypoxia Regions off the Changjiang River Estuary D. Zou et al. https://doi.org/10.1128/spectrum.01947-22
10. Nitrogen loss by nirS-type denitrifying bacterial communities in eutrophic coastal sediments X. Liu et al. https://doi.org/10.1016/j.ibiod.2020.104955
11. Particle-associated denitrification is the primary source of N2O in oxic coastal waters X. Wan et al. https://doi.org/10.1038/s41467-023-43997-3
12. River plume and bottom boundary layer – Hotspots for nitrification in a coastal bay? I. Bartl et al. https://doi.org/10.1016/j.ecss.2018.04.023
13. The effect of bio-irrigation by the polychaete Lanice conchilega on active denitrifiers: Distribution, diversity and composition of nosZ gene M. Yazdani Foshtomi et al. https://doi.org/10.1371/journal.pone.0192391
14. Spatio-temporal shifts in community structure and activity of nirS-type denitrifiers in the sediment cores of Pearl River Estuary H. Xie et al. https://doi.org/10.1371/journal.pone.0231271
15. Effect of thermal stratification on denitrifying bacterial community in a deep drinking water reservoir H. Zhang et al. https://doi.org/10.1016/j.jhydrol.2021.126090
16. The impact of algal blooms on promoting in-situ N2O emissions: A case in Zhanjiang bay, China S. Cai et al. https://doi.org/10.1016/j.jenvman.2024.120935
17. Effects of allochthonous dissolved organic matter input on microbial composition and nitrogen-cycling genes at two contrasting estuarine sites E. Happel et al. https://doi.org/10.1093/femsec/fiz123
18. nirS-Encoding denitrifier community composition, distribution, and abundance along the coastal wetlands of China J. Gao et al. https://doi.org/10.1007/s00253-016-7659-5
19. Functional Gene Diversity and Metabolic Potential of the Microbial Community in an Estuary-Shelf Environment Y. Wang et al. https://doi.org/10.3389/fmicb.2017.01153
20. Extensive nitrification and active ammonia oxidizers in two contrasting coastal systems of the Baltic Sea E. Happel et al. https://doi.org/10.1111/1462-2920.14293
21. Niche differentiation of ammonia and nitrite oxidizers along a salinity gradient from the Pearl River estuary to the South China Sea L. Hou et al. https://doi.org/10.5194/bg-15-5169-2018
22. Nitrogen cycling in China marginal seas: Progress and challenges S. Wu et al. https://doi.org/10.1016/j.marchem.2024.104421
23. Characterizing nitrogen cycling microorganisms and genes in sediments of the Three Gorges Reservoir C. Han et al. https://doi.org/10.1371/journal.pone.0324051
24. Niche adaptation of particle-associated ammonia-oxidizing archaea sustains nitrification under marine deoxygenation L. Li et al. https://doi.org/10.3389/fmicb.2026.1773718
25. Microbial Diversity and Community Structure of Sulfate-Reducing and Sulfur-Oxidizing Bacteria in Sediment Cores from the East China Sea Y. Zhang et al. https://doi.org/10.3389/fmicb.2017.02133
26. OH-isoGDGTs as a paleothermometer for bottom seawater temperature in the eastern China marginal seas Y. Wang et al. https://doi.org/10.1016/j.chemgeo.2025.122768
27. Using water age to study the biogeochemistry of nutrients in a large-river estuary and the adjacent shelf area L. Gao & H. Zong https://doi.org/10.1016/j.jmarsys.2020.103469
28. The Link between Microbial Diversity and Nitrogen Cycling in Marine Sediments Is Modulated by Macrofaunal Bioturbation M. Yazdani Foshtomi et al. https://doi.org/10.1371/journal.pone.0130116
29. Vertical distribution of isoprenoid GDGTs in suspended particles from the East China Sea shelf and implications for sedimentary TEX86H records Y. Wang et al. https://doi.org/10.1016/j.orggeochem.2019.07.004
30. Linking biochemical properties of particles to particle‐attached and free‐living bacterial community structure along the particle density gradient from freshwater to open ocean Y. Zhang et al. https://doi.org/10.1002/2016JG003390
31. Microbial Nitrogen Cycling in Estuaries: From Genes to Ecosystem Processes J. Damashek & C. Francis https://doi.org/10.1007/s12237-017-0306-2
32. Abundance and Diversity of Denitrifying and Anammox Bacteria in Seasonally Hypoxic and Sulfidic Sediments of the Saline Lake Grevelingen Y. Lipsewers et al. https://doi.org/10.3389/fmicb.2016.01661
33. Microbial Diversity and Nitrogen Cycling in Peat and Marine Soils: A Review A. Soratur et al. https://doi.org/10.3390/microbiolres15020052
34. Dual Isotope Measurements Reveal Zoning of Nitrate Processing in the Summer Changjiang (Yangtze) River Plume X. Yan et al. https://doi.org/10.1002/2017GL075951
35. Multi-scale factors affecting composition, diversity, and abundance of sediment denitrifying microorganisms in Yangtze lakes X. Jiang et al. https://doi.org/10.1007/s00253-017-8537-5
36. Effects of Feldspathic Sandstone Addition on Microbial Biomass, Soil Enzyme Activity, and Bacterial Community Structure of Sandy Soil J. Han et al. https://doi.org/10.1080/01490451.2023.2272619
37. Close spatial and metabolic association between heterotrophic and ammonia-oxidizing marine Nitrososphaerota Q. Li et al. https://doi.org/10.1093/ismeco/ycag173
38. Enhanced nitrogen loss from rivers through coupled nitrification-denitrification caused by suspended sediment X. Xia et al. https://doi.org/10.1016/j.scitotenv.2016.10.181
39. Bacterial communities along a 4,500-meter elevation gradient in the sediment of the Yangtze River: what are the driving factors? W. Zhang et al. https://doi.org/10.5004/dwt.2020.24875
40. Effects of illumination on nirS denitrifying and anammox bacteria in the rhizosphere of submerged macrophytes Y. Xiao et al. https://doi.org/10.1016/j.scitotenv.2020.143420
41. Variable Nitrification Rates Across Environmental Gradients in Turbid, Nutrient-Rich Estuary Waters of San Francisco Bay J. Damashek et al. https://doi.org/10.1007/s12237-016-0071-7
42. Water residence time controls seasonal nitrous oxide budget in a semi-enclosed bay: Insights from an improvement estimation method S. Cai et al. https://doi.org/10.1016/j.marpolbul.2024.116701
43. Dark Ammonium Transformations in the Pearl River Estuary During Summer L. Chen et al. https://doi.org/10.1029/2019JG005596
44. Oyster cultivation regulating seasonal nitrate cycling in the estuarine water X. Zhou et al. https://doi.org/10.1016/j.marpolbul.2025.118435
45. Shifts of abundance and community composition of nitrifying microbes along the Changjiang Estuary to the East China Sea Y. Chang et al. https://doi.org/10.1007/s11274-025-04259-0
46. Variation of Isoprenoid GDGTs in the Stratified Marine Water Column: Implications for GDGT-Based TEX86 Paleothermometry J. Guo et al. https://doi.org/10.3389/fmars.2021.715708
47. Contrasting temporal patterns in ammonia-oxidizing archaeal community dynamics in two peri-alpine lakes with different trophic status T. Pollet et al. https://doi.org/10.3354/ame01861
48. Early diagenesis and authigenic mineral formation in mobile muds of the Changjiang Estuary and adjacent shelf B. Zhao et al. https://doi.org/10.1016/j.jmarsys.2017.03.001
49. Potential contributions of nitrifiers and denitrifiers to nitrous oxide sources and sinks in China's estuarine and coastal areas X. Dai et al. https://doi.org/10.5194/bg-19-3757-2022
50. Processes of coastal ecosystem carbon sequestration and approaches for increasing carbon sink Y. Zhang et al. https://doi.org/10.1007/s11430-016-9010-9
51. Distribution characteristics of size-fractionated Chlorophyll a in the coastal area of the Leizhou Peninsula in winter H. Xu et al. https://doi.org/10.3389/fmars.2024.1473950
52. High spatial variations of potential nitrification and N2O production across the Yangtze River and associated major tributaries C. Lan et al. https://doi.org/10.1016/j.watres.2026.126574
53. Denitrification and anammox: Understanding nitrogen loss from Yangtze Estuary to the east China sea (ECS) J. Wang et al. https://doi.org/10.1016/j.envpol.2019.06.025
54. Shifts in the Community Dynamics and Activity of Ammonia‐Oxidizing Prokaryotes Along the Yangtze Estuarine Salinity Gradient J. Gao et al. https://doi.org/10.1029/2017JG004182
55. Genes involved in carbon, nitrogen, and sulfur cycling in an important estuarine ecosystem show coherent shifts in response to changes in environmental conditions S. Preheim et al. https://doi.org/10.1002/lno.12731
56. A potential explanation for the anomalously low nitrate to phosphate ratio in the well-oxygenated East/Japan Sea H. Kim et al. https://doi.org/10.5194/bg-23-4719-2026
57. Insights into the Variations of Hao-Dependent Nitrifying and Nir-Dependent Denitrifying Microbial Communities in Ammonium-Graduated Lake Environments R. Zhao et al. https://doi.org/10.3390/app9163229
58. Major role of ammonia-oxidizing bacteria in N2O production in the Pearl River estuary L. Ma et al. https://doi.org/10.5194/bg-16-4765-2019
59. Sedimentary processes dominate nitrous oxide production and emission in the hypoxic zone off the Changjiang River estuary J. Yang et al. https://doi.org/10.1016/j.scitotenv.2022.154042
60. Overlooked contribution of water column to nitrogen removal in estuarine turbidity maximum zone (TMZ) Y. Zheng et al. https://doi.org/10.1016/j.scitotenv.2021.147736
61. Community Composition and Transcriptional Activity of Ammonia-Oxidizing Prokaryotes of Seagrass Thalassia hemprichii in Coral Reef Ecosystems J. Ling et al. https://doi.org/10.3389/fmicb.2018.00007
62. Metagenomic data highlight shifted nitrogen regime induced by wetland reclamation K. Li et al. https://doi.org/10.1007/s00374-024-01820-1
63. Hurricane Disturbance Stimulated Nitrification and Altered Ammonia Oxidizer Community Structure in Lake Okeechobee and St. Lucie Estuary (Florida) J. Hampel et al. https://doi.org/10.3389/fmicb.2020.01541
64. Hatchery technology restores the spawning ground of phytophilic fish in the urban river of Yangtze Estuary, China X. Huang et al. https://doi.org/10.1007/s11252-020-00971-x
65. How did the bacterial community respond to the level of urbanization along the Yangtze River? Y. Li et al. https://doi.org/10.1039/C9EM00399A
66. Seasonal dynamics of ammonia-oxidizing archaea (AOA) and their contribution to nitrification in wheat rhizospheres Z. He et al. https://doi.org/10.1007/s11104-025-07451-1
67. Illumina MiSeq sequencing reveals the community composition of NirS-Type and NirK-Type denitrifiers in Zhoucun reservoir – a large shallow eutrophic reservoir in northern China S. Zhou et al. https://doi.org/10.1039/C6RA18017E
68. Spatial-temporal dynamics of N-cycle functional genes in a temperate Atlantic estuary (Douro, Portugal) P. Salgado et al. https://doi.org/10.3354/ame01935