TY - JOUR
T1 - Human Activities Dominate Global Trends in Terrestrial Phosphorus Deposition
AU - You, Shiyu
AU - Ma, Jiageng
AU - Zheng, Hua
AU - Liu, Xuejun
AU - Tian, Hanqin
AU - Wu, Yanhong
AU - Zaehle, Sönke
AU - Wang, Yonghong
AU - Shi, Hailong
AU - Li, Rui
AU - Shi, Hao
N1 - Publisher Copyright:
© 2026 American Chemical Society
PY - 2026/4/14
Y1 - 2026/4/14
N2 - Atmospheric deposition of phosphorus (P) has multitudes of environmental implications, but quantifying and validating its spatial and temporal patterns remain highly challenging. Here, we integrated a detailed P emission inventory with atmospheric chemistry transport modeling and a temporally augmented mass-conserving downscaling approach to estimate terrestrial P deposition at 0.1° resolution during 2000–2019. The results reveal a 16.5% increase in global terrestrial P deposition, from 174.6 g ha–1 yr–1 (2.31 Tg yr–1) in 2000 to 202.6 g ha–1 yr–1 (2.69 Tg yr–1) in 2019. Among the natural sources, mineral dust predominated with emissions ranging from 1.31 to 1.50 Tg P yr–1, followed by primary biological aerosol particles (0.14–0.15 Tg P yr–1). Among anthropogenic sources, emissions were led by fossil fuel (1.12–1.62 Tg P yr–1) and biofuel combustion (0.39–0.52 Tg P yr–1), which significantly exceeded contributions from agricultural activities (0.07–0.10 Tg P yr–1). Spatially, the net global increase in P deposition was primarily driven by increased anthropogenic emissions in China (+4.09% per year) and India (+2.98% per year), which outpaced concurrent P emission reductions in the US (−0.40% per year) and Europe (−0.04% per year). Despite the implementation of a series of clean air policies in the two countries, anthropogenic P emissions continued to climb or level off, underscoring the need for systematic monitoring to mitigate potential environmental risks.
AB - Atmospheric deposition of phosphorus (P) has multitudes of environmental implications, but quantifying and validating its spatial and temporal patterns remain highly challenging. Here, we integrated a detailed P emission inventory with atmospheric chemistry transport modeling and a temporally augmented mass-conserving downscaling approach to estimate terrestrial P deposition at 0.1° resolution during 2000–2019. The results reveal a 16.5% increase in global terrestrial P deposition, from 174.6 g ha–1 yr–1 (2.31 Tg yr–1) in 2000 to 202.6 g ha–1 yr–1 (2.69 Tg yr–1) in 2019. Among the natural sources, mineral dust predominated with emissions ranging from 1.31 to 1.50 Tg P yr–1, followed by primary biological aerosol particles (0.14–0.15 Tg P yr–1). Among anthropogenic sources, emissions were led by fossil fuel (1.12–1.62 Tg P yr–1) and biofuel combustion (0.39–0.52 Tg P yr–1), which significantly exceeded contributions from agricultural activities (0.07–0.10 Tg P yr–1). Spatially, the net global increase in P deposition was primarily driven by increased anthropogenic emissions in China (+4.09% per year) and India (+2.98% per year), which outpaced concurrent P emission reductions in the US (−0.40% per year) and Europe (−0.04% per year). Despite the implementation of a series of clean air policies in the two countries, anthropogenic P emissions continued to climb or level off, underscoring the need for systematic monitoring to mitigate potential environmental risks.
KW - GEOS-chem
KW - anthropogenic activities
KW - downscaling
KW - machine learning
KW - phosphorus deposition
UR - https://www.scopus.com/pages/publications/105035699606
U2 - 10.1021/acs.est.5c16208
DO - 10.1021/acs.est.5c16208
M3 - 文章
C2 - 41894602
AN - SCOPUS:105035699606
SN - 0013-936X
VL - 60
SP - 10850
EP - 10860
JO - Environmental Science and Technology
JF - Environmental Science and Technology
IS - 14
ER -