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Abstract: Terrestrial groundwater travels through subterranean estuaries before reaching the sea. Groundwater‐derived nutrients drive coastal water quality, primary production, and eutrophication. We determined how dissolved inorganic nitrogen (DIN), dissolved inorganic phosphorus (DIP), and dissolved organic nitrogen (DON) are transformed within subterranean estuaries and estimated submarine groundwater discharge (SGD) nutrient loads compiling > 10,000 groundwater samples from 216 sites worldwide. Nutrients exhibited complex, nonconservative behavior in subterranean estuaries. Fresh groundwater DIN and DIP are usually produced, and DON is consumed during transport. Median total SGD (saline and fresh) fluxes globally were 5.4, 2.6, and 0.18 Tmol yr−1 for DIN, DON, and DIP, respectively. Despite large natural variability, total SGD fluxes likely exceed global riverine nutrient export. Fresh SGD is a small source of new nutrients, but saline SGD is an important source of mostly recycled nutrients. Nutrients exported via SGD via subterranean estuaries are critical to coastal biogeochemistry and a significant nutrient source to the oceans.

Submarine groundwater discharge (SGD) plays a crucial role in nutrient budgets of coastal systems, encompassing both submarine fresh groundwater discharge (SFGD) and recirculated saline groundwater discharge (RSGD). Despite its significance, the specific importance of these components in mariculture bays has not been thoroughly assessed. Here, utilizing Ra isotopes and water‐salt mass balance model, we show that SFGD flux (1.1 ± 0.4 cm d−1) represented only 17% of the SGD in the Zhenzhu Bay, a typical mariculture bay along the South China Sea. Interestingly, the nutrient contribution from SFGD surpassed that from RSGD, accounting for 82% of the dissolved inorganic nitrogen (DIN) flux within the SGD. Analysis of the monthly satellite Chlorophyll‐a (Chl‐a) data confirmed that the decline in phytoplankton biomass can be linked to the limited dissolved silicate (DSi) transported by SFGD. Additionally, the elevated nitrogen to phosphorus ratio (241:1) and reduced silicon to nitrogen ratio (0.5:1) in SFGD compared to the Redfield ratio suggested that SFGD characterized by nitrogen excess and silica deficient, which likely played a role in transitioning from biogenic element constraints in coastal water. This shift may impact the proportions and functionality of the phytoplankton community, potentially mitigating water eutrophication. These findings underscore the significant influence of SGD on nutrient dynamics and the ecological environment in the Zhenzhu Bay. Plain Language Summary: Submarine groundwater discharge (SGD) is a significant process in coastal regions worldwide. Nutrients by SGD can disrupt the ecological balance of bays, altering nutrient structures and primary productivity in coastal ecosystems. However, this nutrient influx may exacerbate issues such as eutrophication and hypoxia in these waters. Although SGD acts as a significant nutrient source in the Zhenzhu Bay, there remains a scarcity of knowledge in distinguishing between submarine fresh groundwater discharge (SFGD) and recirculated saline groundwater discharge (RSGD), potentially resulting in overestimations of SGD. By utilizing Ra isotopes and a water‐salt mass balance model, we quantified the various components of SGD along with their nutrient fluxes. The study revealed that the persistent discharge of nitrogen‐contaminated fresh groundwater could eventually shift coastal waters from a nitrogen‐limited state to a phosphorus‐limited state. Moreover, the SFGD component under silicon‐limited conditions may restrict primary productivity particularly among freshwater diatom species. These findings contribute to enhancing our comprehension of how nutrients delivered by different SGD components impact marine ecosystems, but long‐term monitoring of SFGD and RSGD components is recommended to evaluate potential hazards and their influence on the ecological environment. Key Points: Nutrient fluxes from submarine fresh groundwater exceeded river by a factor of at least 3 timesSubmarine fresh groundwater discharge (SFGD) contributed more dissolved inorganic nitrogen than recirculated saline groundwater dischargeThe decline in phytoplankton biomass can be linked to the scarcity dissolved silicates in SFGD [ABSTRACT FROM AUTHOR]

The use of 234Th–238U disequilibrium has been widely employed to estimate the sinking flux of particulate organic carbon (POC) from the upper sea and ocean. Here, the deficits of 234Th relative to 238U in the water column and the carbon isotope signature (δ13C) of POC in the East China Sea (ECS) Shelf were measured, which was used to distinguish the fraction of marine and terrestrial POC export fluxes. In the ECS Shelf, very strong deficits of 234Th relative to 238U were observed throughout the water column, with 234Th/238U activity ratios ranging from 0.158 ± 0.045 to 0.904 ± 0.068 (averaging 0.426 ± 0.159). The residence times of particle reactive radionuclide 234Th (τTh–T) in the ECS shelf water varied between 9 and 44 days, which is significantly shorter than that in the continental slope area or the basin area. This phenomenon indicates that there is a more rapid particle scavenging process in the ECS shelf water compared to the continental slope and basin upper water. By applying a two-end-member mixing model based on the δ13C, the fraction of terrestrial POC was estimated to be 0 to 74% (mean: 30 ± 22%) and the fraction of marine POC was in the range of 25% to 100% (mean: 70 ± 22%). Fluxes of marine and terrestrial POC settling to the seafloor exhibited significant spatial differences among different stations, ranging from 11 to 129 mmol C/m2/day and from 2.6 to 38 mmol C/m2/day, respectively. The averaged terrestrial POC fluxes in the southern and northern ECS Shelf were similar (~ 21 to 24 mmol C/m2/day), while the marine POC fluxes in the north (86 ± 37 mmol C/m2/day) were approximately four times higher than those in the south (26 ± 20 mmol C/m2/day). Interestingly, the estimated export flux of both marine and terrestrial POC were approximately one order of magnitude higher than the previously reported burial fluxes of POC (ranging from 1.1 ± 0.1 to 11.4 ± 1.1 mmol C/m2/day) in the underlying bottom sediments, indicating that the majority (> 90%) of both terrestrial and marine POC exported from the upper water column are degraded in the sediments of the ECS Shelf. This "carbon missing" phenomenon can greatly be attributed to rapid decomposition by other processes (including microbial reworking, cross-shelf transport, and possible consumption by benthic organisms). Our findings highlight the dynamic nature of carbon cycling in the continental shelf and the need for further research to understand these processes and improve carbon budget assessments. [ABSTRACT FROM AUTHOR]