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Changes in the cryosphere extent (e.g., glacier, ice sheet, permafrost, and snow) have been speculated to impact (bio)geochemical interactions and element budgets of seawater and pore fluids in Arctic regions. However, this process has rarely been documented in Arctic fjords, which leads to a poor systematic understanding of land-ocean interactions in such a warming-susceptible region. Here, we present the chemical and isotopic (δ 18 O, δD, δ 11 B, and 87 Sr/ 86 Sr) compositions of seawater and pore fluids from five fjords in the Svalbard archipelago. Compared to bottom seawater, the low Cl - concentrations and depleted water isotopic signatures (δ 18 O and δD) of surface seawater and pore fluids delineate freshwater discharge originating from precipitation and/or meltwater of the cryosphere (i.e., glacier, snow, and permafrost). In contrast, the high Cl - concentrations with light water isotopic values in pore fluids from Dicksonfjorden indicate a brine probably resulted from submarine permafrost formation during the late Holocene, a timing supported by the numerical simulation of dissolved Cl - concentration. The freshwater is influenced by the local diagenetic processes such as ion exchanges indicated by δ 11 B signatures as well as interactions with bedrock during fluid migration inferred from pore fluid 87 Sr/ 86 Sr ratios. The interactions with bedrock significantly alter the hydrogeochemical properties of pore fluids in each fjord, yielding spatiotemporal variations. Consequently, land-ocean interactions in combination with the hydrosphere-cryosphere-lithosphere are critical factors for understanding and predicting the hydrology and elemental cycling during global climate change periods in the past, present, and future of the Svalbard archipelago., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.)

Rock weathering and biological cycling hold the development and sustainability of continental ecosystems, yet the interdependence of macro- and micro-nutrients biogeochemical cycles and their implications for ecosystem functioning remains unclear, despite being of particular importance in the context of global changes. This study focuses on the stocks, fluxes and processes constituting the biogeochemical cycle of boron. Vegetation, soils and solutions were monitored for a full year in a temperate beech forest developed on calcareous soil. Despite an overwhelmingly large B pool in soils, this study points to limited influence of weathering emphasizing the importance of vegetation cycling on this site. The biological imprint on the B cycle is marked by (1) a strong 11 B enrichment of solutions compared to the mineral source and (2) systematic correlations observed between B and other strongly recycled elements in all water samples. B isotopes are fractionated within the beech stand with higher values in leaves (23.5‰) and lower in fine roots (-11.7‰), suggesting that the light 10 B isotope is preferentially assimilated during plant growth. B isotopic data are consistent with a Rayleigh-like behaviour during xylem transfer leading to an 11 B enrichment in the higher parts of the trees, putting internal B transfer as the main driver of the large range of isotopic compositions between plant tissues. B apparent isotopic fractionations are observed in the annually produced biomass and total beech stand, albeit with different values: α xylem-biomass  = 0.980 ± 0.009 and 0.990 ± 0.002, respectively, suggesting 11 B transfer from old to new tissue. The developed model also points to an isotopic fractionation factor during B uptake much higher than previously evaluated (0.979 < α uptake  < 0.994). Overall, this study demonstrates that B isotopes appear as a promising tracer of soil-plant interactions with particular emphasis on tree adaptation to B bioavailability in soil., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Boron concentrations and isotopic compositions of atmospheric dust and dissolved depositions were monitored over a two-year period (2012-2013) in the forest ecosystem of Montiers (Northeastern France). This time series allows the determination of the boron atmospheric inputs to this forest ecosystem and contributes to refine our understanding of the sources and processes that control the boron atmospheric cycle. Mean annual dust and dissolved boron atmospheric depositions are comparable in size (13 g·ha -1 ·yr -1 and 16 g·ha -1 ·yr -1 , respectively), which however show significant intra- and interannual variations. Boron isotopes in dust differ from dissolved inputs, with an annual mean value of +1 ‰ and +18 ‰ for, respectively. The notable high boron contents (190-390 μg·g -1 ) of the dust samples are interpreted as resulting from localized spreading of boron-rich fertilizers, thus indicating a significant local impact of regional agricultural activities. Boron isotopes in dissolved depositions show a clear seasonal trend. The absence of correlation with marine cyclic solutes contradicts a control of atmospheric boron by dissolution of seasalts. Instead, the boron data from this study are consistent with a Rayleigh-like evolution of the atmospheric gaseous boron reservoir with possible but limited anthropogenic and/or biogenic contributions.