Abstract

Rivers of the Arctic will become ever more important for the global climate, since they carry a majority of continental dissolved organic carbon flux into the rapidly changing polar ocean. Aqueous organics comprise a wide array of functional groups, several of which are likely to impact coastal and open water biophysical properties. Light attenuation, interfacial films, aerosol formation, gas release and momentum exchange can all be cited. We performed Lagrangian kinetic modeling for the evolution of riverine organic chemistry as the molecules in question make their way from the highlands to Arctic outlets. Classes as diverse as the proteins, sugars, lipids, re-condensates, humics, bio-tracers and small volatiles are all included. Our reduced framework constitutes an idealized northward flow driving a major hydrological discharge rate and primarily representing the Russian Lena. Mountainous, high solute and tundra sources are all simulated, and they meet up at several points between soil and delta process reactors. Turnover rates are parameterized beginning with extrapolated coastal values imposed along a limited tributary network, with connections between different terrestrial sub-ecologies. Temporal variation of our total dissolved matter most closely resembles the observations when we focus on the restricted removal and low initial carbon loads, suggesting relatively slow transformation along the water course. Thus, channel combinations and mixing must play a dominant role. Nevertheless, microbial and photochemical losses help determine the final concentrations for most species. Chemical evolution is distinct for the various functionalities, with special contributions from pre- and post-reactivity in soil and delta waters. Several functions are combined linearly to represent the collective chromophoric dissolved matter, characterized here by its absorption. Tributaries carry the signature of lignin phenols to segregate tundra versus taiga sources, and special attention is paid to the early then marine behaviors of low molecular weight volatiles. Heteropolycondensates comprise the largest percentage of reactive carbon in our simulations due to recombination/accumulation, and they tend to be preeminent at the mouth. Outlet concentrations of individual structures such as amino acids and absorbers lie above threshold values for biophysical influence, on the monolayer and light attenuation. The extent of coastal spreading is examined through targeted regional box modeling, relying on salinity and color for calibration. In some cases, plumes reach the scale of peripheral arctic seas, and amplification is expected during upcoming decades. Conclusions are mapped from the Lena to other boreal discharges, and future research questions are outlined regarding the bonding type versus mass release as permafrost degrades. Dynamic aqueous organic coupling is recommended for polar system models, from headwaters to coastal diluent.

Highlights

  • Boreal rivers are currently the major transporters of dissolved organic carbon (DOC) from land into the Arctic Ocean, and the connection may well become stronger under global warming [1]

  • Structures including the amino acids combined as proteins, photochemically generated volatile organic compounds (VOCs) which are low in molecular weight, plus the colored or chromophoric dissolved organic matter (CDOM) are all likely to imply a biophysical impact on entry into the open sea

  • Dissolved organic levels are most obviously determined by the idealized mixing state

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Summary

Introduction

Boreal rivers are currently the major transporters of dissolved organic carbon (DOC) from land into the Arctic Ocean, and the connection may well become stronger under global warming [1]. It is possible to simulate time evolution along a lengthy river coordinate by accounting for mixing, with seasonal chemical transformations superimposed on fresh water transit times [9,12] This suggests the possibility for incorporating more detail through networks based on realistic hydrology. Concentrations at the river mouth are compared with measurement data given standard statistical formats [17], and through this strategy, we show that the coupled mixing and reactive processes illuminate functionality as well as total solute carbon. The relationship is configured first at a regional scale, based on salinity considerations [19], focused against the Arctic coastline with an estimated spreading distance derived from horizontal diffusivity [19,20,21] It is possible through just a few simple equations to bracket the potential for product concentration patterns to distribute widely depending on lifetime. Detailed mixing chemistry reactive dynamics should be continued from headwaters through tributary–distributary systems out to the turbulent plume regime

Background
Definitions
Early Geometry and Initial DOC Concentrations
Model Description and Mechanism
Total Carbon and Reprocessed Forms
Major Biomacromolecular and Tracer Groups
Aqueous Volatile Organics as a Set of Special Cases
Statistical Comparisons
10.6 Deviation
Summary and Discussion
Full Text
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