Between the land and ocean, diverse coastal ecosystems transform, store, and transport material. Across these interfaces, the dynamic exchange of energy and matter is driven by hydrological and hydrodynamic processes such as river and groundwater discharge, tides, waves, and storms. These dynamics regulate ecosystem functions and Earth’s climate, yet global models lack representation of coastal processes and related feedbacks, impeding their predictions of coastal and global responses to change. Here, we assess existing coastal monitoring networks and regional models, existing challenges in these efforts, and recommend a path towards development of global models that more robustly reflect the coastal interface.

The purpose of this review is to highlight progress in unraveling carbon cycling dynamics across the continuum of landscapes, inland waters, coastal oceans, and the atmosphere. Earth systems are intimately interconnected, yet most biogeochemical studies focus on specific components in isolation. The movement of water drives the carbon cycle, and, as such, inland waters provide a critical intersection between terrestrial and marine biospheres. Inland, estuarine, and coastal waters are well studied in regions near centers of human population in the Northern hemisphere. However, many of the world’s large river systems and their marine receiving waters remain poorly characterized, particularly in the tropics, which contribute to a disproportionately large fraction of the transformation of terrestrial organic matter to carbon dioxide, and the Arctic, where positive feedback mechanisms are likely to amplify global climate change. There are large gaps in current coverage of environmental observations along the aquatic continuum. For example, tidally-influenced reaches of major rivers and near-shore coastal regions around river plumes are often left out of carbon budgets due to a combination of methodological constraints and poor data coverage. We suggest that closing these gaps could potentially alter global estimates of CO2 outgassing from surface waters to the atmosphere by several-fold. Finally, in order to identify and constrain/embrace uncertainties in global carbon budget estimations it is important that we further adopt statistical and modeling approaches that have become well-established in the fields of oceanography and paleoclimatology, for example.

Constraining the fate of dissolved organic matter (DOM) delivered by rivers is a key to understand the global carbon cycle, since DOM mineralization directly influences air‐sea CO ₂ exchange and multiple biogeochemical processes. The Amazon River exports large amounts of DOM, and yet the fate of this material in the ocean remains unclear. Here we investigate the molecular composition and transformations of DOM in the Amazon River‐ocean continuum using ultrahigh resolution mass spectrometry and geochemical and biological tracers. We show that there is a strong gradient in source and composition of DOM along the continuum, and that dilution of riverine DOM in the ocean is the dominant pattern of variability in the system. Alterations in DOM composition are observed in the plume associated with the addition of new organic compounds by phytoplankton and with bacterial and photochemical transformations. The relative importance of each of these drivers varies spatially and is modulated by seasonal variations in river discharge and ocean circulation. We further show that a large fraction (50–76%) of the Amazon River DOM is surprisingly stable in the coastal ocean. This results in a globally significant river plume with a strong terrigenous signature and in substantial export of terrestrially derived organic carbon from the continental margin, where it can be entrained in the large‐scale circulation and potentially contribute to the long‐term storage of terrigenous production and to the recalcitrant carbon pool found in the deep ocean.

Here we present direct measurements of the biological breakdown of ¹³C‐labeled substrates to CO₂ at seven locations along the lower Amazon River, from Óbidos to the mouth. Dark incubation experiments were performed at high and low water periods using vanillin, a lignin phenol derived from vascular plants, and at the high water period using four different ¹³C‐labeled plant litter leachates. Leachates derived from oak wood were degraded most slowly with vanillin monomers, macrophyte leaves, macrophyte stems, and whole grass leachates being converted to CO₂ 1.2, 1.3, 1.7, and 2.3 times faster, respectively, at the upstream boundary, Óbidos. Relative to Óbidos, the sum degradation rate of all four leachates was 3.3 and 2.6 times faster in the algae‐rich Tapajós and Xingu Rivers, respectively. Likewise, the leachates were broken down 3.2 times more quickly at Óbidos when algal biomass from the Tapajós River was simultaneously added. Leachate reactivity similarly increased from Óbidos to the mouth with leachates breaking down 1.7 times more quickly at Almeirim (midway to the mouth) and 2.8 times more quickly across the river mouth. There was no discernible correlation between in situ nutrient levels and remineralization rates, suggesting that priming effects were an important factor controlling reactivity along the continuum. Further, continuous measurements of CO₂, O₂, and conductivity along the confluence of the Tapajós and Amazon Rivers and the Xingu and Jarauçu Rivers revealed in situ evidence for enhanced O₂ drawdown and CO₂ production along the mixing zone of these confluences.