Jeffrey E. Richey

Outgassing from Amazonian rivers and wetlands as a large tropical source of atmospheric CO2

Terrestrial ecosystems in the humid tropics play a potentially important but presently ambiguous role in the global carbon cycle. Whereas global estimates of atmospheric CO2 exchange indicate that the tropics are near equilibrium or are a source with respect to carbon, ground-based estimates indicate that the amount of carbon that is being absorbed by mature rainforests is similar to or greater than that being released by tropical deforestation (about 1.6 Gt C yr-1). Estimates of the magnitude of carbon sequestration are uncertain, however, depending on whether they are derived from measurements of gas fluxes above forests or of biomass accumulation in vegetation and soils. It is also possible that methodological errors may overestimate rates of carbon uptake or that other loss processes have yet to be identified. Here we demonstrate that outgassing (evasion) of CO2 from rivers and wetlands of the central Amazon basin constitutes an important carbon loss process, equal to 1.2 ± 0.3 Mg C ha-1 yr-1. This carbon probably originates from organic matter transported from upland and flooded forests, which is then respired and outgassed downstream. Extrapolated across the entire basin, this flux—at 0.5 Gt C yr-1—is an order of magnitude greater than fluvial export of organic carbon to the ocean. From these findings, we suggest that the overall carbon budget of rainforests, summed across terrestrial and aquatic environments, appears closer to being in balance than would be inferred from studies of uplands alone.

Young organic matter as a source of carbon dioxide outgassing from Amazonian rivers

Rivers are generally supersaturated with respect to carbon dioxide, resulting in large gas evasion fluxes that can be a significant component of regional net carbon budgets. Amazonian rivers were recently shown to outgas more than ten times the amount of carbon exported to the ocean in the form of total organic carbon or dissolved inorganic carbon. High carbon dioxide concentrations in rivers originate largely from in situ respiration of organic carbon, but little agreement exists about the sources or turnover times of this carbon. Here we present results of an extensive survey of the carbon isotope composition (13C and 14C) of dissolved inorganic carbon and three size-fractions of organic carbon across the Amazonian river system. We find that respiration of contemporary organic matter (less than five years old) originating on land and near rivers is the dominant source of excess carbon dioxide that drives outgassing in medium to large rivers, although we find that bulk organic carbon fractions transported by these rivers range from tens to thousands of years in age. We therefore suggest that a small, rapidly cycling pool of organic carbon is responsible for the large carbon fluxes from land to water to atmosphere in the humid tropics.

Storage and Remobilization of Suspended Sediment in the Lower Amazon River of Brazil

In the lower Amazon River, suspended sediment is stored during rising stages of the river and resuspended during falling river stages. The storage and resuspension in the reach are related to the mean slope of the flood wave on the river surface; this slope is smaller during rising river stages than during falling stages. The pattern of storage and resuspension damps out the extreme values of high and low sediment discharge and tends to keep them near the mean value between 3.0 x 106 and 3.5 x 106 metric tons per day. Mean annual discharge of suspended sediment in the lower Amazon is between 1.1 x 109 and 1.3 x 109 metric tons per year.

Exchanges of sediment between the flood plain and channel of the Amazon River in Brazil

Sediment transport through the Brazilian sector of the Amazon River valley, a distance of 2010 km, involves exchanges between the channel and the flood plain that in each direction exceed the annual flux of sediment out of the river at Obidos (∼1200 Mt yr −1 ). The exchanges occur through bank erosion, bar deposition, settling from diffuse overbank flow, and sedimentation in flood-plain channels. We estimated the magnitude of these exchanges for each of 10 reaches of the valley, and combined them with calculations of sediment transport into and out of the reaches based on sediment sampling and flow records to define a sediment budget for each reach. Residuals in the sediment budget of a reach include errors of estimation and erosion or deposition within the channel. The annual supply of sediment entering the channel from bank erosion was estimated to average 1570 Mt yr −1 (1.3 × the Obidos flux) and the amount transferred from channel transport to the bars (380 Mt yr −1 ) and the flood plain (460 Mt yr −1 in channelized flow; 1230 Mt yr −1 in diffuse overbank flow) totaled 2070 Mt yr −1 (1.7 × the Obidos flux). Thus, deposition on the bars and flood plain exceeded bank erosion by 500 Mt yr −1 over a 10–16 yr period. Sampling and calculation of sediment loads in the channel indicate a net accumulation in the valley floor of approximately 200 Mt yr −1 over 16 yr, crudely validating the process-based calculations of the sediment budget, which in turn illuminate the physical controls on each exchange process. Another 300–400 Mt yr −1 are deposited in a delta plain downstream of Obidos. The components of the sediment budget reflect hydrologic characteristics of the valley floor and geomorphic characteristics of the channel and flood plain, which in turn are influenced by tectonic features of the Amazon structural trough.

Loss of organic matter from riverine particles in deltas

Abstract In order to examine the transport and burial of terrigenous organic matter along the coastal zones of large river systems, we assessed organic matter dynamics in coupled river/delta systems using mineral surface area as a conservative tracer for discharged riverine particulate organic matter (POM). Most POM in the rivers studied (n = 6) is tightly associated with suspended mineral material; e.g., it is sorbed to mineral surfaces. Average organic loadings in the Amazon River (0.67 ± 0.14 mg C m−2), the river for which we have the largest dataset, are approximately twice that of sedimentary minerals from the Amazon Delta (∼0.35 mg C m−2). Stable carbon isotope analysis indicate that approximately two-thirds of the total carbon on the deltaic particles is terrestrial. The combined surface-normalized, isotope-distinguished estimate is that >70% of the Amazon fluvial POM is not buried in the delta, consistent with other independent evidence (Aller et al., 1996). Losses of terrestrial POM have also been quantified for the river/delta systems of Columbia in the USA, Fly in New Guinea, and Huange-He in China. If the losses of riverine POM observed in these river/delta systems are representative of rivers worldwide, then the surface-constrained analyses point toward a global loss of fluvial POM in delta regions of ∼0.1 x 1015 g C y−1.

Amazon River Discharge and Climate Variability: 1903 to 1985

Reconstruction of an 83-year record (1903 to 1985) of the discharge of the Amazon River shows that there has been no statistically significant change in discharge over the period of record and that the predominant interannual variability occurs on the 2- to 3-year time scale. Oscillations of river discharge predate significant human influences in the Amazon basin and reflect both extrabasinal and local factors. Cross-spectrum analyses of Amazon flow anomalies with indicators of the El Ni�o-Southern Oscillation phenomenon suggest that the oscillations in the hydrograph are coupled to the tropical Pacific climate cycle.

Nitrogen yields from undisturbed watersheds in the Americas

Yields of total fixed nitrogen and nitrogen fractions are summarized for thirty-one watersheds in which anthropogenic disturbance of the nitrogen cycle, either through land use or atmospheric deposition, is negligible or slight. These yields are taken as representative of background conditions over a broad range of watershed areas, elevations, and vegetation types. The data set focuses on watersheds of the American tropics, but also includes information on the Gambia River (Africa) and some small watersheds in the Sierra Nevada of California. For the tropical watersheds, total nitrogen yield averages 5.1 kg ha -1 y-1. On average, 30% of the total is particulate and 70% is dissolved. Of the dissolved fraction, an average of 50% is organic and 50% is inorganic, of which 20% is ammonium and 80% is nitrate. Yields are substantially lower than previously estimated for background conditions. Yields of all nitrogen fractions are strongly related to runoff, which also explains a large percentage of variance in yield of total nitrogen (r2 = 0.85). For total nitrogen and nitrogen fractions, yield increases at about two-thirds the rate of runoff; concentration decreases as runoff increases. There is a secondary but significant positive relationship between elevation and yield of DIN. Ratios DONAIDN and PN/TN both are related to watershed area rather than runoff; DON/TDN decreases and PN/TN increases toward higher stream orders. The analysis suggests for tropical watersheds the existence of mechanisms promoting strong homeostasis in the yield of N and its fractions for a given moisture regime, as well as predictable downstream change in proportionate representation N fractions. Yields and concentrations for small tropical watersheds are much larger than for the few temperate ones with which comparisons are possible.

Organic Carbon-14 in the Amazon River System

Coarse and fine suspended particulate organic materials and dissolved humic and fulvic acids transported by the Amazon River all contain bomb-produced carbon-14, indicating relatively rapid turnover of the parent carbon pools. However, the carbon-14 contents of these coexisting carbon forms are measurably different and may reflect varying degrees of retention by soils in the drainage basin.

Organic Carbon: Oxidation and Transport in the Amazon River

Spatial and temporal patterns in the organic carbon load (< 1 millimeter) ofthe Amazon River indicate that oxidation was constant throughout the river at any one time but was much greater at rising water than at high water, whereas transport was constant. The total effective efflux, as the sum ofoxidation plus transport in the river, was about 1014 grams of carbon per year. Estimates for other river systems suggest that global riverine carbon fluxes exceed 1015 grams per year. 1348 on Jauary 8, 2021 http://sce.sciencem agorg/ D ow nladed fom Manaus, Brazil, to Iquitos, Peru, in February to March 1977 (R.J.N. and J.T.B.) at the beginning of the rainy season when water levels were rising about 1 m per week. Transect 2 extended 3400 km, from Iquitos, Peru, to Belem, Brazil, in May to June 1977 (J.E.R., R.C.W., and R.F.S.) during peak flooding when the river inundates terrestrial habitats for several kilometers on each side of the normal channel in upstream reaches to 20 to 100 km in downstream reaches. Chemical measurements included particulate organic carbon < 1 mm (POC), dissolved organic carbon (DOC), the organic matter content of seston, and the respiratory oxidation activity (4). The amount of organic matter present in the fine suspended load averaged about 10 percent during both transects (Table 1) (5). The concentration of POC during the rising-water period was 15 to 20 g m-3 upriver and decreased to 8.2 g m-3 downriver at Manaus, whereas at high water the POC concentration reached an upriver maximum of 3.7 g m-3 and exhibited downstream values of 1 to 2 g m-3. During both rising and high water, the DOC concentration was relatively uniform throughout the river, averaging 4.2 and 6.5 g m-3, respectively. The POC and DOC values appear comparable to those of other investigators at single stations with regard to both wetand dry-season values (6). Respiration Tributaries Tributaries

Dissolved organic matter and terrestrial-lotic linkages in the central Amazon basin of Brazil

We evaluate the hypothesis that decomposition and adsorption reactions operating in upland soils of headwater catchments control the concentration and composition of dissolved and fine particulate organic matter in rivers of the Amazon basin. In two contrasting first-order catchments characteristic of the central Amazon basin, we analyzed plant, litter, soil, groundwater, and stream water chemistry. Our results indicate that clear and persistent differences exist in the concentration and elemental composition of dissolved organic matter (DOM) in stream waters and groundwaters from the two catchments, due mainly to corresponding differences in soil texture and chemistry. Within the more oxide and clay rich Oxisols underlying terra firme forest, groundwater DOM concentrations were uniformly low (120 μMC) and C/N ratios averaged 10. Conversely, within the oxide and clay deficient Spodosols underlying campinarana forest, groundwater DOM concentrations were greatly elevated (3000 μMC), and C/N ratios averaged near 60. We found that, in the terra firme/Oxisol terrain, the majority of DOM contributions to the stream derived from the riparian zone, while in the campinarana/Spodosol terrain, upland groundwater contributions could account for the concentration and composition of DOM in the stream. The implications of our findings are that in the terra firme terrains which dominate the region, upland soil profiles are not the site of definitive processes which impart compositional signatures to organic matter carried by the largest rivers of the Amazon basin, as was hypothesized. Instead, we suggest that definitive reactions are focused primarily in the river corridor.