Riverine dissolved organic carbon in Rukarara River Watershed, Rwanda
Graphical abstract
Introduction
The role of inland waters in the global carbon cycle is now widely recognized at the catchment, regional and global scales (Cole et al., 2007; Battin et al., 2009). Streams receive carbon from in-stream and terrestrial production that is processed or exported downstream (Mattsson et al., 2009; Williams et al., 2010; Alvarez-Cobelas et al., 2012). Another source of carbon in rivers is sediment and rock weathering processes in carbonates and gypsum-rich deposits (Salimon et al., 2013). Carbon enters streams mainly through surface runoff and by groundwater as particulate organic carbon (POC), dissolved organic carbon (DOC), and dissolved inorganic carbon (DIC) (Johnson et al., 2006; Aufdenkampe et al., 2011).
This study focuses on DOC since it is the major organic pool in most aquatic ecosystems (Wetzel, 2001). Stream-water DOC is of particular interest because it serves as an important resource for downstream ecosystems (Amon and Meon, 2004; Post et al., 2009; Pagano et al., 2014) and is beneficial for aquatic biota (Sucker and Krause, 2010). Organic carbon in streams serves as an important modulator because it modifies the influences and consequences of other chemicals and processes (Prairie, 2008). However, changes in DOC levels in water are also of environmental concern: high DOC concentration can affect surface water quality, water metabolism, balance between autotrophy and heterotrophy, nutrient uptake and bioavailability of toxic compounds, and the growth of microorganisms (Munson and Gherini, 1993; Delpla et al., 2009; Fernández-Pérez et al., 2005; Erlandsson et al., 2011; Stanley et al., 2012).
DOC concentration in natural waters has changed over the past few decades; for example, in some areas in North America and northern Europe, it may have doubled (Evans et al., 2005; Monteith et al., 2014; SanClements et al., 2012; Pagano et al., 2014). In a few other areas, a decrease or no increase of DOC in waters was reported (Pagano et al., 2014). Regarding the increase of DOC in natural waters, its drivers in some areas are up for debate. Possible factors include changes in air temperature (Freeman et al., 2001), increased precipitation (Worrall and Burt, 2008; Sucker and Krause, 2010), land use changes (Findlay et al., 2001; Sucker and Krause, 2010), increased atmospheric carbon dioxide (Harrison et al., 2008; Sucker and Krause, 2010; Kane et al., 2014) and decreased atmospheric sulfur deposition (Fowler et al., 2005; Sucker and Krause, 2010; Rowe et al., 2014) and atmospheric nitrogen deposition (Singh et al., 2016). Pagano et al. (2014) mention the combined effect of increased atmospheric CO2 concentration and temperature. This increased atmospheric CO2 stimulates plant primary production (Freeman et al., 2004) whereas global warming may influence DOC export by altering decomposition and mineralization of organic matter (Worrall et al., 2003), water budget and discharge, which then increases DOC concentrations (Hongve et al., 2004). Consequently, an increase of DOC in freshwaters may be linked with climate change, it is therefore important to monitor temporal variations of DOC concentration in natural waters to anticipate climate impacts on carbon dynamics and water resources.
Most studies of DOC changes in waters have been performed in temperate ecosystems in North America and Europe. Thus, there is a need to monitor DOC changes in waters in other geographical areas, such as tropical regions, where precipitation and temperature are projected to continue to increase (Paeth et al., 2009). For example, in Rwanda, temperatures have increased 1.4 °C from 1970 to 2008, and this increase is projected to reach 1.5 °C to 3 °C by the 2050s (Hove et al., 2010). Average annual rainfall increased about 10% during the same time interval (Warnest et al., 2012). It follows that changes in climate will alter water budgets in tropical watersheds, with implications for DOC in natural waters. It is important to monitor how hydrological variability can affect DOC in natural waters in tropical watersheds in order to better understand this issue and its implications for the global carbon budget.
Studies suggest that tropical rivers exhibit the highest riverine DOC flux to oceans (Gu et al., 2009; Bouillon et al., 2014), but their inclusion in carbon budgets stems from datasets that are missing well-defined values in the tropics since most studies of riverine DOC have been performed in temperate and arctic rivers (Stedmon et al., 2011; Spencer et al., 2012; Lambert et al., 2015). Recent research (e.g. Palviainen et al., 2016; Ren et al., 2016; Singh et al., 2016) has shown that land cover is a useful predictor of riverine DOC in temperate biomes, but the situation may be different in tropical regions.
The objective of this study is to determine the relationship between stream water DOC loading, hydrological factors, topography and land cover in a tropical watershed for a better understanding of the impact of stream DOC export on watershed carbon budget. This study specifically characterizes the spatial and temporal variation of stream DOC and describes the relationship between stream DOC, water level, water discharge and land cover. It estimates the DOC loading in the Rukarara River and some of its tributaries, and the loss of DOC through fluvial export compared to the net primary productivity of the watershed. We hypothesize that the variability in hydrology and land cover will alter runoff, discharge characteristics and carbon dynamics in tropical watersheds, and this will be expressed in variable export of soil DOC into streams.
Section snippets
Study area
The study was carried out in the Rukarara River Watershed (RRW), a catchment that drains an area of 493.5 km2 (Fig. 1a) in southwestern Rwanda. The catchment landscape is composed of mountainous terrain with elevations from 1541 to 2924 m., and slopes from 0° to 68°. Annual precipitation ranges from 1300 to 1450 mm, and the temperature from 15 °C to 25 °C. The soils are acid (3.6 < pH < 5.0) and mainly of the Ultisol, Entisol, and Inceptisol types. Across the watershed, 13 main streams drain
Stream DOC variation between sites
The results indicate higher concentration of DOC in the natural forest stream compared to the tea plantation and farm streams. The measured DOC means (mg C/L) were 4.98 ± 2.15, 4.06 ± 2.06 and 3.66 ± 1.62 in natural forest, tea, and farm streams, respectively. The DOC concentration at the outlet of the Rukarara River was 5.73 ± 3.75 mg C/L, higher than at all sampled headwater streams (Fig. 3). A two-tailed t-test showed a statistically significant difference between streams in the natural
Between site and temporal variation of stream DOC
Higher stream DOC was found at the natural forest site. This result is explained by the higher DOC in the soil of the natural forest, its high flow path index (Table 2), high TWI values (Table 5) and ridge-like topography in a 500 m buffer zone around the time of concentration sampling point. The large proportion of ridge topography around the sampling site suggests high overland and leakage flow into the stream. The high soil DOC is due to important accumulation of plant biomass in the natural
Conclusions
In this paper, we have investigated on dynamics of stream DOC in the Rukarara River Watershed in Rwanda. The analysis of between site variations of the stream DOC revealed that stream DOC concentration differs significantly between natural forest, tea plantation and farm sites. The stream DOC is positively influenced by land use and land cover, and consequently any change in the land could potentially impact stream DOC. Compared to other watersheds, the RRW showed DOC concentration, flux and
Acknowledgements
The authors would like to thank the University of Rwanda and the Sida Partnership Program for the financial support of this work. The MOD17A3 data product was retrieved from the NASA Land Processes Distributed Active Archive Center (LP DAAC), USGS/Earth Resources Observation and Science (EROS) Center, Oak Ridge, Tennessee, USA, https://daac.ornl.gov/modiswebservice.
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