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Research about Loch Vale

Source-linked reports with geographic coverage including Loch Vale.

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Spatiotemporal dynamics of CO2 gas exchange from headwater mountain streams

Mountain streams play an important role in the global carbon cycle by transporting, metabolizing, and exchanging carbon they receive from the terrestrial environment. The rates at which these processes occur remain highly uncertain because of a paucity of observations and the difficulty of measuring gas exchange rates in steep, turbulent mountain streams. This uncertainty is compounded by large temporal and spatial variability in stream carbon dioxide (CO 2 ) concentrations in mountain environments. In this study, we measured diel, seasonal, and annual variations in CO 2 partial pressure ( p CO 2 ) in seven headwater streams and a groundwater spring in the Colorado Rocky Mountains to determine how CO 2 exchange fluxes ( ) vary with time, annual precipitation, and landscape characteristics. Our results show that temporal variability in p CO 2 and in mountain streams is large and is strongly influenced by solar radiation, the accumulation and melting of seasonal snowpacks, and interannual variations in precipitation. Spatial variations in p CO 2 and were related to landscape characteristics, with soil organic matter, wetlands, and likely groundwater discharge zones having a positive influence. Periglacial features, such as ice and rock glaciers, had a negative influence on stream p CO 2 and . Estimated from streams in an alpine/subalpine region of Colorado was 3.4 kg C m −2 yr −1 normalized to stream surface area (95% CI: 2.1–5.0 kg C m −2 yr −1 ), consistent with recent work on CO 2 exchange from mountain streams in the Swiss Alps. Our results highlight the importance of mountain streams as substantial contributors in the global carbon cycle.

Colorado

Mechanisms for chemostatic behavior in catchments: implications for CO 2 consumption by mineral weathering

Concentrations of weathering products in streams often show relatively little variation compared to changes in discharge, both at event and annual scales. In this study, several hypothesized mechanisms for this “chemostatic behavior” were evaluated, and the potential for those mechanisms to influence relations between climate, weathering fluxes, and CO 2 consumption via mineral weathering was assessed. Data from Loch Vale, an alpine catchment in the Colorado Rocky Mountains, indicates that cation exchange and seasonal precipitation and dissolution of amorphous or poorly crystalline aluminosilicates are important processes that help regulate solute concentrations in the stream; however, those processes have no direct effect on CO 2 consumption in catchments. Hydrograph separation analyses indicate that old water stored in the subsurface over the winter accounts for about one-quarter of annual streamflow, and almost one-half of annual fluxes of Na and SiO 2 in the stream; thus, flushing of old water by new water (snowmelt) is an important component of chemostatic behavior. Hydrologic flushing of subsurface materials further induces chemostatic behavior by reducing mineral saturation indices and increasing reactive mineral surface area, which stimulate mineral weathering rates. CO 2 consumption by carbonic acid mediated mineral weathering was quantified using mass-balance calculations; results indicated that silicate mineral weathering was responsible for approximately two-thirds of annual CO 2 consumption, and carbonate weathering was responsible for the remaining one-third. CO 2 consumption was strongly dependent on annual precipitation and temperature; these relations were captured in a simple statistical model that accounted for 71% of the annual variation in CO 2 consumption via mineral weathering in Loch Vale.

Colorado

Timescales for migration of atmospherically derived sulphate through an alpine/subalpine watershed, Loch Vale, Colorado

Sulphur 35, a cosmogenically produced radioisotope with a short half‐life (87 days), was measured in snowpack during 1993–1997 and at four locations within the Loch Vale watershed during 1995–1997. The four sites include the two main drainages in the watershed, Andrews Creek and Icy Brook, a small south facing catchment flowing into Andrews Creek (Andrews Spring 1), and a similar north facing catchment flowing out of a scree field into Icy Brook (Spring 19). Concentrations ranged from a high of almost 50 mBq/L for a sample from Spring 19 in June 1996 to a concentration near the detection limit for a sample from Andrews Creek in April 1997. Sulphur 35 concentrations were normalized to sulphate (as mBq/mg SO 4 −2 ) and were decay‐corrected to a Julian day of 90 (April 1) for each year. Snowpack had the highest 35 S concentration with an average concentration of 53 mBq/mg SO 4 −2 . Concentrations in the streams were much lower, even when corrected for decay relative to JD 90. The large 35 S concentrations found in Spring 19 were the result of increases in concentration due to sublimation and/or evapotranspiration and were lower than snowpack when normalized to sulphate. Using 35 S concentrations found in snowpack as of JD 90 as a beginning concentration, the fraction of sulphate in streamflow that was derived from atmospheric deposition within the prior water year was estimated. For Icy Brook and Andrews Creek the fraction of the sulphate in streamflow derived from that year's snowpack and precipitation was low prior to the beginning of the main spring melt, reached a maximum during the period of maximum flow, and decreased as the summer progressed. A calculation of the seasonal flux indicated that about 40% of the sulphate that flowed out of the watershed was derived from atmospheric sulphate deposited during the previous year. This suggests that more than half of the sulphate deposited in the watershed by atmospheric processes during the previous year was removed during the following summer. Thus sulphate retention in alpine watersheds like Loch Vale is very limited, and changes in sulphate deposition should be quickly reflected in stream chemistry.

Colorado