J. D. Barker

Abundance and Dynamics of Dissolved Organic Carbon in Glacier Systems

Abstract The biogeochemical cycling of organic carbon (OC) has important implications for aquatic system ecology because the abundance and molecular characteristics of OC influence contaminant transport and bioavailability, and determine its suitability as a substrate for microbial metabolism. There have been few studies of OC cycling in glacier systems and questions remain regarding the abundance, provenance, and biogeochemical transformations of OC in these environments. To address these questions, the abundance and fluorescence characteristics of dissolved organic carbon (DOC) were investigated at John Evans Glacier and Outre Glacier, Canada, and Victoria Upper Glacier, Antarctica. These systems are characterized by different thermal and hydrological regimes, and have different potential DOC sources. Where possible, samples of supraglacial runoff, glacier ice and basal ice, and subglacial meltwater were collected. The DOC concentration in each sample was measured (high-temperature combustion and non-dispersive IR detection), and emission and/or synchronous fluorescence spectroscopy were used to characterize the DOC from each environment. DOC exists in detectable quantities (0.06–46.6 ppm) in all of these glacier systems. The fluorescence characteristics of DOC vary between glaciers, between environments at the same glacier, and over time within a single environment. These results suggest that quality of available OC and glacier hydrological flow routing influence the characteristics of DOC, and that microbial cycling of OC may be active in glacier systems.

Characterization of dissolved organic matter (DOM) from glacial environments using total fluorescence spectroscopy and parallel factor analysis.

Abstract Aquatic dissolved organic matter (DOM) is a major reservoir of reduced organic carbon and has a significant influence on heterotrophic biological productivity and water quality in marine and freshwater environments. Although the forms and transformations of DOM in temperate aquatic and soil environments have been studied extensively, this is not the case for glacial environments. In this study, fluorescent excitation–emission matrices (EEMs), parallel factor analysis (PARAFAC) and cluster analysis were used to characterize the fluorescing components of DOM in ice and water samples from supraglacial, englacial, subglacial and proglacial environments of seven glaciers in the Canadian Arctic, Norway and Antarctica. At least five significant fluorescent DOM fractions were identified, which accounted for 98.2% of the variance in the dataset. These included four protein-like components and one humic-like component. The predominantly proteinaceous character of DOM from these glaciers is very different from the more humic character of DOM described previously from lacustrine, fluvial, estuarine and marine environments. DOM from the sampled glaciers is broadly similar in character despite their geographically distinct locations, different thermal regimes and inter- and intra-site differences in potential organic matter sources. Glacier ice samples had a relatively low ratio of humic-like :protein-like fluorescence while meltwater samples had a higher ratio.

Methylmercury cycling in High Arctic wetland ponds: sources and sinks.

The sources of methylmercury (MeHg; the toxic form of mercury that is biomagnified through foodwebs) to Arctic freshwater organisms have not been clearly identified. We used a mass balance approach to quantify MeHg production in two wetland ponds in the Lake Hazen region of northern Ellesmere Island, NU, in the Canadian High Arctic and to evaluate the importance of these systems as sources of MeHg to Arctic foodwebs. We show that internal production (1.8-40 ng MeHg m(-2) d(-1)) is a much larger source of MeHg than external inputs from direct atmospheric deposition (0.029-0.051 ng MeHg m(-2) d(-1)), as expected. Furthermore, MeHg cycling in these systems is dominated by Hg(II) methylation and MeHg photodemethylation (2.0-33 ng MeHg m(-2) d(-1)), which is a sink for a large proportion of the MeHg produced by Hg(II) methylation in these ponds. We also show that MeHg production in the two study ponds is comparable to what has previously been measured in numerous more southerly systems known to be important MeHg sources, such as temperate wetlands and lakes, demonstrating that wetland ponds in the High Arctic are important sources of MeHg to local aquatic foodwebs.

Variation in Peak Growing Season Net Ecosystem Production Across the Canadian Arctic

Tundra ecosystems store vast amounts of soil organic carbon, which may be sensitive to climatic change. Net ecosystem production, NEP, is the net exchange of carbon dioxide (CO(2)) between landscapes and the atmosphere, and represents the balance between CO(2) uptake by photosynthesis and release by decomposition and autotrophic respiration. Here we examine CO(2) exchange across seven sites in the Canadian low and high Arctic during the peak growing season (July) in summer 2008. All sites were net sinks for atmospheric CO(2) (NEP ranged from 5 to 67 g C m(-2)), with low Arctic sites being substantially larger CO(2) sinks. The spatial difference in NEP between low and high Arctic sites was determined more by CO(2) uptake via gross ecosystem production than by CO(2) release via ecosystem respiration. Maximum gross ecosystem production at the low Arctic sites (average 8.6 μmol m(-2) s(-1)) was about 4 times larger than for high Arctic sites (average 2.4 μmol m(-2) s(-1)). NEP decreased with increasing temperature at all low Arctic sites, driven largely by the ecosystem respiration response. No consistent temperature response was found for the high Arctic sites. The results of this study clearly indicate there are large differences in tundra CO(2) exchange between high and low Arctic environments and this difference should be a central consideration in studies of Arctic carbon balance and climate change.

Trickle or treat: the dynamics of nutrient export from polar glaciers

&NA; Cold‐based polar glacier watersheds contain well‐defined supraglacial, ice‐marginal, and proglacial elements that differ in their degree of hydrologic connectivity, sources of water (e.g., snow, ice, and/or sediment pore water), meltwater residence times, allochthonous and autochthonous nutrient, and sediment loads. We investigated 11 distinct hydrological units along the supraglacial, ice marginal, and proglacial flow paths that drain Joyce Glacier in the McMurdo Dry Valleys of Antarctica. We found that these units play unique and important roles as sources and/or sinks for dissolved inorganic nitrogen and dissolved inorganic phosphorus and for specific fractions of dissolved organic matter (DOM) as waters are routed from the glacier into nutrient‐poor downstream ecosystems. Changes in nutrient export from the glacial system as a whole were observed as the routing and residence times of meltwater changed throughout the melt season. The concentrations of major ions in the proglacial stream were inversely proportional to discharge, such that there was a relatively constant “trickle” of these solutes into downstream ecosystems. In contrast, NO3− concentrations generally increased with discharge, resulting in delivery of episodic pulses of dissolved inorganic nitrogen‐rich water (“treats”) into those same ecosystems during high discharge events. DOM concentrations or fluorescence did not correlate with discharge rate, but high variability in DOM concentrations or fluorescence suggests that DOM may be exported downstream as episodic treats, but with spatial and/or temporal patterns that remain poorly understood. The strong, nutrient‐specific responses to changes in hydrology suggest that polar glacier drainage systems may export meltwater with nutrient compositions that vary within and between melt seasons and watersheds. Because nutrient dynamics identified in this study differ between glacier watersheds with broadly similar hydrology, climate, and geology, we emphasize the need to develop conceptual models of nutrient export that thoroughly integrate the biogeochemical and hydrological processes that control the sources, fate, and export of nutrients from each system.