G. W. Kling’s research while affiliated with University of Michigan and other places

What is this page?


This page lists works of an author who doesn't have a ResearchGate profile or hasn't added the works to their profile yet. It is automatically generated from public (personal) data to further our legitimate goal of comprehensive and accurate scientific recordkeeping. If you are this author and want this page removed, please let us know.

Publications (2)


CO2 produced versus O2 consumed by microbial respiration of DOC kept in the dark (gray), exposed to ultraviolet light (UV; 305 nm, teal), and exposed to visible light (405 nm, orange) for: Imnavait wet sedge tundra (circle symbols), Toolik tussock tundra A (square symbols), Toolik tussock tundra B (diamond symbols), and LTER 395 thermokarst (triangle symbols). Panel (a) shows all of the data, and the region outlined in red is enlarged in panel (b). Data are plotted with the 1:1 line (dashed). Values for CO2 production and O2 consumption are shown as the average ±1 SE of experimental replicates (n = 3). When no error bars are visible, they are smaller than the data point symbols.
(a) Δ¹⁴C composition and (b) δ¹³C composition of CO2 produced from microbial respiration of DOC kept in the dark (circle symbols), exposed to ultraviolet light (UV; 305 nm, diamond symbols), and exposed to visible light (405 nm, square symbols) versus the composition of the initial DOC of dark or light‐exposed permafrost DOC for: Imnavait wet sedge tundra (orange symbols), Toolik tussock tundra A (dark blue symbols), Toolik tussock tundra B (yellow symbols), and LTER 395 thermokarst (teal symbols). Data are plotted with the 1:1 line (dashed). Values for Δ¹⁴C‐CO2 and δ¹³C‐CO2 are shown as the average ±1 SE of experimental replicates (n = 2).
δ¹³C‐CO2 produced from microbial respiration of DOC kept in the dark (circle symbols), exposed to ultraviolet light (UV; 305 nm, diamond symbols), and exposed to visible light (405 nm, square symbols) increased with (a) increasing respiratory quotient and (b) decreasing age of the CO2 from: Imnavait wet sedge tundra (orange symbols), Toolik tussock tundra A (dark blue symbols), Toolik tussock tundra B (yellow symbols), and LTER 395 thermokarst (teal symbols). In panel (a), data were fit using a least‐squares regression where R² = 0.94 and p < 0.01. All values on the x‐axis are shown as the average ±1 SE (n = 3). All values on the y‐axis are shown as the average ±1 SE (n = 2). In panel (b), data were fit using a least‐squares regression where R² = 0.57 and p < 0.05. All values on the x‐ and y‐axes are shown as the average ±1 SE (n = 2).
The difference between CO2 production from microbial respiration in light and dark DOC treatments versus the percentage of DOC that was oxidized by light prior to biological incubations for DOC exposed to ultraviolet light (UV; 305 nm, diamond symbols) and visible light (405 nm, square symbols). Values for the difference between CO2 production from respiration in light and dark DOC treatments are shown as the average ±1 SE of experimental replicates (n = 3).
Controls on the Respiration of Ancient Carbon Draining From Permafrost Soils Into Sunlit Arctic Surface Waters
  • Article
  • Full-text available

May 2024

·

100 Reads

·

1 Citation

E. C. Rieb

·

C. A. Polik

·

·

[...]

·

The thawing of ancient organic carbon stored in arctic permafrost soils, and its oxidation to carbon dioxide (CO2, a greenhouse gas), is predicted to amplify global warming. However, the extent to which organic carbon in thawing permafrost soils will be released as CO2 is uncertain. A critical unknown is the extent to which dissolved organic carbon (DOC) from thawing permafrost soils is respired to CO2 by microbes upon export of freshly thawed DOC to both dark bottom waters and sunlit surface waters. In this study, we quantified the radiocarbon age and ¹³C composition of CO2 produced by microbial respiration of DOC that was leached from permafrost soils and either kept in the dark or exposed to ultraviolet and visible wavelengths of light. We show that permafrost DOC most labile to microbial respiration was as old or older (ages 4,000–11,000 a BP) and more ¹³C‐depleted than the bulk DOC in both dark and light‐exposed treatments, likely indicating respiration of old, ¹³C‐depleted lignin and lipid fractions of the permafrost DOC pool. Light exposure either increased, decreased, or had no effect on the magnitude of microbial respiration of old permafrost DOC relative to respiration in the dark, depending on both the extent of DOC oxidation during exposure to light and the wavelength of light. Together, these findings suggest that photochemical changes affecting the lability of permafrost DOC during sunlight exposure are an important control on the magnitude of microbial respiration of permafrost DOC in arctic surface waters.

Download

Controls on the lability of permafrost DOC to photomineralization. (a) Wavelength‐dependent apparent quantum yield spectrum for photomineralization (φPM,λ) of permafrost DOC. Each data series was fit with a least‐squares exponential model where R² > 0.83, p < 0.05. (b) Apparent quantum yield for photomineralization at 309 nm (φPM,309) versus total dissolved iron concentration in permafrost leachates prior to light exposure. Closed symbols indicate φPM,309 measured following LED exposure at 309 nm. Open symbols indicate φPM,309 estimated from an exponential fit following exposure to broadband light (see section 2). Data in panel (b) were fit using a least‐squares regression where R² = 0.87, t statistic = 7.8, p < 0.001, excluding the open red symbol (see the Supporting Information). Open symbols for Imnavait moist acidic tundra were previously reported (Ward & Cory, 2016). All values are the average ± 1 SE of experimental replicates (n = 2 and 4 for open and closed symbols, respectively; see section 2). φPM,λ at other wavelengths versus dissolved iron are reported in the Supporting Information.
Δ¹⁴C of bulk permafrost DOC was a strong predictor of the Δ¹⁴C‐CO2 produced from photomineralization of DOC. Δ¹⁴C‐CO2 produced from exposure of permafrost DOC to UV (309 nm, diamond symbols) and visible (406 nm, square symbols) light versus Δ¹⁴C of initial, bulk permafrost DOC plotted with the 1:1 line. When all data are fit using a least‐squares regression, R² = 0.66, t statistic = 3.4, p < 0.05. Values for photochemically produced Δ¹⁴C‐CO2 are shown as the average ± 1 SE of experimental replicates (n = 2).
Photomineralization rates were higher for permafrost DOC than for surface water DOC due to higher lability in the visible light region. (a) Wavelength‐dependent water column rates of photomineralization for Imnavait moist acidic tundra permafrost DOC and Imnavait Creek DOC (turquoise vs. black line, respectively). Solid lines show the average photomineralization rate spectrum and the similar color shading shows the upper and lower 95% confidence intervals. Rates of photomineralization were calculated using the different wavelength‐dependent apparent quantum yields for photomineralization (φPM,λ) for Imnavait moist acidic tundra permafrost DOC or Imnavait Creek DOC (Figure S5; see the Supporting Information). The red dashed and solid lines mark the wavelength of peak photomineralization rates (330 nm vs. 402 nm) for Imnavait Creek and Imnavait moist acidic tundra permafrost DOC, respectively. (b) Calculated photomineralization rates increased with an increasing fraction of permafrost DOC in the surface water DOC pool. Percent increase in photomineralization rates as permafrost DOC comprises 0–100% of the DOC pool in Imnavait Creek, Kuparuk River, and Toolik Lake (compared to no permafrost DOC in the DOC pool). Only the φPM,λ was varied in the water column rate calculations, using a “mixed” φPM,λ calculated as a mixture of the φPM,λ for permafrost DOC with the φPM,λ for the surface water DOC (see the Supporting Information). All values are shown as the average ± 1 SE of calculated rates for surface water DOC mixed with each of the five permafrost DOCs in this study (n = 5).
Arctic Amplification of Global Warming Strengthened by Sunlight Oxidation of Permafrost Carbon to CO 2

June 2020

·

157 Reads

·

51 Citations

Once thawed, up to 15% of the ∼1,000 Pg of organic carbon (C) in arctic permafrost soils may be oxidized to carbon dioxide (CO2) by 2100, amplifying climate change. However, predictions of this amplification strength ignore the oxidation of permafrost C to CO2 in surface waters (photomineralization). We characterized the wavelength dependence of permafrost dissolved organic carbon (DOC) photomineralization and demonstrate that iron catalyzes photomineralization of old DOC (4,000‐6,300 a BP) derived from soil lignin and tannin. Rates of CO2 production from photomineralization of permafrost DOC are two‐fold higher than for modern DOC. Given that model predictions of future net loss of ecosystem C from thawing permafrost do not include the loss of CO2 to the atmosphere from DOC photomineralization, current predictions of an average of 208 Pg C loss by 2299 may be too low by ~14%.

Citations (2)


... Taken together these findings suggest that higher background DOC concentrations (in 2022) caused light limitation of autotrophs (similar to dark treatments in Rober et al. 2023), allowing heterotrophs to use available nutrients. The extent to which autotrophic biofilms are able to buffer peatlands against net heterotrophy more broadly may depend on the composition of resources delivered to surface waters with variable hydrology and warming soil conditions (Kendrick et al. 2018;Wickland et al. 2018;Weaver and Jones 2022;Rieb et al. 2024) as well as the changing physical aspects of northern peatlands (Euskirchen et al. 2024), all of which influence concentrations of dissolved organic matter (Kane et al. 2010;Cory and Kling 2018). We might expect greater light attenuation associated with increasing levels of dissolved organic matter to overwhelm the stimulatory effect of nutrients on autotrophic microbes by constraining photosynthesis, favoring heterotrophy and increasing CO 2 emissions. ...

Reference:

Legacy Effects of Plant Community Structure Are Manifested in Microbial Biofilm Development With Consequences for Ecosystem CO 2 Emissions
Controls on the Respiration of Ancient Carbon Draining From Permafrost Soils Into Sunlit Arctic Surface Waters

... Recent global warming has rapidly accelerated temperature increases in the Arctic region [1][2][3][4][5][6][7], leading to the thickening of the active layer and degradation of permafrost [8,9]. This degradation results in the release of previously frozen materials into the atmosphere [6,10,11], hydrosphere [12,13] and biosphere [14][15][16], thereby altering global biogeochemical [17,18] cycles and triggering various climate and environmental impacts [19]. ...

Arctic Amplification of Global Warming Strengthened by Sunlight Oxidation of Permafrost Carbon to CO 2