Abiotic processes control carbon dioxide dynamics in temperate karst lakes

Author:

Vargas-Sánchez Mariana1,Alcocer Javier2,Puche Eric34,Sánchez-Carrillo Salvador3

Affiliation:

1. Graduate Program in Marine Sciences and Limnology, Universidad Nacional Autónoma de México (UNAM), Mexico City, Mexico

2. Tropical Limnology Group, FES-Iztacala, Universidad Nacional Autónoma de México (UNAM), Mexico City, Mexico

3. Biogeochemistry and Microbial Ecology Dep., Museo Nacional de Ciencias Naturales (MNCN-CSIC), Madrid, Spain

4. Cavanilles Insitute of Biodiversity and Evolutionary Biology, Universidad de Valencia, Paterna, Valencia, Spain

Abstract

Inland waters are crucial in the carbon cycle, contributing significantly to the global CO2 fluxes. Carbonate lakes may act as both sources and sinks of CO2 depending on the interactions between the amount of dissolved inorganic carbon (DIC) inputs, lake metabolisms, and geochemical processes. It is often difficult to distinguish the dominant mechanisms driving CO2 dynamics and their effects on CO2 emissions. This study was undertaken in three groundwater-fed carbonate-rich lakes in central Spain (Ruidera Lakes), severely polluted with nitrates from agricultural overfertilization. Diel and seasonal (summer and winter) changes in CO2 concentration (CCO2) DIC, and CO2 emissions-(FCO2)-, as well as physical and chemical variables, including primary production and phytoplanktonic chlorophyll-a were measured. In addition, δ13C-DIC, δ13C-CO2 in lake waters, and δ13C of the sedimentary organic matter were measured seasonally to identify the primary CO2 sources and processes. While the lakes were consistently CCO2 supersaturated and FCO2 was released to the atmosphere during both seasons, the highest CCO2 and DIC were in summer (0.36–2.26 µmol L–1). Our results support a strong phosphorus limitation for primary production in these lakes, which impinges on CO2 dynamics. External DIC inputs to the lake waters primarily drive the CCO2 and, therefore, the FCO2. The δ13C-DIC signatures below –12‰  confirmed the primary geogenic influence on DIC. As also suggested by the high values on the calcite saturation index, the Miller-Tans plot revealed that the CO2 source in the lakes was close to the signature provided by the fractionation of δ13C-CO2 from calcite precipitation. Therefore, the main contribution behind the CCO2 values found in these karst lakes should be attributed to the calcite precipitation process, which is temperature-dependent according to the seasonal change observed in δ13C-DIC values. Finally, co-precipitation of phosphate with calcite could partly explain the observed low phytoplankton production in these lakes and the impact on the contribution to increasing greenhouse gas emissions. However, as eutrophication increases and the soluble reactive phosphorus (SRP) content increases, the co-precipitation of phosphate is expected to be progressively inhibited. These thresholds must be assessed to understand how the CO32− ions drive lake co-precipitation dynamics. Carbonate regions extend over 15% of the Earth’s surface but seem essential in the CO2 dynamics at a global scale.

Funder

Spanish Ministry of Science and Innovation

Programa de Posgrado en Ciencias del Mar y Limnología

CONAHCYT provide a doctoral scholarship to MVS

CSIC

Publisher

PeerJ

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