Highergas transfer velocities for CO2 than CH4 inlakes challenge previous results and commonly made assumptionsand highlight the importance of gas-specific transport in aquaticgreenhouse gas exchange. Large greenhousegas emissions occur via the release of carbondioxide (CO2) and methane (CH4) from the surfacelayer of lakes. Such emissions are modeled from the air-watergas concentration gradient and the gas transfer velocity (k). The links between k and the physicalproperties of the gas and water have led to the development of methodsto convert k between gases through Schmidt numbernormalization. However, recent observations have found that such normalizationof apparent k estimates from field measurements canyield different results for CH4 and CO2. Weestimated k for CO2 and CH4 from measurements of concentration gradients and fluxes in fourcontrasting lakes and found consistently higher (on an average 1.7times) normalized apparent k values for CO2 than CH4. From these results, we infer that several gas-specificfactors, including chemical and biological processes within the watersurface microlayer, can influence apparent k estimates.We highlight the importance of accurately measuring relevant air-watergas concentration gradients and considering gas-specific processeswhen estimating k.

Methane (CH4) emissions (FCH4) from northern freshwater lakes are not only significant but also highly variable in time and one driver variable suggested to be important is precipitation. Rain can have various, potentially large effects on FCH4 across multiple time frames, and verifying the impact of rain on lake FCH4 is key to understand both contemporary flux regulation, and to predict future FCH4 related to possible changes in frequency and intensity of rainfall from climate change. The main objective of this study was to assess the short-term impact of typically occurring rain events with different intensity on FCH4 from various lake types located in hemiboreal, boreal, and subarctic Sweden. In spite of high time resolution automated flux measurements across different depth zones and covering numerous commonly types of rain events in northern areas, in general, no strong impact on FCH4 during and within 24 h after the rainfall could be observed. Only in deeper lake areas and during longer rain events FCH4 was weakly related to rain (R2 = 0.29, p < 0.05), where a minor FCH4 decrease during the rain was identified, suggesting that direct rainwater input, during greater rainfall, may decrease FCH4 by dilution of surface water CH4. Overall, this study indicates that typical rain events in the studied regions have minor direct short-term effects on FCH4 from northern lakes and do not enhance FCH4 from shallow and deeper parts of lakes during and up to 24-h after the rainfall. Instead, other factors such as wind speed, water temperature and pressure changes were more strongly correlated with lake FCH4.

Lakes contribute 9%-19% of global methane (CH4) emissions to the atmosphere. Dissolved molecular oxygen (DO) in lakes can inhibit the production of CH4 and promote CH4 oxidation. DO is therefore often considered an important regulator of CH4 emissions from lakes. Presence or absence of DO in the water above the sediments can affect CH4 production and emissions by (a) influencing if methane production can be fueled by the most reactive organic matter in the top sediment layer or rely on deeper and less degradable organic matter, and (b) enabling CH4 accumulation in deep waters and potentially large emissions upon water column turnover. However, the relative importance of these two DO effects on CH4 fluxes is still unclear. We assessed CH4 fluxes from two connected lake basins in northern boreal Sweden where one was experimentally oxygenated. Results showed no clear difference in summer CH4 emissions attributable to water column DO concentrations. Large amounts of CH4 accumulated in the anoxic hypolimnion of the reference basin but little of this may have been emitted because of incomplete mixing, and effective methane oxidation of stored CH4 reaching oxic water layers. Accordingly, <= 24% of the stored CH4 was likely emitted in the experimental lake. Overall, our results suggest that hypolimnetic DO and water column CH4 storage might have a smaller impact on CH4 emissions in boreal forest lakes than previous estimates, yet potential fluxes associated with water column turnover events remain a significant uncertainty in lake CH4 emission estimates.

Reaching climate goals depends on appropriate and accurate methods to quantify greenhouse gas (GHG) fluxes and to verify that efforts to mitigate GHG emissions are effective. We here highlight critical advantages, limitations, and needs regarding GHG flux measurement methods, identified from an analysis of >13 500 scientific publications regarding three long-lived GHGs, carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O). While existing methods are well-suited for assessing atmospheric changes and local fluxes, they are expensive and have limited accessibility. Further, we are typically forced to choose between methods for very local GHG sources and sinks and their regulation (m(2)-scaled measurements), or methods for aggregated net fluxes at >ha or km(2) scales measurements. The results highlight the key need of accessible and affordable GHG flux measurement methods for the many flux types not quantifiable from fossil fuel use, to better verify inventories and mitigation efforts for transparency and accountability under the Paris agreement. The situation also calls for novel methods, capable of quantifying large scale GHG flux patterns while simultaneously distinguishing local source and sink dynamics and reveal flux regulation, representing key knowledge for quantitative GHG flux modeling. Possible strategies to address the identified GHG flux measurement method needs are discussed. The analysis also generated indications of how GHG flux measurements have been distributed geographically and across flux types, which are reported.

Appropriate methods to measure greenhouse gas (GHG) fluxes are critical for our ability to detect fluxes, understand regulation, make adequate priorities for climate change mitigation efforts, and verify that these efforts are effective. Ideally, we need reliable, accessible, and affordable measurements at relevant scales. We surveyed present GHG flux measurement methods, identified from an analysis of >11000 scientific publications and a questionnaire to sector professionals and analysed method pros and cons versus needs for novel methodology. While existing methods are well-suited for addressing certain questions, this presentation presents fundamental limitations relative to GHG flux measurement needs for verifiable and transparent action to mitigate many types of emissions. Cost and non-academic accessibility are key aspects, along with fundamental measurement performance. These method limitations contribute to the difficulties in verifying GHG mitigation efforts for transparency and accountability under the Paris agreement. Resolving this mismatch between method capacity and societal needs is urgently needed for effective climate mitigation. This type of methodological mismatch is common but seems to get high priority in other knowledge domains. The obvious need to prioritize development of accurate diagnosis methods for effective treatments in healthcare is one example. This presentation provides guidance regarding the need to prioritize the development of novel GHG flux measurement methods.

A major bottleneck regarding the efforts to better quantify greenhouse gas fluxes, map sources and sinks, and understand flux regulation is the shortage of low-cost and accurate-enough measurement methods. The studies of methane (CH4) - a long-lived greenhouse gas increasing rapidly but irregularly in the atmosphere for unclear reasons, and with poorly understood source-sink attribution - suffer from such method limitations. This study presents new calibration and data processing approaches for use of a low-cost CH4 sensor in flux chambers. Results show that the change in relative CH4 levels can be determined at rather high accuracy in the 2-700 ppm mole fraction range, with modest efforts of collecting reference samples in situ and without continuous access to expensive reference instruments. This opens possibilities for more affordable and time-effective measurements of CH4 in flux chambers. To facilitate such measurements, we also provide a description for building and using an Arduino logger for CH4, carbon dioxide (CO2), relative humidity, and temperature.

Aquatic ecosystems are major sources of greenhouse gases (GHGs). Robust measurements of natural GHG emissions are vital for evaluating regional to global carbon budgets and for assessing climate feedbacks of natural emissions to improve climate models. Diffusive and ebullitive (bubble) transport are two major pathways of gas release from surface waters. To capture the high temporal variability of these fluxes in a well-defined footprint, we designed and built an inexpensive device that includes an easily mobile diffusive flux chamber and a bubble counter all in one. In addition to automatically collecting gas samples for subsequent various analyses in the laboratory, this device also utilized a low-cost carbon dioxide (CO2) sensor (SenseAir, Sweden) and methane (CH4) sensor (Figaro, Japan) to measure GHG fluxes. Each of the devices was equipped with an XBee module to enable local radio communication (DigiMesh network) for time synchronization and data readout at a server controller station on the lakeshore. The software of this server controller was operated on a lowcost computer (Raspberry Pi), which has a 3G connection for remote control and monitor functions from anywhere in the world. This study shows the potential of a low-cost automatic sensor network system for studying GHG fluxes on lakes in remote locations.