A widely-used eddy covariance gap-filling method creates systematic bias in carbon balance estimates.

Climate change mitigation requires, besides reductions in greenhouse gas emissions, actions to increase carbon sinks in terrestrial ecosystems. A key measurement method for quantifying such sinks and calibrating models is the eddy covariance technique, but it requires imputation, or gap-filling, of missing data for determination of annual carbon balances of ecosystems. Previous comparisons of gap-filling methods have concluded that commonly used methods, such as marginal distribution sampling (MDS), do not have a significant impact on the carbon balance estimate. By analyzing an extensive, global data set, we show that MDS causes significant carbon balance errors for northern (latitude [Formula: see text]) sites. MDS systematically overestimates the carbon dioxide (CO[Formula: see text]) emissions of carbon sources and underestimates the CO[Formula: see text] sequestration of carbon sinks. We also reveal reasons for these biases and show how a machine learning method called extreme gradient boosting or a modified implementation of MDS can be used to substantially reduce the northern site bias.

Evaluation of Methane Emissions Originating from LNG Ships Based on the Measurements at a Remote Marine Station.

We analyzed pollution plumes originating from ships using liquefied natural gas (LNG) as a fuel. Measurements were performed at a station located on the Utö island in the Baltic Sea during 2015-2021 when vessels passed the station along an adjacent shipping lane and the wind direction allowed the measurements. The ratio of the measured concentration peaks ΔCH4/ΔCO2 ranged from 1% to 9% and from 0.1% to 0.5% for low and high pressure dual fuel engines, respectively. The ratio of the measured concentration peaks of ΔNOx/ΔCO2 varied between 0.5‰ and 8.7‰, which was not explained by engine type. The results were consistent with previously measured on-board or test-bed values for the corresponding ratios of emissions. While the methane emissions from high pressure dual fuel engines were found to fulfill the goal of reducing the climatic impacts of shipping, the emissions originating from low pressure dual fuel engines were found to be substantially high, with a potential for increased climatic impacts compared with using traditional marine fuels. Taking only the global warming potential into account, we can suggest a limit value for the methane emissions; the ratio of the emissions ΔCH4/ΔCO2 originating from LNG powered ships should not exceed 1.4%.

Shipping Remains a Globally Significant Source of Anthropogenic PN Emissions Even after 2020 Sulfur Regulation.

Shipping is the main source of anthropogenic particle emissions in large areas of the globe, influencing climate, air quality, and human health in open seas and coast lines. Here, we determined, by laboratory and on-board measurements of ship engine exhaust, fuel-specific particle number (PN) emissions for different fuels and desulfurization applied in shipping. The emission factors were compared to ship exhaust plume observations and, furthermore, exploited in the assessment of global PN emissions from shipping, utilizing the STEAM ship emission model. The results indicate that most particles in the fresh ship engine exhaust are in ultrafine particle size range. Shipping PN emissions are localized, especially close to coastal lines, but significant emissions also exist on open seas and oceans. The global annual PN produced by marine shipping was 1.2 × 1028 (±0.34 × 1028) particles in 2016, thus being of the same magnitude with total anthropogenic PN emissions in continental areas. The reduction potential of PN from shipping strongly depends on the adopted technology mix, and except wide adoption of natural gas or scrubbers, no significant decrease in global PN is expected if heavy fuel oil is mainly replaced by low sulfur residual fuels. The results imply that shipping remains as a significant source of anthropogenic PN emissions that should be considered in future climate and health impact models.

Effects of drought and meteorological forcing on carbon and water fluxes in Nordic forests during the dry summer of 2018.

The Nordic region was subjected to severe drought in 2018 with a particularly long-lasting and large soil water deficit in Denmark, Southern Sweden and Estonia. Here, we analyse the impact of the drought on carbon and water fluxes in 11 forest ecosystems of different composition: spruce, pine, mixed and deciduous. We assess the impact of drought on fluxes by estimating the difference (anomaly) between year 2018 and a reference year without drought. Unexpectedly, the evaporation was only slightly reduced during 2018 compared to the reference year at two sites while it increased or was nearly unchanged at all other sites. This occurred under a 40 to 60% reduction in mean surface conductance and the concurrent increase in evaporative demand due to the warm and dry weather. The anomaly in the net ecosystem productivity (NEP) was 93% explained by a multilinear regression with the anomaly in heterotrophic respiration and the relative precipitation deficit as independent variables. Most of the variation (77%) was explained by the heterotrophic component. Six out of 11 forests reduced their annual NEP with more than 50 g C m-2 yr-1 during 2018 as compared to the reference year. The NEP anomaly ranged between -389 and +74 g C m-2 yr-1 with a median value of -59 g C m-2 yr-1. This article is part of the theme issue 'Impacts of the 2018 severe drought and heatwave in Europe: from site to continental scale'.

Characteristics of particle emissions and their atmospheric dilution during co-combustion of coal and wood pellets in a large combined heat and power plant.

Coal combustion is one of the most significant anthropogenic CO2 and air pollution sources globally. This paper studies the atmospheric emissions of a power plant fuelled with a mixture of industrial pellets (10.5%) and coal (89.5%). Based on the stack measurements, the solid particle number emission, which was dominated by sub-200 nm particles, was 3.4×1011 MJ-1 for the fuel mixture when electrostatic precipitator (ESP) was cleaning the flue gas. The emission factor was 50 mg MJ-1 for particulate mass and 11 740 ng MJ-1 for the black carbon with the ESP. In the normal operation situation of the power plant, i.e., including the flue-gas desulphurisation and fabric filters (FGD and FF), the particle number emission factor was 1.7×108 MJ-1, particulate mass emission factor 2 mg MJ-1 and black carbon emission factor 14 ng MJ-1. Transmission electron microscopy (TEM) analysis supported the particle number size distribution measurement in terms of particle size and the black carbon concentration. The TEM images of the particles showed variability of the particle sizes, morphologies and chemical compositions. The atmospheric measurements, conducted in the flue-gas plume, showed that the flue-gas dilutes closed to background concentrations in 200 sec. However, an increase in particle number concentration was observed when the flue gas aged. This increase in particle number concentration was interpret as formation of new particles in the atmosphere. In general, the study highlights the importance of detailed particle measurements when utilizing new fuels in existing power plants. Implications: CO2 emissions of energy production decrease when substituting coal with biofuels. The effects of fuels changes on particle emission characteristics have not been studied comprehensively. In this study conducted for a real-scale power plant, co-combustion of wood pellets and coal caused elevated black carbon emissions. However, it was beneficial from the total particle number and particulate mass emission point of view. Flue-gas cleaning can significantly decrease the pollutant concentrations but also changes the characteristics of emitted particles. Atmospheric measurements implicated that the new particle formation in the atmospheric flue-gas plume should be taken into account when evaluating all effects of fuel changes." Are implication statements part of the manuscript?

Early snowmelt significantly enhances boreal springtime carbon uptake.

We determine the annual timing of spring recovery from space-borne microwave radiometer observations across northern hemisphere boreal evergreen forests for 1979-2014. We find a trend of advanced spring recovery of carbon uptake for this period, with a total average shift of 8.1 d (2.3 d/decade). We use this trend to estimate the corresponding changes in gross primary production (GPP) by applying in situ carbon flux observations. Micrometeorological CO2 measurements at four sites in northern Europe and North America indicate that such an advance in spring recovery would have increased the January-June GPP sum by 29 g⋅C⋅m-2 [8.4 g⋅C⋅m-2 (3.7%)/decade]. We find this sensitivity of the measured springtime GPP to the spring recovery to be in accordance with the corresponding sensitivity derived from simulations with a land ecosystem model coupled to a global circulation model. The model-predicted increase in springtime cumulative GPP was 0.035 Pg/decade [15.5 g⋅C⋅m-2 (6.8%)/decade] for Eurasian forests and 0.017 Pg/decade for forests in North America [9.8 g⋅C⋅m-2 (4.4%)/decade]. This change in the springtime sum of GPP related to the timing of spring snowmelt is quantified here for boreal evergreen forests.

The uncertain climate footprint of wetlands under human pressure.

Significant climate risks are associated with a positive carbon-temperature feedback in northern latitude carbon-rich ecosystems, making an accurate analysis of human impacts on the net greenhouse gas balance of wetlands a priority. Here, we provide a coherent assessment of the climate footprint of a network of wetland sites based on simultaneous and quasi-continuous ecosystem observations of CO2 and CH4 fluxes. Experimental areas are located both in natural and in managed wetlands and cover a wide range of climatic regions, ecosystem types, and management practices. Based on direct observations we predict that sustained CH4 emissions in natural ecosystems are in the long term (i.e., several centuries) typically offset by CO2 uptake, although with large spatiotemporal variability. Using a space-for-time analogy across ecological and climatic gradients, we represent the chronosequence from natural to managed conditions to quantify the "cost" of CH4 emissions for the benefit of net carbon sequestration. With a sustained pulse-response radiative forcing model, we found a significant increase in atmospheric forcing due to land management, in particular for wetland converted to cropland. Our results quantify the role of human activities on the climate footprint of northern wetlands and call for development of active mitigation strategies for managed wetlands and new guidelines of the Intergovernmental Panel on Climate Change (IPCC) accounting for both sustained CH4 emissions and cumulative CO2 exchange.

Latent heat exchange in the boreal and arctic biomes.

In this study latent heat flux (λE) measurements made at 65 boreal and arctic eddy-covariance (EC) sites were analyses by using the Penman-Monteith equation. Sites were stratified into nine different ecosystem types: harvested and burnt forest areas, pine forests, spruce or fir forests, Douglas-fir forests, broadleaf deciduous forests, larch forests, wetlands, tundra and natural grasslands. The Penman-Monteith equation was calibrated with variable surface resistances against half-hourly eddy-covariance data and clear differences between ecosystem types were observed. Based on the modeled behavior of surface and aerodynamic resistances, surface resistance tightly control λE in most mature forests, while it had less importance in ecosystems having shorter vegetation like young or recently harvested forests, grasslands, wetlands and tundra. The parameters of the Penman-Monteith equation were clearly different for winter and summer conditions, indicating that phenological effects on surface resistance are important. We also compared the simulated λE of different ecosystem types under meteorological conditions at one site. Values of λE varied between 15% and 38% of the net radiation in the simulations with mean ecosystem parameters. In general, the simulations suggest that λE is higher from forested ecosystems than from grasslands, wetlands or tundra-type ecosystems. Forests showed usually a tighter stomatal control of λE as indicated by a pronounced sensitivity of surface resistance to atmospheric vapor pressure deficit. Nevertheless, the surface resistance of forests was lower than for open vegetation types including wetlands. Tundra and wetlands had higher surface resistances, which were less sensitive to vapor pressure deficits. The results indicate that the variation in surface resistance within and between different vegetation types might play a significant role in energy exchange between terrestrial ecosystems and atmosphere. These results suggest the need to take into account vegetation type and phenology in energy exchange modeling.

Determination of waste decay rate for a large Finnish landfill by calibrating methane generation models on the basis of methane recovery and emissions.

The aim of this study was to determine the methane (CH(4)) generation factor (k) and CH(4) generation potential (L) for bulk waste in order to calibrate a CH(4) generation model (USEPA Landgem 3.02) and provide information on the remaining CH(4) generation potential in a large (54 ha) municipal solid waste landfill located in a boreal climate. The CH(4) generation model was calibrated by actual CH(4) recovery and emission measurement data. Moreover, waste characterisation information from a previous study was considered.The appropriate k for bulk waste was 0.18 in the studied landfill, which indicated a higher rate of degradation than proposed by the Intergovernmental Panel on Climate Change as a default k value of 0.09 for wet conditions in boreal and temperate climes, whereas the calibrated L of 100 m(3)/t was lower than estimated on the basis of a previous waste characterisation study. The results demonstrate the importance of model calibration, as inappropriate model parameters may result in a large discrepancy (approximately 100 % or 119 million m(3) having an energy equivalent of nearly 1.2 TWh) in cumulative CH(4) generation estimates within a 18-year timescale (2012­30) at the studied landfill.

Modeling acclimation of photosynthesis to temperature in evergreen conifer forests.

• In this study, we used a canopy photosynthesis model which describes changes in photosynthetic capacity with slow temperature-dependent acclimations. • A flux-partitioning algorithm was applied to fit the photosynthesis model to net ecosystem exchange data for 12 evergreen coniferous forests from northern temperate and boreal regions. • The model accounted for much of the variation in photosynthetic production, with modeling efficiencies (mean > 67%) similar to those of more complex models. The parameter describing the rate of acclimation was larger at the northern sites, leading to a slower acclimation of photosynthesis to temperature. The response of the rates of photosynthesis to air temperature in spring was delayed up to several days at the coldest sites. Overall photosynthesis acclimation processes were slower at colder, northern locations than at warmer, more southern, and more maritime sites. • Consequently, slow changes in photosynthetic capacity were essential to explaining variations of photosynthesis for colder boreal forests (i.e. where acclimation of photosynthesis to temperature was slower), whereas the importance of these processes was minor in warmer conifer evergreen forests.

Net carbon dioxide losses of northern ecosystems in response to autumn warming.

The carbon balance of terrestrial ecosystems is particularly sensitive to climatic changes in autumn and spring, with spring and autumn temperatures over northern latitudes having risen by about 1.1 degrees C and 0.8 degrees C, respectively, over the past two decades. A simultaneous greening trend has also been observed, characterized by a longer growing season and greater photosynthetic activity. These observations have led to speculation that spring and autumn warming could enhance carbon sequestration and extend the period of net carbon uptake in the future. Here we analyse interannual variations in atmospheric carbon dioxide concentration data and ecosystem carbon dioxide fluxes. We find that atmospheric records from the past 20 years show a trend towards an earlier autumn-to-winter carbon dioxide build-up, suggesting a shorter net carbon uptake period. This trend cannot be explained by changes in atmospheric transport alone and, together with the ecosystem flux data, suggest increasing carbon losses in autumn. We use a process-based terrestrial biosphere model and satellite vegetation greenness index observations to investigate further the observed seasonal response of northern ecosystems to autumnal warming. We find that both photosynthesis and respiration increase during autumn warming, but the increase in respiration is greater. In contrast, warming increases photosynthesis more than respiration in spring. Our simulations and observations indicate that northern terrestrial ecosystems may currently lose carbon dioxide in response to autumn warming, with a sensitivity of about 0.2 PgC degrees C(-1), offsetting 90% of the increased carbon dioxide uptake during spring. If future autumn warming occurs at a faster rate than in spring, the ability of northern ecosystems to sequester carbon may be diminished earlier than previously suggested.

Micrometeorological measurements of methane and carbon dioxide fluxes at a municipal landfill.

Continuous and area-integrating monitoring of methane (CH4) and carbon dioxide (CO2) emissions was performed for 6 and 9 months, respectively, at a municipal landfill in Finland with the micrometeorological eddy covariance (EC) method. The mean CH4 emission from June to December was 0.53 mg m(-2) s(-1), while the CO2 emission between February and December averaged 1.78 mg m(-2) s(-1). The CH4 emissions from the summit area of the landfill, where active waste deposition was going on, were 1.7 times as high as from the slope area with a better surface cover. The variation in emissions over the source area of the measurement was high. Significant seasonal variation, linked to air and soil temperature, was only seen in the CO2 release rates. Results obtained with the EC method were comparable to those measured with closed static chambers. According to the EC measurements, the gas recovery system decreased CH4 fluxes by 69-79%. The ratio of the measured CH4 and CO2 emissions roughly indicated the route of the landfill gas emission, resembling the ratio of the gases measured in the gas wells (1.24) when the emission originated from the area with no oxidizing cover layer and being smaller when CH4 oxidation had taken place.

Ambient air concentrations, source profiles, and source apportionment of 71 different C2-C10 volatile organic compounds in urban and residential areas of Finland.

Ambient air concentrations and source contributions of 71 volatile organic compounds (VOCs) including C2-C10 nonmethane hydrocarbons, halogenated hydrocarbons, and carbonyls were studied at urban and residential sites in Finland. On the basis of the emission profile and concentration measurements, the contributions of different sources were estimated using a chemical mass balance (CMB) receptor model. It was shown that it is possible to apply CMB in the case of a large number of different compounds with different properties. However, the performance of the model varies significantly for the different compounds. According to the CMB analysis, major sources for these VOCs at the urban site were traffic and distant sources. At the residential site, the contribution due to traffic was minor while distant sources, liquid gasoline, and wood combustion made higher contributions. However, different compound groups or compounds were found to have totally different sources. It was also shown that a biogenic compound, isoprene, also has significant anthropogenic sources and that at some locations wood combustion can be an important source for some VOCs usually considered as traffic-related compounds (e.g., benzene).

Nitrous oxide emissions from a municipal landfill.

The first measurements of nitrous oxide (N20) emissions from a landfill by the eddy covariance method are reported. These measurements were compared to enclosure emission measurements conducted at the same site. The average emissions from the municipal landfill of the Helsinki Metropolitan Area were 2.7 mg N m(-2) h(-1) and 6.0 mg N m(-2) h(-1) measured bythe eddy covariance and the enclosure methods, respectively. The N20 emissions from the landfill are about 1 order of magnitude higher than the highest emissions reported from Northern European agricultural soils, and 2 orders of magnitude higher than the highest emissions reported from boreal forest soils. Due to the small area of landfills as compared to other land-use classes, the total N20 emissions from landfills are estimated to be of minor importance for the total emissions from Finland. Expressed as a greenhouse warming potential (GWP100), the N2O emissions make up about 3% of the total GWP100 emission of the landfill. The emissions measured by the two systems were generally of similar magnitude, with enclosure measurements showing a high small-scale spatial variation.

Aromatic hydrocarbon and methyl tert-butyl ether measurements in ambient air of Helsinki (Finland) using diffusive samplers.

The diffusive sampling method was evaluated for measuring benzene, toluene, ethylbenzene, xylenes, styrene, propylbenzene, ethyltoluenes, trimethylbenzenes and methyl tert-butyl ether (MTBE) in the urban air of Helsinki, Finland. Concentrations were measured in 2-week periods at four different sites during the year 2000. Tube type adsorbent tubes were pre-packed with Carbopack-B (60/80). Analysis was conducted using thermal desorption and gas chromatograph coupled to a mass spectrometer. In different seasons, during five diffusive sampling periods, parallel measurements were conducted using pumped and online sampling. The compared techniques agreed reasonably well for other compounds than trimethylbenzenes. Based on comparisons, diffusive uptake rates for ethyltoluenes, styrene, propylbenzene and MTBE were determined, and for trimethylbenzenes, uptake rates were revised. The concentrations of aromatic compounds in Helsinki metropolitan area were also compared to the concentrations of a rural, forested site in Central Finland.