Abstract Woodlands can reduce downstream flooding, but it is not well known how the extent and distribution of woodland affects reductions in peak flow. We used the spatially distributed TOPMODEL to simulate peak flow during a 1 in 50 year storm event for a range of broadleaf woodland scenarios across a 2.6 km 2 catchment in Northern England. Woodland reduced peak flow by 2.6%–15.3% depending on the extent and spatial distribution of woodland cover. Cross slope and riparian woodland resulted in larger reductions in peak flow, 4.9% and 3.3% for a 10‐percentage point increase in woodland cover respectively, compared to a 2.7% reduction for woodland randomly located across the catchment. Our results demonstrate that increased woodland cover can reduce peak flows during a large storm event and suggest that targeted placement of woodland can maximise the effectiveness of natural flood management interventions.
Abstract. Cloud condensation nuclei (CCN) are derived from particles emitted directly into the atmosphere (primary emissions) or from the growth of nanometer-sized particles nucleated in the atmosphere. It is important to separate these two sources because they respond in different ways to gas and particle emission control strategies and environmental changes. Here, we use a global aerosol microphysics model to quantify the contribution of primary and nucleated particles to global CCN. The model considers primary emissions of sea spray, sulfate and carbonaceous particles, and nucleation processes appropriate for the free troposphere and boundary layer. We estimate that 45% of global low-level cloud CCN at 0.2% supersaturation are secondary aerosol derived from nucleation (ranging between 31–49% taking into account uncertainties primary emissions and nucleation rates), the remainder being directly emitted as primary aerosol. The model suggests that 35% of CCN (0.2%) in low-level clouds were created in the free and upper troposphere. In the marine boundary layer 55% of CCN (0.2%) are from nucleation, 45% being entrained from the free troposphere. Both in global and marine boundary layer 10% of CCN (0.2%) is nucleated in the boundary layer. Combinations of model runs show that primary and nucleated CCN are non-linearly coupled. In particular, boundary layer nucleated CCN are strongly suppressed by both primary emissions and entrainment of particles nucleated in the free troposphere. Elimination of all primary emissions reduces global CCN (0.2%) by only 20% and elimination of upper tropospheric nucleation reduces CCN (0.2%) by only 12% because of increased impact of boundary layer nucleation on CCN.
Abstract. It is important to understand the relative contribution of primary and secondary particles to regional and global aerosol so that models can attribute aerosol radiative forcing to different sources. In large-scale models, there is considerable uncertainty associated with treatments of particle formation (nucleation) in the boundary layer (BL) and in the size distribution of emitted primary particles, leading to uncertainties in predicted cloud condensation nuclei (CCN) concentrations. Here we quantify how primary particle emissions and secondary particle formation influence size-resolved particle number concentrations in the BL using a global aerosol microphysics model and aircraft and ground site observations made during the May 2008 campaign of the European Integrated Project on Aerosol Cloud Climate Air Quality Interactions (EUCAARI). We tested four different parameterisations for BL nucleation and two assumptions for the emission size distribution of anthropogenic and wildfire carbonaceous particles. When we emit carbonaceous particles at small sizes (as recommended by the Aerosol Intercomparison project, AEROCOM), the spatial distributions of campaign-mean number concentrations of particles with diameter >50 nm (N50) and >100 nm (N100) were well captured by the model (R2≥0.8) and the normalised mean bias (NMB) was also small (−18% for N50 and −1% for N100). Emission of carbonaceous particles at larger sizes, which we consider to be more realistic for low spatial resolution global models, results in equally good correlation but larger bias (R2≥0.8, NMB = −52% and −29%), which could be partly but not entirely compensated by BL nucleation. Within the uncertainty of the observations and accounting for the uncertainty in the size of emitted primary particles, BL nucleation makes a statistically significant contribution to CCN-sized particles at less than a quarter of the ground sites. Our results show that a major source of uncertainty in CCN-sized particles in polluted European air is the emitted size of primary carbonaceous particles. New information is required not just from direct observations, but also to determine the "effective emission size" and composition of primary particles appropriate for different resolution models.
Human activity has greatly reduced the area of old-growth forest in Europe, with some of the largest remaining fragments in the Carpathian Mountains of south-western Ukraine. We used satellite image analysis to calculate old-growth forest disturbance in this region from 2010 to 2019. Over this period, we identified 1335 ha of disturbance in old-growth forest, equivalent to 1.8% of old-growth forest in the region. During 2015 to 2019, the average annual disturbance rate was 0.34%, varying with altitude, distance to settlements and location within the region. Disturbance rates were 7–8 times lower in protected areas compared to outside of protected areas. Only one third of old-growth forest is currently within protected areas; expansion of the protected area system to include more old-growth forests would reduce future loss. A 2017 law that gave protection to all old-growth forest in Ukraine had no significant impact on disturbance rates in 2018, but in 2019 disturbance rates reduced to 0.19%. Our analysis is the first indication that this new legislation may be reducing loss of old-growth forest in Ukraine.
Abstract. We use a global aerosol microphysics model to estimate the effect of particle formation through activation nucleation in the boundary layer (BL) on cloud droplet number concentration (CDNC) on global and regional scales. The calculations are carried out for years 1850 and 2000 using historical emissions inventories for primary particles and aerosol precursor gases. Predicted CDNC in 2000 are in good agreement with in-situ observations when activation nucleation is included. We find that BL particle formation increases global annual mean CDNC by approximately the same relative amount in both years (16.0% in 1850 and 13.5% in 2000). As a result, global mean changes in cloud albedo are similar with and without BL particle formation. However, there are substantial regional effects of up to 50% enhancement or suppression of the 1850–2000 albedo change. Over most modern-day polluted northern hemisphere regions, including BL particle formation scheme suppresses the 1850–2000 increase in CDNC and cloud albedo because BL particle formation is already large in 1850. Over the Arctic the albedo change is suppressed by 23% in the annual mean and by 43% in summer when BL particle formation is taken into account. The albedo change of the persistent stratocumulus cloud deck west of Chile is enhanced by 49%.
High concentrations of ultrafine particles (UFP, i.e., particles with diameter < 100 nm) impact both human health and Earth's climate. Recent innovations in remote sensing technologies and data retrievals offer the potential for predicting UFP concentrations based on data from satellite‐borne instrumentation. Herein we present a physically based statistical algorithm to estimate UFP concentrations across eastern North America using remotely sensed aerosol optical depth, Ångstrom exponent, ultraviolet solar radiation flux, and ammonia and sulfur dioxide concentrations. The proposed algorithm is built and independently evaluated using an array of in situ observations. The algorithm is able to capture up to 60% of the variability in daily measured UFP number concentrations at a regionally representative reference site and is thus applied to generate seasonal UFP concentration estimates across eastern North America. The resulting UFP concentrations are cross‐evaluated with simulations from a global aerosol microphysics model. There is a negative bias in the model output relative to the satellite‐driven proxy, which is largest (up to 76%) in summer and may be due to overestimation of UFP from the satellite‐based algorithm derived herein, due to the higher availability of remote sensing data in clear‐sky conditions or uncertainty in the model simulation of new particle formation. Nevertheless, the model and algorithm indicate similar spatial and seasonal variability (spatial correlation coefficients of 0.10 to 0.56), indicating the value of the satellite‐based UFP proxy in global and regional model evaluation exercises and in efforts to identify regions where future in situ data collection should be prioritized.
Indonesia has experienced extensive land-cover change and frequent vegetation and land fires in the past few decades. We combined a new land-cover dataset with satellite data on the timing and location of fires to make the first detailed assessment of the association of fire with specific land-cover transitions in Riau, Sumatra. During 1990 to 2017, secondary peat swamp forest declined in area from 40,000 to 10,000 km2 and plantations (including oil palm) increased from around 10,000 to 40,000 km2. The dominant land use transitions were secondary peat swamp forest converting directly to plantation, or first to shrub and then to plantation. During 2001–2017, we find that the frequency of fire is greatest in regions that change land-cover, with the greatest frequency in regions that transition from secondary peat swamp forest to shrub or plantation (0.15 km−2 yr−1). Areas that did not change land cover exhibit lower fire frequency, with shrub (0.06 km−2 yr−1) exhibiting a frequency of fire >60 times the frequency of fire in primary forest. Our analysis demonstrates that in Riau, fire is closely connected to land-cover change, and that the majority of fire is associated with the transition of secondary forest to shrub and plantation. Reducing the frequency of fire in Riau will require enhanced protection of secondary forests and restoration of shrub to natural forest.
Late spring and summer snow cover, the remnants of winter and early spring snowfall, not only possess an intrinsic importance for montane flora and fauna, but also act as a sensitive indicator for climate change. The variability and potential trends in late spring and summer (snowmelt season) snow cover in mountain regions are often poorly documented. May to mid-September Landsat imagery from 1984 to 2022 was used to quantify changes in the snow-covered area of upland regions in the Scottish Highlands. There was substantial annual variability in the area of May to mid-September snow cover combined with a significant decline over the 39-year study period (p = 0.02). Long-term climate data used to show variability in May to mid-September snow cover was positively related to winter snowfall and negatively related to winter and April temperatures. The results from a long-running field survey counting the number of snow patches that survive until the following winter were used to check the veracity of the study. Further, accuracy was estimated through comparison with higher resolution Sentinel-2 imagery, giving a user and producer accuracy rate of 99.8% and 87%, respectively. Projected future warming will further diminish this scarce, valuable habitat, along with its associated plant communities, thus threatening the biodiversity and scenic value of the Scottish Highlands.
Abstract. We have combined the first satellite maps of the global distribution of phytoplankton functional type and new measurements of phytoplankton-specific isoprene productivities, with available remote marine isoprene observations and a global model, to evaluate our understanding of the marine isoprene source and its impacts on organic aerosol abundances. Using satellite products to scale up data on phytoplankton-specific isoprene productivity to the global oceans, we infer a mean "bottom-up" oceanic isoprene emission of 0.31±0.08 (1 σ) Tg/yr. By minimising the mean bias between the model and isoprene observations in the marine atmosphere remote from the continents, we produce a "top-down" oceanic isoprene source estimate of 1.9 Tg/yr. We suggest our reliance on limited atmospheric isoprene data, and limited knowledge of isoprene productivity across the broad range of phytoplankton communities in the oceans as contributors to this difference between the two estimates. Inclusion of secondary organic aerosol (SOA) production from oceanic isoprene in the model with a 2% yield produces small contributions (0.01–1.6%) to observed organic carbon (OC) aerosol mass at three remote marine sites in the Northern and Southern Hemispheres. In addition, we find the seasonal cycle of the isoprene SOA source is out of phase with the observed cycle in OC in the remote Southern Ocean. Based on these findings we suggest an insignificant role for isoprene in modulating remote marine aerosol abundances, giving further support to a recently postulated primary OC source in the remote marine atmosphere.