Old-Growth Forest Disturbance in the Ukrainian Carpathians

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

Identifying European Old-Growth Forests using Remote Sensing: A Study in the Ukrainian Carpathians

Old-growth forests are an important, rare and endangered habitat in Europe. The ability to identify old-growth forests through remote sensing would be helpful for both conservation and forest management. We used data on beech, Norway spruce and mountain pine old-growth forests in the Ukrainian Carpathians to test whether Sentinel-2 satellite images could be used to correctly identify these forests. We used summer and autumn 2017 Sentinel-2 satellite images comprising 10 and 20 m resolution bands to create 6 vegetation indices and 9 textural features. We used a Random Forest classification model to discriminate between dominant tree species within old-growth forests and between old-growth and other forest types. Beech and Norway spruce were identified with an overall accuracy of around 90%, with a lower performance for mountain pine (70%) and mixed forest (40%). Old-growth forests were identified with an overall classification accuracy of 85%. Adding textural features, band standard deviations and elevation data improved accuracies by 3.3%, 2.1% and 1.8% respectively, while using combined summer and autumn images increased accuracy by 1.2%. We conclude that Random Forest classification combined with Sentinel-2 images can provide an effective option for identifying old-growth forests in Europe

A Global Analysis of Deforestation in Moist Tropical Forest Protected Areas.

Protected areas (PAs) have been established to conserve tropical forests, but their effectiveness at reducing deforestation is uncertain. To explore this issue, we combined high resolution data of global forest loss over the period 2000-2012 with data on PAs. For each PA we quantified forest loss within the PA, in buffer zones 1, 5, 10 and 15 km outside the PA boundary as well as a 1 km buffer within the PA boundary. We analysed 3376 tropical and subtropical moist forest PAs in 56 countries over 4 continents. We found that 73% of PAs experienced substantial deforestation pressure, with >0.1% a-1 forest loss in the outer 1 km buffer. Forest loss within PAs was greatest in Asia (0.25% a-1) compared to Africa (0.1% a-1), the Neotropics (0.1% a-1) and Australasia (Australia and Papua New Guinea; 0.03% a-1). We defined performance (P) of a PA as the ratio of forest loss in the inner 1 km buffer compared to the loss that would have occurred in the absence of the PA, calculated as the loss in the outer 1 km buffer corrected for any difference in deforestation pressure between the two buffers. To remove the potential bias due to terrain, we analysed a subset of PAs (n = 1804) where slope and elevation in inner and outer 1 km buffers were similar (within 1° and 100 m, respectively). We found 41% of PAs in this subset reduced forest loss in the inner buffer by at least 25% compared to the expected inner buffer forest loss (P<0.75). Median performance ([Formula: see text]) of subset reserves was 0.87, meaning a reduction in forest loss within the PA of 13%. We found PAs were most effective in Australasia ([Formula: see text]), moderately successful in the Neotropics ([Formula: see text]) and Africa ([Formula: see text]), but ineffective in Asia ([Formula: see text]). We found many countries have PAs that give little or no protection to forest loss, particularly in parts of Asia, west Africa and central America. Across the tropics, the median effectiveness of PAs at the national level improved with gross domestic product per capita. Whilst tropical and subtropical moist forest PAs do reduce forest loss, widely varying performance suggests substantial opportunities for improved protection, particularly in Asia

A small subset of protected areas are a highly significant source of carbon emissions

Protected areas (PAs) aim to protect multiple ecosystem services. However, not all are well protected. For the first time, using published carbon and forest loss maps, we estimate carbon emissions in large forest PAs in tropical countries (N = 2018). We found 36 ± 16 Pg C stored in PA trees, representing 14.5% of all tropical forest biomass carbon. However the PAs lost forest at a mean rate of 0.18% yr(−1) from 2000–2012. Lower protection status areas experienced higher forest losses (e.g. 0.39% yr(−1) in IUCN cat III), yet even highest status areas lost 0.13% yr(−1) (IUCN Cat I). Emissions were not evenly distributed: 80% of emissions derived from 8.3% of PAs (112 ± 49.5 Tg CO(2) yr(−1); n = 171). Unsurprisingly the largest emissions derived from PAs that started with the greatest total forest area; accounting for starting forest area and relating that to carbon lost using a linear model (r(2) = 0.41), we found 1.1% outlying PAs (residuals >2σ; N = 23), representing 1.3% of the total PA forest area, yet causing 27.3% of all PA emissions. These results suggest PAs have been a successful means of protecting biomass carbon, yet a subset causing a disproportionately high share of emissions should be an urgent priority for management interventions

A saturated map of common genetic variants associated with human height

Common single-nucleotide polymorphisms (SNPs) are predicted to collectively explain 40-50% of phenotypic variation in human height, but identifying the specific variants and associated regions requires huge sample sizes(1). Here, using data from a genome-wide association study of 5.4 million individuals of diverse ancestries, we show that 12,111 independent SNPs that are significantly associated with height account for nearly all of the common SNP-based heritability. These SNPs are clustered within 7,209 non-overlapping genomic segments with a mean size of around 90 kb, covering about 21% of the genome. The density of independent associations varies across the genome and the regions of increased density are enriched for biologically relevant genes. In out-of-sample estimation and prediction, the 12,111 SNPs (or all SNPs in the HapMap 3 panel(2)) account for 40% (45%) of phenotypic variance in populations of European ancestry but only around 10-20% (14-24%) in populations of other ancestries. Effect sizes, associated regions and gene prioritization are similar across ancestries, indicating that reduced prediction accuracy is likely to be explained by linkage disequilibrium and differences in allele frequency within associated regions. Finally, we show that the relevant biological pathways are detectable with smaller sample sizes than are needed to implicate causal genes and variants. Overall, this study provides a comprehensive map of specific genomic regions that contain the vast majority of common height-associated variants. Although this map is saturated for populations of European ancestry, further research is needed to achieve equivalent saturation in other ancestries.A large genome-wide association study of more than 5 million individuals reveals that 12,111 single-nucleotide polymorphisms account for nearly all the heritability of height attributable to common genetic variants

A saturated map of common genetic variants associated with human height.

Common single-nucleotide polymorphisms (SNPs) are predicted to collectively explain 40-50% of phenotypic variation in human height, but identifying the specific variants and associated regions requires huge sample sizes1. Here, using data from a genome-wide association study of 5.4 million individuals of diverse ancestries, we show that 12,111 independent SNPs that are significantly associated with height account for nearly all of the common SNP-based heritability. These SNPs are clustered within 7,209 non-overlapping genomic segments with a mean size of around 90 kb, covering about 21% of the genome. The density of independent associations varies across the genome and the regions of increased density are enriched for biologically relevant genes. In out-of-sample estimation and prediction, the 12,111 SNPs (or all SNPs in the HapMap 3 panel2) account for 40% (45%) of phenotypic variance in populations of European ancestry but only around 10-20% (14-24%) in populations of other ancestries. Effect sizes, associated regions and gene prioritization are similar across ancestries, indicating that reduced prediction accuracy is likely to be explained by linkage disequilibrium and differences in allele frequency within associated regions. Finally, we show that the relevant biological pathways are detectable with smaller sample sizes than are needed to implicate causal genes and variants. Overall, this study provides a comprehensive map of specific genomic regions that contain the vast majority of common height-associated variants. Although this map is saturated for populations of European ancestry, further research is needed to achieve equivalent saturation in other ancestries