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    Diversity of prokaryotic microorganisms in alkaline saline soil of the Qarhan Salt Lake area in the Qinghai–Tibet Plateau

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    Active swimming and transphort by currents observed in Japanese eels (Anguilla japonica) acoustically tracked in the western North Pacific

    To our knowledge, this study provides the first recorded information on the active swimming of Japanese eels and on their transport by currents in the open ocean. Specifically, the strong flow of the KC largely dominated the movements of the eels and transported them northeastward while they swam mainly southward, and active swimming contributed a little to their travel trajectories. In contrast, the swimming of eels made a relatively higher contribution to their travel trajectories in the TS area.Our in situ estimates of the mean swimming speeds of Japanese eels (26–41 cm/s) were similar or slightly lower than those of European eels. In the acoustic tracking experiment of European eels considering environmental current vectors, their swimming speeds were 35–58 cm/s in the coastal midwater26. In a laboratory experiment using stamina tunnels with stable temperatures, the optimal swimming speeds of European eels were estimated to be 61–68 cm/s (0.74–1.02 BL/s)56, which were higher than the in situ estimates. The minimum swimming speed of European eels is considered to be 40 cm/s if they will arrive at their spawning area in the Sargasso Sea (distance of 5500 km) in 6 months, and their optimal swimming speeds were sufficient to migrate over the long distance in time for the near-spawning period after escape from their growth habitats56. However, field studies using PSAT tagging also reported that in situ migration speeds (including transport by currents) were less than the optimal swimming speeds and suggested that some European eels could reach their spawning area within the near-spawning periods and that others only arrive in time for the following spawning season19.Our estimated effective swimming speed of Japanese eels, all day and all night over the tracking periods, ranged from 3 to 30 cm/s with individual variations. These estimates were consistent with the swimming speeds (excluding transport by currents) of 2.2–15.1 km/day (2–18 cm/s) estimated in the PSAT study of Japanese eels14. Silver-phase Japanese eels start migrating from their coastal growth habitats in Japan primarily in October to December57, 58, and spawning near the West Mariana Ridge occurs in April to August33, 35. Numerical models assuming that migrating eels use true navigation (readjusted compass) or a constant compass heading (fixed compass from the departure place to the spawning site) indicate that the minimal swimming speed required to arrive at the spawning area within 8 months is 10–12 cm/s37. Our estimated effective swimming speeds of five out of ten eels during the day and eight out of ten eels during the night were similar or higher than these minimal speeds. The low effective swimming speeds frequently observed during the day might be due to the relatively low values observed in the swimming speed at 10 min intervals and the swimming directions often varying during the day. When eels swim with stable orientation, as observed in three of the eels (WE2999_TS, WE3001_TS, and WE3002_TS) during the night, the effective swimming speeds exceeded 25 cm/s. If such a stable orientation is maintained and compensate the low speeds during the day, the eels that leave during autumn and winter will be able to arrive at the spawning area during the next spring to summer.It should also be noted that the swimming speeds in body length per second were significantly higher in shallow water during the night than in deep water during the day. In the open ocean, anguillid species exhibit DVMs during oceanic migration, swimming at depth during the day and in the shallows during the night9,10,11,12,13,14,15,16,17,18,19,20,21,22. These DVMs are likely related to the possible avoidance from visual predators under light conditions19 or maturation control59. Essentially, through the DVMs, the eels encounter low temperatures ( 20 °C) during the same day. Generally, the swimming speeds of fishes are restricted by the ambient water temperature60, and the water temperature encountered through DVMs might influence the horizontal-swimming speeds of Japanese eels.Other factors besides swimming speed are important for the success of eel migrations, such as adapting to mesopelagic zones that silver eels undergo during their spawning migrations. The most important and obvious morphological adaptation in mesopelagic fish is their well-developed eyes, and migrating eels also seem to use this strategy. These fish often have relatively large pupils61, high photosensitive structures, such as tubular eyes62, a pure rod multibank retina63, and maximum rhodopsin absorption to adapt to the blue-green light in the deep sea64. The eyes of catadromous eels displayed enlargement during their transformation into migrating silver-phase eels65, 66 and potentially increase their retinal surface area, which results in the possibility of increased photon capture. In addition, the rhodopsins in the eyes change from a freshwater type with a maximum absorption of ~ 500 nm to a deep-sea type with a maximum absorption of ~ 480 nm67,68,69. Their extreme sensitivity to light is evident through their DVM in mesopelagic water, where the timing of a large descent and ascent in the DVM demonstrated by migrating catadromous eels is precisely synchronized with sunrise and sunset. Furthermore, eels alter their swimming depth in response to the phase of the Moon9, 15, 20, 21, appearing to be capable of perceiving extremely low-intensity moonlight.This study showed that three eels released in the TS area (mainly 300–400-m depth) and one eel in the KC area (near surface) were found to change their swimming direction around the time of the solar culmination when the Sun’s bearing changed. The clockwise and counterclockwise trajectories of these eels corresponded to whether the Sun moved from the east to west in the southern and northern sky, suggesting that they demonstrated horizontal negative phototaxis swimming to avoid sunlight. They might move to avoid high-intensity sunlight horizontally, not vertically, as they gradually increase the swimming depths possibly due to acclimation to cold deep water after release. The daytime swimming depths of the eels became deeper day-by-day after their release (Fig. 4); a similar phenomenon was observed in European eels12, American eels17, and long fin eels13. Recently, Higuchi et al.20 observed that the daytime swimming depths of Japanese eels released in the TS area gradually became deeper until 13 days after their release. These facts indicate that they gradually acclimate to the cold water at the deep depths after release. Since this tracking study was conducted 2–8 days after their release, the daytime swimming depth of eels would not have reached a steady state yet. The relatively high intensity from sunlight at the shallow depths where eels swam immediately after release in the TS area might cause horizontal avoidance behavior from the light.In other cases, many eels, especially those released in the KC area, did not demonstrate the rotational behavior. The eels in the KC area mostly stayed deeper (500–800 m) during the day than the eels in the TS area (stayed at depths of 300–600 m) even during the periods shortly after their release. This is possibly due to higher water temperatures even at the deeper depths in the KC area (Fig. 4). The eels in the TS area did not demonstrate clear rotational behavior at depths of more than 400 m. The PSAT studies have reported that the steady swimming depths during the day were 500–800 m14, 20. Therefore, it was assumed that the rotational behavior observed in some eels was not a regular behavior during their migration. However, the rotational behavior observed in this study suggests that they surely perceive the horizontal direction of Sun’s bearing at 400 m depths at least. Generally, they exhibit DVM precisely synchronizing with sunrise and sunset and surely perceive the change in sunlight intensity at deeper depths9,10,11,12,13,14,15,16,17,18,19,20,21,22. Even though the rotational behavior were not observed below 400 m, it remains unknown whether the eels could not perceive the Sun’s bearing from the light penetrated at depth; thus, further investigation of response to underwater light is required in future.While possible negative phototaxis behaviors were observed in some eels after release around the time of solar culmination, the trajectories of ten eels during the entire period of tracking experiments implied that each eel tended to swim meridionally toward the bearing of the Sun at culmination. We observed that eels released at middle (20°–34° N) and low (12°–13°N) latitudes tended to swim southward and northward in the meridional direction, respectively (Fig. 6A, B). The tendency to move in a north–south swimming direction corresponded to whether the Sun culminated to the north or south: eels swam southward if the culmination occurred in the southern sky, but they swam northward if it occurred in the northern sky (Fig. 6). In the KC area (33°–35° N), the Sun rose in the southeast, passed celestial meridian in the southern sky, and set in the southwest (Fig. 6C). At 20° N in the summer time when the tracking study was conducted, the Sun also passed a celestial meridian in the southern sky, but rose in the northeast and set in the northwest (Fig. 6C). When Sun culmination occurred in the southern sky, the meridional swimming directions tended to be southward (Fig. 6A). However, at 12° to 13° N in the summer time, the Sun rose in the northeast, passed the celestial meridian in the northern sky, and set in the northwest (Fig. 6D). When the Sun at culmination appeared in the northern sky, the meridional swimming directions tended to be northward (Fig. 6B). Furthermore, the swimming behavior by one eel (WE4264_TS) that was released slightly south (14° 15′ N) from the latitude with the Sun passing through the zenith was also indicative of the meridional swimming traits. This eel moved in a northerly direction on the first day, but then it lost its north–south bias in swimming around 14° 30′ N, where the Sun nearly passed through the zenith (Figs. 1 and 6D). These observations imply that the eels might move toward the latitude with the Sun passing through the zenith.Figure 6Swimming trajectories of eels and solar paths in the celestial sphere viewed from east during each tracking period. Swimming trajectories of eels released at (A) 20°N in the tropical–subtropical area and the Kuroshio Current area, and (B) 12°–14°15′N in the tropical–subtropical area. Solar paths through the north (N)–south (S) axis and the zenith at the time of tracking in (C) 20°N in the tropical–subtropical area and the Kuroshio Current area, and (D) 12°–14°15′N in the tropical–subtropical area.Full size imageTheoretically, it is possible for mesopelagic animals to use solar cues for navigation at depths shallower than the asymptotic depth, below which penetrating light rays are symmetrical around the vertical axis and the polarization plane becomes horizontal. For example, the Sargasso Sea, where the two Atlantic catadromous eels spawn1, 3, has extremely transparent water70, and the major axis of radiance distribution still remains tilted in the mesopelagic zone. The angle of maximum radiance of sunlight at 475 nm was 13° at depths of 400 m when the Sun’s elevation was 60° (Fig. 7)52, 53. In highly transparent water, the asymptotic depth could be as high as 1000–1200 m, and the depths below this cannot be utilized for compass use53. Currently, it is not possible to verify whether the Sun culminating to north or south caused the meridional swimming tendencies of eels in this study. Potentially, these meridional swimming tendencies could be due to other orientation clues, such as the geomagnetic field, as discussed for temperate anguillid eels17, 45. Nevertheless, in future studies, it would be worthwhile considering solar cues as a possible candidate factor in the orientation of eels, even when under faint underwater light conditions.Figure 7Optical features of underwater sunlight. (A) Schematic diagram of sunlight penetrating the deep ocean at 90° to the solar bearing. The line of arrows indicates the major axis of the incident beam in a vertical plane perpendicular to the Sun’s bearing. Blue light (around 475 nm) reaches the lowest depths. With increasing depth, the light field alters its character into a less directed distribution and a lower energetic level through scattering and absorption processes. Penetrating light rays are symmetrical around the region below the asymptotic depth. (B) An example of spectral radiance distribution (e. g. 475 nm) at a certain depth. The radiance distribution is shown by an ellipsoid and the major axis is drawn by a line with arrow. The refracted angular deviation (a) of the major axis of underwater radiance distribution from the vertical axis equals the tilt of the electric vector (ee bar) from the horizontal axis53. When the Sun’ s elevation was 60° in the Sargasso Sea, the radiance distributions were measured at three different depths and the tilt of the electric vector were estimated to be 24° at depths of 100 m and 200 m and 13° at depth of 400 m52, 53.Full size imageGiven that eels might be able to use the Sun’s bearing at culmination to orient their meridional swimming direction, this orientation scheme could support a clockwise eel migration route following a partial subtropical gyre2, 37. Japanese eels that departed from the nursery area first transported northeastward via the strong KC. Maintaining southward swimming in the current, they eventually crossed the current and shifted to the southward migration course. When they enter the KC, movement to the left of the bearing of the Sun at culmination (i.e., south) is the typical pattern for the early migration of eels from Japan. The movements of eels observed in the KC were consistent with the expected route; however, eels released at low latitudes of the TS area often swam northward but also westward, which resulted in their traveling an unreasonable distance from the spawning area. This might be due to their behavior during early migration. In this study, eels were transported from Japan and released into the open ocean at low latitudes. They might have swum toward the expected bearing of the Sun at culmination as if they were in the north and moved to the left of the Sun’s bearing along with the North Equatorial Current, which would mimic the early migration of eels leaving Japan and moving along the KC.Among the eels tracked in this study were individuals with impaired swim bladders, yellow-phase eels in the process of hormone-treatment maturation, and silver-phase eels collected from different rivers in different years. Despite these variations, the swimming characteristics of the eels did not differ in terms of their DVM behavior16 and swimming speed. Nevertheless, confirmation of our results using samples with a uniform status in future research would be highly desirable. In this study, the tracked eel position was assumed to be identical to that of the tracking ship and the errors between these two positions could not be evaluated; thus, the positioning of tracked fish also may need to be improved in future studies. Experimental studies, such as tracking of blind, magnetically disturbed, or olfactory-blocked eels, could help obtain or eliminate alternative candidate clues and enhance our understanding of the navigational system of anguillid eels. Controlled laboratory experiments are required to directly quantify the ability of eels to perceive radiance distribution or polarization, along with any associated behaviors. In addition, the internal clock of eels required to perform celestial navigation should be investigated. Meanwhile, the results obtained from this study can enhance our knowledge of the mechanisms underlying the migratory behaviors of eels in the open ocean. More

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    An earlier start of the thermal growing season enhances tree growth in cold humid areas but not in dry areas

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    Doubling of annual forest carbon loss over the tropics during the early twenty-first century

    Global map of forest cover change and its validationWe use a high-resolution map of global forest cover change15 (annual intervals at 30 m spatial resolution; version 1.7) to quantify forest loss across the tropics. The GFC dataset maps where and when forests were converted (naturally and anthropogenically) from 2001 to 2019. Trees are defined as all vegetation taller than 5 m in height, and forests are defined with a tree canopy threshold of at least 30%. The definition of forests includes plantations and tree crops such as oil palm. Forest loss is the mortality or removal of all tree cover within a pixel.Our study uses the v.1.7 product that spans the period 2001–2019 for the analysis. Different methods are used for detecting forest cover loss in two periods (2001–2010 and 2011–2019). This change in detection method as well as in satellite data (Landsat 7 and Landsat 8) might result in inconsistencies of data during the two periods. Therefore, we perform an independent assessment of the v.1.7 product throughout the study period (2001–2019) using stratified random-sample reference data. We randomly sample 18,000 pixels, a much larger sample population than the assessment of the original product (v.1.0, 628 pixels across the tropics; ref. 15), and visually interpret forest loss using Landsat imagery. Specifically, we randomly select 50 path/row locations (World Reference System II) of Landsat imagery in each tropical continent (150 path/row locations in total in the three tropical continents; Supplementary Fig. 6). For each path/row location, we randomly select 20 loss pixels and 10 non-loss pixels in each period of 2001–2005, 2006–2010, 2011–2014 and 2015–2019, with total sampling pixels of ~18,000 ((20 loss + 10 non-loss) × 50 path/row locations × 4 periods × 3 continents). Our study compares the increase in forest carbon loss from the start (~2001) to the end (~2019) of the study period. Thus, we divided the whole 19 yr study period into four subperiods (2001–2005, 2006–2010, 2011–2014 and 2015–2019), with the first five years considered as the start period and the last five years considered as the end period for the comparison. Some path/row locations do not have 20 loss pixels in a specific period; for example, there is no loss detected in some locations of the Sahara. Therefore, we sample 11,198 loss pixels and 6,000 non-loss pixels (Supplementary Data). Finally, we download time-series Landsat imagery covering 1999–2020 to visually interpret these pixels as reference data.Following the suggestion of Global Forest Watch19 and per best practice guidance of ref. 18, we use a stratified random-sample approach for area estimation, which is independent of the method and satellite changes in the GFC data. The sampling reference data (Supplementary Data) are used to estimate loss area:$${it{p}}_{hi} = w_hfrac{{mathop {sum}limits_{j = 1}^{150} {n_{hij} times A_{hi}} }}{{mathop {sum}limits_{j = 1}^{150} {n_{hj} times A_i} }}$$
    (1)
    where phi is the stratified random-sample estimated area for GFC map class h that is classified as reference class i; wh is the proportion of the total area GFC map class h; nhij is the number of pixels in GFC map class h that is classified as reference class i in jth Landsat path/row location; nhj is the total number of pixels in GFC map class h in jth Landsat path/row location; Ahj is the total area in GFC map class h in jth Landsat path/row location; and Aj is the total land area of jth Landsat path/row location.We then calculate the error matrix, which includes overall accuracy (OA), user’s accuracy (UA) and producer’s accuracy (PA), as follows:$${mathrm{OA}} = mathop {sum}limits_{h = 1}^H {p_{hh}}$$
    (2)
    $${mathrm{UA}}_h = frac{{p_{hh}}}{{p_h}}$$
    (3)
    $${mathrm{PA}}_j = frac{{p_{jj}}}{{p_j}}$$
    (4)
    where UAh is the UA for stratum h; ph and pj are the total area in stratum h and j, respectively; and PAj is the PA in stratum j.Using the preceding equations, we estimate OA, UA and PA in the four periods (Supplementary Table 2). In general, OAs are >99%, UAs are >88% and PAs are >72% in each period. The stratified random-sample approach for area estimation is considered the most robust method to investigate loss trends in GFC product and can avoid inconsistencies of the dataset due to changes in detection model and satellite sensors19. Our results show that the forest loss from the stratified random-sample approach is similar to GFC mapped loss, both of which show a consistent increase during the four periods of 2001–2019 (Fig. 1a), confirming the increasing forest carbon loss across the tropics during the early twenty-first century.Forest carbon stocksWe estimate forest (aboveground and belowground) biomass carbon losses by co-locating GFC loss data with corresponding biomass data. Forest biomass maps are not universally reliable, owing to uncertainties and some degree of bias. We use four biomass maps to quantify forest carbon stocks, which helps reduce the uncertainties and bias44. The four maps were developed by refs. 9,48,49,20 and are hereafter referred to as ‘Baccini’, ‘Saatchi’, ‘Avitabile’ and ‘Zarin’ maps, respectively. The Baccini map, derived from Moderate Resolution Imaging Spectroradiometer (MODIS) data, presents aboveground live woody biomass (AGB) across the tropics at 500 m spatial resolution. The Saatchi map, also derived from MODIS data, presents total forest carbon stocks at 1 km spatial resolution across the tropics. The Avitabile map, integrated from the Baccini and Saatchi maps, shows AGB at 1 km resolution across the tropics. The Zarin map, derived from Landsat data, presents AGB across the globe at 30 m resolution.Belowground root biomass (BGB) data are sparse because measurements of BGB are time consuming, laborious and technically challenging50. Thus, we calculate BGB (in Mg ha−1 biomass) from AGB maps (Baccini, Avitabile and Zarin) using an empirical model at the pixel level51:$${mathrm{BGB}} = 0.489 times {mathrm{AGB}}^{0.89}$$
    (5)
    Total forest biomass is calculated as the sum of AGB and BGB. Finally, total forest carbon stocks (MgC ha−1) in live woody forest are estimated as 50% of total biomass20,50. The Saatchi map provides total forest carbon stocks rather than AGB. The total forest carbon stocks are calculated from AGB using the same method mentioned in the preceding50. Thus, we estimate AGB and BGB from total forest carbon stocks in the Saatchi map using the preceding method to separate aboveground and belowground parts of forest carbon stocks.There are inconsistencies in the MODIS-derived biomass maps (Baccini, Saatchi and Avitabile) and Landsat-derived GFC data41, which may underestimate forest carbon loss by the three coarse forest biomass maps (Supplementary Fig. 7). The Zarin map is derived from Landsat data and considers tree cover using GFC data, and tree loss can be co-located with the corresponding biomass20, indicating the consistencies of the Zarin map and GFC. Therefore, to correct the three biomass maps with coarse resolution and reduce the inconsistencies, we resample the Zarin map from 30 m to 500 m (the resolution of the Baccini map) and 1 km (the resolutions of the Avitabile and Baccini maps) and calculate forest carbon loss using the two resampled biomass maps. We then estimate the ratios of forest carbon loss derived from the 30 m biomass map to the forest carbon loss derived from resampled biomass maps in each GFC tile (10° × 10°). The ratios are then used as a scale factor to correct the three biomass maps (Baccini, Saatchi and Avitabile). For the resampling, forest carbon density at 500 m or 1 km is averaged from all 30 m pixels in the corresponding locations.Soil organic carbon stocksDeforestation not only causes forest biomass carbon loss, but also results in loss of SOC10. We calculate SOC loss at 0–30 cm soil depth as:$${mathrm{SOC}}_{{{{mathrm{loss}}}}} = {mathrm{OCS}} times theta$$
    (6)
    where SOCloss is SOC loss resulting from forest loss measured in MgC ha−1, OCS is SOC stocks at 0–30 cm depth measured in MgC ha−1 and θ is the SOC loss rate.We obtain SOC stocks at 0–30 cm depth from SoilGrids (version 2.0), created by the International Soil Reference and Information Centre52. SOC stocks are calculated using a calibrated quantile random forest model at a spatial resolution of 250 m. We further resample the data from 250 m to 30 m using the nearest-neighbour method to match the scale of forest cover loss data.SOC loss rate is affected predominantly by land-use types following forest loss and tree species53. The loss rate data are compiled from a previous meta-analysis, which summarizes the rate of SOC loss resulting from forest loss over the tropics50. SOC losses resulting from primary and secondary forest loss differ (Supplementary Table 3). We use a map of primary humid tropical forests in 2001 developed by ref. 54 to classify primary and secondary forests. The land covers following forest loss are determined according to the driver of forest loss (see Drivers of forest carbon loss). The spatial resolution of the SOC data is coarse compared with GFC data, which may result in inconsistencies in the calculation. However, as SOC loss resulting from forest loss accounts for a small proportion of total forest carbon loss (8%), we ignore the potential inconsistencies.Drivers of forest carbon lossWe determine drivers of tree-cover loss using the dataset generated by ref. 27. This dataset shows the dominant driver of tree-cover loss at each 10 km grid cell for 2001–2019. There are five categories of drivers of tree-cover loss: commodity-driven deforestation, defined as permanent and/or long-term clearing of trees to other land uses (for example, commodity croplands), shifting agriculture, forestry, wildfire and urbanization. Commodity-driven deforestation, shifting agriculture and forestry dominate tropical forest loss27. Thus, wildfire and urbanization are combined and categorized as ‘others’. In tropical Africa, spatial patterns of commodity-driven deforestation are almost similar to that of shifting agriculture, as pointed out by ref. 27, resulting in large uncertainties in separating commodity agriculture from shifting agriculture. Since commodity-driven deforestation is usually for large-scale agricultural plantations, we treat commodity-driven deforestation as loss for large-scale agriculture. Because shifting agriculture is usually smallholder and/or patchy farming systems, we term shifting agriculture as small-scale agriculture, which may include commodity agriculture with similar spatial patterns to shifting agriculture in some regions such as tropical Africa. The driver data are created using decision-tree models trained by ~5,000 high-resolution Google Earth imagery cells, showing overall accuracy of 89 ± 3% from a separate validation of more than 1,500 randomly selected cells. We resample the data from 10 km resolution to 30 m using the nearest-neighbour method to match the scale of forest cover loss data.Interpretation of post-forest-loss land covers in 2020We collect cloudless and very-high-resolution satellite imagery in 2020 from Planet to determine the fate of the agriculture-driven forest loss during 2001–2019. Planet provides two products, RapidEye (at a spatial resolution of 5 m) and Doves (at a spatial resolution of 3 m; 4-band PlanetScope Scene). We randomly sample 500 pixels that show forest loss owing to agriculture expansion during 2001–2005 and 500 pixels that show forest loss owing to agriculture expansion during 2015–2019, then check cloudless satellite imagery in 2020 to visually interpret the land cover of each sampled pixel in 2020. We classify three types of land cover: agricultural land, forest/shrubland and others (Supplementary Fig. 4). Rubber and oil-palm plantations are classified as agricultural lands.Uncertainty and methods for analysisWe use committed emissions of forest carbon, even though some of this carbon will be lost only in later years or transited to other carbon pools or stored as wood products12. Forest carbon loss is defined as gross carbon loss due to forest removal (as indicated by GFC product), including (aboveground and belowground) forest biomass carbon and SOC losses. We calculate only the gross loss of forest carbon stocks while gain of carbon via reforestation and afforestation is not considered.We first estimate reference sample-based forest loss area using sample data:$${mathrm{AS}}_j = {mathrm{AM}}_jmathop {sum}limits_{h = 1}^H {p_{hj}}$$
    (7)
    where ASj and AMj are reference sample-based forest loss areas and mapped forest loss areas in stratum j, respectively.To estimate forest carbon loss (aboveground, belowground and soil carbon) using sample-based forest loss area, we apply a ‘stratify and multiply’ approach21,22 by assigning mean forest carbon density for each stratum. Aboveground and belowground forest carbon losses are estimated using four biomass maps (Baccini, Saatchi, Avitabile and Zarin), and we report ensemble mean ± s.d. from the four maps as our best estimate.Mountain forest carbon loss at different elevations is calculated by overlaying mountain polygon from the Global Mountain Biodiversity Assessment inventory55 (version 1.2) and the 30 m ASTER Global Digital Elevation Model56 (version 3).Although our validation shows that the GFC (v.1.7) product could accurately map forest loss, we cannot reduce the omission and commission errors. In addition, the accuracy of the disturbance year is 75.2%, with 96.7% of the disturbance occurring within one year before or after the estimated disturbance year in GFC product15. Therefore, we calculate 3 yr moving averages of annual forest and related carbon losses for time-series analysis, following the suggestion of the Global Forest Watch19 and refs. 28,38. We use a non-parametric Theil–Sen estimator regression method53 to detect trends in time-series results and test the significance of the trend by Mann–Kendall test57.Reporting SummaryFurther information on research design is available in the Nature Research Reporting Summary linked to this article. More

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    Climate change induced habitat expansion of nutria (Myocastor coypus) in South Korea

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    Large university with high COVID-19 incidence is not associated with excess cases in non-student population

    We used publicly available, daily, county-level COVID-19 cases and deaths from the Pennsylvania Department of Health (PA DOH) (https://www.health.pa.gov/topics/disease/coronavirus/pages/cases.aspx)13,14 for Centre County and the six neighboring counties with which it shares borders: Blair, Clearfield, Clinton, Huntingdon, Mifflin, and Union (Table 1, Fig. 1). Official COVID-19 reporting for these counties began on March 1, 2020 and is ongoing.Table 1 Summary statistics. COVID-19 reporting, census data, SafeGraph mobile-device derived data.Full size tableFigure 1(a) The cumulative COVID-19 case trajectory for Centre County minus the student cases (red line) has the same shape as the outbreak for the neighboring counties. When looking at student cases only (blue line), the curve leads other counties. Centre County cumulative cases including the university (purple line) take on the shape of an early increase because of the student cases. (b) When aggregating cases from students and non-students, Centre County (purple dot) reported about the number of cases expected for its population size, relative to the neighboring counties (black dots). When the university-reported student cases are separated from the non-student residents of the county, cases reported in Centre County non-students (red dots show possible range of total cases) fall below the number of cases we would expect for the population size. Student cases only (blue dot) are high for the student population size.Full size imageWithin Centre County, PSU provided COVID-19 testing for UP students from August 7, 2020 onward and reported anonymized weekly (2020) and daily (2021) confirmed cases, negative test results, and total tests completed for each campus in a public dashboard (Figs. 1a, S1) (https://virusinfo.psu.edu/covid-19-dashboard/)8. Two types of testing were conducted: students who were enrolled in on-campus classes were randomly selected for surveillance testing and all students could use on-demand testing. Through March 23, 2021, a total of 45,092 random tests were conducted for surveillance, of which 462, or 1.0%, were infected. Surveillance testing efforts ranged from 2440 to 4020 weekly tests through the Fall 2020 semester and were designed to consistently test approximately 1% of students throughout the school year.During the same time period, 75,436 on-demand tests were conducted, of which 6093, or 8.1%, were infected. Students living in both on-campus dorms and off-campus apartments had equal access to university-provided testing. Both on-campus and off-campus residences are within Centre County so positive and negative tests results were also included in the overall Centre County reports of COVID-19 cases.Pre-arrival testing was required for students returning to campus from transmission hotspots. Students with positive tests from pre-arrival testing were required to isolate for 10–14 days after their positive test before arriving on campus. Results from pre-arrival testing for students returning to campus in the Fall of 2020 are not included in these data.At the county level, PA DOH reports the total positive, probable, and negative tests for each county. Because PSU is within Centre County, we estimated the number of total positive and negative tests for non-student Centre County residents by subtracting the PSU estimates (from the PSU dashboard) from the Centre County estimates provided by PA DOH. However, not all student tests were reported to DOH. A portion of the on-demand tests conducted for PSU UP students were completed by a third-party vendor, which required student registration. At the time of student registration, an estimated 0–25% of students registered with an address for a family home that did not reflect their residence in Centre County. Their test results were reported to the county of their registered address. This impacts a maximum of 1,166 positive student test results and 10,760 negative student tests.We conducted a sensitivity analysis to assess the uncertainty in reporting around the negative and positive students tests that may have been misallocated due to the reported residence of student tests. We have calculated the minimum and maximum number of affected positive and negative student tests. This uncertainty from student tests impacts non-student values, which are calculated by subtracting student values from county level reports. The calculations are based on a range of a possible 0–1166 positive student tests misallocated to other counties and up to 10,760 misallocated negative student tests. We have used the ranges of misallocated student tests to calculate, for non-student Centre County residents, the full possible range of (1) total cases, (2) reported cases per capita, and (3) tests per capita (Table 1, Fig. 1b). As a result, our estimates of cases and per capita testing among non-student residents in Centre County are imprecise (Table 1).We also used publicly available data from PA DOH data and PSU to calculate COVID-19 deaths per 100,000 for Centre County, the six neighboring counties, and PSU UP.We acquired county-level data on median household income, population size, and college enrollment status from the 2019 United States Census Bureau’s American Community Survey (ACS) 5-year data (https://www.census.gov/data/developers/data-sets/acs-5year.html) for all seven previously mentioned counties in central PA15.We divide the census block groups (CBG) of Centre County into two categories. We first designated ‘student-dominated CBGs’ as CBGs where  > 50% of ACS responses report enrollment as undergraduate students. We consider data from the 19 student-dominated CBGs in Centre County to be representative of the student population in Centre County. In addition to off-campus locations, the 19 student-dominated CBGs include all on-campus dorms. These 19 CBGs are either on or adjacent to PSU’s UP campus and occupy exactly 6 census tracts. The remaining 25 county census tracts were designated as non-student dominated areas.SafeGraph16 receives geolocation data from anonymized mobile devices collected from numerous applications. We analyzed SafeGraph’s mobile device-derived daily visit counts to points of interest (POI), which are fixed locations, such as businesses or attractions. SafeGraph data provide daily counts for total numbers of visits by mobile devices while using at least one application that provides geolocation data to SafeGraph. A “visit” indicates that the device entered the building or spatial perimeter designated as a POI. We acquired daily visit counts for POIs in the seven previously mentioned counties in central PA from January 1, 2019 forward (Table 1) and within Centre County grouped counts into student-dominated CBGs and non-student dominated CBGs. From January 1, 2020 forward, we used SafeGraph data on the median daily minutes that devices spent outside of their home in each county and the student- and non-student dominated CBG divisions in Centre County. The “home location” of each device is defined by its location overnight. Finally, we used SafeGraph’s weekly calculated number of devices residing in each county and the CBGs of Centre County for 2019 to measure SafeGraph’s data representation across the seven counties and the CBGs of Centre County.No administrative permissions were required to obtain these data. Academic researchers can register to receive access to SafeGraph data at no charge for non-commercial purposes only. See Data Availability statement below for details. More

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    Precipitation effects on grassland plant performance are lessened by hay harvest

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