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Motivation: The BioTIME database contains raw data on species identities and abundances in ecological assemblages through time. These data enable users to calculate temporal trends in biodiversity within and amongst assemblages using a broad range of metrics. BioTIME is being developed as a community‐led open‐source database of biodiversity time series. Our goal is to accelerate and facilitate quantitative analysis of temporal patterns of biodiversity in the Anthropocene.Main types of variables included: The database contains 8,777,413 species abundance records, from assemblages consistently sampled for a minimum of 2 years, which need not necessarily be consecutive. In addition, the database contains metadata relating to sampling methodology and contextual information about each record.Spatial location and grain: BioTIME is a global database of 547,161 unique sampling locations spanning the marine, freshwater and terrestrial realms. Grain size varies across datasets from 0.0000000158 km2 (158 cm2) to 100 km2 (1,000,000,000,000 cm2).Time period and grain: BioTIME records span from 1874 to 2016. The minimal temporal grain across all datasets in BioTIME is a year.Major taxa and level of measurement: BioTIME includes data from 44,440 species across the plant and animal kingdoms, ranging from plants, plankton and terrestrial invertebrates to small and large vertebrates.

Potential climate drivers of Arctic tundra vegetation productivity are investigated to understand recent greening and browning trends documented by maximum normalized difference vegetation index (NDVI) (MaxNDVI) and time-integrated NDVI (TI-NDVI) for 1982-2015. Over this period, summer sea ice has continued to decline while oceanic heat content has increased. The increases in summer warmth index (SWI) and NDVI have not been uniform over the satellite record. SWI increased from 1982 to the mid-1990s and remained relatively flat from 1998 onwards until a recent upturn. While MaxNDVI displays positive trends from 1982-2015, TI-NDVI increased from 1982 until 2001 and has declined since. The data for the first and second halves of the record were analyzed and compared spatially for changing trends with a focus on the growing season. Negative trends for MaxNDVI and TI-NDVI were more common during 1999-2015 compared to 1982-1998. Trend analysis within the growing season reveals that sea ice decline was larger in spring for the 1982-1998 period compared to 1999-2015, while fall sea ice decline was larger in the later period. Land surface temperature trends for the 1982-1998 growing season are positive and for 1999-2015 are positive in May-June but weakly negative in July-August. Spring biweekly NDVI trends are positive and significant for 1982-1998, consistent with increasing open water and increased available warmth in spring. MaxNDVI trends for 1999-2015 display significant negative trends in May and the first half of June. Numerous possible drivers of early growing season NDVI decline coincident with warming temperatures are discussed, including increased standing water, delayed spring snow-melt, winter thaw events, and early snow melt followed by freezing temperatures. Further research is needed to robustly identify drivers of the spring NDVI decline.

Linkages between diminishing Arctic sea ice and changes in Arctic terrestrial ecosystems have not been previously demonstrated. Here, the authors use a newly available Arctic Normalized Difference Vegetation Index (NDVI) dataset (a measure of vegetation photosynthetic capacity) to document coherent temporal relationships between near-coastal sea ice, summer tundra land surface temperatures, and vegetation productivity. The authors find that, during the period of satellite observations (1982–2008), sea ice within 50 km of the coast during the period of early summer ice breakup declined an average of 25% for the Arctic as a whole, with much larger changes in the East Siberian Sea to Chukchi Sea sectors (>44% decline). The changes in sea ice conditions are most directly relevant and have the strongest effect on the villages and ecosystems immediately adjacent to the coast, but the terrestrial effects of sea ice changes also extend far inland. Low-elevation (<300 m) tundra summer land temperatures, as indicated by the summer warmth index (SWI; sum of the monthly-mean temperatures above freezing, expressed as °C month−1), have increased an average of 5°C month−1 (24% increase) for the Arctic as a whole; the largest changes (+10° to 12°C month−1) have been over land along the Chukchi and Bering Seas. The land warming has been more pronounced in North America (+30%) than in Eurasia (16%). When expressed as percentage change, land areas in the High Arctic in the vicinity of the Greenland Sea, Baffin Bay, and Davis Strait have experienced the largest changes (>70%). The NDVI has increased across most of the Arctic, with some exceptions over land regions along the Bering and west Chukchi Seas. The greatest change in absolute maximum NDVI occurred over tundra in northern Alaska on the Beaufort Sea coast [+0.08 Advanced Very High Resolution Radiometer (AVHRR) NDVI units]. When expressed as percentage change, large NDVI changes (10%–15%) occurred over land in the North America High Arctic and along the Beaufort Sea. Ground observations along an 1800-km climate transect in North America support the strong correlations between satellite NDVI observations and summer land temperatures. Other new observations from near the Lewis Glacier, Baffin Island, Canada, document rapid vegetation changes along the margins of large retreating glaciers and may be partly responsible for the large NDVI changes observed in northern Canada and Greenland. The ongoing changes to plant productivity will affect many aspects of Arctic systems, including changes to active-layer depths, permafrost, biodiversity, wildlife, and human use of these regions. Ecosystems that are presently adjacent to year-round (perennial) sea ice are likely to experience the greatest changes.

As the Arctic experiences continued warming, significant ecosystem changes, such as the northwards migration of woody species, are underway in tundra landscapes throughout the region. Despite these observable shifts, there remains a gap in our understanding of how climate warming impacts the phenology of tundra plants—specifically, the timing of their growth and reproductive cycles—especially across heterogeneous landscapes. Measuring phenology in the Arctic is challenging, requiring observations throughout the growing season and especially early and late in the season—times when field researchers are typically absent from their study sites. While remote observations offer broad coverage across the biome, they lack the detail needed for accurate phenological interpretations and may introduce significant errors. To address this, time‐lapse cameras (phenocams) present a promising solution, enabling simultaneous, individual‐level observations across disparate sites. In this study, we assess and present the precision, accuracy and practicality of monitoring reproductive phenology using repeat photography in tundra ecosystems by comparing satellite imagery, in situ observations and phenocams deployed on Qikiqtaruk—Herschel Island, Yukon Territory, Canada. Our results show that time‐lapse photography is a powerful tool to detect species‐specific phenology of Arctic vegetation, with an accuracy that is similar to in situ observations conducted by park rangers across the growing season, and at a much higher spatial and temporal detail than satellite data. Especially in the remote Arctic the low cost and ease of deployment across disparate sites throughout the whole year make phenocams an important tool for observing vegetation dynamics in a changing Arctic.

Recently observed Arctic greening trends from normalized difference vegetation index (NDVI) data suggest that shrub growth is increasing in response to increasing summer temperature. An increase in shrub cover is expected to decrease summer albedo and thus positively feed back to climate warming. However, it is unknown how albedo and NDVI are affected by shrub cover and inter-annual variations in the summer climate. Here, we examine the relationship between deciduous shrub fractional cover, NDVI and albedo using field data collected at a tundra site in NE Siberia. Field data showed that NDVI increased and albedo decreased with increasing deciduous shrub cover. We then selected four Arctic tundra study areas and compiled annual growing season maximum NDVI and minimum albedo maps from MODIS satellite data (2000–10) and related these satellite products to tundra vegetation types (shrub, graminoid, barren and wetland tundra) and regional summer temperature. We observed that maximum NDVI was greatest in shrub tundra and that inter-annual variation was negatively related to summer minimum albedo but showed no consistent relationship with summer temperature. Shrub tundra showed higher albedo than wetland and barren tundra in all four study areas. These results suggest that a northwards shift of shrub tundra might not lead to a decrease in summer minimum albedo during the snow-free season when replacing wetland tundra. A fully integrative study is however needed to link results from satellite data with in situ observations across the Arctic to test the effect of increasing shrub cover on summer albedo in different tundra vegetation types.

Vegetation productivity trends for the Arctic tundra are updated for the 1982–2011 period and examined in the context of land surface temperatures and coastal sea ice. Understanding mechanistic links between vegetation and climate parameters contributes to model advancements that are necessary for improving climate projections. This study employs remote sensing data: Global Inventory Modeling and Mapping Studies (GIMMS) Maximum Normalized Difference Vegetation Index (MaxNDVI), Special Sensor Microwave Imager (SSM/I) sea-ice concentrations, and Advanced Very High Resolution Radiometer (AVHRR) radiometric surface temperatures. Spring sea ice is declining everywhere except in the Bering Sea, while summer open water area is increasing throughout the Arctic. Summer Warmth Index (SWI—sum of degree months above freezing) trends from 1982 to 2011 are positive around Beringia but are negative over Eurasia from the Barents to the Laptev Seas and in parts of northern Canada. Eastern North America continues to show increased summer warmth and a corresponding steady increase in MaxNDVI. Positive MaxNDVI trends from 1982 to 2011 are generally weaker compared to trends from 1982–2008. So to better understand the changing trends, break points in the time series were quantified using the Breakfit algorithm. The most notable break points identify declines in SWI since 2003 in Eurasia and 1998 in Western North America. The Time Integrated NDVI (TI-NDVI, sum of the biweekly growing season values of MaxNDVI) has declined since 2005 in Eurasia, consistent with SWI declines. Summer (June–August) sea level pressure (slp) averages from 1999–2011 were compared to those from 1982–1998 to reveal higher slp over Greenland and the western Arctic and generally lower pressure over the continental Arctic in the recent period. This suggests that the large-scale circulation is likely a key contributor to the cooler temperatures over Eurasia through increased summer cloud cover and warming in Eastern North America from more cloud-free skies.

Northern protected areas guard against habitat and species loss but are themselves highly vulnerable to environmental change due to their fixed spatial boundaries. In the low Arctic, Torngat Mountains National Park (TMNP) of Canada, widespread greening has recently occurred alongside warming temperatures and regional declines in caribou. Little is known, however, about how biophysical controls mediate plant responses to climate warming, and available observational data are limited in temporal and spatial scope. In this study, we investigated the drivers of land cover change for the 9700 km2 extent of the park using satellite remote sensing and geostatistical modelling. Random forest classification was used to hindcast and simulate land cover change for four different land cover types from 1985 to 2019 with topographic and surface reflectance imagery (Landsat archive). The resulting land cover maps, in addition to topographic and biotic variables, were then used to predict where future shrub expansion is likely to occur using a binomial regression framework. Land cover hindcasts showed a 235% increase in shrub and a 105% increase in wet vegetation cover from 1985/89 to 2015/19. Shrub cover was highly persistent and displaced wet vegetation in southern, low-elevation areas, whereas wet vegetation expanded to formerly dry, mid-elevations. The predictive model identified both biotic (initial cover class, number of surrounding shrub neighbors), and topographic variables (elevation, latitude, and distance to the coast) as strong predictors of future shrub expansion. A further 51% increase in shrub cover is expected by 2039/43 relative to 2014 reference data. Establishing long-term monitoring plots within TMNP in areas where rapid vegetation change is predicted to occur will help to validate remote sensing observations and will improve our understanding of the consequences of change for biotic and abiotic components of the tundra ecosystem, including important cultural keystone species.

In this study, we utilized NDVI data from the moderate resolution imaging spectroradiometer (MODIS) alongside climatic variables obtained from a reanalyzed dataset to analyze Arctic greening during the summer months (June–September) of the last two decades. This investigation entailed a detailed analysis of these changes across various temporal scales. The data indicated a continuous trend of Arctic greening, evidenced by a 1.8% per decade increment in the NDVI. Notably, significant change points were identified in June 2012 and September 2013. A comparative assessment of NDVI pre- and post-these inflection points revealed an elongation of the Arctic greening trend. Furthermore, an anomalous increase in NDVI of 2% per decade was observed, suggesting an acceleration in greening. A comprehensive analysis was conducted to decipher the correlation between NDVI, temperature, and energy budget parameters to elucidate the underlying causes of these change points. Although the correlation between these variables was relatively low throughout the summer months, a distinct pattern emerged when these periods were dissected and examined in the context of the identified change points. Preceding the change point, a strong correlation (approximately 0.6) was observed between all variables; however, this correlation significantly diminished after the change point, dropping to less than half. This shift implies an introduction of additional external factors influencing the Arctic greening trend after the change point. Our findings provide foundational data for estimating the tipping point in Arctic terrestrial ecosystems. This is achieved by integrating the observed NDVI change points with their relationship with climatic variables, which are essential in comprehensively understanding the dynamics of Arctic climate change, particularly with alterations in tundra vegetation.

The purpose of the present study was to determine the link between planktivorous little auks (Alle alle) and their soil fertilization, the concentration of total, and different forms of phosphorus in the surface layer of the High Arctic soils and the vascular plant composition of the tundra vegetation. Samples of the surface soil layer (0–10 cm) were collected along three pairs of transects (affected and unaffected by little auks) at different locations in Spitsbergen (Svalbard). The surface layer of soils affected by little auks was characterized by a significantly higher mean concentration of Ptot (1.02–1.44 g kg−1) compared to those not affected by seabirds (0.58–0.77 g kg−1). The mean concentration of different forms of P was also generally higher in soils affected by seabirds (i.e., labile P: 0.13–0.34 g kg−1, moderately labile P: 0.31–0.90 g kg−1, stable P: 0.27–0.39 g kg−1) than in unaffected soils (labile P: 0.04–0.18 g kg−1, moderately labile P: 0.30–0.37 g kg−1, stable P: 0.12–0.24 g kg−1); however, the differences were not always significant, most likely due to the high heterogeneity of specific environmental conditions at the local scale such as soil type, soil chemical composition, and vegetation type. Vascular plant cover was significantly and positively related to the concentration of the P forms studied in the soil. The phosphorus gradient significantly altered the composition of the vascular plants and explained 58.4% of its variation. Little auks are an important source of soil phosphorus in terrestrial ecosystems in the High Arctic that significantly affect the cover and composition of vascular plants.

In arctic tundra, large and small mammalian herbivores have substantial impacts on the vegetation community and consequently can affect the magnitude of carbon cycling. However, herbivores are often absent from modern carbon cycle models, partly because relatively few field studies focus on herbivore impacts on carbon cycling. Our objectives were to quantify the impact of 21 years of large herbivore and large and small herbivore exclusion on carbon cycling during peak growing season in a dry heath tundra community. When herbivores were excluded, we observed a significantly greater leaf area index as well as greater vascular plant abundance. While we did not observe significant differences in deciduous dwarf shrub abundance across treatments, evergreen dwarf shrub abundance was greater where large and small herbivores were excluded. Both foliose and fruticose lichen abundance were higher in the large herbivore, but not the small and large herbivore exclosures. Net ecosystem exchange (NEE) likewise indicated the highest carbon uptake in the exclosure treatments and lowest uptake in the control (CT), suggesting that herbivory decreased the capacity of dry heath tundra to take up carbon. Moreover, our calculated NEE for average light and temperature conditions for July 2017, when our measurements were taken, indicated that the tundra was a carbon source in CT, but was a carbon sink in both exclosure treatments, indicating removal of grazing pressure can change the carbon balance of dry heath tundra. Collectively, these findings suggest that herbivore absence can lead to changes in plant community structure of dry heath tundra that in turn can increase its capacity to take up carbon.