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1 uch as vertebrates, reflect changes in wider biodiversity.
2 Speciation is a fundamental process shaping biodiversity.
3 uture socio-economic developments may affect biodiversity.
4 t strategies may successfully conserve urban biodiversity.
5 heir economy and broader wellbeing from this biodiversity.
6 theast Asia, a globally important region for biodiversity.
7 ious threat that wildlife poisoning poses to biodiversity.
8 radles and museums of tropical African plant biodiversity.
9 plate reconfigurations, global climate, and biodiversity.
10 sitions poses a substantial threat to global biodiversity.
11 ogate species for conservation of freshwater biodiversity.
12 diversity tends to correlate positively with biodiversity.
13 e need to take stock of unique Arctic marine biodiversity.
14 ibution to benefit human health and preserve biodiversity.
15 sation is a threat to both mental health and biodiversity.
16 nments; yet we still know little about their biodiversity.
17 e these resources are best spent to conserve biodiversity.
18 CA are poor at capturing the complexities of biodiversity.
19 resources and often does not benefit broader biodiversity.
20 vasive species pose a major threat to global biodiversity.
21 died in isolation but may interact to affect biodiversity.
22 be excluded from salvage logging to conserve biodiversity.
23 e records to describe global patterns of bee biodiversity.
24 considered one of the main threats to global biodiversity.
25 many metals, creating new mining threats for biodiversity.
26 ong the most important global drivers of bee biodiversity.
27 d progress in the way we assess and conserve biodiversity.
28 orld, with consequences for their associated biodiversity.
29 y across biomes is indirectly driven by soil biodiversity.
30 tems, climate stability, and conservation of biodiversity.
31 te adaptation tactics for conserving aquatic biodiversity.
32 ive surrogate for conservation of freshwater biodiversity.
33 crucial to understanding the maintenance of biodiversity.
34 e developing frameworks to assess impacts on biodiversity.
35 tes most likely to be affected by changes to biodiversity.
41 t studies have documented the high levels of biodiversity-across many taxa and biomes-that agricultur
42 at old-growth grasslands support substantial biodiversity and are slow to recover if destroyed by hum
45 ment in the tropics, a region with both high biodiversity and continually intensifying anthropogenic
46 auna in the study region, our study presents biodiversity and distribution data for the regional epi-
47 ojections are likely to affect productivity, biodiversity and distributions of deep-sea fauna, thereb
49 , calling for a need to understand levels of biodiversity and ecosystem responses to climate cycles.
50 recent findings of unprecedented declines in biodiversity and ecosystem services and their negative i
51 targets that account for the complex role of biodiversity and ecosystem services in sustainable devel
53 at are likely to present the highest risk to biodiversity and ecosystems within the APR over the next
56 sampling sites having both information about biodiversity and function, although with different taxon
57 key to understanding the response of forest biodiversity and functioning to climate and land-use cha
58 aryotes constitute a significant fraction of biodiversity and have recently gained more attention, bu
60 marine reserve network paradigm to riverine biodiversity and inland fisheries remains largely untest
61 orces shaping global patterns of present-day biodiversity and its response to ongoing and future abio
62 cs probably caused similar changes in forest biodiversity and should be reflected by conservation act
64 red to prevent further losses to terrestrial biodiversity and the ecosystem services that it provides
68 c activities have led to a global decline in biodiversity, and monitoring studies indicate that both
72 species invasion is an increasing threat to biodiversity, and the extent to which protected areas wo
73 of the factors governing global patterns of biodiversity are key to predicting community responses t
74 nservation areas: protected areas (PAs), Key Biodiversity Areas (KBAs) and Earth's remaining wilderne
75 (ecoregions, 12,056 threatened species, 'Key Biodiversity Areas' and wilderness areas) and ecosystem
76 coinciding with Protected Areas, 7% with Key Biodiversity Areas, and 16% with Remaining Wilderness.
79 yclases comprise the foundation of molecular biodiversity as they generate diverse hydrocarbon scaffo
81 rge-scale environmental forces can influence biodiversity at different levels of biological organizat
84 crocosm study, we provide evidence that soil biodiversity (bacteria, fungi, protists and invertebrate
85 ied the synergies and trade-offs between the biodiversity benefits achieved in the different plans an
87 ate monitoring datasets that allow comparing biodiversity between protected and unprotected sites are
88 s are vital to stream ecosystem function and biodiversity but insufficiently studied with respect to
89 outhern Europe that host increased levels of biodiversity but their persistence is threatened by glob
90 display a secular pattern similar to that of biodiversity, but this similarity was not confirmed when
92 nity can reverse the declines in terrestrial biodiversity caused by habitat conversion, which is a ma
96 lms and taxonomic groups, demonstrating that biodiversity changes at local scale are often complex an
98 Understanding the consequences of ongoing biodiversity changes for ecosystems is a pressing challe
99 financing, plan for climate change and make biodiversity conservation a far stronger part of land, w
100 ractitioners working across sectors, such as biodiversity conservation and food production in farmlan
101 ure, our results have major implications for biodiversity conservation and invasion dynamics in fresh
103 rgeted reactive approaches) might outperform biodiversity conservation as a tool for disease control.
104 d areas (PAs) are the cornerstones of global biodiversity conservation efforts, but to fulfil this ro
105 ecological understanding but can also guide biodiversity conservation in an era of global change.
106 f range limit theory and its applications to biodiversity conservation in the context of changing cli
109 rbance is considered essential for achieving biodiversity conservation outcomes but is rapidly erodin
111 ding of its population-level effects may aid biodiversity conservation through increased regulatory c
112 ed reproductive traits have implications for biodiversity conservation, via prediction of which plant
118 ms and taxonomic groups, and (ii) changes in biodiversity correlate with regional climate and local c
119 sive and often unnoticed consequences of the biodiversity crisis and calls attention to the invisible
122 ions, to generate a new Cambrian to Triassic biodiversity curve with an imputed temporal resolution o
123 e constraints posed by the limited access to biodiversity data, we employ the most comprehensive data
124 racted period of low speciation resulting in biodiversity decline, culminating in extinction events n
127 picuous manifestation of human activity, but biodiversity declines in undisturbed forest represent hi
128 in study-level and cross-study estimates of biodiversity differences, caused by within-study grain a
129 e the primary points of contention regarding biodiversity-disease relationships and suggest that vect
130 These results raise the question of whether biodiversity-disease relationships are more negative at
131 Although natural systems are rapidly losing biodiversity due to numerous human-caused stressors, our
132 these niche-distribution mismatches are for biodiversity dynamics and how they depend on species lif
133 el that expand on the assessed dimensions of biodiversity (e.g., ecosystem structure), and the driver
134 e as strong as other drivers known to impact biodiversity, e.g., grassland management and current lan
135 ng the coverage across different elements of biodiversity (ecoregions, 12,056 threatened species, 'Ke
136 e change poses significant emerging risks to biodiversity, ecosystem function and associated socioeco
137 e intensity affect the relationships between biodiversity, ecosystem functions, and services, we buil
138 tter articulate the interconnections between biodiversity, ecosystem services and sustainable develop
143 evidence for this relationship is drawn from biodiversity-ecosystem functioning experiments in which
145 studies to explore general patterns in soil biodiversity-ecosystem functioning relationships, with o
146 versity-ecosystem functioning relationships, biodiversity effects did not differ significantly betwee
147 we demonstrate a spectral approach to assess biodiversity effects in young forests that provides insi
148 nces among stands enabled us to quantify net biodiversity effects on stem biomass and canopy nitrogen
153 of the largest and longest-running grassland biodiversity experiments (the Jena Experiment in Germany
154 er significantly between the full dataset of biodiversity experiments and the ecologically realistic
156 some ecologists to question the relevance of biodiversity experiments to real-world ecosystems, where
157 developed by the Economics of Ecosystems and Biodiversity for Agriculture and Food (TEEBAgriFood) to
159 f biodiversity will occur is limited because biodiversity forecasts typically focus on individual sna
160 logical Diversity's (CBD's) post-2020 global biodiversity framework and targets will be developed as
163 ilocus amplicon sequencing of eDNA to survey biodiversity from an eighteen-month (2015-2016) time-ser
164 r fisheries and ecological function, but not biodiversity goals, given their degraded state and the l
166 However, the effects of glacier loss on biodiversity have never been quantified across a mountai
167 stern Indian Ocean are identified as a major biodiversity hotspot, with more than 50 bat species.
170 o deep-sea benthos, suggesting that deep-sea biodiversity hotspots are also likely to be microplastic
171 ates to test whether defining and conserving biodiversity hotspots is an effective conservation strat
174 with especially high biodiversity, known as biodiversity 'hotspots', is intuitive because finite res
175 e a leading cause of anthropogenic change in biodiversity; however, context dependencies and interact
176 land than in Estonia, which-according to the biodiversity hypothesis-could relate to differences in e
177 sults highlight that the existing metrics of biodiversity impact assessment in LCA are poor at captur
180 Together, urban environments may support biodiversity in a variety of ways, but species-specific
188 ive species have pervasive impacts on native biodiversity, including population extirpations and spec
189 ed microbiota signature, consisting of lower biodiversity, increased relative abundance of the bacter
190 acts of alternative compensation policies on biodiversity (indicated by native vegetation) and two ec
191 We then investigate a time lag in a real biodiversity indicator using empirical data and explore
192 ecosystems, it is important to consider how biodiversity influences processes such as decomposition.
193 easier to communicate, access, and aggregate biodiversity information, there is a need for a framewor
195 sed the updated model to project terrestrial biodiversity intactness from 2015 to 2050 as a function
202 that the plight of this component of cryptic biodiversity is more dire than previously considered in
206 g biogeographic regions with especially high biodiversity, known as biodiversity 'hotspots', is intui
207 g., ecosystem structure), and the drivers of biodiversity loss (e.g., assessment of species exploitat
208 ctices constitute both the greatest cause of biodiversity loss and the greatest opportunity for conse
210 ver been a greater concern, but attention to biodiversity loss is being eclipsed by the climate crisi
211 y-ecosystem functioning experiments in which biodiversity loss is simulated by randomly assembling co
212 od, limiting our ability to predict how soil biodiversity loss might affect human wellbeing and ecosy
214 that the synergistic impacts of warming and biodiversity loss on ecosystem functioning were mediated
216 y-ecosystem function experiments with random biodiversity loss scenarios have demonstrated that more
217 the local, rather than wider community-with biodiversity loss threatening all environments this pres
219 e, we experimentally crossed host diversity (biodiversity loss) and resource supply to hosts (eutroph
220 Interlocked challenges of climate change, biodiversity loss, and land degradation require transfor
221 ommunity commits to bolder action on abating biodiversity loss, placement of future PAs will be criti
222 erials and products is one of the drivers of biodiversity loss, which in turn affects ecosystem funct
223 drives changes in ecosystem functioning and biodiversity loss, which may ultimately compromise human
229 and to restore), and expected counterfactual biodiversity losses (unregulated vegetation clearing).
230 lance production with conservation could cut biodiversity losses by two-thirds, protecting most endan
232 ight the impending risk of sudden and severe biodiversity losses from climate change and provide a fr
234 udies to assist in mitigating climate-driven biodiversity losses in the 21st century and beyond.
237 used by within-study grain and sample sizes, biodiversity measure, and choice of effect-size metric.
244 Here we use an ensemble of land-use and biodiversity models to assess whether-and how-humanity c
245 a detailed account of the areas where urgent biodiversity monitoring efforts are needed to develop mo
248 anopesticide has limited effects on the soil biodiversity of a target terrestrial agroecosystem, whil
251 varying in space and time; consequently, the biodiversity of soil microorganisms also differs spatial
252 , resulting in negative consequences for the biodiversity of the whole continent, as introduced speci
253 xplore the impact of human activities on the biodiversity of wildlife and livestock with which humans
256 nt is particularly important given that most biodiversity on the planet consists of ectotherms whose
258 teractions has so far focused on quantifying biodiversity outcomes, rather than identifying the under
262 needed to develop more accurate knowledge on biodiversity patterns, offering government and environme
263 icting how global climate change will impact biodiversity patterns, the scarcity of taxon-specific in
268 as struggled to come to consensus on whether biodiversity reduces or increases infectious disease ris
270 traded wildlife products, conservation-based biodiversity research, and identification of blood-meal
274 gical research has brought new insights into biodiversity responses to global environmental change.
277 sate and its critically discussed health and biodiversity risks ask for fast, low cost, on-site sensi
279 n biodiversity, one must understand both how biodiversity scales with city size, and how ecological,
282 influence the ability of forests to support biodiversity, store carbon, mediate water yield and faci
285 t of distributed energy sources for regional biodiversity suggest that trade-offs based on more diver
286 ts, drones, or ground data - allowing global biodiversity targets relating to ecosystem structure to
287 ofoundly reshaped the world's landscapes and biodiversity, the ecological circumstances that facilita
291 rs driving the exposure and vulnerability of biodiversity to land use change, and then examining how
293 The dilution effect predicts increasing biodiversity to reduce the risk of infection, but the ge
296 ecies had greater negative effects on native biodiversity where human population was high and caused
297 ogenic climate change continues the risks to biodiversity will increase over time, with future projec
298 w abruptly this climate-driven disruption of biodiversity will occur is limited because biodiversity
300 al for sustaining agricultural economies and biodiversity, yet stands to lose both from present expos