scholarly article | Q13442814 |
P819 | ADS bibcode | 2018PNAS..115.6506B |
P356 | DOI | 10.1073/PNAS.1711842115 |
P932 | PMC publication ID | 6016768 |
P698 | PubMed publication ID | 29784790 |
P50 | author | Ron Milo | Q25497116 |
P2093 | author name string | Rob Phillips | |
Yinon Bar-On | |||
P2860 | cites work | The encyclopedia of life | Q106239589 |
Toward a census of bacteria in soil | Q21563510 | ||
Prokaryotes: the unseen majority | Q22066200 | ||
Colloquium paper: are we in the midst of the sixth mass extinction? A view from the world of amphibians | Q22066312 | ||
Primary Production of the Biosphere: Integrating Terrestrial and Oceanic Components | Q22299421 | ||
In search of ant ancestors | Q24626727 | ||
Megafauna biomass tradeoff as a driver of Quaternary and future extinctions | Q24642526 | ||
Linking the influence and dependence of people on biodiversity across scales. | Q30376599 | ||
Large mesopelagic fishes biomass and trophic efficiency in the open ocean | Q30442802 | ||
Global covariation of carbon turnover times with climate in terrestrial ecosystems | Q30855036 | ||
Mapping tree density at a global scale | Q30991125 | ||
Global effects of land use on local terrestrial biodiversity | Q31042382 | ||
Feast and famine--microbial life in the deep-sea bed. | Q33298072 | ||
Faster growth of the major prokaryotic versus eukaryotic CO2 fixers in the oligotrophic ocean | Q33587329 | ||
Microbial turnover times in the deep seabed studied by amino acid racemization modelling | Q33916240 | ||
Benchmark map of forest carbon stocks in tropical regions across three continents. | Q33917923 | ||
Nutritional constraints in terrestrial and freshwater food webs. | Q33928182 | ||
Global distribution of microbial abundance and biomass in subseafloor sediment | Q34296356 | ||
Deep subseafloor microbial cells on physiological standby. | Q35546698 | ||
Biological annihilation via the ongoing sixth mass extinction signaled by vertebrate population losses and declines | Q38684436 | ||
The elemental composition of virus particles: implications for marine biogeochemical cycles | Q42212389 | ||
Weighing the deep continental biosphere | Q43777568 | ||
Methyl-compound use and slow growth characterize microbial life in 2-km-deep subseafloor coal and shale beds | Q45354348 | ||
Ecosystem energetic implications of parasite and free-living biomass in three estuaries. | Q45965283 | ||
Unexpectedly large impact of forest management and grazing on global vegetation biomass | Q47572453 | ||
Tara Oceans studies plankton at planetary scale | Q56917885 | ||
Metabolic activity of subsurface life in deep-sea sediments | Q57088060 | ||
Carbon in the biota | Q69726383 | ||
P275 | copyright license | Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International | Q24082749 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 25 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | biomass | Q2945560 |
P304 | page(s) | 6506-6511 | |
P577 | publication date | 2018-05-21 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | The biomass distribution on Earth | |
P478 | volume | 115 |
Q92044609 | A One-Health lens for anthrax |
Q64105315 | A coupled microscopy approach to assess the nano-landscape of weathering |
Q64994268 | A few Ascomycota taxa dominate soil fungal communities worldwide. |
Q91595832 | A genetic toolbox for marine protists |
Q100464450 | A global class reunion with multiple groups feasting on the declining insect smorgasbord |
Q95660507 | A mechanistic explanation of the transition to simple multicellularity in fungi |
Q90001163 | A subfamily roadmap of the evolutionarily diverse glycoside hydrolase family 16 (GH16) |
Q89950149 | Abiotic factors and plant biomass, not plant diversity, strongly shape grassland arthropods under drought conditions |
Q98158629 | Aerobic microbial life persists in oxic marine sediment as old as 101.5 million years |
Q64081228 | An Improved Method for Extracting Viruses From Sediment: Detection of Far More Viruses in the Subseafloor Than Previously Reported |
Q89766174 | Are there 1031 virus particles on Earth, or more, or less? |
Q97073852 | Assessing the evolutionary persistence of ecological relationships: a review and preview |
Q89589926 | Axial changes in wood functional traits have limited net effects on stem biomass increment in European beech (Fagus sylvatica) |
Q91559867 | Bacteria and archaea on Earth and their abundance in biofilms |
Q64068869 | Bacteroidetes use thousands of enzyme combinations to break down glycans |
Q61799125 | Bifacial cambium stem cells generate xylem and phloem during radial plant growth |
Q92996800 | Biodiversity Conservation Requires Management of Feral Domestic Animals |
Q96303664 | Cell Wall Acetylation in Hybrid Aspen Affects Field Performance, Foliar Phenolic Composition and Resistance to Biological Stress Factors in a Construct-Dependent Fashion |
Q91714697 | Cell biomechanics and mechanobiology in bacteria: Challenges and opportunities |
Q100433556 | Clarifying Terrestrial Recycling Pathways |
Q57270686 | Climate warming from managed grasslands cancels the cooling effect of carbon sinks in sparsely grazed and natural grasslands |
Q91260166 | Community-level respiration of prokaryotic microbes may rise with global warming |
Q91465903 | Complex food webs coincide with high genetic potential for chemolithoautotrophy in fractured bedrock groundwater |
Q122983642 | Connecting soils to life in conservation planning, nutrient cycling, and planetary science |
Q76836884 | Conversion of Escherichia coli to Generate All Biomass Carbon from CO2 |
Q89927517 | Desiccation tolerance in streptophyte algae and the algae to land plant transition: Evolution of LEA and MIP protein families within the Viridiplantae |
Q92822541 | Diatoms Are Selective Segregators in Global Ocean Planktonic Communities |
Q91928928 | Direct Cell Mass Measurements Expand the Role of Small Microorganisms in Nature |
Q93239528 | Distinct spread of DNA and RNA viruses among mammals amid prominent role of domestic species |
Q90265283 | Ecology of Subseafloor Crustal Biofilms |
Q96683618 | Economic use of plants is key to their naturalization success |
Q91708126 | Editorial: Root Branching: From Lateral Root Primordium Initiation and Morphogenesis to Function |
Q89518568 | Emergence of life in an inflationary universe |
Q64387050 | Energy metabolism in anaerobic eukaryotes and Earth's late oxygenation |
Q91608129 | Environmental selection shapes the formation of near-surface groundwater microbiomes |
Q58753170 | Feeding the Walls: How Does Nutrient Availability Regulate Cell Wall Composition? |
Q93011997 | First glimpse on attitudes of highly educated consumers towards cell-based meat and related issues in Brazil |
Q92179267 | Fluid geochemistry, local hydrology, and metabolic activity define methanogen community size and composition in deep-sea hydrothermal vents |
Q112593271 | Forest management can mitigate negative impacts of climate and land-use change on plant biodiversity: Insights from the Republic of Korea |
Q130321417 | Fossil vertebrates from southern Zealandia: taonga of international significance |
Q89847185 | From inert matter to the global society life as multi-level networks of processes |
Q92480245 | Fungal community assembly in drought-stressed sorghum shows stochasticity, selection, and universal ecological dynamics |
Q90002985 | Genome mining- and synthetic biology-enabled production of hypermodified peptides |
Q105179581 | Genome-resolved metagenomics reveals site-specific diversity of episymbiotic CPR bacteria and DPANN archaea in groundwater ecosystems |
Q58698242 | Genomic Description of ' Abyssubacteria,' a Novel Subsurface Lineage Within the Candidate Phylum Hydrogenedentes |
Q93130196 | Getting Back to Nature: Feralization in Animals and Plants |
Q104118637 | Global human-made mass exceeds all living biomass |
Q112834452 | Global variation in diversification rate and species richness are unlinked in plants |
Q91842070 | Growing a circular economy with fungal biotechnology: a white paper |
Q98497790 | Herbivore Impacts on Carbon Cycling in Boreal Forests |
Q92157575 | Herbivore corridors sustain genetic footprint in plant populations: a case for Spanish drove roads |
Q105179591 | Huge and variable diversity of episymbiotic CPR bacteria and DPANN archaea in groundwater ecosystems |
Q100514908 | Infectious Diseases, Livestock, and Climate: A Vicious Cycle? |
Q92320852 | Insights into fungal diversity of a shallow-water hydrothermal vent field at Kueishan Island, Taiwan by culture-based and metabarcoding analyses |
Q63491702 | Integrating Material Stock Dynamics Into Economy-Wide Material Flow Accounting: Concepts, Modelling, and Global Application for 1900–2050 |
Q96127231 | Integrative omics analysis of the termite gut system adaptation to Miscanthus diet identifies lignocellulose degradation enzymes |
Q90439092 | Intensive farming drives long-term shifts in avian community composition |
Q94588255 | Is Endothermy an Evolutionary By-Product? |
Q103028618 | Large deep-sea zooplankton biomass mirrors primary production in the global ocean |
Q89582785 | Leveraging Signatures of Plant Functional Strategies in Wood Density Profiles of African Trees to Correct Mass Estimations From Terrestrial Laser Data |
Q64110085 | Marine DNA Viral Macro- and Microdiversity from Pole to Pole |
Q92783840 | Mechanomicrobiology: how bacteria sense and respond to forces |
Q64118888 | Methods to Investigate the Global Atmospheric Microbiome |
Q89931322 | Microbial community analysis using high-throughput sequencing technology: a beginner's guide for microbiologists |
Q64261934 | Microbial dormancy in the marine subsurface: Global endospore abundance and response to burial |
Q90710534 | Microbial residents of the Atlantis Massif's shallow serpentinite subsurface |
Q91045223 | Molecular architecture of softwood revealed by solid-state NMR |
Q94545932 | On the Three Major Recycling Pathways in Terrestrial Ecosystems |
Q91166009 | Oxygenic photosynthesis: history, status and perspective |
Q61443167 | Paleozoic diversification of terrestrial chitin-degrading bacterial lineages |
Q123478311 | Past and present biomass consumption by herbivores and fire across productivity gradients in North America |
Q91148614 | Plant-thickening mechanisms revealed |
Q91555539 | Post-Anthropocene Conservation |
Q93154602 | Revisiting Trade-offs between Rubisco Kinetic Parameters |
Q98513840 | Scale-free vertical tracking microscopy |
Q89630335 | Scientists' warning to humanity on the freshwater biodiversity crisis |
Q92860849 | Scientists' warning to humanity: microorganisms and climate change |
Q91694895 | Serpentinization: Connecting Geochemistry, Ancient Metabolism and Industrial Hydrogenation |
Q93052427 | Shifts in the Active Rhizobiome Paralleling Low Meloidogyne chitwoodi Densities in Fields Under Prolonged Organic Soil Management |
Q57069943 | Sizing Up the Uncultured Microbial Majority |
Q92154164 | Soil nematode abundance and functional group composition at a global scale |
Q93102562 | Soybean Interaction with Engineered Nanomaterials: A Literature Review of Recent Data |
Q92034018 | Substrate specificity, regiospecificity, and processivity in glycoside hydrolase family 74 |
Q94600383 | Tara Oceans: towards global ocean ecosystems biology |
Q64229093 | The Hidden Charm of Life |
Q92650897 | The amphipod crustacean Parhyale hawaiensis: An emerging comparative model of arthropod development, evolution, and regeneration |
Q106533457 | The biomass and biodiversity of the continental subsurface |
Q60959281 | The broiler chicken as a signal of a human reconfigured biosphere |
Q90709556 | The fitness of chemotrophs increases when their catabolic by-products are consumed by other species |
Q112572114 | The fluid city, urbanism as process |
Q64253843 | The global mass and average rate of rubisco |
Q90084933 | The impact of electric generation capacity by renewable and non-renewable energy in Brazilian economic growth |
Q96163001 | The role of ecosystems in mitigation and management of Covid-19 and other zoonoses |
Q60108873 | The scale of life and its lessons for humanity |
Q95841599 | Thinking avant la lettre: A Review of 4E Cognition |
Q90195761 | Thrust and Power Output of the Bacterial Flagellar Motor: A Micromagnetic Tweezers Approach |
Q92212663 | Towards Integrating Evolution, Metabolism, and Climate Change Studies of Marine Ecosystems |
Q93137063 | Towards Quantifying Carrion Biomass in Ecosystems |
Q91816371 | Towards a quantitative view of the global ubiquity of biofilms |
Q90052860 | Trade-offs between multifunctionality and profit in tropical smallholder landscapes |
Q97587569 | Two novel bacteriophage genera from a groundwater reservoir highlight subsurface environments as underexplored biotopes in bacteriophage ecology |
Q89143476 | Two types of cellulose synthesis complex knit the plant cell wall together |
Q92888631 | Uncovering the activities, biological roles, and regulation of bacterial cell wall hydrolases and tailoring enzymes |
Q94550644 | Uncovering the hidden diversity of litter-decomposition mechanisms in mushroom-forming fungi |
Q62927188 | Uniting Discoveries of Abundance-Size Distributions from Soils and Seas |
Q96059339 | Vertebrates on the brink as indicators of biological annihilation and the sixth mass extinction |
Q91991547 | Viromics and infectivity analysis reveal the release of infective plant viruses from wastewater into the environment |
Q58105532 | Virus-virus interactions and host ecology are associated with RNA virome structure in wild birds |
Q92353056 | Weathering in a world without terrestrial life recorded in the Mesoproterozoic Velkerri Formation |
Q98613792 | Widespread energy limitation to life in global subseafloor sediments |
Q90168534 | Wilderness areas halve the extinction risk of terrestrial biodiversity |
Q91683389 | Will organic thermoelectrics get hot? |