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Antagonistic plants preferentially target arbuscular mycorrhizal fungi that are highly connected to mutualistic plants
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ece3.1497openalex-snapshot
Toward accurate molecular identification of species in complex environmental samples: testing the performance of sequence filtering and clustering methods
inferredcites →https://doi.org/10.1002/ece3.2974openalex-snapshot
Fungal‐host diversity among mycoheterotrophic plants increases proportionally to their fungal‐host overlap
inferredcites →https://doi.org/10.1007/978-1-4614-5209-6_4openalex-snapshot
Subterranean Morphology and Mycorrhizal Structures
inferredcites →https://doi.org/10.1007/978-1-4614-5209-6_5openalex-snapshot
Evolution and Diversification
inferredcites →https://doi.org/10.1007/978-1-4614-5209-6_7openalex-snapshot
Species Interactions of Mycoheterotrophic Plants: Specialization and its Potential Consequences
inferredcites →https://doi.org/10.1007/s00572-005-0368-zopenalex-snapshot
Application of network theory to potential mycorrhizal networks
inferredcites →https://doi.org/10.1007/s10530-018-1710-7openalex-snapshot
Biological invasions increase the richness of arbuscular mycorrhizal fungi from a Hawaiian subtropical ecosystem
inferredcites →https://doi.org/10.1016/b978-0-12-372180-8.50042-1openalex-snapshot
AMPLIFICATION AND DIRECT SEQUENCING OF FUNGAL RIBOSOMAL RNA GENES FOR PHYLOGENETICS
inferredcites →https://doi.org/10.1016/j.cub.2006.12.039openalex-snapshot
Specialization, Constraints, and Conflicting Interests in Mutualistic Networks
inferredcites →https://doi.org/10.1016/j.ecocom.2009.03.008openalex-snapshot
Centrality measures and the importance of generalist species in pollination networks
inferredcites →https://doi.org/10.1016/j.soilbio.2011.07.012openalex-snapshot
Global diversity and distribution of arbuscular mycorrhizal fungi
inferredcites →https://doi.org/10.1016/j.tplants.2008.11.004openalex-snapshot
Green plants that feed on fungi: facts and questions about mixotrophy
inferredcites →https://doi.org/10.1016/j.tree.2006.06.018openalex-snapshot
Pathways to mutualism breakdown
inferredcites →https://doi.org/10.1038/nature01054openalex-snapshot
Epiparasitic plants specialized on arbuscular mycorrhizal fungi
inferredcites →https://doi.org/10.1038/ncomms13965openalex-snapshot
Ecological networks are more sensitive to plant than to animal extinction under climate change
inferredcites →https://doi.org/10.1038/ncomms3350openalex-snapshot
Estimating the tolerance of species to the effects of global environmental change
inferredcites →https://doi.org/10.1038/nplants.2015.159openalex-snapshot
Regulation of resource exchange in the arbuscular mycorrhizal symbiosis
inferredcites →https://doi.org/10.1046/j.1461-0248.2001.00230.xopenalex-snapshot
Quantifying biodiversity: procedures and pitfalls in the measurement and comparison of species richness
inferredcites →https://doi.org/10.1073/pnas.1633576100openalex-snapshot
The nested assembly of plant–animal mutualistic networks
inferredcites →https://doi.org/10.1073/pnas.2023989118openalex-snapshot
Insect decline in the Anthropocene: Death by a thousand cuts
inferredcites →https://doi.org/10.1073/pnas.96.16.9178openalex-snapshot
Forty million years of mutualism: Evidence for Eocene origin of the yucca-yucca moth association
inferredcites →https://doi.org/10.1086/284267openalex-snapshot
On the Relationship between Abundance and Distribution of Species
inferredcites →https://doi.org/10.1093/aob/mcab003openalex-snapshot
Partial mycoheterotrophy is common among chlorophyllous plants with Paris-type arbuscular mycorrhiza
inferredcites →https://doi.org/10.1093/aob/mcu228openalex-snapshot
Evidence for phylogenetic correlation of plant–AMF assemblages?
inferredcites →https://doi.org/10.1093/aob/mcx023openalex-snapshot
Genetic diversity patterns of arbuscular mycorrhizal fungi associated with the mycoheterotroph Arachnitis uniflora Phil. (Corsiaceae)
inferredcites →https://doi.org/10.1093/bioinformatics/btq461openalex-snapshot
Search and clustering orders of magnitude faster than BLAST
inferredcites →https://doi.org/10.1093/icb/42.2.352openalex-snapshot
Host Specificity in Ectomycorrhizal Communities: What Do the Exceptions Tell Us?
inferredcites →https://doi.org/10.1098/rsbl.2010.1203openalex-snapshot
The dawn of symbiosis between plants and fungi
inferredcites →https://doi.org/10.1098/rspb.2007.0571openalex-snapshot
Evidence for the existence of a robust pattern of prey selection in food webs
inferredcites →https://doi.org/10.1098/rspb.2007.1622openalex-snapshot
Breakdown and delayed cospeciation in the arbuscular mycorrhizal mutualism
inferredcites →https://doi.org/10.1098/rspb.2016.2093openalex-snapshot
A phosphorus threshold for mycoheterotrophic plants in tropical forests
inferredcites →https://doi.org/10.1111/ele.12235openalex-snapshot
Antagonistic interaction networks are structured independently of latitude and host guild
inferredcites →https://doi.org/10.1111/geb.12920openalex-snapshot
Global distribution patterns of mycoheterotrophy
inferredcites →https://doi.org/10.1111/j.1365-2699.2011.02478.xopenalex-snapshot
Alien plants associate with widespread generalist arbuscular mycorrhizal fungal taxa: evidence from a continental-scale study using massively parallel 454 sequencing
inferredcites →https://doi.org/10.1111/j.1365-294x.2012.05472.xopenalex-snapshot
Mycoheterotrophic interactions are not limited to a narrow phylogenetic range of arbuscular mycorrhizal fungi
inferredcites →https://doi.org/10.1111/j.1461-0248.2005.00868.xopenalex-snapshot
Habitat loss and the structure of plant–animal mutualistic networks
inferredcites →https://doi.org/10.1111/j.1461-0248.2008.01254.xopenalex-snapshot
Preferential allocation to beneficial symbiont with spatial structure maintains mycorrhizal mutualism
inferredcites →https://doi.org/10.1111/j.1469-8137.1994.tb04272.xopenalex-snapshot
The biology of myco‐heterotrophic (‘saprophytic’) plants
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01429.xopenalex-snapshot
The evolutionary ecology of myco‐heterotrophy
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03962.xopenalex-snapshot
Phylogenetic reference data for systematics and phylotaxonomy of arbuscular mycorrhizal fungi from phylum to species level
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.04045.xopenalex-snapshot
The network structure of plant–arbuscular mycorrhizal fungi
inferredcites →https://doi.org/10.1111/j.1574-6941.2011.01103.xopenalex-snapshot
Arbuscular mycorrhizal fungal communities in plant roots are not random assemblages
inferredcites →https://doi.org/10.1111/j.1574-6941.2012.01437.xopenalex-snapshot
New primers to amplify the fungal ITS2 region - evaluation by 454-sequencing of artificial and natural communities
inferredcites →https://doi.org/10.1111/mec.12481openalex-snapshot
Towards a unified paradigm for sequence‐based identification of fungi
inferredcites →https://doi.org/10.1111/mec.14061openalex-snapshot
Phylogenetic relatedness explains highly interconnected and nested symbiotic networks of woody plants and arbuscular mycorrhizal fungi in a Chinese subtropical forest
inferredcites →https://doi.org/10.1111/mec.14924openalex-snapshot
Non‐random association patterns in a plant–mycorrhizal fungal network reveal host–symbiont specificity
inferredcites →https://doi.org/10.1111/nph.12243openalex-snapshot
Fungal community analysis by high‐throughput sequencing of amplified markers – a user's guide
inferredcites →https://doi.org/10.1111/nph.12758openalex-snapshot
Will different OTU delineation methods change interpretation of arbuscular mycorrhizal fungal community patterns?
inferredcites →https://doi.org/10.1111/nph.14249openalex-snapshot
Arbuscular mycorrhizal interactions of mycoheterotrophic Thismia are more specialized than in autotrophic plants
inferredcites →https://doi.org/10.1111/nph.15076openalex-snapshot
The origin and evolution of mycorrhizal symbioses: from palaeomycology to phylogenomics
inferredcites →https://doi.org/10.1111/nph.15876openalex-snapshot
Environmental drivers for cheaters of arbuscular mycorrhizal symbiosis in tropical rainforests
inferredcites →https://doi.org/10.1111/oik.01987openalex-snapshot
Trait‐based partner selection drives mycorrhizal network assembly
inferredcites →https://doi.org/10.1126/sciadv.1500291openalex-snapshot
Below-ground plant–fungus network topology is not congruent with above-ground plant–animal network topology
inferredcites →https://doi.org/10.1126/science.1208473openalex-snapshot
Reciprocal Rewards Stabilize Cooperation in the Mycorrhizal Symbiosis
inferredcites →https://doi.org/10.1126/science.1243092openalex-snapshot
Hyperdominance in the Amazonian Tree Flora
inferredcites →https://doi.org/10.1126/science.298.5594.824openalex-snapshot
Network Motifs: Simple Building Blocks of Complex Networks
inferredcites →https://doi.org/10.1126/science.aab1161openalex-snapshot
Global assessment of arbuscular mycorrhizal fungus diversity reveals very low endemism
inferredcites →https://doi.org/10.1139/b04-056openalex-snapshot
The evolutionary implications of exploitation in mycorrhizas
inferredcites →https://doi.org/10.1146/annurev.ecolsys.38.091206.095818openalex-snapshot
Plant-Animal Mutualistic Networks: The Architecture of Biodiversity
inferredcites →https://doi.org/10.1371/journal.pcbi.1003531openalex-snapshot
Waste Not, Want Not: Why Rarefying Microbiome Data Is Inadmissible
inferredcites →https://doi.org/10.1371/journal.pone.0083241openalex-snapshot
Arbuscular Mycorrhizal Fungal Networks Vary throughout the Growing Season and between Successional Stages
inferredcites →https://doi.org/10.1890/05-0101openalex-snapshot
SIMPLE TROPHIC MODULES FOR COMPLEX FOOD WEBS
inferredcites →https://doi.org/10.1890/15-0132.1openalex-snapshot
How plants connect pollination and herbivory networks and their contribution to community stability
inferredcites →https://doi.org/10.2174/1874213000902010007openalex-snapshot
Indices, Graphs and Null Models: Analyzing Bipartite Ecological Networks
inferredcites →https://doi.org/10.2307/1312122openalex-snapshot
The Keystone-Species Concept in Ecology and Conservation
inferredcites →https://doi.org/10.23943/princeton/9780691131269.001.0001openalex-snapshot
Mutualistic Networks
inferredcites →https://doi.org/10.5941/myco.2013.41.3.121openalex-snapshot
Diversity of Arbuscular Mycorrhizal Fungi and Their Roles in Ecosystems
inferredcites →https://doi.org/10.7208/chicago/9780226118697.001.0001openalex-snapshot
The Geographic Mosaic of Coevolution
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/tax.12765zenodo-depositor-declared
Unravelling the species diversity, phylogeny and biogeography of the mycoheterotrophic Voyrieae (Gentianaceae) and the description of a new species
inferred← citeshttps://doi.org/10.1007/s10265-020-01244-6openalex-snapshot
Evolutionary histories and mycorrhizal associations of mycoheterotrophic plants dependent on saprotrophic fungi
inferred← citeshttps://doi.org/10.70675/7fd34ffezc1d2z441azb463z80173e19b9d2openalex-snapshot
Characterizing and modeling the evolution of host-microbiota interactions
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