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Greenhouse Seedlings of Alnus Showed Low Host Intrageneric Specificity and a Strong Preference for Some Tomentella Ectomycorrhizal Associates

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Outgoing claims: the papers this work cites, builds on, or argues with.

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C omparisons of ectomycorrhizae on pinyon pines (P inus edulis ; P inaceae ) across extremes of soil type and herbivory
inferredcites →https://doi.org/10.1007/978-3-662-03779-9_27openalex-snapshot
Anatomical Characteristics of Identified Ectomycorrhizas: An Attempt Towards a Natural Classification
inferredcites →https://doi.org/10.1007/978-94-011-0511-8_12openalex-snapshot
Extraction of total cellular DNA from plants, algae and fungi
inferredcites →https://doi.org/10.1007/978-94-017-1601-7_19openalex-snapshot
Tripartite associations in an alder: effects of Frankia and Alpova diplophloeus on the growth, nitrogen fixation and mineral acquisition of Alnus tenuifolia
inferredcites →https://doi.org/10.1007/978-94-017-1601-7_22openalex-snapshot
Molecular phylogeny of Alnus (Betulaceae), inferred from nuclear ribosomal DNA ITS sequences
inferredcites →https://doi.org/10.1007/bf00203250openalex-snapshot
Early colonization of red alder and Douglas fir by ectomycorrhizal fungi and Frankia in soils from the Oregon coast range
inferredcites →https://doi.org/10.1007/bf01885276openalex-snapshot
Symbionts of alder nodules in New Zealand
inferredcites →https://doi.org/10.1007/s00374-006-0163-9openalex-snapshot
Contribution of red alder to soil nitrogen input in a silvopastoral system
inferredcites →https://doi.org/10.1007/s00572-001-0148-3openalex-snapshot
Ectomycorrhizae between Alnus acuminata H.B.K. and Naucoria escharoides (Fr.:Fr.) Kummer from Argentina
inferredcites →https://doi.org/10.1007/s00572-002-0158-9openalex-snapshot
Ectomycorrhizal root development in wet Alder carr forests in response to desiccation and eutrophication
inferredcites →https://doi.org/10.1007/s00572-005-0360-7openalex-snapshot
Ectomycorrhizal and arbuscular mycorrhizal colonization of Alnus acuminata from Calilegua National Park (Argentina)
inferredcites →https://doi.org/10.1007/s00572-009-0274-xopenalex-snapshot
Ectomycorrhizal lifestyle in fungi: global diversity, distribution, and evolution of phylogenetic lineages
inferredcites →https://doi.org/10.1007/s00572-011-0366-2openalex-snapshot
Ectomycorrhizal fungi in Mexican Alnus forests support the host co-migration hypothesis and continental-scale patterns in phylogeography
inferredcites →https://doi.org/10.1007/s00572-011-0374-2openalex-snapshot
Diversity and composition of ectomycorrhizal community on seedling roots: the role of host preference and soil origin
inferredcites →https://doi.org/10.1007/s005720050250openalex-snapshot
Plant growth and ectomycorrhiza formation by transplants on deglaciated land near Exit Glacier, Alaska
inferredcites →https://doi.org/10.1016/b978-0-12-633210-0.50008-3openalex-snapshot
Systematics, Isolation, and Culture of Frankia
inferredcites →https://doi.org/10.1016/b978-0-12-633210-0.x5001-1openalex-snapshot
The Biology of Frankia and Actinorhizal Plants
inferredcites →https://doi.org/10.1016/j.mycres.2006.04.007openalex-snapshot
Diversity and community structure of ectomycorrhizal fungi in a wooded meadow
inferredcites →https://doi.org/10.1016/s0580-9517(08)70172-7openalex-snapshot
2 Characterization of Ectomycorrhiza
inferredcites →https://doi.org/10.1016/s0580-9517(08)x7008-4openalex-snapshot
Techniques for the Study of Mycorrhiza
inferredcites →https://doi.org/10.1023/a:1008929520571openalex-snapshot
Isolation of infective and effective Frankia strains from root nodules of Alnus acuminata (Betulaceae)
inferredcites →https://doi.org/10.1023/a:1024938712822openalex-snapshot
Tripartite associations in an alder: effects of Frankia and Alpova diplophloeus on the growth, nitrogen fixation and mineral acquisition of Alnus tenuifolia
inferredcites →https://doi.org/10.1023/a:1024978409187openalex-snapshot
Molecular phylogeny of Alnus (Betulaceae), inferred from nuclear ribosomal DNA ITS sequences
inferredcites →https://doi.org/10.1046/j.1365-294x.1998.00432.xopenalex-snapshot
Chloroplast DNA phylogeography of Alnus glutinosa (L.) Gaertn.
inferredcites →https://doi.org/10.1046/j.1365-294x.1999.00773.xopenalex-snapshot
Community structure of ectomycorrhizal fungi in a Pinus muricata forest: minimal overlap between the mature forest and resistant propagule communities
inferredcites →https://doi.org/10.1046/j.1365-294x.2000.01105.xopenalex-snapshot
Diversity and abundance of resupinate thelephoroid fungi as ectomycorrhizal symbionts in Swedish boreal forests
inferredcites →https://doi.org/10.1046/j.1469-8137.1997.00806.xopenalex-snapshot
Characterization and identification of black alder ectomycorrhizas by PCR/RFLP analyses of the rDNA internal transcribed spacer (ITS)
inferredcites →https://doi.org/10.1046/j.1469-8137.1999.00452.xopenalex-snapshot
Mycorrhizal colonization of Pinus muricata from resistant propagules after a stand‐replacing wildfire
inferredcites →https://doi.org/10.1046/j.1469-8137.2002.00367.xopenalex-snapshot
Ectomycorrhizal fungal taxa differing in response to nitrogen deposition also differ in pure culture organic nitrogen use and natural abundance of nitrogen isotopes
inferredcites →https://doi.org/10.1051/forest:2005027openalex-snapshot
Ectomycorrhizal colonization of Alnus acuminata Kunth in northwestern Argentina in relation to season and soil parameters
inferredcites →https://doi.org/10.1080/15572536.2006.11832672openalex-snapshot
Spatial structure and richness of ectomycorrhizal fungi colonizing bioassay seedlings from resistant propagules in a Sierra Nevada forest: comparisons using two hosts that exhibit different seedling establishment patterns
inferredcites →https://doi.org/10.1086/382795openalex-snapshot
Phylogenetics and Biogeography of Alnus (Betulaceae) Inferred from Sequences of Nuclear Ribosomal DNA ITS Region
inferredcites →https://doi.org/10.1093/bioinformatics/btq461openalex-snapshot
Search and clustering orders of magnitude faster than BLAST
inferredcites →https://doi.org/10.1093/bioinformatics/btr381openalex-snapshot
UCHIME improves sensitivity and speed of chimera detection
inferredcites →https://doi.org/10.1093/molbev/msn083openalex-snapshot
jModelTest: Phylogenetic Model Averaging
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1093/sysbio/syq010openalex-snapshot
New Algorithms and Methods to Estimate Maximum-Likelihood Phylogenies: Assessing the Performance of PhyML 3.0
inferredcites →https://doi.org/10.1093/sysbio/sys029openalex-snapshot
MrBayes 3.2: Efficient Bayesian Phylogenetic Inference and Model Choice Across a Large Model Space
inferredcites →https://doi.org/10.1111/1462-2920.12020openalex-snapshot
Fungal palaeodiversity revealed using high‐throughput metabarcoding of ancient DNA from arctic permafrost
inferredcites →https://doi.org/10.1111/1574-6941.12032openalex-snapshot
New wrinkles in an old paradigm: neighborhood effects can modify the structure and specificity ofAlnus-associated ectomycorrhizal fungal communities
inferredcites →https://doi.org/10.1111/j.1365-2699.2011.02588.xopenalex-snapshot
An arctic community of symbiotic fungi assembled by long‐distance dispersers: phylogenetic diversity of ectomycorrhizal basidiomycetes in Svalbard based on soil and sporocarp DNA
inferredcites →https://doi.org/10.1111/j.1365-294x.1993.tb00005.xopenalex-snapshot
ITS primers with enhanced specificity for basidiomycetes ‐ application to the identification of mycorrhizae and rusts
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01718.xopenalex-snapshot
Species composition of an ectomycorrhizal fungal community along a local nutrient gradient in a boreal forest
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02104.xopenalex-snapshot
Ectomycorrhizal fungi of the Seychelles: diversity patterns and host shifts from the native Vateriopsis seychellarum (Dipterocarpaceae) and Intsia bijuga (Caesalpiniaceae) to the introduced Eucalyptus robusta (Myrtaceae), but not Pinus caribea (Pinaceae)
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.02792.xopenalex-snapshot
Revisiting ectomycorrhizal fungi of the genus Alnus: differential host specificity, diversity and determinants of the fungal community
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.02802.xopenalex-snapshot
Using heterozygosity to estimate a percentage DNA sequence similarity for environmental species’ delimitation across basidiomycete fungi
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03283.xopenalex-snapshot
Phylogenetic and ecological analyses of soil and sporocarp DNA sequences reveal high diversity and strong habitat partitioning in the boreal ectomycorrhizal genus Russula (Russulales; Basidiomycota)
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.12765openalex-snapshot
Large‐scale fungal diversity assessment in the Andean Yungas forests reveals strong community turnover among forest types along an altitudinal gradient
inferredcites →https://doi.org/10.1111/nph.12170openalex-snapshot
Biogeography of ectomycorrhizal fungi associated with alders ( A lnus spp.) in relation to biotic and abiotic variables at the global scale
inferredcites →https://doi.org/10.1111/nph.12638openalex-snapshot
Testing the link between community structure and function for ectomycorrhizal fungi involved in a global tripartite symbiosis
inferredcites →https://doi.org/10.1128/aem.58.5.1569-1576.1992openalex-snapshot
Evidence that some Frankia sp. strains are able to cross boundaries between Alnus and Elaeagnus host specificity groups
inferredcites →https://doi.org/10.1139/b07-017openalex-snapshot
Combining alders, frankiae, and mycorrhizae for the revegetation and remediation of contaminated ecosystems
inferredcites →https://doi.org/10.1139/b81-045openalex-snapshot
Ectomycorrhizal specificity in the genus Alnus
inferredcites →https://doi.org/10.1186/1471-2148-11-40openalex-snapshot
Comparative phylogenies and host specialization in the alder ectomycorrhizal fungi Alnicola, Alpova and Lactarius (Basidiomycota) in Europe
inferredcites →https://doi.org/10.1186/1471-2229-10-244openalex-snapshot
High diversity of root associated fungi in both alpine and arctic Dryas octopetala
inferredcites →https://doi.org/10.14601/phytopathol_mediterr-14998u1.29openalex-snapshot
BIOEDIT: A USER-FRIENDLY BIOLOGICAL SEQUENCE ALIGNMENT EDITOR AND ANALYSIS PROGRAM FOR WINDOWS 95/98/ NT
inferredcites →https://doi.org/10.2136/sssaj1985.03615995004900050041xopenalex-snapshot
Acidification Sources in Red Alder and Douglas Fir Soils‐Importance of Nitrification
inferredcites →https://doi.org/10.2307/2261311openalex-snapshot
Mycorrhizal Functioning. An Integrative Plant Fungal Process.
inferredcites →https://doi.org/10.2307/2265725openalex-snapshot
Biostatistical Analysis
inferredcites →https://doi.org/10.2307/2445327openalex-snapshot
Comparisons of Ectomycorrhizae on Pinyon Pines (Pinus edulis; Pinaceae) Across Extremes of Soil Type and Herbivory
inferredcites →https://doi.org/10.29203/ka.1995.309openalex-snapshot
Community structure and dynamics of wood-rotting Basidiomycetes on decomposing conifer trunks in northern Finland
inferredcites →https://doi.org/10.3732/ajb.0900230openalex-snapshot
Rangewide analysis of fungal associations in the fully mycoheterotrophic Corallorhiza striata complex (Orchidaceae) reveals extreme specificity on ectomycorrhizal Tomentella (Thelephoraceae) across North America
inferredcites →https://doi.org/10.3759/tropics.13.69openalex-snapshot
Molecular identification of ectomycorrhizal fungi associated with Dipterocarpaceae
inferredcites →https://doi.org/10.3852/09-311openalex-snapshot
Description and identification of Alnus acuminata ectomycorrhizae from Argentinean alder stands
inferredcites →https://doi.org/10.3852/mycologia.97.4.762openalex-snapshot
Spore dispersal of a resupinate ectomycorrhizal fungus, Tomentella sublilacina, via soil food webs
inferredcites →https://doi.org/10.5281/zenodo.16261182openalex-snapshot
The systematics of the American species of Alnus (Betulaceae) [concl.]

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.3897/mycokeys.109.132941zenodo-depositor-declared
The diversity and taxonomy of Tomentella (Thelephoraceae, Thelephorales) with descriptions of four new species from Southwestern China
inferred← citeshttps://doi.org/10.1007/978-3-030-15228-4_4openalex-snapshot
Ectomycorrhizal Fungi in South America: Their Diversity in Past, Present and Future Research
inferred← citeshttps://doi.org/10.1007/s00572-023-01112-wopenalex-snapshot
Primary succession of ectomycorrhizal fungi associated with Alnus sieboldiana on Izu-Oshima Island, Japan
inferred← citeshttps://doi.org/10.1007/s10531-018-1512-3openalex-snapshot
Richness, species composition and functional groups in Agaricomycetes communities along a vegetation and elevational gradient in the Andean Yungas of Argentina
inferred← citeshttps://doi.org/10.1007/s13199-017-0512-5openalex-snapshot
Ectomycorrhizal and endophytic fungi associated with Alnus glutinosa growing in a saline area of central Poland
inferred← citeshttps://doi.org/10.1007/s13199-023-00918-8openalex-snapshot
Low specificity and high variability of ectomycorrhizal association in Salix humboldtiana along its southern latitudinal distribution
inferred← citeshttps://doi.org/10.1080/00275514.2021.1911552openalex-snapshot
Phylogenetic relationships among false truffle genera of Paxillaceae—Alpova, Melanogaster, Neoalpova, and Paralpova, gen. nov
inferred← citeshttps://doi.org/10.1080/13416979.2022.2026558openalex-snapshot
Distribution of Frankia and ectomycorrhizal fungi in a denuded volcanic soil exposed by a landslide during heavy rainfall caused by typhoon No. 26 (Wipha) in 2013
inferred← citeshttps://doi.org/10.1111/btp.12394openalex-snapshot
Contracting montane cloud forests: a case study of the Andean alder (Alnus acuminata) and associated fungi in the Yungas
inferred← citeshttps://doi.org/10.31055/1851.2372.v52.n3.18023openalex-snapshot
Tomentella (Thelephorales, Basidiomycota) en bosques de Nothofagaceae de Patagonia, Argentina: micorrizas de nuevas especies
inferred← citeshttps://doi.org/10.3389/fmicb.2022.864198openalex-snapshot
Six New Species of Tomentella (Thelephorales, Basidiomycota) From Tropical Pine Forests in Central Vietnam
inferred← citeshttps://doi.org/10.3389/fmicb.2025.1692695openalex-snapshot
Comparative root associated microbial community analysis of Oreocharis mileensis, a resurrection plant species with extremely small populations
inferred← citeshttps://doi.org/10.3390/jof10070440openalex-snapshot
Four New Species of Tomentella (Thelephorales, Basidiomycota) from Subtropical Forests in Southwestern China
inferred← citeshttps://doi.org/10.3390/jof10110775openalex-snapshot
The Diversity and Taxonomy of Thelephoraceae (Basidiomycota) with Descriptions of Four Species from Southwestern China
inferred← citeshttps://doi.org/10.48130/mycosphere-0026-0019openalex-snapshot
Twenty new species of resupinate Thelephora (Thelephorales, Basidiomycota) from China
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