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Multilocus phylogenetic analysis of true morels ( Morchella ) reveals high levels of endemics in Turkey relative to other regions of Europe
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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/jqs.3390050203openalex-snapshot
European vegetation history: Palaeovegetation maps from pollen data ‐ 13 000 yr BP to present
inferredcites →https://doi.org/10.1006/fgbi.2000.1228openalex-snapshot
Phylogenetic Species Recognition and Species Concepts in Fungi
inferredcites →https://doi.org/10.1007/pl00009992openalex-snapshot
Mycorrhiza-like interaction by Morchella with species of the Pinaceae in pure culture synthesis
inferredcites →https://doi.org/10.1007/s00284-010-9849-1openalex-snapshot
Molecular Characterization of Morchella Species from the Western Himalayan Region of India
inferredcites →https://doi.org/10.1016/0160-9327(96)10019-3openalex-snapshot
Where did all the flowers go? The fate of temperate European flora during glacial periods
inferredcites →https://doi.org/10.1016/0968-0004(90)90252-7openalex-snapshot
PCR protocols — A guide to methods and applications
inferredcites →https://doi.org/10.1016/j.fgb.2010.05.004openalex-snapshot
A multigene molecular phylogenetic assessment of true morels (Morchella) in Turkey
inferredcites →https://doi.org/10.1016/j.fgb.2010.09.006openalex-snapshot
Phylogeny and historical biogeography of true morels (Morchella) reveals an early Cretaceous origin and high continental endemism and provincialism in the Holarctic
inferredcites →https://doi.org/10.1016/j.funbio.2011.10.008openalex-snapshot
A novel plant–fungal mutualism associated with fire
inferredcites →https://doi.org/10.1016/j.ode.2004.07.001openalex-snapshot
Species diversity within the group (Ascomycota: Morchellaceae) in Germany and France
inferredcites →https://doi.org/10.1016/j.ympev.2004.04.012openalex-snapshot
Contribution of RPB2 to multilocus phylogenetic studies of the euascomycetes (Pezizomycotina, Fungi) with special emphasis on the lichen-forming Acarosporaceae and evolution of polyspory
inferredcites →https://doi.org/10.1016/j.ympev.2004.11.014openalex-snapshot
Improving phylogenetic inference of mushrooms with RPB1 and RPB2 nucleotide sequences (Inocybe; Agaricales)
inferredcites →https://doi.org/10.1016/j.ympev.2005.03.010openalex-snapshot
Evolutionary relationships of the cup-fungus genus Peziza and Pezizaceae inferred from multiple nuclear genes: RPB2, β-tubulin, and LSU rDNA
inferredcites →https://doi.org/10.1016/j.ympev.2005.06.016openalex-snapshot
Lower level relationships in the mushroom genus Cortinarius (Basidiomycota, Agaricales): A comparison of RPB1, RPB2, and ITS phylogenies
inferredcites →https://doi.org/10.1016/j.ympev.2006.10.016openalex-snapshot
Phylogenetic comparison of protein-coding versus ribosomal RNA-coding sequence data: A case study of the Lecanoromycetes (Ascomycota)
inferredcites →https://doi.org/10.1016/j.ympev.2008.04.029openalex-snapshot
Evidence for strong inter- and intracontinental phylogeographic structure in Amanita muscaria, a wind-dispersed ectomycorrhizal basidiomycete
inferredcites →https://doi.org/10.1016/s0953-7562(96)80101-8openalex-snapshot
DNA polymorphism in morels: PCR/RFLP analysis of the ribosomal DNA spacers and microsatellite-primed PCR
inferredcites →https://doi.org/10.1038/nature05110openalex-snapshot
Reconstructing the early evolution of Fungi using a six-gene phylogeny
inferredcites →https://doi.org/10.1046/j.1365-2699.2001.00528.xopenalex-snapshot
Shiitake mushrooms and molecular clocks: historical biogeography of Lentinula
inferredcites →https://doi.org/10.1046/j.1461-0248.2003.00477.xopenalex-snapshot
Deterministic Plio‐Pleistocene extinctions in the European cool‐temperate tree flora
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00894.xopenalex-snapshot
Taxonomic misidentification in public DNA databases
inferredcites →https://doi.org/10.1046/j.1523-1739.1996.10051321.xopenalex-snapshot
Implications of Phylogenetic Studies for Conservation of Genetic Diversity in Shiitake Mushrooms
inferredcites →https://doi.org/10.1073/pnas.0709037105openalex-snapshot
Mushroom fruiting and climate change
inferredcites →https://doi.org/10.1080/00275514.1997.12026754openalex-snapshot
Phylogenetic Relationships among Ascomycetous Truffles and the True and False Morels Inferred from 18S and 28S Ribosomal DNA Sequence Analysis
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026092openalex-snapshot
Phylogenetic relationships among ascomycetes: evidence from an RNA polymerse II subunit
inferredcites →https://doi.org/10.1093/sysbio/syp020openalex-snapshot
The Ascomycota Tree of Life: A Phylum-wide Phylogeny Clarifies the Origin and Evolution of Fundamental Reproductive and Ecological Traits
inferredcites →https://doi.org/10.1111/j.1365-294x.2008.04030.xopenalex-snapshot
The ectomycorrhizal fungus Amanita phalloides was introduced and is expanding its range on the west coast of North America
inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04855.xopenalex-snapshot
A global meta‐analysis of Tuber ITS rDNA sequences: species diversity, host associations and long‐distance dispersal
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02728.xopenalex-snapshot
Global patterns of ectomycorrhizal introductions
inferredcites →https://doi.org/10.1127/0029-5035/2009/0088-0011openalex-snapshot
African Morchella crassipes (Ascomycota, Pezizales) revealed by analysis of nrDNA ITS
inferredcites →https://doi.org/10.1128/jcm.02371-07openalex-snapshot
Molecular Phylogenetic Diversity, Multilocus Haplotype Nomenclature, and In Vitro Antifungal Resistance within the Fusarium solani Species Complex
inferredcites →https://doi.org/10.1139/cjm-45-9-769openalex-snapshot
Diversity of the internal transcribed spacer of rDNA in morels
inferredcites →https://doi.org/10.1371/journal.pone.0000059openalex-snapshot
Taxonomic Reliability of DNA Sequences in Public Sequence Databases: A Fungal Perspective
inferredcites →https://doi.org/10.2307/3760722openalex-snapshot
Persistence of Basidiospores and Sclerotia of Ectomycorrhizal Fungi and Morchella in Soil
inferredcites →https://doi.org/10.2307/3761230openalex-snapshot
The Known Morels in Mexico, a Description of a New Blushing Species, Morchella rufobrunnea, and New Data on M. guatemalensis
inferredcites →https://doi.org/10.3732/ajb.89.4.688openalex-snapshot
Using RPB1 sequences to improve phylogenetic inference among mushrooms ( Inocybe , Agaricales)
inferredcites →https://doi.org/10.3732/ajb.91.10.1446openalex-snapshot
Assembling the fungal tree of life: progress, classification, and evolution of subcellular traits
inferredcites →https://doi.org/10.3852/09-186openalex-snapshot
Morchella anatolica(Ascomycota), a new species from southwestern Anatolia, Turkey
inferredcites →https://doi.org/10.3852/09-232openalex-snapshot
Kalapuya brunneagen. & sp. nov. and its relationship to the other sequestrate genera in Morchellaceae
inferredcites →https://doi.org/10.3852/09-294openalex-snapshot
Morchella tomentosa: a unique belowground structure and a new clade of morels
inferredcites →https://doi.org/10.3852/mycologia.97.1.84openalex-snapshot
A Beauveria phylogeny inferred from nuclear ITS and EF1- sequences: evidence for cryptic diversification and links to Cordyceps teleomorphs
inferredcites →https://doi.org/10.3852/mycologia.98.6.1029openalex-snapshot
Systematics of the Pezizomycetes--the operculate discomycetes
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/imafungus.16.152685zenodo-depositor-declared
Unexpected richness and distinct patterns of Morchella (Ascomycota) species diversity in Chongqing, a notable “Furnace City”: unveiling rich diversity in hot regions
inferred← citeshttps://doi.org/10.1002/jemt.24683openalex-snapshot
First report of Morchella galilaea, an autumn species from Pakistan, based on multilocus DNA sequences, light microscopy, and scanning electron microscopy analyses
inferred← citeshttps://doi.org/10.1002/nzb2.70040openalex-snapshot
Ecological Niche Overlap and Environmental Associations Among Species of the Morchella (Morchellaceae, Pezizomycotina) From P.R. China
inferred← citeshttps://doi.org/10.1007/978-1-4939-7018-6_12openalex-snapshot
Minimally Processed Mushrooms
inferred← citeshttps://doi.org/10.1007/978-3-030-73943-0_38openalex-snapshot
Wild Morels in Pakistan: Environmental and Trading Statues
inferred← citeshttps://doi.org/10.1007/s00284-019-01819-0openalex-snapshot
A Novel PCR-Based Approach for Rapid Identification of Morchella sextelata Using Species-Specific Primers
inferred← citeshttps://doi.org/10.1007/s00284-026-04883-5openalex-snapshot
Phylogenetic Identification and Domestication of Wild Morchella Species from Fanjingshan, China
inferred← citeshttps://doi.org/10.1007/s11557-015-1030-6openalex-snapshot
Morchella tridentina, M. rufobrunnea, and M. kakiicolor: a study of three poorly known Mediterranean morels, with nomenclatural updates in section Distantes
inferred← citeshttps://doi.org/10.1007/s11557-016-1180-1openalex-snapshot
Combined phylogenetic and morphological studies of true morels (Pezizales, Ascomycota) in Cyprus reveal significant diversity, including Morchella arbutiphila and M. disparilis spp. nov.
inferred← citeshttps://doi.org/10.1007/s11557-021-01703-xopenalex-snapshot
Two new species of Morchella from Nothofagus forests in Northwestern Patagonia (Chile)
inferred← citeshttps://doi.org/10.1007/s11557-021-01755-zopenalex-snapshot
Has taxonomic vandalism gone too far? A case study, the rise of the pay-to-publish model and the pitfalls of Morchella systematics
inferred← citeshttps://doi.org/10.1007/s11557-022-01846-5openalex-snapshot
South American morels in the Elata group: mitosporic states, distributions, and commentary
inferred← citeshttps://doi.org/10.1007/s12231-015-9326-7openalex-snapshot
Morels of Palas Valley, Pakistan: A Potential Source for Generating Income and Improving Livelihoods of Mountain Communities
inferred← citeshttps://doi.org/10.1016/j.fgb.2012.03.006openalex-snapshot
Multigene molecular phylogenetics reveals true morels (Morchella) are especially species-rich in China
inferred← citeshttps://doi.org/10.1016/j.fldmyc.2017.04.004openalex-snapshot
Morels: the story so far
inferred← citeshttps://doi.org/10.1016/j.funbio.2014.03.008openalex-snapshot
Phylogenetic diversity of true morels (Morchella), the main edible non-timber product from native Patagonian forests of Argentina
inferred← citeshttps://doi.org/10.1016/j.funeco.2024.101373openalex-snapshot
Morchella galilaea – Expanded phylogeography and relaxed seasonality of a globally distributed autumnal morel
inferred← citeshttps://doi.org/10.1038/s41598-019-56321-1openalex-snapshot
RETRACTED ARTICLE: High diversity of Morchella and a novel lineage of the Esculenta clade from the north Qinling Mountains revealed by GCPSR-based study
inferred← citeshttps://doi.org/10.1038/s41598-021-93655-1openalex-snapshot
Retraction Note: High diversity of Morchella and a novel lineage of the Esculenta clade from the north Qinling Mountains revealed by GCPSR-based study
inferred← citeshttps://doi.org/10.1080/00275514.2017.1408294openalex-snapshot
First report of the post-fire morelMorchella exuberansin eastern North America
inferred← citeshttps://doi.org/10.1080/00275514.2018.1533772openalex-snapshot
Four new species of Morchella from the Americas
inferred← citeshttps://doi.org/10.1080/00275514.2018.1543508openalex-snapshot
Ribosomal DNA polymorphisms reveal genetic structure and a phylogeographic pattern in the Burgundy truffleTuber aestivumVittad.
inferred← citeshttps://doi.org/10.1080/00275514.2019.1640012openalex-snapshot
Six new species and two new records of Morchella in China using phylogenetic and morphological analyses
inferred← citeshttps://doi.org/10.1080/00275514.2020.1869489openalex-snapshot
Extended phylogeography of the ancestral Morchella anatolica supports preglacial presence in Europe and Mediterranean origin of morels
inferred← citeshttps://doi.org/10.1080/00275514.2021.2024422openalex-snapshot
Fire as a driver of fungal diversity — A synthesis of current knowledge
inferred← citeshttps://doi.org/10.1080/00275514.2024.2370198openalex-snapshot
Peziza nivalis and relatives—spring fungi of wide distribution
inferred← citeshttps://doi.org/10.1080/00275514.2025.2465094openalex-snapshot
Genetic diversity of true morels ( Morchella ) in Pakistan inferred from multilocus DNA sequence data augmented by a retrospective analysis of Pakistani and Indian morel sequences in GenBank
inferred← citeshttps://doi.org/10.1080/07388551.2017.1333082openalex-snapshot
Artificial cultivation of true morels: current state, issues and perspectives
inferred← citeshttps://doi.org/10.1080/21501203.2015.1016561openalex-snapshot
A review on research advances, issues, and perspectives of morels
inferred← citeshttps://doi.org/10.1111/1462-2920.15692openalex-snapshot
Changes in soil bacteria functional ecology associated with Morchella rufobrunnea fruiting in a natural habitat
inferred← citeshttps://doi.org/10.1111/1750-3841.17219openalex-snapshot
Using a Centroid‐based approach for a reliable identification of morels ( Morchella spp.): A case study for food authentication
inferred← citeshttps://doi.org/10.1128/mmbr.00220-20openalex-snapshot
Mating Systems in True Morels ( Morchella )
inferred← citeshttps://doi.org/10.12677/hjas.2020.103021openalex-snapshot
Research Progress on Genetic Diversity and Cultivation of Morchella
inferred← citeshttps://doi.org/10.15835/nbha4118344openalex-snapshot
Detection of Volatile Aroma Compounds of Morchella by Headspace Gas Chromatography Mass Spectrometry (HS-GC/MS)
inferred← citeshttps://doi.org/10.20289/zfdergi.1072006openalex-snapshot
Farklı bölgelerden toplanan Morchella sp. cinsi mantarların askokarplarında ve toprakta besin elementi kapsamları
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2002834/v1openalex-snapshot
Notes on the morels of South America with comments on their anamorphs
inferred← citeshttps://doi.org/10.21324/dacd.770921openalex-snapshot
Orman Yangınlarının Kuzugöbeği Mantarının (Morchella spp.) Çoğalması Üzerine Etkilerinin Araştırılması: Giresun, Alucra Örneği
inferred← citeshttps://doi.org/10.30550/j.lil/2022.59.1/2022.05.09openalex-snapshot
Nuevo registro de Morchella esculenta (Ascomycota, Pezizales) para la selva paranaense
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1286501openalex-snapshot
Cytological studies reveal high variation in ascospore number and shape and conidia produced directly from ascospores in Morchella galilaea
inferred← citeshttps://doi.org/10.3390/genes13101806openalex-snapshot
DNA Barcoding and Species Classification of Morchella
inferred← citeshttps://doi.org/10.3390/horticulturae10101020openalex-snapshot
Isolation and Molecular Identification of the Pure Culture of Morchella Collected from Türkiye and Its Characteristics
inferred← citeshttps://doi.org/10.3390/horticulturae10121287openalex-snapshot
Whole-Genome Resequencing and Evolutionary Analysis of Wild Morel Mushroom Morchella sp.
inferred← citeshttps://doi.org/10.3390/ijms19092525openalex-snapshot
Opposite Polarity Monospore Genome De Novo Sequencing and Comparative Analysis Reveal the Possible Heterothallic Life Cycle of Morchella importuna
inferred← citeshttps://doi.org/10.3390/jof8090926openalex-snapshot
Unravelling the French National Fungal Database: Geography, Temporality, Taxonomy and Ecology of the Recorded Diversity
inferred← citeshttps://doi.org/10.3390/molecules23092331openalex-snapshot
Validation of Internal Control Genes for Quantitative Real-Time PCR Gene Expression Analysis in Morchella
inferred← citeshttps://doi.org/10.3767/persoonia.2017.39.09openalex-snapshot
A synopsis of the saddle fungi (Helvella: Ascomycota) in Europe – species delimitation, taxonomy and typification
inferred← citeshttps://doi.org/10.3852/11-375openalex-snapshot
Taxonomic revision of true morels ( Morchella ) in Canada and the United States
inferred← citeshttps://doi.org/10.3852/12-056openalex-snapshot
How well do ITS rDNA sequences differentiate species of true morels ( Morchella )?
inferred← citeshttps://doi.org/10.3852/13-065openalex-snapshot
Morchella australianasp. nov., an apparent Australian endemic from New South Wales and Victoria
inferred← citeshttps://doi.org/10.3852/14-166openalex-snapshot
True morels (Morchella, Pezizales) of Europe and North America: evolutionary relationships inferred from multilocus data and a unified taxonomy
inferred← citeshttps://doi.org/10.3852/14-207openalex-snapshot
Mitospore stages of Disciotis, Gyromitra and Morchella in the inland Pacific Northwest USA
inferred← citeshttps://doi.org/10.3852/15-149openalex-snapshot
Two new species of true morels from Newfoundland and Labrador: cosmopolitan Morchella eohespera and parochial M. laurentiana
inferred← citeshttps://doi.org/10.3852/16-100openalex-snapshot
Multilocus phylogenetic and coalescent-based methods reveal dilemma in generic limits, cryptic species, and a prevalent intercontinental disjunct distribution in Geopyxis (Pyronemataceae s. l., Pezizomycetes).
inferred← citeshttps://doi.org/10.3897/mycokeys.52.32335openalex-snapshot
How useful is the current species recognition concept for the determination of true morels? Insights from the Czech Republic
inferred← citeshttps://doi.org/10.46309/biodicon.2023.1252319openalex-snapshot
A macrofungus taxon that is commonly eaten by the folk in Central Anatolia but never reported from Türkiye: Agaricus gennadii var. microsporus (Bohus) Wasser
inferred← citeshttps://doi.org/10.47371/mycosci.2022.08.005openalex-snapshot
Morchella nipponensis sp. nov. (Ascomycota, Pezizales): a paleoendemic species of section Morchella discovered in Japan
inferred← citeshttps://doi.org/10.5248/130.215openalex-snapshot
Morchella galilaea, an autumn species from Turkey
inferred← citeshttps://doi.org/10.5248/131.467openalex-snapshot
Four new morel (Morchella) species in the elata subclade (M. sect. Distantes) from Turkey
inferred← citeshttps://doi.org/10.5248/133.201openalex-snapshot
First record of Morchella pulchella from Pakistan
inferred← citeshttps://doi.org/10.53516/ajfr.1802609openalex-snapshot
New provincial record and habitat characterization of the endangered Morel Morchella steppicola Zerova (Ascomycota) in Çankırı, Turkey
inferred← citeshttps://doi.org/10.5586/am.1094openalex-snapshot
Two species of true morels (the genus Morchella, Ascomycota) recorded in the Ojców National Park (south Poland)
inferred← citeshttps://doi.org/10.5943/cream/9/1/11openalex-snapshot
Morchella tridentina (Ascomycota) from southwestern Turkey based on morphological and molecular evidences
inferred← citeshttps://doi.org/10.6092/issn.2531-7342/9374openalex-snapshot
Morels on the sand dunes of the Emilia-Romagna coast (Northwestern Adriatic Sea, Italy)
inferred← citeshttps://doi.org/10.7287/peerj.7744v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Microbial communities associated with the black morel Morchella sextelata cultivated in greenhouses (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7744v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Microbial communities associated with the black morel Morchella sextelata cultivated in greenhouses (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7744v0.1/reviews/4openalex-snapshot
Peer Review #4 of "Microbial communities associated with the black morel Morchella sextelata cultivated in greenhouses (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7744v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Microbial communities associated with the black morel Morchella sextelata cultivated in greenhouses (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.7744v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Microbial communities associated with the black morel Morchella sextelata cultivated in greenhouses (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.7744openalex-snapshot
Microbial communities associated with the black morel Morchella sextelata cultivated in greenhouses
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