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Host conservatism or host specialization? Patterns of fungal diversification are influenced by host plant specificity inOphiognomonia(Gnomoniaceae: Diaporthales)

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What this work says

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

inferredcites →https://doi.org/10.5061/dryad.74sk3zenodo-depositor-declared

Data from: Host conservatism or host specialization? Patterns of fungal diversification are influenced by host plant specificity in Ophiognomonia (Gnomoniaceae, Diaporthales)

inferredcites →https://doi.org/10.1006/mpev.2000.0888openalex-snapshot

Evolutionary Assembly of the Milkweed Fauna: Cytochrome Oxidase I and the Age of TetraopesBeetles

inferredcites →https://doi.org/10.1007/s10267-007-0347-7openalex-snapshot

A review of the phylogeny and biology of the Diaporthales

inferredcites →https://doi.org/10.1007/s10658-007-9148-2openalex-snapshot

Role of host specificity in the speciation of Ascochyta pathogens of cool season food legumes

inferredcites →https://doi.org/10.1007/s13225-011-0108-yopenalex-snapshot

Occultocarpon, a new monotypic genus of Gnomoniaceae on Alnus nepalensis from China

inferredcites →https://doi.org/10.1007/s13225-012-0200-yopenalex-snapshot

Phylogeny and taxonomy of Ophiognomonia (Gnomoniaceae, Diaporthales), including twenty-five new species in this highly diverse genus

inferredcites →https://doi.org/10.1016/j.fgb.2008.02.001openalex-snapshot

Speciation in fungi

inferredcites →https://doi.org/10.1016/j.funbio.2010.10.007openalex-snapshot

Reclassification of the butternut canker fungus, Sirococcus clavigignenti-juglandacearum, into the genus Ophiognomonia

inferredcites →https://doi.org/10.1016/j.mycres.2007.03.013openalex-snapshot

The type species of Apiognomonia, A. veneta, with its Discula anamorph is distinct from A. errabunda

inferredcites →https://doi.org/10.1016/j.mycres.2007.03.021openalex-snapshot

Phylogenetic placement and taxonomic review of the genus Cryptosporella and its synonyms Ophiovalsa and Winterella (Gnomoniaceae, Diaporthales)

inferredcites →https://doi.org/10.1016/j.tim.2011.11.006openalex-snapshot

Host specificity determinants as a genetic continuum

inferredcites →https://doi.org/10.1016/j.ympev.2012.05.005openalex-snapshot

New molecular markers for fungal phylogenetics: Two genes for species-level systematics in the Sordariomycetes (Ascomycota)

inferredcites →https://doi.org/10.1073/pnas.0607968104openalex-snapshot

Phylogenetic signal in plant pathogen–host range

inferredcites →https://doi.org/10.1086/285902openalex-snapshot

The Red Queen Beats the Jack-Of-All-Trades: The Limitations on the Evolution of Phenotypic Plasticity and Niche Breadth

inferredcites →https://doi.org/10.1086/286195openalex-snapshot

Red Queen Meets Santa Rosalia: Arms Races and the Evolution of Host Specialization in Organisms with Parasitic Lifestyles

inferredcites →https://doi.org/10.1086/314179openalex-snapshot

Genetic Isolation among Host Races of the Anther Smut Fungus Microbotryum violaceum on Three Host Plant Species

inferredcites →https://doi.org/10.1086/345091openalex-snapshot

Explaining Species Richness from Continents to Communities: The Time‐for‐Speciation Effect in Emydid Turtles

inferredcites →https://doi.org/10.1086/645087openalex-snapshot

Inverse‐Gene‐for‐Gene Infection Genetics and Coevolutionary Dynamics

inferredcites →https://doi.org/10.1093/ajcp/15.11.552bopenalex-snapshot

Statistical Methods for Research Workers

inferredcites →https://doi.org/10.1093/bioinformatics/14.9.817openalex-snapshot

MODELTEST: testing the model of DNA substitution.

inferredcites →https://doi.org/10.1093/oso/9780198505235.001.0001openalex-snapshot

The Ecology of Adaptive Radiation

inferredcites →https://doi.org/10.1094/phyto-70-1042openalex-snapshot

Genetics of Pathogenicity inPuccinia coronata:Pathogenic Specialization at the Host Genus Level

inferredcites →https://doi.org/10.1094/phyto-96-0280openalex-snapshot

Importance of the Life Cycle in Sympatric Host Race Formation and Speciation of Pathogens

inferredcites →https://doi.org/10.1098/rspb.2001.1801openalex-snapshot

The niche of higher plants: evidence for phylogenetic conservatism

inferredcites →https://doi.org/10.1101/sqb.1957.022.01.039openalex-snapshot

Concluding Remarks

inferredcites →https://doi.org/10.1111/j.0014-3820.2001.tb01271.xopenalex-snapshot

PATTERNS OF ASSOCIATION BETWEEN CRUCIFERS AND THEIR FLOWER-MIMIC PATHOGENS: HOST JUMPS ARE MORE COMMON THAN COEVOLUTION OR COSPECIATION

inferredcites →https://doi.org/10.1111/j.1096-0031.1993.tb00234.xopenalex-snapshot

ON OUTGROUPS

inferredcites →https://doi.org/10.1111/j.1365-2699.2011.02532.xopenalex-snapshot

Spatial evolutionary and ecological vicariance analysis (SEEVA), a novel approach to biogeography and speciation research, with an example from Brazilian Gentianaceae

inferredcites →https://doi.org/10.1111/j.1420-9101.2007.01462.xopenalex-snapshot

Sympatric genetic differentiation of a generalist pathogenic fungus, Botrytis cinerea, on two different host plants, grapevine and bramble

inferredcites →https://doi.org/10.1111/j.1461-0248.2010.01515.xopenalex-snapshot

Niche conservatism as an emerging principle in ecology and conservation biology

inferredcites →https://doi.org/10.1111/j.1466-822x.2004.00107.xopenalex-snapshot

Ecological niches as stable distributional constraints on mammal species, with implications for Pleistocene extinctions and climate change projections for biodiversity

inferredcites →https://doi.org/10.1111/j.1469-8137.2009.02927.xopenalex-snapshot

Continua of specificity and virulence in plant host–pathogen interactions: causes and consequences

inferredcites →https://doi.org/10.1111/j.1558-5646.1989.tb04220.xopenalex-snapshot

ANALYZING TABLES OF STATISTICAL TESTS

inferredcites →https://doi.org/10.1111/j.1558-5646.2012.01578.xopenalex-snapshot

TWO-STEP INFECTION PROCESSES CAN LEAD TO COEVOLUTION BETWEEN FUNCTIONALLY INDEPENDENT INFECTION AND RESISTANCE PATHWAYS

inferredcites →https://doi.org/10.1126/science.285.5431.1265openalex-snapshot

Conservatism of Ecological Niches in Evolutionary Time

inferredcites →https://doi.org/10.1146/annurev.ecolsys.36.102803.095431openalex-snapshot

Niche Conservatism: Integrating Evolution, Ecology, and Conservation Biology

inferredcites →https://doi.org/10.1186/1471-2148-8-100openalex-snapshot

Cophylogeny of the anther smut fungi and their caryophyllaceous hosts: Prevalence of host shifts and importance of delimiting parasite species for inferring cospeciation

inferredcites →https://doi.org/10.2307/3760218openalex-snapshot

Discula destructiva sp. nov., Cause of Dogwood Anthracnose

inferredcites →https://doi.org/10.3114/sim.2008.62.01openalex-snapshot

Leaf-inhabiting genera of the Gnomoniaceae, Diaporthales

inferredcites →https://doi.org/10.3114/sim.2011.68.10openalex-snapshot

A systematic account of the genus Plagiostoma (Gnomoniaceae, Diaporthales) based on morphology, host-associations, and a four-gene phylogeny

inferredcites →https://doi.org/10.3852/10-002openalex-snapshot

Systematics of genus Gnomoniopsis (Gnomoniaceae, Diaporthales) based on a three gene phylogeny, host associations and morphology

inferredcites →https://doi.org/10.3852/10-134openalex-snapshot

New species, phylogeny, host-associations and geographic distribution of genusCryptosporella(Gnomoniaceae, Diaporthales)

inferredcites →https://doi.org/10.5860/choice.35-4489openalex-snapshot

The plant-book: a portable dictionary of the vascular plants...

What points at this work

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

inferred← citeshttps://doi.org/10.1007/978-3-031-71344-6_14openalex-snapshot

Foliar Endophytic Fungi from Geum peckii in Canada

inferred← citeshttps://doi.org/10.1007/978-3-319-89833-9_2openalex-snapshot

Dimensions of Host Specificity in Foliar Fungal Endophytes

inferred← citeshttps://doi.org/10.1007/s11557-019-01484-4openalex-snapshot

Muyocopron heveae sp. nov. and M. dipterocarpi appears to have host-jumped to rubber

inferred← citeshttps://doi.org/10.1007/s11692-018-9449-8openalex-snapshot

Ecological and Ecomorphological Specialization Are Not Associated with Diversification Rates in Muroid Rodents (Rodentia: Muroidea)

inferred← citeshttps://doi.org/10.1007/s13225-014-0297-2openalex-snapshot

Insights into the genus Diaporthe: phylogenetic species delimitation in the D. eres species complex

inferred← citeshttps://doi.org/10.1016/j.myc.2018.08.001openalex-snapshot

Pathogenicity and taxonomy of Tenuignomonia styracis gen. et sp. nov., a new monotypic genus of Gnomoniaceae on Styrax obassia in Japan

inferred← citeshttps://doi.org/10.1080/00275514.2018.1516969openalex-snapshot

New species and records of Coryneum from China

inferred← citeshttps://doi.org/10.1093/biolinnean/blx043openalex-snapshot

Cladal divergence in fungal Ophiognomonia (Gnomoniaceae: Diaporthales) shows evidence of climatic niche vicariance

inferred← citeshttps://doi.org/10.1093/gbe/evu285openalex-snapshot

More than Skin Deep: Functional Genomic Basis for Resistance to Amphibian Chytridiomycosis

inferred← citeshttps://doi.org/10.1111/efp.12161openalex-snapshot

Recent insights into the pandemic disease butternut canker caused by the invasive pathogen O phiognomonia clavigignenti‐juglandacearum

inferred← citeshttps://doi.org/10.1111/plb.13569openalex-snapshot

Divergent rainforest tree microbiomes between phases of the monsoon cycle, host plants and tissues

inferred← citeshttps://doi.org/10.1139/cjz-2013-0097openalex-snapshot

Re-evaluating niche conservatism versus divergence in the Woodland Salamander genus Plethodon: a case study of the parapatric members of the Plethodon glutinosus species complex

inferred← citeshttps://doi.org/10.12705/636.16openalex-snapshot

Plant diversification in the Espinhaço Range: Insights from the biogeography of Minaria (Apocynaceae)

inferred← citeshttps://doi.org/10.3390/f16040627openalex-snapshot

Identification of the Nut Rot Pathogen Affecting Castanopsis carlesii Based on Morphological and Phylogenetic Analyses

inferred← citeshttps://doi.org/10.3390/jof8080770openalex-snapshot

Morphological and Phylogenetic Analyses Reveal Four New Species of Gnomoniopsis (Gnomoniaceae, Diaporthales) from China

inferred← citeshttps://doi.org/10.3390/plants10051026openalex-snapshot

Foliar Endophytic Fungi from the Endangered Eastern Mountain Avens (Geum peckii, Rosaceae) in Canada

inferred← citeshttps://doi.org/10.3767/003158514x682395openalex-snapshot

Fungal Planet description sheets: 214–280

inferred← citeshttps://doi.org/10.3852/14-353openalex-snapshot

Diversity of Diaporthe species associated with wood cankers of fruit and nut crops in northern California

inferred← citeshttps://doi.org/10.3897/mycokeys.60.46395openalex-snapshot

Taxonomy of two synnematal fungal species from Rhus chinensis, with Flavignomonia gen. nov. described

inferred← citeshttps://doi.org/10.3897/mycokeys.69.54012openalex-snapshot

Tree inhabiting gnomoniaceous species from China, with Cryphogonomonia gen. nov. proposed

inferred← citeshttps://doi.org/10.7717/peerj.573openalex-snapshot

Phylogenetic congruence of lichenised fungi and algae is affected by spatial scale and taxonomic diversity

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