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Words near each other
・ Armin, Prince of Lippe
・ Armillaria camerunensis
・ Armillaria cepistipes
・ Armillaria duplicata
・ Armillaria ectypa
・ Armillaria fellea
・ Armillaria fumosa
・ Armillaria fuscipes
・ Armillaria gallica
・ Armillaria gemina
・ Armillaria griseomellea
・ Armillaria heimii
・ Armillaria hinnulea
・ Armillaria jezoensis
・ Armillaria limonea
Armillaria luteobubalina
・ Armillaria mellea
・ Armillaria melleorubens
・ Armillaria montagnei
・ Armillaria nabsnona
・ Armillaria novae-zelandiae
・ Armillaria omnituens
・ Armillaria pallidula
・ Armillaria paulensis
・ Armillaria pelliculata
・ Armillaria procera
・ Armillaria puiggarii
・ Armillaria root rot
・ Armillaria sinapina
・ Armillaria singula


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Armillaria luteobubalina : ウィキペディア英語版
Armillaria luteobubalina

''Armillaria luteobubalina'', commonly known as the Australian honey fungus, is a species of mushroom in the family Physalacriaceae. Widely distributed in southern Australia, the fungus is responsible for a disease known as ''Armillaria'' root rot, a primary cause of ''Eucalyptus'' tree death and forest dieback. It is the most pathogenic and widespread of the six ''Armillaria'' species found in Australia. The fungus has also been collected in Argentina and Chile. Fruit bodies have cream- to tan-coloured caps that grow up to in diameter and stems that measure up to long by thick. The fruit bodies, which appear at the base of infected trees and other woody plants in autumn (March–April), are edible, but require cooking to remove the bitter taste. The fungus is dispersed through spores produced on gills on the underside of the caps, and also by growing vegetatively through the root systems of host trees. The ability of the fungus to spread vegetatively is facilitated by an aerating system that allows it to efficiently diffuse oxygen through rhizomorphs—rootlike structures made of dense masses of hyphae.
''Armillaria luteobubalina'' was first described in 1978, after having been discovered several years earlier growing in a ''Eucalyptus'' plantation in southeastern Australia. It distinguished itself from other known Australian ''Armillaria'' species by its aggressive pathogenicity. It may take years for infected trees to show signs of disease, leading to an underestimation of disease prevalence. Studies show that the spread of disease in eucalypt forests is associated with infected stumps left following logging operations. Although several methods have been suggested to control the spread of disease, they are largely economically or environmentally unfeasible. Phylogenetic analyses have determined that ''A. luteobubalina'' is closely related to ''A. montagnei'' and that both of these species are in turn closely related to the Brazilian species ''A. paulensis''. The distribution of ''A. luteobubalina'' suggests that it is an ancient species that originated before the separation of the precursor supercontinent Gondwana.
== History and phylogeny ==
''Armillaria luteobubalina'' was first described in 1978 by mycologists Roy Watling and Glen Kile, who studied its effects on a fast-growing plantation of ''Eucalyptus regnans'' near Traralgon, Victoria. The plantation, established in 1963, consisted largely of trees with a mean height of about . A cluster of dead and dying trees discovered in 1973 suggested attack by a virulent primary pathogen, that is, one capable of infecting a host before invasion by other, secondary pathogens. This finding was inconsistent with the pathogenic behaviour of the known ''Armillaria'' species in Australia at the time, ''A. mellea'' and ''A. elegans''. Further study over the next few years showed that the fungus spread by the growth of underground mycelia in root systems, expanding outward from the initial infected stump at an average of per year. Most Australian records of ''Armillaria'' infections referred to ''A. mellea'', based on the presence of black rhizomorphs.〔 For over one hundred years, ''A. mellea'' was thought to be a pleiomorphic (occurring in various distinct forms) species with a widespread distribution and host range, and variable pathogenicity.〔 which led to great confusion among taxonomists and plant pathologists alike.〔 In 1973, Veikko Hintikka reported a technique to distinguish between ''Armillaria'' species by growing them together as single spore isolates on petri dishes and observing changes in the morphology of the cultures.〔 Using similar techniques, mycologists eventually determined that the ''Armillaria mellea'' species complex in Europe and North America in fact consisted of five and ten distinct "biological species", respectively.〔〔
Watling and Kile compared the macroscopic and microscopic characters of the pathogenic ''Armillaria'' with ''A. polymyces'' (now known as ''A. obscura''), ''A. mellea'', ''A. limonea'' and ''A. novae-zelandiae'' and found sufficient differences between them to warrant designating the species as new. Its specific epithet is derived from the Latin ''lutea'' "yellow", and was chosen to highlight an important distinguishing characteristic: the strong yellow colour of the cap and lack of reddish or brown tones in the stem typical of other resident ''Armillaria''.〔
A phylogenetic study of South American ''Armillaria'' species concluded that ''A. luteobubalina'' is in a lineage that includes ''A. montagnei'', and these are sister to a lineage containing ''A. paulensis'',〔 a species known from a single specimen collected in São Paulo, Brazil.〔 Although they are very similar, specimens of ''A. luteobubalina'' have smaller spores than Argentinian specimens of ''A. montagnei'', and their distinctness is well-supported with phylogenetic analysis.〔 Based on analysis of pectic enzymes, ''A. luteobubalina'' is closely related to ''A. limonea'', a species found in New Zealand;〔 this result corroborates phylogenetic analyses reported in 2003〔 and 2006.〔 Molecular analysis of 27 collections of ''A. luteobubalina'' from southwest Western Australia and one from Traralgon revealed four distinct polymorphic groups. The genetic variety suggests it is native to Australia.〔

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