References
- Bright DE, Skidmore RE. A catalogue of Scolytidae and Platypodidae (Coleoptera), Supplement 2 (1995-1999). Ottawa: NRC Research Press; 2002.
- Van der Walt JP. The yeast genus Ambrosiozyma gen. nov. (Ascomycetes). Mycopathol Mycol Appl 1972;46:305-16. https://doi.org/10.1007/BF02052126
- Batra LR. Ambrosia fungi: a taxonomic revision, and nutritional studies of some species. Mycologia 1967;59:976-1017. https://doi.org/10.2307/3757271
- Funk A. Fungal symbionts of the ambrosia beetle Gnathotrichus sulcatus. Can J Bot 1970;48:1445-8. https://doi.org/10.1139/b70-217
- Furniss RL, Carolin VM. Western forest insects. Miscellaneous publication No. 1339. Washington, DC: US Department of Agriculture, Forest Service; 1977.
- Gimenez RA, Etiennot AE. Host range of Platypus mutatus (Chapois, 1865) (Coleoptera: Platypodidae). Entomotropica 2003;18:89-94.
- Babuder G, Pohleven F. Fungal succession in the tunnels of ambrosia beetles in oak wood (Quercus sp.). Res Rep For Wood Sci Technol 1995;47:241-54.
- Ito S. Mass mortality of Quercus species (Fagaceae)-mystery in symbiotic relationships between fungi and ambrosia beetle. Nishi Nippon Branch Mycol Soc Jpn 2000;10:16-22.
- Kaneko S. Mass death of oaks in Japan. In: IUFRO XX World Congress; 1995 Aug 6-12; Tampere, Finland.
- Masuya H, Kaneko S, Yamaoka Y. A new Ophiostoma species isolated from Japanese oak infested by Platypus quercivorus. Mycoscience 1998;39:347-50. https://doi.org/10.1007/BF02464020
- Murata M, Yamada T, Matsuda Y, Ito S. Discoloured and non-conductive sapwood among six Fagaceae species inoculated with Raffaelea quercivora. For Pathol 2007;37:73-9. https://doi.org/10.1111/j.1439-0329.2007.00480.x
- Kinuura H, Kobayashi M. Death of Quercus crispula by inoculation with adult Platypus quercivorus (Coleoptera: Platypodidae). Appl Entomol Zool 2006;41:123-8. https://doi.org/10.1303/aez.2006.123
- Hong KJ, Kwon YD, Park SW, Lyu DP. Platypus koryoensis (Murayama)(Platypodidae: Coleoptera), the vector of oak wilt disease. Korean J Appl Entomol 2006;45:113-7.
- Beaver RA. Insect-fungus relationships in the bark and ambrosia beetles. In: Wilding N, Collins NM, Hammond PM, Webber JF, editors. Insect-fungus interactions. London: Academic Press; 1989. p. 121-43.
- Paine TD, Raffa KF, Harrington TC. Interactions among scolytid bark beetles, their associated fungi, and live host conifers. Annu Rev Entomol 1997;42:179-206. https://doi.org/10.1146/annurev.ento.42.1.179
- Kim KH, Choi YJ, Seo ST, Shin HD. Raffaelea quercusmongolicae sp. nov. associated with Platypus koryoensis on oak in Korea. Mycotaxon 2009;110:189-97. https://doi.org/10.5248/110.189
- Torii M, Matsuda Y, Seo ST, Kim KH, Ito S, Moon MJ, Kim SH, Yamada T. The effect of Raffaelea quercus-mongolicae inoculations on the formation of non-conductive sapwood of Quercus mongolica. Mycobiology 2014;42:210-4. https://doi.org/10.5941/MYCO.2014.42.2.210
- Suh DY, Hyun MW, Choi IJ, Kim SH, Seo ST, Kim KH. Filamentous fungi and yeasts isolated from Platypus koryoensis and the beetle infested oak tree in Korea. In: Proceeding of Asian Mycological Congress 2011 & The 12th International Marine and Freshwater Mycology Symposium; 2011 Aug 7- 11; Incheon, Korea. Seoul: The Korean Society of Mycology; 2011. p. 196.
- Suh DY, Hyun MW, Kim SH, Seo ST, Kim KH. Filamentous fungi isolated from Platypus koryoensis, the insect vector of oak wilt disease in Korea. Mycobiology 2014;39:313-6.
- Muller FM, Werner KE, Kasai M, Francesconi A, Chanock SJ, Walsh TJ. Rapid extraction of genomic DNA from medically important yeasts and filamentous fungi by high-speed cell disruption. J Clin Microbiol 1998;36:1625-9.
- White TJ, Bruns T, Lee S, Taylor J. Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In: Innis MA, Gelfand DH, Sninsky JJ, White TJ, editors. PCR protocols: a guide to methods and applications. New York: Academic Press; 1990. p. 315-22.
- O'Donnell K, Nirenberg HI, Aoki T, Cigelnik E. A multigene phylogeny of the Gibberella fujikuroi species complex: detection of additional phylogenetically distinct species. Mycoscience 2000;41:61-78. https://doi.org/10.1007/BF02464387
- Swofford DL. Paup*: phylogenetic analysis using parsimony (*and other methods). Ver. 4.0. B5. Sunderland (MA): Sinauer Associates; 2001.
- Kimura M. A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. J Mol Evol 1980;16:111-20. https://doi.org/10.1007/BF01731581
- Yoon JH, Park JE, Suh DY, Hong SB, Ko SJ, Kim SH. Comparison of dyes for easy detection of extracellular cellulases in fungi. Mycobiology 2007;35:21-4. https://doi.org/10.4489/MYCO.2007.35.1.021
- van der Walt JP, Nakase T. Candida homilentoma, a new yeast from South African insect sources. Antonie Van Leeuwenhoek 1973;39:449-53. https://doi.org/10.1007/BF02578887
- Kurtzman CP, Fell JW, Boekhout T. The yeasts: a taxonomic study. 5th ed. London: Elsevier; 2011. p. 1107-8.
- Endoh R, Suzuki M, Benno Y. Pichia rarassimilans sp. nov., a novel yeast species isolated from body surface of the ambrosia beetle Platypus quercivorus. J Gen Appl Microbiol 2008;54:181-6. https://doi.org/10.2323/jgam.54.181
- Endoh R, Suzuki M, Benno Y. Ambrosiozyma kamigamensis sp. nov. and A. neoplatypodis sp. nov., two new ascomycetous yeasts from ambrosia beetle galleries. Antonie Van Leeuwenhoek 2008;94:365-76. https://doi.org/10.1007/s10482-008-9253-z
- Endoh R, Suzuki M, Benno Y, Futai K. Candida kashinagacola sp. nov., C. pseudovanderkliftii sp. nov. and C. vanderkliftii sp. nov., three new yeasts from ambrosia beetle-associated sources. Antonie Van Leeuwenhoek 2008;94:389-402. https://doi.org/10.1007/s10482-008-9256-9
- Endoh R, Suzuki M, Okada G, Takeuchi Y, Futai K. Fungus symbionts colonizing the galleries of the ambrosia beetle Platypus quercivorus. Microb Ecol 2011;62:106-20. https://doi.org/10.1007/s00248-011-9838-3
- Suh DY, Kim SH, Son SY, Seo ST, Kim KH. A new record of Candida kashinagacola (synonym Ambrosiozyma kashinagacola) from galleries of Platypus koryoensis, the oak wilt disease vector, in Korea. Mycobiology 2013;41:245-7. https://doi.org/10.5941/MYCO.2013.41.4.245