58 results on '"Coleine C"'
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2. Global consortium for the classification of fungi and fungus-like taxa
- Author
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Hyde, K.D., Abdel-Wahab, M.A., Abdollahzadeh, J., Abeywickrama, P.D., Absalan, S., Afshari, N., Ainsworth, A.M., Akulov, O.Y., Aleoshin, V.V., Al-Sadi, A.M., Alvarado, P., Alves, A., Alves-Silva, G., Amalfi, M., Amira, Y., Amuhenage, T.B., Anderson, J., Antonín, V., Aouali, S., Aptroot, A., Apurillo, C.C.S., Araújo, J.P.M., Ariyawansa, H.A., Armand, A., Arumugam, E., Asghari, R., Assis, D.M.A., Atienza, V., Avasthi, S., Azevedo, E., Bahkali, A.H., Bakhshi, M., Banihashemi, Z., Bao, D.F., Baral, H.O., Barata, M., Barbosa, F., Barbosa, R.N., Barreto, R.W., Baschien, C., Belamesiatseva, D.B., Bennett Reuel, M., Bera, I., Bezerra, J.D.P., Bezerra, J.L., Bhat, D.J., Bhunjun, C.S., Bianchinotti, M.V., Błaszkowski, J., Blondelle, A., Boekhout, T., Bonito, G., Boonmee, S., Boonyuen, N., Bregant, C., Buchanan, P., Bundhun, D., Burgaud, G., Burgess, T., Buyck, B., Cabarroi-Hernández, M., Cáceres, M.E.S., Caeiro, M.F., Cai, L., Cai, M.F., Calabon, M.S., Calaça, F.J.S., Callalli, M., Camara, M.P.S., Cano-Lira, J.F., Cantillo, T., Cao, B., Carlavilla, J.R., Carvalho, A., Castañeda-Ruiz, R.F., Castlebury, L., Castro-Jauregui, O., Catania, M.D.V., Cavalcanti, L.H., Cazabonne, J., Cedeño-Sanchez, M.L., Chaharmiri-Dokhaharani, S., Chaiwan, N., Chakraborty, N., Chaverri, P., Cheewangkoon, R., Chen, C., Chen, C.Y., Chen, K.H., Chen, J., Chen, Q., Chen, W.H., Chen, Y.P., Chethana, K.W.T., Coleine, C., Condé, T.O., Corazon-Guivin, M.A., Cortés-Pérez, A., Costa-Rezende, D.H., Courtecuisse, R., Crouch, J.A., Crous, P.W., Cui, B.K., Cui, Y.Y., da Silva, D.K.A., da Silva, G.A., da Silva, I.R., da Silva, R.M.F., da Silva Santos, A.C., Dai, D.Q., Dai, Y.C., Damm, U., Darmostuk, V., Daroodi, Z., Das, K., Davoodian, N., Davydov, E.A., Dayarathne, M.C., Decock, C., de Groot, M.D., De Kesel, A., dela Cruz, T.E.E., De Lange, R., Delgado, G., Denchev, C.M., Denchev, T.T., de Oliveira, N.T., de Silva, N.I., de Souza, F.A., Dentinger, B., Devadatha, B., Dianese, J.C., Dima, B., Diniz, A.G., Dissanayake, A.J., Dissanayake, L.S., Doğan, H.H., Doilom, M., Dolatabadi, S., Dong, W., Dong, Z.Y., Dos Santos, L.A., Drechsler-Santos, E.R., Du, T.Y., Dubey, M.K., Dutta, A.K., Egidi, E., Elliott, T.F., Elshahed, M.S., Erdoğdu, M., Ertz, D., Etayo, J., Evans, H.C., Fan, X.L., Fan, Y.G., Fedosova, A.G., Fell, J., Fernandes, I., Firmino, A.L., Fiuza, P.O., Flakus, A., Fragoso de Souza, C.A., Frisvad, J.C., Fryar, S.C., Gabaldón, T., Gajanayake, A.J., Galindo, L.J., Gannibal, P.B., García, D., García-Sandoval, S.R., Garrido-Benavent, I., Garzoli, L., Gautam, A.K., Ge, Z.W., Gené, D.J., Gentekaki, E., Ghobad-Nejhad, M., Giachini, A.J., T.b., Gibertoni, Góes-Neto, A., Gomdola, D., Gomes de Farias, A.R., Gorjón, S.P., Goto, B.T., Granados-Montero, M.M., Griffith, G.W., Groenewald, J.Z., Groenewald, M., Grossart, H.P., Gueidan, C., Gunarathne, A., Gunaseelan, S., Gusmão, L.F.P., Gutierrez, A.C., Guzmán-Dávalos, L., Haelewaters, D., Halling, R., Han, Y.F., Hapuarachchi, K.K., Harder, C.B., Harrington, T.C., Hattori, T., He, M.Q., He, S., He, S.H., Healy, R., Herández-Restrepo, M., Heredia, G., Hodge, K.T., Holgado-Rojas, M., Hongsanan, S., Horak, E., Hosoya, T., Houbraken, J., Huang, S.K., Huanraluek, N., Hur, J.S., Hurdeal, V.G., Hustad, V.P., Iotti, M., Iturriaga, T., Jafar, E., Janik, P., Jayalal, R.G.U., Jayasiri, S.C., Jayawardena, R.S., Jeewon, R., Jerônimo, G.H., Jesus, A.L., Jin, J., Johnston, P.R., Jones, E.B.G., Joshi, Y., Justo, A., Kaishian, P., Kakishima, M., Kaliyaperumal, M., Kang, G.P., Kang, J.C., Karimi, O., Karpov, S.A., Karunarathna, S.C., Kaufmann, M., Kemler, M., Kezo, K., Khyaju, S., Kirchmair, M., Kirk, P.M., Kitaura, M.J., Klawonn, I., Kolarik, M., Kong, A., Kuhar, F., Kukwa, M., Kumar, S., Kušan, I., Lado, C., Larsson, K.H., Latha, K.P.D., Lee, H.B., Leonardi, M., Leontyev, D.L., Lestari, A.S., Li, C.J.Y., Li, D.W., Li, H., Li, H.Y., Li, L., Li, Q.R., Li, W.L., Li, Y., Li, Y.C., Liao, C.F., Liimatainen, K., Lim, Y.W., Lin, C.G., Linaldeddu, B.T., Linde, C.C., Linn, M.M., Liu, F., Liu, J.K., Liu, N.G., Liu, S., Liu, S.L., Liu, X.F., Liu, X.Y., Liu, X.Z., Liu, Z.B., Lu, L., Lu, Y.Z., Luangharn, T., Luangsa-ard, J.J., Lumbsch, H.T., Lumyong, S., Luo, L., Luo, M., Luo, Z.L., Ma, J., Machado, A.R., Madagammana, A.D., Madrid, H., Magurno, F., Magyar, D., Mahadevan, N., Maharachchikumbura, S.S.N., Maimaiti, Y., Malosso, E., Manamgoda, D.S., Manawasinghe, I.S., Mapook, A., Marasinghe, D.S., Mardones, M., Marin-Felix, Y., Márquez, R., Masigol, H., Matočec, N., May, Tom W., McKenzie, E.H.C., Meiras-Ottoni, A., Melo, R.F.R., Mendes, A.R.L., Mendieta, S., Meng, Q.F., Menkis, A., Menolli, N Jr., Mešić, A., Meza Calvo, J.G., Mikhailov, K.V., Miller, S.L., Moncada, B., Moncalvo, J.M., Monteiro, J.S., Monteiro, M., Mora-Montes, H.M., Moreau, P.A., Mueller, G.M., Mukhopadyay, S., Murugadoss, R., Nagy, L.G., Najafiniya, M., Nanayakkara, C.M., Nascimento, C.C., Nei, Y., Neves, M.A., Neuhauser, S., Niego, A.G.T., Nilsson, R.H., Niskanen, T., Niveiro, N., Noorabadi, M.T., Noordeloos, M.E., Norphanphoun, C., Nuñez Otaño, N.B., O’Donnell, R.P., Oehl, F., Olariaga, I., Orlando, F.P., Pang, K.L., Papp, V., Pawłowska, J., Peintner, U., Pem, D., Pereira, Olinto Liparini, Perera, R.H., Perez-Moreno, J., Perez-Ortega, S., Péter, G., Phillips, A.J.L., Phonemany, M., Phukhamsakda, C., Phutthacharoen, K., Piepenbring, M., Pires-Zottarelli, C.L.A., Poinar, G., Pošta, A., Prieto, M., Promputtha, I., Quandt, C.A., Radek, R., Rahnama, K., Raj, K.N.A., Rajeshkumar, K.C., Rämä, Teppo, Rambold, G., Ramírez-Cruz, V., Rasconi, S., Rathnayaka, A.R., Raza, M., Ren, G.C., Robledo, G.L., Rodriguez-Flakus, P., Ronikier, A., Rossi, W., Ryberg, M., Ryvarden, L.R., Salvador-Montoya, C.A., Samant, B., Samarakoon, B.C., Samarakoon, M.C., Sánchez-Castro, I., Sánchez-García, M., Sandoval-Denis, M., Santiago, A.L.C.M.A., Santamaria, B., Santos, A.C.S., Sarma, V.V., Savchenko, A., Savchenko, K., Saxena, R.K., Scholler, M., Schoutteten, N., Seifollahi, E., Selbmann, Laura, Selcuk, F., Senanayake, I.C., Seto, K., Shabashova, T.G., Shen, H.W., Shen, Y.M., Silva-Filho, A.G.S., Simmons, D.R., Singh, R., Sir, E.B., Song, C.G., Souza-Motta C.M. Sruthi, O.P., Stadler, M., Stchigel, A.M., Stemler, J., Stephenson, S.L., Strassert, J.F.H., Su, H.L., Su, L., Suetrong, S., Sulistyo, B., Sun, Y.F., Sun, Y.R., Svantesson, S., Sysouphanthong, P., Takamatsu, S., Tan, T.H., Tanaka, Kazuaki, Tang, A.M.C., Tang, X., Tanney, J.B., Tavakol, N.M., Taylor, J.E., Taylor, P.W.J., Tedersoo, L., Tennakoon, D.S., Thamodini, G.K., Thines, Marco, Thiyagaraja, V., Thongklang, N., Tiago, P.V., Tian, Q., Tian, W.H., Tibell, L., Tibell, S., Tibpromma, S., Tkalčec, Z., Tomšovský, M., Toome-Heller, M., Torruella, G., Tsurykau, A., Udayanga, Dhanushka, Ulukapi, M., Untereiner, W.A., Uzunov, B.A., Valle, L.G., Van Caenegem, W., Van den Wyngaert, S., Van Vooren, N., Velez, P., Verma, R.K., Vieira, L.C., Vieira, W.A.S., Vizzini, A., Walker, A., Walker, A.K., Wanasinghe, D.N., Wang, C.G., Wang, K., Wang, S.X., Wang, X.Y., Wang, Y., Wannasawang, N., Wartchow, F., Wei, D.P., Wei, X.L., White, J.F., Wijayawardene, N.N., Wijesinghe, S.N., Wijesundara, D.S.A., Wisitrassameewong, K., Worthy, F.R., Wu, F., Wu, G., Wu, H.X., Wu, N., Wu, W.P., Wurzbacher, C., Xiao, Y.P., Xiong, Y.R., Xu, L.J., Xu, R., Xu, R.F., Xu, R.J., Xu, T.M., Yakovchenko, L., Yan, J.Y., Yang, H., Yang, J., Yang, Z.L., Yang, Y.H., Yapa, N., Yasanthika, E., Youssef, N.H., Yu, F.M., Yu, Q., Yu, X.D., Yu, Y.X., Yu, Z.F., Yuan, H.S., Yuan, Y., Yurkov, Andrey, Zafari, D., Zamora, Juan Carlos, Zare, Rasoul, Zeng, M., Zeng, N.K., Zeng, X.Y., Zhang, F., Zhang, H., Zhang, J.F., Zhang, J.Y., Zhang, Q.Y., Zhang, S.N., Zhang, W., Zhang, Y., Zhang, Y.X., Zhao, C.L., Zhao, H., Zhao, Q., Zhao, R.L., Zhou, L.W., Zhou, M., Zhurbenko, M.P., Zin, H.H., Zucconi, L., Hyde, K.D., Abdel-Wahab, M.A., Abdollahzadeh, J., Abeywickrama, P.D., Absalan, S., Afshari, N., Ainsworth, A.M., Akulov, O.Y., Aleoshin, V.V., Al-Sadi, A.M., Alvarado, P., Alves, A., Alves-Silva, G., Amalfi, M., Amira, Y., Amuhenage, T.B., Anderson, J., Antonín, V., Aouali, S., Aptroot, A., Apurillo, C.C.S., Araújo, J.P.M., Ariyawansa, H.A., Armand, A., Arumugam, E., Asghari, R., Assis, D.M.A., Atienza, V., Avasthi, S., Azevedo, E., Bahkali, A.H., Bakhshi, M., Banihashemi, Z., Bao, D.F., Baral, H.O., Barata, M., Barbosa, F., Barbosa, R.N., Barreto, R.W., Baschien, C., Belamesiatseva, D.B., Bennett Reuel, M., Bera, I., Bezerra, J.D.P., Bezerra, J.L., Bhat, D.J., Bhunjun, C.S., Bianchinotti, M.V., Błaszkowski, J., Blondelle, A., Boekhout, T., Bonito, G., Boonmee, S., Boonyuen, N., Bregant, C., Buchanan, P., Bundhun, D., Burgaud, G., Burgess, T., Buyck, B., Cabarroi-Hernández, M., Cáceres, M.E.S., Caeiro, M.F., Cai, L., Cai, M.F., Calabon, M.S., Calaça, F.J.S., Callalli, M., Camara, M.P.S., Cano-Lira, J.F., Cantillo, T., Cao, B., Carlavilla, J.R., Carvalho, A., Castañeda-Ruiz, R.F., Castlebury, L., Castro-Jauregui, O., Catania, M.D.V., Cavalcanti, L.H., Cazabonne, J., Cedeño-Sanchez, M.L., Chaharmiri-Dokhaharani, S., Chaiwan, N., Chakraborty, N., Chaverri, P., Cheewangkoon, R., Chen, C., Chen, C.Y., Chen, K.H., Chen, J., Chen, Q., Chen, W.H., Chen, Y.P., Chethana, K.W.T., Coleine, C., Condé, T.O., Corazon-Guivin, M.A., Cortés-Pérez, A., Costa-Rezende, D.H., Courtecuisse, R., Crouch, J.A., Crous, P.W., Cui, B.K., Cui, Y.Y., da Silva, D.K.A., da Silva, G.A., da Silva, I.R., da Silva, R.M.F., da Silva Santos, A.C., Dai, D.Q., Dai, Y.C., Damm, U., Darmostuk, V., Daroodi, Z., Das, K., Davoodian, N., Davydov, E.A., Dayarathne, M.C., Decock, C., de Groot, M.D., De Kesel, A., dela Cruz, T.E.E., De Lange, R., Delgado, G., Denchev, C.M., Denchev, T.T., de Oliveira, N.T., de Silva, N.I., de Souza, F.A., Dentinger, B., Devadatha, B., Dianese, J.C., Dima, B., Diniz, A.G., Dissanayake, A.J., Dissanayake, L.S., Doğan, H.H., Doilom, M., Dolatabadi, S., Dong, W., Dong, Z.Y., Dos Santos, L.A., Drechsler-Santos, E.R., Du, T.Y., Dubey, M.K., Dutta, A.K., Egidi, E., Elliott, T.F., Elshahed, M.S., Erdoğdu, M., Ertz, D., Etayo, J., Evans, H.C., Fan, X.L., Fan, Y.G., Fedosova, A.G., Fell, J., Fernandes, I., Firmino, A.L., Fiuza, P.O., Flakus, A., Fragoso de Souza, C.A., Frisvad, J.C., Fryar, S.C., Gabaldón, T., Gajanayake, A.J., Galindo, L.J., Gannibal, P.B., García, D., García-Sandoval, S.R., Garrido-Benavent, I., Garzoli, L., Gautam, A.K., Ge, Z.W., Gené, D.J., Gentekaki, E., Ghobad-Nejhad, M., Giachini, A.J., T.b., Gibertoni, Góes-Neto, A., Gomdola, D., Gomes de Farias, A.R., Gorjón, S.P., Goto, B.T., Granados-Montero, M.M., Griffith, G.W., Groenewald, J.Z., Groenewald, M., Grossart, H.P., Gueidan, C., Gunarathne, A., Gunaseelan, S., Gusmão, L.F.P., Gutierrez, A.C., Guzmán-Dávalos, L., Haelewaters, D., Halling, R., Han, Y.F., Hapuarachchi, K.K., Harder, C.B., Harrington, T.C., Hattori, T., He, M.Q., He, S., He, S.H., Healy, R., Herández-Restrepo, M., Heredia, G., Hodge, K.T., Holgado-Rojas, M., Hongsanan, S., Horak, E., Hosoya, T., Houbraken, J., Huang, S.K., Huanraluek, N., Hur, J.S., Hurdeal, V.G., Hustad, V.P., Iotti, M., Iturriaga, T., Jafar, E., Janik, P., Jayalal, R.G.U., Jayasiri, S.C., Jayawardena, R.S., Jeewon, R., Jerônimo, G.H., Jesus, A.L., Jin, J., Johnston, P.R., Jones, E.B.G., Joshi, Y., Justo, A., Kaishian, P., Kakishima, M., Kaliyaperumal, M., Kang, G.P., Kang, J.C., Karimi, O., Karpov, S.A., Karunarathna, S.C., Kaufmann, M., Kemler, M., Kezo, K., Khyaju, S., Kirchmair, M., Kirk, P.M., Kitaura, M.J., Klawonn, I., Kolarik, M., Kong, A., Kuhar, F., Kukwa, M., Kumar, S., Kušan, I., Lado, C., Larsson, K.H., Latha, K.P.D., Lee, H.B., Leonardi, M., Leontyev, D.L., Lestari, A.S., Li, C.J.Y., Li, D.W., Li, H., Li, H.Y., Li, L., Li, Q.R., Li, W.L., Li, Y., Li, Y.C., Liao, C.F., Liimatainen, K., Lim, Y.W., Lin, C.G., Linaldeddu, B.T., Linde, C.C., Linn, M.M., Liu, F., Liu, J.K., Liu, N.G., Liu, S., Liu, S.L., Liu, X.F., Liu, X.Y., Liu, X.Z., Liu, Z.B., Lu, L., Lu, Y.Z., Luangharn, T., Luangsa-ard, J.J., Lumbsch, H.T., Lumyong, S., Luo, L., Luo, M., Luo, Z.L., Ma, J., Machado, A.R., Madagammana, A.D., Madrid, H., Magurno, F., Magyar, D., Mahadevan, N., Maharachchikumbura, S.S.N., Maimaiti, Y., Malosso, E., Manamgoda, D.S., Manawasinghe, I.S., Mapook, A., Marasinghe, D.S., Mardones, M., Marin-Felix, Y., Márquez, R., Masigol, H., Matočec, N., May, Tom W., McKenzie, E.H.C., Meiras-Ottoni, A., Melo, R.F.R., Mendes, A.R.L., Mendieta, S., Meng, Q.F., Menkis, A., Menolli, N Jr., Mešić, A., Meza Calvo, J.G., Mikhailov, K.V., Miller, S.L., Moncada, B., Moncalvo, J.M., Monteiro, J.S., Monteiro, M., Mora-Montes, H.M., Moreau, P.A., Mueller, G.M., Mukhopadyay, S., Murugadoss, R., Nagy, L.G., Najafiniya, M., Nanayakkara, C.M., Nascimento, C.C., Nei, Y., Neves, M.A., Neuhauser, S., Niego, A.G.T., Nilsson, R.H., Niskanen, T., Niveiro, N., Noorabadi, M.T., Noordeloos, M.E., Norphanphoun, C., Nuñez Otaño, N.B., O’Donnell, R.P., Oehl, F., Olariaga, I., Orlando, F.P., Pang, K.L., Papp, V., Pawłowska, J., Peintner, U., Pem, D., Pereira, Olinto Liparini, Perera, R.H., Perez-Moreno, J., Perez-Ortega, S., Péter, G., Phillips, A.J.L., Phonemany, M., Phukhamsakda, C., Phutthacharoen, K., Piepenbring, M., Pires-Zottarelli, C.L.A., Poinar, G., Pošta, A., Prieto, M., Promputtha, I., Quandt, C.A., Radek, R., Rahnama, K., Raj, K.N.A., Rajeshkumar, K.C., Rämä, Teppo, Rambold, G., Ramírez-Cruz, V., Rasconi, S., Rathnayaka, A.R., Raza, M., Ren, G.C., Robledo, G.L., Rodriguez-Flakus, P., Ronikier, A., Rossi, W., Ryberg, M., Ryvarden, L.R., Salvador-Montoya, C.A., Samant, B., Samarakoon, B.C., Samarakoon, M.C., Sánchez-Castro, I., Sánchez-García, M., Sandoval-Denis, M., Santiago, A.L.C.M.A., Santamaria, B., Santos, A.C.S., Sarma, V.V., Savchenko, A., Savchenko, K., Saxena, R.K., Scholler, M., Schoutteten, N., Seifollahi, E., Selbmann, Laura, Selcuk, F., Senanayake, I.C., Seto, K., Shabashova, T.G., Shen, H.W., Shen, Y.M., Silva-Filho, A.G.S., Simmons, D.R., Singh, R., Sir, E.B., Song, C.G., Souza-Motta C.M. Sruthi, O.P., Stadler, M., Stchigel, A.M., Stemler, J., Stephenson, S.L., Strassert, J.F.H., Su, H.L., Su, L., Suetrong, S., Sulistyo, B., Sun, Y.F., Sun, Y.R., Svantesson, S., Sysouphanthong, P., Takamatsu, S., Tan, T.H., Tanaka, Kazuaki, Tang, A.M.C., Tang, X., Tanney, J.B., Tavakol, N.M., Taylor, J.E., Taylor, P.W.J., Tedersoo, L., Tennakoon, D.S., Thamodini, G.K., Thines, Marco, Thiyagaraja, V., Thongklang, N., Tiago, P.V., Tian, Q., Tian, W.H., Tibell, L., Tibell, S., Tibpromma, S., Tkalčec, Z., Tomšovský, M., Toome-Heller, M., Torruella, G., Tsurykau, A., Udayanga, Dhanushka, Ulukapi, M., Untereiner, W.A., Uzunov, B.A., Valle, L.G., Van Caenegem, W., Van den Wyngaert, S., Van Vooren, N., Velez, P., Verma, R.K., Vieira, L.C., Vieira, W.A.S., Vizzini, A., Walker, A., Walker, A.K., Wanasinghe, D.N., Wang, C.G., Wang, K., Wang, S.X., Wang, X.Y., Wang, Y., Wannasawang, N., Wartchow, F., Wei, D.P., Wei, X.L., White, J.F., Wijayawardene, N.N., Wijesinghe, S.N., Wijesundara, D.S.A., Wisitrassameewong, K., Worthy, F.R., Wu, F., Wu, G., Wu, H.X., Wu, N., Wu, W.P., Wurzbacher, C., Xiao, Y.P., Xiong, Y.R., Xu, L.J., Xu, R., Xu, R.F., Xu, R.J., Xu, T.M., Yakovchenko, L., Yan, J.Y., Yang, H., Yang, J., Yang, Z.L., Yang, Y.H., Yapa, N., Yasanthika, E., Youssef, N.H., Yu, F.M., Yu, Q., Yu, X.D., Yu, Y.X., Yu, Z.F., Yuan, H.S., Yuan, Y., Yurkov, Andrey, Zafari, D., Zamora, Juan Carlos, Zare, Rasoul, Zeng, M., Zeng, N.K., Zeng, X.Y., Zhang, F., Zhang, H., Zhang, J.F., Zhang, J.Y., Zhang, Q.Y., Zhang, S.N., Zhang, W., Zhang, Y., Zhang, Y.X., Zhao, C.L., Zhao, H., Zhao, Q., Zhao, R.L., Zhou, L.W., Zhou, M., Zhurbenko, M.P., Zin, H.H., and Zucconi, L.
- Abstract
The Global Consortium for the Classification of Fungi and fungus-like taxa is an international initiative of more than 550 mycologists to develop an electronic structure for the classification of these organisms. The members of the Consortium originate from 55 countries/regions worldwide, from a wide range of disciplines, and include senior, mid-career and early-career mycologists and plant pathologists. The Consortium will publish a biannual update of the Outline of Fungi and fungus-like taxa, to act as an international scheme for other scientists. Notes on all newly published taxa at or above the level of species will be prepared and published online on the Outline of Fungi website (https://www.outlineoffungi.org/), and these will be finally published in the biannual edition of the Outline of Fungi and fungus-like taxa. Comments on recent important taxonomic opinions on controversial topics will be included in the biannual outline. For example, ‘to promote a more stable taxonomy in Fusarium given the divergences over its generic delimitation’, or ‘are there too many genera in the Boletales?’ and even more importantly, ‘what should be done with the tremendously diverse ‘dark fungal taxa?’ There are undeniable differences in mycologists’ perceptions and opinions regarding species classification as well as the establishment of new species. Given the pluralistic nature of fungal taxonomy and its implications for species concepts and the nature of species, this consortium aims to provide a platform to better refine and stabilise fungal classification, taking into consideration views from different parties. In the future, a confidential voting system will be set up to gauge the opinions of all mycologists in the Consortium on important topics. The results of such surveys will be presented to the International Commission on the Taxonomy of Fungi (ICTF) and the Nomenclature Committee for Fungi (NCF) with opinions and percentages of votes for and against. Criticisms based
- Published
- 2023
3. Global consortium for the classification of fungi and fungus-like taxa
- Author
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Hyde, KD, Abdel-Wahab, MA, Abdollahzadeh, J, Abeywickrama, PD, Absalan, S, Afshari, N, Ainsworth, AM, Akulov, OY, Aleoshin, VV, Al-Sadi, AM, Alvarado, P, Alves, A, Alves-Silva, G, Amalfi, M, Amira, Y, Amuhenage, TB, Anderson, J, Antonín, V, Aouali, S, Aptroot, A, Apurillo, CCS, Araújo, JPM, Ariyawansa, HA, Armand, A, Arumugam, E, Asghari, R, Assis, DMA, Atienza, V, Avasthi, S, Azevedo, E, Bahkali, AH, Bakhshi, M, Banihashemi, Z, Bao, DF, Baral, HO, Barata, M, Barbosa, F, Barbosa, RN, Barreto, RW, Baschien, C, Belamesiatseva, DB, Bennett Reuel, M, Bera, I, Bezerra, JDP, Bezerra, JL, Bhat, DJ, Bhunjun, CS, Bianchinotti, MV, Błaszkowski, J, Blondelle, A, Boekhout, T, Bonito, G, Boonmee, S, Boonyuen, N, Bregant, C, Buchanan, P, Bundhun, D, Burgaud, G, Burgess, T, Buyck, B, Cabarroi-Hernández, M, Cáceres, MES, Caeiro, MF, Cai, L, Cai, MF, Calabon, MS, Calaça, FJS, Callalli, M, Cano-Lira, JF, Cantillo, T, Cao, B, Carlavilla, JR, Carvalho, A, Castañeda-Ruiz, RF, Castlebury, L, Castro-Jauregui, O, Catania, MDV, Cavalcanti, LH, Cazabonne, J, Cedeño-Sanchez, ML, Chaharmiri-Dokhaharani, S, Chaiwan, N, Chakraborty, N, Chaverri, P, Cheewangkoon, R, Chen, C, Chen, CY, Chen, KH, Chen, J, Chen, Q, Chen, WH, Chen, YP, Chethana, KWT, Coleine, C, Condé, TO, Corazon-Guivin, MA, Cortés-Pérez, A, Costa-Rezende, DH, Courtecuisse, R, Crouch, JA, Crous, PW, Cui, BK, Cui, YY, da Silva, DKA, da Silva, GA, da Silva, IR, da Silva, RMF, da Silva Santos, AC, Dai, DQ, Dai, YC, Damm, U, Darmostuk, V, Daroodi, Zoha, Das, K, Davoodian, N, Davydov, EA, Dayarathne, MC, Decock, C, de Groot, MD, De Kesel, A, dela Cruz, TEE, De Lange, R, Delgado, G, Denchev, CM, Denchev, TT, de Oliveira, NT, de Silva, NI, de Souza, FA, Dentinger, B, Devadatha, B, Dianese, JC, Dima, B, Diniz, AG, Dissanayake, AJ, Dissanayake, LS, Doğan, HH, Doilom, M, Dolatabadi, S, Dong, W, Dong, ZY, Dos Santos, LA, Drechsler-Santos, ER, Du, TY, Dubey, MK, Dutta, AK, Egidi, E, Elliott, TF, Elshahed, MS, Erdoğdu, M, Ertz, D, Etayo, J, Evans, HC, Fan, XL, Fan, YG, Fedosova, AG, Fell, J, Fernandes, I, Firmino, AL, Fiuza, PO, Flakus, A, Fragoso de Souza, CA, Frisvad, JC, Fryar, SC, Gabaldón, T, Gajanayake, AJ, Galindo, LJ, Gannibal, PB, García, D, García-Sandoval, SR, Garrido-Benavent, I, Garzoli, L, Gautam, AK, Ge, ZW, Gené, DJ, Gentekaki, E, Ghobad-Nejhad, M, Giachini, AJ, Gibertoni, TB, Góes-Neto, A, Gomdola, D, Gomes de Farias, AR, Gorjón, SP, Goto, BT, Granados-Montero, MM, Griffith, GW, Groenewald, JZ, Groenewald, M, Grossart, HP, Gueidan, C, Gunarathne, A, Gunaseelan, S, Gusmão, LFP, Gutierrez, AC, Guzmán-Dávalos, L, Haelewaters, D, Halling, R, Han, YF, Hapuarachchi, KK, Harder, CB, Harrington, TC, Hattori, T, He, MQ, He, S, He, SH, Healy, R, Herández-Restrepo, M, Heredia, G, Hodge, KT, Holgado-Rojas, M, Hongsanan, S, Horak, E, Hosoya, T, Houbraken, J, Huang, SK, Huanraluek, N, Hur, JS, Hurdeal, VG, Hustad, VP, Iotti, M, Iturriaga, T, Jafar, E, Janik, P, Jayalal, RGU, Jayasiri, SC, Jayawardena, RS, Jeewon, R, Jerônimo, GH, Jesus, AL, Jin, J, Johnston, PR, Jones, EBG, Joshi, Y, Justo, A, Kaishian, P, Kakishima, M, Kaliyaperumal, M, Kang, GP, Kang, JC, Karimi, O, Karpov, SA, Karunarathna, SC, Kaufmann, M, Kemler, M, Kezo, K, Khyaju, S, Kirchmair, M, Kirk, PM, Kitaura, MJ, Klawonn, I, Kolarik, M, Kong, A, Kuhar, F, Kukwa, M, Kumar, S, Kušan, I, Lado, C, Larsson, KH, Latha, KPD, Lee, HB, Leonardi, M, Leontyev, DL, Lestari, AS, Li, CJY, Li, DW, Li, H, Li, HY, Li, L, Li, QR, Li, WL, Li, Y, Li, YC, Liao, CF, Liimatainen, K, Lim, YW, Lin, CG, Linaldeddu, BT, Linde, CC, Linn, MM, Liu, F, Liu, JK, Liu, NG, Liu, S, Liu, SL, Liu, XF, Liu, XY, Liu, XZ, Liu, ZB, Lu, L, Lu, YZ, Luangharn, T, Luangsaard, JJ, Lumbsch, HT, Lumyong, S, Luo, L, Luo, M, Luo, ZL, Ma, J, Machado, AR, Madagammana, AD, Madrid, H, Magurno, F, Magyar, D, Mahadevan, N, Maharachchikumbura, SSN, Maimaiti, Y, Malosso, E, Manamgoda, DS, Manawasinghe, IS, Mapook, A, Marasinghe, DS, Mardones, M, Marin-Felix, Y, Márquez, R, Masigol, H, Matočec, N, May, T, McKenzie, EHC, Meiras-Ottoni, A, Melo, RFR, Mendes, ARL, Mendieta, S, Meng, QF, Menkis, A, Menolli Jr, N, Mešić, A, Meza Calvo, JG, Mikhailov, KV, Miller, SL, Moncada, B, Moncalvo, JM, Monteiro, JS, Monteiro, M, Mora-Montes, HM, Moreau, PA, Mueller, GM, Mukhopadyay, S, Murugadoss, R, Nagy, LG, Najafiniya, M, Nanayakkara, CM, Nascimento, CC, Nei, Y, Neves, MA, Neuhauser, S, Niego, AGT, Nilsson, RH, Niskanen, T, Niveiro, N, Noorabadi, MT, Noordeloos, (Machiel E.), Norphanphoun, C, Nuñez Otaño, NB, O’Donnell, RP, Oehl, F, Olariaga, I, Orlando, FP, Pang, KL, Papp, V, Pawłowska, J, Peintner, U, Pem, D, Pereira, OL, Perera, RH, Perez-Moreno, J, Perez-Ortega, S, Péter, G, Phillips, AJL, Phonemany, M, Phukhamsakda, C, Phutthacharoen, K, Piepenbring, M, Pires-Zottarelli, CLA, Poinar, G, Pošta, A, Prieto, M, Promputtha, I, Quandt, CA, Radek, R, Rahnama, K, Raj, KNA, Rajeshkumar, KC, Rämä, T, Rambold, G, Ramírez-Cruz, V, Rasconi, S, Rathnayaka, AR, Raza, M, Ren, GC, Robledo, GL, Rodriguez-Flakus, P, Ronikier, A, Rossi, W, Ryberg, M, Ryvarden, LR, Salvador‑Montoya, CA, Samant, B, Samarakoon, BC, Samarakoon, MC, Sánchez-Castro, I, Sánchez-García, M, Sandoval-Denis, M, Santiago, ALCMA, Santamaria, B, Santos, ACS, Sarma, VV, Savchenko, A, Savchenko, K, Saxena, RK, Scholler, M, Schoutteten, N, Seifollahi, E, Selbmann, L, Selcuk, F, Senanayake, IC, Shabashova, TG, Shen, HW, Shen, YM, SilvaFilho, AGS, Simmons, DR, Singh, R, Sir, EB, Song, Chang-Ge, Souza-Motta, CM, Sruthi, OP, Stadler, M, Stchigel, AM, Stemler, J, Stephenson, SL, Strassert, JFH, Su, HL, Su, L, Suetrong, S, Sulistyo, B, Sun, YF, Sun, YR, Svantesson, Sten, Sysouphanthong, P, Takamatsu, S, Tan, TH, Tanaka, K, Tang, AMC, Tang, X, Tanney, JB, Tavakol, NM, Taylor, JE, Taylor, PWJ, Tedersoo, L, Tennakoon, DS, Thamodini, GK, Thines, M, Thiyagaraja, V, Thongklang, N, Tiago, PV, Tian, Q, Tian, WH, Tibell, L, Tibell, S, Tibpromma, S, Tkalčec, Z, Tomšovský, M, Toome-Heller, M, Torruella, G, Tsurykau, A, Udayanga, D, Ulukapi, M, Untereiner, WA, Uzunov, BA, Valle, LG, Van Caenegem, W, Van den Wyngaert, S, Van Vooren, N, Velez, P, Verma, RK, Vieira, LC, Vieira, WAS, Vizzini, A, Walker, A, Walker, AK, Wanasinghe, DN, Wang, CG, Wang, K, Wang, SX, Wang, XY, Wang, Y, Wannasawang, N, Wartchow, F, Wei, DP, Wei, XL, White, JF, Wijayawardene, NN, Wijesinghe, SN, Wijesundara, DSA, Wisitrassameewong, K, Worthy, FR, Wu, F, Wu, G, Wu, HX, Wu, N, Wu, WP, Wurzbacher, C, Xiao, YP, Xiong, YR, Xu, LJ, Xu, R, Xu, RF, Xu, RJ, Xu, TM, Yakovchenko, L, Yan, JY, Yang, H, Yang, J, Yang, ZL, Yang, YH, Yapa, N, Yasanthika, E, Youssef, NH, Yu, FM, Yu, Q, Yu, YX, Yu, ZF, Yuan, HS, Yuan, Y, Yurkov, A, Zafari, D, Zamora, JC, Zare, R, Zeng, M, Zeng, NK, Zeng, XY, Zhang, F, Zhang, H, Zhang, JF, Zhang, JY, Zhang, QY, Zhang, SN, Zhang, W, Zhang, Y, Zhang, YX, Zhao, CL, Zhao, H, Zhao, Q, Zhao, RL, Zhou, LW, Zhou, M, Zhurbenko, MP, Zin, HH, Zucconi, L, Hyde, KD, Abdel-Wahab, MA, Abdollahzadeh, J, Abeywickrama, PD, Absalan, S, Afshari, N, Ainsworth, AM, Akulov, OY, Aleoshin, VV, Al-Sadi, AM, Alvarado, P, Alves, A, Alves-Silva, G, Amalfi, M, Amira, Y, Amuhenage, TB, Anderson, J, Antonín, V, Aouali, S, Aptroot, A, Apurillo, CCS, Araújo, JPM, Ariyawansa, HA, Armand, A, Arumugam, E, Asghari, R, Assis, DMA, Atienza, V, Avasthi, S, Azevedo, E, Bahkali, AH, Bakhshi, M, Banihashemi, Z, Bao, DF, Baral, HO, Barata, M, Barbosa, F, Barbosa, RN, Barreto, RW, Baschien, C, Belamesiatseva, DB, Bennett Reuel, M, Bera, I, Bezerra, JDP, Bezerra, JL, Bhat, DJ, Bhunjun, CS, Bianchinotti, MV, Błaszkowski, J, Blondelle, A, Boekhout, T, Bonito, G, Boonmee, S, Boonyuen, N, Bregant, C, Buchanan, P, Bundhun, D, Burgaud, G, Burgess, T, Buyck, B, Cabarroi-Hernández, M, Cáceres, MES, Caeiro, MF, Cai, L, Cai, MF, Calabon, MS, Calaça, FJS, Callalli, M, Cano-Lira, JF, Cantillo, T, Cao, B, Carlavilla, JR, Carvalho, A, Castañeda-Ruiz, RF, Castlebury, L, Castro-Jauregui, O, Catania, MDV, Cavalcanti, LH, Cazabonne, J, Cedeño-Sanchez, ML, Chaharmiri-Dokhaharani, S, Chaiwan, N, Chakraborty, N, Chaverri, P, Cheewangkoon, R, Chen, C, Chen, CY, Chen, KH, Chen, J, Chen, Q, Chen, WH, Chen, YP, Chethana, KWT, Coleine, C, Condé, TO, Corazon-Guivin, MA, Cortés-Pérez, A, Costa-Rezende, DH, Courtecuisse, R, Crouch, JA, Crous, PW, Cui, BK, Cui, YY, da Silva, DKA, da Silva, GA, da Silva, IR, da Silva, RMF, da Silva Santos, AC, Dai, DQ, Dai, YC, Damm, U, Darmostuk, V, Daroodi, Zoha, Das, K, Davoodian, N, Davydov, EA, Dayarathne, MC, Decock, C, de Groot, MD, De Kesel, A, dela Cruz, TEE, De Lange, R, Delgado, G, Denchev, CM, Denchev, TT, de Oliveira, NT, de Silva, NI, de Souza, FA, Dentinger, B, Devadatha, B, Dianese, JC, Dima, B, Diniz, AG, Dissanayake, AJ, Dissanayake, LS, Doğan, HH, Doilom, M, Dolatabadi, S, Dong, W, Dong, ZY, Dos Santos, LA, Drechsler-Santos, ER, Du, TY, Dubey, MK, Dutta, AK, Egidi, E, Elliott, TF, Elshahed, MS, Erdoğdu, M, Ertz, D, Etayo, J, Evans, HC, Fan, XL, Fan, YG, Fedosova, AG, Fell, J, Fernandes, I, Firmino, AL, Fiuza, PO, Flakus, A, Fragoso de Souza, CA, Frisvad, JC, Fryar, SC, Gabaldón, T, Gajanayake, AJ, Galindo, LJ, Gannibal, PB, García, D, García-Sandoval, SR, Garrido-Benavent, I, Garzoli, L, Gautam, AK, Ge, ZW, Gené, DJ, Gentekaki, E, Ghobad-Nejhad, M, Giachini, AJ, Gibertoni, TB, Góes-Neto, A, Gomdola, D, Gomes de Farias, AR, Gorjón, SP, Goto, BT, Granados-Montero, MM, Griffith, GW, Groenewald, JZ, Groenewald, M, Grossart, HP, Gueidan, C, Gunarathne, A, Gunaseelan, S, Gusmão, LFP, Gutierrez, AC, Guzmán-Dávalos, L, Haelewaters, D, Halling, R, Han, YF, Hapuarachchi, KK, Harder, CB, Harrington, TC, Hattori, T, He, MQ, He, S, He, SH, Healy, R, Herández-Restrepo, M, Heredia, G, Hodge, KT, Holgado-Rojas, M, Hongsanan, S, Horak, E, Hosoya, T, Houbraken, J, Huang, SK, Huanraluek, N, Hur, JS, Hurdeal, VG, Hustad, VP, Iotti, M, Iturriaga, T, Jafar, E, Janik, P, Jayalal, RGU, Jayasiri, SC, Jayawardena, RS, Jeewon, R, Jerônimo, GH, Jesus, AL, Jin, J, Johnston, PR, Jones, EBG, Joshi, Y, Justo, A, Kaishian, P, Kakishima, M, Kaliyaperumal, M, Kang, GP, Kang, JC, Karimi, O, Karpov, SA, Karunarathna, SC, Kaufmann, M, Kemler, M, Kezo, K, Khyaju, S, Kirchmair, M, Kirk, PM, Kitaura, MJ, Klawonn, I, Kolarik, M, Kong, A, Kuhar, F, Kukwa, M, Kumar, S, Kušan, I, Lado, C, Larsson, KH, Latha, KPD, Lee, HB, Leonardi, M, Leontyev, DL, Lestari, AS, Li, CJY, Li, DW, Li, H, Li, HY, Li, L, Li, QR, Li, WL, Li, Y, Li, YC, Liao, CF, Liimatainen, K, Lim, YW, Lin, CG, Linaldeddu, BT, Linde, CC, Linn, MM, Liu, F, Liu, JK, Liu, NG, Liu, S, Liu, SL, Liu, XF, Liu, XY, Liu, XZ, Liu, ZB, Lu, L, Lu, YZ, Luangharn, T, Luangsaard, JJ, Lumbsch, HT, Lumyong, S, Luo, L, Luo, M, Luo, ZL, Ma, J, Machado, AR, Madagammana, AD, Madrid, H, Magurno, F, Magyar, D, Mahadevan, N, Maharachchikumbura, SSN, Maimaiti, Y, Malosso, E, Manamgoda, DS, Manawasinghe, IS, Mapook, A, Marasinghe, DS, Mardones, M, Marin-Felix, Y, Márquez, R, Masigol, H, Matočec, N, May, T, McKenzie, EHC, Meiras-Ottoni, A, Melo, RFR, Mendes, ARL, Mendieta, S, Meng, QF, Menkis, A, Menolli Jr, N, Mešić, A, Meza Calvo, JG, Mikhailov, KV, Miller, SL, Moncada, B, Moncalvo, JM, Monteiro, JS, Monteiro, M, Mora-Montes, HM, Moreau, PA, Mueller, GM, Mukhopadyay, S, Murugadoss, R, Nagy, LG, Najafiniya, M, Nanayakkara, CM, Nascimento, CC, Nei, Y, Neves, MA, Neuhauser, S, Niego, AGT, Nilsson, RH, Niskanen, T, Niveiro, N, Noorabadi, MT, Noordeloos, (Machiel E.), Norphanphoun, C, Nuñez Otaño, NB, O’Donnell, RP, Oehl, F, Olariaga, I, Orlando, FP, Pang, KL, Papp, V, Pawłowska, J, Peintner, U, Pem, D, Pereira, OL, Perera, RH, Perez-Moreno, J, Perez-Ortega, S, Péter, G, Phillips, AJL, Phonemany, M, Phukhamsakda, C, Phutthacharoen, K, Piepenbring, M, Pires-Zottarelli, CLA, Poinar, G, Pošta, A, Prieto, M, Promputtha, I, Quandt, CA, Radek, R, Rahnama, K, Raj, KNA, Rajeshkumar, KC, Rämä, T, Rambold, G, Ramírez-Cruz, V, Rasconi, S, Rathnayaka, AR, Raza, M, Ren, GC, Robledo, GL, Rodriguez-Flakus, P, Ronikier, A, Rossi, W, Ryberg, M, Ryvarden, LR, Salvador‑Montoya, CA, Samant, B, Samarakoon, BC, Samarakoon, MC, Sánchez-Castro, I, Sánchez-García, M, Sandoval-Denis, M, Santiago, ALCMA, Santamaria, B, Santos, ACS, Sarma, VV, Savchenko, A, Savchenko, K, Saxena, RK, Scholler, M, Schoutteten, N, Seifollahi, E, Selbmann, L, Selcuk, F, Senanayake, IC, Shabashova, TG, Shen, HW, Shen, YM, SilvaFilho, AGS, Simmons, DR, Singh, R, Sir, EB, Song, Chang-Ge, Souza-Motta, CM, Sruthi, OP, Stadler, M, Stchigel, AM, Stemler, J, Stephenson, SL, Strassert, JFH, Su, HL, Su, L, Suetrong, S, Sulistyo, B, Sun, YF, Sun, YR, Svantesson, Sten, Sysouphanthong, P, Takamatsu, S, Tan, TH, Tanaka, K, Tang, AMC, Tang, X, Tanney, JB, Tavakol, NM, Taylor, JE, Taylor, PWJ, Tedersoo, L, Tennakoon, DS, Thamodini, GK, Thines, M, Thiyagaraja, V, Thongklang, N, Tiago, PV, Tian, Q, Tian, WH, Tibell, L, Tibell, S, Tibpromma, S, Tkalčec, Z, Tomšovský, M, Toome-Heller, M, Torruella, G, Tsurykau, A, Udayanga, D, Ulukapi, M, Untereiner, WA, Uzunov, BA, Valle, LG, Van Caenegem, W, Van den Wyngaert, S, Van Vooren, N, Velez, P, Verma, RK, Vieira, LC, Vieira, WAS, Vizzini, A, Walker, A, Walker, AK, Wanasinghe, DN, Wang, CG, Wang, K, Wang, SX, Wang, XY, Wang, Y, Wannasawang, N, Wartchow, F, Wei, DP, Wei, XL, White, JF, Wijayawardene, NN, Wijesinghe, SN, Wijesundara, DSA, Wisitrassameewong, K, Worthy, FR, Wu, F, Wu, G, Wu, HX, Wu, N, Wu, WP, Wurzbacher, C, Xiao, YP, Xiong, YR, Xu, LJ, Xu, R, Xu, RF, Xu, RJ, Xu, TM, Yakovchenko, L, Yan, JY, Yang, H, Yang, J, Yang, ZL, Yang, YH, Yapa, N, Yasanthika, E, Youssef, NH, Yu, FM, Yu, Q, Yu, YX, Yu, ZF, Yuan, HS, Yuan, Y, Yurkov, A, Zafari, D, Zamora, JC, Zare, R, Zeng, M, Zeng, NK, Zeng, XY, Zhang, F, Zhang, H, Zhang, JF, Zhang, JY, Zhang, QY, Zhang, SN, Zhang, W, Zhang, Y, Zhang, YX, Zhao, CL, Zhao, H, Zhao, Q, Zhao, RL, Zhou, LW, Zhou, M, Zhurbenko, MP, Zin, HH, and Zucconi, L
- Abstract
The Global Consortium for the Classification of Fungi and fungus-like taxa is an international initiative of more than 550 mycologists to develop an electronic structure for the classification of these organisms. The members of the Consortium originate from 55 countries/regions worldwide, from a wide range of disciplines, and include senior, mid-career and early-career mycologists and plant pathologists. The Consortium will publish a biannual update of the Outline of Fungi and funguslike taxa, to act as an international scheme for other scientists. Notes on all newly published taxa at or above the level of species will be prepared and published online on the Outline of Fungi website (https://www.outlineoffungi.org/), and these will be finally published in the biannual edition of the Outline of Fungi and fungus-like taxa. Comments on recent important taxonomic opinions on controversial topics will be included in the biannual outline. For example, ‘to promote a more stable taxonomy in Fusarium given the divergences over its generic delimitation’, or ‘are there too many genera in the Boletales?’ and even more importantly, ‘what should be done with the tremendously diverse ‘dark fungal taxa?’ There are undeniable differences in mycologists’ perceptions and opinions regarding species classification as well as the establishment of new species. Given the pluralistic nature of fungal taxonomy and its implications for species concepts and the nature of species, this consortium aims to provide a platform to better refine and stabilise fungal classification, taking into consideration views from different parties. In the future, a confidential voting system will be set up to gauge the opinions of all mycologists in the Consortium on important topics. The results of such surveys will be presented to the International Commission on the Taxonomy of Fungi (ICTF) and the Nomenclature Committee for Fungi (NCF) with opinions and percentages of votes for and against. Criticisms based o
- Published
- 2023
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4. Global consortium for the classification of fungi and fungus-like taxa
- Author
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Hyde, K. D., Abdel-Wahab, M. A., Abdollahzadeh, J., Abeywickrama, P. D., Absalan, S., Afshari, N., Ainsworth, A. M., Akulov, O. Y., Aleoshin, V. V., Al-Sadi, A. M., Alvarado, P., Alves, A., Alves-Silva, G., Amalfi, M., Amira, Y., Amuhenage, T. B., Anderson, J. L., Antonín, V., Aouali, S., Aptroot, A., Apurillo, C. C. S., Araújo, J. P.M., Ariyawansa, H. A., Armand, A., Arumugam, E., Asghari, R., Assis, D. M.A., Atienza, V., Avasthi, S., Azevedo, E., Bahkali, A. H., Bakhshi, M., Banihashemi, Z., Bao, D. F., Baral, H. O., Barata, M., Barbosa, F. R., Barbosa, R. N., Barreto, R. W., Baschien, C., Belamesiatseva, D. B., Reuel, M. Bennett, Bera, I., Bezerra, J. D. P., Bezerra, J. L., Bhat, D. J., Bhunjun, C. S., Bianchinotti, M. V., Błaszkowski, J., Blondelle, A., Boekhout, T., Bonito, G., Boonmee, S., Boonyuen, N., Bregant, C., Buchanan, P., Bundhun, D., Burgaud, G., Burgess, T., Buyck, B., Cabarroi-Hernández, M., Cáceres, M. E. S., Caeiro, M. F., Cai, L., Cai, M. F., Calabon, M. S., Calaça, F. J. S., Callalli, M., Camara, M. P. S., Cano-Lira, J. F., Cantillo, T., Cao, B., Carlavilla, J. R., Carvalho, A., Castañeda-Ruiz, R. F., Castlebury, L., Castro-Jauregui, O., Catania, M. D., Cavalcanti, L. H., Cazabonne, J., Cedeño-Sanchez, M. L., Chaharmiri-Dokhaharani, S., Chaiwan, N., Chakraborty, N., Chaverri, P., Cheewangkoon, R., Chen, C., Chen, C. Y., Chen, K. H., Chen, J., Chen, Q., Chen, W. H., Chen, Y. P., Chethana, K. W. T., Coleine, C., Condé, T. O., Corazon-Guivin, M. A., Cortés-Pérez, A., Costa-Rezende, D. H., Courtecuisse, R., Crouch, J. A., Crous, P. W., Cui, B. K., Cui, Y. Y., da Silva, D. K. A., da Silva, G. A., da Silva, I. R., da Silva, R. M. F., da Silva Santos, A. C., Dai, D. Q., Dai, Y. C., Damm, U., Darmostuk, V., Zoha, Daroodi, Das, K., Davoodian, N., Davydov, E. A., Dayarathne, M. C., Decock, C., de Groot, M. D., De Kesel, A., de la Cruz, T. E. E., De Lange, R., Delgado, G., Denchev, C. M., Denchev, T. T., de Oliveira, N. T., de Silva, N. I., de Souza, F. A., Dentinger, B., Devadatha, B., Dianese, J. C., Dima, B., Diniz, A. G., Dissanayake, A. J., Dissanayake, L. S., Doğan, H. H., Doilom, M., Dolatabadi, S., Dong, W., Dong, Z. Y., Dos Santos, L. A., Drechsler-Santos, E. R., Du, T. Y., Dubey, M. K., Dutta, A. K., Egidi, E., Elliott, T. F., Elshahed, M. S., Erdoğdu, M., Ertz, D., Etayo, J., Evans, H. C., Fan, X. L., Fan, Y. G., Fedosova, A. G., Fell, J., Fernandes, I., Firmino, A. L., Fiuza, P. O., Flakus, A., de Souza, C. A.Fragoso, Frisvad, J. C., Fryar, S. C., Gabaldón, T., Gajanayake, A. J., Galindo, L. J., Gannibal, P. B., García, D., García-Sandoval, S. R., Garrido-Benavent, I., Garzoli, L., Gautam, A. K., Ge, Z. W., Gené, D. J., Gentekaki, E., Ghobad-Nejhad, M., Giachini, A. J., Gibertoni, T. B., Góes-Neto, A., Gomdola, D., de Farias, A. R. Gomes, Gorjón, S. P., Goto, B. T., Granados-Montero, M. M., Griffith, G. W., Groenewald, J. Z., Groenewald, M., Grossart, H. P., Gueidan, C., Gunarathne, A., Gunaseelan, S., Gusmão, L. F.P., Gutierrez, A. C., Guzmán-Dávalos, L., Haelewaters, D., Halling, R., Han, Y. F., Hapuarachchi, K. K., Harder, C. B., Harrington, T. C., Hattori, T., He, M. Q., He, S., He, S. H., Healy, R., Herández-Restrepo, M., Heredia, G., Hodge, K. T., Holgado-Rojas, M., Hongsanan, S., Horak, E., Hosoya, T., Houbraken, J., Huang, S. K., Huanraluek, N., Hur, J. S., Hurdeal, V. G., Hustad, V. P., Iotti, M., Iturriaga, T., Jafar, E., Janik, P., Jany, J. L., Jayalal, R. G.U., Jayasiri, S. C., Jayawardena, R. S., Jeewon, R., Jerônimo, G. H., Jesus, A. L., Jin, J., Johnston, P. R., Jones, E. B.G., Joshi, Y., Justo, A., Kaishian, P., Kakishima, M., Kaliyaperumal, M., Kang, G. P., Kang, J. C., Karakehian, J. M., Karimi, O., Karpov, S. A., Karunarathna, S. C., Kaufmann, M., Kemler, M., Kezo, K., Khyaju, S., Kirchmair, M., Kirk, P. M., Kitaura, M. 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S., Yuan, Y., Yurkov, A., Zafari, D., Zamora, J. C., Zare, R., Zeng, M., Zeng, N. K., Zeng, X. Y., Zhang, F., Zhang, H., Zhang, J. F., Zhang, J. Y., Zhang, Q. Y., Zhang, S. N., Zhang, W., Zhang, Y., Zhao, C. L., Zhao, H., Zhao, Q., Zhao, R. L., Zhou, L. W., Zhou, M., Zhurbenko, M. P., Zin, H. H., Zucconi, L., Hyde, K. D., Abdel-Wahab, M. A., Abdollahzadeh, J., Abeywickrama, P. D., Absalan, S., Afshari, N., Ainsworth, A. M., Akulov, O. Y., Aleoshin, V. V., Al-Sadi, A. M., Alvarado, P., Alves, A., Alves-Silva, G., Amalfi, M., Amira, Y., Amuhenage, T. B., Anderson, J. L., Antonín, V., Aouali, S., Aptroot, A., Apurillo, C. C. S., Araújo, J. P.M., Ariyawansa, H. A., Armand, A., Arumugam, E., Asghari, R., Assis, D. M.A., Atienza, V., Avasthi, S., Azevedo, E., Bahkali, A. H., Bakhshi, M., Banihashemi, Z., Bao, D. F., Baral, H. O., Barata, M., Barbosa, F. R., Barbosa, R. N., Barreto, R. W., Baschien, C., Belamesiatseva, D. B., Reuel, M. Bennett, Bera, I., Bezerra, J. D. P., Bezerra, J. L., Bhat, D. J., Bhunjun, C. S., Bianchinotti, M. V., Błaszkowski, J., Blondelle, A., Boekhout, T., Bonito, G., Boonmee, S., Boonyuen, N., Bregant, C., Buchanan, P., Bundhun, D., Burgaud, G., Burgess, T., Buyck, B., Cabarroi-Hernández, M., Cáceres, M. E. S., Caeiro, M. F., Cai, L., Cai, M. F., Calabon, M. S., Calaça, F. J. S., Callalli, M., Camara, M. P. S., Cano-Lira, J. F., Cantillo, T., Cao, B., Carlavilla, J. R., Carvalho, A., Castañeda-Ruiz, R. F., Castlebury, L., Castro-Jauregui, O., Catania, M. D., Cavalcanti, L. H., Cazabonne, J., Cedeño-Sanchez, M. L., Chaharmiri-Dokhaharani, S., Chaiwan, N., Chakraborty, N., Chaverri, P., Cheewangkoon, R., Chen, C., Chen, C. Y., Chen, K. H., Chen, J., Chen, Q., Chen, W. H., Chen, Y. P., Chethana, K. W. T., Coleine, C., Condé, T. O., Corazon-Guivin, M. A., Cortés-Pérez, A., Costa-Rezende, D. H., Courtecuisse, R., Crouch, J. A., Crous, P. W., Cui, B. K., Cui, Y. Y., da Silva, D. K. A., da Silva, G. A., da Silva, I. R., da Silva, R. M. F., da Silva Santos, A. C., Dai, D. Q., Dai, Y. C., Damm, U., Darmostuk, V., Zoha, Daroodi, Das, K., Davoodian, N., Davydov, E. A., Dayarathne, M. C., Decock, C., de Groot, M. D., De Kesel, A., de la Cruz, T. E. E., De Lange, R., Delgado, G., Denchev, C. M., Denchev, T. T., de Oliveira, N. T., de Silva, N. I., de Souza, F. A., Dentinger, B., Devadatha, B., Dianese, J. C., Dima, B., Diniz, A. G., Dissanayake, A. J., Dissanayake, L. S., Doğan, H. H., Doilom, M., Dolatabadi, S., Dong, W., Dong, Z. Y., Dos Santos, L. A., Drechsler-Santos, E. R., Du, T. Y., Dubey, M. K., Dutta, A. K., Egidi, E., Elliott, T. F., Elshahed, M. S., Erdoğdu, M., Ertz, D., Etayo, J., Evans, H. C., Fan, X. L., Fan, Y. G., Fedosova, A. G., Fell, J., Fernandes, I., Firmino, A. L., Fiuza, P. O., Flakus, A., de Souza, C. A.Fragoso, Frisvad, J. C., Fryar, S. C., Gabaldón, T., Gajanayake, A. J., Galindo, L. J., Gannibal, P. B., García, D., García-Sandoval, S. R., Garrido-Benavent, I., Garzoli, L., Gautam, A. K., Ge, Z. W., Gené, D. J., Gentekaki, E., Ghobad-Nejhad, M., Giachini, A. J., Gibertoni, T. B., Góes-Neto, A., Gomdola, D., de Farias, A. R. Gomes, Gorjón, S. P., Goto, B. T., Granados-Montero, M. M., Griffith, G. W., Groenewald, J. Z., Groenewald, M., Grossart, H. P., Gueidan, C., Gunarathne, A., Gunaseelan, S., Gusmão, L. F.P., Gutierrez, A. C., Guzmán-Dávalos, L., Haelewaters, D., Halling, R., Han, Y. F., Hapuarachchi, K. K., Harder, C. B., Harrington, T. C., Hattori, T., He, M. Q., He, S., He, S. H., Healy, R., Herández-Restrepo, M., Heredia, G., Hodge, K. T., Holgado-Rojas, M., Hongsanan, S., Horak, E., Hosoya, T., Houbraken, J., Huang, S. K., Huanraluek, N., Hur, J. S., Hurdeal, V. G., Hustad, V. P., Iotti, M., Iturriaga, T., Jafar, E., Janik, P., Jany, J. L., Jayalal, R. G.U., Jayasiri, S. C., Jayawardena, R. S., Jeewon, R., Jerônimo, G. H., Jesus, A. L., Jin, J., Johnston, P. R., Jones, E. B.G., Joshi, Y., Justo, A., Kaishian, P., Kakishima, M., Kaliyaperumal, M., Kang, G. P., Kang, J. C., Karakehian, J. M., Karimi, O., Karpov, S. A., Karunarathna, S. C., Kaufmann, M., Kemler, M., Kezo, K., Khyaju, S., Kirchmair, M., Kirk, P. M., Kitaura, M. J., Klawonn, I., Kolarik, M., Kong, A., Kuhar, F., Kukwa, M., Kumar, S., Kušan, I., Lado, C., Larsson, K. H., Latha, K. P.D., Lee, H. B., Leonardi, M., Leontyev, D. L., Lestari, A. S., Li, C. J.Y., Li, D. W., Li, H. Y., Li, L., Li, Q. R., Li, W. L., Li, Y., Li, Y. C., Liao, C. F., Liimatainen, K., Lim, Y. W., Lin, C. G., Linaldeddu, B. T., Linde, C. C., Linn, M. M., Liu, F., Liu, J. K., Liu, N. G., Liu, S., Liu, X. F., Liu, X. Z., Liu, Z. B., Lu, L., Lu, Y. Z., Luangharn, T., Luangsa-ard, J. J., Lumbsch, H. T., Lumyong, S., Luo, L., Luo, M., Luo, Z. L., Ma, J., Machado, A. R., Madagammana, A. D., Madrid, H., Magurno, F., Magyar, D., Mahadevan, N., Maharachchikumbura, S. S.N., Maimaiti, Y., Malosso, E., Manamgoda, D. S., Manawasinghe, I. S., Mapook, A., Marasinghe, D. S., Mardones, M., Marin-Felix, Y., Márquez, R., Masigol, H., Matočec, N., May, T. W., McKenzie, E. H.C., Meiras-Ottoni, A., Melo, R. F.R., Mendes-Alvarenga, R. L., Mendieta, S., Meng, Q. F., Menkis, A., Menolli, N., Mešić, A., Calvo, J. G.Meza, Mikhailov, K. V., Miller, S. L., Moncada, B., Moncalvo, J. M., Monteiro, J. S., Monteiro, M., Mora-Montes, H. M., Moreau, P. A., Mueller, G. M., Mukhopadyay, S., Murugadoss, R., Nagy, L. G., Najafiniya, M., Nanayakkara, C. M., Nascimento, C. C., Nei, Y., Neves, M. A., Neuhauser, S., Niego, A. G.T., Nilsson, R. H., Niskanen, T., Niveiro, N., Noorabadi, M. T., Noordeloos, M. E., Norphanphoun, C., Otaño, N. B.Nuñez, O’Donnell, R. P., Oehl, F., Olariaga, I., Orlando, O. P., Pang, K. L., Papp, V., Pawłowska, J., Peintner, U., Pem, D., Pereira, O. L., Perera, R. H., Perez-Moreno, J., Perez-Ortega, S., Péter, G., Phillips, A. J.L., Phonemany, M., Phukhamsakda, C., Phutthacharoen, K., Piepenbring, M., Pires-Zottarelli, C. L.A., Poinar, G., Pošta, A., Prieto, M., Promputtha, I., Quandt, C. A., Radek, R., Rahnama, K., Raj, K. N.A., Rajeshkumar, K. C., Rämä, T., Rambold, G., Ramírez-Cruz, V., Rasconi, S., Rathnayaka, A. R., Raza, M., Ren, G. C., Robledo, G. L., Rodriguez-Flakus, P., Ronikier, A., Rossi, W., Ryberg, M., Ryvarden, L. R., Salvador-Montoya, C. A., Samant, B., Samarakoon, B. C., Samarakoon, M. C., Sánchez-Castro, I., Sánchez-García, M., Sandoval-Denis, M., Santamaria, B., Santiago, A. L.C.M.A., Sarma, V. V., Savchenko, A., Savchenko, K., Saxena, R. K., Scholler, M., Schoutteten, N., Seifollahi, E., Selbmann, L., Selcuk, F., Senanayake, I. C., Shabashova, T. G., Shen, H. W., Shen, Y. M., Silva-Filho, A. G.S., Simmons, D. R., Singh, R., Sir, E. B., Song, C. G., Souza-Motta, C. M., Sruthi, O. P., Stadler, M., Stchigel, A. M., Stemler, J., Stephenson, S. L., Strassert, J. F.H., Su, H. L., Su, L., Suetrong, S., Sulistyo, B., Sun, Y. R., Svantesson, S., Sysouphanthong, P., Takamatsu, S., Tan, T. H., Tanaka, K., Tang, A. M.C., Tang, X., Tanney, J. B., Tavakol, N. M., Taylor, J. E., Taylor, P. W.J., Tedersoo, L., Tennakoon, D. S., Thamodini, G. K., Thines, M., Thiyagaraja, V., Thongklang, N., Tiago, P. V., Tian, Q., Tian, W. H., Tibell, L., Tibell, S., Tibpromma, S., Tkalčec, Z., Tomšovský, M., Toome-Heller, M., Torruella, G., Tsurykau, A., Udayanga, D., Ulukapi, M., Untereiner, W. A., Uzunov, B. A., Valle, L. G., Van Caenegem, W., Van den Wyngaert, S., Van Vooren, N., Velez, P., Verma, R. K., Vieira, L. C., Vieira, W. A.S., Vizzini, A., Walker, A., Walker, A. K., Wanasinghe, D. N., Wang, C. G., Wang, K., Wang, S. X., Wang, X. Y., Wang, Y., Wannasawang, N., Wartchow, F., Wei, D. P., Wei, X. L., White, J. F., Wijayawardene, N. N., Wijesinghe, S. N., Wijesundara, D. S.A., Wisitrassameewong, K., Worthy, F. R., Wu, F., Wu, G., Wu, H. X., Wu, N., Wu, W. P., Wurzbacher, C., Xiao, Y. P., Xiong, Y. R., Xu, B., Xu, L. J., Xu, R., Xu, T. M., Yakovchenko, L., Yan, J. Y., Yang, H. D., Yang, J., Yang, Z. L., Yang, Y. H., Yapa, N., Yasanthika, E., Youssef, N. H., Yu, F. M., Yu, Q., Yu, X. D., Yu, Y. X., Yu, Z. F., Yuan, H. S., Yuan, Y., Yurkov, A., Zafari, D., Zamora, J. C., Zare, R., Zeng, M., Zeng, N. K., Zeng, X. Y., Zhang, F., Zhang, H., Zhang, J. F., Zhang, J. Y., Zhang, Q. Y., Zhang, S. N., Zhang, W., Zhang, Y., Zhao, C. L., Zhao, H., Zhao, Q., Zhao, R. L., Zhou, L. W., Zhou, M., Zhurbenko, M. P., Zin, H. H., and Zucconi, L.
- Abstract
The Global Consortium for the Classification of Fungi and fungus-like taxa is an international initiative of more than 550 mycologists to develop an electronic structure for the classification of these organisms. The members of the Consortium originate from 55 countries/regions worldwide, from a wide range of disciplines, and include senior, mid-career and early-career mycologists and plant pathologists. The Consortium will publish a biannual update of the Outline of Fungi and fungus-like taxa, to act as an international scheme for other scientists. Notes on all newly published taxa at or above the level of species will be prepared and published online on the Outline of Fungi website (https://www.outlineoffungi.org/), and these will be finally published in the biannual edition of the Outline of Fungi and fungus-like taxa. Comments on recent important taxonomic opinions on controversial topics will be included in the biannual outline. For example, 'to promote a more stable taxonomy in Fusarium given the divergences over its generic delimitation', or 'are there too many genera in the Boletales?' and even more importantly, 'what should be done with the tremendously diverse 'dark fungal taxa?' There are undeniable differences in mycologists' perceptions and opinions regarding species classification as well as the establishment of new species. Given the pluralistic nature of fungal taxonomy and its implications for species concepts and the nature of species, this consortium aims to provide a platform to better refine and stabilise fungal classification, taking into consideration views from different parties. In the future, a confidential voting system will be set up to gauge the opinions of all mycologists in the Consortium on important topics. The results of such surveys will be presented to the International Commission on the Taxonomy of Fungi (ICTF) and the Nomenclature Committee
- Published
- 2023
5. Antarctolichenia onofrii gen. nov. sp. nov. from Antarctic Endolithic Communities Untangles the Evolution of Rock-Inhabiting and Lichenized Fungi in Arthoniomycetes
- Author
-
Muggia L, Coleine C, De Carolis, R, Cometto A, Selbmann L, Muggia, L, Coleine, C, Carolis, De, R, Cometto, A, and Selbmann, L
- Subjects
Microbiology (medical) ,Stichococcus ,QH301-705.5 ,algae ,Lichenostigmatales ,melanization ,microbial communities ,phylogeny ,Plant Science ,Article ,Algae ,Lichenostigmatale ,Phylogenetics ,Genus ,Biology (General) ,Ecology, Evolution, Behavior and Systematics ,biology ,Ecology ,microbial communitie ,Dothideomycetes ,biology.organism_classification ,Type species ,Taxon ,Arthoniomycetes - Abstract
Microbial endolithic communities are the main and most widespread life forms in the coldest and hyper-arid desert of the McMurdo Dry Valleys and other ice-free areas across Victoria Land, Antarctica. There, the lichen-dominated communities are complex and self-supporting assemblages of phototrophic and heterotrophic microorganisms, including bacteria, chlorophytes, and both free-living and lichen-forming fungi living at the edge of their physiological adaptability. In particular, among the free-living fungi, microcolonial, melanized, and anamorphic species are highly recurrent, while a few species were sometimes found to be associated with algae. One of these fungi is of paramount importance for its peculiar traits, i.e., a yeast-like habitus, co-growing with algae and being difficult to propagate in pure culture. In the present study, this taxon is herein described as the new genus Antarctolichenia and its type species is A. onofrii, which represents a transitional group between the free-living and symbiotic lifestyle in Arthoniomycetes. The phylogenetic placement of Antarctolichenia was studied using three rDNA molecular markers and morphological characters were described. In this study, we also reappraise the evolution and the connections linking the lichen-forming and rock-inhabiting lifestyles in the basal lineages of Arthoniomycetes (i.e., Lichenostigmatales) and Dothideomycetes.
- Published
- 2021
6. SHOWCAVE: a multidisciplinary research project to quantify and mitigate the environmental impacts in tourist caves
- Author
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Isaia, Marco, Arca, A., Valentina Balestra, Rossana Bellopede, Biagioli, F., Cina, Alberto, Cinus, Daniela, Coleine, C., Cossu, Q. A., Regibus, Claudio, Del Piano, D., Duce, P., Ferrara, R., Mammola, Stefano, Manzino A. M., PAOLA MARINI, Maschio, Paolo Felice, Nanni, Veronica, Nicolosi, Giuseppe, Pavia, Marco, Piano, Elena, Poli, A., Prigione, V. P., Selbmann, Laura, Thun Honenstein Ursula, Turrini, M. C., Vagnoni, E., Varese, C., Ventura, A., Vigna, Bartolomeo, and Zanellati, A.
- Subjects
caves ,show caves ,multidisciplinary research ,environmental impacts - Published
- 2021
7. Shed light in the dark lineages of the fungal tree of life—stres
- Author
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Selbmann, L, Benkő, Z, Coleine, C, de Hoog, S, Donati, C, Druzhinina, I, Emri, T, Ettinger, CL, Gladfelter, AS, Gorbushina, AA, Grigoriev, IV, Grube, M, Gunde-Cimerman, N, Karányi, ZÁ, Kocsis, B, Kubressoian, T, Miklós, I, Miskei, M, Muggia, L, Northen, T, Novak-Babič, M, Pennacchio, C, Pfliegler, WP, Pòcsi, I, Prigione, V, Riquelme, M, Segata, N, Schumacher, J, Shelest, E, Sterflinger, K, Tesei, D, U’ren, JM, Varese, GC, Vázquez-Campos, X, Vicente, VA, Souza, EM, Zalar, P, Walker, AK, Stajich, JE, Selbmann, L, Benkő, Z, Coleine, C, de Hoog, S, Donati, C, Druzhinina, I, Emri, T, Ettinger, CL, Gladfelter, AS, Gorbushina, AA, Grigoriev, IV, Grube, M, Gunde-Cimerman, N, Karányi, ZÁ, Kocsis, B, Kubressoian, T, Miklós, I, Miskei, M, Muggia, L, Northen, T, Novak-Babič, M, Pennacchio, C, Pfliegler, WP, Pòcsi, I, Prigione, V, Riquelme, M, Segata, N, Schumacher, J, Shelest, E, Sterflinger, K, Tesei, D, U’ren, JM, Varese, GC, Vázquez-Campos, X, Vicente, VA, Souza, EM, Zalar, P, Walker, AK, and Stajich, JE
- Abstract
The polyphyletic group of black fungi within the Ascomycota (Arthoniomycetes, Dothideomycetes, and Eurotiomycetes) is ubiquitous in natural and anthropogenic habitats. Partly because of their dark, melanin-based pigmentation, black fungi are resistant to stresses including UV-and ionizing-radiation, heat and desiccation, toxic metals, and organic pollutants. Consequently, they are amongst the most stunning extremophiles and poly-extreme-tolerant organisms on Earth. Even though ca. 60 black fungal genomes have been sequenced to date, [mostly in the family Herpotrichiellaceae (Eurotiomycetes)], the class Dothideomycetes that hosts the largest majority of extremophiles has only been sparsely sampled. By sequencing up to 92 species that will become reference genomes, the “Shed light in The daRk lineagES of the fungal tree of life” (STRES) project will cover a broad collection of black fungal diversity spread throughout the Fungal Tree of Life. Interestingly, the STRES project will focus on mostly unsampled genera that display different ecologies and life-styles (e.g., ant-and lichen-associated fungi, rock-inhabiting fungi, etc.). With a resequencing strategy of 10-to 15-fold depth coverage of up to ~550 strains, numerous new reference genomes will be established. To identify metabolites and functional processes, these new genomic resources will be enriched with metabolomics analyses coupled with transcriptomics experiments on selected species under various stress conditions (salinity, dryness, UV radiation, oligotrophy). The data acquired will serve as a reference and foundation for establishing an encyclopedic database for fungal metagenomics as well as the biology, evolution, and ecology of the fungi in extreme environments.
- Published
- 2020
8. Draft Genome Sequences of the Antarctic Endolithic Fungi Rachicladosporium antarcticum CCFEE 5527 and Rachicladosporium sp. CCFEE 5018
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Coleine, C, Masonjones, S, Selbmann, L, Zucconi, L, Onofri, S, Pacelli, C, and Stajich, JE
- Abstract
The draft genome sequences of Rachicladosporium antarcticum CCFEE 5527 and Rachicladosporium sp. CCFEE 5018 are the first sequenced genomes from this genus, which comprises rock-inhabiting fungi. These endolithic strains were isolated from inside rocks collected from the Antarctic Peninsula and Battleship Promontory (McMurdo Dry Valleys), Antarctica, respectively.
- Published
- 2017
9. Fecal microbiota transplantation ameliorates high-fat diet-induced memory impairment in mice.
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Pereira LTG, Vilela WR, Bellozi PMQ, Engel DF, de Paula GC, de Andrade RR, Mortari MR, de Melo Teixeira M, Coleine C, Figueiredo CP, de Bem AF, and Amato AA
- Subjects
- Animals, Male, Mice, Hippocampus, Glucose Intolerance, Diet, High-Fat adverse effects, Fecal Microbiota Transplantation methods, Mice, Inbred C57BL, Memory Disorders prevention & control, Memory Disorders etiology, Gastrointestinal Microbiome physiology
- Abstract
Gut dysbiosis is linked to metabolic and neurodegenerative diseases and comprises a plausible link between high-fat diet (HFD) and brain dysfunction. Here we show that gut microbiota modulation by either antibiotic treatment for 5 weeks or a brief 3-day fecal microbiota transplantation (FMT) regimen from low-fat (control) diet-fed mice decreased weight gain, adipose tissue hypertrophy, and glucose intolerance induced by HFD in C57BL/6 male mice. Notably, gut microbiota modulation by FMT completely reversed impaired recognition memory induced by HFD, whereas modulation by antibiotics had less pronounced effect. Improvement in recognition memory by FMT was accompanied by decreased HFD-induced astrogliosis in the hippocampal cornu ammonis region. Gut microbiome composition analysis indicated that HFD diminished microbiota diversity compared to control diet, whereas FMT partially restored the phyla diversity. Our findings reinforce the role of the gut microbiota on HFD-induced cognitive impairment and suggest that modulating the gut microbiota may be an effective strategy to prevent metabolic and cognitive dysfunction associated with unfavorable dietary patterns., (© 2024 International Society for Neurochemistry.)
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- 2024
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10. Three novel woody litter inhabiting fungi in Didymosphaeriaceae, Phaeoseptaceae and Synnemasporellaceae from Zhujiangyuan Nature Reserve, Yunnan Province, P.R. China.
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Zhang GQ, Wijayawardene NN, Han LH, Kumla J, Suwannarach N, Li Q, Elgorban AM, Moussa IM, Coleine C, and Dai DQ
- Abstract
Zhujiangyuan Nature Reserve, located in Qujing City, Yunnan Province, China, is reported with high fauna and floral diversity, while the fungal diversity of the region is poorly documented. During the summer season in 2023, decaying wood-inhabiting microfungi were collected from different microhabitats. The novel species were identified based on morphological characteristics and phylogenetic analyses (based on combined datasets of ITS, LSU, SSU, tef 1-α, and rpb 2 regions). Two species belong to Dothideomycetes ( viz. , Spegazziniazhujiangyuanensis sp. nov. and Phaeoseptumzhujiangyuanense sp. nov. in Pleosporales) while the other one resides in Sordariomycetes ( Synnemasporellafanii sp. nov. in Diaporthales). The results are in conformity with the earlier studies that predicted higher fungal diversity in this region., Competing Interests: The authors have declared that no competing interests exist., (Gui-Qing Zhang, Nalin N. Wijayawardene, Li-Hong Han, Jaturong Kumla, Nakarin Suwannarach, Qiang Li, Abdallah M. Elgorban, Ihab M. Moussa, Claudia Coleine, Dong-Qin Dai.)
- Published
- 2024
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11. Metagenomics untangles potential adaptations of Antarctic endolithic bacteria at the fringe of habitability.
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Coleine C, Albanese D, Ray AE, Delgado-Baquerizo M, Stajich JE, Williams TJ, Larsen S, Tringe S, Pennacchio C, Ferrari BC, Donati C, and Selbmann L
- Subjects
- Antarctic Regions, Metagenome, Metagenomics, Bacteria genetics, Bacteria metabolism, Microbiota
- Abstract
Survival and growth strategies of Antarctic endolithic microbes residing in Earth's driest and coldest desert remain virtually unknown. From 109 endolithic microbiomes, 4539 metagenome-assembled genomes were generated, 49.3 % of which were novel candidate bacterial species. We present evidence that trace gas oxidation and atmospheric chemosynthesis may be the prevalent strategies supporting metabolic activity and persistence of these ecosystems at the fringe of life and the limits of habitability., Competing Interests: Declaration of competing interest The authors declare that they have no competing interests., (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)
- Published
- 2024
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12. Novel endolithic bacteria of phylum Chloroflexota reveal a myriad of potential survival strategies in the Antarctic desert.
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Williams TJ, Allen MA, Ray AE, Benaud N, Chelliah DS, Albanese D, Donati C, Selbmann L, Coleine C, and Ferrari BC
- Subjects
- Antarctic Regions, Fungi genetics, Cold Temperature, Sugars, Bacteria genetics, Chloroflexi
- Abstract
The ice-free McMurdo Dry Valleys of Antarctica are dominated by nutrient-poor mineral soil and rocky outcrops. The principal habitat for microorganisms is within rocks (endolithic). In this environment, microorganisms are provided with protection against sub-zero temperatures, rapid thermal fluctuations, extreme dryness, and ultraviolet and solar radiation. Endolithic communities include lichen, algae, fungi, and a diverse array of bacteria. Chloroflexota is among the most abundant bacterial phyla present in these communities. Among the Chloroflexota are four novel classes of bacteria, here named Candidatus Spiritibacteria class. nov. (=UBA5177), Candidatus Martimicrobia class. nov. (=UBA4733), Candidatus Tarhunnaeia class. nov. (=UBA6077), and Candidatus Uliximicrobia class. nov. (=UBA2235). We retrieved 17 high-quality metagenome-assembled genomes (MAGs) that represent these four classes. Based on genome predictions, all these bacteria are inferred to be aerobic heterotrophs that encode enzymes for the catabolism of diverse sugars. These and other organic substrates are likely derived from lichen, algae, and fungi, as metabolites (including photosynthate), cell wall components, and extracellular matrix components. The majority of MAGs encode the capacity for trace gas oxidation using high-affinity uptake hydrogenases, which could provide energy and metabolic water required for survival and persistence. Furthermore, some MAGs encode the capacity to couple the energy generated from H
2 and CO oxidation to support carbon fixation (atmospheric chemosynthesis). All encode mechanisms for the detoxification and efflux of heavy metals. Certain MAGs encode features that indicate possible interactions with other organisms, such as Tc-type toxin complexes, hemolysins, and macroglobulins.IMPORTANCEThe ice-free McMurdo Dry Valleys of Antarctica are the coldest and most hyperarid desert on Earth. It is, therefore, the closest analog to the surface of the planet Mars. Bacteria and other microorganisms survive by inhabiting airspaces within rocks (endolithic). We identify four novel classes of phylum Chloroflexota , and, based on interrogation of 17 metagenome-assembled genomes, we predict specific metabolic and physiological adaptations that facilitate the survival of these bacteria in this harsh environment-including oxidation of trace gases and the utilization of nutrients (including sugars) derived from lichen, algae, and fungi. We propose that such adaptations allow these endolithic bacteria to eke out an existence in this cold and extremely dry habitat., Competing Interests: The authors declare no conflict of interest.- Published
- 2024
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13. Dryland microbiomes reveal community adaptations to desertification and climate change.
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Coleine C, Delgado-Baquerizo M, DiRuggiero J, Guirado E, Harfouche AL, Perez-Fernandez C, Singh BK, Selbmann L, and Egidi E
- Subjects
- Conservation of Natural Resources, Climate Change, Soil, Hot Temperature, Ecosystem, Microbiota
- Abstract
Drylands account for 45% of the Earth's land area, supporting ~40% of the global population. These regions support some of the most extreme environments on Earth, characterized by extreme temperatures, low and variable rainfall, and low soil fertility. In these biomes, microorganisms provide vital ecosystem services and have evolved distinctive adaptation strategies to endure and flourish in the extreme. However, dryland microbiomes and the ecosystem services they provide are under threat due to intensifying desertification and climate change. In this review, we provide a synthesis of our current understanding of microbial life in drylands, emphasizing the remarkable diversity and adaptations of these communities. We then discuss anthropogenic threats, including the influence of climate change on dryland microbiomes and outline current knowledge gaps. Finally, we propose research priorities to address those gaps and safeguard the sustainability of these fragile biomes., (© The Author(s) 2024. Published by Oxford University Press on behalf of the International Society for Microbial Ecology.)
- Published
- 2024
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14. Outdoor climate drives diversity patterns of dominant microbial taxa in caves worldwide.
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Biagioli F, Coleine C, Delgado-Baquerizo M, Feng Y, Saiz-Jimenez C, and Selbmann L
- Subjects
- Caves microbiology, Bacteria metabolism, Geography, Microbiota, Mycobiome
- Abstract
The cave microbiota is assumed to be shaped by indoor microclimate, biotic and abiotic factors, which are largely dependent from outside environmental conditions; however, this knowledge is available at local or regional scales only. To address this knowledge gap, we reanalyzed over 1050 bacterial and fungal communities of caves worldwide, and found that outdoor temperature and rainfall play a critical role in explaining differences in microbial diversity patterns of global caves, selecting specific dominant taxa across gradients of growing aridity conditions with arid climate leading to a reduction in total cave microbial diversity. Moreover, we found that fungal (from 186 to 1908 taxa) and bacterial (from 467 to 1619 taxa) diversity increased under temperate-tropical and temperate-continental climatic regions, respectively, highlighting an opposite preference for the two microbial compartments. We hypothesized that outdoor geographical, climatic variables and lithology are critical epistatic drivers in assembling microbial communities and their dominant taxa, whose ecological responses could be useful to predict the fate of these subterranean environments in the context of climate change. Our work elucidates the intimate connection between caves microbiota and surface ecosystems highlighting the sensitivity of cave microbial communities to climatic changes and environmental degradation. This work also provides a natural benchmark for the biogeographic information for caves globally and for protection strategies aiming at conservation of underground environments., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.)
- Published
- 2024
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15. Assessing critical thresholds in terrestrial microbiomes.
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Egidi E, Coleine C, Delgado-Baquerizo M, and Singh BK
- Subjects
- Microbiota
- Published
- 2023
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16. Geography and environmental pressure are predictive of class-specific radioresistance in black fungi.
- Author
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Aureli L, Coleine C, Delgado-Baquerizo M, Ahren D, Cemmi A, Di Sarcina I, Onofri S, and Selbmann L
- Subjects
- Gamma Rays, Geography, Fungi genetics, Radiation, Ionizing
- Abstract
Black fungi are among the most resistant organisms to ionizing radiation on Earth. However, our current knowledge is based on studies on a few isolates, while the overall radioresistance limits across this microbial group and the relationship with local environmental conditions remain largely undetermined. To address this knowledge gap, we assessed the survival of 101 strains of black fungi isolated across a worldwide spatial distribution to gamma radiation doses up to 100 kGy. We found that intra and inter-specific taxonomy, UV radiation, and precipitation levels primarily influence the radioresistance in black fungi. Altogether, this study provides insights into the adaptive mechanisms of black fungi to extreme environments and highlights the role of local adaptation in shaping the survival capabilities of these extreme-tolerant organisms., (© 2023 The Authors. Environmental Microbiology published by Applied Microbiology International and John Wiley & Sons Ltd.)
- Published
- 2023
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17. Geology and elevation shape bacterial assembly in Antarctic endolithic communities.
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Larsen S, Coleine C, Albanese D, Stegen JC, Selbmann L, and Donati C
- Abstract
Ice free areas of continental Antarctica are among the coldest and driest environments on Earth, and yet, they support surprisingly diverse and highly adapted microbial communities. Endolithic growth is one of the key adaptations to such extreme environments and often represents the dominant life-form. Despite growing scientific interest, little is known of the mechanisms that influence the assembly of endolithic microbiomes across these harsh environments. Here, we used metagenomics to examine the diversity and assembly of endolithic bacterial communities across Antarctica within different rock types and over a large elevation range. While granite supported richer and more heterogeneous communities than sandstone, elevation had no apparent effect on taxonomic richness, regardless of rock type. Conversely, elevation was clearly associated with turnover in community composition, with the deterministic process of variable selection driving microbial assembly along the elevation gradient. The turnover associated with elevation was modulated by geology, whereby for a given elevation difference, turnover was consistently larger between communities inhabiting different rock types. Overall, selection imposed by elevation and geology appeared stronger than turnover related to other spatially-structured environmental drivers. Our findings indicate that at the cold-arid limit of life on Earth, geology and elevation are key determinants of endolithic bacterial heterogeneity. This also suggests that warming temperatures may threaten the persistence of such extreme-adapted organisms., (Copyright © 2023. Published by Elsevier B.V.)
- Published
- 2023
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18. Seasonality Is the Main Determinant of Microbial Diversity Associated to Snow/Ice around Concordia Station on the Antarctic Polar Plateau.
- Author
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Stoppiello GA, Coleine C, Moeller R, Ripa C, Billi D, and Selbmann L
- Abstract
The French-Italian Concordia Research Station, situated on the Antarctic Polar Plateau at an elevation of 3233 m above sea level, offers a unique opportunity to study the presence and variation of microbes introduced by abiotic or biotic vectors and, consequently, appraise the amplitude of human impact in such a pristine environment. This research built upon a previous work, which explored microbial diversity in the surface snow surrounding the Concordia Research Station. While that study successfully characterized the bacterial assemblage, detecting fungal diversity was hampered by the low DNA content. To address this knowledge gap, in the present study, we optimized the sampling by increasing ice/snow collected to leverage the final DNA yield. The V4 variable region of the 16S rDNA and Internal Transcribed Spacer (ITS1) rDNA was used to evaluate bacterial and fungal diversity. From the sequencing, we obtained 3,352,661 and 4,433,595 reads clustered in 930 and 3182 amplicon sequence variants (ASVs) for fungi and bacteria, respectively. Amplicon sequencing revealed a predominance of Basidiomycota (49%) and Ascomycota (42%) in the fungal component; Bacteroidota (65.8%) is the main representative among the bacterial phyla. Basidiomycetes are almost exclusively represented by yeast-like fungi. Our findings provide the first comprehensive overview of both fungal and bacterial diversity in the Antarctic Polar Plateau's surface snow/ice near Concordia Station and to identify seasonality as the main driver of microbial diversity; we also detected the most sensitive microorganisms to these factors, which could serve as indicators of human impact in this pristine environment and aid in planetary protection for future exploration missions.
- Published
- 2023
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19. Water availability creates global thresholds in multidimensional soil biodiversity and functions.
- Author
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Zhang J, Feng Y, Maestre FT, Berdugo M, Wang J, Coleine C, Sáez-Sandino T, García-Velázquez L, Singh BK, and Delgado-Baquerizo M
- Subjects
- Animals, Humans, Water, Biodiversity, Invertebrates, Ecosystem, Soil chemistry
- Abstract
Soils support an immense portion of Earth's biodiversity and maintain multiple ecosystem functions which are essential for human well-being. Environmental thresholds are known to govern global vegetation patterns, but it is still unknown whether they can be used to predict the distribution of soil organisms and functions across global biomes. Using a global field survey of 383 sites across contrasting climatic and vegetation conditions, here we showed that soil biodiversity and functions exhibited pervasive nonlinear patterns worldwide and are mainly governed by water availability (precipitation and potential evapotranspiration). Changes in water availability resulted in drastic shifts in soil biodiversity (bacteria, fungi, protists and invertebrates) and soil functions including plant-microbe interactions, plant productivity, soil biogeochemical cycles and soil carbon sequestration. Our findings highlight that crossing specific water availability thresholds can have critical consequences for the provision of essential ecosystem services needed to sustain our planet., (© 2023. The Author(s), under exclusive licence to Springer Nature Limited.)
- Published
- 2023
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20. Positive fungal interactions are key drivers in Antarctic endolithic microcosms at the boundaries for life sustainability.
- Author
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Biagioli F, Coleine C, Buzzini P, Turchetti B, Sannino C, and Selbmann L
- Abstract
In the ice-free areas of Victoria Land in continental Antarctica, where the conditions reach the limits for life sustainability, highly adapted and extreme-tolerant microbial communities exploit the last habitable niches inside porous rocks (i.e. cryptoendolithic communities). These guilds host the main standing biomass and principal, if not sole, contributors to environmental/biogeochemical cycles, driving ecosystem processes and functionality in these otherwise dead lands. Although knowledge advances on their composition, ecology, genomic and metabolic features, a large-scale perspective of occurring interactions and interconnections within and between endolithic fungal assemblages is still lacking to date. Unravelling the tight relational network among functional guilds in the Antarctic cryptoendolithic communities may represent a main task. Aiming to fill this knowledge gap, we performed a correlation-network analysis based on amplicon-sequencing data of 74 endolithic microbiomes collected throughout Victoria Land. Endolithic communities' compositional pattern was largely dominated by Lichenized fungi group (83.5%), mainly represented by Lecanorales and Lecideales, followed by Saprotrophs (14.2%) and RIF+BY (2.4%) guilds led by Tremellales and Capnodiales respectively. Our findings highlighted that fungal functional guilds' relational spectrum was dominated by cooperative interactions led by lichenised and black fungi, deeply engaged in community trophic sustain and protection, respectively. On the other hand, a few negative correlations found may help in preserving niche boundaries between microbes living in such strict spatial association., (© The Author(s) 2023. Published by Oxford University Press on behalf of FEMS.)
- Published
- 2023
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21. Highly diverse and unknown viruses may enhance Antarctic endoliths' adaptability.
- Author
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Ettinger CL, Saunders M, Selbmann L, Delgado-Baquerizo M, Donati C, Albanese D, Roux S, Tringe S, Pennacchio C, Del Rio TG, Stajich JE, and Coleine C
- Subjects
- Antarctic Regions, Bicycling, Climate, Acclimatization, Microbiota genetics
- Abstract
Background: Rock-dwelling microorganisms are key players in ecosystem functioning of Antarctic ice free-areas. Yet, little is known about their diversity and ecology, and further still, viruses in these communities have been largely unexplored despite important roles related to host metabolism and nutrient cycling. To begin to address this, we present a large-scale viral catalog from Antarctic rock microbial communities., Results: We performed metagenomic analyses on rocks from across Antarctica representing a broad range of environmental and spatial conditions, and which resulted in a predicted viral catalog comprising > 75,000 viral operational taxonomic units (vOTUS). We found largely undescribed, highly diverse and spatially structured virus communities which had predicted auxiliary metabolic genes (AMGs) with functions indicating that they may be potentially influencing bacterial adaptation and biogeochemistry., Conclusion: This catalog lays the foundation for expanding knowledge of virosphere diversity, function, spatial ecology, and dynamics in extreme environments. This work serves as a step towards exploring adaptability of microbial communities in the face of a changing climate. Video Abstract., (© 2023. The Author(s).)
- Published
- 2023
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22. Tourism affects microbial assemblages in show caves.
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Piano E, Biagioli F, Nicolosi G, Coleine C, Poli A, Prigione V, Zanellati A, Addesso R, Varese GC, Selbmann L, and Isaia M
- Subjects
- Humans, Caves microbiology, Bacteria, Archaea, Fungi, Tourism, Microbiota
- Abstract
Anthropogenic disturbance on natural ecosystems is growing in frequency and magnitude affecting all ecosystems components. Understanding the response of different types of biocoenosis to human disturbance is urgently needed and it can be achieved by adopting a metacommunity framework. With the aid of advanced molecular techniques, we investigated sediment communities of Fungi, Bacteria and Archaea in four Italian show caves, aiming to disentangle the effects induced by tourism on their diversity and to highlight changes in the driving forces that shape their community composition. We modelled diversity measures against proxies of tourism pressure. With this approach we demonstrate that the cave tourism has a direct effect on the community of Bacteria and an indirect influence on Fungi and Archaea. By analysing the main driving forces influencing the community composition of the three microbial groups, we highlighted that stochastic factors override dispersal-related processes and environmental selection in show caves compared to undisturbed areas. Thanks to this approach, we provide new perspectives on the dynamics of microbial communities under human disturbance suggesting that a proper understanding of the underlying selective mechanisms requires a comprehensive and multi-taxonomic approach., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Marco Isaia reports financial support was provided by Government of Italy Ministry of Education University and Research. Elena Piano reports financial support was provided by PON Research and Innovation., (Copyright © 2023 Elsevier B.V. All rights reserved.)
- Published
- 2023
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23. Rock Traits Drive Complex Microbial Communities at the Edge of Life.
- Author
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Coleine C, Delgado-Baquerizo M, Zerboni A, Turchetti B, Buzzini P, Franceschi P, and Selbmann L
- Subjects
- Planets, Earth, Planet, Antarctic Regions, Ecosystem, Exobiology
- Abstract
Antarctic deserts are among the driest and coldest ecosystems of the planet; there, some microbes survive under these extreme conditions inside porous rocks, forming the so-called endolithic communities. Yet the contribution of distinct rock traits to support complex microbial assemblies remains poorly determined. Here, we combined an extensive Antarctic rock survey with rock microbiome sequencing and ecological networks and found that contrasting combinations of microclimatic and rock traits such as thermal inertia, porosity, iron concentration, and quartz cement can help explain the multiple complex microbial assemblies found in Antarctic rocks. Our work highlights the pivotal role of rocky substrate heterogeneity in sustaining contrasting groups of microorganisms, which is essential to understand life at the edge on Earth and for the search for life on other rocky planets such as Mars.
- Published
- 2023
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24. Microbial diversity and proxy species for human impact in Italian karst caves.
- Author
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Biagioli F, Coleine C, Piano E, Nicolosi G, Poli A, Prigione V, Zanellati A, Varese C, Isaia M, and Selbmann L
- Subjects
- Humans, Anthropogenic Effects, Bacteria, Archaea, Fungi, Caves microbiology, Microbiota
- Abstract
To date, the highly adapted cave microbial communities are challenged by the expanding anthropization of these subterranean habitats. Although recent advances in characterizing show-caves microbiome composition and functionality, the anthropic effect on promoting the establishment, or reducing the presence of specific microbial guilds has never been studied in detail. This work aims to investigate the whole microbiome (Fungi, Algae, Bacteria and Archaea) of four Italian show-caves, displaying different environmental and geo-morphological conditions and one recently discovered natural cave to highlight potential human-induced microbial traits alterations. Results indicate how show-caves share common microbial traits in contrast to the natural one; the first are characterized by microorganisms related to outdoor environment and/or capable of exploiting extra inputs of organic matter eventually supplied by tourist flows (i.e. Chaetomium and Phoma for fungi and Pseudomonas for bacteria). Yet, variation in microalgae assemblage composition was reported in show-caves, probably related to the effect of the artificial lighting. This study provides insights into the potential microbiome cave contamination by human-related bacteria (e.g. Lactobacillus and Staphylococcus) and commensal/opportunistic human associated fungi (e.g. Candida) and dermatophytes. This work is critical to untangle caves microbiome towards management and conservation of these fragile ecosystems., (© 2023. The Author(s).)
- Published
- 2023
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25. Snow Surface Microbial Diversity at the Detection Limit within the Vicinity of the Concordia Station, Antarctica.
- Author
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Napoli A, Coleine C, Ulrich NJ, Moeller R, Billi D, and Selbmann L
- Abstract
The Concordia Research Station provides a unique location for preparatory activities for future human journey to Mars, to explore microbial diversity at subzero temperatures, and monitor the dissemination of human-associated microorganisms within the pristine surrounding environment. Amplicon sequencing was leveraged to investigate the microbial diversity of surface snow samples collected monthly over a two-year period, at three distances from the Station (10, 500, and 1000 m). Even when the extracted total DNA was below the detection limit, 16S rRNA gene sequencing was successfully performed on all samples, while 18S rRNA was amplified on 19 samples out of 51. No significant relationships were observed between microbial diversity and seasonality (summer or winter) or distance from the Concordia base. This suggested that if present, the anthropogenic impact should have been below the detectable limit. While harboring low microbial diversity, the surface snow samples were characterized by heterogeneous microbiomes. Ultimately, our study corroborated the use of DNA sequencing-based techniques for revealing microbial presence in remote and hostile environments, with implications for Planetary Protection during space missions and for life-detection in astrobiology relevant targets.
- Published
- 2022
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26. Unearthing terrestrial extreme microbiomes for searching terrestrial-like life in the Solar System.
- Author
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Coleine C and Delgado-Baquerizo M
- Subjects
- Earth, Planet, Solar System, Exobiology, Microbiota
- Abstract
The possibility of life elsewhere in the universe has fascinated humankind for ages. To the best of our knowledge, life, as we know it, is limited to planet Earth; yet current investigation suggests that life might be more common than previously thought. In this review, we explore extreme terrestrial analogue environments in the search for some notable examples of extreme organisms, including overlooked microbial groups such as viruses, fungi, and protists, associated with limits of life on Earth. This knowledge is integral to provide the foundational principles needed to predict what sort of Earth-like organisms we might find in the Solar System and beyond, and to understand the future and origins of life on Earth., Competing Interests: Declaration of interests The authors declare no competing interests., (Copyright © 2022 Elsevier Ltd. All rights reserved.)
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- 2022
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27. Fungi are key players in extreme ecosystems.
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Coleine C, Stajich JE, and Selbmann L
- Subjects
- Earth, Planet, Extreme Environments, Fungi, Ecosystem, Extremophiles
- Abstract
Extreme environments on Earth are typically devoid of macro life forms and are inhabited predominantly by highly adapted and specialized microorganisms. The discovery and persistence of these extremophiles provides tools to model how life arose on Earth and inform us on the limits of life. Fungi, in particular, are among the most extreme-tolerant organisms with highly versatile lifestyles and stunning ecological and morphological plasticity. Here, we overview the most notable examples of extremophilic and stress-tolerant fungi, highlighting their key roles in the functionality and balance of extreme ecosystems. The remarkable ability of fungi to tolerate and even thrive in the most extreme environments, which preclude most organisms, have reshaped current concepts regarding the limits of life on Earth., Competing Interests: Declaration of interests No interests are declared., (Copyright © 2022 Elsevier Ltd. All rights reserved.)
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- 2022
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28. The poly-extreme tolerant black yeasts are prevalent under high ultraviolet light and climatic seasonality across soils of global biomes.
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Coleine C, Selbmann L, Singh BK, and Delgado-Baquerizo M
- Subjects
- Humans, Soil, Soil Microbiology, Ultraviolet Rays, Ascomycota, Ecosystem
- Abstract
Black yeasts are among the most stress-tolerant organisms of the planet, thriving under all types of terrestrial habitats and extreme environments. Yet, their global patterns and ecology remain far less studied, limiting our capacity to identify the main environmental drivers of these important organisms across biomes. To fill this knowledge gap, we analysed topsoils from 235 terrestrial ecosystems across and within globally distributed climate groups (i.e. dry, temperate and continental). We found that soils are important repositories of black yeasts, and that ultraviolet light, fine soil texture, and precipitation seasonality are the most consistent environmental factors associated with their diversity across biomes. Finally, we identified Exophiala and Cladophialophora as the most dominant black yeasts genera in soils across the globe. These findings provide novel evidence of global distribution of black yeasts and their key environmental predictors, giving new insights for speculating the evolution and spreading of these extreme-tolerant organisms throughout both natural and human associated extreme environments., (© 2022 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd.)
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- 2022
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29. Rocks support a distinctive and consistent mycobiome across contrasting dry regions of Earth.
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Coleine C, Delgado-Baquerizo M, Albanese D, Singh BK, Stajich JE, Selbmann L, and Egidi E
- Subjects
- Desert Climate, Earth, Planet, Fungi genetics, Soil Microbiology, Mycobiome
- Abstract
Rock-dwelling fungi play critical ecological roles in drylands, including soil formation and nutrient cycling; however, we know very little about the identity, function and environmental preferences of these important organisms, and the mere existence of a consistent rock mycobiome across diverse arid regions of the planet remains undetermined. To address this knowledge gap, we conducted a meta-analysis of rock fungi and spatially associated soil communities, surveyed across 28 unique sites spanning four major biogeographic regions (North America, Arctic, Maritime and Continental Antarctica) including contrasting climates, from cold and hot deserts to semiarid drylands. We show that rocks support a consistent and unique mycobiome that was different from that found in surrounding soils. Lichenized fungi from class Lecanoromycetes were consistently indicative of rocks across contrasting regions, together with ascomycetous representatives of black fungi in Arthoniomycetes, Dothideomycetes and Eurotiomycetes. In addition, compared with soil, rocks had a lower proportion of saprobes and plant symbiotic fungi. The main drivers structuring rock fungi distribution were spatial distance and, to a larger extent, climatic factors regulating moisture and temperature (i.e. mean annual temperature and mean annual precipitation), suggesting that these paramount and unique communities might be particularly sensitive to increases in temperature and desertification., (© The Author(s) 2022. Published by Oxford University Press on behalf of FEMS.)
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- 2022
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30. Endolithic Bacterial Diversity in Lichen-Dominated Communities Is Shaped by Sun Exposure in McMurdo Dry Valleys, Antarctica.
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Mezzasoma A, Coleine C, Sannino C, and Selbmann L
- Subjects
- Antarctic Regions, Biodiversity, Humans, Sunlight, Cyanobacteria genetics, Lichens
- Abstract
The diversity and composition of endolithic bacterial diversity of several locations in McMurdo Dry Valleys (Continental Antarctica) were explored using amplicon sequencing, targeting the V3 and V4 of the 16S region. Despite the increasing interest in edaphic factors that drive bacterial community composition in Antarctic rocky communities, few researchers focused attention on the direct effects of sun exposure on bacterial diversity; we herein reported significant differences in the northern and southern communities. The analysis of β-diversity showed significant differences among sampled localities. For instance, the most abundant genera found in the north-exposed rocks were Rhodococcus and Blastococcus in Knobhead Mt.; Ktedonobacter and Cyanobacteria Family I Group I in Finger Mt.; Rhodococcus and Endobacter in University Valley; and Segetibacter and Tetrasphaera in Siegfried Peak samples. In south-exposed rocks, instead, the most abundant genera were Escherichia/Shigella and Streptococcus in Knobhead Mt.; Ktedonobacter and Rhodococcus in Finger Mt.; Ktedonobacter and Roseomonas in University Valley; and Blastocatella, Cyanobacteria Family I Group I and Segetibacter in Siegfried Peak. Significant biomarkers, detected by the Linear discriminant analysis Effect Size, were also found among north- and south-exposed communities. Besides, the large number of positive significant co-occurrences may suggest a crucial role of positive associations over competitions under the harsher conditions where these rock-inhabiting microorganisms spread. Although the effect of geographic distances in these extreme environments play a significant role in shaping biodiversity, the study of an edaphic factor, such as solar exposure, adds an important contribution to the mosaic of microbial biodiversity of Antarctic bacterial cryptoendolithic communities., (© 2021. The Author(s).)
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- 2022
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31. Endolithic microbial composition in Helliwell Hills, a newly investigated Mars-like area in Antarctica.
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Coleine C, Biagioli F, de Vera JP, Onofri S, and Selbmann L
- Subjects
- Antarctic Regions, Bacteria genetics, Biodiversity, Fungi genetics, Microbiota
- Abstract
The diversity and composition of Antarctic cryptoendolithic microbial communities in the Mars-analogue site of Helliwell Hills (Northern Victoria Land, Continental Antarctica) are investigated, for the first time, applying both culture-dependent and high-throughput sequencing approaches. The study includes all the domains of the tree of life: Eukaryotes, Bacteria and Archaea to give a complete overview of biodiversity and community structure. Furthermore, to explore the geographic distribution of endoliths throughout the Victoria Land (Continental Antarctica), we compared the fungal and bacterial community composition and structure of endolithically colonized rocks, collected in >30 sites in 10 years of Italian Antarctic Expeditions. Compared with the fungi and other eukaryotes, the prokaryotic communities were richer in species, more diverse and highly heterogeneous. Despite the diverse community compositions, shared populations were found and were dominant in all sites. Local diversification was observed and included prokaryotes as members of Alphaproteobacteria and Crenarchaeota (Archaea), the last detected for the first time in these cryptoendolithic communities. Few eukaryotes, namely lichen-forming fungal species as Lecidella grenii, were detected in Helliwell Hills only. These findings suggest that geographic distance and isolation in these remote areas may promote the establishment of peculiar locally diversified microorganisms., (© 2021 Society for Applied Microbiology and John Wiley & Sons Ltd.)
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- 2021
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32. Amplicon Sequencing of Rock-Inhabiting Microbial Communities from Joshua Tree National Park, USA.
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Coleine C, Selbmann L, Pombubpa N, and Stajich JE
- Abstract
Endolithic microorganisms have been reported to date in hot and cold drylands worldwide, where they represent the prevailing life forms ensuring ecosystem functionality, playing a paramount role in global biogeochemical processes. We report here an amplicon sequencing characterization of rocks collected from Joshua Tree National Park (JTNP), USA.
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- 2021
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33. Pre-Cambrian roots of novel Antarctic cryptoendolithic bacterial lineages.
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Albanese D, Coleine C, Rota-Stabelli O, Onofri S, Tringe SG, Stajich JE, Selbmann L, and Donati C
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- Antarctic Regions, Bacteria genetics, History, Ancient, Mars, Bacteria classification, Ecosystem, Phylogeny
- Abstract
Background: Cryptoendolithic communities are microbial ecosystems dwelling inside porous rocks that are able to persist at the edge of the biological potential for life in the ice-free areas of the Antarctic desert. These regions include the McMurdo Dry Valleys, often accounted as the closest terrestrial counterpart of the Martian environment and thought to be devoid of life until the discovery of these cryptic life-forms. Despite their interest as a model for the early colonization by living organisms of terrestrial ecosystems and for adaptation to extreme conditions of stress, little is known about the evolution, diversity, and genetic makeup of bacterial species that reside in these environments. Using the Illumina Novaseq platform, we generated the first metagenomes from rocks collected in Continental Antarctica over a distance of about 350 km along an altitudinal transect from 834 up to 3100 m above sea level (a.s.l.)., Results: A total of 497 draft bacterial genome sequences were assembled and clustered into 269 candidate species that lack a representative genome in public databases. Actinobacteria represent the most abundant phylum, followed by Chloroflexi and Proteobacteria. The "Candidatus Jiangella antarctica" has been recorded across all samples, suggesting a high adaptation and specialization of this species to the harshest Antarctic desert environment. The majority of these new species belong to monophyletic bacterial clades that diverged from related taxa in a range from 1.2 billion to 410 Ma and are functionally distinct from known related taxa., Conclusions: Our findings significantly increase the repertoire of genomic data for several taxa and, to date, represent the first example of bacterial genomes recovered from endolithic communities. Their ancient origin seems to not be related to the geological history of the continent, rather they may represent evolutionary remnants of pristine clades that evolved across the Tonian glaciation. These unique genomic resources will underpin future studies on the structure, evolution, and function of these ecosystems at the edge of life. Video abstract.
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- 2021
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34. Culture-Dependent and Amplicon Sequencing Approaches Reveal Diversity and Distribution of Black Fungi in Antarctic Cryptoendolithic Communities.
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Selbmann L, Stoppiello GA, Onofri S, Stajich JE, and Coleine C
- Abstract
In the harshest environmental conditions of the Antarctic desert, normally incompatible with active life, microbes are adapted to exploit the cryptoendolithic habitat (i.e., pore spaces of rocks) and represent the predominant life-forms. In the rocky niche, microbes take advantage of the thermal buffering, physical stability, protection against UV radiation, excessive solar radiation, and water retention-of paramount importance in one of the driest environments on Earth. In this work, high-throughput sequencing and culture-dependent approaches have been combined, for the first time, to untangle the diversity and distribution of black fungi in the Antarctic cryptoendolithic microbial communities, hosting some of the most extreme-tolerant microorganisms. Rock samples were collected in a vast area, along an altitudinal gradient and opposite sun exposure-known to influence microbial diversity-with the aim to compare and integrate results gained with the two approaches. Among black fungi, Friedmanniomyces endolithicus was confirmed as the most abundant taxon. Despite the much stronger power of the high-throughput sequencing, several species were not retrieved with DNA sequencing and were detectable by cultivation only. We conclude that both culture-dependent and -independent analyses are needed for a complete overview of black fungi diversity. The reason why some species remain undetectable with molecular methods are speculated upon. The effect of environmental parameters such as sun exposure on relative abundance was clearer if based on the wider biodiversity detected with the molecular approach.
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- 2021
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35. Metabolomics of Dry Versus Reanimated Antarctic Lichen-Dominated Endolithic Communities.
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Fanelli G, Coleine C, Gevi F, Onofri S, Selbmann L, and Timperio AM
- Abstract
Cryptoendolithic communities are almost the sole life form in the ice-free areas of the Antarctic desert, encompassing among the most extreme-tolerant organisms known on Earth that still assure ecosystems functioning, regulating nutrient and biogeochemical cycles under conditions accounted as incompatible with active life. If high-throughput sequencing based studies are unravelling prokaryotic and eukaryotic diversity, they are not yet characterized in terms of stress adaptations and responses, despite their paramount ecological importance. In this study, we compared the responses of Antarctic endolithic communities, with special focus on fungi, both under dry conditions (i.e., when dormant), and after reanimation by wetting, light, and optimal temperature (15 °C). We found that several metabolites were differently expressed in reanimated opposite sun exposed communities, suggesting a critical role in their success. In particular, the saccharopine pathway was up-regulated in the north surface, while the spermine/spermidine pathway was significantly down-regulated in the shaded exposed communities. The carnitine-dependent pathway is up-regulated in south-exposed reanimated samples, indicating the preferential involvement of the B-oxidation for the functioning of TCA cycle. The role of these metabolites in the performance of the communities is discussed herein.
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- 2021
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36. Beyond the extremes: Rocks as ultimate refuge for fungi in drylands.
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Coleine C, Stajich JE, de Los Ríos A, and Selbmann L
- Subjects
- Adaptation, Physiological, Antarctic Regions, Biodiversity, Climate Change, Droughts, Geologic Sediments microbiology, Lichens, Desert Climate, Extreme Environments, Fungi classification, Fungi isolation & purification
- Abstract
In an era of rapid climate change and expansion of desertification, the extremely harsh conditions of drylands are a true challenge for microbial life. Under drought conditions, where most life forms cannot survive, rocks represent the main refuge for life. Indeed, the endolithic habitat provides thermal buffering, physical stability, and protection against incident ultraviolet (UV) radiation and solar radiation and, to some extent, ensures water retention to microorganisms. The study of these highly specialized extreme-tolerant and extremophiles may provide tools for understanding microbial interactions and processes that allow them to keep their metabolic machinery active under conditions of dryness and oligotrophy that are typically incompatible with active life, up to the dry limits for life. Despite lithobiontic communities being studied all over the world, a comprehensive understanding of their ecology, evolution, and adaptation is still nascent. Herein, we survey the fungal component of these microbial ecosystems. We first provide an overview of the main defined groups (i.e., lichen-forming fungi, black fungi, and yeasts) of the most known and studied Antarctic endolithic communities that are almost the only life forms ensuring ecosystem functionality in the ice-free areas of the continent. For each group, we discuss their main traits and their diversity. Then, we focus on the fungal taxonomy and ecology of other worldwide endolithic communities. Finally, we highlight the utmost importance of a global rock survey in order to have a comprehensive view of the diversity, distribution, and functionality of these fungi in drylands, to obtain tools in desert area management, and as early alarm systems to climate change.
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- 2021
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37. Shed Light in the DaRk LineagES of the Fungal Tree of Life-STRES.
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Selbmann L, Benkő Z, Coleine C, de Hoog S, Donati C, Druzhinina I, Emri T, Ettinger CL, Gladfelter AS, Gorbushina AA, Grigoriev IV, Grube M, Gunde-Cimerman N, Karányi ZÁ, Kocsis B, Kubressoian T, Miklós I, Miskei M, Muggia L, Northen T, Novak-Babič M, Pennacchio C, Pfliegler WP, Pòcsi I, Prigione V, Riquelme M, Segata N, Schumacher J, Shelest E, Sterflinger K, Tesei D, U'Ren JM, Varese GC, Vázquez-Campos X, Vicente VA, Souza EM, Zalar P, Walker AK, and Stajich JE
- Abstract
The polyphyletic group of black fungi within the Ascomycota (Arthoniomycetes, Dothideomycetes, and Eurotiomycetes) is ubiquitous in natural and anthropogenic habitats. Partly because of their dark, melanin-based pigmentation, black fungi are resistant to stresses including UV- and ionizing-radiation, heat and desiccation, toxic metals, and organic pollutants. Consequently, they are amongst the most stunning extremophiles and poly-extreme-tolerant organisms on Earth. Even though ca. 60 black fungal genomes have been sequenced to date, [mostly in the family Herpotrichiellaceae (Eurotiomycetes)], the class Dothideomycetes that hosts the largest majority of extremophiles has only been sparsely sampled. By sequencing up to 92 species that will become reference genomes, the "Shed light in The daRk lineagES of the fungal tree of life" (STRES) project will cover a broad collection of black fungal diversity spread throughout the Fungal Tree of Life. Interestingly, the STRES project will focus on mostly unsampled genera that display different ecologies and life-styles (e.g., ant- and lichen-associated fungi, rock-inhabiting fungi, etc.). With a resequencing strategy of 10- to 15-fold depth coverage of up to ~550 strains, numerous new reference genomes will be established. To identify metabolites and functional processes, these new genomic resources will be enriched with metabolomics analyses coupled with transcriptomics experiments on selected species under various stress conditions (salinity, dryness, UV radiation, oligotrophy). The data acquired will serve as a reference and foundation for establishing an encyclopedic database for fungal metagenomics as well as the biology, evolution, and ecology of the fungi in extreme environments.
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- 2020
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38. Expansion of shrubs could result in local loss of soil bacterial richness in Western Greenland.
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Canini F, Zucconi L, Coleine C, D'Alò F, Onofri S, and Geml J
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- Arctic Regions, Bacteria genetics, Greenland, RNA, Ribosomal, 16S genetics, Soil Microbiology, Ecosystem, Soil
- Abstract
Climate warming in Greenland is facilitating the expansion of shrubs across wide areas of tundra. Given the close association between plants and soil microorganisms and the important role of soil bacteria in ecosystem functioning, it is of utmost importance to characterize microbial communities of arctic soil habitats and assess the influence of plant edaphic factors on their composition. We used 16S rRNA gene amplicons to explore the bacterial assemblages of three different soil habitats representative of a plant coverage gradient: bare ground, biological soil crusts dominated by mosses and lichens and vascular vegetation dominated by shrubs. We investigated how bacterial richness and community composition were affected by the vegetation coverage, and soil pH, moisture and carbon (C), nitrogen (N) and phosphorus (P) contents. Bacterial richness did not correlate with plant coverage complexity, while community structure varied between habitats. Edaphic variables affected both the taxonomic richness and community composition. The high number of Amplicon Sequence Variants (ASVs) indicators of bare ground plots suggests a risk of local bacterial diversity loss due to expansion of vascular vegetation., (© FEMS 2020.)
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- 2020
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39. Uncovered Microbial Diversity in Antarctic Cryptoendolithic Communities Sampling three Representative Locations of the Victoria Land.
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Coleine C, Pombubpa N, Zucconi L, Onofri S, Turchetti B, Buzzini P, Stajich JE, and Selbmann L
- Abstract
The endolithic niche represents an ultimate refuge to microorganisms in the Mars-like environment of the Antarctic desert. In an era of rapid global change and desertification, the interest in these border ecosystems is increasing due to speculation on how they maintain balance and functionality at the dry limits of life. To assure a reliable estimation of microbial diversity, proper sampling must be planned in order to avoid the necessity of re-sampling as reaching these remote locations is risky and requires tremendous logistical and economical efforts. In this study, we seek to determine the minimum number of samples for uncovering comprehensive bacterial and fungal diversity, comparing communities in strict vicinity to each other. We selected three different locations of the Victoria Land (Continental Antarctica) at different altitudes and showing sandstone outcrops of a diverse nature and origin-Battleship promontory (834 m above sea level (a.s.l.), Southern VL), Trio Nunatak (1,470 m a.s.l., Northern VL) and Mt New Zealand (3,100 m a.s.l., Northern VL). Overall, we found that a wider sampling would be required to capture the whole amplitude of microbial diversity, particularly in Northern VL. We concluded that the inhomogeneity of the rock matrix and the stronger environmental pressure at higher altitudes may force the communities to a higher local diversification.
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- 2020
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40. Specific adaptations are selected in opposite sun exposed Antarctic cryptoendolithic communities as revealed by untargeted metabolomics.
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Coleine C, Gevi F, Fanelli G, Onofri S, Timperio AM, and Selbmann L
- Subjects
- Allantoin metabolism, Antarctic Regions, Extreme Environments, Melanins metabolism, Selection, Genetic, Stress, Physiological, Adaptation, Physiological, Metabolome, Microbiota, Sunlight
- Abstract
Antarctic cryptoendolithic communities are self-supporting borderline ecosystems spreading across the extreme conditions of the Antarctic desert and represent the predominant life-form in the ice-free areas of McMurdo Dry Valleys, accounted as the closest terrestrial Martian analogue. Components of these communities are highly adapted extremophiles and extreme-tolerant microorganisms, among the most resistant known to date. Recently, studies investigated biodiversity and community composition in these ecosystems but the metabolic activity of the metacommunity has never been investigated. Using an untargeted metabolomics, we explored stress-response of communities spreading in two sites of the same location, subjected to increasing environmental pressure due to opposite sun exposure, accounted as main factor influencing the diversity and composition of these ecosystems. Overall, 331 altered metabolites (206 and 125 unique for north and south, respectively), distinguished the two differently exposed communities. We also selected 10 metabolites and performed two-stage Receiver Operating Characteristic (ROC) analysis to test them as potential biomarkers. We further focused on melanin and allantoin as protective substances; their concentration was highly different in the community in the shadow or in the sun. These results clearly indicate that opposite insolation selected organisms in the communities with different adaptation strategies in terms of key metabolites produced., Competing Interests: The authors have declared that no competing interests exist.
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- 2020
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41. Peculiar genomic traits in the stress-adapted cryptoendolithic Antarctic fungus Friedmanniomyces endolithicus.
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Coleine C, Masonjones S, Sterflinger K, Onofri S, Selbmann L, and Stajich JE
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- Antarctic Regions, Exophiala genetics, Stress, Physiological genetics, Ascomycota genetics, Genome, Fungal genetics
- Abstract
Friedmanniomyces endolithicus is a highly melanized fungus endemic to the Antarctic, occurring exclusively in endolithic communities of the ice-free areas of the Victoria Land, including the McMurdo Dry Valleys, the coldest and most hyper-arid desert on Earth and accounted as the Martian analog on our planet. F. endolithicus is highly successful in these inhospitable environments, the most widespread and commonly isolated species from these peculiar niches, indicating a high degree of adaptation. The nature of its extremo tolerance has not been previously studied. To investigate this, we sequenced genome of F. endolithicus CCFEE 5311 to explore gene content and genomic patterns that could be attributed to its specialization. The predicted functional potential of the genes was assigned by similarity to InterPro and CAZy domains. The genome was compared to phylogenetically close relatives which are also melanized fungi occurring in extreme environments including Friedmanniomyces simplex, Baudoinia panamericana, Acidomyces acidophilus, Hortaea thailandica and Hortaea werneckii. We tested if shared genomic traits existed among these species and hyper-extremotolerant fungus F. endolithicus. We found that some characters for stress tolerance such as meristematic growth and cold tolerance are enriched in F. endolithicus that may be triggered by the exposure to Antarctic prohibitive conditions., Competing Interests: Declaration of Competing Interest The authors report no conflicts of interest. The authors alone are responsible for the content and the writing of the paper., (Copyright © 2020 British Mycological Society. Published by Elsevier Ltd. All rights reserved.)
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- 2020
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42. Draft Genome Sequence of the Yeast Rhodotorula sp. Strain CCFEE 5036, Isolated from McMurdo Dry Valleys, Antarctica.
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Coleine C, Masonjones S, Onofri S, Selbmann L, and Stajich JE
- Abstract
A draft genome sequence was assembled and annotated of the basidiomycetous yeast Rhodotorula sp. strain CCFEE 5036, isolated from Antarctic soil communities. The genome assembly is 19.07 megabases and encodes 6,434 protein-coding genes. The sequence will contribute to understanding the diversity of fungi inhabiting polar regions., (Copyright © 2020 Coleine et al.)
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- 2020
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43. Metagenomes in the Borderline Ecosystems of the Antarctic Cryptoendolithic Communities.
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Coleine C, Albanese D, Onofri S, Tringe SG, Pennacchio C, Donati C, Stajich JE, and Selbmann L
- Abstract
Antarctic cryptoendolithic communities are microbial ecosystems dwelling inside rocks of the Antarctic desert. We present the first 18 shotgun metagenomes from these communities to further characterize their composition, biodiversity, functionality, and adaptation. Future studies will integrate taxonomic and functional annotations to examine the pathways necessary for life to evolve in the extremes., (Copyright © 2020 Coleine et al.)
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- 2020
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44. Endolithic Fungal Species Markers for Harshest Conditions in the McMurdo Dry Valleys, Antarctica.
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Coleine C, Pombubpa N, Zucconi L, Onofri S, Stajich JE, and Selbmann L
- Abstract
The microbial communities that inhabit lithic niches inside sandstone in the Antarctic McMurdo Dry Valleys of life's limits on Earth. The cryptoendolithic communities survive in these ice-free areas that have the lowest temperatures on Earth coupled with strong thermal fluctuations, extreme aridity, oligotrophy and high levels of solar and UV radiation. In this study, based on DNA metabarcoding, targeting the fungal Internal Transcribed Spacer region 1 (ITS1) and multivariate statistical analyses, we supply the first comprehensive overview onto the fungal diversity and composition of these communities sampled over a broad geographic area of the Antarctic hyper-arid cold desert. Six locations with surfaces that experience variable sun exposure were sampled to compare communities from a common area across a gradient of environmental pressure. The Operational Taxonomic Units (OTUs) identified were primarily members of the Ascomycota phylum, comprised mostly of the Lecanoromycetes and Dothideomycetes classes. The fungal species Friedmanniomyces endolithicus , endemic to Antarctica, was found to be a marker species to the harshest conditions occurring in the shady, south exposed rock surfaces. Analysis of community composition showed that sun exposure was an environmental property that explained community diversity and structured endolithic colonization., Competing Interests: The authors declare no conflict of interest.
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- 2020
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45. Altitude and fungal diversity influence the structure of Antarctic cryptoendolithic Bacteria communities.
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Coleine C, Stajich JE, Pombubpa N, Zucconi L, Onofri S, Canini F, and Selbmann L
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- Antarctic Regions, DNA, Bacterial genetics, Genetic Variation, Phylogeny, Sequence Analysis, DNA, Soil Microbiology, Altitude, Bacteria classification, Biodiversity, Fungi classification, Microbiota
- Abstract
Endolithic growth within rocks is a critical adaptation of microbes living in harsh environments where exposure to extreme temperature, radiation, and desiccation limits the predominant life forms, such as in the ice-free regions of Continental Antarctica. The microbial diversity of the endolithic communities in these areas has been sparsely examined. In this work, diversity and composition of bacterial assemblages in the cryptoendolithic lichen-dominated communities of Victoria Land (Continental Antarctica) were explored using a high-throughput metabarcoding approach, targeting the V4 region of 16S rDNA. Rocks were collected in 12 different localities (from 14 different sites), along a gradient ranging from 1000 to 3300 m a.s.l. and at a sea distance ranging from 29 to 96 km. The results indicate Actinobacteria and Proteobacteria are the dominant taxa in all samples and defined a 'core' group of bacterial taxa across all sites. The structure of bacteria communities is correlated with the fungal counterpart and among the environmental parameters considered, altitude was found to influence bacterial biodiversity, while distance from sea had no evident influence., (© 2019 Society for Applied Microbiology and John Wiley & Sons Ltd.)
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- 2019
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46. Draft Genome Sequence of an Antarctic Isolate of the Black Yeast Fungus Exophiala mesophila .
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Coleine C, Selbmann L, Masonjones S, Onofri S, Zucconi L, and Stajich JE
- Abstract
A 30.43-Mb draft genome sequence with 10,355 predicted protein-coding genes was produced for the ascomycete fungus Exophiala mesophila strain CCFEE 6314, a black yeast isolated from Antarctic cryptoendolithic communities. The sequence will be of importance for identifying differences among extremophiles and mesophiles and cataloguing the global population diversity of this organism., (Copyright © 2019 Coleine et al.)
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- 2019
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47. Responses of the Black Fungus Cryomyces antarcticus to Simulated Mars and Space Conditions on Rock Analogs.
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Pacelli C, Selbmann L, Zucconi L, Coleine C, de Vera JP, Rabbow E, Böttger U, Dadachova E, and Onofri S
- Subjects
- Ascomycota radiation effects, Ascomycota ultrastructure, DNA Damage, Melanins analysis, Spectrum Analysis, Raman, Ultraviolet Rays, Ascomycota physiology, Extraterrestrial Environment, Mars
- Abstract
The BIOMEX (BIOlogy and Mars Experiment) is part of the European Space Agency (ESA) space mission EXPOSE-R2 in Low-Earth Orbit, devoted to exposing microorganisms for 1.5 years to space and simulated Mars conditions on the International Space Station. In preparing this mission, dried colonies of the Antarctic cryptoendolithic black fungus Cryomyces antarcticus CCFEE 515, grown on martian and lunar analog regolith pellets, were subjected to several ground-based preflight tests, Experiment Verification Tests, and Science Verification Tests (SVTs) that were performed to verify (i) the resistance of our model organism to space stressors when grown on extraterrestrial rock analogs and (ii) the possibility of detecting biomolecules as potential biosignatures. Here, the results of the SVTs, the last set of experiments, which were performed in ultraviolet radiation combined with simulated space vacuum or simulated martian conditions, are reported. The results demonstrate that C. antarcticus was able to tolerate the conditions of the SVT experiment, regardless of the substratum in which it was grown. DNA maintained high integrity after treatments and was confirmed as a possible biosignature; melanin, which was chosen to be a target for biosignature detection, was unambiguously detected by Raman spectroscopy.
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- 2019
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48. Antarctic Cryptoendolithic Fungal Communities Are Highly Adapted and Dominated by Lecanoromycetes and Dothideomycetes.
- Author
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Coleine C, Stajich JE, Zucconi L, Onofri S, Pombubpa N, Egidi E, Franks A, Buzzini P, and Selbmann L
- Abstract
Endolithic growth is one of the most spectacular microbial adaptations to extreme environmental constraints and the predominant life-form in the ice-free areas of Continental Antarctica. Although Antarctic endolithic microbial communities are known to host among the most resistant and extreme-adapted organisms, our knowledge on microbial diversity and composition in this peculiar niche is still limited. In this study, we investigated the diversity and structure of the fungal assemblage in the cryptoendolithic communities inhabiting sandstone using a meta-barcoding approach targeting the fungal Internal Transcribed Sequence region 1 (ITS1). Samples were collected from 14 sites in the Victoria Land, along an altitudinal gradient ranging from 1,000 to 3,300 m a.s.l. and from 29 to 96 km distance to coast. Our study revealed a clear dominance of a 'core' group of fungal taxa consistently present across all the samples, mainly composed of lichen-forming and Dothideomycetous fungi. Pareto-Lorenz curves indicated a very high degree of specialization (F
0 approximately 95%), suggesting these communities are highly adapted but have limited ability to recover after perturbations. Overall, both fungal community biodiversity and composition did not show any correlation with the considered abiotic parameters, potentially due to strong fluctuations of environmental conditions at local scales.- Published
- 2018
- Full Text
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49. Sun Exposure Shapes Functional Grouping of Fungi in Cryptoendolithic Antarctic Communities.
- Author
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Coleine C, Zucconi L, Onofri S, Pombubpa N, Stajich JE, and Selbmann L
- Abstract
Antarctic cryptoendolithic microbial communities dominate ice-free areas of continental Antarctica, among the harshest environments on Earth. The endolithic lifestyle is a remarkable adaptation to the exceptional environmental extremes of this area, which is considered the closest terrestrial example to conditions on Mars. Recent efforts have attempted to elucidate composition of these extremely adapted communities, but the functionality of these microbes have remained unexplored. We have tested for interactions between measured environmental characteristics, fungal community membership, and inferred functional classification of the fungi present and found altitude and sun exposure were primary factors. Sandstone rocks were collected in Victoria Land, Antarctica along an altitudinal gradient from 834 to 3100 m a.s.l.; differently sun-exposed rocks were selected to test the influence of this parameter on endolithic settlement. Metabarcoding targeting the fungal internal transcribed spacer region 1 (ITS1) was used to catalogue the species found in these communities. Functional profile of guilds found in the samples was associated to species using FUNGuild and variation in functional groups compared across sunlight exposure and altitude. Results revealed clear dominance of lichenized and stress-tolerant fungi in endolithic communities. The main variations in composition and abundance of functional groups among sites correlated to sun exposure, but not to altitude.
- Published
- 2018
- Full Text
- View/download PDF
50. Taxonomic annotation of public fungal ITS sequences from the built environment - a report from an April 10-11, 2017 workshop (Aberdeen, UK).
- Author
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Nilsson RH, Taylor AFS, Adams RI, Baschien C, Johan Bengtsson-Palme, Cangren P, Coleine C, Heide-Marie Daniel, Glassman SI, Hirooka Y, Irinyi L, Reda Iršėnaitė, Pedro M Martin-Sanchez, Meyer W, Seung-Yoon Oh, Jose Paulo Sampaio, Seifert KA, Sklenář F, Dirk Stubbe, Suh SO, Summerbell R, Svantesson S, Martin Unterseher, Cobus M Visagie, Weiss M, Woudenberg JH, Christian Wurzbacher, den Wyngaert SV, Yilmaz N, Andrey Yurkov, Kõljalg U, and Abarenkov K
- Abstract
Recent DNA-based studies have shown that the built environment is surprisingly rich in fungi. These indoor fungi - whether transient visitors or more persistent residents - may hold clues to the rising levels of human allergies and other medical and building-related health problems observed globally. The taxonomic identity of these fungi is crucial in such pursuits. Molecular identification of the built mycobiome is no trivial undertaking, however, given the large number of unidentified, misidentified, and technically compromised fungal sequences in public sequence databases. In addition, the sequence metadata required to make informed taxonomic decisions - such as country and host/substrate of collection - are often lacking even from reference and ex-type sequences. Here we report on a taxonomic annotation workshop (April 10-11, 2017) organized at the James Hutton Institute/University of Aberdeen (UK) to facilitate reproducible studies of the built mycobiome. The 32 participants went through public fungal ITS barcode sequences related to the built mycobiome for taxonomic and nomenclatural correctness, technical quality, and metadata availability. A total of 19,508 changes - including 4,783 name changes, 14,121 metadata annotations, and the removal of 99 technically compromised sequences - were implemented in the UNITE database for molecular identification of fungi (https://unite.ut.ee/) and shared with a range of other databases and downstream resources. Among the genera that saw the largest number of changes were Penicillium , Talaromyces , Cladosporium, Acremonium , and Alternaria , all of them of significant importance in both culture-based and culture-independent surveys of the built environment.
- Published
- 2018
- Full Text
- View/download PDF
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