• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

欧洲肉座菌属物种第二部分:具透明子囊孢子的物种。

European species of Hypocrea part II: species with hyaline ascospores.

作者信息

Jaklitsch Walter M

机构信息

Department of Systematic and Evolutionary Botany, Faculty Centre of Biodiversity, University of Vienna, Rennweg 14, 1030 Vienna, Austria.

出版信息

Fungal Divers. 2011 May;48(1):1-250. doi: 10.1007/s13225-011-0088-y.

DOI:10.1007/s13225-011-0088-y
PMID:21994484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3189789/
Abstract

To date 75 species of Hypocrea/Trichoderma forming teleomorphs are recognised in Europe. The 56 hyaline-spored species are here described in detail and illustrated in colour plates, including cultures and anamorphs. This number includes 16 new holomorphs, two new teleomorphs and nine anamorphs of species previously described as teleomorphs. Phylogenetic placement and relationships of the species are shown on the strict consensus tree, based on sequences of RNA polymerase II subunit b (rpb2) and translation elongation factor 1 alpha (tef1) exon, comprising 135 species of the genus Hypocrea/Trichoderma. All available holotypes of species described from Europe including some from North America have been examined. A dichotomous key to the species is provided primarily utilising ecological and morphological traits of the teleomorphs and, where necessary, morphology of the anamorphs and cultures, and growth rates. Species descriptions are subdivided among five chapters, arranged primarily according to the larger phylogenetic clades, viz. section Trichoderma with 13 species, the pachybasium core group with 13 species including four species with stipitate stromata ('Podostroma'), species forming large effused stromata with 10 species including the section Hypocreanum, 9 species of the Brevicompactum, Lutea and Psychrophila clades, and 11 residual species of various smaller clades or of unknown phylogenetic placement. Finally, a list comprising dubious names and species excluded from Hypocrea that are relevant for Europe, or species claimed to occur in Europe by other authors is provided. Hypocrea minutispora is by far the most common species in Europe. For H. moravica, H. subalpina and H. tremelloides the anamorphs are newly described. The anamorphs of the latter two species and H. sambuci produce hyaline conidia on unusual structures new to Trichoderma. These three species form a new subclade of the morphologically strikingly different section Longibrachiatum, which is currently only represented by H. schweinitzii in Europe as a holomorph. The subclade is not named yet formally due to low statistical support. H. fungicola f. raduli is described as the new species H. austriaca, while H. hypomycella was found not to belong to Hypocrea. The typification of H. pilulifera, H. tremelloides and H. lutea has been clarified. Gliocladium deliquescens, the anamorph of H. lutea, is combined in Trichoderma. Species are epitypified where appropriate. Anamorph names are established prospectively to avoid numerous new combinations in future when they may be possibly used as holomorphic names if the ICBN is altered accordingly.

摘要

迄今为止,在欧洲已识别出75种形成有性型的肉座菌属/木霉属真菌。本文详细描述了其中56种产透明孢子的物种,并配有彩色图谱说明,包括培养物和无性型。这个数字包括16个新的全型、2个新的有性型以及9个先前被描述为有性型的物种的无性型。基于RNA聚合酶II亚基b(rpb2)和翻译延伸因子1α(tef1)外显子的序列,构建了包含135种肉座菌属/木霉属真菌的严格合意树,展示了这些物种的系统发育位置和关系。已检查了所有来自欧洲(包括一些来自北美的)已描述物种的可用模式标本。提供了一个分种检索表,主要利用有性型的生态和形态特征,并在必要时结合无性型、培养物的形态以及生长速率。物种描述分为五章,主要根据较大的系统发育分支进行排列,即:木霉组有13个物种;厚基核组有13个物种,其中包括4个具柄子座的物种(“柄座菌属”);形成大型平铺子座的物种有10个,包括肉座菌组;短密孢组、黄孢组和嗜冷组有9个物种;以及11个来自各种较小分支或系统发育位置未知的剩余物种。最后,列出了与欧洲相关的可疑名称和从肉座菌属中排除的物种,或其他作者声称在欧洲出现的物种。微小肉座菌是欧洲迄今为止最常见的物种。对于摩拉维亚肉座菌、亚高山肉座菌和银耳状肉座菌,其无性型是新描述的。后两个物种和接骨木肉座菌的无性型在木霉属中不常见的结构上产生透明分生孢子。这三个物种形成了形态上显著不同的长枝组的一个新亚分支,目前在欧洲作为全型仅由施氏肉座菌代表。由于统计支持率低,该亚分支尚未正式命名。拟食菌肉座菌蕨类变种被描述为新物种奥地利肉座菌,而拟菌肉座菌被发现不属于肉座菌属。已阐明了丸形肉座菌、银耳状肉座菌和黄肉座菌的模式指定。黄肉座菌的无性型消解粘帚霉被归并入木霉属。在适当的情况下对物种进行了后选模式指定。前瞻性地建立无性型名称,以避免未来在国际植物命名法规相应变更时可能用作全型名称而产生大量新组合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/13ef74ea8669/13225_2011_88_Fig32_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/25839d087c70/13225_2011_88_Fig1a_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/971a6c725bd0/13225_2011_88_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/596e2b85be8c/13225_2011_88_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/172b90d05ce6/13225_2011_88_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/2c4da18aa269/13225_2011_88_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/bee6d04244c6/13225_2011_88_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/a2bfb13647c0/13225_2011_88_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/c9f317912696/13225_2011_88_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/3536a877ab04/13225_2011_88_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/1c80e04f4f13/13225_2011_88_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/f3a98bf87a95/13225_2011_88_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/26364a9ac80a/13225_2011_88_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/86b267497374/13225_2011_88_Fig13_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/5a87f5cc3634/13225_2011_88_Fig14_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/2925e1b7427f/13225_2011_88_Fig15_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/2f1cf5e6ede5/13225_2011_88_Fig17_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/af019f8d3376/13225_2011_88_Fig18_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/f04e8e6e07aa/13225_2011_88_Fig19_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/a63e5d9a0ce8/13225_2011_88_Fig20_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/8186e457fc32/13225_2011_88_Fig21_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/06f62cda1fa7/13225_2011_88_Fig22_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/b66d9b04ad9e/13225_2011_88_Fig23_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/e0322b9d37b0/13225_2011_88_Fig24_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/63bdd47b46a8/13225_2011_88_Fig25_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/6bb70977c8fa/13225_2011_88_Fig26_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/a20b98499025/13225_2011_88_Fig27_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/d75acbb430f7/13225_2011_88_Fig28_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/d7c2a06501c7/13225_2011_88_Fig29_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/c34a88fa4af4/13225_2011_88_Fig30_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/3aa12f7ff04f/13225_2011_88_Fig31_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/13ef74ea8669/13225_2011_88_Fig32_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/25839d087c70/13225_2011_88_Fig1a_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/971a6c725bd0/13225_2011_88_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/596e2b85be8c/13225_2011_88_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/172b90d05ce6/13225_2011_88_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/2c4da18aa269/13225_2011_88_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/bee6d04244c6/13225_2011_88_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/a2bfb13647c0/13225_2011_88_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/c9f317912696/13225_2011_88_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/3536a877ab04/13225_2011_88_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/1c80e04f4f13/13225_2011_88_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/f3a98bf87a95/13225_2011_88_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/26364a9ac80a/13225_2011_88_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/86b267497374/13225_2011_88_Fig13_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/5a87f5cc3634/13225_2011_88_Fig14_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/2925e1b7427f/13225_2011_88_Fig15_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/2f1cf5e6ede5/13225_2011_88_Fig17_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/af019f8d3376/13225_2011_88_Fig18_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/f04e8e6e07aa/13225_2011_88_Fig19_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/a63e5d9a0ce8/13225_2011_88_Fig20_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/8186e457fc32/13225_2011_88_Fig21_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/06f62cda1fa7/13225_2011_88_Fig22_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/b66d9b04ad9e/13225_2011_88_Fig23_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/e0322b9d37b0/13225_2011_88_Fig24_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/63bdd47b46a8/13225_2011_88_Fig25_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/6bb70977c8fa/13225_2011_88_Fig26_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/a20b98499025/13225_2011_88_Fig27_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/d75acbb430f7/13225_2011_88_Fig28_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/d7c2a06501c7/13225_2011_88_Fig29_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/c34a88fa4af4/13225_2011_88_Fig30_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/3aa12f7ff04f/13225_2011_88_Fig31_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e44b/3688327/13ef74ea8669/13225_2011_88_Fig32_HTML.jpg

相似文献

1
European species of Hypocrea part II: species with hyaline ascospores.欧洲肉座菌属物种第二部分:具透明子囊孢子的物种。
Fungal Divers. 2011 May;48(1):1-250. doi: 10.1007/s13225-011-0088-y.
2
European species of Hypocrea Part I. The green-spored species.欧洲 Hypocrea 种 Part I. 绿孢种。
Stud Mycol. 2009;63:1-91. doi: 10.3114/sim.2009.63.01.
3
Hypocrea crystalligena sp. nov., a common European species with a white-spored Trichoderma anamorph.新种结晶肉座菌,一种具有白色孢子木霉无性型的常见欧洲物种。
Mycologia. 2006 May-Jun;98(3):499-513. doi: 10.3852/mycologia.98.3.499.
4
Taxonomy and phylogenetic relationships of nine species of Hypocrea with anamorphs assignable to Trichoderma section Hypocreanum.具有 assignable 到 Trichoderma 节 Hypocreanum 无性型的 Hypocrea 九个种的分类和系统发育关系。
Stud Mycol. 2006;56:39-65. doi: 10.3114/sim.2006.56.02.
5
Hypocrea/Trichoderma species with pachybasium-like conidiophores: teleomorphs for T. minutisporum and T. polysporum and their newly discovered relatives.具有厚壁孢梗束状分生孢子梗的Hypocrea/Trichoderma 种:T. minutisporum 和 T. polysporum 的有性型及其新发现的亲缘种。
Mycologia. 2004 Mar-Apr;96(2):310-42.
6
Hypocrea/Trichoderma: species with conidiophore elongations and green conidia.Hypocrea/Trichoderma:具有分生孢子梗伸长和绿色分生孢子的物种。
Mycologia. 2003 Nov-Dec;95(6):1100-40.
7
Hypocrea rufa/Trichoderma viride: a reassessment, and description of five closely related species with and without warted conidia.红栓菌/绿色木霉:重新评估及五组密切相关种的描述,包括有和无疣状分生孢子。
Stud Mycol. 2006;56:135-77. doi: 10.3114/sim.2006.56.04.
8
Hypocrea britdaniae and H. foliicola: two remarkable new European species.Hypocrea britdaniae 和 H. foliicola:两个显著的欧洲新物种。
Mycologia. 2012 Sep-Oct;104(5):1213-21. doi: 10.3852/11-429. Epub 2012 Apr 13.
9
Three European species of Hypocrea with reddish brown stromata and green ascospores.三种欧洲的肉座菌属物种,具红棕色子座和绿色子囊孢子。
Mycologia. 2008 Sep-Oct;100(5):796-815. doi: 10.3852/08-039.
10
Hypocrea seppoi, a new stipitate species from Finland.芬兰新发现的具柄肉座菌——塞氏肉座菌
Karstenia. 2008;48(1):1-11. doi: 10.29203/ka.2008.423.

引用本文的文献

1
Trichoderma: a multifunctional agent in plant health and microbiome interactions.木霉:植物健康与微生物组相互作用中的多功能因子
BMC Microbiol. 2025 Jul 12;25(1):434. doi: 10.1186/s12866-025-04158-2.
2
Exploring diversity in the Western Ghats of India: phylogenetic analysis, metabolomics insights and biocontrol efficacy against Maydis Leaf Blight disease.探索印度西高止山脉的多样性:系统发育分析、代谢组学见解及对玉米大斑病的生物防治效果
Front Microbiol. 2024 Dec 20;15:1493272. doi: 10.3389/fmicb.2024.1493272. eCollection 2024.
3
What are the 100 most cited fungal genera?

本文引用的文献

1
Exploring the species diversity of Trichoderma in Norwegian drinking water systems by DNA barcoding.通过 DNA 条形码技术探索挪威饮用水系统中的木霉属物种多样性。
Mol Ecol Resour. 2008 Nov;8(6):1178-88. doi: 10.1111/j.1755-0998.2008.02280.x. Epub 2008 Aug 20.
2
Hypocrea atroviridis sp. nov., the teleomorph of Trichoderma atroviride.Hypocrea atroviridis sp. nov.,即深绿木霉的有性型。
Mycologia. 2003 Jan-Feb;95(1):27-40. doi: 10.1080/15572536.2004.11833129.
3
Hypocrea/Trichoderma: species with conidiophore elongations and green conidia.
被引用次数最多的100个真菌属有哪些?
Stud Mycol. 2024 Jul;108:1-411. doi: 10.3114/sim.2024.108.01. Epub 2024 Jul 15.
4
Sclerotia degradation by Trichoderma-mycoparasitic; an effective and sustainable trend in the drop lettuce disease control caused by Sclerotinia sclerotiorum.木霉寄生对菌核的降解:一种防治由核盘菌引起的生菜菌核病的有效且可持续的趋势。
Arch Microbiol. 2024 Jun 3;206(7):286. doi: 10.1007/s00203-024-04014-3.
5
Genetic diversity and antagonistic properties of Trichoderma strains from the crop rhizospheres in southern Rajasthan, India.印度拉贾斯坦邦南部作物根际木霉菌株的遗传多样性与拮抗特性
Sci Rep. 2024 Apr 14;14(1):8610. doi: 10.1038/s41598-024-58302-5.
6
and Its Benefits.及其益处。
J Fungi (Basel). 2023 Oct 8;9(10):994. doi: 10.3390/jof9100994.
7
Biochemical and Biotechnological Insights into Fungus-Plant Interactions for Enhanced Sustainable Agricultural and Industrial Processes.关于真菌-植物相互作用以促进可持续农业和工业进程的生化与生物技术见解。
Plants (Basel). 2023 Jul 19;12(14):2688. doi: 10.3390/plants12142688.
8
What was old is new again: Phenotypic screening of a unique fungal library yields pyridoxatin, a promising lead against extensively resistant (AB5075).旧物新用:对一个独特真菌文库进行表型筛选得到了吡哆他汀,这是一种对抗广泛耐药菌(AB5075)的有前景的先导化合物。
Phytochem Lett. 2023 Jun;55:88-96. doi: 10.1016/j.phytol.2023.04.002. Epub 2023 Apr 21.
9
Endophytic species from rubber trees native to the Brazilian Amazon, including four new species.来自巴西亚马逊地区本土橡胶树的内生菌物种,包括四个新物种。
Front Microbiol. 2023 Apr 18;14:1095199. doi: 10.3389/fmicb.2023.1095199. eCollection 2023.
10
Species: Our Best Fungal Allies in the Biocontrol of Plant Diseases-A Review.物种:植物病害生物防治中我们最好的真菌盟友——综述
Plants (Basel). 2023 Jan 17;12(3):432. doi: 10.3390/plants12030432.
Hypocrea/Trichoderma:具有分生孢子梗伸长和绿色分生孢子的物种。
Mycologia. 2003 Nov-Dec;95(6):1100-40.
4
Trichoderma brevicompactum sp. nov.短小木霉(Trichoderma brevicompactum)新种
Mycologia. 2004 Sep-Oct;96(5):1059-73.
5
Hypocrea/Trichoderma species with pachybasium-like conidiophores: teleomorphs for T. minutisporum and T. polysporum and their newly discovered relatives.具有厚壁孢梗束状分生孢子梗的Hypocrea/Trichoderma 种:T. minutisporum 和 T. polysporum 的有性型及其新发现的亲缘种。
Mycologia. 2004 Mar-Apr;96(2):310-42.
6
Hypocrea seppoi, a new stipitate species from Finland.芬兰新发现的具柄肉座菌——塞氏肉座菌
Karstenia. 2008;48(1):1-11. doi: 10.29203/ka.2008.423.
7
IMI descriptions of fungi and bacteria set 129.真菌和细菌的IMI描述第129套。
Mycopathologia. 1996 Jul;135(1):37-71. doi: 10.1007/BF00436574.
8
Trichoderma asperellum sensu lato consists of two cryptic species.广义里氏木霉包含两个隐种。
Mycologia. 2010 Jul-Aug;102(4):944-66. doi: 10.3852/09-243.
9
European species of Hypocrea Part I. The green-spored species.欧洲 Hypocrea 种 Part I. 绿孢种。
Stud Mycol. 2009;63:1-91. doi: 10.3114/sim.2009.63.01.
10
Trichoderma evansii and T. lieckfeldtiae: two new T. hamatum-like species.伊氏木霉和利氏木霉:两个新的类哈茨木霉物种。
Mycologia. 2009 Jan-Feb;101(1):142-56. doi: 10.3852/08-161.