identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
9E2BEFC173D856DCA035342FB5D4251A.text	9E2BEFC173D856DCA035342FB5D4251A.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Trichoderma hailarense G. Z. Zhang 2022	<div><p>Trichoderma hailarense G.Z. Zhang sp. nov.</p><p>Fig. 3</p><p>Etymology.</p><p>The specific epithet " Trichoderma hailarense " refers to the locality, the Hailar River Basin in Inner Mongolia of China where the holotype was found.</p><p>Typification.</p><p>China. Inner Mongolia, Hailar River Basin, 618 m (altitude), isolated from soil, 17 September 2016, G.Z. Zhang (Holotype WT 17901).</p><p>Diagnosis.</p><p>Phylogenetically, Trichoderma hailarense formed a distinct clade and is related to T. gamsii and T. neokoningii (Fig. 1). The sequence similarity of rpb2 with T. gamsii S488 and T. neokoningii CBS120070 was 97.32% and 96.86%, respectively and the sequence similarity of tef1 -α with T. gamsii S488 and T. neokoningii CBS120070 was 97.43% and 96.66%, respectively. Colonies of T. hailarense did not form conidia on PDA and conidia of T. hailarense on other media were obovoid, delicately roughened and easily distinguished from those of T. gamsii and T. neokoningii .</p><p>Teleomorph.</p><p>Unknown.</p><p>Growth optimal at 30 °C, slow at 35 °C on all media. Colony radius after 72 h at 30 °C 53-56 mm on PDA, 54-56 mm on CMD, 33-37 mm on MEA and 33-36 mm on SNA. Colony radius after 72 h at 35 °C 13-15 mm on PDA, 10-14 mm on CMD, 9-12 mm on MEA and 10-12 mm on SNA. Aerial mycelia abundant, arachnoid on PDA after 72 h at 25 °C under 12 h photoperiod. Conidiation started around the inoculation point after 7 days on PDA, with relatively few or small conidia. Diffusing pigment or distinctive odour absent. Conidiation started around the inoculation point after 7 days on MEA, forming a few large pustules, cream yellow. On SNA, aerial mycelia were few, forming a few large pustules around the inoculation point in age, cream-yellow. Conidiophores and branches narrow and flexuous, tending to be regularly verticillate, forming a pyramidal structure, with each branch terminating in a cruciate whorl of up to five phialides. Phialides, lageniform, (8.0-)9.4-13.1(-15.5) × (2.5-)3.0-3.5(-3.6) μm (mean = 11.2 × 3.3 μm), base 1.8-2.5 μm (mean = 2.1 μm); phialide length/width ratio (2.33-)2.7-4.4(-5.9) (mean = 3.4). Conidia obovoid, (4.2-)4.3-4.7(-4.9) × (3.4-)3.6-3.9(-4.1) μm (mean = 4.5 × 3.7 μm), length/width ratio 1.1-1.4 (mean = 1.2), delicately roughened. Chlamydospores: (7.0-)7.5-8.2(-8.5) × (6.5-)7.0-7.5(-8.3) μm .</p><p>Distribution.</p><p>China. Inner Mongolia.</p><p>Additional specimen examined.</p><p>China. Inner Mongolia, Hulun Buir, 610 m (altitude), isolated from soil, 17 September 2016, J.D. Hu (WT17905).</p><p>Notes.</p><p>Phylogenetically Trichoderma hailarense is related to T. gamsii and T. neokoningii (Fig. 1) and does not meet the sp ∃!(rpb2 99≅ tef1 97) standard for T. gamsii or T. neokoningii . Morphologically, colonies of T. gamsii and T. neokoningii on PDA formed conidia sporadically or in hemispherical pustules and conidia of T. gamsii and T. neokoningii were ellipsoidal to oblong, smooth-walled (Jaklitsch et al. 2006). However, colonies of T. hailarense did not form conidia on PDA and conidia of T. hailarense on other media were obovoid, delicately roughened and easily distinguished from those of T. gamsii and T. neokoningii .</p></div>	https://treatment.plazi.org/id/9E2BEFC173D856DCA035342FB5D4251A	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Zhang, Guang-Zhi;Yang, He-Tong;Zhang, Xin-Jian;Zhou, Fang-Yuan;Wu, Xiao-Qing;Xie, Xue-Ying;Zhao, Xiao-Yan;Zhou, Hong-Zi	Zhang, Guang-Zhi, Yang, He-Tong, Zhang, Xin-Jian, Zhou, Fang-Yuan, Wu, Xiao-Qing, Xie, Xue-Ying, Zhao, Xiao-Yan, Zhou, Hong-Zi (2022): Five new species of Trichoderma from moist soils in China. MycoKeys 87: 133-157, DOI: http://dx.doi.org/10.3897/mycokeys.87.76085, URL: http://dx.doi.org/10.3897/mycokeys.87.76085
78B37AB88A2152F5B56306B4AA0094BE.text	78B37AB88A2152F5B56306B4AA0094BE.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Trichoderma macrofasciculatum G. Z. Zhang 2022	<div><p>Trichoderma macrofasciculatum G.Z. Zhang sp. nov.</p><p>Fig. 4</p><p>Etymology.</p><p>The specific epithet " Trichoderma macrofasciculatum " refers to the morphological feature of the conidiation, conidiophores aggregated into large fascicles in concentric rings.</p><p>Typification.</p><p>China, Sichuan, Nine-Village Valley, 2405 m (altitude), isolated from soil, 24 September 2016, G.Z. Zhang (Holotype WT 37805).</p><p>Diagnosis.</p><p>Phylogenetically, Trichoderma macrofasciculatum WT37805 and WT37810 formed a distinct clade and is related to T. polysporum C.P.K. 3131 in the Polysporum clade, but the similarities of rpb2 and tef1 -α between these two species were only 96.41% and 92.81%, respectively. Trichoderma macrofasciculatum cannot grow at 35 °C as T. polysporum and the former formed large and white pustules in concentric rings at 25 °C, elongations were rarely observed and conidia had few guttules, which are distinct from T. polysporum .</p><p>Teleomorph.</p><p>Unknown.</p><p>Growth optimum at 20 °C, slow or limited at 30 °C, absent at 35 °C. Colony radius after 72 h at 25 °C 21-24 mm on PDA, 23-27 mm on CMD, 17-20 mm on MEA and 12-16 mm on SNA. Aerial mycelia abundant on PDA and MEA after incubation for 72 h at 25 °C under a 12 h photoperiod. Conidiation typically in pustules in concentric rings on PDA, solitary or aggregated, producing a Protocrea farinose to granular mat. Diameter of pustules up to 2.2 mm, pompon-like, white. Diffusing pigment and distinct odour absent. Conidiation on MEA typically in pustules in concentric rings, pompon-like as on PDA. On CMD, aerial mycelia sparsely developed. Conidiation aggregated in sporadic pustules near the colony margin, white. On SNA, aerial mycelia few and conidiation not observed. Conidiophores and branches irregularly branched in a dendriform structure, with each branch terminating in a cruciate whorl of up to five phialides. Hyphal septa clearly visible. Phialides flask-shaped, often curved, (4.9-)5.6-7.8(-8.8) × (2.8-)3.0-3.2(-3.4) μm (mean = 6.7 × 3.1 μm), 1.8-2.6 μm (mean = 2.2 μm) near the base; phialide length/width ratio (1.5-)1.8-2.4(-2.8) (mean = 2.1). Conidia subglobose to ellipsoid, hyaline, smooth, with one or few distinctly verrucose, (2.6-)2.8-3.3(-3.6) × (2.4-)2.5-2.7(-2.9) μm (mean = 3.0 × 2.6 μm), length/width ratio 1.0-1.3 (mean = 1.2). Chlamydospores not observed.</p><p>Distribution.</p><p>China, Sichuan Province.</p><p>Additional material examined.</p><p>China, Sichuan, Nine-Village Valley, 2405 m (altitude), isolated from soil, 24 September 2016, G.Z. Zhang (WT 37810) .</p><p>Notes.</p><p>Phylogenetically Trichoderma macrofasciculatum WT 37805 is related to T. polysporum C.P.K. 3131 in the Polysporum clade (Fig. 1), but the similarities of rpb2 and tef1 -α between these two species were only 96.41% and 92.81% respectively, with 94 and 41 bp differences amongst 1311 and 1152 bp. Trichoderma macrofasciculatum cannot grow at 35 °C as T. polysporum and the former formed large and white pustules in concentric rings at 25 °C, elongations were rarely observed and conidia had few guttules, which are distinct from T. polysporum (Lu et al. 2004).</p></div>	https://treatment.plazi.org/id/78B37AB88A2152F5B56306B4AA0094BE	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Zhang, Guang-Zhi;Yang, He-Tong;Zhang, Xin-Jian;Zhou, Fang-Yuan;Wu, Xiao-Qing;Xie, Xue-Ying;Zhao, Xiao-Yan;Zhou, Hong-Zi	Zhang, Guang-Zhi, Yang, He-Tong, Zhang, Xin-Jian, Zhou, Fang-Yuan, Wu, Xiao-Qing, Xie, Xue-Ying, Zhao, Xiao-Yan, Zhou, Hong-Zi (2022): Five new species of Trichoderma from moist soils in China. MycoKeys 87: 133-157, DOI: http://dx.doi.org/10.3897/mycokeys.87.76085, URL: http://dx.doi.org/10.3897/mycokeys.87.76085
DE284B67F38459E092E805DCBFD3BCE4.text	DE284B67F38459E092E805DCBFD3BCE4.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Trichoderma nordicum G. Z. Zhang 2022	<div><p>Trichoderma nordicum G.Z. Zhang sp. nov.</p><p>Fig. 5</p><p>Etymology.</p><p>“nord” means found in the north of China.</p><p>Holotype.</p><p>China, Beijing, Yu-yuan-tan Park, 43 m (altitude), isolated from soil, 27 October 2016, G.Z. Zhang (Holotype WT 13001), ex-type culture ACCC 39713.</p><p>Diagnosis.</p><p>Phylogenetically Trichoderma nordicum is related to T. paratroviride, but the sequence similarities of rpb2 and tef1 -α were 98.15% and 94.43%, respectively. That does not meet the sp ∃!(rpb2 99≅ tef1 97) standard for T. paratroviride or other known Trichoderma species. Morphologically, conidiophores of T. paratroviride consisting of a main axis and often distantly-spaced side branches, not re-branching. Conidiophores of T. nordicum are branched in a more complex manner; conidia are larger than those of T. paratroviride .</p><p>Teleomorph.</p><p>Unknown.</p><p>Growth optimal at 25 °C, slow or limited at 30 °C, absent at 35 °C. Colonies grew fast on PDA, CMD and MEA and slow on SNA. Colony radius after 72 h at 25 °C 67-71 mm on PDA, 68-71 mm on CMD, 51-55 mm on MEA and 21-24 mm on SNA. Aerial mycelia sparse on PDA after 72 h at 25 °C under 12 h photoperiod and conidiation developed within 48 h beginning at the inoculation point and progressed around, grey-white at first and slowly turning green. Diffusing pigment or distinctive odour absent. Aerial mycelia sparse and flocculence on MEA after 72 h at 20 °C under 12 h photoperiod. Conidia developed within 48 h beginning near the colony margin on MEA, grey-white at first and slowly turning green, transparent liquid secreted. Aerial mycelia few on SNA and CMD after 72 h at 25 °C, conidia formed around the inoculation point and in distinct concentric rings after 96 h under 12 h photoperiod on SNA and CMD, diffusing pigment not produced. Conidiophores and branches narrow and flexuous, tending to be regularly verticillate forming a pyramidal structure, each branch terminating in a cruciate whorl of up to five phialides. Phialides, lageniform, (6.2-)7.2-10.3(-12.9) × (2.6-)2.9-3.2(-3.4) μm (mean = 8.8 × 3.1 μm), 1.6-2.3 μm (mean = 1.9 μm) near the base; phialide length/width ratio (2.1-)2.4-3.4(-4.3) (mean = 2.9). On PDA, phialides curved, distinguished from those on other media. Conidia, globose to obovoidal, (4.1-)4.4-4.8(-5.0) × (4.0-)4.1-4.4(-4.6) μm (mean = 4.6 × 4.3 μm), length/width ratio 1.0-1.2 (mean = 1.1). Chlamydospores sometimes present, (8.7-)9.8 × 10.4(-12.5) μm .</p><p>Distribution.</p><p>China, Beijing and Hebei.</p><p>Additional specimen examined.</p><p>China. Hebei, Bai-yang Lake, 19 m (altitude), isolated from soil, 15 September 2016, J.S. Li (WT 61001).</p><p>Notes.</p><p>Phylogenetically, Trichoderma nordicum is related to T. paratroviride (Fig. 1), but the sequence similarities of rpb2 and tef1 -α were 98.15% and 94.43%, respectively. That does not meet the sp ∃!(rpb2 99≅ tef1 97) standard for T. paratroviride or other known Trichoderma species. Morphologically, conidiophores of T. paratroviride consist of a main axis and often distantly-spaced side branches, not re-branching. Conidiophores of T. nordicum are branched in a more complex manner; conidia are larger than those of T. paratroviride (Jaklitsch and Voglmayr 2015).</p></div>	https://treatment.plazi.org/id/DE284B67F38459E092E805DCBFD3BCE4	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Zhang, Guang-Zhi;Yang, He-Tong;Zhang, Xin-Jian;Zhou, Fang-Yuan;Wu, Xiao-Qing;Xie, Xue-Ying;Zhao, Xiao-Yan;Zhou, Hong-Zi	Zhang, Guang-Zhi, Yang, He-Tong, Zhang, Xin-Jian, Zhou, Fang-Yuan, Wu, Xiao-Qing, Xie, Xue-Ying, Zhao, Xiao-Yan, Zhou, Hong-Zi (2022): Five new species of Trichoderma from moist soils in China. MycoKeys 87: 133-157, DOI: http://dx.doi.org/10.3897/mycokeys.87.76085, URL: http://dx.doi.org/10.3897/mycokeys.87.76085
51ECA4846FB65DD388CFFFE20CD94506.text	51ECA4846FB65DD388CFFFE20CD94506.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Trichoderma shangrilaense G. Z. Zhang 2022	<div><p>Trichoderma shangrilaense G.Z. Zhang sp. nov.</p><p>Fig. 6</p><p>Etymology.</p><p>" Trichoderma shangrilaense " was originally found at Shangrila in Yunnan Province of China.</p><p>Typification.</p><p>China. Yunnan, Pudacuo National Park, 3611 m (altitude), isolated from soil, 21 June 2016, G.Z. Zhang (Holotype WT 34004), Ex-type culture ACCC 39714.</p><p>Diagnosis.</p><p>Phylogenetically, Trichoderma shangrilaense is related to T. parapiluliferum (CBS 120921) (Fig. 1), but the sequence similarity of rpb2 between these two species was 98.93% and the sequence similarity of tef1 -α was 96.35%. That does not meet the sp ∃!(rpb2 99≅ tef1 97) standard for T. parapiluliferum or other known Trichoderma species. Conidiophore main axis of T. shangrilaense fertile to apex, conidia obovoid to ellipsoid, easily distinguished from that of T. parapiluliferum .</p><p>Teleomorph.</p><p>Unknown.</p><p>Growth optimal at 20 °C, slow, limited at 25 °C and absent at 30 °C or 35 °C. Colony radius after 72 h at 20 °C 19-21 mm on PDA, 23-24 mm on CMD, 19-21 mm on MEA and 8-11 mm on SNA. Aerial mycelia abundant, compact on PDA after 7 days at 20 °C under 12 h photoperiod, conidiation not easily formed and a yellow diffusing pigment developed near the inoculation point; conidiation formed unequal in size, white pustules after 14 days. Conidiophores and branches narrow and flexuous, forming a dendriform structure and irregularly branched, not rebranched, main axis to 4.3-5.0 µm wide, fertile to apex. Phialides, flask-shaped, often curved, (4.5-)5.7-9.0(-11.1) × (2.9-)3.2-3.5(-4.1) μm (mean = 7.4 × 3.4 μm), 1.6-3.4 μm wide (mean = 2.6 μm) near the base; phialide length/width ratio (1.5-)2.0-2.6(-3.0) (mean = 2.3). Conidia, obovoid to ellipsoidal, smooth, (3.3-)3.5-4.0(-4.4) × (2.8-)3.0-3.3(-3.5) μm (mean = 3.8 × 3.19 μm), length/width ratio 1.1-1.4 (mean = 1.2). Chlamydospores not observed.</p><p>Colony radius 28-33 mm, aerial mycelia abundant and floccose after 7 days at 20 °C under 12 h photoperiod. Conidiation slowly developing on MEA. After about 14 days, pompon-like, white fascicles developed. No diffusing pigment observed. On CMD after 7 days at 20 °C under 12 h photoperiod, colony radius 28-33 mm, aerial mycelia few. Conidiation formed flat or cushion-shaped pustules near the colony margin after 21 days and a yellow diffusing pigment developed near the inoculation point. On SNA after 7 days at 20 °C under 12 h photoperiod, colony mycelia sparse and no conidiation formed. After 10 days, pustules scattered around the periphery of the colony. Diffusing pigment not developed.</p><p>Distribution.</p><p>China. Yunnan and Sichuan.</p><p>Additional specimen examined.</p><p>China. Sichuan, Huanglong Nature Reserve, 3561 m (altitude), isolated from soil, 25 September 2016, Z. Li (WT 34012).</p><p>Notes.</p><p>Phylogenetically, Trichoderma shangrilaense is related to T. parapiluliferum (CBS 120921) (Fig. 1), but the sequence similarity of rpb2 between these two species was 98.93% and the sequence similarity of tef1 -α was 96.35%. The sequence similarity of tef1 -α with the ex-type culture G.J.S. 91-60 (GenBank accession no. AY937444) was only 92%. Optimum temperature for growth of T. shangrilaense was 20 °C, no growth occurred at 30 °C as in T. parapiluliferum and conidiation structures consist of flat or cushion-shaped pustules, formed near the colony margin on MEA, SNA and CMD. Conidiophore main axis of Trichoderma parapiluliferum has conspicuous spiral sterile apical elongations, conidia ellipsoidal to oblong (Lu et al. 2004). Conidiophore main axis of T. shangrilaense fertile to apex, conidia obovoid to ellipsoid, easily distinguished from that of T. parapiluliferum .</p></div>	https://treatment.plazi.org/id/51ECA4846FB65DD388CFFFE20CD94506	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Zhang, Guang-Zhi;Yang, He-Tong;Zhang, Xin-Jian;Zhou, Fang-Yuan;Wu, Xiao-Qing;Xie, Xue-Ying;Zhao, Xiao-Yan;Zhou, Hong-Zi	Zhang, Guang-Zhi, Yang, He-Tong, Zhang, Xin-Jian, Zhou, Fang-Yuan, Wu, Xiao-Qing, Xie, Xue-Ying, Zhao, Xiao-Yan, Zhou, Hong-Zi (2022): Five new species of Trichoderma from moist soils in China. MycoKeys 87: 133-157, DOI: http://dx.doi.org/10.3897/mycokeys.87.76085, URL: http://dx.doi.org/10.3897/mycokeys.87.76085
929D624BE67C535990831E7A60EF07CB.text	929D624BE67C535990831E7A60EF07CB.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Trichoderma vadicola G. Z. Zhang 2022	<div><p>Trichoderma vadicola G.Z. Zhang sp. nov.</p><p>Fig. 7</p><p>Etymology.</p><p>The specific epithet " Trichoderma vadicola ", from the noun “vadum”, reflects the ecological environment and means that the species inhabits shallow water.</p><p>Typification.</p><p>China. Shandong, 2 m (altitude), isolated from soil, 13 August 2016, G.Z. Zhang (Holotype WT 10708), Ex-type culture ACCC 39716.</p><p>Diagnosis.</p><p>Phylogenetically, Trichoderma vadicola is related to T. caerulescens in the Viride clade (Fig. 1), but the sequence similarity of tef1 -α and rpb2 between these species was all 95%. Morphologically, colonies of T. vadicola and T. caerulescens on PDA have similar features, such as abundant aerial hyphae, forming strands and a whitish hairy or floccose mat. However, the former Trichoderma vadicola formed no or relatively few conidia and the latter forming greyish-bluish patches around the plug. On CMD, T. caerulescens peculiar greyish-blue pigment formed after 1-2 months and conidiophores simply or slightly branched; the former had no observed diffusing pigment and conidiophores branched in a complex manner in pyramidal structure or tree-like.</p><p>Teleomorph.</p><p>Unknown.</p><p>Growth optimal at 25 °C, no grow at 35 °C on all media. Colony radius after 72 h at 25 °C 25-29 mm on PDA, 24-27 mm on CMD, 23-26 mm on MEA and 22-26 mm on SNA. Aerial mycelia abundant on PDA after 72 h at 25 °C under 12 h photoperiod, forming strands and floccose mat. Conidiation not formed or relatively few. No diffusing pigment or distinctive odour was produced. On MEA after 72 h at 25 °C under 12 h photoperiod, aerial mycelia abundant, floccose. After 7 days, mycelia covered the plate and conidia appeared, effuse, granuliform. On CMD after 72 h at 25 °C under 12 h photoperiod, aerial mycelia not observed. After 7 days, mycelia covered the plate and conidia developed near the colony margin. On SNA after 72 h at 25 °C under 12 h photoperiod, aerial mycelia not observed. After 7 days, mycelia covered the plate, aerial mycelia floccose and conidia formed, effuse. Conidiophores and branches regularly verticillate, formed a pyramidal structure, each branch terminating in a cruciate whorl of 3-5 phialides. Phialides lageniform, (8.3-)9.9-12.3(-15.1) × (2.0-)2.6-3.2(-3.4) μm (mean = 11.1 × 2.9 μm), 1.1-2.9 μm wide (mean = 1.9 μm) near the base; phialide length/width ratio (2.7-)3.2-4.6(-6.6) (mean = 3.9). Conidia subglobose or obovoidal, (3.5-)3.7-4.3(-4.8) × (3.2-)3.4-3.6(-3.8) μm (mean = 4.0 × 3.5 μm), length/width ratio 1.0-1.3 (mean = 1.1). Chlamydospores not observed.</p><p>Distribution.</p><p>China. Shandong and Yunnan Provinces.</p><p>Additional specimen examined.</p><p>China. Yunnan, Shangri-La, Pudacuo National Park, 3551 m (altitude), isolated from soil, 21 September 2016, H.T. Yang (WT 10713).</p><p>Notes.</p><p>Phylogenetically, Trichoderma vadicola is related to T. caerulescens in the Viride clade (Fig. 1), but the sequence similarity of tef1 -α and rpb2 between these species was all 95%, with 62 and 60 bp differences amongst 1218 and 1130 bp, respectively. Morphologically, colonies of T. vadicola and T. caerulescens on PDA have similar features, such as abundant aerial hyphae, forming strands and a whitish hairy or floccose mat. However, the former Trichoderma vadicola formed no or relatively few conidia, with the latter forming greyish-bluish patches around the plug. On CMD, T. caerulescens formed peculiar greyish-blue pigment after 1-2 months and conidiophores simply or slightly branched (Jaklitsch et al. 2012); the former had no observed diffusing pigment and conidiophores branched in a complex manner in pyramidal structure or tree-like.</p></div>	https://treatment.plazi.org/id/929D624BE67C535990831E7A60EF07CB	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Zhang, Guang-Zhi;Yang, He-Tong;Zhang, Xin-Jian;Zhou, Fang-Yuan;Wu, Xiao-Qing;Xie, Xue-Ying;Zhao, Xiao-Yan;Zhou, Hong-Zi	Zhang, Guang-Zhi, Yang, He-Tong, Zhang, Xin-Jian, Zhou, Fang-Yuan, Wu, Xiao-Qing, Xie, Xue-Ying, Zhao, Xiao-Yan, Zhou, Hong-Zi (2022): Five new species of Trichoderma from moist soils in China. MycoKeys 87: 133-157, DOI: http://dx.doi.org/10.3897/mycokeys.87.76085, URL: http://dx.doi.org/10.3897/mycokeys.87.76085
