Trichoderma hailarense G.Z. Zhang, 2022

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, pp. 133-157 : 133

publication ID

https://dx.doi.org/10.3897/mycokeys.87.76085

persistent identifier

https://treatment.plazi.org/id/9E2BEFC1-73D8-56DC-A035-342FB5D4251A

treatment provided by

MycoKeys by Pensoft

scientific name

Trichoderma hailarense G.Z. Zhang
status

sp. nov.

Trichoderma hailarense G.Z. Zhang sp. nov.

Fig. 3 View Figure 3

Etymology.

The specific epithet " Trichoderma hailarense " refers to the locality, the Hailar River Basin in Inner Mongolia of China where the holotype was found.

Typification.

China. Inner Mongolia, Hailar River Basin, 618 m (altitude), isolated from soil, 17 September 2016, G.Z. Zhang (Holotype WT 17901).

Diagnosis.

Phylogenetically, Trichoderma hailarense formed a distinct clade and is related to T. gamsii and T. neokoningii (Fig. 1 View Figure 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 .

Teleomorph.

Unknown.

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.

Distribution.

China. Inner Mongolia.

Additional specimen examined.

China. Inner Mongolia, Hulun Buir, 610 m (altitude), isolated from soil, 17 September 2016, J.D. Hu (WT17905).

Notes.

Phylogenetically Trichoderma hailarense is related to T. gamsii and T. neokoningii (Fig. 1 View Figure 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 .