Jenniferia thomisidarum Mongkolsamrit, Noisripoom & Tasanathai, 2022

Mongkolsamrit, Suchada, Noisripoom, Wasana, Tasanathai, Kanoksri, Kobmoo, Noppol, Thanakitpipattana, Donnaya, Khonsanit, Artit, Petcharad, Booppa, Sakolrak, Baramee & Himaman, Winanda, 2022, Comprehensive treatise of Hevansia and three new genera Jenniferia, Parahevansia and Polystromomyces on spiders in Cordycipitaceae from Thailand, MycoKeys 91, pp. 113-149 : 113

publication ID

https://dx.doi.org/10.3897/mycokeys.91.83091

persistent identifier

https://treatment.plazi.org/id/070A1D30-91F8-599B-AC8C-CF07E933BA18

treatment provided by

MycoKeys by Pensoft

scientific name

Jenniferia thomisidarum Mongkolsamrit, Noisripoom & Tasanathai
status

sp. nov.

Jenniferia thomisidarum Mongkolsamrit, Noisripoom & Tasanathai sp. nov.

Fig. 7 View Figure 7

Typification.

Thailand, Nakhon Ratchasima Province, Khao Yai National Park, 14°26'20.72"N, 101°22'20.02"E, on spider (Non-web builder, Araneae, Thomisidae , Diaea cf. dorsata ) attached to the underside of a dicot leaf of forest plants, 23 July 2009, K. Tasanathai, P. Srikitikulchai, S. Mongkolsamrit, R. Ridkaew, MY5032.01 (BBH 29502, holotype), ex-type culture BCC 37881 isolated from ascospores.

Etymology.

Named after the host belonging to the family Thomisidae ( Araneae).

Description.

Spider hosts covered by dense greyish-brown mycelium (199C-D). Sexual morph: Stromata non-stipitate. Perithecia growing in subiculum, aggregated in clusters, superficial, obpyriform, 850-1100 × 300-400 µm, ostiole pale brown. Asci cylindrical, 8-spored, 520-700 µm long, 4-6 µm broad, with cap 2-6 µm thick. Ascospores hyaline, whole ascospores with septate part-spores alternately connected with thread-like structures, three-terminal cells on each end with six alternating pairs of cells and filament, eighteen cells per ascospore, up to 680 µm long, each cell narrowly fusiform, 10-20 × 1-2 µm, filiform regions, 30-50 × 0.2-0.8 µm. Asexual morph: Synnemata arising from the mycelial mat, numerous, greyish-brown, cylindrical to clavate, erect up to 800 µm long, 30-100 µm broad. Conidiogenous cells producing at the upper part of synnemata, mostly monophialidic or some polyphialidic. Phialides cylindrical, (7)10-15(16) × 2-4(5) µm, tapering into a distinct neck, (1)1.5-3.5(5) × 1-1.5 µm. Conidia hyaline, fusiform, cylindrical, (3)8.5-10.5(12) × 1-3 µm.

Culture characteristics.

Colonies on OA attaining a diam. of (12)14-15 mm in 21 days, cottony with high mycelium density, white, reverse pale orange (165D), poor sporulation. Phialides arising from aerial hyphae, solitary, awl-shaped, lecanicillium-like, 20-40 × 1-2 µm. Conidia in chains, hyaline, fusiform, cylindrical, smooth, (3)7.5-10.5(12) × (1.5)2-2.5(3) µm.

Colonies on PDA attaining a diam. of 8-10 mm in 21 days, cottony with high mycelium density in the middle of colonies, mycelium with low density around the margin of colonies, pale orange, reverse moderate orange (167D), poor sporulation. Phialides arising from aerial hyphae, solitary, awl-shaped, lecanicillium-like, 10-35 × 1-2 µm. Conidia in the chains, hyaline, fusiform, cylindrical, smooth, (3)6.5-9.5(10) × (1.5)2-2.5(3) µm.

Host.

Spiders ( Araneae, Thomisidae , Diaea cf. dorsata ).

Habitat.

Specimens were found on the underside of dicot leaves of forest plants.

Additional materials examined.

Thailand, Nakhon Ratchasima Province, Khao Yai National Park , 14°26'20.72"N, 101°22'20.02"E, on spider (Non-web builder, Araneae, Thomisidae , Diaea cf. dorsata ) attached to the underside of a dicot leaf of forest plants, 23 July 2009, K. Tasanathai, P. Srikitikulchai, S. Mongkolsamrit, R. Ridkaew, MY5032.02 ( BBH 29502 View Materials , paratype), ex-paratype culture BCC 37882 View Materials GoogleMaps isolated from conidia; idem, 7 August 2011, K. Tasanathai, P. Srikitikulchai, S. Mongkolsamrit, A. Khonsanit, W. Noisripoom, K. Sansatchanon, MY6813 ( BBH 30660 View Materials , culture BCC 48932 View Materials ) GoogleMaps ; idem, 3 August 2011, K. Tasanathai, P. Srikitikulchai, S. Mongkolsamrit, A. Khonsanit, W. Noisripoom, K. Sansatchanon, MY6866 ( BBH 30690 View Materials ), culture BCC 49257 View Materials GoogleMaps ; idem, 9 August 2012, K. Tasanathai, S. Mongkolsamrit, A. Khonsanit, W. Noisripoom, MY7598 ( BBH 32822 View Materials ), culture BCC 54482 View Materials GoogleMaps ; MY7599 ( BBH 32823 View Materials ), culture BCC 54483 View Materials ; MY7600 ( BBH 32824 View Materials ), culture BCC 32824 View Materials ; idem, 26 June 2012, K. Tasanathai, P. Srikitikulchai, S. Mongkolsamrit, A. Khonsanit, W. Noisripoom, K. Sansatchanon, R. Somnuk, MY8636 ( BBH 35789 View Materials ), culture BCC 64182 View Materials ; idem, 7 August 2013, P. Srikitikulchai, S. Mongkolsamrit, A. Khonsanit, W. Noisripoom, MY8878 (BBH 336396), culture BCC 66224 View Materials .

Notes. In sexual morph specimens found in nature, Jenniferia thomisidarum resembles J. griseocinerea by the formation of non-stipitate ascomata. The perithecia of both species are superficial and aggregate in clusters, challenging the identification of the species rank. The ascospores are of the same type by septate part-spores alternately connected with thread-like structures along the whole ascospore (Fig. 2d View Figure 2 ). Ascospores in J. thomisidarum are longer than those reported for J. griseocinerea (Table 2 View Table 2 ). Jenniferia thomisidarum differs from J. griseocinerea in the size and shape of the perithecia and asci. In J. thomisidarum , perithecia and asci are larger and longer than those reported for J. griseocinerea (850- 1100 × 300-400 µm vs. 650-850 × 250-320 µm; 520-700 × 4-6 µm vs. 375-460 × 5-6 µm). The perithecia in J. thomisidarum are obpyriform, while perithecia in J. griseocinerea are ovoid.