cover
Contact Name
Ahmad Dwi Setyawan
Contact Email
editors@smujo.id
Phone
-
Journal Mail Official
editors@smujo.id
Editorial Address
Jl. Ir. Sutami 36A Surakarta 57126, Central Java, Indonesia Tel. +62-271-7994097, Tel. & Fax.: +62-271-663375
Location
Kota surakarta,
Jawa tengah
INDONESIA
Nusantara Bioscience
ISSN : 20873948     EISSN : 20873956     DOI : https://doi.org/10.13057/nusbiosci
Core Subject : Education,
Aims and Scope Nusantara Bioscience (Nusantara Biosci) encourages submission of manuscripts dealing with all aspects of biological sciences that emphasize issues germane to biological and nature conservation.
Arjuna Subject : Umum - Umum
Articles 552 Documents
Macrofungal diversity of Sarıkamış Allahuekber Mountains National Park (Kars/Erzurum, Türkiye) MUSTAFA EMRE AKÇAY; YUSUF UZUN
Nusantara Bioscience Vol. 18 No. 2 (2026)
Publisher : Smujo International

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.13057/nusbiosci/n180203

Abstract

Abstract. Akçay ME, Uzun Y. 2026. Macrofungal diversity of Sarıkamış Allahuekber Mountains National Park (Kars/Erzurum, Türkiye). Nusantara Bioscience 18 (2): n180203. https://doi.org/10.13057/nusbiosci/n180203. Macrofungal inventories in protected mountain forests provide baseline data for biodiversity monitoring and conservation planning. This study presents a historical inventory of macrofungi documented in Sarıkamış Allahuekber Mountains National Park, northeastern Türkiye, based on specimens collected from 49 localities during 2011-2016 and examined using macro- and micromorphological characters. The field campaign comprised approximately 75 survey days and yielded 920 specimens. After a cautious reassessment of doctoral-thesis material under current nomenclature, 240 species were retained; records requiring molecular reassessment were excluded. Accepted names and author citations were cross-checked against Index Fungorum and MycoBank, together with recent Turkish checklist sources. The retained taxa belong to 5 classes, 12 order-level categories, 54 family-level categories and 117 genera. These taxa represent new records for the national park in the published literature, not national-level new records for Türkiye. The inventory links taxa with habitat, locality, date, collection number, Turkish vernacular name and edibility/use-value code. Scots pine forests and pine-derived substrates accounted for 292 of 416 voucher-linked records. Because sampling effort was not standardized, seasonal and habitat patterns are interpreted as collection-record frequencies. The study provides a reference point for future effort-standardized surveys and conservation planning in this protected high-altitude Scots pine ecosystem.
Network analysis identifies a shared flagellar-associated candidate module in five selected Gram-negative pathogen strains YITAO XIANG; XIAOCHAN LIU; LI YU; FANGZHEN LUO
Nusantara Bioscience Vol. 18 No. 2 (2026)
Publisher : Smujo International

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.13057/nusbiosci/n180202

Abstract

Abstract. Xiang Y, Liu X, Yu L, Luo F. 2026. Network analysis identifies a shared flagellar-associated candidate module in five selected Gram-negative pathogen strains. Nusantara Bioscience 18 (2): n180202. https://doi.org/10.13057/nusbiosci/n180202. We compared score-filtered STRING functional-association networks from five selected flagellated Gram-negative pathogen reference strains: Burkholderia cenocepacia J2315, Enterobacter cloacae ATCC 13047, Escherichia coli JJ1886, Legionella pneumophila Philadelphia 1, and Pseudomonas aeruginosa UCBPP-PA14. Here, shared denotes an exact normalized node label present in all five networks and does not imply formal orthology. The five connected networks contained 51, 94, 157, 117, and 222 nodes. Their exact five-way connected-node intersection comprised 20 labels, and the same 20 were recovered from the full filtered-node sets. The raw preferred-name intersection expanded to 21 only because one Burkholderia flhA mapping referred to a non-flagellar alcohol dehydrogenase annotation. Under a within-network top-decile rule, only flgG and fliM were shared-central across all five networks. A within-species MMseqs2 audit across five fixed 50-assembly panels showed broad presence of the primary 20 labels and little change after restriction to strict ANI-pass assemblies. The selected-reference fliC label remained detectable in 50/50, 50/50, 47/50, 50/50, and 50/50 assemblies, yet a broader flagellin-family audit revealed marked cross-species heterogeneity, so shared label identity was not interpreted as molecular equivalence. The historical 18-protein set was retained only as secondary conditional STRING-coherence evidence. Because the study includes only five selected flagellated pathogen strains and no commensal, non-pathogenic, or non-flagellated controls, the results support a hypothesis-generating shared flagellar/motility-associated module rather than a pathogen-specific core.