Achnanthidium petuniabuktianum, Pinseel & Vijver & Kopalova, 2015
publication ID |
https://doi.org/ 10.11646/phytotaxa.226.1.6 |
DOI |
https://doi.org/10.5281/zenodo.13636350 |
persistent identifier |
https://treatment.plazi.org/id/038B878A-AE13-FF8D-15E7-FF6C34DCFACE |
treatment provided by |
Felipe |
scientific name |
Achnanthidium petuniabuktianum |
status |
sp. nov. |
Achnanthidium petuniabuktianum sp. nov. ( Figs 2–32 View FIGURES 2–26 View FIGURES 27–32 )
Frustules rectangular, only slightly arched in girdle view ( Figs 2 View FIGURES 2–26 , 27 & 32 View FIGURES 27–32 ). Cingulum composed of three open, unperforated copulae ( Figs 27, 32 View FIGURES 27–32 ). Valvocopula typically showing two indentations at one third from the valve apex ( Fig. 32 View FIGURES 27–32 ). Mantle areolae slit–like ( Figs 27 & 32 View FIGURES 27–32 ). Valves linear with broadly rounded apices. Valve dimensions (n=20): length: 8.9–20.1 μm, width 1.9–2.9 μm. Raphe valve ( Figs 3–11 View FIGURES 2–26 , Figs 20–26 View FIGURES 2–26 ): valves concave. Axial area broad, linear, slightly narrowing towards the distal raphe endings ( Figs 20–22 View FIGURES 2–26 ). Central area broad, forming a clear rectangular fascia ( Figs 20–22 View FIGURES 2–26 ). Shortened marginal striae occasionally present in the central area ( Fig. 22 View FIGURES 2–26 ). Central striae slightly more widely spaced ( Fig. 22 View FIGURES 2–26 ). External raphe branches straight, filiform, slightly broadening towards the central area terminating in simple, straight to weakly bent proximal raphe endings ( Figs 20–22 View FIGURES 2–26 ). External distal raphe endings terminating just beyond the last apical striae, distinctly unilaterally hooked ( Figs 20–23 View FIGURES 2–26 ). Internal proximal raphe endings slightly bent in opposite directions, internal distal raphe endings straight terminating into small helictoglossae ( Figs 24–26 View FIGURES 2–26 ). Distal raphe endings hardly discernible in LM. Striae, 39–44 in 10 μm, hardly visible in LM. In SEM, striae clearly parallel throughout the entire valve, composed of one to two transapically elongated areolae ( Fig. 20–23 View FIGURES 2–26 ). Rapheless valve ( Figs 12–19 View FIGURES 2–26 , Figs 27–31 View FIGURES 27–32 ): valves convex. Axial area very broad, slightly narrowing towards the distal raphe endings ( Figs 27–28 & 30 View FIGURES 27–32 ). Central area almost absent, formed by a slightly widening axial area ( Fig. 28 View FIGURES 27–32 ). Central striae slightly more widely spaced ( Fig. 28 View FIGURES 27–32 ). Central area occasionally lacking marginal striae thus forming a clear fascia ( Fig. 27 View FIGURES 27–32 ). Striae, 38–42 in 10 μm, hardly discernible in LM. In SEM, striae parallel throughout, composed of usually one, rarely two, transapically elongated areolae ( Figs 27–28, 30 View FIGURES 27–32 ).
Type:— NORWAY, SVALBARD ARCHIPELAGO. Spitsbergen: Petuniabukta, Mathiessondalen, epiphyton on moss from a wetland adjacent to a lake, sample SPITS 2013 /029, 30 m a.s.l., 78.56317° N and 16.58725° E, E. Pinseel, 26 July 2013 (holotype BR!, slide no. 4177, Botanic Garden Meise, Belgium; isotype PLP!, slide no. 288, University of Antwerp , Belgium) GoogleMaps .
Etymology:— The specific epithet petuniabuktianum refers to the fjord area, Petuniabukta, where the new taxon was found.
Ecology, distribution and associated diatom flora: —So far, A. petuniabuktianum has only been found in Petuniabukta (Spitsbergen, Svalbard Archipelago). The new species is described from a wetland adjacent to a small lake characterized by an alkaline pH (8.1) and a moderately high conductivity value (761 μS/cm). At the type locality, this taxon was solely observed in association with moss vegetation, both submerged and terrestrial (wetland). A second population was observed in an epilithon sample of a shallow pond in the terminal moraine of a glacier. Due to logistic constraints, physicochemical measurements of this locality could not be obtained. In all cases, the abundances of this taxon were low (0.5–3.8% of all counted valves). The associated diatom flora was dominated by species of the A. minutissimum complex, Denticula tenuis Kützing (1844: 43) , D. kuetzingii Grunow (1862: 546) , Staurosirella aff. lapponica (Grunow in Van Heurck 1881: 45) D.M. Williams & Round (1987: 274), two at present unidentified Encyonopsis Krammer (1997: 91) taxa and Nitzschia cf. perminuta (Grunow in Van Heurck 1881: 68) Peragallo (1903: 672).
BR |
Embrapa Agrobiology Diazothrophic Microbial Culture Collection |
PLP |
Institute of Himalayan Bioresource Technology |
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.
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