Navicula gogorevii Chudaev, Glushchenko, Kulikovskiy & Kociolek, 2020
publication ID |
https://doi.org/ 10.11646/phytotaxa.428.1.6 |
DOI |
https://doi.org/10.5281/zenodo.13875909 |
persistent identifier |
https://treatment.plazi.org/id/03FD87F2-FFCD-BE44-FF5A-FC8CFCBBF7FB |
treatment provided by |
Felipe |
scientific name |
Navicula gogorevii Chudaev, Glushchenko, Kulikovskiy & Kociolek |
status |
sp. nov. |
Navicula gogorevii Chudaev, Glushchenko, Kulikovskiy & Kociolek , sp. nov. ( Figs 1–26 View FIGURES 1–14 View FIGURES 15–20 View FIGURES 21–26 )
Description.
LM ( Figs 1–14 View FIGURES 1–14 ). Valves lanceolate with widely rounded apices, length 67.6–97.5 μm, width 11.4–13.1 μm. Axial area moderately narrow, linear, slightly widening towards the centre. Central area transversely expanded, variable in shape, occupying 1/2–4/5 of valve width, often with irregular border due to unequal shortening of central striae. Striae radiate at the valve centre, becoming convergent towards valve ends, 16.0–18.6/10 μm. Areolae well distinguishable in LM, 21.2–23.6/10 μm. Raphe slightly lateral, terminal fissures curved to the secondary valve side, central pores enlarged, straight or rare slightly deflected to the primary side. Central nodule asymmetrically expanded to the primary valve side.
SEM, external views ( Figs 15–20 View FIGURES 15–20 ). Areolae open into distinct longitudinal grooves, separated by longitudinal siliceous strips, curved around central area and straight on the rest of the valve ( Figs 19 View FIGURES 15–20 , black arrow). The margins of the grooves do not close up, so separate areolae are visible through the slits ( Fig. 20 View FIGURES 15–20 , black arrow). Proximal grooves are interrupted by the central area. Grooves’ endings at central area and valve apices are pointed ( Figs 17, 20 View FIGURES 15–20 , white arrowheads). Raphe-sternum is at the same level as the valve surface. Raphe slit is slightly lateral. Central pores enlarged (sometimes slightly asymmetrically), drop-shaped, undeflected or slightly deflected to the valve primary side ( Figs 17, 18 View FIGURES 15–20 , white arrows). Terminal fissures sickle-shaped, lying mostly on the valve face ( Figs 19, 20 View FIGURES 15–20 , white arrows). Pinhole-like openings of apical areolae are arranged in one row at the primary side of valve apex ( Figs 19, 20 View FIGURES 15–20 , black arrowheads).
SEM, internal views ( Figs 21–26 View FIGURES 21–26 ). Virgae and vimines lie on the same level, so transapical depressions (alveolae) are not formed. Areola openings are roundish-square to round. Internal width of areolae is larger than the external, so external slit-like openings are visible at the bottom of the areolae ( Figs 25, 26 View FIGURES 21–26 ). Hymenes were not preserved during the material treatment. Raphe slits open obliquely to the secondary valve side and are visible only at the valve centre and apices ( Figs 23, 24, 26 View FIGURES 21–26 , white arrows). Proximal raphe endings straight, positioned on the slight widening of rapheridge, with a short intermissio ( Figs 23, 24 View FIGURES 21–26 , white arrows). Distal raphe endings are well-developed and terminate as straight or slightly deflected helictoglossae ( Figs 25, 26 View FIGURES 21–26 , black arrows). Accessory rib prominent, unilaterally widened to the primary valve side ( Figs 23, 24 View FIGURES 21–26 , black arrows), separated from raphe ridge by shallow longitudinal furrow ( Figs 23, 24 View FIGURES 21–26 , black arrowheads). The widening of accessory rib (central nodule) gradually turns into the central area ( Figs 23, 24 View FIGURES 21–26 , white arrowheads). Raphe-sternum widens at the apices forming well-developed terminal areas with cushion-like thickenings at the ends of accessory rib ( Figs 25, 26 View FIGURES 21–26 white arrowheads). Internal openings of apical areolae are apically elongated and larger than the external ones ( Figs 25, 26 View FIGURES 21–26 , black arrowheads).
Type: — VIETNAM. Ba Bể Lake, Bắc Kạn Province, benthos, N22°23.605´E105°36.856´, was collected by E.S. Gusev & M.S. Kulikovskiy, 29.04.2015 (in collection of Maxim Kulikovskiy at the Herbarium of the Institute of Plant Physiology Russian Academy of Science, Moscow, Russia), holotype here designated, slide no. 02168 = Fig. 3 View FIGURES 1–14 ).
Etymology: —Species epithet honors the well-known Russian diatomologist Dr. Rinat Gogorev, Komarov Botanical Institute, Saint-Petersburg.
Distribution. As yet known only from the type locality.
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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