Nitzschia nandorii Olszynski , Zakrzewski & Zelazna-Wieczorek, 2024

Olszynski, Rafal M., Zakrzewski, Piotr K., Rimet, Frederic, Sulkowska, Julia, Peszek, Lukasz & Zelazna-Wieczorek, Joanna, 2024, Morphology and phylogeny of Nitzschia nandorii sp. nov. (Bacillariophyceae), a new small-celled lanceolate species from a post-mining reservoir, PhytoKeys 241, pp. 1-26 : 1

publication ID

https://dx.doi.org/10.3897/phytokeys.241.117406

persistent identifier

https://treatment.plazi.org/id/76218E52-AED5-5ECF-9972-4C572630D3AE

treatment provided by

PhytoKeys by Pensoft

scientific name

Nitzschia nandorii Olszynski , Zakrzewski & Zelazna-Wieczorek
status

sp. nov.

Nitzschia nandorii Olszynski, Zakrzewski & Zelazna-Wieczorek sp. nov.

Figs 2 View Figure 2 , 3A-AE View Figure 3 , 4 View Figure 4 -6 View Figure 6

Holotype.

Slide number: D.BOF2.191022, Algae Collection Department of Algology and Mycology, University of Lodz. The holotype is illustrated in Fig. 3K View Figure 3 (designated here).

Isotype.

Slide number: SZCZ 29106, Szczecin Diatomological Collection, University of Szczecin, Poland.

Type locality.

Poland. Greater Poland Voivodeship, Bogdałów. Post-mining reservoir Bogdałów. 52°2'53.938"N, 18°35'49.646"E.

Morphology description.

Nitzschia nandorii sp. nov. possesses two conical-shaped chloroplasts arranged apically with a central, longitudinal groove (Fig. 2 View Figure 2 , see: Suppl. material 8). Frustules are small, distended, and broadly lanceolate with short protracted and subcapitate apices. Valves are 9.0-12.0 µm length and 2.5-3.3 µm width. The ratio of length and width is 3.44-4.80 (Fig. 3A View Figure 3 -AE). Striae 40-46 in 10 µm (based on SEM analysis) and indiscernible in LM. Fibulae are visible 11-16 in 10 µm. Externally, the valve face is flat and without costae (Figs 4 View Figure 4 , 5 View Figure 5 ). Striae are uniseriate, and transapically becoming more arched to the apices (Figs 4 View Figure 4 , 5 View Figure 5 ). Two longitudinal rows of areolae are present along the edge of the valve on the raphe canal with a doublet of pores closest to the raphe and second with a single pore near the junction of the raphe canal and valve face (Fig. 4 View Figure 4 ). Distal raphe endings are strongly hooked and deflected in different directions depending on the valve. Polar raphe fissures deflected to the proximal mantle overlap on it (Figs 4 View Figure 4 , 5A-D View Figure 5 ). The central raphe fissures are missing (Fig. 5A, B, E, F View Figure 5 , see: Suppl. material 9). The proximal mantle possesses three rows of areolae (Figs 5C View Figure 5 , 6B View Figure 6 , see: Suppl. material 9). The first two are arranged to mirror pores on the raphe canal and open to the raphe canal (Fig. 5C View Figure 5 ). The third with areolae covered by hymenes (Fig. 6D View Figure 6 ) and open to frustule interior (Fig. 5C View Figure 5 , see: Suppl. material 9). The distal mantle is narrow with a scalloped edge (Figs 4D View Figure 4 , 6C View Figure 6 ). Valvocopula is smooth and possesses opened pores (Fig. 4D View Figure 4 ). Internally, the fibulae are roughly equidistant so that the central fibulae are not further apart than any of the others (Fig. 6A View Figure 6 ). Distal raphe fissures terminate with small helictoglossa internally (Fig. 6E View Figure 6 ).

Gene sequences.

sequences were deposited in the GenBank: D.LDZ8 (SSU rDNA: PP082029, rbcL: PP073739, and psbC: PP073738), D.LDZ12 (SSU rDNA: PP082030, rbcL: PP073741, and psbC: PP073740)

PhycoBank registration.

http://phycobank.org/104257.

Molecular phylogeny.

The phylogenetic reconstructions based on the ML and BI strategy for the concatenated SSU- rbcL - psbC matrix, as well as separate SSU, rbcL, and psbC analysis, were performed. The three-genes tree placed strains D.LDZ8 and D.LDZ12 (Fig. 7 View Figure 7 , green box) within the clade including the Nitzschia Lanceolatae section, which is characterized by double rows of areolae on the raphe canal, with very high node support (BI = 1; ML = 100) (Fig. 7 View Figure 7 , grey box). Moreover, the tree topology distinguished the strains described here, i.e., N. nandorii sp. nov., from N. fonticola ( N. cf. romana syn. N. fonticola ) both in BI and ML phylogenetic reconstructions with the strong division support (BI = 1; ML = 100). Phylogenetic trees reconstructed using separate DNA markers, i.e., rbcL (Fig. 8 View Figure 8 ), psbC (see Suppl. materials 10, 11), and SSU (see Suppl. materials 12, 13), and the concatenated analysis distinct N. nandorii sp. nov., as a separate clade in Lanceolate section. The rbcL tree topology (Fig. 8 View Figure 8 ) was included in the main manuscript here, due to its higher taxon sampling.

Etymology.

The species name comes from the main character of the TV series " What We Do in the Shadows " Nandor the Relentless, and the name of the authors’ cat (RMO, PKZ).

Differential diagnosis.

Nitzschia nandorii sp. nov. is a species with a small cell size that can be overlooked or misidentified with other taxa, especially when they occur in one sample. The valve shape of the small specimens of N. fonticola can be misidentified with N. nandorii sp. nov., however visible striation and the wider relative spacing between the central fibulae compared to the rest of the fibulae in N. fonticola distinguish these two taxa ( Lange-Bertalot 1976; Krammer and Lange-Bertalot 1997; Lange-Bertalot et al. 2017). The valve outline of N. dealpina Lange-Bertalot & G. Hofmann 1993 is similar to N. nandorii sp. nov., but these taxa can be distinguished due to the lower stria and fibula density per 10 µm in N. dealpina . Furthermore, N. dealpina occurs in an environment with a high concentration of calcium bicarbonate while N. nandorii has so far only been identified in an environment with a moderate concentration of these ions ( Lange-Bertalot 1993; Krammer and Lange-Bertalot 1997; Rumrich et al. 2000; Lange-Bertalot et al. 2017; Olszyński et al. 2019). The smaller forms of N. alpinobacillum Lange-Bertalot, 1993, which also possess two rows of pores on the raphe canal ( Lange-Bertalot 1993; Rumrich et al. 2000; Lange-Bertalot et al. 2017), have similar outlines to the N. nandorii sp. nov., but have denser striation and fibulae. N. nandorii sp. nov. can be easily misidentified with a small N. lacuum Lange-Bertalot 1980. Both taxa have similar valve size and stria and fibula density. Neither has a central nodule or a relatively wide gap between central fibulae. However, N. lacuum has different proportions between length and width and, therefore, is more elongated and has more protracted apices than N. nandorii sp. nov. ( Lange-Bertalot 1980, 1993; Lange-Bertalot et al. 2017). N. bryophila (Hustedt) Hustedt 1943 has a similar valve outline to N. nandorii sp. nov. However, the frustules of N. bryophila are bigger, apices are more elongated and have clearly visible striations. Fibulae are less dense in N. bryophila than in N. nandorii sp. nov. ( Lange-Bertalot and Metzeltin 1996; Krammer and Lange-Bertalot 1997). N. bacillum Husted, 1922 has a similar valve outline to N. nandorii sp. nov. In some cases a small form of N. bacillum can be misidentified with newly described species. However, N. bacillum has visible striations and particular areolae can be observed. A character which is visible in SEM and distinguishes this species from N. nandorii sp. nov. is a single row of areolae on the raphe canal ( Lange-Bertalot 1993). Another similar species to N. nandorii sp. nov. is N. rosenstockii Lange-Bertalot, 1980. This taxa has specific apices which are short, beak-like and point rounded. In some cases, the valve outline can be similar to N. nandorii sp. nov. However, N. rosenstockii can be easily distinguished in LM from N. nandorii sp. nov. by the valve outline, characteristic valve ends, a higher number of fibulae in 10 µm, and the presence of striae discontinuity in the central part of valves ( Lange-Bertalot 1980). For more details see Table 2 View Table 2 .