Nitzschia australodesertorum Lehmkuhl, T. Ludwig & C. Bicudo, 2019

Lehmkuhl, Elton A., Morales, Eduardo A., Tremarin, Priscila I., Bartozek, Elaine C. R., Zorzal-Almeida, Stéfano, Ludwig, Thelma A. V. & Bicudo, Carlos E. De M., 2019, Two new species of Nitzschia (Bacillariaceae, Bacillariophyta) from tropical reservoirs of southeastern Brazil, Phytotaxa 399 (1), pp. 83-99 : 89-93

publication ID

https://doi.org/ 10.11646/phytotaxa.399.1.9

persistent identifier

https://treatment.plazi.org/id/039787F7-FF89-9F23-F0C8-FAAFFA53FDD3

treatment provided by

Felipe

scientific name

Nitzschia australodesertorum Lehmkuhl, T. Ludwig & C. Bicudo
status

sp. nov.

Nitzschia australodesertorum Lehmkuhl, T. Ludwig & C. Bicudo sp. nov. ( Figs 32–52 View FIGURES 32–52 , 59–68 View FIGURES 59–63 View FIGURES 64–68 )

LM: Frustules with nitzschioid symmetry ( Figs 41, 51, 52 View FIGURES 32–52 ), rectangular in girdle view ( Figs 51–52 View FIGURES 32–52 ). Valves linear-elliptic to elliptic ( Figs 32–50 View FIGURES 32–52 ). Apices protracted, subcapitate ( Figs 37, 40–42, 47, 48, 50 View FIGURES 32–52 ) to capitate ( Figs 32–36, 38, 39, 43–46, 49 View FIGURES 32–52 ). Fibulae unevenly spaced, sometimes with variable shape in the same specimen, forked ( Figs 32–34, 37–40, 42, 43, 45, 47–50 View FIGURES 32–52 ), slightly extended across the valve ( Figs 32, 34, 36–43, 47, 50 View FIGURES 32–52 ), rounded ( Figs 36, 37, 41, 44–46, 48, 50 View FIGURES 32–52 ), short rectangular ( Figs 32–38, 40, 43, 44, 46–49 View FIGURES 32–52 ). Gap present between the two central fibulae, evident (arrows, figs 32, 35, 43–45, 49, 51, 52) or not evident ( Figs 33, 34, 36–42, 46–48, 50 View FIGURES 32–52 ). Fibulae distant, every 1–3 striae. Striae parallel at the valve centre, becoming curved from one-third of the valve length until the apices. Areolae rounded, delicate, visible under LM.

Dimensions: length: 16–20 μm; width: 3–4.5 μm; 9–12 fibulae in 10 μm; 24–25 striae in 10 μm; 24–28 areolae in 10 μm (n = 50).

SEM/TEM: Internal valve face flat ( Figs 59–63 View FIGURES 59–63 ). Marginal keel rising from the valve face ( Figs 61 View FIGURES 59–63 , 64 View FIGURES 64–68 ). Raphe continuous ( Fig 61 View FIGURES 59–63 ), located at the marginal keel between the valve face and the mantle ( Figs 60, 61 View FIGURES 59–63 , 64 View FIGURES 64–68 ). Terminal raphe slits ending in a small helictoglossa at each pole ( Figs 59, 61 View FIGURES 59–63 , 64, 65 View FIGURES 64–68 ). Fibulae rounded or short rectangular ( Figs 59, 62, 63 View FIGURES 59–63 ). Gap present in the central fibulae, evident (arrow Fig. 63 View FIGURES 59–63 ) or not evident ( Fig 59 View FIGURES 59–63 , 66 View FIGURES 64–68 ). Interfibular space circular, smaller than the fibulae ( Figs 59, 62, 63 View FIGURES 59–63 ). Striae formed by single rows of areolae ( Figs 59–63 View FIGURES 59–63 , 66–68 View FIGURES 64–68 ), straight at the valve centre, becoming curved from one-third of the valve length until the apices ( Figs 59, 60 View FIGURES 59–63 , 66 View FIGURES 64–68 ). Internal virgae flat ( Figs 59–63 View FIGURES 59–63 ). Areolae rounded to elliptical, showing different sizes along the valve face ( Figs 59–68 View FIGURES 59–63 View FIGURES 64–68 ). Elongated areolae bordering the opposite raphe side ( Figs 59–67 View FIGURES 59–63 View FIGURES 64–68 ), occluded by hymenes ( Figs 67, 68 View FIGURES 64–68 ). Mantle on the keel side with two areolae forming each stria; thicker virgae at mantle margin ( Figs 59–61 View FIGURES 59–63 , 64, 65 View FIGURES 64–68 ).

Etymology: the epithet refers to its resemblance to N. desertorum Hustedt (1949: 50) and its occurrence in the southern region.

Diagnosis: Nitzschia australodesertorum differs from N. desertorum by the presence of a gap between the central fibulae, and by the even density of fibulae throughout the whole margin. It differs from N. supralitorea by the valve outline linear-elliptic to elliptic, presence of a gap between the central fibulae, the lower density of fibulae, and the higher striae density.

Type: — BRAZIL, São Paulo State: Municipality São Paulo, Tatu reservoir, from surface sediments, 22º39′12′′S, 47º16′59′′W, 18 July 2013 (Holotype SP! 469268, depicted in Fig. 42 View FIGURES 32–52 ).

Ecology: Nitzschia australodesertorum was recorded from seven samples of surface sediments, phytoplankton, and periphyton of Tatu reservoir, which ranged from oligo to mesotrophic conditions (see Table 3 for the abiotic characterization of Tatu reservoir). The greatest relative abundance of this species was registered from surface sediments (20.3%) and phytoplankton (3.3%). Tatu is considered a river-like reservoir due to its low residence time ( Mansor 2005), high turbidity during intense rainfalls, and the presence of banks of macrophytes along its margin.

Achnanthidium catenatum (Bily & Marvan) Lange-Bertalot (1999: 271) (18.4%) and A. minutissimum (13.2%) were the most abundant species from surface sediments, co-occurring with Nitzschia amphibia , N. australodesertorum , N. acidoclinata , N. palea , N. pusilluhasta , N. recta Hantzsch ex Rabenhorst (1862: 1283) , N. semirobusta , N. subacicularis , and N. terrestris . Other co-occurring species that were abundant in the phytoplankton during the winter were A. exiguum (Grunow) Czarnecki (1994: 157) (25.6%), A. minutissimum (17.3%) and Fragilaria sp. (17.3%). Nitzschia amphibia , N. clausii , N. palea , and N. pusilluhasta were also registered but with a low abundance (<2%).

Kingdom

Animalia

Phylum

Platyhelminthes

Class

Monogenea

Order

Capsalidea

Family

Capsalidae

Genus

Nitzschia

Loc

Nitzschia australodesertorum Lehmkuhl, T. Ludwig & C. Bicudo

Lehmkuhl, Elton A., Morales, Eduardo A., Tremarin, Priscila I., Bartozek, Elaine C. R., Zorzal-Almeida, Stéfano, Ludwig, Thelma A. V. & Bicudo, Carlos E. De M. 2019
2019
Loc

Achnanthidium catenatum (Bily & Marvan)

Lange-Bertalot, H. 1999: )
Czarnecki, D. B. 1994: )
Rabenhorst, L. 1862: )
1999
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