Bracteacoccus ruber Novis & Visnovsky, 2012

Novis, Phil M. & Visnovsky, Gabriel, 2012, Novel alpine algae from New Zealand: Chlorophyta, Phytotaxa 39, pp. 1-30 : 16

publication ID

https://doi.org/ 10.11646/phytotaxa.39.1.1

DOI

https://doi.org/10.5281/zenodo.4894706

persistent identifier

https://treatment.plazi.org/id/0391A571-2119-C67D-78AD-FC984EA4FADD

treatment provided by

Felipe

scientific name

Bracteacoccus ruber Novis & Visnovsky
status

sp. nov.

Bracteacoccus ruber Novis & Visnovsky , sp. nov. ( Figs 2A–G View FIGURE 2 )

Cellulae sphaericae, 5.0–24.0(–60.0) µm latae, unicae vel in greges laxos irregulars aggregatae. Paries cellularis laevis, in cellulis immaturis <0.5 µm crassus, sed in cellulis maturis magnis usque ad 5.0 µm crassus. Chloroplasti numerosi discoideo–polygonii pyrenoidibus carentes, parietales sed interdum ad interioribus cellulae plicati. Autosporis 2–4–8–16 per sporangium regenerans. Cellulae in culturis vetustioribus in cytoplasmate praecipue quum luci valda objectata pigmentationem evolventes, imprimis in area nucleum proxime ambiente.

Type:— NEW ZEALAND: Westland : Mt Philistine, 1400 m, preserved cultured specimen from sample collected 30 November 2007, CHR610485 View Materials .

Cells spherical, 5.0–24.0(–60.0) µm wide, single or in loose, irregular groups. Cell wall smooth, <0.5 µm thick in young cells, but up to 5.0 µm thick in large, mature cells ( Fig. 2C View FIGURE 2 ). Numerous discoidal–polygonal chloroplasts lacking pyrenoids, parietal but occasionally folded towards the cell interior ( Fig. 2A View FIGURE 2 ). Reproduction through autospores, 2–4–8–16 per sporangium ( Fig. 2D View FIGURE 2 ). Zoospores not observed. Cells in older cultures develop red pigmentation in the cytoplasm, especially immediately surrounding the nucleus and when exposed to strong light (compare Figs 2F and G View FIGURE 2 ). DNA sequence data for 18 S showed the species to belong to Bracteacoccus , but without close affinities ( Fig. 7 View FIGURE 7 ).

Habitat:— Alpine herbfield soil.

Distribution:— New Zealand.

Etymology:— Referring to the red pigmentation developed by older cultures.

Observations:— Data for rbc L failed to reconstruct Bracteacoccus as a clade ( Fig. 9 View FIGURE 9 ); the phylogenetic conclusions are therefore drawn from 18S data. The size and red colouration of B. ruber resemble those reported for B. minor (Chodat) Petrová 1931 , but the two are not closest relatives according to DNA sequences. Fučíková et al. (2011) suggest that Bracteacoccus ( Tereg 1923) and Pseudomuriella ( Hanagata 1998) are morphologically cryptic genera. However, our strain of Bracteacoccus is clearly related to B. aerius ( Bischoff & Bold 1963) UTEX 1250 , which falls in the Bracteacoccus clade of Fučíková et al. The large cells with multilayered wall suggest B. giganteus ( Bischoff & Bold 1963) , but 18S rDNA sequences clearly distinguish this from B. ruber ( Fig. 7 View FIGURE 7 ).

Capacity to develop the red colouration was found to diminish over time following isolation from field material, especially if the population underwent a culture cycle in liquid medium before replating on agar. A crude spectrophotometer test indicated that the pigment absorbs in the UV spectrum (data not shown).

Cultures:— LCR-CG8.

S

Department of Botany, Swedish Museum of Natural History

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