Progonoia diatreta Lobban, 2015
publication ID |
https://doi.org/ 10.11646/phytotaxa.234.3.5 |
persistent identifier |
https://treatment.plazi.org/id/03CD1837-EC37-FF84-00A8-1511FD32F8CB |
treatment provided by |
Felipe |
scientific name |
Progonoia diatreta Lobban |
status |
sp. nov. |
Progonoia diatreta Lobban , sp. nov. ( Figs 6 View FIGURES 4–6 , 18–29 View FIGURES 18–26 View FIGURES 27–29 )
Synonyms: Navicula musca sensu Peragallo & Peragallo (1897 –1908: 79–80, pl. 14, figs 14–16), Oestrupia musca sensu Hendey (1964: 228 , pl. 29, fig. 17)
Differing from P. musca in having rings of small pores around the external edges of the areolae rather than simple large, uniseriate openings, and in having externally a wide, sculpted space between the two alveolae.
Type:— GUAM. Apra Harbor Guam: Outhouse Beach, 13° 27’ 50” N, 144° 39’ 27” E, calcareous sand sample GU52O-4, ca. 12 m deep, C. Lobban & M. Schefter, 13 December 2010 (holotype: CAS! frustule located 17.6 mm E and 8.5 mm S of reference mark on slide 1696, accession # [627432], slide # [223050], illustrated in Fig. 18 View FIGURES 18–26 . Isotypes: GUAM! slides 1695 and 1697 in Guam Diatom Herbarium. Isotypes: GUAM! slides 821 (GU44P-5) and 1115 (GU52Q-2) in Guam Diatom Herbarium.
Etymology:— Diatreta L., n. pl. noun in apposition = filigree; from diatetrum = artisan, with reference to the elegant pattern of external pores around the areolae. [A more appropriate English analogy would be a doily, but I could find no Latin or Greek translation that conveys the sense of the elaborate pattern of holes.]
Description:— LM ( Figs 6 View FIGURES 4–6 , 18–20 View FIGURES 18–26 ): Valves elliptical-lanceolate, length 51–86 μm, width 19–25 μm, somewhat constricted in the middle to 15–19 μm, but axial area continuous across the central part of the valve ( Figs 18–20 View FIGURES 18–26 ). Axial area occupies only about one quarter of the width of the valve; it is slightly depressed except for two narrow strips alongside the raphe slits from the central area halfway to the poles. Raphe is straight, central endings slightly expanded. Striae 7–8 in 10 μm, uniseriate, alveolate, with two chambers apparently separated by a sculpted, hyaline space rather than just a longitudinal rib ( Fig. 6 View FIGURES 4–6 vs. Fig. 5 View FIGURES 4–6 ). SEM ( Figs 21–29 View FIGURES 18–26 View FIGURES 27–29 ): The external valve face is elaborately perforated and sculpted ( Figs 21–26 View FIGURES 18–26 ). The perforations include a series of large pores along the edge of the mantle, two series of small circular and C-shaped pores around the edges of the two alveoli ( Figs 22, 26 View FIGURES 18–26 ), often with additional pores in the middle of the alveolus (especially in the longer cells: Figs 23–26 View FIGURES 18–26 ), and a series of medium-sized, curved pores along the axial ends of the alveoli. The sculpted areas include the majority of the axial area and small patches offset between the two series of alveoli ( Figs 24 View FIGURES 18–26 , arrow, and 26). Internally ( Figs 27–29 View FIGURES 27–29 ), alveoli extend between fingers of the basal siliceous layer that are connected by an internal partition that separated the alveoli in adjacent striae. The alveoli are apparently divided by cross walls that formed a continuous longitudinal “rib.” In this species there also appear to be short transapical partial walls in both directions from the cross wall (inferred from the markings on the membrane) ( Figs 27 and 29 View FIGURES 27–29 ). In spite of the appearance of the outer surface, the chambers are separated only by a thin wall. The junction between the basal siliceous layer and the alveolar membrane is perforated by a line of tiny pores ( Figs 28 and 29 View FIGURES 27–29 ). The middle part of the alveoli is thicker, such that there was a ridge on both sides ( Figs 27–29 View FIGURES 27–29 ). The external raphe central endings are expanded and pore-like ( Figs 23–25 View FIGURES 18–26 ); internally they end in a beak-like double helictoglossa ( Fig. 28 View FIGURES 27–29 ). External terminal endings deflect to the same side and end on the valve mantle ( Fig. 26 View FIGURES 18–26 ); internal endings are straight, with a very small helicoglossa ( Fig. 29 View FIGURES 27–29 ). Girdle bands ( Figs 24–26 View FIGURES 18–26 ) are striate, the striae 21–25 in 10 μm.
Additional records:— The following records from the literature are probably this species, as indicated by the record of small pores along the sides of the alveoli, and cited above under synonymy: Peragallo & Peragallo (1897 – 1908, pl. 14, figs 14–16, as Navicula musca ) and Hendey (1964, pl. 29, fig. 17, as Oestrupia musca ). Hustedt’s (1955) drawing does not show pores at all but the large space separating the alveoli suggests that this, too, may be P. diatreta ; I was unable to find any specimens in subsamples of his material and he gave no description in either Hustedt (1955) or Hustedt (1935) to indicate his concept of the species. The following records cannot be identified to species because the photographs do not show the surface pores: López Fuerte et al. (2010, pl. 18, figs 21, 22), and Al-Yamani & Saburova (2011, pl. 62, figs a–c, both as Oestrupia musca ).
CAS |
California Academy of Sciences |
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.
Kingdom |
|
Phylum |
|
Class |
|
Order |
|
Family |
|
Genus |