Lithophyllum yemenense, Basso & Caragnano & Gall & Rodondi, 2015

Basso, Daniela, Caragnano, Annalisa, Gall, Line Le & Rodondi, Graziella, 2015, The genus Lithophyllum in the north-western Indian Ocean, with description of L. yemenense sp. nov., L. socotraense sp. nov., L. subplicatum comb. et stat. nov., and the resumed L. affine, L. kaiseri, and L. subreduncum (Rhodophyta, Corallinales), Phytotaxa 208 (3), pp. 183-200 : 195-196

publication ID

https://doi.org/ 10.11646/phytotaxa.208.3.1

DOI

https://doi.org/10.5281/zenodo.13642567

persistent identifier

https://treatment.plazi.org/id/03C43948-EC63-492E-B3C8-FCCBFA6D1240

treatment provided by

Felipe

scientific name

Lithophyllum yemenense
status

sp. nov.

Lithophyllum yemenense sp. nov.

Figures 11–12 View FIGURE 11 View FIGURE 12 ; Table 3

HOLOTYPE: sample DB567 (tetrasporangial plant, Fig. 11 View FIGURE 11 ; legit Caragnano: Balhaf, Yemen, iii.2008), including histological slides DB567-13y2, DB567-13y4, conserved in TRH ( TRH-A3882 ).

ETYMOLOGY: the specific epithet is dedicated to the Arabian country where samples were collected.

TYPE LOCALITY: Balhaf, Yemen, on biogenic calcareous rock, 2 m depth.

MATERIAL EXAMINED: Red Sea : Yemen, Kamaran, 1.5 m (legit Caragnano: DB575-576, 28.ix.2009) ; Indian Ocean : Gulf of Aden, Yemen, Balhaf, 2–3 m (leg. Benzoni: DB559 , ix 2006; DB563, xi.2006; leg. Caragnano: DB568-570, iii.2008; DB657, DB659, DB660, DB692, xi.2008) ; Yemen, Socotra Is., 9 m (leg. Caragnano: DB612 , iii.2010) .

GEOGRAPHIC DISTRIBUTION: L. yemenense is distributed in the Red Sea, Gulf of Aden and Arabian Sea. The occurrence of L. yemenense outside this area is unknown.

HABIT AND VEGETATIVE STRUCTURE: The coralline may be attached on corals or other biogenic substrate or form unattached nodules (rhodoliths). Thallus non-endophytic, encrusting, lumpy to fruticose. The protuberances, up to about 10 mm long and about 2–5 mm wide, have a smooth surface, are cylindrical or compressed, branched, sometimes fused and apically enlarged and flattened ( Fig. 11A View FIGURE 11 ).

Plant structure pseudoparenchymatous ( Fig. 11B–E View FIGURE 11 ). Basal or ventral layer (= hypothallium) dimerous, hypothallial cells 7–20 μm long and 10–15 μm in diameter ( Fig. 11E View FIGURE 11 ). Peripheral region (= perithallium) composed of cell filaments curving outwards towards the thallus surface, 5–30 μm long and 7–14 μm in diameter ( Fig. 11B–E View FIGURE 11 ). Cells of adjacent filaments joined by secondary pit connections, cell fusions not observed ( Fig. 11C View FIGURE 11 ). Palisade cells not observed. Single trichocytes 15–45 μm long and about 10–18 μm in diameter occurring in the perithallium and at the thallus surface ( Fig. 11C View FIGURE 11 ). Single epithallial cells flattened, about 7–13 μm in diameter and 2–5 μm long ( Fig. 11D View FIGURE 11 ; Tab. 3).

REPRODUCTION: Uniporate tetrasporangial conceptacles flush or weakly protruding above the surrounding thallus surface, conceptacle chamber 250–300 μm in diameter and 80–120 μm high, with a pore-canal 50–61 μm long ( Fig. 11B, F View FIGURE 11 ; Tab. 3). Floor of the conceptacle chamber with a central columella, 11–14 cells below the thallus surface. Roof filaments 4–6 cells long, including the terminal epithallial cell ( Fig. 11F View FIGURE 11 ).

Gametangial thalli dioecious; carpogonia and spermatangia produced in separate uniporate conceptacles ( Fig. 12 View FIGURE 12 ). Spermatangial filaments unbranched, arising from the male conceptacle chamber floor ( Fig. 12A View FIGURE 12 ). Mature male conceptacle roof weakly raised above the surrounding thallus surface or flush, composed of 5–7 layers of cells above the chamber. Male conceptacle chambers 250–315 μm in diameter and 40–45 μm high, plus a pore canal 38–55 μm long ( Fig. 12A View FIGURE 12 , Tab. 3).

Female conceptacles chamber about 170 μm in diameter. Carposporangial conceptacle chamber 325 μm in diameter, 125 μm high, with a pore-canal about 75 μm long ( Fig. 12B View FIGURE 12 , Tab. 3). Carposporophyte composed of a central fusion cell and short peripheral gonimoblast filaments bearing terminal carposporangia ( Fig. 12B View FIGURE 12 ).

REPRESENTATIVE SEQUENCES: KP696789 (LSU), KP976401 (CO1) & KP976408 (psb A).

A ML phylogenetic analysis inferred from psb A ( Fig. 13 View FIGURE 13 ) revealed that the two last species ( L. socotraense and L. yemenense ) were only distantly related to the specimens so far sequenced for this gene and available in GenBank.

TRH

Norwegian University of Science and Technology - Herbarium

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