Chenopodium hoggarense Uotila & C. Chatel., 2022

Chatelain, Cyrille, Uotila, Pertti, Benhouhou, Salima, Mombrial, Florian, Mesbah, Melilia, Baa, Soumaya & Benghanem, Abdelkader Nabil, 2022, Chenopodium hoggarense (Amaranthaceae), a new species from Algeria and Chad, Willdenowia 52 (1), pp. 75-81 : 75-79

Chenopodium hoggarense Uotila & C. Chatel. , sp. nov. – Fig. 1 , 2 , 3 (A–D).

Holotype: Algeria, Assekrem, pente Sud menant à l’hermitage (Hoggar) pt 7 , 23°15'37"N, 05°38'02"E, 2700 m, 24 Oct 2019, Chatelain, Benhouhou, Mombrial, Mesbah, Baa & Benghanem CM874 ( G [ G00408262 ]! [ Fig. 1 ]; isotypes: ENSA!, G [ G00408265 ]!, H [ H1777033 ]! ).

Diagnosis — Small annuals, strongly smelling like rotting fish (trimethylamine) and densely covered with vesicular hairs as in Chenopodium vulvaria L., but differing from that species by red colour sometimes present on stem and leaves, erect stem with short branches, leaves much longer than broad and often mucronate to cuspidate at apex, inflorescence mostly leafless in upper 1/3 of stem and branches, paniculate, of mostly well-spaced, dense glomerules, perianth deeply split into lobes, lobes apically winged abaxially and truncate at apex.

Description — Small annuals, strongly smelling like rotting fish (trimethylamine), whitish because of dense indumentum of vesicular hairs, especially in young parts, sometimes with red colour on stems, leaf margins and perianth segments. Stem erect, green with red longitudinal stripes, 10–16(–18) cm tall, hard, branched in lower half; branches spreading to erectopatent, straight, short, usually without secondary branches. Leaves erectopatent to erect; petiole 3–5 mm long; blade trullate to ovate to elliptic-ovate, entire or very slightly 3-lobed, 9–11 × 6–7 mm, becoming ± glabrescent on upper surface and often red at least on margin when old, base obtuse, margin entire or with a few obscure teeth, apex acute to mucronate to cuspidate; upper leaves narrowly elliptic to lanceolate ( Fig. 3 A ). Inflorescence occupying most of plant height, composed of paniculately arranged, mostly well-spaced, dense glomerules, mostly leafless in upper 1/3 of stem and branch length, in leaf axils in lower parts. Perianth lobes 5, basally united for 1/4–2/5 of their length, 0.7–1 mm long, densely farinose, free parts spreading in fruit, abaxially with a narrow, wing-like keel in apical part, midrib strong, visible adaxially, margin broad, membranous, minutely ciliate, apex truncate, sometimes red; receptacle cupuliform to obconic ( Fig. 3 B –D ). Stamens 5; anthers 0.3–0.4 mm long. Stigmas 2, very short, c. 0.2 mm long. Fruits mostly falling without perianth; pericarp fairly thin, quite easily scraped off. Seeds lenticular with weakly acute margin, 1.2–1.3 × 1.1–1.2 mm, 0.4–0.5 mm thick, testa finely radially rugose to almost smooth.

Distribution and habitat — Chenopodium hoggarense is known from Algeria, the Hoggar mountains, and Chad, the Tibesti mountains (Fig. 4). In 2019 it grew as a very large population in the Hoggar Assekrem plateau at altitudes of 2000–2700 m; occasionally it was also seen on rocky slopes of the plateau covered by bushes of Pentzia monodiana Maire, Crambe kralikii Coss. subsp. kralikii and occasionally Senecio hoggariensis Batt. & Trab. Habitats were barren rocky, sandy soil ( Fig. 5 ), practically without other vegetation except for scattered Euphorbia dracunculoides Lam., Rumex vesicarius L. and Stipa parviflora Desf. Earlier finds are from the same area and mostly from similar habitats and altitudes, but also from cultivated places and lower altitude (1060 m, 1928, Maire 1062, MPU). The find from Tibesti, Toussidié , is from 2000 m.

Chenopodium hoggarense could be an endemic species for the isolated mountains of the Sahara. Maire (1933) described 58 new taxa from the Hoggar, but they did not all prove to be endemic. It is difficult to estimate the number of taxa endemic to the Hoggar even now, but it probably does not exceed 20 among the total of 350–399 species reported from the area ( Lebrun 1981; Chenoune 2005; Médail & Quézel 2018: 108). Also, C. hoggarense is probably endemic to a wider area, at least for the Hoggar and Tibesti mountains.

Etymology — the specific epithet refers to the Hoggar mountains, the core area and locality of the type collection of the species.

Remarks — Chenopodium hoggarense shares some common features with C. vulvaria , such as the smell of trimethylamine and dense cover of vesicular hairs. However, it differs from C. vulvaria in many taxonomically essential morphological features, among others in its growth habit, presence of red colour, leaf shape, inflorescence and perianth characters (Table 1; Fig. 3 ). The red colour detected in 2019 on the plants of C. hoggarense may be a stress response to the extreme circumstances in the high altitude; it was not seen in the other specimens studied. Despite its smell, C. hoggarense is not necessarily closely related to C. vulvaria , which is an isolated species and phylogenetically sister to the other species of Chenopodium s.str. ( Fuentes-Bazan & al. 2012; Mandák & al. 2018). A similar smell has also been reported from some other, unrelated and geographically separated Chenopodium species, such as C. hircinum Schrad. (South America), C. frutescens C. A. Mey. (Siberia and Central Asia), C. sosnowskyi Kapeller (E Turkey, Caucasus and Iran), C. detestans Kirk (New Zealand) and some other taxa (see Mosyakin & Iamonico 2017; Lomonosova & Uotila in press; and references therein). However, in C. vulvaria and C. hoggarense the smell is probably stronger than in other species and, at least in C. vulvaria, can still be detected from herbarium specimens that are several years old. The specimens of C. hoggarense collected in 2019 still had a very strong smell in the autumn of 2020, but by the autumn of 2021 the smell was only weakly detected by moistening and rubbing the leaves of the specimens.

Chenopodium hoggarense could resemble small plants with ± entire leaves of some members of the polymorphic species aggregate C. album L. (sensu lato) but differs from them in the smell (not known, or at least not evidently perceptible, in C. album), dense cover of vesicular hairs (usually sparser in C. album), leaf shape with mucronate to cuspidate apex (mostly acute in C. album) and perianth characters.

In the Hoggar in 1928, R. Maire collected plants that he identified as Chenopodium vulvaria. He also determined specimens collected by Th. Monod from the same area during “Mission Saharienne Augiéras-Draper 1927–1928” as the same species. On the basis of these specimens, Maire (1933: 80) reported C. vulvaria from the summit of Atakor and several other places in the Hoggar at altitudes of 1060–3000 m. He recorded it as very abundant on slopes and rocky plateaux of the high mountains in the upper and lower Mediterranean levels, from which it descended along wadis to the tropical level, particularly in cultivated places.

Maire (1933) also noted morphological differences of the Hoggar plants from the Mediterranean Chenopodium vulvaria and even provided a description of the former (“40–60 cm tall, rather short and ascending branches, elongated inflorescence, leaves often lobed, resembling C. opulifolium Schrad.”), but he neither named the taxon nor discussed the importance of this observation. The description “leaves often lobed” corresponds to only two of his specimens (Maire 1067 from Hoggar and Maire 1063 from Tefedest), but the others have typical, ± entire leaves of C. hoggarense. Laperrine’s specimen (MPU276164) may indicate that also C. opulifolium Schrad. ex W. D. J. Koch & Ziz could have grown in the area: it was named by the collector as “Aggaouit” (the Tuareg name for C. opulifolium). However, Maire corrected the identification to C. vulvaria, with an addition “Taouit (non Aggaouit)”.

Ozenda (2004: 225) mentioned Chenopodium vulvaria as an alien plant from the central Sahara; the drawing included in his flora corresponds rather well to C. hoggarense by its leaf shape and deeply lobed perianth, but the habit is not so typical, possibly due to damage from grazing animals.

Additional specimens examined

ALGERIA: Wilaya de Tamanrasset: Coudia du Hoggar, 1927, Monod 144 ( P [ P04940923 ]), Monod 151 ( P [ P04940920 ]), Monod 153 ( P [ P04940921 ]); Hoggar, Laperrine s.n., in herb. Maire ( MPU [ MPU276163 ]); Atakor-n-Ahaggar , 19 Mar 1928, Maire 1061 ( MPU [ MPU276161 ]; Montibus Ahaggar , im-Amgel in cultis, 1060 m, 4 Apr 1928, Maire 1062 ( MPU [ MPU276167 ]); Montibus Ahaggar, Issekkaressem , in lapidosis basalticis 2070 m, 22 Mar 1928, Maire 1068 ( P [ P04940924 ]); Hoggar-Massif, Umgebung des guelta Afilal , 2050 m, Felsen, Sand und Sumpf, 24 Mar 1980, Podlech 33352 ( G); Hoggar-Massif, Assekrem Südhänge , 2520 m, 25 Mar 1980, Podlech 33397 ( G); Assekrem , Nov 1953, Quézel s.n. ( MPU [ MPU276159 ]); Hoggar au-dessus de 2000 m, s.d., Lhote s.n. ( MPU [ MPU276162 ]). — CHAD: Tibesti, Toussidé , 2000 m, in lapidosis basalticis, Mar 1931 Dalloni s.n. ( P [ P04940922 ]) [image seen]; Tibesti, 12 Nov 1940, Monod 7829 ( IFAN [ IFAN26382 ] [image seen]); both specimens from Chad represent basal parts of injured plants only.

Figures

Fig. 1. Holotype of Chenopodium hoggarense (G [G00408262]).

Fig. 2. Chenopodium hoggarense, flowering and fruiting branches. – Algeria, rocky plateau of Assekrem, 2700 m, 24 Oct 2019, photograph by S. Benhouhou.

Fig. 3. A–D: Chenopodium hoggarense; A: leaves; B: perianth, apical view; C: perianth, lateral view; D: perianth, basal view. – E: Chenopodium vulvaria, young perianth, lateral view. – Scale bars:A = 5 mm; B–E = 1 mm. – Based on the holotype. – Drawings by C. Chatelain.

Fig. 5. A: Algeria, rocky plateau of Assekrem, 2700 m, view to south, 24 Oct 2019; B: same locality, habitat of Chenopodium hoggarense, 24 Oct 2019. – Photographs by S. Benhouhou.