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International audience; Date palm (Phoenix dactyliferaL.) is the mainstay of oasis agriculture in the Saharan region. It is cultivated in a large part of the Mediterranean coastal area of the Sahara and in most isolated oases in the Algerian desert. We sampled 10 oases in Algeria to understand the structure of date palm diversity from the coastal area to a very isolated desert location. We used 18 microsatellite markers and a chloroplast minisatellite to characterize 414 individual palm trees corresponding to 114 named varieties. We found a significant negative inbreeding coefficient, suggesting active farmer selection for heterozygous individuals. Three distinct genetic clusters were identified, a ubiquitous set of varieties found across the different oases, and two clusters, one of which was specific to the northern area, and the other to the drier southern area of the Algerian Sahara. The ubiquitous cluster presented very striking chloroplast diversity, signing the frequency of haplotypes found in Saudi Arabia, the most eastern part of the date palm range. Exchanges of Middle Eastern and Algerian date palms are known to have occurred and could have led to the introduction of this particular chlorotype. However, Algerian nuclear diversity was not of eastern origin. Our study strongly suggests that the peculiar chloroplastic diversity of date palm is maintained by farmers and could originate from date palms introduced from the Middle East a long time ago, which since then, hasbeen strongly introgressed. This study illustrates the complex structure of date palm diversity in Algerian oases and the role of farmers in shaping such cryptic diversity.

Attalea blepharopus Mart. in Orb., Voy. Amér. Mér. 7(3): 116. 1847. Ξ Scheelea blepharopus (Mart.) Burret in Notizbl. Bot. Gart. Berlin-Dahlem 10: 541. 1829. Lectotypus (designated here): BOLIVIA: “ Yuracares ” (Martius, 1847: tab. V, fig. 2; tab. XXXIC); isolecto-: P [P01797296]!) (Fig. 1). Epitypus (designated here): BOLIVIA. Cochabamba: Prov. Villa Tunari, Isinota, 16°44’07’’S 65°38’07’’W; 203 m, 10.IV.2015, Moraes & Pintaud 2518 (LPB!; isoepi-: BOLV!, G!, NY!, P!) (Fig. 2). Solitary, monoecious, arborescent, medium-sized palm, 12-19 m high, 50-58 cm diameter, stem 6-8 m, covered by persistent and woody leaf bases on obliquely-8 ranked with thick fibrous margins that form a net of fibers 1-5 mm wide. Leaves sessile leaves 18-21 ascending and arching distally, 7-8 m long, apical leaves upright, green lustrous adaxially, glaucous abaxially; sheath ca. 140 cm long × 40 cm wide at base; petiole 50 cm long, rachis 6.6-7.6 m long, slightly carinate adaxially, rounded abaxially, initially with a dense appressed grey-white indumentum, aging thin and glaucous white adaxially, thin, appressed, dark reddish-brown abaxially; prophyll not seen. Pinnae 185-195 per side, rather stiff, regularly arranged and inserted on one plane, lanceolate to subulate, lower segments hanging, upper ones held distichously on distal part of rachis, 120-130 cm long and 8-10 cm wide, very thin waxy-glaucous indumentum on stomata lines, elongated, basal pulvinulus prominent, swollen, shallowly channeled, light green, apex not bifid, basal pinnae: 2.5-3 cm × 135 cm, medial pinnae: 8.2-9.4 cm × 124- 126 cm and apical pinnae: 1-1.5 cm × 43 cm; proximal five pinnae densely grouped, subsequent segments not grouped and progressively more distant (1.5 to 8 cm from each other). Inflorescences (2 staminate and one pistillate, 1 infructescence and 15-20 old ones on same individual) erect; staminate inflorescence with peduncular bract fusiform in bud stage, boat-shaped, widely open at anthesis, fibrous, plicate, deeply sulcate, dark reddish brown with thin, appressed, finely lepidote indumentum, ca. 2 m long; peduncle subulate, dorsoventrally compressed, erect, slightly recurved, glabrous, pale yellow at anthesis, ca. 100 cm long; rachis 55-62 cm long, terete, pale yellow at anthesis, glabrous; rachillae 180-193, ascending-spreading, stiff and spirally arranged on the rachis, swollen base, finely covered with a silvery-white indumentum made of stellate-hairy scales, flower pits spirally arranged, basal rachillae 18-25.3 cm long with 322-334 flowers, medial rachillae 22.5-24.3 cm long with 250-262 flowers and terminal rachillae 12-14 cm long with 248-259 flowers; staminate flowers inserted solitary, total length of 14-17 mm, sessile, cream and strongly scented at anthesis; sepals 3 connate basally, triangular, membranous, glabrous, 4-6 mm long; petals (3) free, slightly divergent and flexuose, firm fleshy, 14-16 mm long, caducous immediately after anthesis; stamens (6), filament length 1-1.5 mm, deltate, basifixed, connective narrow: thecae contiguous, yellow, anthers 2-3 mm long, linear sagittate, apex obtuse, base auriculate, dehiscence latrorse, pistillode length ca. 0.5 mm, trifid; pistillate inflorescence with peduncular bract erect, slightly recurved, peduncle ca. 50 cm, dorso-ventrally compressed, pale yellow, appressed, lepidote reddish-brown indumentum, 25-30 peduncular bracteoles, 2-9 cm long, triangular-winged, apiculate to mucronate, central part glabrous, lateral wings covered with an appressed lepidote, reddish-brown indumentum; rachis 88-92 cm long, 5-7 cm wide, elliptic in cross section, dorso-ventrally compressed, pale yellow, sparse reddish-brown, lepidote, appressed indumentum; terminal rachilla 15-18 cm long, basal diameter 2.6-3.1 cm; length of basal pistillate part 8-9 cm with 24-27 pistillate flowers, length of apical staminate part 7-9 cm with 20-50 staminate flowers; pistillate flowers spirally arranged, rachillae ascending, 160-175, dorso-ventrally compressed, zigzag in form, pale yellow, glabrous, subtending bract 4-8 cm long, triangular-winged, acuminate, membranaceous, phylotaxys alternate, pistillate flower receptacle rounded, superficial, triangular-acuminate; length of pistillate portion of basal rachillae 8-11 cm with 7-9 pistillate flowers, median rachillae 13-17 cm with 9-16 flowers and apical rachillae 7-13 cm with 4-8 flowers; pistillate flowers with pedicel of 1.5-2 mm, pale yellow turning brown, ovoid, 2.4-3 cm long, sepals free, concave-deltate, cartilaginous, pale yellow, turning brown, glabrous adaxially, glabrescent abaxially, initially with a whitish-brown lepidote appressed indumentum, triangularacute, glabrous, 2.7-2.8 cm long; petals concave-deltate, cartilaginous, pale yellow, turning brown, glabrous adaxially, glabrescent abaxially, initially with a thin, felt-like, white, lepidote indumentum, triangular-acute, glabrous, 2-4 cm long; staminodial ring free from corolla, cupular, cartilaginous, whitish-brown, lepidote, appressed indumentum, 9 mm heigth, 16 mm external diameter and 1.5-2 mm thickness; gynoecium pyriform, 3-carpellate, ovary 11 mm high, 16 mm width, covered with a brown floccose lepidote indumentum, stylar column of 7 mm, trifid, stigma angular, subulate, pale yellow, finely covered with a silvery-white indumentum made of stellate-hairy scales, apex pointed; inserted alternatespiral; floral bracteole deltate, cartilaginous, brown, glossy dark brown, cartilaginous, margin ciliate; basal rachillae total length of 0-3 cm, 0-12 cm long of proximal sterile part, 6 mm long of distal sterile part, with 20-30 staminate flowers, 8-9 cm total length of median rachillae with 25-35 flowers and 7 mm of total length for apical rachillae without flowers; staminate flowers not seen; staminate flowers in triads, 10 mm long, pedicel 1 mm. Infructescence with fruits densely packed, remaining perianth cupular, brown, 1.8-2.6 × 4.2-44 cm, greyish-brown, lepidote, appressed, partially caducous external indumentum, staminodial ring adnation free, plate-like, irregularly split, looking densely ciliate for the emergence of abaxial indumentum, light brown turning dark brown, hard, cartilaginous, glabrous adaxially, covered with a dense felt-like brown indumentum abaxially, 7-8 mm high; sepal concave-deltate, brown, cartilaginous, glabrous adaxially, with an appressed brown-lepidote indumentum abaxially, 2.6 cm length; petals broadly triangular acute, same color, texture and indumentum as sepals, 2.4 cm length. Barrelshaped fruits, 6.4-7.5 × 4.8-5.1 cm, beak narrowly conical with a broad flat base, brown, silvery-grey lepidote appressed indumentum, ca. 9 mm long, trifid; exocarp covered with a dense brown lepidote indumentum, orange-brown to light brown, thickness 4 mm, fibers rounded in cross section, solitary, dispersed, longitudinally arranged, anastomosing, orange-brown; mesocarp 4-5 mm thick, orange, fleshy and fibrous, fibers filiform in middle mesocarp, flattened, bristle in inner mesocarp, fibers thickness very thin in middle mesocarp, 0.2-0.3 mm wide in inner mesocarp, arrangement of fibers very abundant in middle mesocarp, numerous, longitudinal in inner mesocarp, orange in middle mesocarp, dark glossy brown in inner mesocarp, inner mesocarp fibers adnate to the endocarp; endocarp narrowly ellipsoid; seeds 1-2, elliptical, 3.5-4 cm long. Seedling slender cylindrical, radicle axial, 2.6 mm diameter; four 1st adventitious roots, 2nd adventitious roots lateral forming a cross. Vernacular names. – “Corokke” (Yuracaré), “Palla” (colonos). Uses. – The Palla palm is utilized mostly for roofing (leaves) and oil (extracted from seeds). It has a number of minor uses. The mesocarp is edible but very fibrous. The Yuracaré use this species more frequently than colonial residents and other recent settlers. It was reported by the 80 % of Yuracaré people as the most used tree palm species (Montoya & Moraes, 2014). Distribution and ecology. – Attalea blepharopus is found in alluvial rainforest and primary floodplain forest of Cochabamba and La Paz departments of Bolivia. It grows in forests where other distinctive palms are also found: Astrocaryum gratum F. Kahn & B. Millán (dominant), Attalea princeps Mart., Iriartea deltoidea Ruiz & Pav., Oenocarpus bataua Mart., Socratea exorrhiza (Mart.) H. Wendl., as well as with other species such as Inga sp. (Fabaceae), Theobroma sp. (Malvaceae), Virola sp. (Myristicaceae), and Triplaris sp. (Polygonaceae). Mature fruits and flowers at anthesis were observed simultaneously present in April. The species growth in rocky alluvium deposits of the Rio Chapare and tributaries in the upper Amazon drainage. Populations are well represented in the region of western Amazonia in Bolivia. The presence of Attalea blepharopus was somehow ignored because it has been undercollected in previous field surveys. Nevertheless its prescence from eastern La Paz department was co渟rmed by photographic records and from Cochabamba by a previous collections in fruits (Balslev 8235). The conservation status of this species is currently under evaluation and will be published in the upcoming “Red Book of Threatened Plants Bolivia - Volume II: Lowlands”. Notes. – Attalea blepharopus has remained a poorly known species since its description by MARTIUS (1847). The original d’Orbigny type in Berlin was destroyed and a throughout search in various herbaria led to the conclusion that the only available material are the drawing cited in the protologue. Therefore we designate these as lectotype including a duplicated at P. A recent collection made by the authors with complete material of leaves, pistillate and staminate flowers, fruits and seedlings is here designated as epitype (Moraes & Pintaud 2518). As we are in the process of better understanding the species diversity within the genus Attalea Kunth and have listed approximately 700 descriptors, we consider necessary to clearly fix the morphology of this species by designating an epitype that comes along with several observations and pictures in the field (Fig. 2). Attalea species with regularly-arranged pinnae have been poorly studied in southwestern Amazonia, although GLASS- MAN (1999) recognized a high variation among species and mentioned a complex of species. In the lowlands of Bolivia the lack of study is not an exception. When assigning the name Scheelea blepharopus, BURRET (1929) emphasized mostly the male inflorescence regardless of the original description of Martius and he did not take into account the combination of the features that were the basis for the species epithet “blepharopus”. Field observations allowed to note that the lower margins of the leaf rachis have several thick and long fibers on both sides giving the margins a ciliate aspect: “petiolo margine fibris longis strictis ciliato” (Fig. 2B), as stated by MARTIUS (1847) in the epithet “blepharopus”. It was also noted the corolla staminodial ring in the fruit: “staminodial ring adnation free, platelike, irregularly split, looking densely ciliate for the emergence of abaxial indumentum”. Important morphological characters that allow to separate A. blepharopus from related species, i.e. Attalea peruviana Zona, A. bassleriana (Burret) Zona, A. moorei (Glassman) Zona, that are typical of the NW Amazon, and mostly concentrated in northern Bolivia are: sessile leaves (petiole absent), glaucous leaf abaxially, orange and fleshy mesocarp, 1-6 pistillate flowers per rachillae, thick rachillae of staminate inflorescence with spirally inserted flowers, endocarp with scattered fibers, and peduncular bract relatively thin and shallowly sulcate. Additional material examined. – BOLIVIA. Cochabamba: 1.5 km NE of San Benito village, next to the Isiboro river, 120 km NE of Cochabamba, 127 m, 16°31’53’’S, 65°29’32’’W, 23.III.2010, Balslev 8235 (AAU, USZ)., Published as part of Moraes, Mónica R. & Pintaud, Jean-Christophe, 2016, Attalea blepharopus Mart. (Arecaceae) from Bolivia revisited since Martius, pp. 27-32 in Candollea 71 (1) on pages 29-32, DOI: 10.15553/c2016v711a6, http://zenodo.org/record/5721492

Moraes, Mónica R., Pintaud, Jean-Christophe (2016): Attalea blepharopus Mart. (Arecaceae) from Bolivia revisited since Martius. Candollea 71 (1): 27-32, DOI: 10.15553/c2016v711a6

A revision of the large-flowered group of Basselinia Vieill. sect. Taloua H. E. Moore & Uhl (Arecaceae). Condollea 66: 147-154. In English, English and French abstracts. The genus Basselinia Vieill. is endemic to New Caledonia and currently comprises 13 species. It was divided in two sections, sect. Basselinia H. E. Moore & Uhl which includes 5, mostly small and often caespitose species, and sect. Taloua H. E. Moore & Uhl, which includes 7 large and solitary species. One species, Basselinia glabrata Becc., remains unplaced to section because it had been once excluded from Basselinia and placed in a separate genus, Alloschmidia H. E. Moore, prior to the sectional treatment of Basselinia. Section Taloua H. E. appears morphologically the least specialized group of Basselinia, and within it, the large-flowered group of species retains the most plesiomorphic characteristics, in habit, inflorescence and floral structure. This group includes three species, one newly described here, Basselinia moorei J.-C. Pintaud & F. W. Stauffer, and two others, Basselinia velutina Becc. and Basselinia sordida H. E. Moore. Morphology, ecology and distribution of these species are addressed here.