Introduction

SectionArachisis the largest and more diverse taxonomic section of the homonymous genus (^{Krapovickas et Gregory 1994}; ^{Valls et Simpson 2005}). It is composed of 31 species arranged in six different genomes: A, B, D, F, G and K, with two different basic chromosome numbers (x= 9, 10) and ploidy (2x and 4x) levels (^{Smartt et al., 1978}; Gregory et Gregory, 1979; ^{Fernández et Krapovickas 1994}; ^{Stalker, 1991}; ^{Seijo et al., 2004}, 2007; ^{Robledo et Seijo, 2008}, 2010; Robledo et al., 2009; ^{Silvestri et al., 2015}). Germplasm of these wild species (mainly with 2n= 2x= 20) is economically important, because they are the most related to the cultivated peanut (2n= 4x= 40, AABB) and have several potentially useful agronomic traits for genetic improvement of the crop (Simpson, 2001; Stalker et al., 2016).

Intense germplasm collections were carried out in Argentina, Brazil and Uruguay enlarging the number of accessions maintained in the genebanks of different National or International Institutions to the present day. Even though several exploration missions for wildArachisspecies were done in Bolivia, most of them concentrated in the 70´s - 80´s and early 90’s (^{Valls et al., 1995}), logistic difficulties for travelling by land and the enormous effort that required the expeditions at that time resulted in a sparse picture of many of the collection points. Despite the comparatively few expeditions, most of the species of sectionArachiswere found in Bolivia, and most of them are endemic, indicating that this country is a large center of diversity for this group of plants and deserves more attention.

Under the hypothesis that underexplored areas have new and diverse populations/species ofArachis, we conducted a series of explorations since 2000, mainly in the Santa Cruz department of Bolivia, with the objective of increasing the documentation of the genus diversity. Those explorations were only possible thanks to the collaboration of researchers from the Instituto de Botánica del Nordeste in Corrientes (Argentina) with those from the Herbario Nacional de Bolivia in La Paz (LPB), Herbario Nacional Forestal Martín Cardenas (BOLV) in Cochabamba, and Herbarium of the Museo de Historia Natural Noel Kempff-Mercado in Santa Cruz de la Sierra (USZ), all from Bolivia; also, with the collaboration of researchers from Texas A&M AgriLife Research, USA and Embrapa Genetic Resources and Biotechnology (CEN, Brazil). Herbarium acronyms follow ^{Thiers (2021}).

A first result of these explorations is the finding ofArachispopulations that undoubtedly belong to a new B genome species of sectionArachis. While searching forArachisspecies in the Planalto Chiquitano, Velazco Province, Santa Cruz Department, several new populations ofA. magna(e.g.J. G. Seijo, V. G. Solís Neffa, A. Schinini & R. Almada 2996, 3022andJ. G. Seijo & V. G. Solís Neffa 3257,3289; all at LPB and CTES) were found. Also, some other populations were found (likeJ. G. Seijo, V. G. Solís Neffa, M. Grabiele & W. Reynoso 3637,3640,3649,3653,3664,3790) that resembleA. magnain the aerial organs, although they looked larger and somewhat different. A closer look to the above-ground vegetative organs revealed that the distal portion of the leaflets in the main axis of well developed plants was wider and less acute than inA. magna, and the margin of the leaflets was conspicuously whitish, due to presence of a dense layer of long hairs. Also, in most of the populations the color of the standard petal was pale orange compared to the intense orange tone commonly observed inA. magnaand otherArachisspecies of the B genome. The great surprise came after sifting the soil. The fruit articles recovered were completely different from those expected forA. magna, with reticulated morphology. They were very large, with a smooth epicarp, and with air chambers in the mesocarp, that gave them a bullated external appearance (Fig. 1 G-H).

Further studies of the morphology, cytogenetics, molecular marker profiles and cross compatibility of these accessions with bullated fruits provided evidence that they belong to a new species of sectionArachis. Here we present its formal description in the following section.

Arachis inflataSeijo, Atahuachi, C. E. Simpson & Krapov.sp. nov.Fig. 1.

Morphologically similar to Arachis magna Krapov., W. C. Greg. & C. E. Simpson, but differing by the generally larger plants, less acute leaflets and with whitish margin, and bullated, not reticulated, fruits, with conspicuous air chambers in the mesocarp.

Fig. 1 Arachis inflata(Seijo et al. 3637). A: Main axis and a lateral branch of a young plant. Note remains of the fruit (that harbored the seed that gave rise to the plant) in the roots. B: Stem. C: Lateral branch apex. D: Main stem apex. E: Detail of the apex of a leaflet, lower surface. F: Petiole, rachis, midvein and lower surface of the leaflets. G: Fruit article external view, the exocarp with a bullated aspect. H: Inside view of half fruit article with the seed removed. Note the bullated aspect in the inner surface of the fruit article and the air chambers in the mesocarp (some of them were manually opened). Drawings by Liliana Gómez. Fig. 1. Arachis inflata(Seijo et al. 3637). A: Eje principal y rama lateral de una planta joven. Se observan restos del fruto (que contenía la semilla que dio origen a la panta) en las raíces. B: Tallo. C: Ápice de la rama lateral. D: Ápice del eje principal. E: Detalle del ápice del folíolo, superficie inferior. F: Pecíolo, raquis, nervadura central y superficie inferior del folíolo. G: Vista externa de un artejo del fruto, el exocarpo con aspecto ampollado. H: Vista interna de una mitad de artejo con la semilla removida. Se observa el aspecto ampollado en la cara interna de artejo y las cámaras de aire en el mesocarpo (algunas de ellas fueron manualmente abiertas). Ilustración realizada por Liliana Gómez.  

Typus. Bolivia. Santa Cruz: Prov. Ñuflo de Chávez, 4,2 km S de San Antonio de Lomerío, camino a San Juan de Lomerío, 16º48’01”S, 61º50’24”W, 343 m, 21-I-2005,J. G. Seijo, V. G. Solís Neffa, M. Grabiele & W. Reynoso 3637(holotypusCTES,isotypusLPB).

Annual herb, weak axonomorphic root. Mainstem erect, up to 90 cm long, usually flowers toward the apex and with few long branches at the base. Lateral branches prostrated, up to 1.50 m long, stems green, rounded, or somewhat angular, quadrangular in dried specimens, villous, with wavy hairs 1.5-2 mm long, and few scattered bristles. Leaves tetrafoliolate. On the main-stem, stipules with the fused portion 14-20 mm long, the free part 28-40 mm long, 2.5-3 mm wide at the base; petiole 35-55 mm long; rachis 10-20 mm long; leaflets oblong, apex sub-acute, the basal pair 45-52 mm long, 18-24 mm wide, and the apical one 52-63 mm long, 22-28 mm wide. On lateral branches, the fused part of the stipules 5-13 mm long, and the free part 15-22 mm long, 2.5-3.5 mm wide; petiole 12-22 mm long; rachis 5-9 mm long; leaflets oblong to cordate, obtuse to sub-acute, proximal pair 23-30 mm long, 15-20 mm wide, distal one 28-33 mm long, 19-22 wide. The fused part of the stipules villous, with long wavy hairs and long bristles, the free portion glabrous in most of the surface with few long hairs and bristles toward the base, margins ciliate. Petiole and rachis canaliculated, villous and with bristles; leaflets with the adaxial surface glabrous, abaxial face with sparse adpressed 1 mm long hairs, and wavy 1-2 mm long hairs in the midvein, margin densely ciliate with antrorse white hairs and few 1 mm long erect bristles. Flowers in two-four flowered spikes, hypanthium 30-60 mm long, light pink, covered with 1-2 mm long wavy hairs. Calyx light pink, villous with some sparse long bristles; upper lip 4-5 mm long; lower lip falcate, narrow, 5-6 mm long. Standard petal 9-10 mm long, pale orange, with orange lines on the front and yellow throat, wings yellow and keel whitish. Peg violaceous, villous in the aerial part, with wavy 1-2 mm long and scattered 1-2 mm long adpressed hairs. Fruit subterranean, biarticulated, articles ellipsoid, 15-25 mm long, 10-14 mm wide, without beak, surface smooth, bullated due to air chambers in the mesocarp. Shell thick, up to 5 mm.

Chromosome number: 2n= 20, without large heterochromatic bands in the typical accessionSeijo et al. 3637(Seijo unpublished).

Geographic distribution   and habitat:It grows in Santa Cruz Department (Bolivia), Ñuflo de Chávez and Velasco provinces, Lomerío region, in the southern portion of the Planalto Chiquitano, and the northern part of the San Julian River Basin, which in turn drains into the Mamoré River. Most populations were found in the undergrowth of cerrado vegetation or in the transition between cerrado vegetation and open grassy patches, close to lagoons or water courses, in sandy soils.

Etymology: The specific epithet refers to the air chambers present in the mesocarp that gives the fruits articles an inflated aspect.

Paratype:BOLIVIA. Santa Cruz:Prov. Ñuflo de Chávez, Camino de San Antonio de Lomerío a San Juan de Lomerío, 16º48’02”S, 61º50’26”W, 328 m, 29-XI-2007,Atahuachi et al. 1390(BOLV, CTES); 6,9 km S de San Antonio de Lomerío, 16º48’30”S, 61º51’10”W, 390 m, 31-I-2005,Seijo et al. 3640(CTES, LPB, UCZ); id., 16º48’36”S, 61º51’12”W, 29-XI-2007,Atahuachi et al. 1391(BOLV, CTES); 18,1 km S de San Antonio, 16º52’04”S, 61º50’16”W, 417 m, 21-I-2005,Seijo et al. 3649(CTES, LPB); id., Itotoca, 16º52’05”S, 61º50’13”W, 383 m, 29-XI-2007,Atahuachi et al. 1393(BOLV, CTES); 23,1 km S de San Antonio, 16º54’S, 61º49’W, 21-I-2005,Seijo et al. 3653(CTES, LPB); 39,8 km S de San Antonio, 16º58’31”S, 61º48’28”W, 290 m, 21-I-2005,Seijo et al. 3664(CTES, LPB). Prov. Velasco, 31,2 km S de San Rafael, 17º01’S, 60º36’W, 302 m, 8-IV-2004,Seijo & Solís Neffa 3292(CTES); 89,4 km NE de San Ignacio, 16º15’23”S, 60º15’52W, 280 m, 25-I-2005,Seijo et al. 3715(CTES, LPB); 32 km S de San Rafael, camino a San José, 17º01’S, 60º36’W, 288 m, 1-II-2005,Seijo et al.3790 (CTES, LPB); camino San Rafael-Las Petas, Hacienda San Jorge, 16º38’18”S, 59º59’31”W, 212 m, 30-XI-2007,Atahuachi et al. 1405(BOLV, CTES).

Obs. 1: The area ofA. inflatais associated with the Planalto Chiquitano, overlaps the SW area ofA. magnaand extends southward to the San Julian River. The above-ground vegetative appearance is similar in both species, however, they are easily distinguished by the morphology of the fruit: whileA. magnahas the classical reticulated ones,A. inflatahas fruits that bear conspicuous air chambers in the mesocarp, giving the external appearance of a bullated surface. The later character of the fruit is unique in the genusArachis. Another difference is the color of the standard petal, while inA. inflatait is pale orange, inA. magnais of a more intense tone of orange. The leaflet margin is different as well, inA. magnais poorly distinguishable while inA. inflatais conspicuously whitish, due to the presence of abundant long hairs.

Obs. 2:Arachis inflatadoes not have large heterochromatic bands in its chromosomes and has a typical karyotype of the B genome species, resembling that ofA. magnaandA. ipaënsis(Seijo et al. unpublished).Crossing data gave the following pollen stain results withA. inflata×A. ipaënsis(K 30076) 61.3%;A. magna(V 13761) 45.4%;A. glandulifera(K 30091) 11.8%;A. krapovickasii(Wm 1291) 8.6%;A. batizocoi(K 9484) 2.93%. These data help to solidify the separation ofA. inflatainto a new species.

Obs. 3: Moretzhon et al. (2012) studied the genetic relationships among species of sectionArachis, including the accessionSeijo et al. 3292ofA. inflata, by using intron sequences of a few nuclear genes and SSR markers. This accession ofA. inflatagrouped closely with an accession ofA. williamsiiin the cluster made on intron sequences, but with a set ofA. magna(sister to accession V14750) in the distance tree made on SSRs markers. This data confirm thatA. inflatabelongs to the B genome and that there is a very low genetic distance among species in this group.