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KEW BULLETIN 62: 605–608 (2007) 605

A new species of Acacia (Leguminosae: Mimosoideae)


endemic to Bolivia
M. Atahuachi B.1 & Lourdes Rico2

Summary. A new species of Acacia (Leguminosae: Mimosoideae), A. riograndensis Atahuachi & L. Rico, endemic to
the valley of the Rio Grande in Bolivia is described and illustrated. Affinities to closely related species are
discussed.

Key words. Acacia, Leguminosae, Mimosoideae, Bolivia, endemic.

Introduction Small to medium-sized tree 3 – 12 m tall with a


Thirty-one species of Acacia are recorded from Bolivia single bole. Bark whitish, superficially fissured.
in the most recent published account (Killeen et al. Shoots lacking prickles, glabrous, slightly glossy,
1993) of which eight are introduced and sometimes orange-brown. Stipules 1.5 – 2 mm long, weakly
naturalised, seven are near endemics, being found spinescent, setiform, late caducous. Leaves crowded
also in adjacent areas of Paraguay and Argentina, and on short side shoots or brachyblasts, bipinnate, 4 –
one is endemic (A. feddeana Harms). Here, we 5.5 cm long, almost glabrous; petioles 0.5 – 1 cm
describe a second endemic species discovered during long, channelled on upper surface, extrafloral
ongoing fieldwork to document the endemic plants nectary lacking, rachis 0.5 – 2.5 cm long, channelled
of the dry central valleys of Bolivia. along upper surface, leaf with 3 – 5(– 7) pairs of 1 –
1.5(– 2) cm long pinnae, the apex of the rachis
extending beyond the terminal pinnae pair as a
Acacia riograndensis Atahuachi & L. Rico sp. nov. pointed mucro 1.2 – 1.6 mm long, the rachis
subgeneris Aculeiferum Vassal sectionis Monacantheae charged between the first, and sometimes the
Vassal. A. compactae Rose e Mexico similis sed floribus terminal pair of pinnae with an elliptic disciform or
eburnis (non albis), leguminibus 0.5 – 1.4 cm (non 1 shallow crateriform extrafloral nectary, this 0.5 – 0.6
– 2.2 cm), latis, inter semina constrictis, exocarpio × 0.25 – 0.35 mm. Leaflets (12 –)17 – 23 pairs per
rubro (non ochraceo) distincta. Arbor usque ad 12 pinna, 1 × 2.3(– 3) mm, narrow-linear, apex rounded,
m, sine aculeis; stipulae spinescentes, 1.5 – 2 mm base asymmetric, the midrib near the anterior
longae, tarde caducae; flores in spiculis 1.7 – 3.8(– 6) margin, inconspicuous, secondary veins not visible,
cm longis dispositi; pedunculi sine bracteis; stamina almost glabrous but sparsely ciliate and densely
sine glande apicale; ovarium glabrum stipitatum, covered with translucent punctate glandular
stipite 2 mm longo; nectarium interstaminale non est; structures. Inflorescences axillary, solitary, 3.8 – 6 cm
stylus sub anthesi supra stamina exsertus; legumina long including a peduncle of 0.7 – 1.5 cm long, c. 1
ex ambobis lateribus dehiscentia. Ab ea, species – 1.7 cm in diam. at anthesis, glabrous, without
ceterae austroamericanae spinis persistentibus veris bracts. Flowers cream in colour, sessile, floral bracts
vel stipulis foliosis dignoscendae. Typus Bolivia, Dept. 0.75 – 1 mm long, spathulate, internally glabrous,
Cochabamba, Prov. Campero, Pasorapa, en la bajada externally pubescent towards the apex with
de Buena Vista hacia el Río Grande, 27 Dec. 2004, J. translucent trichomes, persistent after anthesis;
R. I. Wood, M. Atahuachi & M. Mercado 21251, calyx campanulate, pale green-yellow, puberulent
(holotypus BOLV; isotypi K, LPB). externally, hairs translucent, (1.5 –)2 mm long, 5-

Accepted for publication January 2007.


1 Herbario Nacional Forestal ‘Martin Cardenas’, Centro de Biodiversidad y Genetica, Facultad de Ciencias y Tecnologia, Universidad Mayor de San Simon,
Cochabamba, Casilla 538, Bolivia.
2 Herbarium, Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AB, UK.

© The Board of Trustees of the Royal Botanic Gardens, Kew, 2007


606 KEW BULLETIN VOL. 62(4)

lobed, ciliate at the apex; corolla campanulate, 5 – 6 Acacia sensu lato based primarily on the pollen which
mm long, 5-lobed, puberulent, more densely so occurs in 16-grained polyads of colporate grains.
before anthesis; stamens more than 100 per flower, Amongst the South American species of Acacia with
free, 7.5 – 8(– 10) mm long, inserted on a 0.7 mm spicate inflorescences, A. riograndensis is unique in
long stemonozone, anthers eglandular, dorsifixed having late falling spinescent stipules. All other
and with longitudinal dehiscence; gynoecium 6 – 8.5 species in South America have either persistent true
mm long, ovary 2.5 mm long, glabrous, with a stipe spines or foliaceous stipules. Among neotropical
1.8 – 2 mm long, lacking an intrastaminal nectary, Acacias, A. riograndensis most closely resembles A.
style 3.5 mm long, exserted beyond the anthers. compacta Rose from the semi-arid Teotitlán-Cuicatlán
Pods 9.5 – 12 cm long, 5 – 14 mm wide, dehiscent valley of south-central Mexico, an area similarly rich
along both sutures, flat, constricted between the in cacti species at elevations between 500 and 850 m.
seeds, apex mucronate, base acute without a stipe, In A. riograndensis the flowers are cream in colour,
exocarp membranous or weakly coriaceous, reddish, and the pod only 0.5 – 1.4 cm wide. In addition the
slightly reticulate, glabrescent, endocarp pale tan pod is constricted between the seeds, which are
coloured. Seeds (2 –)3 – 8(– 10) per pod, 9 – 11 × 6 – reddish-brown in colour. In contrast in A. compacta
7 × 2 mm, ellipsoid, pleurogram U-shaped, open, the flowers are whitish and the pod 1 – 2.2 cm in
testa slightly glossy, reddish brown. Fig. 1. width but not constricted between the seeds which
are yellowish-brown in colour. A full description and
HABITAT AND DISTRIBUTION. Acacia riograndensis is illustration of A. compacta is given in Rico &
known from only two collections both from the same Rodríguez (1998).
area in the Río Grande valley below Pasorapa. Several Within Bolivia, Acacia riograndensis resembles A.
other narrowly restricted endemic plants, including visco Lorentz ex Griseb. in leaf characters, but can
an undescribed species of Varronia (Boraginaceae), be distinguished from that species by its spicate
Brongniartia ulbrichiana Harms, Bougainvillea inflorescence and leaves with more pairs of pinnae
berberidifolia Heimerl, Myrocarpus emarginatus A. L. B. and longer and wider fruit. A. bonariensis Gill. is also
Sartori & A. M. G. Azevedo and Espostoa guentheri vegetatively similar to A. riograndensis but has shoots
(Kupper) Buxb. are recorded from this area. Based with scattered prickles and more persistent
on the first author’s field observations it is locally spinescent stipules, as well as fruits that are not
common in relatively undisturbed, open, seasonally constricted between the seeds and differ in size.
dry tropical forest, between 1300 and 1500 m on dry, Finally, although the striking whitish bark of A.
freely drained, rocky river terraces with minimal soil. feddeana is similar to that of A. riograndensis, these
There is little ground vegetation but common trees two species can be readily distinguished based on
and shrubs in the area include Schinopsis haenkeana leaf, inflorescence and pod characters. A. feddeana
Engl. (‘soto’), Athyana weinmannifolia Radkl. (‘sotillo’), consistently has a single pair of pinnae per leaf
Cochlospermum tetraporum Hallier f. (‘calapierna’), while A. riograndensis has leaves with 3 – 5(– 7) pairs
Jatropha spp., Bougainvillea spp., Loxopterygium of pinnae. The infloresence of A. riograndensis is
grisebachii Hieron. ex Griseb. (‘Sotomara’) and long-spicate with numerous flowers while in A.
numerous cacti including Neoraimondia herzogiana feddeana it is few-flowered and compact-oblong. The
(Backeb.) Buxb. & Krainz. pods of A. feddeana are broader and more robust
BOLIVIA. Cochabamba, Prov. Campero, camino de than those of A. riograndensis with coriaceous valves
Pasorapa pasando (“a”) Buena Vista, 1300 m, 24 Nov. which are hardly constricted between the seeds.
1999, C. Antezana et al. 1325 (BOLV); ibid, camino de Furthermore, A. riograndensis generally forms an
Pasorapa, en la bajada de Buena Vista hacia el Río erect single-stemmed tree up to 12 m, while A.
Grande, 18°36'32"S, 64°32'85"W, 1447 m, 27 Dec. feddeana is usually a much smaller and more
2004, J. R. I. Wood, M. Atahuachi & M. Mercado 21251 branched treelet (to 4 m) that is consistently multi-
(holotype BOLV; isotypes K, LPB). stemmed from the base. These two endemic
CONSERVATION STATUS. Although Acacia riograndensis is Bolivian Acacias occupy distinct ranges. A. feddeana
locally abundant and apparently under no immediate is frequent over wide areas of semi-arid bushland at
threat from human settlement, its total range is 2300 – 2900 m in the valleys of the Río Tumusla and
highly restricted and the species is thus globally rare, the Río San Juan del Oro in Nor Chichas Province
particularly as there are plans to construct a bridge (Potosi), Nor and Sud Cinti Provinces (Chuquisaca)
over the Río Grande in the area, thus opening the and Mendez Province (Tarija) (Killeen et al. 1993:
site to access by vehicular traffic. 425; Torrico et al. 1994; Wood pers. comm.), being
PHENOLOGY. Acacia riograndensis flowers in November especially abundant between El Puente and
and December. Iscayachi. A. riograndensis is restricted to 1300 – 1500
NOTES. Acacia riograndensis is placed in subgenus m in the Río Grande valley further north in
Aculeiferum Vassal section Monocanthea Vassal of Cochabamba Department.

© The Board of Trustees of the Royal Botanic Gardens, Kew, 2007


A NEW SPECIES OF ACACIA ENDEMIC TO BOLIVIA 607

M C

H G

Fig. 1. Acacia riograndensis. A habit with inflorescences × 0.65; B spinescent stipules showing canaliculate petiole and extrafloral
nectary × 5; C leaflet upper surface × 13; D apex of leaf rachis showing extrafloral nectary and mucro × 5; E flower and floral bract × 5;
F calyx opened out × 10; G corolla opened out × 10; H longitudinal section of base of flower showing the receptacle ×13; J gynoecium
× 5; K seed front and side view × 2; L pod × 0.65; M open pod valve showing seed × 0.65. From J. R. I. Wood, M. Atahuachi & M.
Mercado 21251. DRAWN BY ROSEMARY WISE.

© The Board of Trustees of the Royal Botanic Gardens, Kew, 2007


608 KEW BULLETIN VOL. 62(4)

Acknowledgements
We thank Rosemary Wise for the illustration, John
Wood for preparing the Latin diagnosis, Colin
Hughes, Gwilym Lewis and John Wood for assistance
in assembling the manuscript, and the Darwin
Initiative, Department for the Environment, Food
and Rural Affairs (DEFRA), U.K. which funded the
fieldwork on which this publication is based.

References
Killeen T. J., García, E. & Beck, S. G.(1993). Guía de
Árboles de Bolivia. Herbario Nacional de Bolivia &
Missouri Botanical Garden. La Paz, Bolivia.
Rico, A. M. de L. & Rodríguez, A. (1998). Mimosaceae
R. Br. Tribu Acacieae. Flora del valle de Tehuacán –
Cuicatlán. Fasc. 20: 1 – 27. Universidad Nacional
Autonoma de Mexico, Mexico City.
Torrico, G., Peca, C., Beck, S. G. & García, E. (1994).
Leñosas útiles de Potosi-Proyecto FAO/
Holanda/CDF “Desarrollo Forestal Comunal en el
Altiplano Boliviano. Potosi, Bolivia.

© The Board of Trustees of the Royal Botanic Gardens, Kew, 2007

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