Introduction
Coulteria Kunth as proposed by Lewis (2005), and later confirmed by Gagnon et al. (2013; 2016) based on molecular studies, is a genus of dioecious shrubs and trees of the family Leguminosae, subfamily Caesalpinioideae. The flowers typically have a lower cucullate sepal with a glandular-pectinate margin, a flat, papyraceous, indehiscent or late dehiscent (along one suture) fruit, leaflets which are pellucid-punctate, and a style which has a groove in its adaxial suture from base to stigma (Contreras, 1991; Sotuyo et al., 2017). The genus has a distinctive seed chemistry, producing phenylalanine substituted derivatives via the shikimic acid metabolic pathway (Larsen et al., 1975; Kite and Lewis, 1994) and the presence of prismatic crystals in ray cells and chambered axial parenchyma in its wood (Gasson et al., 2009). Coulteria occurs across Central America and Mexico and also in parts of northern South America. In Mexico, Coulteria glabra (Britton & Rose) J.L. Contr., Sotuyo & G.P. Lewis and C. pumila (Britton & Rose) Sotuyo & G.P. Lewis occur across Northwestern Mexico, the first in Colima and Jalisco and the latter in Sonora. Coulteria pringlei (Britton & Rose) J.L. Contr., Sotuyo & G.P. Lewis reaches Northeastern Mexico, from the Sierra Gorda de Xichú, Guanajuato to Tamaulipas, while C. platyloba (S. Watson) N. Zamora can be found with a great morphological variation along the Pacific Coast, from Guerrero to the Tehuantepec Isthmus. Within the Río Balsas Depression and the Tehuacán-Cuicatlán Valley, five or six species occur. In the Yucatán Peninsula, the Caribbean Islands, Central and northern South America, at least three species are found. Morphological variation within Coulteria has always been considered part of broadly distributed species, tolerating a wide geological heterogeneity and growing in a range of dry vegetation types including seasonally dry tropical forest, deciduous woodland and dry thorn scrub (Sotuyo et al., 2017). Our botanical explorations in central and southern Mexico, especially in the Río Balsas Depression, during the last 25 years have led us to reconsider the morphological variation throughout the distribution range, resulting in the discovery of several new legume taxa. The objective of this work is to describe and illustrate a new species of Coulteria from Infiernillo, Michoacán, Mexico, a Protected Natural Area with the category of Biosphere Reserve since 2007.
Material and Methods
The morphological description of the new species was based on macroscopic characters from herbarium specimens (FCME and MEXU, Universidad Nacional Autónoma de México (UNAM), acronyms according to Thiers, 2020) and field collected samples. The specimens examined from Guerrero and Michoacán were compared with the original descriptions and photographs of the different species described in the genus.
Coulteria species are dioecious, female and male flowers occur in separate individuals, and to study flower micromorphology in detail, a JEOL JSM35 (JEOL, Cd. Mx., Mexico) electron microscope (SEM) was used at the Instituto de Ciencias del Mar y Limnología, Universidad Nacional Autónoma de México. Closed buds of the new species were dissected and prepared for SEM by dehydrating in an EtOH series. Pollen grains were prepared for SEM by the standard method described by Erdtman (1952). All samples were dry-mounted on metal stubs using double-sided tape and then coated with gold. The distribution map of Coulteria delgadoana and other closely related Coulteria species was based on curated GBIF data (2020a, b, c), generated using R v. 4.0.2 (R Core Team, 2020) and ggplot2 (Wickham 2016). The conservation status was assessed using GeoCAT software (Bachman et al., 2011) to estimate the extent of occurrence (EOO) and the area of occupancy (AOO) of the species, followed by applying the IUCN (2019) categories and criteria for conservation status assessment.
Results
We recorded a new species of Coulteria from the Infiernillo area (Guerrero and Michoacán, Mexico) in the Río Balsas Depression. The Río Balsas Depression or Río Balsas Basin is a large region that occupies portions of eight states of Mexico (Jalisco, Michoacán, Mexico, Guerrero, Morelos, Tlaxcala, Oaxaca and Puebla). The area is found between the Trans-Mexican Volcanic Belt to the North, the Sierra Madre del Sur to the South and a geological subprovince, the Sierra Norte de Oaxaca to the East. Interrelations between vegetations, evapotranspiration and flows of water in the soil are complex. The Balsas River, especially on its flanks of the Sierra Madre del Sur, contains a diverse endemic biota, some genera have the highest concentration of species in the area (e.g. Bursera Jacq. ex L., Becerra, 2003), clearly linked to environmental conditions, orogeny, volcanism and glaciations. Other endemic species in the Río Balsas Depression can show an amalgam of isolated lineages or species, each occupying different ecological environments (Sotuyo et al., 2007). Coulteria delgadoana Sotuyo & J.L. Contr., sp. nov. is related to Coulteria glabra (Table 1). The two species are similar in the number of leaflet pairs per pinna and per leaf, as well as in leaflet indumentum and fruit size, but can be distinguished by size of the male inflorescence, and the length of the fruit stipe, amongst other characters discussed below.
Taxonomy
Coulteria delgadoana Sotuyo & J.L. Contr., sp. nov., Figs. 1-3.
TYPE: MEXICO. Guerrero, municipio Coahuayutla de Guerrero, La Garita, 6 km al SE de Infiernillo, 77 m, 18°14'38.98''N, 101°54'6.38''W, 18.IX.1979, J. C. Soto and G. Ramírez 1660 (holotype: MEXU, isotypes: MEXU, more will be distributed to ENCB, FCME, IZTA, XAL).
Coulteria delgadoana is similar to C. glabra, a species from Colima and Jalisco, but it can be distinguished by its longer male inflorescences (generally more than 15 cm long), smaller flowers, its glabrous leaflets with prominent reticulate venation, and its glabrous ochreous-chestnut coloured fruit with violet tints.
Dioecious trees or shrubs, 4-6 m high; bark smooth grey, young branches puberulous; leaves 5.5-17 cm long, glabrous, paripinnate; stipules triangular, 0.3-0.4 × 0.5-0.7 mm, densely pubescent, caducous; petiole (1.8-)3.1-8 cm long; rachis 3.5-13.1 cm long; pinnae (1-)2-4 pairs, (5.5-)9-17(-30) cm long; leaflets (3-)4-7 pairs, opposite, the proximal leaflets broadly ovate, the distal ones ovate to ovate-lanceolate, (1.6-)3-6 × (1.3-)2-3.5 cm, base cordate, apex obtuse, acute or rounded, margin entire, glabrous or inconspicuously pubescent, punctate, reticulate venation prominent on both surfaces, median vein displaced towards the proximal margin, discolorous, the adaxial surface bright green, the abaxial surface opaque light green; inflorescence axillary, racemose, pedunculate, glabrous, peduncle reddish; male inflorescences (5.5-)11-43(-58) cm; flowers pedicellate, (2.5-)4.2-8.9 mm long, articulated at ⅔ or more of their length from the base, glabrous, bracts caducous, not seen; calyx green, its tube obliquely obconic, puberulent, 2.8-4.5 × 1.8-3 mm; sepals red, adaxial sepals oblong, 3.7-6(-6.7) × 2.1-3(-3.5) mm, apex acute, slightly concave, glandular fimbriolate, vesicular-pubescent on both surfaces, lateral sepals ovate to oblong-ovate, 3-3.5 × 1.7-2.8 mm, apex rounded, glandular fimbriolate, indumentum as on the adaxial sepals, abaxial sepal cucullate, 6-9(-11) × 4.5-6(-7) mm, apex acute, glandular pectinate, pubescent, vesiculate on both surfaces; petals yellow, adaxial petal broadly ovate, 2.5-4.5 × 3-5.5 mm, strongly reflexed, apex rounded or wavy, margin ciliate, base decurrent at the claw, vesiculate, claw 1.3-3.2 × 1.5-2.6 mm, incurved, margin ciliate-pilose abaxially; lateral petal oblong-ovate, 3.7(7.8) × (1.2-)2-6.3(-7.9) mm, apex rounded, margin entire, base oblique, cuneate or rounded, ciliate, glandular-granulate, claw (0.6-)1-1.5(-1.8) × 1.2(-3) mm, hairy on the abaxial surface; abaxial petal ovate-obovate, 2.9-6(-7.8) × 1.7-4.4(-6) mm, base cuneate, apex rounded or obliquely truncated, margin entire, sometimes ciliated, glandular-granulate, vesiculate, claw 0.6-1.2 × 1.3 mm; stamen filaments curved or straight, (2.3-)3-7 mm, villose up to ½ of their length from the base; anthers oblong ovate, (0.8-)0.9-1.2 × 1.2(-1.4) mm, dorsifixed; pollen grains spheroidal, tricolporate, reticulate, pores elliptic, unibaculate; ovary vestigial, 1.2-1.5 mm long, ciliate on the adaxial suture, stipe 0.4-1 mm long, style reduced, 0.5-0.7 mm long; ovules not observed; female inflorescences 1.8-7.7 cm long, bracts early caducous, subulate, 1-2 × 0.6 mm, pedicels 3.1-4.5 mm long, curved, articulated at ⅔ of their length from the base, pubescent; calyx green, pubescent, vesiculate, tube slightly oblique obconic, 2.5-2.9 × 1.4-2 mm, sepals red, adaxial sepals ovate, 3-4.3 × 2.1-2.6, apex rounded, glandular fimbriolate, vesicular on the abaxial surface; lateral sepals elliptic, 2.5-3.2 × 1.5-2 mm, apex obtuse, glandular-fimbriolate; abaxial sepal cucullate, 6-7.5 × 4-5 mm, entire for ⅓ of its length from the base, the remaining ⅔ glandular-pectinate, all sepals densely pubescent and glandular-granulate on both surfaces; petals yellow, adaxial petal broadly obovate, 2.7-3.8 × 2.6-4 mm, curved as in the male flowers, apex truncate or sinuous, margin entire, base attenuate towards the claw, glandular-granulate, vesiculate, claw 2-2.3 × 1.6-2.2 mm, incurved, ciliate-tomentose on the adaxial surface; lateral petals obovate, 3.5-4.5 × 2.3-3.8, apex truncate, margin entire or wavy, base cuneate, glandular-granular, claw 0.7-1.4 mm long, villose at the base adaxially; abaxial petals obovate, 3.9-4.7 × 2.3-3.6 mm, apex rounded, margin entire, base cuneate, glandular-granulate, claw 0.6-1 mm long, ciliate; stamen filaments almost straight, (2.9)3.5-4.3 mm long, villose up to ½ of their length from the base; anthers oblong-elliptic, 0.7-0.9 × 0.4-0.6 mm, erect, sub-dorsifixed, without pollen; ovary oblong, 3.2-5.5 mm, base oblique, stipe 0.5-1 mm; style well-developed, curved, 1.5-2.2 mm, stigma infundibuliform, with a groove in its adaxial suture; ovules 4-5 per ovary; fruit flat, oblong-ovate, 8.5-13.6 × (2.5-)3-3.7 cm, apex obtuse or rounded, base obtuse, septate between the seeds, stipe (6-)8-11 mm long, valves ochre-chestnut coloured, subchartaceous, glabrous, indehiscent; seeds 3-5 per fruit, ovate, laterally compressed, 10-15 × 8.6-13.3 × 2.2-3.2(-3.7) mm, olive with brown marks, darker at the margin, testa cross-fissurate transversally.
Etymology: the new species is dedicated to Alfonso Octavio Delgado Salinas, teacher and friend, a research leader in Mexican botany, and expert in the legume genus Phaseolus L. and other related groups.
Distribution, habitat and phenology: the new species is known only from the Infiernillo region in the states of Guerrero and Michoacán, Mexico. The species grows in deciduous tropical forest, on slopes with rocky soils, and along seasonally streams, at elevations of 77-348 m. Flowering from April to June; in fruit from May to October, the fruits remain attached to the tree until the next flowering season.
Conservation status: based on the extent of occurrence (EOO) estimated at 718,697 km2, and the area of occupancy (AOO) of 24 km2, we propose a conservation assessment of Endangered (EN) in accordance with IUCN (2019) categories and criteria. If we consider only the area of occupancy, this would result in a higher category of threat because Coulteria delgadoana has a fragmented distribution across two Mexican states and is recorded from only four locations, all subject to the threats from human settlement, road construction and local agriculture.
Specimens examined: MEXICO. Guerrero, municipio Coahuayutla de Guerrero, La Garita, 6 km al SE de Infiernillo, 77 m, 18°14'38.98''N, 101°54'6.38''W, 18.IX.1979, J. C. Soto and G. Ramírez 1660 (MEXU); 2 km al E de La Garita camino a Platanillo, 335 m, 18°14'21.39''N, 101°53'16.89''W, 13.VI.1998, J. L. Contreras 2386 (FCME), 2386 bis (FCME); Matamoros de Guerrero, 4.67 km al NO, 21.VI.1999, J. Calónico-Soto 15181 (MEXU); Matamoros de Guerrero, 2.7 km al N, 330 m, 18°30'53''N, 101°50'29''W, 17.IX.1999, J. Calónico-Soto 15954 (MEXU); Las Balsas, 1.32 km al SO, 230 m, 18°32'56''N, 101°50'2''W, 19.XI.1999, J. Calónico-Soto 18981 (MEXU); El Rincón del Bejuco, 15.5 km al O de Juntas Cuajarán, 274 m, 18°28'59.0''N, 101°32'28.0''W, 27.VII.2011, J. C. Soto 19194 (MEXU). Michoacán, municipio Arteaga, 17 km por la carretera a Infiernillo, 348 m, 18°25'19.40''N, 101°56'50.24''W, 01.VI.1990, J. L. Contreras 2762 (FCME); 20 km por la carretera a Infiernillo, 265 m, 18°25'18.77''N, 101°55'30.89''W, 01.VI.1990, J. L. Contreras 2764 (MEXU), 2765 (MEXU), 2766 (FCME); Infiernillo, 114 m, 18°17'30.06''N, 101°54'15.82''W, 18.IX.1979, J. C. Soto et al. 1638 (MEXU).
Hereafter, we present an identification key to distinguish C. delgadoana and its morphologically most closely related species.
Taxonomic key for Coulteria delgadoana and related species
1a. Trees; leaflets glabrous or inconspicuously pubescent, with prominent reticulate venation, ovate, 3-6 × 2-3.5 cm; fruit 8.5-13.6 × (2.5-)3-3.7 cm, oblong-ovate, glabrous, 3-5-seeded; in deciduous tropical forest in Infiernillo region in Guerrero and Michoacán, Mexico ..................................... C. delgadoana Sotuyo & J.L. Contr.
1b. Trees or shrubs; leaflets orbicular, ovate, elliptic, oblong-lanceolate to obovate, indument absent or if present, diverse, on one or both surfaces, venation reticulate but not prominent; fruit oblong to oblong-elliptic, mostly to 3.7-7.2 × 1.9-3.2 cm long, pubescent, 1-3-seeded; from Sonora to Guerrero along the west coast plains or low sierra slopes, in Central and Northeast Mexico, in Tamaulipas, San Luis Potosí, Querétaro, Guanajuato Hidalgo, Michoacán, Morelos, Puebla, and Oaxaca ............................................................…. 2
2a. Trees; leaflets glabrous, oblong-lanceolate, 3-6 × 1.5-3 cm; fruit 7-14 × 3-4 cm, oblong, glabrous, 2-3-seeded; on low rocky bluffs in dry seasonal forest, Colima and Jalisco .............................................................................. C. glabra (Britton & Rose) J.L. Contr., Sotuyo & G.P. Lewis
2b. Shrubs or small trees; leaflets tomentulose to inconspicuously pubescent, densely pubescent to glabrous, orbicular to elliptic or obovate lanceolate ....................... 3
3a. Shrubs; leaflets tomentulose, orbicular to elliptic, 0.79-2.6(-2.8) × 0.79-1.5(-1.9) cm; fruit 3.7-7.2 × 1.9-3.2 cm, oblong-elliptic, tomentulose, 2-3-seeded; in deciduous tropical forest in the Tehuacán-Cuicatlán Valley (Puebla and Oaxaca) .…............................................................................ C. rosalindamedinae R. Torres, Saynes & Tenorio
3b. Shrubs or small trees; leaflets strigilose to glabrous or densely pubescent, orbiculate or oblong elliptic, glabrous or densely pubescent ................................................. 4
4a. Shrubs or small trees; leaflets densely pubescent below, oblong to obovate, 1.7-8.5 × 1.2-4.5 cm; fruit 5-7 × 2.5-3 cm, oblong to elliptic, mucronate, densely pubescent on both surfaces, 1-3-seeded; in dry forest and bushland, in Guanajuato, Hidalgo, Querétaro, San Luis Potosí and Tamaulipas ...................................................................................... C. pringlei J.L. Contr., Sotuyo & G.P. Lewis
4b. Shrubs; leaflets glabrous to sparsely strigilose, orbiculate 0.6-2.7 × 0.6-2.5 cm; fruit glabrous to scarcely strigilose 2-4.5 × 2.2-1.5 cm, 1-2-seeded; in xerophilous scrub or deciduous tropical forest, Sonora ...................................... C. pumila (Britton & Rose) Sotuyo & G.P. Lewis
Discussion
We observed that the closest morphological affinity of the new species is with Coulteria glabra. Coulteria delgadoana is a species restricted to the Infiernillo area, most of the specimens correspond to Guerrero. However, in the past it was thought that the distribution of C. glabra and C. platyloba were broader, our study shows that the Coulteria species have restricted distributions within the Río Balsas Depression. The flowers as well as the fruit in Coulteria are basic structures for the taxonomic determination of the species in the group. In the genus, the flowers are unisexual, the individuals are dioecious, with separate male and female individuals as occurs in other genera as Conzattia Rose. Female flowers have a well-developed pistil, but the stamens have reduced anthers and no pollen. Male flowers have a rudimentary pistil that does not exceed the height of the calyx tube and the anthers develop normally. Coulteria delgadoana cohabits with C. lewisii Sotuyo & J. L. Contr. in the Infiernillo area, the latter can be distinguished by the size of the flowers (ca. 2 cm in length plus the calyx tube), the sericeous indumentum of the young leaves that changes to tomentose when mature, as well as a glabrous fruit.