Senna atomaria |
Senna |
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flor de San Jose, flor de san josé, palo zorillo |
senna |
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Habit | Shrubs or trees, to 20 m. Leaves mesophyllous to slightly sclerophyllous, 8.5–28.5 cm, hairy, sometimes densely; stipules caducous; extrafloral nectaries 0; leaflet pairs 2–5, blades bicolored, usually obovate to elliptic, sometimes ovate, 20–130 × 10–60 mm. | Herbs, annual, biennial, or perennial, shrubs, or trees, unarmed; roots without bacterial nodules. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Stems | erect, glabrous or pubescent. |
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Leaves | alternate, even-pinnate, mesophyllous to sclerophyllous, rarely phyllodic; stipules present, caducous or persistent; petiolate; extrafloral nectaries 0 or 1–8, on petioles, on rachis between proximal pair of leaflets only, or between proximal and subsequent pairs of leaflets, sessile or stipitate, glandlike and concave; leaflets (or phyllodes) 2–28, blade margins usually entire, surfaces glabrous or pubescent. |
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Racemes | 5–55-flowered, not spikelike; bracts early caducous, to 5 mm. |
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Inflorescences | 1–40+-flowered, axillary, racemes, sometimes aggregated into compound racemes, erect; bracts present, usually early or late caducous, rarely persistent at anthesis; bracteoles absent. |
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Pedicels | 13–28 mm. |
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Flowers | asymmetric, enantiostylous; calyx greenish to yellow; corolla yellow-orange, slightly dark-veined, longest petal 12–23 mm, highly asymmetric, 1 or both lower petals highly modified, strongly concave and folded over stamens (flag-shaped); androecium slightly heterantherous, stamens 7 (similar in shape and size, abaxial ones slightly longer), staminodes 3; anthers 2.8–5 mm, dehiscing by 2 short slits, apical appendage 0; gynoecium incurved, ovules 46–70; ovary glabrate, sometimes becoming hairy after fertilization; style stout. |
caesalpinioid, monosymmetric or asymmetric, enantiostylous; calyx usually early or late caducous, rarely persistent after anthesis, bowl- or vase-shaped, lobes 5, greenish to yellowish; corolla yellow to yellow-orange, petals subequal, blades narrowed to claw; stamens 6–10, often heterantherous, with 1 adaxial set of 3 staminodes, 1 middle set of 4 short stamens and 1 abaxial set of 2 or 3 long stamens, or not heterantherous and stamens similar in shape and only slightly different in size; filaments stiff, or arcuate, glabrous, nearly same length as anthers; anthers stiff, basifixed, dehiscing by 1 or 2 apical pores or short slits; ovary shortly stipitate, incurved, linear, usually hairy, rarely glabrous; style linear or incurved, usually terminating in minute stigmatic tip. |
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Fruits | legumes, stipitate, flat to cylindrical, straight or curved [spiral], often corrugated over seeds, indehiscent or partly dehiscent, glabrous or pubescent. |
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Legumes | pendulous, flat, straight, 220–370 × 80–140 mm, woody, indehiscent or splitting transversely into woody segments. |
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Seeds | reddish brown, obovoid to oblong-obovoid. |
10–20, ovoid, obovoid, ellipsoid to rhomboid, or pyriform, usually areolate. |
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x | = 12, 13, 14. |
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Senna atomaria |
Senna |
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Phenology | Flowering late winter–late spring. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Habitat | Disturbed habitats. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Elevation | 0–20 m. (0–100 ft.) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Distribution |
FL; Mexico (Baja California Sur, Campeche, Chiapas, Colima, Guerrero, Jalisco, México, Michoacán, Nayarit, Oaxaca, Quintana Roo, San Luis Potosí, Sinaloa, Sonora, Tabasco, Tamaulipas, Veracruz, Yucatán); Central America (including Caribbean Islands); South America (Colombia, Ecuador, Venezuela) [Introduced in North America]
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North America; Mexico; Central America; South America; West Indies; Bermuda; Australia [Introduced in Asia, Africa, Atlantic Islands, Indian Ocean Islands, Pacific Islands] |
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Discussion | As with other trees from deciduous and semi-deciduous vegetation, Senna atomaria is covered with flowers before developing the foliage (H. S. Irwin and R. C. Barneby 1982). In the flora area, it occurs naturalized only very locally in Collier County (R. P. Wunderlin et al., http://florida.plantatlas.usf.edu/). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Species 300–350 (25 in the flora). Senna was segregated from the large Cassia and placed in subtribe Cassiinae, together with Cassia in the narrow sense and Chamaecrista (H. S. Irwin and R. C. Barneby 1981, 1982). A number of Senna species have been used as purgatives or laxatives, several other species have been cultivated as ornamentals (L. T. F. Colladon 1816; M. A. Luckow 1996), and some have become invasive weeds (Irwin and Barneby 1982). Senna is a remarkable example of floral specialization in relation to buzz pollination (that is, pollen-collecting bees vibrate flowers; S. L. Buchmann 1974). The nectarless flowers of Senna display a wide range of traits typical of buzz-pollinated flowers: poricidal anthers, heteranthery, point-tipped stigma, and enantiostyly (deflection of the carpel to the left or right) often accompanied by asymmetric corolla and androecium (B. Marazzi et al. 2007; Marazzi and P. K. Endress 2008). Another characteristic feature of Senna is the conspicuous glandlike extrafloral nectaries (EFNs) on leaves and, sometimes, also at the base of pedicels in 80% of the species (Irwin and Barneby 1982; Marazzi and M. J. Sanderson 2010). Less well known are recently reported cryptic EFNs embedded within stipules, bracts, and sepals in species previously thought to lack extrafloral nectaries (Marazzi et al. 2013). Extrafloral nectaries offer nectar to ants in return for their protection from insect herbivores (R. R. Fleet and B. L. Young 2000). Senna is a relatively old genus with several fossil fruits described from the Eocene (P. S. Herendeen 1992; L. Calvillo Canadell and S. R. S. Cevallos-Ferriz 2005), and probably diverged from its sister Cassia in the narrow sense about 50 million years ago (Marazzi and Sanderson). The current classification of Senna (Irwin and Barneby 1982), recognizing 35 series in six sections [Astroites H. S. Irwin & Barneby, Chamaefistula (de Candolle ex Colladon) H. S. Irwin & Barneby, Paradictyon H. S. Irwin & Barneby, Peiranisia (Rafinesque) H. S. Irwin & Barneby, Psilorhegma (Vogel) H. S. Irwin & Barneby, and Senna], has been adopted worldwide but received little support in molecular phylogenetic studies, as only sect. Psilorhegma is monophyletic (Marazzi et al. 2006). In North America, all of the sections are represented except for the monospecific Astroites and Paradictyon from central Mexico and South America, respectively. Several ornamental species are cultivated in warmer areas of North America and may escape, especially in Arizona, California, and Florida, including Senna bacillaris (Linnaeus f.) H. S. Irwin & Barneby, S. corymbosa, S. didymobotrya (Fresenius) H. S. Irwin & Barneby, S. multijuga (Richard) H. S. Irwin & Barneby, S. spectabilis (de Candolle) H. S. Irwin & Barneby, and S. surattensis. Currently, S. corymbosa and S. surattensis are considered naturalized in North America, along with at least another six introduced species. A few of the introductions have regionally been recognized as problematic invasive plants (S. multiglandulosa in California and S. pendula in Florida), and two other species (S. obtusifolia and S. occidentalis) are considered noxious weeds in many countries worldwide. Two species, Senna bicapsularis (Linnaeus) Roxburgh and S. italica Miller, have been excluded since all specimens examined were misidentified. Specimens known in North America as S. bicapsularis have been confirmed to represent misidentifications or misappli (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 11. | FNA vol. 11. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Parent taxa | Fabaceae > subfam. Caesalpinioideae (excluding Mimosoid clade) > Senna | Fabaceae > subfam. Caesalpinioideae (excluding Mimosoid clade) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sibling taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Synonyms | Cassia atomaria, C. emarginata | Cassia section senna, Cassia subg. senna | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Name authority | (Linnaeus) H. S. Irwin & Barneby: Mem. New York Bot. Gard. 35: 588. (1982) | Miller: Gard. Dict. Abr. ed. 4, vol. 3. (1754) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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