Chamaecrista nictitans |
Chamaecrista fasciculata |
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partridge pea, sensitive partridge or wild sensitive pea, sensitive partridge pea, sensitive pea, wild sensitive-pea |
partridge pea, partridge sensitive-pea, showy partridgepea, sleepingplant |
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Habit | Herbs, annual, rarely over-wintering, to 0.8(–1)[–1.2] m. | Herbs, annual, rarely overwintering, to 1.4 m; roots not rhizomelike. | ||||||||
Stems | erect, incurved ascending. |
erect. |
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Leaves | (1.5–)2–8(–9)[15–21] cm; petiole (1.5–)2–7 mm; extrafloral nectary 1(or 2), near mid petiole, stipitate; leaflets (6–)8–28(–32)[–40] pairs, blades usually straight, sometimes falcate, linear, narrowly oblong, or oblong-elliptic, (3–)4–26 × 1–3 mm. |
2.5–11 cm; petiole (2–)2.5–9 mm; extrafloral nectary 1(–3), sessile or shortly stipitate; leaflets (7 or)8–22(–26) pairs, blades linear-oblong, oblong, oblong-oblanceolate, or -elliptic, apex mucronulate to subacute, (5.5–)7–20(–23) × (1.3–)1.5–5(–6) mm. |
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Racemes | 1(or 2)-flowered, axillary. |
1–4(or 6)-flowered, supra-axillary. |
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Pedicels | 0.5–4[–16] mm; bracteoles mid pedicel. |
(6–)8–22(–26) mm; bracteoles distal to mid pedicel. |
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Flowers | calyx greenish, sepal venation reticulate; corolla yellow, sometimes fading pinkish, petals to 3.5–8(–9)[–16] mm; stamens [2–]4–8[or 9]; anthers yellow-orange or red, to (1.4–)1.6–3[–9.5] mm, different sizes; ovary usually hairy throughout, rarely glabrate. |
calyx greenish, sepal venation reticulate; corolla yellow, fading brown or orange, rarely whitish, 2–4 petals with reddish maculate at claw, to 10–23 mm; stamens 10; anthers all or some yellow, yellow and red-tipped, red, red-brown, or red-violet, to (5.5–)6–10.5 mm; ovary often hairy, sometimes glabrous. |
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Legumes | straight, linear-oblong, [14–](15–)18–48(–56)[–78] × [2.4–]2.5–5.5(–5.8) mm. |
straight or curved, linear-oblong, (3–)3.5–6.5(–10) × (25–)30–75(–85) mm. |
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Seeds | [1.9–](2.2–)2.4–3.4[–3.7] mm. |
(2.8–)3.2–4.8(–6.3) mm. |
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2n | = 16. |
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Chamaecrista nictitans |
Chamaecrista fasciculata |
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Phenology | Flowering mid spring–early fall(–winter). | |||||||||
Habitat | Open woods, fields, roadsides, inland and coastal dunes, coastal prairies, disturbed hardwood prairies, tallgrass prairies, sandy patches in shortgrass prairies, pine-savannas, usually in dry, sandy soils. | |||||||||
Elevation | 0–1400 m. [0–4600 ft.] | |||||||||
Distribution |
United States; Mexico; Central America; West Indies; South America (Argentina, Brazil, Paraguay, Peru)
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AL; AR; CT; DC; DE; FL; GA; IA; IL; IN; KS; KY; LA; MA; MD; MI; MN; MO; MS; NC; NE; NJ; NM; NY; OH; OK; PA; RI; SC; SD; TN; TX; VA; VT; WI; WV; ON
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Discussion | Varieties 13 (3 in the flora). Chamaecrista nictitans is distinguished from the closely similar C. fasciculata (and C. deeringiana) by its globose-ovoid floral buds, which are ovoid-acuminate in the latter two species. All three varieties in the flora area belong to subsp. nictitans and are characterized by two to nine fertile stamens, while all other varieties have ten fertile stamens (they belong to the other subspecies): subsp. brachypoda (Bentham) H. S. Irwin & Barneby, subsp. disadena (Steudel) H. S. Irwin & Barneby, and subsp. patellaria (Colladon) H. S. Irwin & Barneby (H. S. Irwin and R. C. Barneby 1982). The key to varieties in the flora is adapted from Irwin and Barneby. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Due to its high morphological variation, Chamaecrista fasciculata has been characterized by a history of shifting species and infraspecific taxonomic boundaries. Even its current definition is not satisfactory (H. S. Irwin and R. C. Barneby 1982), especially considering the high similarity (and probably very close relationship) with other partially sympatric species of Chamaecrista, such as C. chamaecristoides, which occurs in Texas, and C. deeringiana in the southeastern United States. Chamaecrista fasciculata also closely resembles C. nictitans but can be distinguished by its ovoid-acuminate floral buds, which are globose-ovoid in C. nictitans. Chamaecrista fasciculata is the first non-papilionoid legume to become a model species in genomics (S. R. Singer et al. 2009). It has been used to address research questions ranging from climate change (J. R. Etterson 2004) to specialized pollination biology (C. B. Fenster 1995) and ant-plant interactions (M. T. Rutter and M. D. Rauser 2004; R. S. Rios et al. 2008). Cassia chamaecrista Linnaeus is a rejected name that pertains here. (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 | ||||||||||
Sibling taxa | ||||||||||
Subordinate taxa | ||||||||||
Synonyms | Cassia nictitans | Cassia fasciculata, C. brachiata, C. chamaecrista var. robusta, C. depressa, C. fasciculata var. depressa, C. fasciculata var. ferrisiae, C. fasciculata var. macrosperma, C. fasciculata var. puberula, C. fasciculata var. robusta, C. fasciculata var. rostrata, C. mississippiensis, C. triflora, C. venosa, C. bellula, C. brachiata, C. camporum, C. depressa, C. fasciculata var. macrosperma, C. ferrisiae, C. littoralis, C. mississippiensis, C. puberula, C. robusta, C. rostrata, C. tracyi | ||||||||
Name authority | (Linnaeus) Moench: Methodus, 272. (1794) | (Michaux) Greene: Pittonia 3: 242. (1897) — (as fascicularis) | ||||||||
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