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false indigo

savanna false indigo or indigo-bush

Habit Shrubs, rarely subshrubs, unarmed, often gland-dotted; sometimes rhizomatous, pungently fragrant when bruised. Shrubs, 0.3–1.4 m; arising from compact, woody root.
Stems

usually erect, sometimes spreading, glabrous or pubescent.

finely longitudinally grooved and ridged, gland-dotted, strigulose to glabrate.

Leaves

alternate, odd-pinnate;

stipules present;

petiolate;

leaflets (7–)9–45(–63), opposite or subopposite, stipels present, petiolulate, blade margins entire or crenulate, veins usually obscured abaxially, midvein mucronate, surfaces gland-dotted or eglandular, pubescent or glabrous.

(8–)12–20(–26) cm;

stipules sometimes persistent, linear or setaceous, (1–)1.5–2(–2.5) mm;

petiole (6–)8–15(–20) mm, gland-dotted, puberulent or glabrous;

rachis sparsely gland-dotted, puberulent or glabrous;

leaflets (11–)15–31(–35), stipels acicular or setaceous, 0.8–1.8 mm, petiolule 0.7–1.5(–1.8) mm, gland-dotted, mostly puberulent or glabrous, blade elliptic to oblong or ovate to suborbiculate, (10–)15–25(–35) × (7–)9–15(–18) mm, base truncate or round to subcordate, margins usually revolute, entire or inconspicuously crenulate, apex round to obtuse or emarginate, surfaces sparsely to conspicuously gland-dotted, usually glabrous or glabrate, sometimes sparsely pubescent abaxially;

midvein terminated by a slender mucro, (0.2–)0.4–1 mm.

Racemes

(1–)3–5(–8)-branched, 10–20(–30) cm;

rachis sparsely gland-dotted, puberulent;

bracteoles linear to narrowly subulate, 1.5–2.5(–3) mm, usually eglandular, sparsely pubescent or sparsely ciliate.

Inflorescences

50–120+-flowered, terminal, racemes, usually solitary or clustered, rarely paniculiform (A. paniculata);

bracts present, caducous, entire or crenulate, often gland-dotted;

bracteoles caducous, entire.

Pedicels

spreading to ascending, sometimes obscure, articulate to hypanthium.

0.4–1 mm, eglandular, sparsely pubescent.

Flowers

non-papilionaceous, reduced to a single banner petal enveloping androecium and gynoecium;

calyx persistent, slightly zygomorphic, greenish to reddish or purplish, sometimes drying blackish, cylindric, funnelform, campanulate, turbinate, conic, or obconic, lobes 5, obscure or distinct, not accrescent;

banner petal purple, reddish purple, purplish, blue, lavender, violet, violet-blue, or white, glabrous;

stamens 10, monadelphous basally, at least at early anthesis, or distinct, exserted;

anthers dorsifixed, relatively small, dehiscing longitudinally;

ovary slightly compressed, ovoid;

styles slender, often exserted;

stigma terminal, capitate.

calyx tube turbinate to narrowly campanulate or cylindric, 1.7–2.2 mm, distal 1/3–2/3 rarely gland-dotted, glabrous;

lobes: abaxial lobe acuminate, slightly longer, adaxial lobes triangular to acuminate, 0.4–1.2(–1.5) mm, margins densely ciliate;

banner bright blue, broadly obovate to obcordate, (4–)5–6 × 3–3.5(–4) mm, distinctly clawed, margins entire or finely erose;

filaments 5–8 mm, distinct;

anthers yellow;

ovary pubescent.

Fruits

legumes, often persistent through next growing season, sessile or shortly stipitate, straight, curved, or bent, falcate or D-shaped, slightly compressed and asymmetrical, oblong to obovoid or claviform, indehiscent, dispersed with calyx, glabrous or pubescent.

Legumes

sessile or stipitate, 4–5.5 × 2–2.5 mm, margins curved outward abaxially, straight adaxially, at least distal 1/2–2/3 gland-dotted, glabrous.

Seeds

1(or 2), laterally compressed, ovoid to oblong.

olive brown or brown, 2–2.3 × 1–1.5 mm, smooth, lustrous.

x

= 10.

Amorpha

Amorpha confusa

Phenology Flowering (May–)Jun–Jul.
Habitat Pine woodlands, savannas, and road banks in outer Atlantic Coastal Plain.
Elevation 0–50 m. (0–200 ft.)
Distribution
from USDA
North America; nw Mexico [Introduced in Europe, Asia, Africa]
[BONAP county map]
from FNA
NC; Pine woodlands; savannas; and road banks in outer Atlantic Coastal Plain
[BONAP county map]
Discussion

Species 16 (15 in the flora).

Amorpha is notable among papilionoid legumes for having a non-papilionaceous corolla consisting solely of a banner petal, although deviation from the normal papilionoid floral form is common throughout Amorpheae. Even though recognition of the genus has never been in question, due to its easily distinguished floral characters, delimitation of species within the genus has long caused consternation among taxonomists. The range and intergradation of morphological variation have resulted in a prodigious list of recognized species, varieties, and forms, most often associated with the A. fruticosa complex. Early taxonomic treatments failed to result in a satisfactory circumscription of the genus (C. K. Schneider 1907; P. A. Rydberg 1919–1920; E. J. Palmer 1931), but the insightful and thorough work of R. L. Wilbur (1975), closely followed by D. Isely (1998) and here, was a marked improvement.

The “amorphoid” clade of Amorpheae, to which Amorpha belongs, has been strongly supported as monophyletic in molecular analyses (M. McMahon and L. Hufford 2004), although most relationships among genera in the clade remain unclear. Analyses of chloroplast, ribosomal DNA, and low-copy nuclear gene sequence data indicated that Amorpha may not be monophyletic because either Errazurizia rotundata or Parryella filifolia, or both, are nested within it (McMahon and Hufford 2004, 2005; McMahon 2005). Some of these analyses have indicated that E. rotundata and P. filifolia are sister species (combined analyses of chloroplast trnK, matK, ITS/5.8S rDNA, nuclear CNGC4), which may or may not be nested in Amorpha; other analyses indicated that E. rotundata is nested among Amorpha species while P. filifolia may or may not be (trnK, matK analyzed alone, CNGC4 analyzed alone). These conflicting outcomes leave the relationship of these two species to each other and to Amorpha unclear. Preliminary analyses of additional nuclear gene data sets have also indicated that E. rotundata and P. filifolia are nested in Amorpha but have not clarified whether or not they are sister species (S. C. K. Straub and J. J. Doyle 2014). Morphological evidence also supports the close association of E. rotundata (originally described as P. rotundata Wooton), P. filifolia, and Amorpha. Parryella filifolia lacks a corolla, and the corolla of E. rotundata is either absent or consists of a single petal, which suggests a closer association in terms of floral evolution to Amorpha than to the other 5-petaled genera of Amorpheae, an observation supported by developmental studies (McMahon and Hufford 2005). W. F. Mahler (1965) hypothesized a close relationship of Amorpha, E. rotundata, and P. filifolia based on shared pollen characteristics.

The phylogenetic relationships among Amorpha species remain unclear due to lack of molecular variation in non-coding chloroplast, nuclear rDNA spacer regions, and nuclear gene intron sequence data. Preliminary results from phylogenetic analyses, including DNA sequence data from most species of the genus, indicate that A. californica is the earliest diverging species in the genus and that A. georgiana and A. nana are closely related; however, the relationships among the other species of the genus are thus far unresolved (S. C. K. Straub and J. J. Doyle 2014). The lack of molecular variation may be indicative of a rapid radiation in the genus or of continued gene flow and partial genetic homogenization through hybridization and introgression, possibly mediated by widespread species. Ongoing genetic work has suggested that polyploidy is more common in Amorpha than previously recognized. Amorpha fruticosa has long been known to be a tetraploid, and new information from nuclear gene DNA sequences and microsatellites now indicates that A. confusa, A. crenulata, and A. roemeriana may also be tetraploids, although this is yet to be confirmed by chromosome counts (Straub et al. 2009; Straub and Doyle). Clearly, further work is needed to resolve species relationships within Amorpha, to update species concepts within the genus, and to determine whether or not Amorpha is monophyletic as circumscribed or if Errazurizia rotundata and P. filifolia should be added to Amorpha.

Amorpha has been a group of interest for many years in the search for biologically active compounds. In the area of medicinal biochemistry, anti-tumor and anti-inflammatory compounds have been isolated from A. fruticosa (L. Li et al. 1993; J. Y. Cho et al. 2000). Antimicrobial agents have been identified in both A. fruticosa and A. nana (L. A. Mitscher et al. 1981, 1985). Amorpha fruticosa has also been investigated for its insecticidal and insect repellant properties (R. C. Roark 1947). The glands on the fruits of this species have been shown to contain compounds that poison numerous types of insects through ingestion or contact (for example, chinch bug, cotton aphid, pea aphid, spotted cucumber beetle, mosquito larvae) and also insect repellant properties (for example, striped cucumber beetle, flour beetles, dog fleas, and houseflies; C. H. Brett 1946, 1946b).

Native Americans of the Great Plains employed several of the more common Amorpha species for a variety of uses. Amorpha fruticosa was used for bedding, horse feed, and arrow shafts, and stems were arranged on the ground to create a clean place to put butchered meat (M. R. Gilmore 1919; P. A. Vestal and R. E. Schultes 1939; D. J. Rogers 1980). Amorpha canescens was used to treat stomach pain, intestinal worms, eczema, neuralgia, and rheumatism, and powdered leaves were applied to wounds (W. J. Hoffman 1891; Gilmore 1909, 1919; Hu. H. Smith 1928). The leaves were also mixed with buffalo fat and smoked or used to make tea (Gilmore 1919). The dried leaves of A. nana were used to treat catarrh (F. H. Elmore 1944).

A few Amorpha species are found regularly in cultivation, the most common being A. fruticosa and A. canescens, while A. californica, A. herbacea, and A. nana are less commonly part of the horticultural trade. Amorpha fruticosa has also been used in the United States and abroad for soil stabilization, erosion control, and in windbreaks, and has been investigated as a potential forage and biomass production crop (S. Karrenberg et al. 2003; L. R. DeHaan et al. 2006; K. Török et al. 2003). Cultivation of A. fruticosa has led to its escape and naturalization in many parts of Europe and Asia.

Amorpha apiculata Wiggins is known from Baja California, Mexico.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Amorpha confusa is known presently only from Brunswick and Columbus counties; it is believed to be extirpated in adjacent South Carolina. The taxon is a Federal species of concern and is listed as threatened in North Carolina. It is usually encountered growing in loamy soils, most often of the Foreston soil series.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Key
1. Petioles and rachises with spinelike glands; Arizona, California, Oregon.
A. californica
1. Petioles and rachises without spinelike glands; widespread in United States, southernmost Canada.
→ 2
2. Subshrubs or shrubs, rarely perennial herbs, (0.1–)0.3–1.4(–3) m; petioles 0.5–15(–20) mm; leaflet margins usually slightly to conspicuously revolute.
→ 3
3. Shrubs mostly canescent, rarely glabrous; eglandular or sparsely gland-dotted; c United States, s, c Canada.
A. canescens
3. Shrubs not canescent; usually densely gland-dotted; widespread in n, c, se United States, s, c Canada.
→ 4
4. Leaflet midveins terminated by a swollen mucro; shrubs mostly densely puberulent to pubescent, when glabrous, then plants of Florida.
→ 5
5. Leaflet blades (6–)8–18(–24) cm, margins entire or inconspicuously crenulate; petioles (0.5–)1–10(–13) mm.
A. herbacea
5. Leaflet blades (8–)15–25(–30) cm, margins crenulate; petioles (3–)8–15.
A. crenulata
4. Leaflet midveins terminated by a slender mucro; shrubs usually glabrous or sparsely pubescent and not of Florida.
→ 6
6. Petioles (6–)8–15(–20) mm; racemes branched, 10–20(–30) cm; banners bright blue.
A. confusa
6. Petioles 1–8(–10) mm; racemes usually unbranched, (2–)3–20(–30) cm; banners reddish purple, rarely lavender.
→ 7
7. Leaflet blades (3–)6–15(–18) cm; petioles 1–3(–5) mm; filaments distinct; anthers yellow; ovaries pubescent; se United States.
A. georgiana
7. Leaflet blades (1.5–)3–7(–10) cm; petioles (2–)4–8(–10) mm; filaments connate basally; anthers purplish; ovaries glabrous; n, c United States, sc Canada.
A. nana
2. Shrubs or suffrutescent herbs, 1–3(–4) m; petioles (5–)10–60(–90) mm; leaflet margins flat or slightly revolute.
→ 8
8. Calyx lobes as long as or longer than tubes, adaxial calyx lobes usually not rounded.
A. schwerinii
8. Calyx lobes as long as or distinctly shorter than tubes, adaxial calyx lobes usually rounded or leaflets with conspicuous raised venation and paniculiform inflorescence if calyx lobes not rounded.
→ 9
9. Leaflet veins conspicuous, distinctly raised abaxially; racemes paniculiform.
A. paniculata
9. Leaflet veins obscure, not raised abaxially; racemes 1–8(–12)-branched.
→ 10
10. Leaflet midveins terminated by a swollen mucro.
→ 11
11. Leaflets (9–)13–19(or 21), blades 4–10(–12) mm wide, mucro 0.1–0.2 mm, petiolules distinctly warty-glandular; banners bright blue to deep violet-blue; legumes 4.5–6 mm.
A. laevigata
11. Leaflets (7 or)9–13(–17), blades (7–)15–25(–38) mm wide, mucro 0.2–0.8 mm, petiolules gland-dotted, rarely eglandular; banners purple; legumes 6–9 mm.
→ 12
12. Racemes (4–)6–12(–20) cm; calyx obviously gland-dotted on distal 1/3; Texas.
A. roemeriana
12. Racemes (8–)10–20 cm; calyx not obviously gland-dotted on distal 1/4; Arkansas, Oklahoma.
A. ouachitensis
10. Leaflet midveins terminated by a slender or slightly swollen mucro.
→ 13
13. Calyx lobes 0–0.6(–0.8) mm.
A. glabra
13. Calyx lobes 0.2–1.4 mm.
→ 14
14. Foliage and calyx drying blackish; leaflet blades distinctly shiny adaxially.
A. nitens
14. Foliage and calyx not drying blackish; leaflet blades not shiny adaxially.
A. fruticosa
Source FNA vol. 11. Authors: Shannon C. K. Straub, James L. Reveal†, Alan S. Weakley. FNA vol. 11.
Parent taxa Fabaceae > subfam. Faboideae Fabaceae > subfam. Faboideae > Amorpha
Sibling taxa
A. californica, A. canescens, A. crenulata, A. fruticosa, A. georgiana, A. glabra, A. herbacea, A. laevigata, A. nana, A. nitens, A. ouachitensis, A. paniculata, A. roemeriana, A. schwerinii
Subordinate taxa
A. californica, A. canescens, A. confusa, A. crenulata, A. fruticosa, A. georgiana, A. glabra, A. herbacea, A. laevigata, A. nana, A. nitens, A. ouachitensis, A. paniculata, A. roemeriana, A. schwerinii
Synonyms A. georgiana var. confusa
Name authority Linnaeus: Sp. Pl. 2: 713. (1753): Gen. Pl. ed. 5, 319. (1754) (Wilbur) S. C. K. Straub: Sorrie & Weakley, J. Bot. Res. Inst. Texas 3: 154. (2009)
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