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fewflower tick trefoil, fewflower tickclover

Habit Herbs, perennial, unarmed; roots ± woody, often partly subtuberous or tuberous.
Stems

ascending to erect or spreading, terete, usually pubescent, rarely glabrous.

monomorphic; ascending or spreading, branched or unbranched, 20–60 cm, uncinate-puberulent and sparsely pilose.

Leaves

whorled or alternate, usually odd-pinnate, rarely unifoliolate;

stipules present, usually scarious, rarely thinly papery, striate, glabrate or hairy;

petiolate;

leaflets usually 3, rarely 1 [5 or 7], stipels present or absent, sometimes partly or wholly, filiform, usually reduced, scarious, blade margins entire, rarely undulate, ciliate, surfaces pubescent.

3-foliolate, usually 4–6 and alternate;

stipules caducous, subulate to narrowly ovate, 1.5–5 mm, apex acute;

petiole 5.5–6.5 cm;

leaflets often estipellate, sometimes stipellate, surfaces appressed-pubescent;

lateral blade oblique, slightly smaller than terminal;

terminal blade broadly obovate to rhombic, 3–9 × 4–6.5 cm, apex acute or short-acuminate.

Inflorescences

2–26-flowered, terminal, sometimes also axillary, sometimes a fertile shoot separately arising from basal part of vegetative stem, pseudoracemes, sometimes in panicles, lax-flowered, branched or unbranched;

bracts caducous, primary ones subtending flower cluster with secondary bracts each subtending 1 pedicel.

usually terminal, mostly unbranched, sometimes axillary from distal leaf axils and relatively short;

rachis white-pilose and densely uncinate-puberulent;

primary bract linear to narrowly ovate, 1–4 mm.

Pedicels

densely uncinate-puberulent or glabrous.

stout, 2–7 mm, uncinate-puberulent.

Flowers

papilionaceous;

calyx broadly campanulate, lobes 5, usually appearing 4-lobed, adaxial pair connate except apically, with 2 minute teeth, lobes shorter than tube;

corolla pink, pink-purple, or white [orange, red], banner clawed or tapering proximally, blade usually broadly obovate, often with pair of spots (false nectar guides) at base;

wing and keel petals clawed, keel usually connate along abaxial margin of blade (distinct in H. pauciflorum);

stamens 10, monadelphous;

anthers dorsifixed;

ovary stipitate.

calyx 1.5–1.8 mm, white-puberulent, hairs rather abundant, long, stiff;

corolla white, 4.5–6.5 mm, keel distinct, not connate along abaxial margin (exposing reproductive organs).

Fruits

loments, distinctly stipitate, stipe exserted from calyx, greater than 5 mm, glabrous or puberulent, compressed, very deeply incised abaxially, straight or shallowly undulate adaxially, 1–4-jointed, lateral faces densely uncinate-puberulent;

segments obliquely depressed or very shallowly obovate or obtriangular;

sutures glabrate, abaxial suture very deeply incised, adaxial distinctly thickened, connections between segments (isthmi) less than 1/5 as broad as pod.

Seeds

2–5, flat, obliquely depressed-obovate, broadest 2/3 distance towards anterior end, without rim-aril around hilum;

cotyledons of seedlings hypogeous, remaining underground being enclosed in loment-segment, rarely epigeous.

Loments

1 or 2(or 3)-articulate;

segments asymmetrically obtriangular, 9–14 × 6–8 mm;

stipe 5–9 mm, uncinate-puberulent.

x

= 11.

2n

= 22.

Hylodesmum

Hylodesmum pauciflorum

Phenology Flowering summer–fall.
Habitat Rich, moist woodlands, bottomlands or slopes, drier uplands.
Elevation 10–300 m. (0–1000 ft.)
Distribution
North America; n Mexico; Asia; n Africa
[BONAP county map]
from FNA
AL; AR; DC; DE; FL; GA; IL; IN; KS; KY; LA; MD; MO; MS; NC; NJ; NY; OH; OK; SC; TN; TX; VA; WV
[WildflowerSearch map]
[BONAP county map]
Discussion

Species ca. 11 (3 in the flora).

Plants of Hylodesmum and Desmodium are alike in having three-foliolate leaves and uncinate-puberulent loments that are easily separable into 1-seeded segments; Hylodesmum differs from Desmodium in having calyx lobes shorter than the tubes, monadelphous stamens, long-stipitate loments with abaxial sutures incised to the adaxial sutures, shallowly obtriangular segments, and seeds without a rim-aril around the hilum.

Phylogenetic relationships between the three North American species were illustrated in the phylogenetic trees in K. Ohashi et al. (2018b) and discussed by Li H. C. et al. (2019).

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

Hylodesmum pauciflorum can be locally abundant in mesic woods with rich soil, although it is less common than the other two members of the genus in the flora area. The stems are initially upright and are weak; they are often bent by wind and rain as the season progresses. The absence of fusion of the keel petals is unusual for the tribe; apparently, the pollination biology of H. pauciflorum has never been examined.

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

Key
1. Inflorescences usually terminal, sometimes axillary; corollas white; keel petals distinct (reproductive organs exposed); loment stipe uncinate-puberulent; stipels sometimes present.
H. pauciflorum
1. Inflorescences terminal or on peduncles from bases of plants; corollas usually pink or pink-purple, rarely white; keel petals connate along abaxial margin (enclosing reproductive organs); loment stipe glabrous or glabrate; stipels usually absent, rarely present.
→ 2
2. Inflorescences terminal; pedicels 3–8 mm, stout; terminal leaflet blades broadly ovate, apex abruptly acuminate; stipules often persistent; loment stipe 4–10 mm.
H. glutinosum
2. Inflorescences on peduncles arising from bases of plants; pedicels 10–25 mm, slender; terminal leaflet blades rhombic, elliptic, obovate, or orbiculate, apex acute or short- acuminate; stipules deciduous; loment stipe (5–)10–22 mm.
H. nudiflorum
Source FNA vol. 11. Author: Hiroyoshi Ohashi. FNA vol. 11.
Parent taxa Fabaceae > subfam. Faboideae Fabaceae > subfam. Faboideae > Hylodesmum
Sibling taxa
H. glutinosum, H. nudiflorum
Subordinate taxa
H. glutinosum, H. nudiflorum, H. pauciflorum
Synonyms Podocarpium, Desmodium Hedysarum pauciflorum, Desmodium pauciflorum, Meibomia pauciflora
Name authority H. Ohashi & R. R. Mill: Edinburgh J. Bot. 57: 173. (2000) (Nuttall) H. Ohashi & R. R. Mill: Edinburgh J. Bot. 57: 181. (2000)
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