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keys to the vascular plants of east texas - Botanical Research ...

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896 POACEAE/DICHANTHELIUM<br />

glabrous except for nodes, summits <strong>of</strong> leaf sheaths, and margins <strong>of</strong> leaf blades near base; nodes<br />

glabrous or bearded with long spreading hairs; ligule absent or � 1 mm long; leaf blades usually<br />

3–10(–15) mm wide; spikelets 1.5–2.4(–2.6) mm long. Often in low sandy woods, moist, or<br />

<strong>of</strong>ten boggy areas, less commonly in drier habitats; widespread in <strong>the</strong> e 1/2 <strong>of</strong> TX; se Canada<br />

and e 1/2 <strong>of</strong> <strong>the</strong> U.S. w <strong>to</strong> MI and TX, also AZ, CA, and OR. Apr–Jun, also late summer–fall.<br />

Dichan<strong>the</strong>lium dicho<strong>to</strong>mum and its relatives comprise one <strong>of</strong> <strong>the</strong> most confusing species complexes<br />

known. Countless different approaches have been taken regarding <strong>the</strong>ir taxonomy, with<br />

<strong>the</strong> numerous intergrading morphological entities variously treated as varieties, subspecies, or<br />

distinct species, or not formally recognized (e.g., Diggs et al. 1999). Jones et al. (1997) and Hatch<br />

(2002) recognized five infraspecific taxa in TX, one <strong>of</strong> which is here treated as a separate species<br />

(D. tenue). Based on work by LeBlond (2001) and Freckmann and Lelong (2003a), we are<br />

tentatively recognizing six for <strong>the</strong> state. While we are following Freckmann and Lelong (2003a)<br />

in recognizing <strong>the</strong>se taxa as subspecies, we would prefer <strong>to</strong> treat <strong>the</strong>m at <strong>the</strong> varietal level as<br />

partially done by LeBlond (2001)—see Turner and Nesom (2000) for an explanation <strong>of</strong> infraspecific<br />

ranks. However, this would necessitate making new combinations which we cannot justify<br />

without a thorough study <strong>of</strong> <strong>the</strong> entire group. The following key <strong>to</strong> subspecies is slightly modified<br />

from Freckmann and Lelong (2003) and LeBlond (2001). However, <strong>the</strong>re is substantial intergradation<br />

between <strong>the</strong>se subspecies and difficulty should be anticipated when trying <strong>to</strong><br />

separate <strong>the</strong>m. The fruits are reportedly dispersed by ants, which are apparently attracted <strong>to</strong> a<br />

substance (possibly an oil) found under <strong>the</strong> first glume (Gaddy 1986).<br />

1. Lower nodes hairy.<br />

2. Spikelets 1.5–1.8 mm long; upper floret 0.6–0.8 mm wide ________________________ subsp. microcarpon<br />

2. Spikelets usually 1.8–2.5 mm long; upper floret 0.7–1 mm wide.<br />

3. Spikelets usually glabrous; midculm leaf blades usually 5–7 mm wide ____________ subsp. dicho<strong>to</strong>mum<br />

3. Spikelets pubescent; midculm leaf blades usually 7–14 mm wide ___________________ subsp. nitidum<br />

1. Lower nodes glabrous.<br />

4. Larger leaf blades more than (7–)10 mm wide; leaf sheaths <strong>of</strong>ten with pale glandular spots<br />

between <strong>the</strong> prominent veins; spikelets 1.9–2.6 mm long, acute <strong>to</strong> beaked ___________ subsp. yadkinense<br />

4. Larger leaf blades less than 10 mm wide; leaf sheaths without glandular spots; spikelets 1.5–<br />

2.3 mm long, obtuse <strong>to</strong> subacute.<br />

5. Culms weak, ultimately reclining or sprawling over o<strong>the</strong>r <strong>plants</strong>, <strong>of</strong>ten flattened ________ subsp. lucidum<br />

5. Culms erect, terete.<br />

6. Leaf blades usually ascending or erect; spikelets broadly ellipsoid or obovoid, 1.5–1.8<br />

(–2.1) mm long, <strong>of</strong>ten purplish at <strong>the</strong> base; <strong>plants</strong> <strong>of</strong> wet pine savannahs and open<br />

swamps ____________________________________________________________ subsp. roanokense<br />

6. Leaf blades usually spreading; spikelets ellipsoid, 1.8–2.3 mm long, rarely purplish at <strong>the</strong><br />

base; <strong>plants</strong> <strong>of</strong> wet-mesic <strong>to</strong> dry woods and thickets _______________________ subsp. dicho<strong>to</strong>mum<br />

subsp. dicho<strong>to</strong>mum. Wet-mesic <strong>to</strong> dry, well-drained woodland sites, sandy soils; Henderson, Leon,<br />

and Limes<strong>to</strong>ne (BRIT) cos.; Hatch et al. (1990) cited regions 1, 2, 3, 4, and 5; se Canada and e 1/2 <strong>of</strong><br />

<strong>the</strong> U.S. w <strong>to</strong> MI and TX. [Panicum barbulatum Michx., Panicum dicho<strong>to</strong>mum L., Panicum<br />

dicho<strong>to</strong>mum var. barbulatum (Michx.) A.W. Wood] This is a quite variable taxon (LeBlond 2001).<br />

subsp. lucidum (Ashe) Freckmann & Lelong, (bright, shining, clear). Wet woods and o<strong>the</strong>r wet<br />

areas; Leon, New<strong>to</strong>n, Robertson, Rusk, and San Jacin<strong>to</strong> (TAES—annotated by S. Hatch) cos.;<br />

mainly se US from NJ s <strong>to</strong> FL w <strong>to</strong> TX. [D. lucidum (Ashe) LeBlond, Panicum dicho<strong>to</strong>mum var.<br />

lucidum (Ashe) Lelong, Panicum lucidum Ashe] LeBlond (2001) recognized this taxon as a distinct<br />

species and noted that “<strong>the</strong> densely papillose fertile lemma and palea readily separate” it<br />

from all o<strong>the</strong>r members <strong>of</strong> <strong>the</strong> D. dicho<strong>to</strong>mum complex.<br />

subsp. microcarpon (Muhl. ex Elliott) Freckmann & Lelong, (small-fruited). Low or wet woods;<br />

Bowie, Camp, Cass, Hardin, Harrison, Hous<strong>to</strong>n, Jasper (BRIT), Angelina, Brazos, Leon, Liberty,<br />

Nacogdoches, New<strong>to</strong>n, Polk, Robertson, Rusk, Shelby, Smith (TAES—annotated by S. Hatch),

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