Atriplex covillei
Atriplex fruticulosa
Coville's orach
ball saltbush, ballscale, little oak orach
terete, sparsely scurfy when young.
simple or much branched, scurfy, finally glabrate.
petiole to 1/2 as long as blade (becoming subsessile distally);
blade green or finally stramineous, (10–)20–50 × 6–30 mm, firm, base abruptly acute to narrowly cuneate, apex acute to attenuate, sparsely scurfy.
numerous, proximal ones mostly short petiolate, distal ones sessile;
blade narrowly lanceolate to elliptic, 5–15(–20) × 2–4 mm, mostly acute at both ends, margin entire, densely gray scurfy.
in sessile glomerules in distal axils, often mixed with pistillate ones, staminate calyx deeply 5-cleft;
lobes obtuse, not appendaged.
in short, dense, interrupted terminal spikes.
with calyx of (1–)3(–5) hyaline sepals.
in small, axillary clusters.
dark reddish brown, 1–1.5 mm.
dark brown, 1.4–1.7 mm.
bracteoles sessile or stipitate, 6–12 × 4–7 mm, margin mostly 3-lobed, with elongate terminal lobe triangular to lanceolate, 2 short rounded lobes at base or sides merely rounded at base, united to beyond middle.
bracteoles sessile or subsessile, broadly obovate to suborbicular in profile, slightly if at all compressed, 3–5 mm and almost as wide, united to middle, narrowly margined and acutely dentate beyond middle, sides tooth-crested or muricate, ± indurate.
Atriplex covillei
Atriplex fruticulosa
Endolepis covillei was treated within the synonymy of Atriplex phyllostegia (Torrey) S. Watson by H. M. Hall and F. E. Clements (1923).
H. C. Stutz et al. (1993) placed Atriplex covillei within Endolepis, based in large part on the presence of a perianth subtending the pistil within the fruiting bracteoles and on the lack of Kranz anatomy in the leaves. The pattern of venation is, nevertheless, very similar to that in species with Kranz anatomy. The presence of perianth scales in the pistillate flowers of A. covillei has been regarded as evidence of relationship with A. suckleyi. Despite placement of these taxa within Endolepis by Stutz et al. Atriplex covillei is possibly more closely allied to the morphologically similar and partially sympatric A. phyllostegia than it is to strongly dissimilar and the distantly disjunct A. suckleyi. Stutz and his associates placed great emphasis on the presence of reduced perianth segments subtending the pistil within the fruiting bracteoles of A. covillei. Calyces per se, otherwise known only in A. suckleyi and A. pleiantha, probably have arisen independently. Their presence does not necessarily indicate a close relationship. Stutz et al. pointed to other differences aside from the calyx of the pistillate flowers, and it is apparent that the two entities can stand as distinct species. To segregate A. covillei within a separate genus and to ally it with a species to which its relationships are obscure at best, stretches logic beyond reason.
(Discussion copyrighted by Flora of North America; reprinted with permission.)
H. M. Hall and F. E. Clements (1923) indicated a close relationship between Atriplex fruticulosa and A. coulteri. Both species are described as being perennial by D. Taylor and D. H. Wilken (1993), wherein A. coulteri was inadvertently left out of the key. Perhaps the size of the fruiting bracteoles, 3–5 mm in A. fruticulosa and 2–3 mm in A. coulteri, is diagnostic. Hall and Clements pointed to differences in habit of the plant, which vary from the erect woody forms represented by the type collection (and known only from them?) to the evidently more common phase in which the leafy stems are spreading or prostrate, and herbaceous throughout except at the very base, where they are attached to a more or less woody root crown.
In some fruiting bracteoles the faces are bicristate as in the thornberi phase of Atriplex elegans, in which the teeth radiate around much of the bracteole margin, not mainly from above the middle as in the present species.
(Discussion copyrighted by Flora of North America; reprinted with permission.)
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