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ivesia, mousetail

Habit Herbs, perennial, rosetted, tufted, or matted, sometimes forming hanging clumps, often aromatic, (0.1–)0.3–6(–6.5) dm, sparsely to densely hirsute, sericeous, villous, or pilose, sometimes glabrate, sparsely to densely glandular-puberulent to stipitate-glandular; caudices simple or branched, branches usually relatively short, rarely elongate (I. cryptocaulis), taproot slender to stout, sometimes fusiform and fleshy. Plants usually rosetted or tufted, rarely ± matted (I. kingii var. eremica), not forming hanging clumps, not aromatic; taproot stout to fusiform and fleshy.
Stems

(1–)2–20+, prostrate or pendent to erect, green, grayish, or reddish.

(0.3–)1–4.5(–5.5) dm.

Leaves

winter-marcescent, primarily basal, cauline 0–10(–15), well developed to vestigial, usually alternate (cauline opposite in I. muirii, I. webberi), odd-pinnate;

stipules persistent, sometimes absent, basally adnate to petiole, linear to lanceolate or elliptic, margins usually entire, cauline sometimes lobed;

petiole present;

blade narrowly oblong to filiform, planar to cylindric, 0.5–20(–25) cm, foliaceous, leaflets (3–)7–161, sometimes separate, more often overlapping at least distally, sometimes tightly imbricate, terminal distinct or, more often, confluent with distalmost lateral ones, ovate or obovate to orbiculate or ± flabellate, often oriented in 3-dimensions, leaflet arrangement appearing verticillate, margins flat, palmately incised from 1/4 to completely to base into teeth or linear or oblanceolate to oval or obovate lobes, venation palmate.

Basal leaves

loosely to tightly cylindric (± mousetail-like in I. argyrocoma and I. kingii var. eremica);

stipules present or absent;

leaflets loosely or, sometimes, tightly overlapping, individually distinguishable or not, lobed to base, sometimes entire;

terminal leaflets indistinct, sparsely to densely hairy or glabrate.

Cauline leaves

(1–)2–10(–15), not paired;

blade ± well developed.

Inflorescences

terminal, (1–)3–100(–250)-flowered, ± cymes, open or of 1–several loose to capitate glomerules;

bracts present, reduced;

bracteoles absent.

open to congested, flowers arranged individually and/or in glomerules, these usually ± capitate.

Pedicels

present, straight to sigmoid.

remaining ± straight (rarely ± curved in I. argyrocoma).

Flowers

4–15 mm diam.;

epicalyx bractlets (0–)5;

hypanthium patelliform to campanulate or cupulate to turbinate, 0.5–3(–4) mm;

sepals 5 (usually 4 in I. campestris), spreading, lanceolate to broadly ovate or deltate;

petals 5 (usually 4 in I. campestris), golden to pale yellow to white, sometimes pink-tinged (red in I. multifoliolata), linear or narrowly oblanceolate to obovate, sometimes obcordate;

stamens 5–20(–40), usually shorter than petals;

filaments not forming tube;

torus ± flat to conic, or turbinate (in sect. Comarella), rarely elongate and stipelike (I. arizonica);

carpels 1–20(–40), glabrous, styles subterminal, usually ± filiform, sometimes rough-thickened proximally;

ovule 1.

hypanthium shallowly cupulate or campanulate to turbinate, rarely patelliform (I. pityocharis);

petals not medially reflexed, light yellow to white, sometimes pink-tinged, ± clawed, apices rounded or truncate to emarginate;

stamens usually 20 (10–15 in I. unguiculata, 12–20 in I. campestris), anthers ± as long as to longer than wide, laterally dehiscent;

carpels (1–)2–20.

Fruits

aggregated achenes, individually deciduous, 1–20+, obliquely ovoid to reniform, 0.8–3 mm, sometimes rugose and/or carunculate, glabrous;

hypanthium persistent;

sepals persistent, erect;

styles tardily deciduous, jointed.

Achenes

vertical, smooth, not carunculate.

x

= 7.

Ivesia

Ivesia sect. Unguiculatae

Distribution
from USDA
w United States; nw Mexico
[BONAP county map]
w United States; nw Mexico
Discussion

Species 30 (30 in the flora).

The often aromatic (resin-scented) ivesioid genera (Horkelia, Horkeliella, and Ivesia) have generally been assumed to be derived from Potentilla in the broad sense, an interpretation confirmed by molecular analyses (T. Eriksson et al. 1998, 2003; C. Dobeš and J. Paule 2010; M. H. Töpel et al. 2012). Continued recognition of the three genera (and Duchesnea) accordingly creates a paraphyletic Potentilla; the senior author does not accept the dictum that paraphyletic groups are inherently unnatural and finds it more useful to continue recognizing the ivesioid genera as here circumscribed.

In spite of the morphologic and ecologic extremes encompassed within Ivesia, spanning the continuum from planar-leaved desert chasmophytes to alpine species with mousetail-like leaves, molecular phylogenetic analyses of representatives from all sections of Ivesia, Horkelia, and Horkeliella result in a monophyletic near-polytomy, indicating rapid morphologic radiation not matched by molecular divergence (C. Dobeš and J. Paule 2010; M. H. Töpel et al. 2012). This interpretation is not fully supported by M. Töpel et al., but until the lack of concordance between molecular-based clades and even the most well-defined morphology-based groups is addressed, any conclusions based on molecular analysis alone are inconclusive.

The hypothesis on which the sequence of species used here is based is that the ivesiod genera represent a threshold-crossing radiation in response to the late Tertiary development of xeric conditions in western North America, with adaptations that allow drought-avoidance or minimize water loss. A recurrent trend is the progressive reduction in size and number of floral parts occurring independently in multiple lineages. The end product is a flower in which the nectariferous, patelliform hypanthium itself becomes the main pollinator attractor. Much of this evolutionary radiation has occurred in the various island-like habitats that characterize the arid West, with the result that the ivesioid genera include a high percentage of narrowly endemic species.

In the following descriptions, stems refer to flowering stems, with length including the inflorescence. For chasmophytic (growing on cliffs) species in sect. Setosae, terms such as decumbent are in reference to the vertical rock face. The inflorescence is composed of the branched portion of the flowering stem, including the proximalmost branched node. Cauline leaves are on the portion of the flowering stem proximal to the inflorescence. Planar leaves are those in which the leaflets are largely arranged in a single plane on both sides of the rachis; in cylindric leaves the lobes of deeply incised leaflets are arranged evenly around the rachis and thus appear verticillate. Well-developed blades of cauline leaves are similar to those of basal leaves, though progressively reduced distally; vestigial blades are reduced to a simple lobe, which, with the stipules, has the appearance of a 3-lobed bract. Leaf incisions are referred to as teeth if less than half to base, as lobes if more than half. Counts of leaflet lobes are of ultimate segments, including teeth, not just of primary segments incised to the base or nearly so. Inflorescence structure is described at peak anthesis; at early anthesis flowers are often more congested than indicated here and sometimes become more distant in fruit. Pedicels at proximal nodes are often significantly longer than others; those in most sections remain more or less straight in fruit or bend proximal to the flower, in contrast to those of sect. Setosae that generally become strongly curved or even sigmoid. Petal color is described at peak of flowering; yellow petals often fade afterward. Vestiture descriptions are primarily of non-glandular hairs; subsessile glands or evidently septate-glandular trichomes are universal in Ivesia, though often sparse or hidden by dense non-glandular vestiture.

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

Species 8 (8 in the flora).

Section Unguiculatae encompasses a series of species that have radiated in montane meadows in California, from Siskiyou and Trinity counties through the Sierra Nevada to the San Bernardino Mountains, and in the Carson, Virginia, and Pine Nut ranges in adjacent Nevada; one variety of Ivesia argyrocoma is endemic to the Sierra San Pedro Mártir in Baja California, Mexico. The species occur in seasonally wet/dry meadows and flats, including some specific substrate types of localized occurrence that often support suites of endemic species. The most widespread species in the section, I. kingii, has adapted to alkali-crusted valley bottoms extending across the Great Basin to western Utah.

Members of sect. Unguiculatae are nearly glabrous to densely sericeous but lack the conspicuous glandularity and distinctive ivesioid smell that characterize sects. Ivesia and Setosae. The taproot is often elongate and fleshy-thickened, which is apparently an adaption for when the preferred habitat becomes seasonally desiccated. Leaves are cylindric with deeply lobed leaflets. Flowers are usually aggregated into multiple few- to many-flowered glomerules; sometimes they are individually arranged in diffuse inflorescences. Petals are white to pale yellow but never golden yellow and are often conspicuously clawed. Stamens are commonly 20 except in Ivesia campestris and I. unguiculata.

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

Key

Key to sections of Ivesia

1. Pedicels usually becoming ± curved, often sigmoid; basal leaves planar or loosely to tightly cylindric, leaflets separate to overlapping, toothed 1/4–3/4 or lobed to base; achenes often rugose, ± carunculate (except I. cryptocaulis); flowers arranged ± individually (or ± glomerate in I. paniculata and I. rhypara); plants usually ± petrophytic, often forming hanging clumps in vertical rock crevices.
sect. Setosae
1. Pedicels remaining ± straight; basal leaves loosely to tightly cylindric (sometimes weakly planar in I. longibracteata), leaflets ± overlapping, lobed to base (except I. multifoliolata); achenes smooth, not carunculate; flowers arranged individually or in 1–several loose to capitate glomerules; plants usually not petrophytic (except I. longibracteata), not forming hanging clumps
→ 2
2. Stamens 5; petals not or scarcely clawed
→ 3
2. Stamens 10–20; petals often clawed
→ 4
3. Inflorescences usually ± congested, sometimes becoming open in fruit, flowers arranged in 1+ loose to capitate glomerules; hypanthia shallowly cupulate or campanulate, sometimes turbinate; petals usually narrowly oblanceolate or spatulate to broadly obovate, sometimes linear, not medially reflexed, usually yellow, sometimes white (I. utahensis); stems (0.2–)0.3–2(–4) dm.
sect. Ivesia
3. Inflorescences open, flowers arranged individually; hypanthia patelliform; petals linear to oblanceolate or narrowly elliptic, medially reflexed, yellow or red; stems (1.8–)2–6(–6.5) dm.
sect. Comarella
4. Cauline leaves (0–)1; stems 0.3–1(–1.5) dm; petals golden yellow.
sect. Ivesia
4. Cauline leaves (1–)2–10(–15); stems (0.3–)1–4.5(–5.5) dm; petals light yellow to white, sometimes pink-tinged
→ 5
5. Basal leaves not mousetail-like, loosely to tightly cylindric, individual leaflets distinguishable, sparsely to densely hairy or glabrate.
sect. Unguiculatae
5. Basal leaves mousetail-like, tightly to very tightly cylindric, individual leaflets not or scarcely distinguishable, densely hairy
→ 6
6. Stamens 20; carpels (1–)2–20; inflorescences: flowers arranged individually and/or in glomerules; anthers white to yellowish, ± as long as to longer than wide.
sect. Unguiculatae
6. Stamens 15; carpels 1; inflorescences: flowers arranged individually; anthers purple, shorter than wide.
sect. Stellariopsis
1. Filaments flattened; leaflets (1–)2–3.5 mm, tightly overlapping; plants silvery; stems prostrate to ascending, (0.3–)1–2.5(–3) dm; cauline leaves (1–)2–3; San Bernardino Mountains, s California.
I. argyrocoma
1. Filaments filiform; leaflets (1.5–)2–15(–20) mm, loosely overlapping (tightly so in some I. kingii); plants green to grayish or silvery; stems prostrate-decumbent to erect, (0.5–)1–4(–5.5) dm; cauline leaves 2–15; w United States
→ 2
2. Stamens 10–20, filaments 0.6–1.1 mm; leaflets 15–20(–25) per side; c, s Sierra Nevada, California
→ 3
2. Stamens 20, filaments (1–)1.5–4 mm; leaflets 15–50(–60) per side; n California to Utah
→ 4
3. Petals 5, white, often tinged with pink; sepals heavily purple-mottled; inflorescences (15–)30–100(–200)-flowered; c Sierra Nevada.
I. unguiculata
3. Petals 4(–5), light yellow; sepals green; inflorescences 5–20(–40)-flowered; s Sierra Nevada.
I. campestris
4. Flowers arranged in tight glomerules of 5–20 flowers; pedicels 1–3(–15) mm
→ 5
4. Flowers arranged individually or in loose glomerules of 2–10 flowers; pedicels (1–)2–20(–25) mm
→ 6
5. Petals white; petiole hairs usually spreading, 1–4 mm; hypanthia campanulate to shallowly turbinate, 1.5–3 mm, often nearly as deep as wide.
I. sericoleuca
5. Petals light yellow; petiole hairs ascending, ± 1(–3) mm; hypanthia cupulate, 1–2 mm, 1/2–2/3 as deep as wide.
I. aperta
6. Petals oblanceolate to narrowly spatulate; hypanthia cupulate to turbinate, 1.5–3 mm, often nearly as deep as wide; on ultramafic-derived soil; n California.
I. pickeringii
6. Petals spatulate or obovate to orbiculate; hypanthia shallowly cupulate to patelliform, 0.5–2.5 mm, ± 1/2 as deep as wide; on alkaline soil or in non-alkaline meadows; Great Basin and n Mojave Desert
→ 7
7. Leaflets 15–60 per side, hairs absent or 0.2–0.5(–1) mm, ± appressed; carpels 2–9; alkali-crusted flats, e California, Nevada, sw Utah.
I. kingii
7. Leaflets 5–25 per side, hairs 1–3 mm, spreading to ascending; carpels 8–20; meadows in sagebrush, Pine Nut Mountains, Nevada.
I. pityocharis
Source FNA vol. 9, p. 219. Authors: Barbara Ertter, James L. Reveal. FNA vol. 9, p. 237.
Parent taxa Rosaceae > subfam. Rosoideae > tribe Potentilleae Rosaceae > subfam. Rosoideae > tribe Potentilleae > Ivesia
Subordinate taxa
I. sect. Comarella, I. sect. Ivesia, I. sect. Setosae, I. sect. Stellariopsis, I. sect. Unguiculatae
I. aperta, I. argyrocoma, I. campestris, I. kingii, I. pickeringii, I. pityocharis, I. sericoleuca, I. unguiculata
Synonyms Horkelia subg. I., Potentilla section I., Potentilla subg. I. Horkelia unranked Unguiculatae, Horkelia unranked Eremicae, I. unranked Eremicae, I. section Eremicae, I. unranked Unguiculatae
Name authority Torrey & A. Gray: in War Department [U.S.], Pacif. Railr. Rep. 6(3): 72, plate 11. (1858) (Rydberg) O. Stevens: in N. L. Britton et al., N. Amer. Fl. 22(7): 8. (1959)
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