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New Mexico fleabane
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large-flower daisy, large-flower fleabane, onestem fleabane, Rocky Mountain alpine fleabane
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| Perennials, 20–70 cm; taprooted, caudices woody. |
Perennials, 2–25 cm; rhizomatous, fibrous-rooted, caudices or rhizomes crownlike or branches relatively short and thick. |
erect, moderately to densely strigose (hairs appressed to ascending, 0.1–0.8(–2) mm, sometimes spreading at bases or throughout), eglandular or glands minute, non-capitate. |
erect to decumbent-ascending, sparsely to moderately pilose to villoso-hirsute, often stipitate-glandular over all or part. |
basal (sometimes persistent) and cauline; blades oblanceolate, margins usually deeply pinnatifid (lobes in 2–5 pairs), sometimes dentate to entire, faces strigose, eglandular; basal 10–60 × 6–35 mm, cauline gradually reduced distally. |
basal (persistent) and cauline (petioles equaling or shorter than blades); blades oblanceolate to obovate or spatulate, 10–60(–90) × 3–8(–14) mm, cauline abruptly or gradually reduced distally, margins entire (apices rounded), faces sparsely hirsutulous or villous to sparsely strigose or glabrate, sometimes sparsely glandular. |
3.5–5 × 7–12 mm. |
5–8(–10) × 8–20 mm. |
70–150; corollas white, drying white, (2–)6–15 mm, laminae reflexing. |
50–130; corollas blue to pink or purplish, rarely white, 7–11(–15) mm (mostly 1–2 mm wide), laminae coiling. |
2.5–3.3 mm (throats somewhat white-indurate, not inflated). |
2.4–4(–5) mm. |
in 3–4 series, strigose to hirsute (hairs arising mostly from midregion), usually minutely glandular, rarely eglandular. |
in 2–3 series (green or purplish), moderately to densely woolly-villous (hairs flattened, cross walls sometimes reddish), minutely glandular at least apically. |
(1–)5–15(–30) in loosely corymbiform arrays. |
1. |
1–1.3 mm, 2(–4)–nerved, faces sparsely strigose; pappi: (outer 0) inner (readily falling) of (8–)10–12 bristles. |
1.8–2.4 mm, 2-nerved, faces strigose; pappi: outer of setae, inner of (7–)10–18(–22) bristles. |
= 18, 36. |
= 18, 27. |
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| Flowering (Jul–)Aug–Oct(–Dec). |
Flowering Jul–Aug(–Sep). |
| Open, rocky sites, from grasslands into oak or pine woodlands, often with madrono, juniper, or fir |
Rocky sites, meadows, alpine or near timberline |
| (900–)1500–2700(–3000) m ((3000–)4900–8900(–9800) ft) |
2900–4200 m (9500–13800 ft) |
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AZ; NM; Mexico (Chihuahua, Sonora)
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AZ; CO; ID; MT; NM; OR; UT; WY; AB; BC
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Relatively large, pinnatifid leaves are typical of Erigeron neomexicanus; plants with nearly entire leaves can be identified by the strongly perennial habit, white, reflexing rays, and 10–12 readily falling pappus bristles. Erigeron neomexicanus and E. oreophilus were treated by A. Cronquist (1947) as varieties of one species, and their morphologic similarity and the closeness of their geographic ranges support that hypothesis. But relatively few collections are found that could be regarded as intermediates, and both forms sometimes grow in proximity, apparently without a range of intermediates. In some Arizona mountain ranges, apparently only one or the other taxon occurs. Still, the possibility exists that these are populational segregants of a single species (see further comments in G. L. Nesom 1989d). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
S. A. Spongberg (1971) recognized only the triploid populations as Erigeron grandiflorus and assigned the diploid ones to E. simplex. He hypothesized that the triploids incorporate genomic elements from an ancestor other than E. simplex. Based on his comments and annotations, however, triploids in southern Canada and the western United States apparently differ from the much more widespread diploids only quantitatively, having involucres and florets at the higher end of size ranges. Morphologic distinctions between the ploidal races do not provide a basis for consistent distinction. Spongberg (p. 200) also noted that “because of the intergrading of morphologic features of plants of Erigeron grandiflorus...the single most important criterion indicative of this taxon is highly irregular [in shape] and greatly abortive pollen.” These pollen features result from meiotic anomalies associated with the triploid condition. Specimen citations by A. Cronquist (1947) for Erigeron grandiflorus were mostly from collections of the species treated here as E. porsildii. He also cited two collections from southwestern Alberta; those and the type collection of E. grandiflorus (from the same region) are disjunct by more than 1500 kilometers from the more northern range of E. porsildii and instead lie at the northern extremity of the range of what previously has generally been identified as E. simplex. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
| FNA vol. 20, p. 277. |
FNA vol. 20, p. 324. |
| Asteraceae > tribe Astereae > Erigeron |
Asteraceae > tribe Astereae > Erigeron |
E. abajoensis, E. acomanus, E. acris, E. aequifolius, E. algidus, E. aliceae, E. allocotus, E. alpiniformis, E. anchana, E. annuus, E. aphanactis, E. arenarioides, E. argentatus, E. arisolius, E. arizonicus, E. asperugineus, E. aureus, E. barbellulatus, E. basalticus, E. bellidiastrum, E. bigelovii, E. biolettii, E. blochmaniae, E. bloomeri, E. breweri, E. caespitosus, E. calvus, E. canaani, E. canus, E. cascadensis, E. cavernensis, E. cervinus, E. chrysopsidis, E. clokeyi, E. compactus, E. compositus, E. concinnus, E. consimilis, E. corymbosus, E. coulteri, E. cronquistii, E. davisii, E. decumbens, E. denalii, E. disparipilus, E. divergens, E. eatonii, E. elatior, E. elatus, E. elegantulus, E. elmeri, E. engelmannii, E. evermannii, E. eximius, E. filifolius, E. flabellifolius, E. flagellaris, E. flettii, E. foliosus, E. formosissimus, E. garrettii, E. geiseri, E. glabellus, E. glacialis, E. glaucus, E. goodrichii, E. gracilis, E. grandiflorus, E. greenei, E. heliographis, E. hessii, E. howellii, E. humilis, E. hyperboreus, E. hyssopifolius, E. inornatus, E. jonesii, E. kachinensis, E. karvinskianus, E. klamathensis, E. kuschei, E. lackschewitzii, E. lanatus, E. lassenianus, E. latus, E. leibergii, E. leiomerus, E. lemmonii, E. linearis, E. lobatus, E. lonchophyllus, E. maguirei, E. mancus, E. maniopotamicus, E. mariposanus, E. melanocephalus, E. miser, E. modestus, E. muirii, E. multiceps, E. nanus, E. nauseosus, E. nematophyllus, E. nivalis, E. ochroleucus, E. oreganus, E. oreophilus, E. ovinus, E. oxyphyllus, E. pallens, E. parishii, E. parryi, E. peregrinus, E. petrophilus, E. philadelphicus, E. pinnatisectus, E. piperianus, E. piscaticus, E. poliospermus, E. porsildii, E. pringlei, E. procumbens, E. pulchellus, E. pulcherrimus, E. pumilus, E. purpuratus, E. pygmaeus, E. quercifolius, E. radicatus, E. reductus, E. religiosus, E. rhizomatus, E. robustior, E. rybius, E. rydbergii, E. salishii, E. salmonensis, E. sanctarum, E. saxatilis, E. sceptrifer, E. scopulinus, E. serpentinus, E. sionis, E. sivinskii, E. sparsifolius, E. speciosus, E. strigosus, E. subglaber, E. subtrinervis, E. supplex, E. tenellus, E. tener, E. tenuis, E. tracyi, E. trifidus, E. tweedyi, E. uintahensis, E. uncialis, E. uniflorus, E. untermannii, E. ursinus, E. utahensis, E. vagus, E. velutipes, E. vernus, E. versicolor, E. vetensis, E. vicinus, E. vreelandii, E. watsonii, E. wilkenii, E. yukonensis |
E. abajoensis, E. acomanus, E. acris, E. aequifolius, E. algidus, E. aliceae, E. allocotus, E. alpiniformis, E. anchana, E. annuus, E. aphanactis, E. arenarioides, E. argentatus, E. arisolius, E. arizonicus, E. asperugineus, E. aureus, E. barbellulatus, E. basalticus, E. bellidiastrum, E. bigelovii, E. biolettii, E. blochmaniae, E. bloomeri, E. breweri, E. caespitosus, E. calvus, E. canaani, E. canus, E. cascadensis, E. cavernensis, E. cervinus, E. chrysopsidis, E. clokeyi, E. compactus, E. compositus, E. concinnus, E. consimilis, E. corymbosus, E. coulteri, E. cronquistii, E. davisii, E. decumbens, E. denalii, E. disparipilus, E. divergens, E. eatonii, E. elatior, E. elatus, E. elegantulus, E. elmeri, E. engelmannii, E. evermannii, E. eximius, E. filifolius, E. flabellifolius, E. flagellaris, E. flettii, E. foliosus, E. formosissimus, E. garrettii, E. geiseri, E. glabellus, E. glacialis, E. glaucus, E. goodrichii, E. gracilis, E. greenei, E. heliographis, E. hessii, E. howellii, E. humilis, E. hyperboreus, E. hyssopifolius, E. inornatus, E. jonesii, E. kachinensis, E. karvinskianus, E. klamathensis, E. kuschei, E. lackschewitzii, E. lanatus, E. lassenianus, E. latus, E. leibergii, E. leiomerus, E. lemmonii, E. linearis, E. lobatus, E. lonchophyllus, E. maguirei, E. mancus, E. maniopotamicus, E. mariposanus, E. melanocephalus, E. miser, E. modestus, E. muirii, E. multiceps, E. nanus, E. nauseosus, E. nematophyllus, E. neomexicanus, E. nivalis, E. ochroleucus, E. oreganus, E. oreophilus, E. ovinus, E. oxyphyllus, E. pallens, E. parishii, E. parryi, E. peregrinus, E. petrophilus, E. philadelphicus, E. pinnatisectus, E. piperianus, E. piscaticus, E. poliospermus, E. porsildii, E. pringlei, E. procumbens, E. pulchellus, E. pulcherrimus, E. pumilus, E. purpuratus, E. pygmaeus, E. quercifolius, E. radicatus, E. reductus, E. religiosus, E. rhizomatus, E. robustior, E. rybius, E. rydbergii, E. salishii, E. salmonensis, E. sanctarum, E. saxatilis, E. sceptrifer, E. scopulinus, E. serpentinus, E. sionis, E. sivinskii, E. sparsifolius, E. speciosus, E. strigosus, E. subglaber, E. subtrinervis, E. supplex, E. tenellus, E. tener, E. tenuis, E. tracyi, E. trifidus, E. tweedyi, E. uintahensis, E. uncialis, E. uniflorus, E. untermannii, E. ursinus, E. utahensis, E. vagus, E. velutipes, E. vernus, E. versicolor, E. vetensis, E. vicinus, E. vreelandii, E. watsonii, E. wilkenii, E. yukonensis |
| E. delphiniifolius var. euneomexicanus, E. delphiniifolius subsp. neomexicanus |
E. simplex |
| A. Gray: Proc. Amer. Acad. Arts 19: 2. (1883) |
Hooker: Fl. Bor.-Amer. 2: 18, plate 123. (1834) |
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