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Merten's or wood or woodland saxifrage, Mertens' saxifrage, wood saxifrage, woodland saxifrage

saxifrage

Habit Plants solitary or in clumps, not stoloniferous, with caudex or short-rhizomatous. Herbs perennial (biennial in S. adscendens, annual in S. tridactylites), sometimes rhizomatous, sometimes stoloniferous; caudex not fleshy, scaly, sometimes with bulbils; herbage hairy or stipitate-glandular, sometimes glabrous.
Flowering stems

± erect, leafy, 1–40[–100] cm.

Leaves

basal and cauline, (basal persistent, cauline ± inconspicuous);

petiole rounded, 2–20 mm;

blade round to reniform, irregularly shallowly lobed, 20–80(–100) mm, thin, margins serrate, stipitate glandular-ciliate, apex obtuse to rounded, surfaces sparsely hairy.

in basal rosette and cauline, alternate (opposite in S. nathorstii, S. oppositifolia), cauline reduced;

stipules absent;

petiole absent or present;

blade obovate, oblong, oblong-obovate, elliptic, linear, spatulate, or oblanceolate to ovate, reniform, or round, lobed or unlobed, base cuneate to cordate, ultimate margins entire, crenate, serrate, or dentate, (with lime-secreting hydathodes in S. aizoides, S. nathorstii, S. oppositifolia, S. paniculata), apex acute to obtuse or rounded;

venation pinnate or palmate.

Inflorescences

30+-flowered, open, much-branched thyrses, usually some or all flowers replaced by bulbils (sometimes bulbils absent), 15–40 cm, dark purple-tipped stipitate-glandular;

bracts (± inconspicuous), petiolate or sessile.

thyrses or, sometimes, cymes, sometimes solitary flowers, terminal from terminal bud in rosette, 2–200[–1000]-flowered, (some or all flowers replaced by bulbils in S. cernua, S. mertensiana), usually bracteate (ebracteate in S. nathorstii, S. oppositifolia); (bracts leaflike).

Flowers

sepals reflexed (at least in fruit), ovate to elliptic, margins eciliate, surfaces sparsely stipitate-glandular or glabrous;

petals white, not spotted, narrowly ovate to elliptic, (3–)4–6 mm, longer than sepals;

filaments strongly club-shaped;

ovary superior.

[bilaterally symmetric], bisexual (unisexual and plants sometimes gynodioecious, or plants dioecious in S. eschscholtzii);

hypanthium free from or 1/4–3/4 adnate to ovary, free from ovary to 0.5 mm, green or pink to purple, (0.1–4 mm);

sepals 5, green, sometimes reddish at tips, sometimes ± purple;

petals absent or (1–)5, white, cream, yellow, orange, red, pink, or purple, often yellow-, orange-, or red-spotted;

nectary disc present or not;

stamens 10, (distinct);

filaments linear and ± flattened (club-shaped in S. mertensiana);

ovary superior to ± inferior, sometimes appearing more superior in fruit, 2-locular, carpels usually (1/4–)1/2 connate proximally or ± distinct;

placentation axile (when connate 1/2+ their length) or appearing marginal;

styles 2;

stigmas 2.

Capsules

2(–3)-beaked (± folliclelike in S. oppositifolia).

Seeds

brown, oblong, ellipsoid, or ovoid, smooth, tuberculate, or papillate.

x

= 6, 8, 11, 13, 14.

2n

= 36, ca. 48, 50.

Saxifraga mertensiana

Saxifraga

Phenology Flowering spring–summer.
Habitat Moist to wet stream banks, mossy cliffs and slopes, waterfall spray zones
Elevation 0-2500 m (0-8200 ft)
Distribution
from FNA
AK; CA; ID; MT; OR; WA; AB; BC
[WildflowerSearch map]
[BONAP county map]
from USDA
North America; South America; Eurasia; n Africa; mostly north-temperate; arctic; and montane regions
[BONAP county map]
Discussion

Plants of Saxifraga mertensiana bear bulbils in the axils of basal leaves.

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

Antiphylla Haworth; Heterisia Rafinesque ex Small; Hirculus Haworth; Leptasea Haworth; Lobaria Haworth; Muscaria Haworth

Species ca. 390 (25 in the flora).

Saxifraga has had differing treatments (e.g., J. K. Small and P. A. Rydberg 1905b; H. G. A. Engler and E. Irmscher 1916; P. E. Elvander 1984; D. A. Webb and R. J. Gornall 1989). Most have been based on morphology and cytology. Relationships among species are difficult to assess. The broad Linnaean concept of the genus had been accepted by most recent authors. Molecular phylogenetic data (summarized by D. E. Soltis et al. 2001) show that Saxifraga as traditionally understood is polyphyletic and should be divided into two main groups, Saxifraga in the narrow sense and Micranthes Haworth, the treatment followed here. Other taxa, notably the North American Cascadia, must also be recognized. Cascadia differs from both Saxifraga and Micranthes in its lax, trailing stems and only cauline leaves, its carpels connate only proximally and each independently adnate to the hypanthium, and its spiny seeds; its ovules are bitegmic as in Saxifraga; ovules are unitegmic (except for sect. Merkianae) in Micranthes. In addition, Saxifraga and Micranthes differ by the following traits: leaves basal and cauline (these sometimes reduced and bractlike) in the former versus basal only (or proximally crowded) in the latter (the flowering stems being leafless); carpels usually connate more than one-half versus less than one-half, although there is variation in both genera for this trait; seeds smooth, tuberculate, or papillate versus longitudinally ribbed; and pollen striate or granular versus reticulate (L. Brouillet and R. J. Gornall 2007).

Saxifraga in the narrow sense, as adopted here, includes most sections of the traditional genus as well as a majority of the species. In North America fewer species belong to Saxifraga than to Micranthes. Eight species of Saxifraga are endemic to North America. A single introduced species has established itself in the flora area; other garden species have usually not escaped or were ephemeral. The following species are excluded from this treatment: S. cymbalaria Linnaeus (misidentification of S. sibthorpii Boissier, a garden plant, not established), S. ×geum Linnaeus and S. umbrosa Linnaeus (both misidentifications of S. hirsuta specimens), and S. hirsuta Linnaeus (not established). The report of S. stolonifera Meerburgh (syn. S. sarmentosa Linnaeus f.) from California is old; there has been no recent collection, and that species also is excluded here.

There is extensive occurrence of polyploidy and dysploidy throughout Saxifraga (P. E. Elvander 1984; D. A. Webb and R. J. Gornall 1989).

The stigmas and styles are typically two; occasional flowers on plants in some species have three or, rarely, four stigmas and styles. In addition, ovary position in some taxa can change from mostly inferior at flowering to superior in fruit. Ovary position is described at flowering. Capsules usually have two connate carpels that are distally distinct; in rare cases, carpels are distinct nearly to the base and fruits are folliclelike. Only such exceptions are indicated in descriptions, the usual case being assumed.

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

Key
1. Inflorescences with all or some flowers replaced by bulbils
→ 2
1. Inflorescences without bulbils
→ 3
2. Basal leaves usually ephemeral (gradually dying through growing season), leaf blade (3-)5-18(-20) mm, 3-7(-9)-lobed, margins entire; inflorescences with bulbils often replacing all flowers or all flowers except terminal; bracts conspicuous; sepals erect.
S. cernua
2. Basal leaves persistent, leaf blade 20-80(-100) mm, irregularly lobed, margins serrate; inflorescences with bulbils replacing at least some flowers; bracts ± inconspicuous; sepals reflexed (at least in fruit).
S. mertensiana
3. Ovaries 1/2+ inferior (sometimes appearing more superior in fruit)
→ 4
3. Ovaries ± superior to ca. 1/2 inferior
→ 13
4. Petals yellow to orange
→ 5
4. Petals white, cream, pink, or purple, yellowish, greenish, or pink tinged
→ 6
5. Plants mat- or cushion-forming, not stoloniferous; leaf blade margins usually spinose-ciliate; inflorescences glabrous or clear-tipped stipitate-glandular.
S. aizoides
5. Plants in clumps, stoloniferous; leaf blade margins glandular-ciliate; inflorescences purplish-tipped stipitate-glandular.
S. flagellaris
6. Petioles absent; leaf blades leathery, lime-secreting hydathodes present.
S. paniculata
6. Petioles usually present; leaf blades thin or ± fleshy (not leathery), lime-secreting hydathodes absent
→ 7
7. Leaf blades spatulate, obovate, oblanceolate, or elliptic to ovate
→ 8
7. Leaf blades reniform to orbiculate or round
→ 10
8. Plants perennial, densely cushion- or loosely mat-forming.
S. cespitosa
8. Plants biennial or annual, solitary or tufted
→ 9
9. Plants biennial, basal leaves persistent; petals (2-)3-6 mm.
S. adscendens
9. Plants annual, basal leaves usually withered at flowering; petals 2.5-3 mm.
S. tridactylites
10. Plants usually densely (sometimes loosely) tufted, not rhizomatous
→ 11
10. Plants loosely (sometimes densely) tufted or matted, sometimes solitary, rhizomatous
→ 12
11. Cauline leaves 3-5 (proximal similar to basal leaves); hypanthium V-shaped in longisection, glabrous or sparsely short stipitate-glandular; sepals 0.7-1 mm wide.
S. debilis
11. Cauline leaves 1-3 (dissimilar from basal leaves, reduced); hypanthium U-shaped in longisection, sparsely to densely long stipitate-glandular; sepals 1.5-2.1 mm wide.
S. hyperborea
12. Plants green; leaf blades (5-)7.4-11.2(-20) mm, 5-7(-11)-lobed, lobes obtuse, sometimes acute; inflorescences capitate thyrses (flowers subsessile), (3-)5-15(-18) cm; bracts 5-10, leaflike, 3-7-lobed, densely surrounding inflorescence; petals broadly elliptic to obovate.
S. bracteata
12. Plants green to purple; leaf blades (2.6-)3.7-5.2(-7.4) mm, 3-5(-7)-lobed, lobes rounded, sometimes ± obtuse; inflorescences cymes (flowers pedicellate), 1.7-7 cm; bracts 2-3, reduced, unlobed or 1-3-lobed, not surrounding inflorescence; petals oblong to elliptic.
S. rivularis
13. Leaves mostly opposite, with lime-secreting hydathodes
→ 14
13. Leaves alternate, without lime-secreting hydathodes
→ 15
14. Leaf blades oblong to obovate, 2-5 mm; petals purple to pink, rarely white, often drying violet.
S. oppositifolia
14. Leaf blades oblanceolate to elliptic, 5-9 mm; petals salmon to flesh colored, sometimes red or orange, rarely yellow, sometimes violet tinged.
S. nathorstii
15. Petals yellow to greenish yellow (rarely purple), rarely orange- or red-spotted, sometimes fading when dried
→ 16
15. Petals white or cream to purple, sometimes yellow-, orange-, or red-, or purple-spotted, sometimes drying to cream or pale yellow
→ 21
16. Plants loosely tufted and rhizomatous or in solitary clumps and stoloniferous
→ 17
16. Plants mat- or cushion-forming, rhizomatous
→ 18
17. Plants loosely tufted, not stoloniferous or sometimes shortly so; leaf blade margins eciliate or sparsely reddish brown-ciliate, surfaces glabrous or sparsely reddish brown-villous; sepal margins reddish brown-ciliate.
S. hirculus
17. Plants in solitary clumps, stoloniferous; leaf blade margins glandular-ciliate, surfaces glabrous; sepal margins stipitate glandular-ciliate.
S. flagellaris
18. Flowers unisexual; leaf blade margins stiffly bristly-ciliate.
S. eschscholtzii
18. Flowers bisexual; leaf blade margins ciliate (but not stiffly bristly) or eciliate
→ 19
19. Petals greenish yellow, 2-3 mm.
S. aleutica
19. Petals bright golden or pale yellow, rarely purple, 4-8 mm
→ 20
20. Sepals erect to spreading, margins eciliate or sparsely ciliate; petals pale yellow, rarely purple.
S. serpyllifolia
20. Sepals strongly reflexed, margins eciliate to glandular-ciliate; petals bright golden yellow.
S. chrysantha
21. Sepals reflexed (at least in fruit).
S. mertensiana
21. Sepals erect or ascending to spreading
→ 22
22. Plants solitary or tufted; leaf blades round to reniform, 3-7(-9)-lobed
→ 23
22. Plants mat-forming; leaf blades linear or lanceolate to elliptic or oblong, oblanceolate, or obovate to spatulate or cuneate, unlobed or with 1-3 apical teeth or lobes
→ 24
23. Leaf blades lobed less than halfway to midvein; petioles (5-)10-60 (-90) mm.
S. cernua
23. Leaf blades lobed usually more than halfway to midvein; petioles 5-15 mm.
S. radiata
24. Leaf blades usually with 1-3 apical teeth or lobes
→ 25
24. Leaf blades unlobed
→ 27
25. Leaf apex long spinose-mucronate, margins softly glandular- ciliate.
S. tricuspidata
25. Leaf apex mucronate or not, margins stiffly ciliate
→ 26
26. Leaf blades spatulate, apex mucronate, margins not cartilaginous, unlobed or minutely 3-toothed or -lobed apically; petals red- or orange-spotted distally.
S. vespertina
26. Leaf blades broadly obovate, apex not or slightly mucronate, margins cartilaginous, prominently 3-lobed apically; petals not spotted.
S. taylorii
27. Leaf blades linear, linear-lanceolate, or oblanceolate to narrowly elliptic or cuneate, apex acute, spinose-mucronate
→ 28
27. Leaf blades linear or oblong to oblanceolate or spatulate, apex rounded or obtuse, sometimes mucronate (but not spinose-mucronate)
→ 29
28. Leaf blade margins stiffly ciliate.
S. bronchialis
28. Leaf blade margins softly glandular-ciliate.
S. tricuspidata
29. Petals usually pale yellow, rarely purple, not spotted.
S. serpyllifolia
29. Petals white to cream, yellow-, orange-, or red- spotted
→ 30
30. Petals yellow-spotted proximally, red- or orange-spotted distally.
S. vespertina
30. Petals usually yellow-spotted, sometimes sparsely red-spotted proximally.
S. cherlerioides
Source FNA vol. 8, p. 146. FNA vol. 8, p. 132. Authors: Luc Brouillet, Patrick E. Elvander†.
Parent taxa Saxifragaceae > Saxifraga Saxifragaceae
Sibling taxa
S. adscendens, S. aizoides, S. aleutica, S. bracteata, S. bronchialis, S. cernua, S. cespitosa, S. cherlerioides, S. chrysantha, S. debilis, S. eschscholtzii, S. flagellaris, S. hirculus, S. hyperborea, S. nathorstii, S. oppositifolia, S. paniculata, S. radiata, S. rivularis, S. serpyllifolia, S. taylorii, S. tricuspidata, S. tridactylites, S. vespertina
Subordinate taxa
S. adscendens, S. aizoides, S. aleutica, S. bracteata, S. bronchialis, S. cernua, S. cespitosa, S. cherlerioides, S. chrysantha, S. debilis, S. eschscholtzii, S. flagellaris, S. hirculus, S. hyperborea, S. mertensiana, S. nathorstii, S. oppositifolia, S. paniculata, S. radiata, S. rivularis, S. serpyllifolia, S. taylorii, S. tricuspidata, S. tridactylites, S. vespertina
Synonyms S. mertensiana var. eastwoodiae
Name authority Bongard: Mém. Acad. Imp. Sci. St.-Pétersbourg, Sér. 6, Sci. Math. 2: 141. 1832 , Linnaeus: Sp. Pl. 1: 398. (1753): Gen. Pl. ed. 5, 189. 1754 ,
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