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Draba fladnizensis Wulf.

Place: Endalen

Place: Endalen

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Place: Endalen

Life span

Perennial, but probably not long-lived.

Growth form

Solitary herb with basal caudex, sometimes with some leaf remains, mainly sheaths and mid-veins, from previous seasons, branching into comparatively few, small, densely to loosely clustered rosettes forming small tussocks. Each rosette potentially with one flowering stem, up to 10 stems per tussock.

Leaf

Leaf rosettes mostly 2–3 cm but occasionally up to 10 cm broad. Leaves pale green, narrowly oblanceolate to nearly linear, acute, up to 14 × 2 mm, entire, mid-vein very prominent. Both upper and lower leaf surfaces glabrous or rarely with sparse long, stout, simple and forked hairs; margin with long, stout, simple, and sometimes forked hairs, rarely glabrous. Hairs on leaf surfaces and margins pointing strongly forward.

Inflorescence

Flowering stems erect, sometimes short at the beginning of the flowering (1–2 cm), but elongating during and after flowering to 5–15 cm, glabrous, often red-tinged, and often with one leaf (besides bracts). Inflorescence a raceme elongating in the fruit stage to 2–3.5 cm, with 3–10(–15) flowers. Pedicels slender, attached at an angle of 40–60° with the stem but regularly curved upwards, 2–6 mm, less than half the fruit length, glabrous.

Flower

Flowers radially symmetric, with four sepals and petals. Sepals green or red tinged, up to 2 × 1 mm (i.e., twice as long as broad), with conspicuous white margins. Petals white, erectopatent (making the flower half-open), broadly spathulate, notched, 2–2.5 × 1–1.5 mm, usually less than twice as long as sepals, not contiguous.

Fruit

Fruit a silicule, pale or dark green, sometimes strongly purplish or reddish tinged, erect, elliptic or rarely lanceolate, 4–7 × 1.5–2 mm, glabrous. Style short, up to 0.3 mm. Seeds 7–10 in each room, dark brown, ca. 1 × 0.75 mm.

Reproduction

Reproducing only by seeds. Flowering and seed-set is regular in most years; mature seeds are often observed. Draba fladnizensis is known to be highly selfing (Brochmann 1993). Grundt et al. (2006) found sterility barriers between populations of D. fladnizensis to be quite frequent in the circumpolar area. Crosses between several populations from Svalbard and populations from S Norway and Alaska were included.

Comparison

Draba fladnizensis is characterized by having only simple and sometimes forked, forward pointing hairs on the leaves, and glabrous stems and fruits. The only other white-flowered Draba in Svalbard with a predominance of simple hairs on the leaves (and glabrous stems and fruits), is D. lactea. This species, however, nearly always have some very small, multibranched hairs on the outer parts of the lower surface of leaves, and also much broader leaves with less strengthened mid-vein, larger petals (3.5—4 mm long vs. 2—2.5 mm), a more corymbose panicle, and fruits lanceolate or ovate vs. mostly elliptic.

Habitat

Draba fladnizensis is clearly a thermophilous species with an affinity for sites with higher insolation rates. Occurs in sparsely vegetated environments such as crevices and rock ledges, gravelly slopes and ridges. On dry to very dry substrates of well drained soils of mixed or coarse texture and with circumneutral to basic reaction. The growth sites are usually exposed or semi-exposed, with little snow cover in winter and little competition. Little grazed by reindeer and geese.

Distribution

Restricted to the middle arctic tundra zone in the fjord regions, perhaps with 1–2 sites in the northern arctic tundra zone, and to the weakly and clearly continental sections, perhaps with 1–2 sites in the transitional section. Only known from Spitsbergen with sites in the Isfjorden, Kongsfjorden, and Wijdefjorden areas, and a single, isolated site in Sørkapp Land. Not recorded from Bjørnøya.

Comments

Draba fladnizensis is an arctic−alpine, diploid (2n = 16) species distributed throughout the Arctic and in the majority of temperate mountain ranges in Europe, Asia, and North America. It is recognizable everywhere and monomorphic, so that no feature has been found to distinguish, e.g., European, Asian, or American plants. Grundt et al. (2006) have, however, shown that this morphologically and cytologically uniform species include several cryptic species separated by sterility barriers, present both within and between regions (e.g., N Europe and Alaska).

Several authors concerned with the American plants have claimed transitions between D. fladnizensis and D. lactea to be common (e.g., Hultén 1945, 1968; Scoggan 1978). Such claims are unfounded; natural hybrids are unknown and artificial hybrids sterile. The claims are based on an erroneous morphological concept of the two species (i.e., much D. lactea misidentified as D. fladnizensis). Other authors have assumed the diploid D. fladnizensis to be parental, together with the diploid D. nivalis, in the predominantly hexaploid D. lactea (e.g., Knaben 1966). Also this claim seems to be unfounded and based on a provisional viewpoint that the hybridization behind the hexaploid D. lactea must have taken place among species present in the North Atlantic regions. Grundt et al. (2004) rather point towards an origin from the Beringian diploid and tetraploid (2n = 16, 32) D. palanderiana.

Even if D. fladnizensis is monomorphic, a few plants from Svalbard have been difficult to place within this global uniform pattern. They are from two populations from inner Wijdefjorden on Spitsbergen, found in 2010. They have a leaf pubescence different from any D. fladnizensis inspected worldwide, and are under investigation.

Literature

Brochmann, C. 1993. Reproductive strategies of diploid and polyploid populations of Arctic Draba (Brassicaceae). – Plant Systematics and Evolution 185: 55−83.

Grundt, H.H., Kjølner, S., Borgen, L., Rieseberg, L.H. & Brochmann, C. 2006. High biological species diversity in the arctic flora. – Proceedings of the National Academy of Sciences 103: 972−975.

Grundt, H.H., Popp, M., Brochmann, C. & Oxelman, B. 2004. Polyploid origins in a circumpolar complex in Draba (Brassicaceae) inferred from cloned nuclear DNA sequences and fingerprints. – Molecular and Phylogenetic Evolution 32: 695–710.

Hultén, E. 1945. Flora of Alaska and Yukon. V. Dicotyledoneae. Rhoeadales, Sarraceniales, Rosales I (Crassulaceae, Saxifragaceae). – Acta Universitas Lundensis, n. s., sect. 2, 41, 1: 797–978.

Hultén, E. 1968. Comments on the flora of Alaska and Yukon. – Arkiv för Botanik, ser. 2, 7, 1. 147 pp.

Knaben, G. 1966. Cytotaxonomical studies in some Draba species. – Botaniska Notiser 119: 427–444.

Scoggan, H.J. 1978. The Flora of Canada. 3. Dicotyledoneae (Saururaceae to Violaceae) (pp. 547–1115). – National Museum of Natural Sciences, National Museums of Canada, Ottawa.


 

Frøplante: Frø av denne arten er lagret i Svalbard globale frøhvelv, og deres spireevne vil bli sjekket med jevne mellomrom. (Alsos et al. In prep).

Scientific name, meaning and origin:

Draba: From greek drabe, sharp or besk, birning. Name on honningkarse hos Dioskorides, 70.

fladnizensis: From Flattnitz in Kärnten, Austria.

See all

Draba fladnizensis

English name:White Artic Whitlow-grass
German name:Fladnitzer Felsenblümchen
Norwegian name:Alperublom
Familiy:Brassicaceae

Scientific data:


Groupe:
Lifeform:Perennial shrub
Worldwide distribution:
Distribution on Svalbard:
Diploid/Polyploid:Diploid
Chromosome number (2n):16
Pollination vector:
Main mode of pollination:
Source: Brochmann, C. & Steen, S.W, 1999 - Sex and genes in the flora of Svalbard