Species
Veronica flavida
Etymology
Veronica: Named after Saint Veronica, who gave Jesus her veil to wipe his brow as he carried the cross through Jerusalem, perhaps because the common name of this plant is 'speedwell'. The name Veronica is often believed to derive from the Latin vera 'truth' and iconica 'image', but it is actually derived from the Macedonian name Berenice which means 'bearer of victory'.
flavida: pale yellow
Current Conservation Status
2012 - Not Threatened
Conservation status of New Zealand indigenous vascular plants, 2012
The conservation status of all known New Zealand vascular plant taxa at the rank of species and below were reassessed in 2012 using the New Zealand Threat Classification System (NZTCS). This report includes a statistical summary and brief notes on changes since 2009 and replaces all previous NZTCS lists for vascular plants. Authors: Peter J. de Lange, Jeremy R. Rolfe, Paul D. Champion, Shannel P. Courtney, Peter B. Heenan, John W. Barkla, Ewen K. Cameron, David A. Norton and Rodney A. Hitchmough. File size: 792KB
Previous Conservation Status
2009 - Not Threatened
2004 - Not Threatened
Authority
Veronica flavida (Bayly, Kellow et de Lange) Garn.-Jones
Family
Plantaginaceae
Brief Description
Bushy small tree with pairs of yellowish narrow leaves and upright flower spikes inhabiting upland western Northland. Leaves to 135mm long, by 29mm wide, central vein yellowish. Leaf bud without a gap. Flowers white, with a tube around equal the teeth of the green base, in erect spikes 4-25cm long.
Flora Category
Vascular - Native
Structural Class
Dicotyledonous Trees & Shrubs
Synonyms
Hebe flavida Bayly, Kellow et de Lange
Distribution
Endemic to Northland, North Island, where it occurs with certainty between Warawara Forest and
Waikaraka Valley in the north and Tangihua Forest in the south.
Habitat
Grows mostly in upland areas, above approximately 250 m a.s.l., often in cloud forest.
Features
Small tree (usually) or bushy shrub to 8 m tall. Branches erect, old stems brown or grey; branchlets green, puberulent to pubescent, hairs uniform; internodes (2.5-) 6-20 (-27) mm; leaf decurrencies evident (sometimes weakly). Leaf bud distinct; sinus absent. Leaves erecto-patent to patent; lamina linear-lanceolate to narrowly elliptic or oblanceolate, thin or subcoriaceous, flat or slightly m-shaped in transverse section (30-) 50-100 (-135) x (6-) 10-20 (-29) mm; apex acuminate or acute; brochidodromous secondary veins evident in fresh leaves; margin narrowly cartilaginous. puberulent, entire or distantly denticulate; upper surface light to dark green (with midrib and base of lamina usually yellow), dull, with few or without evident stomata, hairy along midrib; lower surface light green, hairy along midrib and sometimes covered with minute glandular hairs (when young) or rarely glabrous. Inflorescences with 60-140 (-155) flowers, lateral, unbranched (although one small secondary branch seen on one inflorescence of WELT 80664), (4-) 7-16 (-24.5) cm; peduncle
(0.7-) 1-3 (-4.5) cm; rachis (2.8 -) 5.5-14 (-20.5) cm. Bracts alternate, lanceolate or narrowly deltoid, acute, hairy outside. Flowers hermaphrodite. Pedicels 1.5-4.2 mm. Calyx 2.1-2.7 mm; lobes linear or narrowly deltoid, acute or acuminate, hairy outside. Corolla tube hairy inside and sometimes outside (near base of corolla lobes), 1.5-3 x 1.7-2.7 mm, funnelform, shorter than or equalling calyx (usually asymmetrically divided - anterior side is approximately equal to calyx, but posterior is shorter); lobes white or tinged mauve to pink at anthesis (sometimes very faintly), lanceolate (sometimes narrowly) or
ovate or elliptic, subacute (usually) or obtuse, suberect to patent, longer than corolla tube, sometimes sparsely hairy inside. Stamen filaments 5.5-6.8 mm; anthers violet or purple or blue, 1.5-2.5 mm. Ovary sometimes hairy, approximately 0.8-1 mm; ovules approximately 9-13 per locule; style 4-7.2 mm, sometimes hairy. Capsules, obtuse or subacute, 2.5-4 x (2-) 2.5-3.5 mm, sometimes hairy, loculicidal split extending ½-¾-way to base. Seeds flattened (sometimes strongly), more or less broad ellipsoid to discoid, pale brown, (0.8-) 0.9-1.4 (-1.6) x 0.7-1.2 mm, Micropylar rim 0.1-0.3 mm.
Similar Taxa
The three, species it most closely resembles are V. stricta (of which var. stricta occurs in Northland). V. rivalis and V. ligustrifolia. V. stricta has a similar shrubby habit and superficial appearance (although it doesn't grow as tall as V. flavida often does), but is readily distinguished by its flowers, which have corolla tubes much longer than the calyces. V. rivalis has flowers similar to V. flavida, with short corolla tubes, but differs most substantially in having leaves that are generally narrower both in absolute terms and in proportion to their length (they are (3-) 4-9(-12) wide, and linear or linear-lanceolate), and in that it is a low-growing shrub, usually not exceeding 1.2 m in height, that apparently grows exclusively on riverbanks, in the zone of vegetation subjected to occasional flooding. Differences from V. ligustrifolia are less clear-cut, but V. flavida often has longer leaves that are more conspicuously tapered toward the apex and a larger habit, and usually occupies more upland habitats. Flavonoid chemistry distinguishes V. flavida from all samples of V. stricta and V. rivalis, but not consistently from samples of V. ligustrifolia (Mitchell et al. in prep.). See also ‘Taxonomic Notes’ below.
Flowering
January-June
Flower Colours
White
Fruiting
March-June (-September)
Propagation Technique
Easy from fresh seed and semi-hardwood cuttings. A fast growing species which often forms a small tree 5-6 m tall.
Threats
Chromosome No.
2n = 40
Endemic Taxon
Yes
Endemic Genus
No
Endemic Family
No
Life Cycle and Dispersal
Seeds are wind dispersed (Thorsen et al., 2009).
Taxonomic notes
A new species described herein. It is distinguished from most species bythe combination of: a shrub to tree habit (up to approximately8 m tall, with trunk 10 cm dbh); no leaf bud sinus; corolla tubes shorter than or equalling calyx; mostly subacute corolla lobes; leaves with the upper surface of the petiole and base of midvein usually conspicuously yellow; and inflorescences that are usually held erect, even in fruit.
Specimens of V. flavida are not uniform in appearance. They vary in leaf shape and size, inflorescence length, and in the hairiness of stems, ovaries, undersides of leaf midribs and outer surfaces of calyx lobes. On some specimens the leaves are tightly arranged and restricted to the apices of branchlets, whereas on others the leaves are more widely spaced along the branchlets; these features probably vary with plant age and the degree of exposure of both whole plants and individual branches. Some herbarium specimens that might be V. flavida cannot be identified
with certainty without flowers, or without further information on habit or habitat. These include narrow-leaved, lowland specimens from Herekino (e.g. CHR 316527) and Warawara Forest (AK 175866) that might be V. rivalis or V. flavida.
Lowland specimens from Waipoua Forest, near the mouth of Ohae Stream (e.g. WELT 83433, AK 153629) and Kararoa Road (e.g. WELT 81935), are only tentatively identified as V. flavida, and their relationships to V. ligustrifolia and V. rivalis are worthy of further consideration. These specimens have reasonably long, broad leaves, and flowers (where present) with short corolla tubes. Some from Ohae Stream have flavonoid profiles generally similar to V. flavida, but in cultivation in Wellington have different flowering times and paler leaves than any other specimens of V. flavida. Vegetation around Ohae Stream is highly modified, and these Veronica’s might not be indigenous there.
Attribution
Description adapted by M. Ward from Bayly & Kellow (2006).
References and further reading
Bayly, M.J., Kellow, A.V. 2006. An illustrated guide to New Zealand Hebes. Wellington, N.Z.: Te Papa press pg. 194-195.
Mitchell, K. A., Markham, K. R. and Bayly, M. J. (2001). Flavonoid characters contributing to the taxonomic revision of the Hebe parviflora complex. Phytochemistry 56: 453-61.
Thorsen, M. J.; Dickinson, K. J. M.; Seddon, P. J. 2009. Seed dispersal systems in the New Zealand flora. Perspectives in Plant Ecology, Evolution and Systematics 11: 285-309
This page last updated on 13 Nov 2019