Hebe perbella de Lange
Vascular – Native
Trees & Shrubs - Dicotyledons
2n = 40
Current conservation status
The threat classification status of all known New Zealand vascular plant taxa at the rank of species and below were reassessed in 2017 using the New Zealand Threat Classification System (NZTCS) – more information about this can be found on the NZTCS website This report includes a statistical summary and brief notes on changes since 2012 and replaces all previous NZTCS lists for vascular plants. Authors: By Peter J. de Lange, Jeremy R. Rolfe, John W. Barkla, Shannel P. Courtney, Paul D. Champion, Leon R. Perrie, Sarah M. Beadel, Kerry A. Ford, Ilse Breitwieser, Ines Schönberger, Rowan Hindmarsh-Walls, Peter B. Heenan and Kate Ladley. Please note, threat classifications are often suggested by authors when publications fall between NZTCS assessment periods – a suggested threat classification status has not been assessed by the NZTCS panel.
2017 | Threatened – Nationally Endangered | Qualifiers: RR, Sp
Previous conservation statuses
2012 | Threatened – Nationally Endangered | Qualifiers: DP, RR, Sp
2009 | Threatened – Nationally Endangered | Qualifiers: DP, RR, Sp
2004 | Threatened – Nationally Vulnerable
Bushy shrub bearing pairs of narrow leaves and spikes of pinkish flowers on reddish stems inhabiting upland western Northland. Leaves dark green, to 110mm long by 25mm wide, tapering to a rounded tip. Leaf bud without a gap at base. Flower spikes to 15cm long.
Endemic. North Island. Known only from the west coast of Northland from Kaitaia to the Waima Forest
Montane cloud forest where it grows on rock outcrops and cliff faces, also at the base of scrub fringing steep sided streams and gorges, and in one site growing from dense Astelia colonies on an exposed rock outcrop.
Erect shrub, up to 1 m tall in exposed sites, occasionally reaching 1.8 m in dense vegetation. Mature branchlets purple-grey, fading to grey on 2–3-year-old wood; branchlets fleshy, green, greenish-purple, sometimes spotted red, drying purple-black, flattened and ridged, minutely puberulent, hairs bifarious; leaf decurrencies prominent as a narrow medial ridge, this often tinged pink or red; internodes 2–10× diameter. Leaf bud strongly flattened, olive-green, midrib and lamina margin pink; sinus absent. Leaves (63–)87–110(–220) × (9–)10–14(–23) mm, patent to erecto patent, lamina lanceolate or oblanceolate, firmly fleshy, adaxial surface dark green, midrib orange green or pale green above, usually pink below, minutely eglandular/glandular hairy, adaxial lamina surface glossy, ± glabrous, except for sparse minute eglandular hairs at leaf base, abaxial surface dull pale green, apex cream, obtuse to subacute, base attenuate; margin entire, glabrous, often tinged pink. Inflorescences with 15–80 flowers, lateral, racemose, simple, occasionally double branched from basal bracts, rarely ternate, 60–100(–150) mm long, flowers usually crowded on rachis, sometimes widely spaced, spiraled. Peduncle and rachis with minute spreading eglandular hairs, usually reddish brown, fading to pinkish green at fruit maturation, sometimes yellow-green, peduncle 40–100 mm long. Basal bracts foliose, olive-green, usually falcate, lanceolate 7–19 mm long, upper bracts 3–4 mm long, violet-maroon, linear, acute, margins involute, minutely puberulent. Pedicels spreading 2–5 mm long, reddish brown, rarely pink. Flowers protandrous, hermaphrodite, faintly sweet-scented, usually single but occasionally peloric near raceme apex. Calyx 4–5-lobed, 2.6–3.3 mm long, violet fading to lilac, narrowly lanceolate to lanceolate, acuminate, overlapping at edges, outer surface with scattered minute sessile glands; margin ± alternating glandular-eglandular ciliolate. Corolla violet-red, violet, occasionally pink or dark carmine, maturing mauve, usually fading to off white following anthesis, tube 1.8–2.2 × 1.8–2.8 mm, narrow, usually included within calyx lobes, inner surface ± glabrous, lobes (4.8–)5.0–6.5 × (2.0–)2.5–3.0 mm, erect to suberect, becoming reflexed following anthesis, narrowly lanceolate, lanceolate to narrowly ovate, subauriculate and minutely ciliolate at base, acute. Stamen filaments 7–10 mm long, pink or violet-red fading to white with age, curving outwards after dehiscence, base minutely puberulent; anthers 2.0–2.8 mm long, blue to purple, acute, pollen cream. Nectarial disc glabrous, fleshy, dark green. Style 8–10 mm long, violet-red, glabrous, stigma capitate, pink. Ovary 1.0 × 0.6 mm, pale pink, cylindrical, sparsely to distinctly puberulent especially in lower third and along septal grooves; hairs eglandular. Peloric flowers scarce, confined to distil portion of racemes; in structure similar to single flowers but fused for length of calyx and corolla tube, otherwise with 8 corolla lobes, 2 stamens, 2 fused pistils, and 2 fused ovaries. Capsule latiseptate, 7–8 × 5–6 mm, amber to amber-brown, rhombic to ovate, sharply acute, sparsely to distinctly hairy, septicidal to base, loculicidal for 1/3–½ length. Seeds 1.8 × 2.0 mm, amber, ovate, slightly papillate with a narrow marginal wing.
Veronica saxicola is a closely related species (see de Lange & Rolfe 2008). From V. perbella, V. saxicola is distinguished by its ecology, smaller stature, shorter and wider leaves with dull rather than glossy upper leaf surfaces, less colourful flowers that open pale lavender or lilac soon fading to white, shorter corolla tube, broader lanceolate to ovate, subacute corolla lobes, mostly glabrous ovaries, and glabrous capsules. Veronica saxicola also has a different flavonoid chemistry to V. perbella. Veronica perbella is superficially similar to V. adamsii from which it differs by its diploid (2n = 40) rather than tetraploid (2n = 80) chromosome number, absence of a leaf-bud sinus, and sparsely pubescent ovaries.
March to December (often with two distinct peaks in April and October)
April to February
Seeds are wind dispersed (Thorsen et al., 2009).
Very easily grown from fresh seed and semi hardwood cuttings.
This species is very uncommon throughtout its range. A detailed assessment of the threats facing this species is given by de Lange & Rolfe (2008). Often the habitats it occupies are a few square metres in extent, and so it is very vulnerable to weed invasion, animal browse, and because it colonises freshly disturbed ground within forest, natural succession to forest can be a threat in some locations. In many of its habitats it is threatened by goat browse. Some northern populations are threatened by weeds and residential development.
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’.
perbella: From the Latin per ‘very, exceedingly’ and bellus ‘beautiful’
Plants from Maungaraho Rock previously included in Veronica (Hebe) perbella (de Lange 1998) were later described as a new, allied species, Veronica (Hebe) saxicola (de Lange & Rolfe 2008).
Fact sheet prepared for NZPCN by P.J. de Lange (13 October 2008). Description from de Lange & Rolfe (2008).
References and further reading
de Lange, P.J. 1998: Hebe perbella (Scrophulariaceae) - a new and threatened species from western Northland, North Island, New Zealand. New Zealand Journal of Botany 36: 399-406.
de Lange, P.J.; Rolfe, J.R. 2008: Hebe saxicola (Plantaginaceae) – a new threatened species from western Northland, North Island, New Zealand. New Zealand Journal of Botany 46: 531-545.
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
NZPCN Fact Sheet citation
Please cite as: de Lange, P.J. (Year at time of access): Veronica perbella Fact Sheet (content continuously updated). New Zealand Plant Conservation Network. https://www.nzpcn.org.nz/flora/species/veronica-perbella/ (Date website was queried)