Classification
 Nomenclature
Scientific Name:
Veronica birleyi N.E.Br., Kew Bull. 8: 345 (1911)
Synonymy:
  • Parahebe birleyi (N.E.Br.) W.R.B.Oliv., Rec. Domin. Mus. 1: 230 (1944)
  • Hebejeebie birleyi (N.E.Br.) Heads, Bot. Soc. Otago Newsl. 36: 11 (2003)
Holotype: Top Ridge of Mt Bonpland, near L. Wakatipu, 2435 m, Feb 1908, L. S. Gibbs 1172, K. Isotypes: AK 8415, BM
  • = Veronica grahamii Petrie, Trans. & Proc. New Zealand Inst. 45: 273 (1913) – as Grahami
Lectotype (designated by Garnock-Jones & Lloyd 2004): Peak N. of Copeland Pass, 7000 ft, In Mar 1913, WELT 41402; Copeland Pass, 6800 ft, Graham, 5 Feb 1913, WELT 41403, 6115; Peak N. of Copeland Pass, Nr Mt. Cook, 7000 ft, Graham, 4 Mar 1912, WELT5121
Etymology:
Birleyi, after Harry Birley, climber, alpine guide, and explorer, of Glenorchy, who guided the collector of the holotype, Miss L.S. Gibbs (Godley 2004).
 Description

Low sub-shrub to 0.2 m tall. Stems decumbent to ascending, eglandular-pubescent, rarely a few glandular hairs as well; hairs uniform. Leaf bud indistinct; leaves separating while small, opposite-decussate, erecto-patent to spreading; lamina sub-coriaceous, elliptic, oblong, orbicular, broadly obovate, to obtriangular, 4–12 mm long, 2.5–11.0 mm wide, dull dark green to purplish-green above and beneath; veins obscure; surfaces densely eglandular-hairy above and beneath, occasionally with a few long, glandular hairs as well; margins ciliate, deeply crenate to lobed; lobes in 1–3 pairs; apex obtuse, rounded, truncate, or retuse; base cuneate; petiole 0–1 mm long. Inflorescence a lateral raceme 2–5 mm long or a solitary bibracteate flower; flowers distant, 2–3 or rarely solitary, all bisexual; bracts opposite, narrowly spathulate, > pedicels; pedicels erecto-patent, 0.3–1.5 mm long, eglandular-hairy all around. Calyx lobes 4, sub-acute or obtuse, 4–6 mm long, equal, mixed eglandular- and glandular-hairy. Corolla 7–10 mm diameter; tube white and greenish-yellow, 3–4 mm long, < calyx, glabrous; lobes 5, sometimes 4, white, spreading to recurved, unequal, elliptic to orbicular, 3–5 mm long, obtuse to rounded; nectar guides absent. Stamen filaments white, 2–3 mm long; anthers pink, magenta, or purplish. Style glabrous, 1.0–1.5 mm long. Capsules angustiseptate, emarginate, glabrous, 3–4 mm long, 3–4 mm at widest point. Seeds elliptic to obovate, flattened, smooth, buff to brown, 0.6–1.0 mm long.

 Recognition

V. birleyi and three similar species, V. spectabilis, V. densifolia, and V. trifida, are placed together in the snow hebe group. Veronica birleyi is distinctive. The unusual combination of broad, blunt, dull dark green, hairy leaves, often purplish (especially beneath), white solitary flowers, or 2 to 3 together, and short stamens and style enclosed in the corolla tube, is shared only with V. spectabilis, to which it is probably closely related. So far as is known, V. spectabilis plants are generally larger, and differ in having a higher proportion of glandular hairs on the leaves and inflorescences, longer inflorescences (10–25 mm long), much larger flowers (18–25 mm diameter), usually with 4 corolla lobes, and hairy capsules. In V. spectabilis the longer peduncles and pedicels tend to cause the flowers to be more exserted than they are in V. birleyi. The related V. trifida and V. densifolia are similar, but have bronze or yellowish leaves, which are narrower, and in V. densifolia usually entire.

(See: Morphological features to distinguish the snow hebes in Veronica sensu lato: i.e. Chionohebe, Hebejeebie, Parahebe p.p.​​​​​​​)

Morphological features to distinguish the snow hebes in Veronica (sensu lato: i.e. Chionohebe, Hebejeebie, Parahebe p.p.). Species are ordered according to similarity of their habit.

 

birleyi

spectabilis

trifida

densifolia

thomsonii

pulvinaris

chionohebe

ciliolata

Habit

lax sub-shrub

lax sub-shrub

lax sub-shrub

lax sub-shrub

cushion plant

cushion plant

cushion plant

cushion plant

Stem hairs

eglandular & a few glandular, spreading

mixed glandular & eglandular, spreading

eglandular, retrorse

eglandular, retrorse

glabrous

glabrous

glabrous

glabrous

Leaf size (mm)

4.0–12 × 2.5–11

4.5–13 × 2.5–6.0

2–10 × 1–7

2–6.5 × 0.7–3

1.7–4.7 × 0.7–2.6

1.8–4.8 × 0.5–2

1.75–5 × 0.75–2.25

1.75–4.5 × 0.8–2.8

Leaf margins

deeply crenate to lobed

deeply crenate to lobed

shallowly toothed to lobed, rarely entire

usually entire, rarely 1–2 teeth or lobes

entire

entire

entire

entire

Lamina

subcoriaceous, flat; margin not thickened, smooth

subcoriaceous, flat; margin not thickened, smooth

subcoriaceous, flat; margin not thickened, smooth

coriaceous, keeled, with thickened papillate margin

thin, flat; margin not thickened, smooth

thin, flat; margin not thickened, smooth

thin, flat; margin not thickened, smooth

thin, flat; margin not thickened, smooth

Leaf hairs: adaxial

scattered eglandular

mixed eglandular & glandular

glabrous

glabrous

eglandular: in broad band across middle, occasionally scattered distally

eglandular appressed: scattered or in a central patch on distal half

absent

absent or isolated and scattered in distal ½

Leaf hairs: abaxial

scattered eglandular

mixed eglandular & glandular

glabrous

glabrous

glabrous, or stiff, eglandular, isolated distal hairs

glabrous or eglandular appressed scattered distally

absent or isolated in distal ½

absent or isolated and scattered in distal ½

Leaf hairs: margin

eglandular-ciliate

mixed eglandular & glandular-ciliate

long glandular-ciliate

stiff eglandular-ciliate

ciliate in basal ⅔ with apical tuft

eglandular appressed: ciliate

absent or scattered cilia

ciliate throughout or in basal or distal half, usually with apical tuft

Sexual system

cosexual

cosexual

cosexual

cosexual

dioecious

dioecious

dioecious

dioecious

Inflorescence

2–3 flowers, sometimes solitary bibracteolate

2–3 flowers, sometimes solitary bibracteolate

2–3 flowers, sometimes solitary bibracteolate

solitary bibracteolate

solitary bibracteolate

solitary bibracteolate

solitary bibracteolate

solitary bibracteolate

Peduncle (mm)

2–4

5–15

2–10

0

0

0

0

0

Pedicel (mm)

0.3–1.5

2.5–5

0.5–7

0

0

0

0

0

Calyx lobes

4

4

4

5

5

5

5

5

Corolla lobes

(4–)5(–6)

4(–5)

5(–6)

5(–6)

5

5

5

5

Corolla diameter (mm)

7–10

18–25

15–20

7–16

2.5–5

2.5–6

1.5–4.1

2.1–6.5

Corolla shape

funnelform

funnelform

funnelform

funnelform

rotate

rotate

rotate

rotate

Capsule size (mm)

3–4 × 3–4

4–5 × 4–5

4.5–6 × 2.5–3

2.7–5 × 1.7–4.25

1.5–3 × 1–2

1–3 × 1.2–2.7

1.9–2.5 × 1.5–1.9

2.5–3.5 × 1.4–3.1

Capsule hairs

glabrous

mixed glandular & eglandular-hairy at apex

glandular-ciliate, sometimes glabrous

glabrous

glabrous to densely hairy at apex

eglandular-hairy, especially at apex

absent

absent or apical

 Distribution

South Island: Canterbury, Westland, Otago (Remarkables), Southland (Eyre Mountains), Fiordland; mostly along and close to the main divide from Mt Westland to Mt Tūtoko.

 Habitat

Nival rock crevices. Recorded elevations range from 1830 to 2835 m.

 Biostatus
Indigenous (Endemic)
 Phenology

Flowers: December–March; fruits: January–March.

 Cytology

2n = 42 (Hair 1970).

 Notes

Veronica birleyi is classified in V. subg. Pseudoveronica sect. Hebe and informally in the “snow hebe” group (Albach & Meudt 2010). It has not been included in molecular phylogenetic studies so far; records under the name Parahebe birleyi refer to material of V. spectabilis. Morphological similarities suggest a close relationship to V. spectabilis, and it is likely these are allopatric sister species. Its wider relationships are with V. trifida and V. densifolia and the cushion snow hebes (e.g., V. pulvinaris).

V. birleyi is one of a trio that attains the highest altitudes of flowering plants in New Zealand, about 2900 m (the others are V. epacridea and  Ranunculus grahamii).

 Bibliography
Albach, D.C.; Meudt, H.M. 2010: Phylogeny of Veronica in the Southern and Northern Hemispheres based on plastid, nuclear ribosomal and nuclear low-copy DNA. Molecular Phylogenetics and Evolution 54: 457–471.
Brown, N.E. 1911: Veronica birleyi N.E. Brown. Kew Bulletin 8: 345.
de Lange, P.J.; Rolfe, J.R.; Barkla J.W.; Courtney, S.P.; Champion, P.D.; Perrie, L.R.; Beadel, S.N.; Ford, K.A.; Breitwieser, I.; Schönberger, I.; Hindmarsh-Walls, R.; Heenan, P.B.; Ladley, K. 2018: Conservation status of New Zealand indigenous vascular plants, 2017. New Zealand Threat Classification Series. No. 22. [Not Threatened]
de Lange, P.J.; Rolfe, J.R.; Champion, P.D.; Courtney, S.P.; Heenan, P.B.; Barkla, J.W.; Cameron, E.K.; Norton, D.A.; Hitchmough, R.A. 2013: Conservation status of New Zealand indigenous vascular plants, 2012. New Zealand Threat Classification Series 3. Department of Conservation, Wellington. [as Hebejeebie birleyi (N.E.Br.) Heads] [Not Threatened]
Garnock-Jones, P.J. 2023: Veronica. In: Breitwieser, I. (ed.) Flora of New Zealand – Seed Plants. Fascicle 9. Manaaki Whenua Press, Lincoln.
Garnock-Jones, P.J.; Albach, D.; Briggs, B.G. 2007: Botanical names in Southern Hemisphere Veronica (Plantaginaceae): sect. Detzneria, sect. Hebe, and sect. Labiatoides. Taxon 56: 571–582.
Garnock-Jones, P.J.; Lloyd, D.G. 2004: A taxonomic revision of Parahebe (Plantaginaceae) in New Zealand. New Zealand Journal of Botany 42: 181–232.
Godley, E.J. 2004: Biographical Notes (55): Lilian Suzette Gibbs (1870–1925) and Harry Birley (c.1863–1924). New Zealand Botanical Society Newsletter 77: 22–23.
Hair, J.B. 1970: Contributions to a chromosome atlas of the New Zealand flora — 13. Parahebe and Pygmea (Scrophulariaceae). New Zealand Journal of Botany 8: 255–259.
Heads, M.J. 2003: Hebejeebie (Plantaginaceae), a new genus from the South Island, New Zealand, and Mt. Kosciusko, SE Australia . Botanical Society of Otago Newsletter 36: 10–12.
Oliver, W.R.B. 1944: The Veronica-like species of New Zealand. Records of the Dominion Museum, Wellington 1: 228–231.
Petrie, D. 1913: Descriptions of new species and varieties of native phanerogams. Transactions and Proceedings of the New Zealand Institute 45: 265–275.