Classification
 Nomenclature
Scientific Name:
Veronica trifida Petrie, Trans. & Proc. New Zealand Inst. 55: 437 (1924)
Synonymy:
  • Parahebe trifida (Petrie) W.R.B.Oliv., Rec. Domin. Mus. 1: 230 (1944)
  • Hebejeebie trifida (Petrie) Heads, Bot. Soc. Otago Newsl. 36: 11 (2003)
Holotype: Garvie Range, Speden & Darton, WELT 5120 (Petrie Herbarium)
Etymology:
The epithet trifida is a reference to the commonly trifid leaves that are characteristic of the species, although the leaves sometimes have five teeth or lobes.
 Description

Low sprawling or creeping sub-shrub to 0.2 m tall. Stems prostrate, ascending at tips, eglandular-pubescent; hairs uniform. Leaf bud indistinct; leaves separating while very small, opposite-decussate to sub-distichous, erecto-patent. Lamina thin to sub-coriaceous, elliptic, obovate, oblong, oblanceolate, or spathulate, rarely sub-orbicular, 2–10 mm long, 1–7 mm wide, glossy green or bronze-green above and beneath; veins not evident; surfaces glabrous; margin sparsely glandular-ciliate, rarely some eglandular hairs as well, serrate, crenate or lobed; teeth or lobes in 1–3 pairs; apex obtuse, rounded, or sub-acute; base cuneate; petiole 1–2 mm long. Inflorescence a lateral raceme, 15–25 mm long; flowers crowded or distant, 2–3 or solitary and bibracteate; peduncle 2–10 mm long, all bisexual; bracts opposite or alternate, elliptic or obovate, >pedicels; pedicels sub-erect, 0.5–7.0 mm long, mixed glandular- and eglandular-hairy all around. Calyx lobes 4, rarely reduced 5th lobe present, obtuse to sub-acute, 4.0–5.5 mm long, equal, glandular-hairy with a few eglandular hairs. Corolla 15–20 mm diameter; tube white, rarely purplish, greenish-yellow at the base, 3–4 mm long, < calyx, glabrous; lobes 5, sometimes 6, white, rarely purplish, erecto-patent to recurved, unequal, elliptic to obovate or orbicular, 6–11 mm long, obtuse to rounded; nectar guides absent. Stamen filaments white or greenish, 2–3 mm long; anthers purple, sometimes magenta or pink. Style glabrous, 2.5–4.0 mm long. Capsule angustiseptate, emarginate, glabrous or with a few glandular hairs, 4.5–6.0 mm long, 2.5–3.5 mm at widest point. Seeds ellipsoid to obovoid, flattened, smooth, pale brown to brown, 0.8–1.2 mm long.

 Recognition
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: Otago (Hector Mountains, Old Man Range, Garvie Mountains, Umbrella Mountains, Lammermoor Range), Southland (Cecil Peak).

 Habitat

Alpine seepages and flushes of melt-water associated with summer snow-banks, edges of water races, boggy ground. Recorded elevations range from 1070 to 1840 m.

 Biostatus
Indigenous (Endemic)
 Hybridisation

Where the ranges of V. trifida and V. chionohebe meet (Garvie Mountains, Old Man Range) hybrids between them are quite frequent (Garnock-Jones & Lloyd 2004). Such plants are lax, softly woody sub-shrubs to about 5 cm tall; leaves entire, margin ciliate and glandular-ciliate; flowers solitary, axillary, bibracteate; pedicel c. 0.8 mm long; calyx 3-nerved with a few cilia, both glandular and eglandular, 3 mm long; calyx lobes 5, regular or 1 smaller, obovate-elliptic, with glandular and eglandular cilia (glandular distally); corolla rotate, 7 mm diameter, tube c. 2.5 mm (< calyx).

 Phenology

Flowers: December–February: fruits: January–April (and probably persisting longer).

 Cytology

2n = 42 (Hair 1970).

 Notes

Veronica trifida is classified in V. subg. Pseudoveronica sect. Hebe and informally in the “snow hebe” group (Albach & Meudt 2010).

Analysis of ITS sequence data indicates V. trifida is sister species to V. densifolia, and its next nearest relative is V. spectabilis (and probably V. birleyi). These species are morphologically similar in growth form, leaf lobing (when present), inflorescences, five- to six-lobed corollas, and short stamens and styles. The ITS tree topology suggests this group is sister to a large clade of shrubby hebes, sun hebes and speedwell hebes, but field observations and phylogenetic analysis of chloroplast DNA indicate they hybridise with the cushion snow hebes, and that process probably includes chloroplast exchange. Thus cpDNA sequences of V. densifolia and V. spectabilis cluster with those of V. pulvinaris and V. thomsonii, whereas those of V. trifida cluster with V. ciliolata, V. chionohebe (with which hybrids are observed in the field), and another accession of V. thomsonii.

The leaves often dry black in herbarium specimens, but retain their glossy surface. The margins of the corolla lobes are finely fimbriate or erose.

The earlier V. trifida Gilibert, Flora Lithuanica 1, 121 (1785), based on a different type, is not a legitimate name because the work it is published in is listed in Opera Utique Oppressa (http://www.bgbm.org/iapt/nomenclature/code/saintlouis/0116AppendixV.htm).

 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.
de Lange, P.J.; Norton, D.A.; Courtney, S.P.; Heenan, P.B.; Barkla, J.W.; Cameron, E.K.; Hitchmough, R.; Townsend, A.J. 2009: Threatened and uncommon plants of New Zealand (2008 revision). New Zealand Journal of Botany 47: 61–96. [as Hebejeebie trifida (Petrie) Heads] [Naturally uncommon]
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. [Naturally Uncommon]
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 trifida (Petrie) Heads] [Naturally Uncommon]
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.
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. 1924: Descriptions of new native flowering-plants. Transactions and Proceedings of the New Zealand Institute 55: 434–437.