Species
Cardamine latior
Etymology
Cardamine: From the Greek name kárdamon, referring to an Indian spice
Common Name(s)
Auckland Islands bitter cress
Current Conservation Status
2012 - At Risk - Naturally Uncommon
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 - At Risk - Naturally Uncommon
2004 - Range Restricted
Qualifiers
2012 - IE, OL
2009 - RR, OL
Authority
Cardamine latior Heenan
Family
Brassicaceae
Flora Category
Vascular - Native
CARLAT
The
National Vegetation Survey (NVS) Databank is a physical archive and electronic databank containing records of over 94,000 vegetation survey plots - including data from over 19,000 permanent plots. NVS maintains a standard set of species code abbreviations that correspond to standard scientific plant names from the Ngä Tipu o Aotearoa - New Zealand Plants database.
Structural Class
Dicotyledonous Herbs other than Composites
Synonyms
None. First described in December 2008
Distribution
Endemic. Auckland Islands (Auckland and Adams Islands)
Habitat
Recorded growing among boulders and fellfield, particularly at higher altitudes on mountain top screes
Features
Perennial herb, caespitose, with many leaves forming a small, compact rosette. Leaves pinnate, up to 40–50 mm long, glabrous, green, ± coriaceous; petiole 8–12 mm long, 1.7–1.8 mm wide, winged and sheathing at base. Leaflets 11–15, in pairs and usually overlapping in distal part of leaf, alternate and distant in lower part of leaf, reniform, orbicular to broadly elliptic, hydathodes prominent on margin and in axil of petiolule, margin entire, base cordate, ± truncate to obtuse, apex obtuse to rounded; terminal leaflet lamina 3.5–4.7 × 3.5–4.1 mm, with 2 conspicuous lateral lobes; lateral leaflet lamina 1.5–2.5 × 0.7–2.2 mm; petiolules up to 0.5 mm long, often ± absent. Cauline leaves occasionally present subtending only the lower 1–2 flowers; similar to rosette leaves, but with fewer leaflets and smaller in all parts. Inflorescence usually up to 50 mm long, occ. 145 mm in sheltered sites, 1.2–1.6 mm diam. at base, glabrous, compact and not elongating after flowering, fastigiate, racemose, flowers usually
crowded in upper half. Pedicels 5–10(–17) mm long, 0.8–1.2 mm diam., usually erect. Sepals 2.0–2.4 × 0.7–1.2 mm, oblong to elliptic, glabrous, margin white and membranous, apex obtuse to rounded, base truncate. Petals 3.2–4.0 × 1.2–1.5 mm, white, pale pink or purple, limb obovate; apex obtuse to rounded; base cuneate to attenuate, tapering to an
indistinct claw. Filaments 6, 1.6–2.4 mm long; anthers 0.4–0.5 mm long. Ovary 1.5–2.6 mm
long, 0.5–0.6 mm diam., terete, glabrous; stigma 0.3–0.5 mm diam. Siliques 12–23 × 1.7–2.2 mm, crowded, erect, beak 0.7–1.4 mm long; replum 0.9–1.1 mm wide; septum with a prominent central vein. Seeds 1.4–2.1 mm long, 1.1–1.5 mm wide, 0.4–0.5 mm thick, rounded or oblong, red-brown.
Similar Taxa
Distinguished from the Campbell Island endemic Cardamine subcarnosa by shorter leaves with more leaflets, leaflets that overlap, more prominent leaf margin and axil hydathodes, short inflorescences, distinctly erect and broader siliques, and the septum with a distinct central vein.
Flowering
October – December
Flower Colours
Red / Pink,White
Fruiting
October – February
Propagation Technique
Not known from cultivation. Probably easy but likely to dislike high temperatures and humidity
Threats
Rated as Naturally Uncommon because this species is naturally confined to a restricted geographic area of <1000 km²
Endemic Taxon
Yes
Endemic Genus
No
Endemic Family
No
Life Cycle and Dispersal
Seeds are dispersed by ballistic projection, water and attachment (Thorsen et al., 2009).
Where To Buy
Not Commercially Available
Attribution
Description from: Heenan (2008)
References and further reading
Heenan, P.B. (2008). N.Z.Journal of Bot. 46(4): 559–566
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 2009 Vol. 11 No. 4 pp. 285-309
This page last updated on 25 May 2014