A NSW Government website

Prostanthera gilesii, a shrub - critically endangered species listing

01 Dec 2017

The NSW Threatened Species Scientific Committee, established under the Biodiversity Conservation Act 2016 (the Act), has made a Final Determination to list the shrub Prostanthera gilesii Althofer ex B.J.Conn & T.C.Wilson as a CRITICALLY ENDANGERED SPECIES in Part 1 of Schedule 1 of the Act. Listing of Critically Endangered species is provided for by Part 4 of the Act.

NSW Threatened Species Scientific Committee - final determination

The NSW Threatened Species Scientific Committee has found that:

1. Prostanthera gilesii Althofer ex B.J.Conn & T.C.Wilson (family Lamiaceae) is described as a “small, compact, spreading shrub, up to 1 m high, with the populations formed by a tangle of individual plants. Branchlets ± terete, moderately hairy on distal internodes and nodes with antrorse hairs, becoming sparsely hairy, glands indistinct. Leaves dark green, glossy, paler below, aromatic; petiole 1–2 mm long; lamina narrowly ovate to elliptic, 15–26 mm long, 5–10 mm wide, a few hairs on midrib, otherwise glabrous, margin entire; apex obtuse; venation indistinct, midrib slightly raised on abaxial surface. Inflorescence in groups of 3–4, sometimes 6 flowers; calyx green; outer surface glabrous, moderately glandular; inner surface of tube glabrous, lobes densely hairy near margin and apex; corolla 12–15 mm long, white to yellowish white, with purple to dark mauve markings on the inner surface of the tube and base of adaxial median lobe-pair, with pale orange marking on base of abaxial median lobe; hairs crinkled. Fruiting calyx not or only slightly enlarged (only immature fruits seen). Mature mericarps and seeds not seen” (PlantNET 2017).

2. Prostanthera gilesii is endemic to New South Wales (NSW) and is currently only known from Mount Canobolas, approximately 13 km west south west of Orange in central western NSW (Conn and Wilson 2015). There are two known populations within the Mount Canobolas State Conservation Area (Conn and Wilson 2015).

3. The largest population of Prostanthera gilesii occurs along a creek-line in wet sclerophyll forest dominated by tall  Eucalyptus dalrympleana subsp.  dalrympleana, with scattered  E. canobolensis and  E. dives. The understory consists predominantly of  Mirbelia oxylobioides,  Cassinia longifolia,  Pteridium esculentum,  Polyscias sambucifolia and thickets of exotic Blackberry ( Rubus fruticosus agg.). The soil is a deep basaltic clay-loam (krasnozem) with alluvial deposits on the lower slopes. The second, smaller population of  P. gilesii occurs in a steep rock crevice of a trachyte rocky outcrop. The crevice is fed by seepage and the soil is likely to be formed from rock scree and detritus. The surrounding vegetation is heath with the occasional small tree of  Exocarpos cupressiformis (native cherry) and  Eucalyptus canobolensis. The heath is dominated by  Pteridium esculentum,  Mirbelia oxylobioides,  Phebalium sp.,  Calytrix tetragona and  Kunzea parvifolia.

4. Little is known about the ecology of Prostanthera gilesii. Mature plants characteristically form a tangled divaricate mass, making it difficult to estimate the numbers of individuals.  Prostanthera gilesii easily readily roots from layered stems and may be clonal, suggesting that genetic diversity within the species is low. Notes associated with past collections (AVH 2016) indicate  P. gilesii may not readily set seed, and Conn and Wilson (2015) did not describe the mature mericarps or seed as none was seen on the specimens examined.

5. The number of mature individuals of Prostanthera gilesii is extremely low, estimated to be fewer than 50 plants (name withheld  in litt. January 2016).

6. The geographic distribution of Prostanthera gilesii is very highly restricted. The area of occupancy (AOO) and extent of occurrence were both estimated to be 4 km2 . The AOO is based on 2 x 2 km grid cells, the scale recommended for assessing AOO by IUCN (2016).

7. There are a number of threats currently affecting Prostanthera gilesii including competition from weeds, disturbance from feral pigs ( Sus scrofa), human visitation and soil pathogens (name withheld  in litt. January 2016; S. Woodhall pers. comm. Dec 2016). Blackberry ( Rubus fruticosus agg.) infestations surround and encroach upon the larger  P. gilesii population and although the smaller population is currently free of exotic plant species, Blackberry occurs nearby. Blackberry is likely to compete with P. gilesii, provide habitat for feral pigs and may build fuel loads that could potentially increase the severity of fire (name withheld  in litt. January 2016). Other exotic plants in nearby areas of Mt Canobolas include English Ivy ( Hedera helix), Elderberry ( Sambucus nigra), Radiata Pine ( Pinus radiata) and English Holly ( Ilex aquifolium) (name withheld i n litt. January 2016). Damage caused by feral pigs is evident in the nearby riparian zone of the creek-line site (name withheld  in litt. January 2016). Feral pigs cause substantial soil disturbance, introduce weeds and spread soil borne diseases. The pathogenic soil fungus  Phytophthora was detected in the population following observations of dieback in several  Prostanthera gilesii plants. Whilst it was not the highly pathogenic species  Phytophthora cinnamomi, most  Phytophthora species are potentially pathogenic given the right environment and host (Botanic Gardens Trust  in litt. August 2015). Human visitation to both sites may lead to the spread of  Phytophthora sp., trampling of the plants and the introduction of weeds. In addition, unauthorised collection of plant material has occurred (name withheld  in litt. January 2016). The response of  Prostanthera gilesii to fire is unknown, however the persistence of this species is likely to be dependent on an appropriate fire regime and associated fire mitigation activities. ‘Invasion and establishment of exotic vines and scramblers’, ‘Loss and degradation of native plant and animal habitat by invasion of escaped garden plants, including aquatic plants’ and ‘Predation, habitat degradation, competition and disease transmission by Feral Pigs,  Sus scrofa Linnaeus 1758’ are listed as Key Threatening Processes under the Act.

8. Prostanthera gilesii Althofer ex B.J.Conn & T.C. Wilson is eligible to be listed as a Critically Endangered species as, in the opinion of the Scientific Committee, it is facing an extremely high risk of extinction in Australia in the immediate future as determined in accordance with the following criteria as prescribed by the  Biodiversity Conservation Regulation 2017:

Clause 4.3 - Restricted geographic distribution of species and other conditions (Equivalent to IUCN criterion B)

The geographic distribution of the species is:
(a)for critically endangered speciesvery highly restricted.
and the following conditions apply:
(d) the population or habitat of the species is severely fragmented or nearly all the mature individuals of the species occur within a small number of locations,
(e)there is a projected or continuing decline in the following:
 (iii) habitat area, extent or quality

Clause 4.5 - Low total numbers of mature individuals of species (Equivalent to IUCN criterion D)

The total number of mature individuals of the species is:
(a)for critically endangered species
extremely low.

Dr Marco Duretto
Chairperson
NSW Threatened Species Scientific Committee

Exhibition period: 01/12/17 – 26/01/18
Proposed Listing date: 01/12/17

References:

AVH (2016) Australia’s Virtual Herbarium, Council of Heads of Australasian Herbaria (accessed 25 October 2016).

Conn BJ, Wilson TC (2015) Two new species of Prostanthera (Lamiaceae) in New South Wales. Telopea 18, 463–474.

IUCN Standards and Petitions Subcommittee (2016) Guidelines for Using the IUCN Red ListCategories and Criteria. Version 12. Prepared by the Standards and Petitions Subcommittee.

PlantNET (The NSW Plant Information Network System) Royal Botanic Gardens and Domain Trust, Sydney (accessed 7 August 2017).

Contact us

Threatened Species Scientific Committee

Email: [email protected]