Hibiscus verecundus McLay & Albr., 2023

McLay, Todd G. B., Barker, Robyn M. & Albrecht, David E., 2023, Morphological and environmental variation within Hibiscus krichauffianus (Malvaceae), and the recognition of two new species, H. verecundus and H. calcareus, Australian Systematic Botany 36 (6), pp. 457-477 : 471-473

publication ID

https://doi.org/ 10.1071/SB23003

persistent identifier

https://treatment.plazi.org/id/340B7504-FFBC-FFAD-465C-78E2FA4B230D

treatment provided by

Felipe

scientific name

Hibiscus verecundus McLay & Albr.
status

sp. nov.

Hibiscus verecundus McLay & Albr. View in CoL , sp. nov.

Type: Queensland , Poison Valley Track , White Mountains National Park, 13 Apr. 2000, K. R. McDonald KRM463 (holo: BRI AQ 496863 View Materials ! [Supplementary Fig. S3]; iso: DNA D0156915!) .

[ Hibiscus krichauffianus auct . non F.Muell.: F. J. H. von Mueller, Fragm. 6(46): 169 (1868), as ‘ H. krichauffi ’; E. J.Thompson et al., White Mountains Scientific Study Report, Geogr. Monogr. Ser. 9: 106 (2003); F. A.Zich et al., Australian Tropical Rainforest Plants Ed. 7 (2018); G. P.Guymer, Malvaceae View in CoL in G. K.Brown & P.D.Bostock, Census Queensland Fl. 2020 (2021), http://www.data.qld.gov.au/dataset/ census-of-the-queensland-flora-2020, accessed Aug. 2023].

Low, spreading, usually decumbent subshrub to 0.5 m tall. Branchlets very densely covered with sessile to shortly stalked stellate hairs 0.5–1 mm in diameter, indumentum yellowish-brown on younger branchlets, sometimes fading to white with age. Stipules persistent or abscising with age, filiform to filiform–subulate, 1.5–6 mm long, 0.1–0.17 mm wide. Mature leaves simple and unlobed, petiolate; petiole 5–15 mm long, densely to very densely covered with sessile or shortly stalked stellate hairs; lamina ovate to broadly ovate, rarely elliptic–ovate, flat to weakly concave or weakly folded, 9–52 mm long, 8–33 mm wide; base broadly cuneate, obtuse or truncate; margins serrate to dentate, rarely crenate; apex obtuse or occasionally acute; adaxial surface green to dark green, abaxial surface paler (except in young leaves); abaxial main and lateral veins raised and obvious or obscured by hairs; stellate hairs on adaxial surface moderate to dense, 0.4–0.8(–1) mm in diameter, sessile to shortly stalked, multiradiate with 5–18 rays; stellate hairs on abaxial surface moderate to very dense, 0.3–1 mm in diameter, sessile to shortly stalked, multiradiate with 7–22 rays. Flowers solitary in leaf axils; combined peduncle and pedicel 3–22 mm long, usually elongating in fruit, abscission line sometimes obvious, one-third to one-half the length from the base, indumentum as for young stems and petioles, pedicel broadening distally. Epicalyx lobes 5–7, narrowly

5 Note this specimen is currently identified as Melhania oblongifolia on the Australasian Virtual Herbarium ( AVH) site, but this is incorrect (https:// avh.ala.org.au/occurrences/fc878fa7-9670-4272-a8d1-c6932c6a4757, viewed 15 November 2022).

linear or subulate, 6–10 mm long, to ~ 1 mm wide, one-half to three-quarters the length of the calyx at anthesis, free to base or fused basally for up to ~ 0.5 mm, straight, not recurved apically, with moderate to dense stellate hairs abaxially. Calyx 9–15 mm long at anthesis, enlarging to 20 mm long in fruit; lobes narrowly triangular to triangular, 4.5–7 mm long at anthesis, enlarging to 12 mm long in fruit, abaxial indumentum of dense to very dense stellate hairs, adaxial indumentum of appressed or ascending 1- or 2-armed hairs intermixed with stellate hairs particularly distally. Petals 15–28 mm long, adnate to staminal column at base but otherwise free, light pink or white, sometimes drying pale yellow, lacking basal spot, glabrous adaxially, with sparse to moderate stellate hairs abaxially toward the margin on one side. Staminal column ~ 15.5 mm long, apex irregularly 5-lobed, with the stamens distributed singly along the distal 4–7 mm of the column; staminal filaments 2.5–5 mm long; anthers yellow. Style 5-branched, with branches 2.5–4 mm long, exserted 4–6 mm beyond the apex of the staminal column. Stigmas capitate, ~ 0.5 mm wide, distinctly hairy, hairs ~ 0.25 mm long. Ovary 5-locular, with hairs 0.4–0.9 mm long. Capsule ovoid to ellipsoid, 6–10 mm long, usually very shortly beaked, densely covered with stout shiny simple appressed hairs, the apical hairs erect, 1–1.5 mm long and extending beyond apex of capsule. Seeds angular–reniform with the two abaxial sides flat to convex, 1.7–2.3 mm long and almost forming a right angle at the junction, dark brown, with a short patchy indumentum of simple appressed white to yellowish-brown hairs with a minute persistent tubercle base, 0.25–0.4 mm long; funicular remnants brown, membranous and wing-like, one centrally placed and one on either side of the hilum, the central one occasionally detaching. ( Fig. 2 b, 3 b, 4 b.)

Distribution and habitat

Hibiscus verecundus is endemic to eastern central Queensland. Scattered populations occur within an area bound by Emerald in the south, Mt Garnet in the north, Duaringa in the east and Muttaburra in the west. Most occurrences are within the Leichhardt, Kennedy South and Kennedy North botanical regions, with fewer records from adjoining parts of the Cook, Burke and Mitchell botanical regions ( Fig. 1, orange circles).

The species occurs in shrublands, woodlands and forests featuring an overstorey of Acacia (especially A. shirleyi Maiden , and also A. rhodoxylon Maiden and A. catenulata C.T.White ), or Eucalyptus (e.g. E. persistens L.A.S.Johnson & K.D.Hill , E. melanophloia F.Muell. , E. thozetiana (F.Muell. ex Maiden) R.T.Baker , E. drepanophylla F.Muell. ex Benth. and E. similis, Maiden ) or Corymbia (e.g. C. citriodora (Hook.) K.D.Hill & L.A.S.Johnson , C. trachyphloia (F.Muell.) K.D.Hill & L.A.S.Johnson and C. clarksoniana (D.J.Carr & S.G.M.Carr) K.D.Hill & L.A.S.Johnson ). One specimen was collected in the remnants of semi-deciduous vine thicket. The

species occurs over a range of topographical positions including on ridges, plains, hillslopes, rocky outcrops, escarpments and gullies, and is typically associated with shallow soils overlying sandstone, laterite or basalt.

Phenology

Flowering specimens have been collected in January, March, April, May, June and November. Flowering is likely dependent on rainfall that predominantly occurs in summer within the geographic range of Hibiscus verecundus , but a reasonable amount of rainfall can occur in any month in the region.

Conservation status

Following International Union for Conservation of Nature (2012) threat assessment definitions, Hibiscus verecundus has an approximate Extent of Occurrence ( EOO) of 15 400 km 2 and occurs in several nature reserves (Epping Forest National Park, White Mountains National Park and Blackwood National Park). The species has a much smaller Area of Occupancy ( AOO) of 180 km 2 based on ~25 collections and populations seen by the authors are generally small (<10 plants) (but due to the small stature of the species individual plants could easily be overlooked). The conservation status is possibly of Least Concern but could be Vulnerable. Until further surveying is undertaken to obtain a more accurate estimation of population number and size, and population decline, the species should be considered Data Deficient.

Etymology

The species epithet is the Latin adjective verecundus , meaning modest or shy ( Lewis and Short 1879), referring both to the fact that this entity was overlooked despite being very distinct from Hibiscus krichauffianus and to the difficulty in finding this species in the field.

Affinities

Specimens of Hibiscus verecundus have previously been included within H. krichauffianus , though whether the two species are particularly closely related is uncertain. Hibiscus verecundus is readily distinguished from H. krichauffianus by the branchlet indumentum colour (yellowish-brown, sometimes fading to white, cf. white or silvery sometimes fading to yellowish-white in H. krichauffianus ), narrower stipules (0.1–0.17 mm wide, cf.> 0.16 mm in H. krichauffianus ), adaxial leaf lamina colour (green to dark green, cf. typically silvery-white in H. krichauffianus ), free or slightly basally fused epicalyx lobes (fused for up to 0.5 mm, cf. fused for 1–4 mm in H. krichauffianus ) that remain straight in fruiting specimens (cf. recurved or incurved in H. krichauffianus ) and seeds that are angular in profile (cf. rounded in profile in H. krichauffianus ), with an indumentum of shorter, more rigid appressed hairs (cf. longer wispy hairs that are not regularly appressed in H. krichauffianus ), and with a central and two marginal flaps of tissue associated with the hilum (cf. with only two marginal flaps in H. krichauffianus ). Hibiscus verecundus has a low usually decumbent habit, whereas in H. krichauffianus the stems are mostly erect or ascending. The habitat of H. verecundus is also completely different from that of H. krichauffianus , the former occurring in woodlands, forests and shrublands (rarely vine-thickets), whereas the latter occurs in more arid environments, typically on sand dunes.

Populations of the highly variable species Hibiscus sturtii and H. leptocladus occur within the distributional range of H. verecundus and could possibly be confused with this. Both H. sturtii and H. leptocladus represent species complexes that are currently undergoing taxonomic revision. Members of the H. sturtii complex have epicalyx lobes that are distinctly fused basally for> 4 mm (or if rarely less then the epicalyx lobes are never narrowly linear), whereas in H. verecundus the epicalyx lobes are free at the base or virtually so. The leaves of H. sturtii var. campylochlamys F.Muell. ex Benth. are similar to those of H. verecundus and the two taxa could be confused when flowers are lacking. Members of the H. leptocladus complex differ from H. verecundus in the erect or ascending habit, petals with a dark basal spot, capsules that never have a dense covering of appressed hairs throughout and the non-appressed seed hairs.

Notes

Due to the risk of damaging the few open flowers present on herbarium specimens (three specimens), some measurements, particularly of the androecium and gynoecium, are based on a small sample and may not truly reflect the range of variation in this species. Only chasmogamous flowers were seen in this species though an extensive field-based investigation has not been undertaken. This contrasts with Hibiscus krichauffianus that can have cleistogamous flowers.

Specimens examined (25 specimens seen)

QUEENSLAND. White Mountain National Park – NW of Warang, 3 Apr. 2000, B. S. Wannan 1736 & T . Daniel ( BRI, CANB); Red soil tableland south of Jervoise homestead, 9 June 1999, E. Addicott 248 ( BRI, MBA); On Myola Road , 48 km from Powlathanga homestead, 13 Mar. 1988, P. I. Forster 3665 & M. P . Bolton ( BRI); ~ 40 miles [~ 64 km] S of Mt Garnet , 24 June 1967, S. A. Morain 6 ( BRI); ~ 45 miles [~ 72 km] SE of Mt Garnet , 23 Jan. 1967, S. A. Morain 283 ( BRI); 15 km NE of Mt Cooper homestead in St Pauls Scrub, 15 June 1992, E. J. Thompson CHA145 View Materials & P. R . Sharpe ( BRI); Collinsville Coal Pty. Ltd. Mine lease area, near Collinsville and Scottville, 11 Nov. 1984, H. S. Thompson s.n. ( CANB); 3.5 km SW of Scott homestead, 3 Apr. 1992, E. J. Thompson BUC841 View Materials A & B. K . Simon ( BRI); 31.7 km from Gregory Development Rd into eastern Disney, 14 June 1997, S. Thompson 373 ( BRI); 48 km N of Belyando Crossing , 11 Dec. 1999, K. R. McDonald 190 ( BRI); SSW of junction of Belyando & Suttor Rivers, 24 May 1945, S. T. Blake 15714 & L. J . Webb ( BRI); 10 km W of St Anns homestead, 11 June 1992, E. J. Thompson BUC626 View Materials & P. R . Sharpe ( BRI, K); Vine Creek Holding, NW of Mt Coolon, 12 June 1997, R. J. Cumming 16035 ( BRI); Cometville (= Comet), 1879, P’A. O’Shanesy s.n. ( MEL); Dawson Range, 1.6 km S of Baralaba – Woorabinda Road, 26 Mar. 2005, A. R. Bean 23521 ( BRI); Dawson Highway, ~ 10 km W of Dawson River crossing, 2009, G. Harvey s.n. ( CANB); Humboldt , S of Blackwater, 7 Jan. 1997, R. J. Fensham 2991 ( BRI); Humboldt , S of Blackwater, 8 Jan. 1997, R. J. Fensham 2990 ( BRI); Terang Holdings , 4 km NE of South Blackwater Mine administration, 24 Nov. 1998, T. S. Ryan 1264 ( BRI); South Blackwater Mine , Laleham, 3 Jan. 1986, E. J. Thompson s.n. ( BRI); ~ 10 km due NNW of ‘ Exevale’ along the Pipeline – Eungella Dam Road, Nebo Shire, 18 Mar. 2003, A. B. Pollock 1564 & I. G . Champion ( BRI); Harrybrandt Station , 7 km W of Dingo / Mt Flora, Beef Road, 24 Jan. 1998, S. Thompson 566 & I . Fox ( BRI); Blackdown Tableland , 9 Apr. 1982, S. Pearson 471 ( BRI). Bullock Creek , NNW of Torrens Creek township, 27 Apr. 1990, R. J. Cumming 9553 ( BRI) .

K

Royal Botanic Gardens

R

Departamento de Geologia, Universidad de Chile

BRI

Queensland Herbarium

F

Field Museum of Natural History, Botany Department

J

University of the Witwatersrand

H

University of Helsinki

E

Royal Botanic Garden Edinburgh

A

Harvard University - Arnold Arboretum

G

Conservatoire et Jardin botaniques de la Ville de Genève

P

Museum National d' Histoire Naturelle, Paris (MNHN) - Vascular Plants

B

Botanischer Garten und Botanisches Museum Berlin-Dahlem, Zentraleinrichtung der Freien Universitaet

S

Department of Botany, Swedish Museum of Natural History

T

Tavera, Department of Geology and Geophysics

CANB

Australian National Botanic Gardens

MBA

Environmental Protection Agency

I

&quot;Alexandru Ioan Cuza&quot; University

M

Botanische Staatssammlung München

NE

University of New England

N

Nanjing University

L

Nationaal Herbarium Nederland, Leiden University branch

W

Naturhistorisches Museum Wien

MEL

Museo Entomologico de Leon

Kingdom

Plantae

Phylum

Tracheophyta

Class

Magnoliopsida

Order

Malvales

Family

Malvaceae

Genus

Hibiscus

Loc

Hibiscus verecundus McLay & Albr.

McLay, Todd G. B., Barker, Robyn M. & Albrecht, David E. 2023
2023
Loc

Hibiscus krichauffianus auct

White Mountains Scientific Study Report 2003: 106
Mueller 1868: 169
1868
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