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===Overview: ===
<i>Archontophoenix</i> H. Wendland & O. Drude is a
genus of single-stemmed, pinnate-leaved, monoecious, Arecoid
palms endemic to eastern Australia.
The genus was established in 1875 by Hermann Wendland and
Oscar Drude in the journal Linnaea. Though no type species
was designated at the time of publication, the accepted
lectotype is <i>A. alexandrae</i>
(F. Mueller) H. Wendland & Drude
(=<i>Ptychosperma alexandrae</i> F. Mueller) which was
described in the same publication.
A number of other names have been applied to the genus; for
example <i>Seaforthia, Ptychosperma</i>, <i>Loroma</i> and <i>Jessenia</i>.
The genus is rather undifferentiated and the species do not
display a great degree of variation. The main features of the
genus include: solitary habit; tall erect trunk; leaf bases
forming an elongate crownshaft; leaves paripinnate; pinnae
linear-acute with a prominent midrib raised on both surfaces;
inflorescence infrafoliar at maturity, protandrous, branched
to three or four orders; two bracts which fully enclose the
inflorescence in bud, the prophyll attached at the base of
the peduncle, fully enclosing the peduncular bract which is
attached slightly above the attachment of the prophyll;
bracts are completely deciduous immediately prior to floral
maturity; flowers unisexual and borne in triads throughout
most of the rachillae, staminate flowers only in the distal
portion; peduncle short; rachis elongate, angled proximally,
becoming terete distally; rachillae zig-zagged throughout or
distally; staminate flowers asymmetrical in bud; petals thin,
angled, valvate, opening widely at anthesis; stamens 9-34;
anthers dorsifixed near the middle; pistillode about as long
as stamens; pistillate flowers smaller than the staminate,
globose; stigma trifid; staminodes three; gynoecium
unilocular, uniovulate; fruit one-seeded, conic-ovoid to
elliptical, red at maturity; stigmatic remains apical or
nearly so; mesocarp with thin to thick fibres; endocarp thin,
brittle to crustaceous, non-operculate; hilum elongate;
endosperm ruminate; embryo basal; germination
adjacent-ligular; eophyll bifid.
Variation between the species is primarily expressed in the
following characteristics: degree of enlargement of the base
of the trunk; colour of the crownshaft - from shades of green
to red/purple; degree of lateral twist in the leaf the pinnae
in near-horizontal to vertical orientation; whether
silver/grey scales or ramenta are present or absent on the
lower surface of the pinnae; size and degree of branching of
the inflorescence; colour of the flowers white/cream to
lilac; number of stamens - 9-34; whether the filament is
desexed or not; size of the fruit - 8-26 mm long; texture of
the epicarp - smooth or pebbled; position of the stigmatic
remains apical or eccentric; thickness, type and degree of
branching of the fibres within the mesocarp; the degree of
adherence of the raphe fibres to the seed; and the degree to
which the mesocarpic fibres are embedded in the endocarp.
Distribution of the genus in along the eastern coast of
Australia, from Durras Mountain, New South Wales [35&deg
10'S] to Cape York, Queensland [10&#176; 40'S], in coastal and
near coastal lowlands and ranges, from sea-level to 1200 m
altitude. Lowland and moderate altitude populations are
continuous for many kilometres where conditions permit
(e.g. <i>A. alexandrae</i>, <i>A. cunninghamiana</i> and
<i>A. tuckeri</i>, whilst other species have small populations which
are isolated and remote from others (e.g. <i>A. myolensis</i> and
<i>A. maxima</i>).
Main habitats include rainforest, wet sclerophyll, gallery
forest, moist vineforest and swampforest; and occasionally in
seasonally dry forests such as deciduous or semi-evergreen
vineforests. Soil types are varied, derived from granite,
basalt, metamorphics, siliceous sand and schists.
===The Species: ===
The taxonomic history of
<i>A. cunninghamiana</i> began in
1857 when W. Hooker described <i>Seaforthia elegans</i> in
Botanical Magazine. There was some confusion in regards to
the true identity of the taxon which he intended to describe;
some of the accompanying illustrations depicted what we now
know as <i> Ptychosperma elegans</i>
as well as <i>A. cunninghamiana</i>. The following year,
Hermann Wendland clarified the situation with his description
of <i>Ptychosperma cunninghamiana</i>  in Botanische
Zeitung. Subsequently Wendland and Drude renamed it
<i> Archontophoenix cunninghamiana</i>
in 1875 in Linnaea when they created
<i>Archontophoenix</i> as a new genus.
<i> A. alexandrae</i>
was first described in 1866 as <i>Ptychosperma alexandrae</i>
by Ferdinand von Mueller in Fragmenta Phytographiae
Australiae.
The early history of this species is not as
complex as <i>A. cunninghamiana</i>; Wendland and Drude
transferred it to <i>Archontophoenix</i> in Linnaea in 1875.
Two subspecies of <i> A. alexandrae</i> have been named, <i> A. alexandrae</i>
var. <i>schizanthera</i> by Wendland & Drude in the same publication,
and <i> A. alexandrae</i>
var. <i>beatricea</i> ( the latter originally as <i>P. beatricea</i>
by von Mueller in 1882), both of which now appear to be
unnecessary considering the overall variability of that
species.
(by John Dowe from '''''Palms & Cycads''''' No. 39, Apr-Jun 1993)
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[[Category:Palms|Archontophoenix]]
[[Category:Palms|Archontophoenix]]
[[Category:Palm|Archontophoenix]]
     

Latest revision as of 13:43, 9 July 2024

Overview:[edit]

Archontophoenix H. Wendland & O. Drude is a genus of single-stemmed, pinnate-leaved, monoecious, Arecoid palms endemic to eastern Australia. The genus was established in 1875 by Hermann Wendland and Oscar Drude in the journal Linnaea. Though no type species was designated at the time of publication, the accepted lectotype is A. alexandrae (F. Mueller) H. Wendland & Drude (=Ptychosperma alexandrae F. Mueller) which was described in the same publication. A number of other names have been applied to the genus; for example Seaforthia, Ptychosperma, Loroma and Jessenia.

The genus is rather undifferentiated and the species do not display a great degree of variation. The main features of the genus include: solitary habit; tall erect trunk; leaf bases forming an elongate crownshaft; leaves paripinnate; pinnae linear-acute with a prominent midrib raised on both surfaces; inflorescence infrafoliar at maturity, protandrous, branched to three or four orders; two bracts which fully enclose the inflorescence in bud, the prophyll attached at the base of the peduncle, fully enclosing the peduncular bract which is attached slightly above the attachment of the prophyll; bracts are completely deciduous immediately prior to floral maturity; flowers unisexual and borne in triads throughout most of the rachillae, staminate flowers only in the distal portion; peduncle short; rachis elongate, angled proximally, becoming terete distally; rachillae zig-zagged throughout or distally; staminate flowers asymmetrical in bud; petals thin, angled, valvate, opening widely at anthesis; stamens 9-34; anthers dorsifixed near the middle; pistillode about as long as stamens; pistillate flowers smaller than the staminate, globose; stigma trifid; staminodes three; gynoecium unilocular, uniovulate; fruit one-seeded, conic-ovoid to elliptical, red at maturity; stigmatic remains apical or nearly so; mesocarp with thin to thick fibres; endocarp thin, brittle to crustaceous, non-operculate; hilum elongate; endosperm ruminate; embryo basal; germination adjacent-ligular; eophyll bifid.

Variation between the species is primarily expressed in the following characteristics: degree of enlargement of the base of the trunk; colour of the crownshaft - from shades of green to red/purple; degree of lateral twist in the leaf the pinnae in near-horizontal to vertical orientation; whether silver/grey scales or ramenta are present or absent on the lower surface of the pinnae; size and degree of branching of the inflorescence; colour of the flowers white/cream to lilac; number of stamens - 9-34; whether the filament is desexed or not; size of the fruit - 8-26 mm long; texture of the epicarp - smooth or pebbled; position of the stigmatic remains apical or eccentric; thickness, type and degree of branching of the fibres within the mesocarp; the degree of adherence of the raphe fibres to the seed; and the degree to which the mesocarpic fibres are embedded in the endocarp. Distribution of the genus in along the eastern coast of Australia, from Durras Mountain, New South Wales [35&deg 10'S] to Cape York, Queensland [10° 40'S], in coastal and near coastal lowlands and ranges, from sea-level to 1200 m altitude. Lowland and moderate altitude populations are continuous for many kilometres where conditions permit (e.g. A. alexandrae, A. cunninghamiana and A. tuckeri, whilst other species have small populations which are isolated and remote from others (e.g. A. myolensis and A. maxima).

Main habitats include rainforest, wet sclerophyll, gallery forest, moist vineforest and swampforest; and occasionally in seasonally dry forests such as deciduous or semi-evergreen vineforests. Soil types are varied, derived from granite, basalt, metamorphics, siliceous sand and schists.

The Species:[edit]

The taxonomic history of A. cunninghamiana began in 1857 when W. Hooker described Seaforthia elegans in Botanical Magazine. There was some confusion in regards to the true identity of the taxon which he intended to describe; some of the accompanying illustrations depicted what we now know as Ptychosperma elegans as well as A. cunninghamiana. The following year, Hermann Wendland clarified the situation with his description of Ptychosperma cunninghamiana in Botanische Zeitung. Subsequently Wendland and Drude renamed it Archontophoenix cunninghamiana in 1875 in Linnaea when they created Archontophoenix as a new genus. A. alexandrae was first described in 1866 as Ptychosperma alexandrae by Ferdinand von Mueller in Fragmenta Phytographiae Australiae.

The early history of this species is not as complex as A. cunninghamiana; Wendland and Drude transferred it to Archontophoenix in Linnaea in 1875. Two subspecies of A. alexandrae have been named, A. alexandrae var. schizanthera by Wendland & Drude in the same publication, and A. alexandrae var. beatricea ( the latter originally as P. beatricea by von Mueller in 1882), both of which now appear to be unnecessary considering the overall variability of that species.

(by John Dowe from Palms & Cycads No. 39, Apr-Jun 1993)