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Revision ab281457

Added by Andreas Müller almost 12 years ago

move taxonX files to palmae folder

View differences:

.gitattributes
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app-import/src/main/resources/images/palmae/KPALM00000073.jpg -text
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app-import/src/main/resources/images/protologue_links_palmae.xls -text
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app-import/src/main/resources/log4j.properties -text
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app-import/src/main/resources/palmae/taxonX/palm_tc_100446.xml -text
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app-import/src/main/resources/palmae/taxonX/palm_tc_101019.xml -text
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app-import/src/main/resources/palmae/taxonX/palm_tc_101020.xml -text
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app-import/src/main/resources/palmae/taxonX/palm_tc_101021.xml -text
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app-import/src/main/resources/palmae/taxonX/palm_tc_101022.xml -text
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app-import/src/main/resources/palmae/taxonX/palm_tc_101023.xml -text
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app-import/src/main/resources/palmae/taxonX/palm_tc_101024.xml -text
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app-import/src/main/resources/palmae/taxonX/palm_tc_101025.xml -text
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app-import/src/main/resources/palmae/taxonX/palm_tc_101026.xml -text
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app-import/src/main/resources/sdd/Cicad.sdd11.xml -text
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app-import/src/main/resources/sdd/Cicad2.sdd11.xml -text
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app-import/src/main/resources/sdd/Cichorieae-DA-export-sdd.xml -text
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app-import/src/main/resources/sdd/phlebo.sdd.xml -text
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app-import/src/main/resources/specimen/SynthesysSpecimenExample.xls -text
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app-import/src/main/resources/specimenABCD/multiABCD.xml -text
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app-import/src/main/resources/taxonX/palm_tc_100446.xml -text
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app-import/src/main/resources/taxonX/palm_tc_101019.xml -text
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app-import/src/main/resources/taxonX/palm_tc_101020.xml -text
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app-import/src/main/resources/taxonX/palm_tc_101021.xml -text
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app-import/src/main/resources/taxonX/palm_tc_101022.xml -text
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app-import/src/main/resources/taxonX/palm_tc_101023.xml -text
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app-import/src/main/resources/taxonX/palm_tc_101024.xml -text
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app-import/src/main/resources/taxonX/palm_tc_101025.xml -text
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app-import/src/main/resources/taxonX/palm_tc_101026.xml -text
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app-import/src/main/resources/tcs/Cichorium_tcs.xml -text
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app-import/src/main/resources/tcs/tcsXmlTest.xml -text
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cdm-col/format/meta.tpl.txt -text
app-import/src/main/resources/palmae/taxonX/palm_tc_100446.xml
1
<taxonx xmlns:dc="http://digir.net/schema/conceptual/darwin/core/2.0" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
2
<taxonxHeader>
3
<mods:mods>
4
<mods:titleInfo><mods:title>Genera Palmarum. The evolution and classification of palms</mods:title></mods:titleInfo>
5
<mods:name>
6
<mods:namePart type="family">Dransfield</mods:namePart>
7
<mods:namePart type="given">J.</mods:namePart>
8
<mods:namePart type="family">Uhl</mods:namePart>
9
<mods:namePart type="given">N.</mods:namePart>
10
<mods:namePart type="family">Asmussen</mods:namePart>
11
<mods:namePart type="given">C.</mods:namePart>
12
<mods:namePart type="family">Baker</mods:namePart>
13
<mods:namePart type="given">W.J.</mods:namePart>
14
<mods:namePart type="family">Harley</mods:namePart>
15
<mods:namePart type="given">M.</mods:namePart>
16
<mods:namePart type="family">Lewis</mods:namePart>
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<mods:namePart type="given">C.</mods:namePart>
18
</mods:name>
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<mods:originInfo>
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<mods:dateIssued>2008</mods:dateIssued><mods:publisher>Kew Publishing, Royal Botanic Gardens Kew</mods:publisher></mods:originInfo>
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</mods:mods>
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</taxonxHeader>
23
<taxonxBody>
24
<treatment rank="genus">
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<div type="diagnosis"><p>Spectacular pinnate-leaved palms endemic to Lord Howe Island, where they occur in huge populations; distinctive in the robust pendulous spicate inflorescences and staminate flowers with large numbers of stamens.</p></div>
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<nomenclature>
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<name>Howea</name>
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<author>Becc.</author> 
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<citation>Malesia 1: 66 (1877)</citation>
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<type>Lectotype; Howea belmoreana; (C.Moore &amp; F.Muell.) Becc.</type>
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<type_loc></type_loc>
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<synonymy>
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<name>Grisebachia</name>
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<author>Drude and H. Wendl.</author>
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<bibref>Drude and H. Wendl., Nachr. Königl. Ges. Wiss. Georg-Augusts-Univ. 1875: 55 (1875) (non Klotzsch 1838).</bibref>
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<type>Lectotype; Grisebachia belmoreana; (C.Moore &amp; F.Muell.) H.Wendl. &amp; Drude</type>
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</synonymy>
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<synonymy>
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<name>Denea</name>
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<author>O.F. Cook</author>
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<bibref>O.F. Cook, J. Wash. Acad. Sci.16: 395 (1926).</bibref>
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</synonymy>
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</nomenclature>
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<div type="etymology"><p>Derived from Lord Howe Island, which in turn commemorates Admiral Lord Richard Howe (1726–1799).</p></div>
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<div type="description"><p>Moderate, solitary, unarmed, pleonanthic, monoecious palms. Stem erect, bare, conspicuously marked with close, horizontal or oblique leaf scars, the base sometimes expanded into a knob. Leaves pinnate, neatly abscising but not forming a crownshaft; sheath well developed, splitting longitudinally opposite the petiole, disintegrating into an interwoven mass of fine fibres; petiole short to moderately long, flattened or slightly channelled adaxially, abaxially ± angled, sparsely to densely scaly; rachis ± rounded to angled abaxially, adaxially angled, scaly as the petiole; leaflets numerous, single-fold, regularly arranged, curved or stiffly ascending, acute, acuminate or minutely bifid, adaxially with sparse scattered scales, abaxially ± glabrous or rather densely dotted with scales and bearing abundant floccose indumentum and ramenta along the midrib, transverse veinlets obscure. Inflorescences interfoliar, sometimes becoming infrafoliar after leaf fall, short or almost as long as the leaves, spicate, solitary or compound with up to 3–8 borne together on a common axillary boss, erect at first, later pendulous, protandrous; peduncle ± elliptic in cross-section, much shorter than or ± equalling the rachis, densely scaly; prophyll tubular, membranous; peduncular bract inserted near to or some distance from the prophyll, enclosing the inflorescence until anthesis, ± membranous, tubular, later splitting down its length, disintegrating and falling, leaving a low collar; rachis robust, scaly, densely covered with spirally arranged, ± spreading, low, rounded or triangular, rigid, coriaceous bracts, each forming a lip to a floral pit, enclosing a triad of flowers, except at the very tips where pits enclosing paired staminate flowers; floral bracteoles ± sepal-like. Staminate flowers partially exserted one at a time from the pit at anthesis; sepals 3, distinct, imbricate, usually keeled, ± rounded, the margins toothed; corolla with a stalk-like base ± as long as the sepals, and 3 ovate, valvate lobes; stamens 30–70 or more, filaments elongate, variously connate at the base for much of their length, the connective sometimes prolonged into a point, anthers elongate, ± latrorse; pistillode absent. Pollen ellipsoidal, asymmetric to pyriform; aperture a distal sulcus; ectexine tectate, finely perforate-rugulate, or granular-rugulate, especially on proximal face, aperture margin finely perforate-rugulate; infratectum columellate; longest axis 37–52 µm [2/2]. Pistillate flowers ± globular; sepals 3, distinct, imbricate, rounded, the margins toothed; petals 3, distinct, basally strongly imbricate, the tips briefly valvate; staminodes 3–6, forming a low, irregularly lobed, membranous ring, or irregularly separated as triangular or bifid flanges; gynoecium unilocular, uniovulate, tipped with 3 short stigmas ± reflexed at anthesis, ovule laterally attached, campylotropous. Fruit ovoid, sometimes faintly ridged, 1-seeded, shiny dark green at first, turning dull yellowish-green or reddish-brown, perianth whorls persistent, stigmatic remains apical; epicarp smooth, mesocarp rather thinly fleshy with abundant longitudinal fibres, endocarp cartilaginous, not adhering to the seed. Seed laterally attached, raphe extending 1/3 the length of the seed or less, endosperm homogeneous; embryo basal. Germination adjacent-ligular; eophyll bifid. Cytology: 2n = 32.</p></div>
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<div type="distribution"><p>Two easily distinguished species endemic to Lord Howe Island.</p></div>
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<div type="anatomy"><p>Leaf (Tomlinson 1961), root (Seubert 1998a,1998b), and fruit (Essig 2002). </p></div>
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<div type="relationships"><p>Howea is strongly supported as monophyletic(Savolainen et al. 2006, Baker et al. in prep.). For relationships,see Linospadix. </p></div>
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<div type="uses"><p>Both species, but especially Howea forsteriana, are important as commercially grown ornamentals.</p></div>
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<div type="taxonomic accounts"><p>Bailey (1939a). </p></div>
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<div type="fossil record"><p>No generic records found.</p></div>
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<div type="discussion"><p>The two species of Howea are the largest palms in theLinospadicinae. Howea belmoreana is distinguished by curvedleaves with erect leaflets and by a single spike in each leaf axil,while H. forsteriana has rather flat leaves with drooping leafletsand several spikes in each leaf axil. Flowers and fruits matureslowly so that several inflorescences in different stages areoften present on a single tree.
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Recent research has demonstrated that Howea speciated sympatrically on Lord Howe Island and is thus a rare convincing example of this controversial mode of speciation (Savolainen et al. 2006). 
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</p></div>
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<div type="vernacular"><p>Kentia palms, Howea palms, sentry palms. </p></div>
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<div type="biology_ecology"><p>Howea forsteriana is abundant on the island in lowland forest on sandy areas; H. belmoreana can be found as scattered individuals with H. forsteriana, but becomes abundant at higher elevations up to about 450 m above sea level. Wind has been shown to be the primary pollinator, one of the few proven examples in the palms (Savolainen et al. 2006). </p></div>
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<div type="conservation"><p></p></div>
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</treatment>
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</taxonxBody>
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</taxonx>
app-import/src/main/resources/palmae/taxonX/palm_tc_101019.xml
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<taxonx xmlns:dc="http://digir.net/schema/conceptual/darwin/core/2.0" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
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<taxonxHeader>
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<mods:mods>
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<mods:titleInfo><mods:title>Genera Palmarum. The evolution and classification of palms</mods:title></mods:titleInfo>
5
<mods:name>
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<mods:namePart type="family">Dransfield</mods:namePart>
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<mods:namePart type="given">J.</mods:namePart>
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<mods:namePart type="family">Uhl</mods:namePart>
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<mods:namePart type="given">N.</mods:namePart>
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<mods:namePart type="family">Asmussen</mods:namePart>
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<mods:namePart type="given">C.</mods:namePart>
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<mods:namePart type="family">Baker</mods:namePart>
13
<mods:namePart type="given">W.J.</mods:namePart>
14
<mods:namePart type="family">Harley</mods:namePart>
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<mods:namePart type="given">M.</mods:namePart>
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<mods:namePart type="family">Lewis</mods:namePart>
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<mods:namePart type="given">C.</mods:namePart>
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</mods:name>
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<mods:originInfo>
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<mods:dateIssued>2008</mods:dateIssued><mods:publisher>Kew Publishing, Royal Botanic Gardens Kew</mods:publisher></mods:originInfo>
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</mods:mods>
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</taxonxHeader>
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<taxonxBody>
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<treatment rank="genus">
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<div type="diagnosis"><p>Very variable small to very robust, solitary or clustered pinnate-leaved palms from Sulawesi eastwards to Fiji and Australia, with conspicuous crownshafts and often conspicuous praemorse leaflets; the inflorescences bear triads (and hence fruit) throughout the length of the rachillae.</p></div>
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<nomenclature>
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<name>Hydriastele</name>
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<author>H. Wendl. and Drude</author> 
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<citation>Linnaea 39: 180, 208 (1875).</citation>
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<type>Type; Hydriastele wendlandiana; (F.Muell.) H.Wendl. &amp; Drude</type>
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<synonymy>
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<name>Adelonenga</name>
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<author>Hook.f. in Benth. and Hook.f.</author>
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<bibref>Hook.f. in Benth. and Hook.f., Gen. pl. 3: 885 (1883).</bibref>
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<type>Lectotype; Adelonenga variabilis; (Becc.) Becc.</type>
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</synonymy>
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<synonymy>
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<name>Gronophyllum</name>
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<author>Scheff.</author>
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<bibref>Scheff., Ann. Jard. Bot. Buitenzorg 1: 135 (1876).</bibref>
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<type>Type; Gronophyllum microcarpum; Scheff.</type>
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</synonymy>
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<synonymy>
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<name>Gulubia</name>
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<author>Becc.</author>
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<bibref>Becc., Ann. Jard. Bot. Buitenzorg 2: 128, 131, 134 (1885).</bibref>
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<type>Lectotype; Gulubia moluccana; (Becc.) Becc.</type>
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</synonymy>
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<synonymy>
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<name>Gulubiopsis</name>
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<author>Becc.</author>
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<bibref>Becc., Bot. Jahrb. Syst. 59: 11 (1924).</bibref>
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<type>Type; Gulubiopsis palauensis; Becc.</type> 
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</synonymy>
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<synonymy>
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<name>Leptophoenix</name>
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<author>Becc.</author>
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<bibref>Becc., Ann. Jard. Bot. Buitenzorg 2: 82 (1885).</bibref>
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<type>Lectotype; Leptophoenix pinangoides; (Becc.) Becc.</type>
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</synonymy>
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<synonymy>
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<name>Nengella</name>
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<author>Becc.</author>
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<bibref>Becc., Malesia 1: 32 (1877).</bibref>
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<type>Lectotype; Nengella montana; Becc.</type>
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</synonymy>
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<synonymy>
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<name>Paragulubia</name>
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<author>Burret</author>
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<bibref>Burret, Notizbl. Bot. Gart. Berlin-Dahlem 13: 84 (1936).</bibref>
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<type>Type; Paragulubia macrospadix; Burret</type>
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</synonymy>
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<synonymy>
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<name>Siphokentia</name>
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<author>Burret</author>
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<bibref>Burret, Notizbl. Bot. Gart. Berlin-Dahlem 10: 198 (1927).</bibref>
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<type>Type; Siphokentia beguinii; Burret</type>
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</synonymy>
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<synonymy>
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<name>Kentia</name>
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<author>Blume</author>
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<bibref>Blume, Bull. Sci. Phys. Nat. Néerl. 1: 64 (1838) (non Kentia Adans. 1763).</bibref>
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<type>Type; Kentia procera; Blume</type>
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</synonymy>
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</nomenclature>
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<div type="etymology"><p>Hydrias — water nymph, stele — column or pillar, perhaps referring to the erect slender stems of those species growing near water.</p></div>
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<div type="description"><p>Small, moderate or tall, solitary or clustered, unarmed, pleonanthic, monoecious palms. Stems erect, slender to robust, bare, conspicuously ringed with leaf scars. Leaves entire-bifid or pinnate, neatly abscising; sheaths elongate, forming a well-defined crownshaft, usually densely scaly or tomentose, and/or waxy, a ligule-like prolongation sometimes present opposite or at the base of the petiole; petiole short to long, adaxially channelled, abaxially rounded, usually conspicuously scaly; rachis adaxially channelled or angled near the base, distally angled, abaxially rounded, usually scaly as the petiole; leaflets regularly arranged, or grouped, pendulous or horizontal or ascending, straight or curved, single-fold or several-fold, the terminal pair usually broad, several-fold, the rest parallel sided or somewhat wedge-shaped, apically acute, bifid or conspicuously praemorse, adaxial and abaxial surfaces bearing scattered minute scales, abaxially sometimes with scattered ramenta along the main veins, sometimes also with bands of deciduous chaffy scales along major ribs, transverse veinlets conspicuous or obscure. Inflorescences infrafoliar, branching to 1–3 orders or rarely spicate, usually horsetail-like, protandrous or protogynous; peduncle short, winged at the base, sometimes becoming swollen; prophyll compressed, entirely enclosing the inflorescence in bud, 2-keeled, with a conspicuous apical beak, thin, papery when dry, glabrous or scaly, soon drying on exposure, splitting longitudinally on the abaxial face and abscising together with the peduncular bract; peduncular bract 1 rarely 2, similar to and entirely enclosed by the prophyll, tubular, enclosing the inflorescence in bud; subsequent bracts inconspicuous; rachis (where present) longer or shorter than the peduncle, bearing inconspicuous rachis bracts subtending few to many crowded, ± spirally arranged first-order branches, the proximal bearing a few branches or all unbranched; rachillae elongate, usually ± straight or curved, of ± equal length, tending to curve downwards, bearing throughout their length spirally arranged or opposite and decussate pairs of triads of cream-coloured or pinkish-tinged flowers, except at the very tip where bearing solitary or paired staminate flowers; rachilla bracts very inconspicuous, low, ± rounded. Staminate flowers fleshy, asymmetrical; calyx sessile or with a short stalk-like base, sepals 3, short, triangular, ± distinct or joined into a cup for ca. 1/2 their length; petals 3, fleshy, distinct, except at the very base, valvate except in Hydriastele palauensis where margins not meeting triangular, asymmetric; aperture a distal sulcus or trichotomosulcus; in bud, 4–5 times as long as the calyx, narrow, triangular, 1 usually larger ectexine tectate, coarsely perforate, foveolate, coarsely perforate-than the other 2; stamens 6–24, epipetalous, filaments very short, fleshy, rugulate or rarely scabrate verrucate, aperture margin similar; longest variously epipetalous and connate, anthers elongate, erect, basifixed, axis ranging from 33–70 µm; post-meiotic tetrads tetragonal or latrorse, connective sometimes prolonged into a short point; pistillode tetrahedral [22/47]. Pistillate flowers globose or ± conical in bud, smaller absent. Pollen ellipsoidal, bi-symmetric; aperture a distal sulcus, brevi-, ± than the staminate; sepals 3, distinct, rounded or triangular, broadly same length as long axis or, frequently, extended; ectexine semi-tectate imbricate or connate in a ring with 3 low triangular lobes; petals 3, and coarsely (rarely finely) reticulate, muri of reticulum sometimes distinct or connate, not more than to at least twice as long as the sepals, perforate, aperture margins similar; or pollen ellipsoidal or oblate-rounded or triangular, basally broadly imbricate or connate in a ring, apically rounded except for very small triangular valvate tips or with conspicuous triangular valvate tips, closely appressed in bud, the tips persisting or eroding into fibres in fruit; staminodes 3(–6), tooth-like, minute; gynoecium ± globose or ovoid, unilocular, uniovulate, stigmas 3, low, sessile or fleshy, reflexed, ovule laterally attached near apex of locule, hemianatropus (?always). Fruit globose to narrowly ellipsoidal, straight or curved, bright red to purplish-black, sometimes drying ridged, sometimes briefly beaked, stigmatic remains apical, perianth whorls persistent, the petal tips sometimes reflexed or appressed to the fruit; epicarp smooth or slightly pebbled, mesocarp thin, with abundant tannin cells, and longitudinal fibre bundles, endocarp thin, crustose or obsolescent. Seed ovoid or globose, laterally or basally attached with elongate or rounded hilum, raphe branches sparse, anastomosing, endosperm homogeneous or shallowly to deeply ruminate; embryo basal. Germination adjacent-ligular; eophyll bifid with entire or minutely to strongly praemorse tips. Cytology: 2n = 32.</p></div>
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<div type="distribution"><p>About 47 species in Sulawesi, Moluccas, New Guinea, Bismarck Archipelago, northern Australia, Fiji, Vanuatu and Palau. </p></div>
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<div type="anatomy"><p>Fruit (Essig 1982). </p></div>
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<div type="relationships"><p>Hydriastele is moderately to highly supported as a monophyletic genus following the recent inclusion of three genera, Gronophyllum, Gulubia and Siphokentia, in synonymy (Baker and Loo 2004, Asmussen et al. 2006, Loo et al. 2006, Norup et al. 2006, Baker et al. in prep.). The relationships of Hydriastele remain unclear, but it is worth noting that, in the most densely sampled studies, the genus does not resolve within the western Pacific clade of Areceae, despite its distribution (Norup et al. 2006, Baker et al. in prep.). Lewis and Doyle (2002) resolve Hydriastele as sister to the western Pacific clade. </p></div>
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<div type="uses"><p>Essig (1982) records the use of trunks for floorboards and side panels of houses in New Guinea. Stems have been split and used as spears. Several species are cultivated as ornamentals. </p></div>
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<div type="taxonomic accounts"><p>Baker and Loo (2004). See also Essig (1982), Baker et al. (2000d), Burret (1936a, 1936b) and Essig and Young (1985). </p></div>
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<div type="fossil record"><p>Fossil leaf material referred to Kentites (= Hydriastele) from the Tertiary of Italy (Bureau 1896) was placed in the synonomy of Phoenicites by Read and Hickey (1972). Any link with extant Hydriastele is almost certainly spurious, particularly as the generic name Kentia has been so misapplied in the past. </p></div>
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<div type="discussion"><p>Uhl and Dransfield (1987) indicated that generic delimitation among the Papuasian members of Arecinae was problematic. In the first edition of Genera Palmarum, four Papuasian genera were assigned to Arecinae, together with Areca, Nenga, Pinanga and Loxococcus. Uhl and Dransfield placed emphasis on aspects of floral morphology that seemed to be correlated with protandry and protogyny. Species in which the pistillate flowers have large triangular petals closely adpressed in bud (Gronophyllum and Siphokentia) seemed to be protandrous, whereas those with inconspicuous rounded petals with minute triangular tips (Hydriastele and Gulubia) seemed to be protogynous. This apparently neat correlation was, however, based on very few observations of the sequence of flowering and was in the most part inferred. Furthermore, this delimitation resulted in genera of sometimes disparate habit. Recent phylogenetic studies (Loo et al. 2006) strongly support the monophyly of the Papuasian clade. Within the clade, however, only Hydriastele is monophyletic; Gronophyllum and Gulubia are polyphyletic with members of both genera resolving in a number of separate, highly supported groups with members of other genera within the clade. The position of Siphokentia is ambiguous but this genus, along with Hydriastele, is deeply nested within the clade. It has not been possible to find morphological characters that differentiate most of the groupings resolved in the molecular studies, and thus it is not possible to alter the generic delimitation to reflect the molecular phylogeny. For these reasons, we have followed Baker and Loo’s proposal (2004) to accept a single genus, for which the earliest name is Hydriastele. </p></div>
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<div type="vernacular"><p>Pinang salea (Hydriastele microcarpa). </p></div>
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<div type="biology_ecology"><p>Lowland to upland tropical rain forest. One species, Hydriastele rheophytica, occurs as a rheophyte in western New Guinea, and has very slender leaflets (Dowe and Ferrero 2000). Several species are recorded from limestone and others from ultramafic rock. Pollination has been studied by Essig (1973) who showed that curculionid beetles are probably the pollinators in H. microspadix. </p></div>
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<div type="conservation"><p></p></div>
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</treatment>
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</taxonxBody>
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</taxonx>
app-import/src/main/resources/palmae/taxonX/palm_tc_101020.xml
1
<taxonx xmlns:dc="http://digir.net/schema/conceptual/darwin/core/2.0" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
2
<taxonxHeader>
3
<mods:mods>
4
<mods:titleInfo>
5
<mods:title>A synopsis of the genus Hydriastele (Arecaceae)</mods:title>
6
</mods:titleInfo>
7
<mods:name>
8
<mods:namePart type="family">Baker</mods:namePart>
9
<mods:namePart type="given">W.J.</mods:namePart>
10
<mods:namePart type="family">Loo</mods:namePart>
11
<mods:namePart type="given">A.H.B.</mods:namePart>
12
</mods:name>
13
<mods:originInfo>
14
<mods:publisher>Kew Bulletin, Vol. 59, No. 1, pp. 61-68</mods:publisher>
15
<mods:dateIssued>2004</mods:dateIssued>
16
</mods:originInfo>
17
</mods:mods>
18
</taxonxHeader>
19
<taxonxBody>
20
<treatment rank="species">
21
<nomenclature>
22
<name>Hydriastele affinis</name>
23
<author>(Becc.) W.J.Baker and Loo</author>
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<citation>Kew Bull. 59: 62 (2004)</citation>
25
<type>Indonesia, Papua, Kapaor; Beccari; s.n.</type>
26
<type_loc>Holotype FI</type_loc>
27
<synonymy>
28
<name>Nenga affinis</name>
29
<author>Becc.</author>
30
<bibref>Becc., Malesia 1: 29 (1877)</bibref>
31
</synonymy>
32
<synonymy>
33
<name>Leptophoenix affinis</name>
34
<author>(Becc.) Becc.</author>
35
<bibref>(Becc.) Becc., Ann. Jard. Bot. Buitenzorg 2: 82 (1885)</bibref>
36
</synonymy>
37
<synonymy>
38
<name>Nengella affinis</name>
39
<author>(Becc.) Burret</author>
40
<bibref>(Becc.) Burret, Notizbl. Bot. Gart. Berlin-Dahlem 13: 316 (1936)</bibref>
41
</synonymy>
42
<synonymy>
43
<name>Gronophyllum affine</name>
44
<author>(Becc.) Essig and B. E. Young</author>
45
<bibref>(Becc.) Essig and B. E. Young, Principes 29: 136 (1985)</bibref>
46
</synonymy>
47
</nomenclature>
48
<div type="introduction"><p></p></div>
49
<div type="etymology"><p></p></div>
50
<div type="vernacular"><p></p></div>
51
<div type="diagnosis"><p></p></div>
52
<div type="description"><p></p></div>
53
<div type="distribution"><p></p></div>
54
<div type="biology_ecology"><p></p></div>
55
<div type="conservation"><p></p></div>
56
<div type="uses"><p></p></div>
57
<div type="discussion"><p></p></div>
58
<div type="materials_examined"><p></p></div>
59
</treatment>
60
</taxonxBody>
61
</taxonx>
app-import/src/main/resources/palmae/taxonX/palm_tc_101021.xml
1
<taxonx xmlns:dc="http://digir.net/schema/conceptual/darwin/core/2.0" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
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<taxonxHeader>
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<mods:mods>
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<mods:titleInfo>
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<mods:title>A synopsis of the genus Hydriastele (Arecaceae)</mods:title>
6
</mods:titleInfo>
7
<mods:name>
8
<mods:namePart type="family">Baker</mods:namePart>
9
<mods:namePart type="given">W.J.</mods:namePart>
10
<mods:namePart type="family">Loo</mods:namePart>
11
<mods:namePart type="given">A.H.B.</mods:namePart>
12
</mods:name>
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<mods:originInfo>
14
<mods:publisher>Kew Bulletin, Vol. 59, No. 1, pp. 61-68</mods:publisher>
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<mods:dateIssued>2004</mods:dateIssued>
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</mods:originInfo>
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</mods:mods>
18
</taxonxHeader>
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<taxonxBody>
20
<treatment rank="species">
21
<nomenclature>
22
<name>Hydriastele aprica</name>
23
<author>(B.E.Young) W.J.Baker and Loo</author>
24
<citation>Kew Bull. 59: 62 (2004)</citation>
25
<type>Papua New Guinea, Sandaun, Telefomin; Essig and Young; 74082</type>
26
<type_loc>Holotype LAE</type_loc>
27
<synonymy>
28
<name>Gronophyllum apricum</name>
29
<author>B. E. Young</author>
30
<bibref>B. E. Young, Principes 29: 139 (1985)</bibref>
31
</synonymy>
32
</nomenclature>
33
<div type="introduction"><p></p></div>
34
<div type="etymology"><p></p></div>
35
<div type="vernacular"><p></p></div>
36
<div type="diagnosis"><p></p></div>
37
<div type="description"><p></p></div>
38
<div type="distribution"><p></p></div>
39
<div type="biology_ecology"><p></p></div>
40
<div type="conservation"><p></p></div>
41
<div type="uses"><p></p></div>
42
<div type="discussion"><p></p></div>
43
<div type="materials_examined"><p></p></div>
44
</treatment>
45
</taxonxBody>
46
</taxonx>
app-import/src/main/resources/palmae/taxonX/palm_tc_101022.xml
1
<taxonx xmlns:dc="http://digir.net/schema/conceptual/darwin/core/2.0" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
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<taxonxHeader>
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<mods:mods>
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<mods:titleInfo>
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<mods:title>A synopsis of the genus Hydriastele (Arecaceae)</mods:title>
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</mods:titleInfo>
7
<mods:name>
8
<mods:namePart type="family">Baker</mods:namePart>
9
<mods:namePart type="given">W.J.</mods:namePart>
10
<mods:namePart type="family">Loo</mods:namePart>
11
<mods:namePart type="given">A.H.B.</mods:namePart>
12
</mods:name>
13
<mods:originInfo>
14
<mods:publisher>Kew Bulletin, Vol. 59, No. 1, pp. 61-68</mods:publisher>
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<mods:dateIssued>2004</mods:dateIssued>
16
</mods:originInfo>
17
</mods:mods>
18
</taxonxHeader>
19
<taxonxBody>
20
<treatment rank="species">
21
<nomenclature>
22
<name>Hydriastele beccariana</name>
23
<author>Burret</author>
24
<citation>Repert. Spec. Nov. Regni Veg. 24: 292 (1928)</citation>
25
<type>Indonesia, Papua, Noord R.; Versteeg; 1662</type>
26
<type_loc>Holotype B†; isotypes BO, L</type_loc>
27
</nomenclature>
28
<div type="introduction"><p></p></div>
29
<div type="etymology"><p></p></div>
30
<div type="vernacular"><p></p></div>
31
<div type="diagnosis"><p></p></div>
32
<div type="description"><p></p></div>
33
<div type="distribution"><p></p></div>
34
<div type="biology_ecology"><p></p></div>
35
<div type="conservation"><p></p></div>
36
<div type="uses"><p></p></div>
37
<div type="discussion"><p></p></div>
38
<div type="materials_examined"><p></p></div>
39
</treatment>
40
</taxonxBody>
41
</taxonx>
app-import/src/main/resources/palmae/taxonX/palm_tc_101023.xml
1
<taxonx xmlns:dc="http://digir.net/schema/conceptual/darwin/core/2.0" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
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<taxonxHeader>
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<mods:mods>
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<mods:titleInfo>
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<mods:title>A synopsis of the genus Hydriastele (Arecaceae)</mods:title>
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</mods:titleInfo>
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<mods:name>
8
<mods:namePart type="family">Baker</mods:namePart>
9
<mods:namePart type="given">W.J.</mods:namePart>
10
<mods:namePart type="family">Loo</mods:namePart>
11
<mods:namePart type="given">A.H.B.</mods:namePart>
12
</mods:name>
13
<mods:originInfo>
14
<mods:publisher>Kew Bulletin, Vol. 59, No. 1, pp. 61-68</mods:publisher>
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<mods:dateIssued>2004</mods:dateIssued>
16
</mods:originInfo>
17
</mods:mods>
18
</taxonxHeader>
19
<taxonxBody>
20
<treatment rank="species">
21
<nomenclature>
22
<name></name>
23
<author>(Burret) W.J.Baker and Loo</author>
24
<citation>Kew Bull. 59: 62 (2004)</citation>
25
<type>Indonesia, Maluku, Halmahera, Soa Toberoe; Beguin; 1995</type>
26
<type_loc>Holotype B†; isotype BO</type_loc>
27
<synonymy>
28
<name>Siphokentia beguinii</name>
29
<author>Burret</author>
30
<bibref>Burret, Notizbl. Bot. Gart. Berlin-Dahlem 10: 198 (1927)</bibref>
31
</synonymy>
32
<synonymy>
33
<name>Siphokentia pachypus</name>
34
<author>Burret</author>
35
<bibref>Burret, Notizbl. Bot. Gart. Berlin- Dahlem 10: 199 (1927)</bibref>
36
<type>Indonesia, Maluku, Halmahera, Weda; Beguin; 2349</type>
37
<type_loc>Holotype Bt; isotype BO</type_loc>
38
</synonymy>
39
</nomenclature>
40
<div type="introduction"><p></p></div>
41
<div type="etymology"><p></p></div>
42
<div type="vernacular"><p></p></div>
43
<div type="diagnosis"><p></p></div>
44
<div type="description"><p></p></div>
45
<div type="distribution"><p></p></div>
46
<div type="biology_ecology"><p></p></div>
47
<div type="conservation"><p></p></div>
48
<div type="uses"><p></p></div>
49
<div type="discussion"><p></p></div>
50
<div type="materials_examined"><p></p></div>
51
</treatment>
52
</taxonxBody>
53
</taxonx>
app-import/src/main/resources/palmae/taxonX/palm_tc_101024.xml
1
<taxonx xmlns:dc="http://digir.net/schema/conceptual/darwin/core/2.0" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
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<taxonxHeader>
3
<mods:mods>
4
<mods:titleInfo>
5
<mods:title>A synopsis of the genus Hydriastele (Arecaceae)</mods:title>
6
</mods:titleInfo>
7
<mods:name>
8
<mods:namePart type="family">Baker</mods:namePart>
9
<mods:namePart type="given">W.J.</mods:namePart>
10
<mods:namePart type="family">Loo</mods:namePart>
11
<mods:namePart type="given">A.H.B.</mods:namePart>
12
</mods:name>
13
<mods:originInfo>
14
<mods:publisher>Kew Bulletin, Vol. 59, No. 1, pp. 61-68</mods:publisher>
15
<mods:dateIssued>2004</mods:dateIssued>
16
</mods:originInfo>
17
</mods:mods>
18
</taxonxHeader>
19
<taxonxBody>
20
<treatment rank="species">
21
<nomenclature>
22
<name>Hydriastele brassii</name>
23
<author>(Burret) W.J.Baker and Loo</author>
24
<citation>Kew Bull. 59: 63 (2004)</citation>
25
<type>Papua New Guinea, Western, Palmer R.; Brass; 7093</type>
26
<type_loc>Holotype B†; isotypes A, BRI, BO, L</type_loc>
27
<synonymy>
28
<name>Gronophyllum brassii</name>
29
<author>Burret</author>
30
<bibref>Burret, J. Arnold Arbor. 20: 205 (1939)</bibref>
31
</synonymy>
32
</nomenclature>
33
<div type="introduction"><p></p></div>
34
<div type="etymology"><p></p></div>
35
<div type="vernacular"><p></p></div>
36
<div type="diagnosis"><p></p></div>
37
<div type="description"><p></p></div>
38
<div type="distribution"><p></p></div>
39
<div type="biology_ecology"><p></p></div>
40
<div type="conservation"><p></p></div>
41
<div type="uses"><p></p></div>
42
<div type="discussion"><p></p></div>
43
<div type="materials_examined"><p></p></div>
44
</treatment>
45
</taxonxBody>
46
</taxonx>
app-import/src/main/resources/palmae/taxonX/palm_tc_101025.xml
1
<taxonx xmlns:dc="http://digir.net/schema/conceptual/darwin/core/2.0" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
2
<taxonxHeader>
3
<mods:mods>
4
<mods:titleInfo>
5
<mods:title>A synopsis of the genus Hydriastele (Arecaceae)</mods:title>
6
</mods:titleInfo>
7
<mods:name>
8
<mods:namePart type="family">Baker</mods:namePart>
9
<mods:namePart type="given">W.J.</mods:namePart>
10
<mods:namePart type="family">Loo</mods:namePart>
11
<mods:namePart type="given">A.H.B.</mods:namePart>
12
</mods:name>
13
<mods:originInfo>
14
<mods:publisher>Kew Bulletin, Vol. 59, No. 1, pp. 61-68</mods:publisher>
15
<mods:dateIssued>2004</mods:dateIssued>
16
</mods:originInfo>
17
</mods:mods>
18
</taxonxHeader>
19
<taxonxBody>
20
<treatment rank="species">
21
<nomenclature>
22
<name></name>
23
<author>(Dowe and M.D.Ferrero) W.J.Baker and Loo</author>
24
<citation>Kew Bull. 59: 63 (2004)</citation>
25
<type>Papua New Guinea, Sandaun, Bewani Mts; Dowe et al.; 514 </type>
26
<type_loc>Holotype BRI</type_loc>
27
<synonymy>
28
<name>Gronophyllum cariosum</name>
29
<author>Dowe and M. D. Ferrero</author>
30
<bibref>Dowe and M. D. Ferrero, Palms 44: 161 (2000)</bibref>
31
</synonymy>
32
</nomenclature>
33
<div type="introduction"><p></p></div>
34
<div type="etymology"><p></p></div>
35
<div type="vernacular"><p></p></div>
36
<div type="diagnosis"><p></p></div>
37
<div type="description"><p></p></div>
38
<div type="distribution"><p></p></div>
39
<div type="biology_ecology"><p></p></div>
40
<div type="conservation"><p></p></div>
41
<div type="uses"><p></p></div>
42
<div type="discussion"><p></p></div>
43
<div type="materials_examined"><p></p></div>
44
</treatment>
45
</taxonxBody>
46
</taxonx>
app-import/src/main/resources/palmae/taxonX/palm_tc_101026.xml
1
<taxonx xmlns:dc="http://digir.net/schema/conceptual/darwin/core/2.0" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
2
<taxonxHeader>
3
<mods:mods>
4
<mods:titleInfo>
5
<mods:title>A synopsis of the genus Hydriastele (Arecaceae)</mods:title>
6
</mods:titleInfo>
7
<mods:name>
8
<mods:namePart type="family">Baker</mods:namePart>
9
<mods:namePart type="given">W.J.</mods:namePart>
10
<mods:namePart type="family">Loo</mods:namePart>
11
<mods:namePart type="given">A.H.B.</mods:namePart>
12
</mods:name>
13
<mods:originInfo>
14
<mods:publisher>Kew Bulletin, Vol. 59, No. 1, pp. 61-68</mods:publisher>
15
<mods:dateIssued>2004</mods:dateIssued>
16
</mods:originInfo>
17
</mods:mods>
18
</taxonxHeader>
19
<taxonxBody>
20
<treatment rank="species">
21
<nomenclature>
22
<name>Hydriastele carrii</name>
23
<author>Burret,</author>
24
<citation>Notizbl. Bot. Gart. Berlin-Dahlem 13: 326 (1936)</citation>
25
<type>Papua New Guinea, Central, Boridi; Carr; s.n.</type>
26
<type_loc>Holotype B†</type_loc>
27
</nomenclature>
28
<div type="introduction"><p></p></div>
29
<div type="etymology"><p></p></div>
30
<div type="vernacular"><p></p></div>
31
<div type="diagnosis"><p></p></div>
32
<div type="description"><p></p></div>
33
<div type="distribution"><p></p></div>
34
<div type="biology_ecology"><p></p></div>
35
<div type="conservation"><p></p></div>
36
<div type="uses"><p></p></div>
37
<div type="discussion"><p></p></div>
38
<div type="materials_examined"><p></p></div>
39
</treatment>
40
</taxonxBody>
41
</taxonx>
app-import/src/main/resources/taxonX/palm_tc_100446.xml
1
<taxonx xmlns:dc="http://digir.net/schema/conceptual/darwin/core/2.0" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
2
<taxonxHeader>
3
<mods:mods>
4
<mods:titleInfo><mods:title>Genera Palmarum. The evolution and classification of palms</mods:title></mods:titleInfo>
5
<mods:name>
6
<mods:namePart type="family">Dransfield</mods:namePart>
7
<mods:namePart type="given">J.</mods:namePart>
8
<mods:namePart type="family">Uhl</mods:namePart>
9
<mods:namePart type="given">N.</mods:namePart>
10
<mods:namePart type="family">Asmussen</mods:namePart>
11
<mods:namePart type="given">C.</mods:namePart>
12
<mods:namePart type="family">Baker</mods:namePart>
13
<mods:namePart type="given">W.J.</mods:namePart>
14
<mods:namePart type="family">Harley</mods:namePart>
15
<mods:namePart type="given">M.</mods:namePart>
16
<mods:namePart type="family">Lewis</mods:namePart>
17
<mods:namePart type="given">C.</mods:namePart>
18
</mods:name>
19
<mods:originInfo>
20
<mods:dateIssued>2008</mods:dateIssued><mods:publisher>Kew Publishing, Royal Botanic Gardens Kew</mods:publisher></mods:originInfo>
21
</mods:mods>
22
</taxonxHeader>
23
<taxonxBody>
24
<treatment rank="genus">
25
<div type="diagnosis"><p>Spectacular pinnate-leaved palms endemic to Lord Howe Island, where they occur in huge populations; distinctive in the robust pendulous spicate inflorescences and staminate flowers with large numbers of stamens.</p></div>
26
<nomenclature>
27
<name>Howea</name>
28
<author>Becc.</author> 
29
<citation>Malesia 1: 66 (1877)</citation>
30
<type>Lectotype; Howea belmoreana; (C.Moore &amp; F.Muell.) Becc.</type>
31
<type_loc></type_loc>
32
<synonymy>
33
<name>Grisebachia</name>
34
<author>Drude and H. Wendl.</author>
35
<bibref>Drude and H. Wendl., Nachr. Königl. Ges. Wiss. Georg-Augusts-Univ. 1875: 55 (1875) (non Klotzsch 1838).</bibref>
36
<type>Lectotype; Grisebachia belmoreana; (C.Moore &amp; F.Muell.) H.Wendl. &amp; Drude</type>
37
</synonymy>
38
<synonymy>
39
<name>Denea</name>
40
<author>O.F. Cook</author>
41
<bibref>O.F. Cook, J. Wash. Acad. Sci.16: 395 (1926).</bibref>
42
</synonymy>
43
</nomenclature>
44
<div type="etymology"><p>Derived from Lord Howe Island, which in turn commemorates Admiral Lord Richard Howe (1726–1799).</p></div>
45
<div type="description"><p>Moderate, solitary, unarmed, pleonanthic, monoecious palms. Stem erect, bare, conspicuously marked with close, horizontal or oblique leaf scars, the base sometimes expanded into a knob. Leaves pinnate, neatly abscising but not forming a crownshaft; sheath well developed, splitting longitudinally opposite the petiole, disintegrating into an interwoven mass of fine fibres; petiole short to moderately long, flattened or slightly channelled adaxially, abaxially ± angled, sparsely to densely scaly; rachis ± rounded to angled abaxially, adaxially angled, scaly as the petiole; leaflets numerous, single-fold, regularly arranged, curved or stiffly ascending, acute, acuminate or minutely bifid, adaxially with sparse scattered scales, abaxially ± glabrous or rather densely dotted with scales and bearing abundant floccose indumentum and ramenta along the midrib, transverse veinlets obscure. Inflorescences interfoliar, sometimes becoming infrafoliar after leaf fall, short or almost as long as the leaves, spicate, solitary or compound with up to 3–8 borne together on a common axillary boss, erect at first, later pendulous, protandrous; peduncle ± elliptic in cross-section, much shorter than or ± equalling the rachis, densely scaly; prophyll tubular, membranous; peduncular bract inserted near to or some distance from the prophyll, enclosing the inflorescence until anthesis, ± membranous, tubular, later splitting down its length, disintegrating and falling, leaving a low collar; rachis robust, scaly, densely covered with spirally arranged, ± spreading, low, rounded or triangular, rigid, coriaceous bracts, each forming a lip to a floral pit, enclosing a triad of flowers, except at the very tips where pits enclosing paired staminate flowers; floral bracteoles ± sepal-like. Staminate flowers partially exserted one at a time from the pit at anthesis; sepals 3, distinct, imbricate, usually keeled, ± rounded, the margins toothed; corolla with a stalk-like base ± as long as the sepals, and 3 ovate, valvate lobes; stamens 30–70 or more, filaments elongate, variously connate at the base for much of their length, the connective sometimes prolonged into a point, anthers elongate, ± latrorse; pistillode absent. Pollen ellipsoidal, asymmetric to pyriform; aperture a distal sulcus; ectexine tectate, finely perforate-rugulate, or granular-rugulate, especially on proximal face, aperture margin finely perforate-rugulate; infratectum columellate; longest axis 37–52 µm [2/2]. Pistillate flowers ± globular; sepals 3, distinct, imbricate, rounded, the margins toothed; petals 3, distinct, basally strongly imbricate, the tips briefly valvate; staminodes 3–6, forming a low, irregularly lobed, membranous ring, or irregularly separated as triangular or bifid flanges; gynoecium unilocular, uniovulate, tipped with 3 short stigmas ± reflexed at anthesis, ovule laterally attached, campylotropous. Fruit ovoid, sometimes faintly ridged, 1-seeded, shiny dark green at first, turning dull yellowish-green or reddish-brown, perianth whorls persistent, stigmatic remains apical; epicarp smooth, mesocarp rather thinly fleshy with abundant longitudinal fibres, endocarp cartilaginous, not adhering to the seed. Seed laterally attached, raphe extending 1/3 the length of the seed or less, endosperm homogeneous; embryo basal. Germination adjacent-ligular; eophyll bifid. Cytology: 2n = 32.</p></div>
46
<div type="distribution"><p>Two easily distinguished species endemic to Lord Howe Island.</p></div>
47
<div type="anatomy"><p>Leaf (Tomlinson 1961), root (Seubert 1998a,1998b), and fruit (Essig 2002). </p></div>
48
<div type="relationships"><p>Howea is strongly supported as monophyletic(Savolainen et al. 2006, Baker et al. in prep.). For relationships,see Linospadix. </p></div>
49
<div type="uses"><p>Both species, but especially Howea forsteriana, are important as commercially grown ornamentals.</p></div>
50
<div type="taxonomic accounts"><p>Bailey (1939a). </p></div>
51
<div type="fossil record"><p>No generic records found.</p></div>
52
<div type="discussion"><p>The two species of Howea are the largest palms in theLinospadicinae. Howea belmoreana is distinguished by curvedleaves with erect leaflets and by a single spike in each leaf axil,while H. forsteriana has rather flat leaves with drooping leafletsand several spikes in each leaf axil. Flowers and fruits matureslowly so that several inflorescences in different stages areoften present on a single tree.
53
Recent research has demonstrated that Howea speciated sympatrically on Lord Howe Island and is thus a rare convincing example of this controversial mode of speciation (Savolainen et al. 2006). 
54
</p></div>
55
<div type="vernacular"><p>Kentia palms, Howea palms, sentry palms. </p></div>
56
<div type="biology_ecology"><p>Howea forsteriana is abundant on the island in lowland forest on sandy areas; H. belmoreana can be found as scattered individuals with H. forsteriana, but becomes abundant at higher elevations up to about 450 m above sea level. Wind has been shown to be the primary pollinator, one of the few proven examples in the palms (Savolainen et al. 2006). </p></div>
57
<div type="conservation"><p></p></div>
58
</treatment>
59
</taxonxBody>
60
</taxonx>
app-import/src/main/resources/taxonX/palm_tc_101019.xml
1
<taxonx xmlns:dc="http://digir.net/schema/conceptual/darwin/core/2.0" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
2
<taxonxHeader>
3
<mods:mods>
4
<mods:titleInfo><mods:title>Genera Palmarum. The evolution and classification of palms</mods:title></mods:titleInfo>
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<mods:name>
6
<mods:namePart type="family">Dransfield</mods:namePart>
7
<mods:namePart type="given">J.</mods:namePart>
8
<mods:namePart type="family">Uhl</mods:namePart>
9
<mods:namePart type="given">N.</mods:namePart>
10
<mods:namePart type="family">Asmussen</mods:namePart>
11
<mods:namePart type="given">C.</mods:namePart>
12
<mods:namePart type="family">Baker</mods:namePart>
13
<mods:namePart type="given">W.J.</mods:namePart>
14
<mods:namePart type="family">Harley</mods:namePart>
15
<mods:namePart type="given">M.</mods:namePart>
16
<mods:namePart type="family">Lewis</mods:namePart>
17
<mods:namePart type="given">C.</mods:namePart>
18
</mods:name>
19
<mods:originInfo>
20
<mods:dateIssued>2008</mods:dateIssued><mods:publisher>Kew Publishing, Royal Botanic Gardens Kew</mods:publisher></mods:originInfo>
21
</mods:mods>
22
</taxonxHeader>
23
<taxonxBody>
24
<treatment rank="genus">
25
<div type="diagnosis"><p>Very variable small to very robust, solitary or clustered pinnate-leaved palms from Sulawesi eastwards to Fiji and Australia, with conspicuous crownshafts and often conspicuous praemorse leaflets; the inflorescences bear triads (and hence fruit) throughout the length of the rachillae.</p></div>
26
<nomenclature>
27
<name>Hydriastele</name>
28
<author>H. Wendl. and Drude</author> 
29
<citation>Linnaea 39: 180, 208 (1875).</citation>
30
<type>Type; Hydriastele wendlandiana; (F.Muell.) H.Wendl. &amp; Drude</type>
31
<synonymy>
32
<name>Adelonenga</name>
33
<author>Hook.f. in Benth. and Hook.f.</author>
34
<bibref>Hook.f. in Benth. and Hook.f., Gen. pl. 3: 885 (1883).</bibref>
35
<type>Lectotype; Adelonenga variabilis; (Becc.) Becc.</type>
36
</synonymy>
37
<synonymy>
38
<name>Gronophyllum</name>
39
<author>Scheff.</author>
40
<bibref>Scheff., Ann. Jard. Bot. Buitenzorg 1: 135 (1876).</bibref>
41
<type>Type; Gronophyllum microcarpum; Scheff.</type>
42
</synonymy>
43
<synonymy>
44
<name>Gulubia</name>
45
<author>Becc.</author>
46
<bibref>Becc., Ann. Jard. Bot. Buitenzorg 2: 128, 131, 134 (1885).</bibref>
47
<type>Lectotype; Gulubia moluccana; (Becc.) Becc.</type>
48
</synonymy>
49
<synonymy>
50
<name>Gulubiopsis</name>
51
<author>Becc.</author>
52
<bibref>Becc., Bot. Jahrb. Syst. 59: 11 (1924).</bibref>
53
<type>Type; Gulubiopsis palauensis; Becc.</type> 
54
</synonymy>
55
<synonymy>
56
<name>Leptophoenix</name>
57
<author>Becc.</author>
58
<bibref>Becc., Ann. Jard. Bot. Buitenzorg 2: 82 (1885).</bibref>
59
<type>Lectotype; Leptophoenix pinangoides; (Becc.) Becc.</type>
60
</synonymy>
61
<synonymy>
62
<name>Nengella</name>
63
<author>Becc.</author>
64
<bibref>Becc., Malesia 1: 32 (1877).</bibref>
65
<type>Lectotype; Nengella montana; Becc.</type>
66
</synonymy>
67
<synonymy>
68
<name>Paragulubia</name>
69
<author>Burret</author>
70
<bibref>Burret, Notizbl. Bot. Gart. Berlin-Dahlem 13: 84 (1936).</bibref>
71
<type>Type; Paragulubia macrospadix; Burret</type>
72
</synonymy>
73
<synonymy>
74
<name>Siphokentia</name>
75
<author>Burret</author>
76
<bibref>Burret, Notizbl. Bot. Gart. Berlin-Dahlem 10: 198 (1927).</bibref>
77
<type>Type; Siphokentia beguinii; Burret</type>
78
</synonymy>
79
<synonymy>
80
<name>Kentia</name>
81
<author>Blume</author>
82
<bibref>Blume, Bull. Sci. Phys. Nat. Néerl. 1: 64 (1838) (non Kentia Adans. 1763).</bibref>
83
<type>Type; Kentia procera; Blume</type>
84
</synonymy>
85
</nomenclature>
86
<div type="etymology"><p>Hydrias — water nymph, stele — column or pillar, perhaps referring to the erect slender stems of those species growing near water.</p></div>
87
<div type="description"><p>Small, moderate or tall, solitary or clustered, unarmed, pleonanthic, monoecious palms. Stems erect, slender to robust, bare, conspicuously ringed with leaf scars. Leaves entire-bifid or pinnate, neatly abscising; sheaths elongate, forming a well-defined crownshaft, usually densely scaly or tomentose, and/or waxy, a ligule-like prolongation sometimes present opposite or at the base of the petiole; petiole short to long, adaxially channelled, abaxially rounded, usually conspicuously scaly; rachis adaxially channelled or angled near the base, distally angled, abaxially rounded, usually scaly as the petiole; leaflets regularly arranged, or grouped, pendulous or horizontal or ascending, straight or curved, single-fold or several-fold, the terminal pair usually broad, several-fold, the rest parallel sided or somewhat wedge-shaped, apically acute, bifid or conspicuously praemorse, adaxial and abaxial surfaces bearing scattered minute scales, abaxially sometimes with scattered ramenta along the main veins, sometimes also with bands of deciduous chaffy scales along major ribs, transverse veinlets conspicuous or obscure. Inflorescences infrafoliar, branching to 1–3 orders or rarely spicate, usually horsetail-like, protandrous or protogynous; peduncle short, winged at the base, sometimes becoming swollen; prophyll compressed, entirely enclosing the inflorescence in bud, 2-keeled, with a conspicuous apical beak, thin, papery when dry, glabrous or scaly, soon drying on exposure, splitting longitudinally on the abaxial face and abscising together with the peduncular bract; peduncular bract 1 rarely 2, similar to and entirely enclosed by the prophyll, tubular, enclosing the inflorescence in bud; subsequent bracts inconspicuous; rachis (where present) longer or shorter than the peduncle, bearing inconspicuous rachis bracts subtending few to many crowded, ± spirally arranged first-order branches, the proximal bearing a few branches or all unbranched; rachillae elongate, usually ± straight or curved, of ± equal length, tending to curve downwards, bearing throughout their length spirally arranged or opposite and decussate pairs of triads of cream-coloured or pinkish-tinged flowers, except at the very tip where bearing solitary or paired staminate flowers; rachilla bracts very inconspicuous, low, ± rounded. Staminate flowers fleshy, asymmetrical; calyx sessile or with a short stalk-like base, sepals 3, short, triangular, ± distinct or joined into a cup for ca. 1/2 their length; petals 3, fleshy, distinct, except at the very base, valvate except in Hydriastele palauensis where margins not meeting triangular, asymmetric; aperture a distal sulcus or trichotomosulcus; in bud, 4–5 times as long as the calyx, narrow, triangular, 1 usually larger ectexine tectate, coarsely perforate, foveolate, coarsely perforate-than the other 2; stamens 6–24, epipetalous, filaments very short, fleshy, rugulate or rarely scabrate verrucate, aperture margin similar; longest variously epipetalous and connate, anthers elongate, erect, basifixed, axis ranging from 33–70 µm; post-meiotic tetrads tetragonal or latrorse, connective sometimes prolonged into a short point; pistillode tetrahedral [22/47]. Pistillate flowers globose or ± conical in bud, smaller absent. Pollen ellipsoidal, bi-symmetric; aperture a distal sulcus, brevi-, ± than the staminate; sepals 3, distinct, rounded or triangular, broadly same length as long axis or, frequently, extended; ectexine semi-tectate imbricate or connate in a ring with 3 low triangular lobes; petals 3, and coarsely (rarely finely) reticulate, muri of reticulum sometimes distinct or connate, not more than to at least twice as long as the sepals, perforate, aperture margins similar; or pollen ellipsoidal or oblate-rounded or triangular, basally broadly imbricate or connate in a ring, apically rounded except for very small triangular valvate tips or with conspicuous triangular valvate tips, closely appressed in bud, the tips persisting or eroding into fibres in fruit; staminodes 3(–6), tooth-like, minute; gynoecium ± globose or ovoid, unilocular, uniovulate, stigmas 3, low, sessile or fleshy, reflexed, ovule laterally attached near apex of locule, hemianatropus (?always). Fruit globose to narrowly ellipsoidal, straight or curved, bright red to purplish-black, sometimes drying ridged, sometimes briefly beaked, stigmatic remains apical, perianth whorls persistent, the petal tips sometimes reflexed or appressed to the fruit; epicarp smooth or slightly pebbled, mesocarp thin, with abundant tannin cells, and longitudinal fibre bundles, endocarp thin, crustose or obsolescent. Seed ovoid or globose, laterally or basally attached with elongate or rounded hilum, raphe branches sparse, anastomosing, endosperm homogeneous or shallowly to deeply ruminate; embryo basal. Germination adjacent-ligular; eophyll bifid with entire or minutely to strongly praemorse tips. Cytology: 2n = 32.</p></div>
88
<div type="distribution"><p>About 47 species in Sulawesi, Moluccas, New Guinea, Bismarck Archipelago, northern Australia, Fiji, Vanuatu and Palau. </p></div>
89
<div type="anatomy"><p>Fruit (Essig 1982). </p></div>
90
<div type="relationships"><p>Hydriastele is moderately to highly supported as a monophyletic genus following the recent inclusion of three genera, Gronophyllum, Gulubia and Siphokentia, in synonymy (Baker and Loo 2004, Asmussen et al. 2006, Loo et al. 2006, Norup et al. 2006, Baker et al. in prep.). The relationships of Hydriastele remain unclear, but it is worth noting that, in the most densely sampled studies, the genus does not resolve within the western Pacific clade of Areceae, despite its distribution (Norup et al. 2006, Baker et al. in prep.). Lewis and Doyle (2002) resolve Hydriastele as sister to the western Pacific clade. </p></div>
91
<div type="uses"><p>Essig (1982) records the use of trunks for floorboards and side panels of houses in New Guinea. Stems have been split and used as spears. Several species are cultivated as ornamentals. </p></div>
92
<div type="taxonomic accounts"><p>Baker and Loo (2004). See also Essig (1982), Baker et al. (2000d), Burret (1936a, 1936b) and Essig and Young (1985). </p></div>
93
<div type="fossil record"><p>Fossil leaf material referred to Kentites (= Hydriastele) from the Tertiary of Italy (Bureau 1896) was placed in the synonomy of Phoenicites by Read and Hickey (1972). Any link with extant Hydriastele is almost certainly spurious, particularly as the generic name Kentia has been so misapplied in the past. </p></div>
94
<div type="discussion"><p>Uhl and Dransfield (1987) indicated that generic delimitation among the Papuasian members of Arecinae was problematic. In the first edition of Genera Palmarum, four Papuasian genera were assigned to Arecinae, together with Areca, Nenga, Pinanga and Loxococcus. Uhl and Dransfield placed emphasis on aspects of floral morphology that seemed to be correlated with protandry and protogyny. Species in which the pistillate flowers have large triangular petals closely adpressed in bud (Gronophyllum and Siphokentia) seemed to be protandrous, whereas those with inconspicuous rounded petals with minute triangular tips (Hydriastele and Gulubia) seemed to be protogynous. This apparently neat correlation was, however, based on very few observations of the sequence of flowering and was in the most part inferred. Furthermore, this delimitation resulted in genera of sometimes disparate habit. Recent phylogenetic studies (Loo et al. 2006) strongly support the monophyly of the Papuasian clade. Within the clade, however, only Hydriastele is monophyletic; Gronophyllum and Gulubia are polyphyletic with members of both genera resolving in a number of separate, highly supported groups with members of other genera within the clade. The position of Siphokentia is ambiguous but this genus, along with Hydriastele, is deeply nested within the clade. It has not been possible to find morphological characters that differentiate most of the groupings resolved in the molecular studies, and thus it is not possible to alter the generic delimitation to reflect the molecular phylogeny. For these reasons, we have followed Baker and Loo’s proposal (2004) to accept a single genus, for which the earliest name is Hydriastele. </p></div>
95
<div type="vernacular"><p>Pinang salea (Hydriastele microcarpa). </p></div>
96
<div type="biology_ecology"><p>Lowland to upland tropical rain forest. One species, Hydriastele rheophytica, occurs as a rheophyte in western New Guinea, and has very slender leaflets (Dowe and Ferrero 2000). Several species are recorded from limestone and others from ultramafic rock. Pollination has been studied by Essig (1973) who showed that curculionid beetles are probably the pollinators in H. microspadix. </p></div>
97
<div type="conservation"><p></p></div>
98
</treatment>
99
</taxonxBody>
100
</taxonx>
app-import/src/main/resources/taxonX/palm_tc_101020.xml
1
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<taxonxHeader>
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<mods:namePart type="family">Baker</mods:namePart>
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<mods:namePart type="given">W.J.</mods:namePart>
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</taxonxHeader>
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<taxonxBody>
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<treatment rank="species">
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<nomenclature>
22
<name>Hydriastele affinis</name>
23
<author>(Becc.) W.J.Baker and Loo</author>
24
<citation>Kew Bull. 59: 62 (2004)</citation>
25
<type>Indonesia, Papua, Kapaor; Beccari; s.n.</type>
26
<type_loc>Holotype FI</type_loc>
27
<synonymy>
28
<name>Nenga affinis</name>
29
<author>Becc.</author>
30
<bibref>Becc., Malesia 1: 29 (1877)</bibref>
31
</synonymy>
32
<synonymy>
33
<name>Leptophoenix affinis</name>
34
<author>(Becc.) Becc.</author>
35
<bibref>(Becc.) Becc., Ann. Jard. Bot. Buitenzorg 2: 82 (1885)</bibref>
36
</synonymy>
37
<synonymy>
38
<name>Nengella affinis</name>
39
<author>(Becc.) Burret</author>
40
<bibref>(Becc.) Burret, Notizbl. Bot. Gart. Berlin-Dahlem 13: 316 (1936)</bibref>
41
</synonymy>
42
<synonymy>
43
<name>Gronophyllum affine</name>
44
<author>(Becc.) Essig and B. E. Young</author>
45
<bibref>(Becc.) Essig and B. E. Young, Principes 29: 136 (1985)</bibref>
46
</synonymy>
47
</nomenclature>
48
<div type="introduction"><p></p></div>
49
<div type="etymology"><p></p></div>
50
<div type="vernacular"><p></p></div>
51
<div type="diagnosis"><p></p></div>
52
<div type="description"><p></p></div>
53
<div type="distribution"><p></p></div>
54
<div type="biology_ecology"><p></p></div>
55
<div type="conservation"><p></p></div>
56
<div type="uses"><p></p></div>
57
<div type="discussion"><p></p></div>
58
<div type="materials_examined"><p></p></div>
59
</treatment>
60
</taxonxBody>
61
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app-import/src/main/resources/taxonX/palm_tc_101021.xml
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<nomenclature>
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<name>Hydriastele aprica</name>
23
<author>(B.E.Young) W.J.Baker and Loo</author>
24
<citation>Kew Bull. 59: 62 (2004)</citation>
25
<type>Papua New Guinea, Sandaun, Telefomin; Essig and Young; 74082</type>
26
<type_loc>Holotype LAE</type_loc>
27
<synonymy>
28
<name>Gronophyllum apricum</name>
29
<author>B. E. Young</author>
30
<bibref>B. E. Young, Principes 29: 139 (1985)</bibref>
31
</synonymy>
32
</nomenclature>
33
<div type="introduction"><p></p></div>
34
<div type="etymology"><p></p></div>
35
<div type="vernacular"><p></p></div>
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<div type="diagnosis"><p></p></div>
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<div type="description"><p></p></div>
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<div type="materials_examined"><p></p></div>
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</treatment>
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app-import/src/main/resources/taxonX/palm_tc_101022.xml
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<nomenclature>
22
<name>Hydriastele beccariana</name>
23
<author>Burret</author>
24
<citation>Repert. Spec. Nov. Regni Veg. 24: 292 (1928)</citation>
25
<type>Indonesia, Papua, Noord R.; Versteeg; 1662</type>
26
<type_loc>Holotype B†; isotypes BO, L</type_loc>
27
</nomenclature>
28
<div type="introduction"><p></p></div>
29
<div type="etymology"><p></p></div>
30
<div type="vernacular"><p></p></div>
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<div type="description"><p></p></div>
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37
<div type="discussion"><p></p></div>
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<div type="materials_examined"><p></p></div>
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</treatment>
40
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41
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app-import/src/main/resources/taxonX/palm_tc_101023.xml
1
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12
</mods:name>
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<mods:publisher>Kew Bulletin, Vol. 59, No. 1, pp. 61-68</mods:publisher>
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<name></name>
23
<author>(Burret) W.J.Baker and Loo</author>
24
<citation>Kew Bull. 59: 62 (2004)</citation>
25
<type>Indonesia, Maluku, Halmahera, Soa Toberoe; Beguin; 1995</type>
26
<type_loc>Holotype B†; isotype BO</type_loc>
27
<synonymy>
28
<name>Siphokentia beguinii</name>
29
<author>Burret</author>
30
<bibref>Burret, Notizbl. Bot. Gart. Berlin-Dahlem 10: 198 (1927)</bibref>
31
</synonymy>
32
<synonymy>
33
<name>Siphokentia pachypus</name>
34
<author>Burret</author>
35
<bibref>Burret, Notizbl. Bot. Gart. Berlin- Dahlem 10: 199 (1927)</bibref>
36
<type>Indonesia, Maluku, Halmahera, Weda; Beguin; 2349</type>
37
<type_loc>Holotype Bt; isotype BO</type_loc>
38
</synonymy>
39
</nomenclature>
40
<div type="introduction"><p></p></div>
41
<div type="etymology"><p></p></div>
42
<div type="vernacular"><p></p></div>
43
<div type="diagnosis"><p></p></div>
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<div type="description"><p></p></div>
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<div type="distribution"><p></p></div>
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<div type="biology_ecology"><p></p></div>
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<div type="conservation"><p></p></div>
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<div type="uses"><p></p></div>
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<div type="discussion"><p></p></div>
50
<div type="materials_examined"><p></p></div>
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</treatment>
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app-import/src/main/resources/taxonX/palm_tc_101024.xml
1
<taxonx xmlns:dc="http://digir.net/schema/conceptual/darwin/core/2.0" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
2
<taxonxHeader>
3
<mods:mods>
4
<mods:titleInfo>
5
<mods:title>A synopsis of the genus Hydriastele (Arecaceae)</mods:title>
6
</mods:titleInfo>
7
<mods:name>
8
<mods:namePart type="family">Baker</mods:namePart>
9
<mods:namePart type="given">W.J.</mods:namePart>
10
<mods:namePart type="family">Loo</mods:namePart>
11
<mods:namePart type="given">A.H.B.</mods:namePart>
12
</mods:name>
13
<mods:originInfo>
14
<mods:publisher>Kew Bulletin, Vol. 59, No. 1, pp. 61-68</mods:publisher>
15
<mods:dateIssued>2004</mods:dateIssued>
16
</mods:originInfo>
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</mods:mods>
18
</taxonxHeader>
19
<taxonxBody>
20
<treatment rank="species">
21
<nomenclature>
22
<name>Hydriastele brassii</name>
23
<author>(Burret) W.J.Baker and Loo</author>
24
<citation>Kew Bull. 59: 63 (2004)</citation>
25
<type>Papua New Guinea, Western, Palmer R.; Brass; 7093</type>
26
<type_loc>Holotype B†; isotypes A, BRI, BO, L</type_loc>
27
<synonymy>
28
<name>Gronophyllum brassii</name>
29
<author>Burret</author>
30
<bibref>Burret, J. Arnold Arbor. 20: 205 (1939)</bibref>
31
</synonymy>
32
</nomenclature>
33
<div type="introduction"><p></p></div>
34
<div type="etymology"><p></p></div>
35
<div type="vernacular"><p></p></div>
36
<div type="diagnosis"><p></p></div>
37
<div type="description"><p></p></div>
38
<div type="distribution"><p></p></div>
39
<div type="biology_ecology"><p></p></div>
40
<div type="conservation"><p></p></div>
41
<div type="uses"><p></p></div>
42
<div type="discussion"><p></p></div>
43
<div type="materials_examined"><p></p></div>
44
</treatment>
45
</taxonxBody>
46
</taxonx>
app-import/src/main/resources/taxonX/palm_tc_101025.xml
1
<taxonx xmlns:dc="http://digir.net/schema/conceptual/darwin/core/2.0" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
2
<taxonxHeader>
3
<mods:mods>
4
<mods:titleInfo>
5
<mods:title>A synopsis of the genus Hydriastele (Arecaceae)</mods:title>
6
</mods:titleInfo>
7
<mods:name>
8
<mods:namePart type="family">Baker</mods:namePart>
9
<mods:namePart type="given">W.J.</mods:namePart>
10
<mods:namePart type="family">Loo</mods:namePart>
11
<mods:namePart type="given">A.H.B.</mods:namePart>
12
</mods:name>
13
<mods:originInfo>
14
<mods:publisher>Kew Bulletin, Vol. 59, No. 1, pp. 61-68</mods:publisher>
15
<mods:dateIssued>2004</mods:dateIssued>
16
</mods:originInfo>
17
</mods:mods>
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</taxonxHeader>
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<taxonxBody>
20
<treatment rank="species">
21
<nomenclature>
22
<name></name>
23
<author>(Dowe and M.D.Ferrero) W.J.Baker and Loo</author>
24
<citation>Kew Bull. 59: 63 (2004)</citation>
25
<type>Papua New Guinea, Sandaun, Bewani Mts; Dowe et al.; 514 </type>
26
<type_loc>Holotype BRI</type_loc>
27
<synonymy>
28
<name>Gronophyllum cariosum</name>
29
<author>Dowe and M. D. Ferrero</author>
30
<bibref>Dowe and M. D. Ferrero, Palms 44: 161 (2000)</bibref>
31
</synonymy>
32
</nomenclature>
33
<div type="introduction"><p></p></div>
34
<div type="etymology"><p></p></div>
35
<div type="vernacular"><p></p></div>
36
<div type="diagnosis"><p></p></div>
37
<div type="description"><p></p></div>
38
<div type="distribution"><p></p></div>
39
<div type="biology_ecology"><p></p></div>
40
<div type="conservation"><p></p></div>
41
<div type="uses"><p></p></div>
42
<div type="discussion"><p></p></div>
43
<div type="materials_examined"><p></p></div>
44
</treatment>
45
</taxonxBody>
46
</taxonx>
app-import/src/main/resources/taxonX/palm_tc_101026.xml
1
<taxonx xmlns:dc="http://digir.net/schema/conceptual/darwin/core/2.0" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
2
<taxonxHeader>
3
<mods:mods>
4
<mods:titleInfo>
5
<mods:title>A synopsis of the genus Hydriastele (Arecaceae)</mods:title>
6
</mods:titleInfo>
7
<mods:name>
8
<mods:namePart type="family">Baker</mods:namePart>
9
<mods:namePart type="given">W.J.</mods:namePart>
10
<mods:namePart type="family">Loo</mods:namePart>
11
<mods:namePart type="given">A.H.B.</mods:namePart>
12
</mods:name>
13
<mods:originInfo>
14
<mods:publisher>Kew Bulletin, Vol. 59, No. 1, pp. 61-68</mods:publisher>
15
<mods:dateIssued>2004</mods:dateIssued>
16
</mods:originInfo>
17
</mods:mods>
18
</taxonxHeader>
19
<taxonxBody>
20
<treatment rank="species">
21
<nomenclature>
22
<name>Hydriastele carrii</name>
23
<author>Burret,</author>
24
<citation>Notizbl. Bot. Gart. Berlin-Dahlem 13: 326 (1936)</citation>
25
<type>Papua New Guinea, Central, Boridi; Carr; s.n.</type>
26
<type_loc>Holotype B†</type_loc>
27
</nomenclature>
28
<div type="introduction"><p></p></div>
29
<div type="etymology"><p></p></div>
30
<div type="vernacular"><p></p></div>
31
<div type="diagnosis"><p></p></div>
32
<div type="description"><p></p></div>
33
<div type="distribution"><p></p></div>
34
<div type="biology_ecology"><p></p></div>
35
<div type="conservation"><p></p></div>
36
<div type="uses"><p></p></div>
37
<div type="discussion"><p></p></div>
38
<div type="materials_examined"><p></p></div>
39
</treatment>
40
</taxonxBody>
41
</taxonx>

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