Cuspidaria
publication ID |
https://doi.org/10.5252/adansonia2023v45a12 |
DOI |
https://doi.org/10.5281/zenodo.8015269 |
persistent identifier |
https://treatment.plazi.org/id/039687DC-FFD2-9128-8F08-C2B9FA14A8FF |
treatment provided by |
Felipe (2023-06-05 14:07:06, last updated 2024-11-26 07:53:52) |
scientific name |
Cuspidaria |
status |
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VIII. Cuspidaria View in CoL View at ENA - Tynanthus clade
TAXONOMIC INFORMATION. — This clade contains two genera, Cuspidaria and Tynanthus , both with four phloem wedges in transversal section. While the circumscription of Tynanthus has remained constant in different classification systems, Cuspidaria currently includes species from three previously recognized genera (see Fischer et al. 2004; Table 1 View TABLE ), Cuspidaria, Arrabidaea , and Pyrostegia .
TOTAL NUMBER OF SPECIES IN THIS CLADE. — 35 species belonging to Cuspidaria (21) and Tynanthus (14) ( Lohmann & Taylor 2014; Medeiros & Lohmann 2015; Kaehler et al. 2019).
STUDIED SPECIES. — Four species, Cuspidaria convoluta (Vell.) A.H.Gentry , C. pulchra (Cham.) L.G.Lohmann , Tynanthus cognatus (Cham.) Miers , and T. elegans (Vell.) L.G.Lohmann.
Regular phloem
Thin to thick fiber bands, assemblages present ( Fig. 11D View FIG ). Mostly thin fiber bands in T. cognatus ( Fig. 11D View FIG ).
Variant phloem
General configuration. Fibrous ( Fig. 11 View FIG A-C, E, F), with axial elements in a tangential arrangement of one row of sieve tubes, surrounded by a sieve-tube-centric phloem parenchyma ( Fig. 11 View FIG A-C). A band of parenchyma sometimes present ( Fig. 11F View FIG ).
Sieve-tube elements. As seen in transverse section, each sieve element is associated with 2-3 (sometimes over 4) companion cells that occur at the same side of the sieve element ( Fig. 11B, E View FIG ). The sieve elements generally occur in multiples of 2-3 (up to 5) radially elongated cells ( Fig. 11B View FIG ). Solitary sieve elements are also present in Cuspidaria ( Fig. 11F View FIG ). As seen in transverse section, the sieve elements are of variable length, from 400 µm to approximately 1 mm and their end walls are inclined, bearing compound sieve plates with 12- 30 sieve areas ( Fig. 11G View FIG ).
Axial parenchyma. The phloem parenchyma is typically sieve-tube-centric, surrounding the groups of sieve elements ( Fig. 11B, C, E, F View FIG ). In Cuspidaria convoluta , lignified lines of phloem parenchyma cross the entire phloem wedge ( Fig. 11C View FIG yellow arrows); some non-lignified lines are also found occasionally in this species ( Fig. 11F View FIG ).
Fibers. Fibers are very abundant, forming background tissue ( Fig. 11 View FIG A-C, F).
Rays. The limiting rays are lignified to both xylem and phloem faces ( Fig. 11A View FIG ), with a radial row non-lignified between them. The wedge rays have randomly alternating portions lignified and non-lignified. The lignified portions never bear crystals and are differentiated very close to the cambium.
Crystals. Acicular and navicular crystals are present solely on the non-lignified portions of the phloem and ray parenchyma.
Periderm
A single periderm is formed. The phellem is stratified, composed of thin and thick-walled cells in alternation. The phelloderm is thick, with over three cell layers, non-stratified ( Table 2 View TABLE ). In Tynanthus the lenticels are non-stratified, with unlignified filling tissue ( Table 2 View TABLE ). In Cuspidaria the lenticels are stratified, with a closing layer of lignified cells ( Table 2 View TABLE ).
FISCHER E., THEISEN I. & LOHMANN L. G. 2004. - Bignoniaceae. in KUBITZKI K. & KADEREIT J. K. (eds), The Families and Genera of Vascular Plants. VII. Dicotyledons. Lamiales (except Acanthaceae including Avicenniaceae). Springer-Verlag, Heidelberg: 9 - 38.
KAEHLER M., MICHELANGELI F. A. & LOHMANN L. G. 2019. - Fine tuning the circumscription of Fridericia (Bignonieae, Bignoniaceae). Taxon 68: 751 - 770. https: // doi. org / 10.1002 / tax. 12121
LOHMANN L. G. & TAYLOR C. M. 2014. - A new generic classification of tribe Bignonieae (Bignoniaceae). Annals of the Missouri Botanical Garden 99: 348 - 489. https: // doi. org / 10.3417 / 2003187
MEDEIROS M. C. M. P. & LOHMANN L. G. 2015. - Taxonomic revision of Tynanthus (Bignonieae, Bignoniaceae). Phytotaxa 216: 1 - 60. https: // doi. org / 10.11646 / phytotaxa. 216.1.1
FIG. 11. — Secondary phloem of the Cuspidaria-Tynanthus clade: A-F, transverse sections; G, longitudinal tangential section; A, overall view of the phloem at the wedge and interwedges. Fibrous variant phloem, Tynanthus cognatus; B, detail of the variant phloem. Sieve tubes radially elongated (*), generally in tangential multiples, surrounded by sieve-tube-centric parenchyma, all embedded in a matrix of fibers. Two to four companion cells per sieve tube, lying on their corner (arrows), Tynanthus cognatus; C, Fibrous phloem. Sieve tubes (*) solitary or in tangential multiples.Sieve-tube centric parenchyma, Cuspidaria convoluta; D-F, comparison of the sieve tube dimensions on regular and variant portion of Tynanthus cognatus; D, regular phloem with thin fiber bands and assemblages (arrows); E, variant phloem. Sieve tubes with two to four (or more) companion cells, lying at the same corner of the sieve tube; F, Variant phloem of Cuspidaria convoluta. Sieve tubes (*) solitary or in multiples. Parenchyma band present (arrows); G, sieve tubes are lower than 1 mm, with inclined, compound sieve plates. Rays varying from 2 to 8-seriate. Scale bars: A, G, 200 μm; B, C, 100 μm; D-F, 50 μm.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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