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Pollen morphology of the Euphorbiaceae with special reference to taxonomy

01 Jan 1962-
TL;DR: The morphology of the pollen grains of the Stenolobeae is in agreement with the opinion of PAX, that any separation of these Australian genera is an artificial one.
Abstract: In the present study pollen morphology of the Euphorbeaceae is treated as an additional character in taxonomy. Besides the greater part of the genera occurring in the system of PAX and K. HOFFMANN (1931), most of the genera published after 1931 are studied. The pollen grains have been described with the aid of a terminology as simple as possible. In principle the terminology of IVERSEN and TROELS-SMITH has been followed, although in addition, many improvements of ERDTMAN have been used. One of the simplifications is the rejection of POTONIE’s term sculpture. All elements occurring on the endexine are called structure elements; all structure elements together form the structure of a pollen grain. For the sake of consequence endexine apertures and extexine apertures are discussed separately. Different pollen grains are placed in different pollen types. If the differences are of minor importance, the pollen grains are placed in subtypes. Several types can have some characters in common. To express the correspondences, these types are assembled in configurations. As the pollen types in Phyllanthoideae and Crotonoideae differ distinctly, the division of the Euphorbiaceae in these subfamilies is maintained in the discussion of the results. The Phyllanthodieae can be separated in three large groups of pollen types ( Antidesma configuration, Amanoa configuration and Aristogeitonia configuration), which agrees with the grouping of PAX in 1924. The remaining small configurations belong in taxonomic respect to the genera of the Antidesma configuration. In the Crotonoideae many genera possess pollen grains with a croton-pattern. These genera should be treated as a single group. Besides this natural group, the Plukenetiinae possess pollen grains which are clearly distinguished from other genera in the Crotonoideae. Pollen grains of Omphalea are similar to those in the Plukenetia configuration. This pollen-morphological result agrees with the opinion of CROIZAT. The remaining pollen grains in the Crotonoideae are less easy to differentiate in groups. One of the largest configurations is the Mallotus configuration, which includes most genera of the Acalypheae and several genera or other tribes. The Hippomane configuration is another large one. This configuration comprises the tribes Hippomaneae and Euphorbieae. The pollen grains of both tribes are very similar. The genus Pachystroma is pollen-morphologically as well as taxonomically related to the tribe Hippomaneae. Pera, treated as a separate tribe by PAX and K. HOFFMANN, is related by its pollen grains to some genera in the Acalypheae. Dalechampia is habitually related to the genera in the Plukenetiinae. Pollenmorphological data, however, do not support this relation. The pollen grains of Dalechampia are not similar to any other pollen type. The morphology of the pollen grains of the Stenolobeae is in agreement with the opinion of PAX, that any separation of these Australian genera is an artificial one.
Citations
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Journal ArticleDOI
TL;DR: The glossary of pollen and spore terminology was first presented to the international palynological community as the final outcome of the Working Group onPalynological Terminology at the 8th International Palynological Congress in Aix-en-Provence in 1992 and became widely accepted as reference guide for palynologists to assist in the preparation of accurate and consistent descriptions of their material.

1,985 citations


Additional excerpts

  • ...Atrium (Punt, 1962) Synonym of fastigium....

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Journal ArticleDOI
Jan Muller1
TL;DR: The fossil record for angiosperm pollen types which are comparable to recent taxa is evaluated, following a similar survey published in 1970, with special attention paid to the dating of the sediments.
Abstract: The fossil record for angiosperm pollen types which are comparable to recent taxa is evaluated, following a similar survey published in 1970. Special attention is paid to the dating of the sediments. Evidence for 139 families is considered to be reliable, for others the records are cited as provisional, pending the accumulation of more evidence. Some published records are shown to be erroneous.

919 citations

Journal ArticleDOI
TL;DR: These data provide greatly increased support for the recent additions of Aneulophus, Bhesa, Centroplacus, Ploiarium, and Rafflesiaceae to Malpighiales; sister relations of Phyllanthaceae + Picrodendraceae, monophyly of Hypericaceae, and polyphyly of Clusiaceae.
Abstract: The eudicot order Malpighiales contains ∼16000 species and is the most poorly resolved large rosid clade. To clarify phylogenetic relationships in the order, we used maximum likelihood, Bayesian, and parsimony analyses of DNA sequence data from 13 gene regions, totaling 15604 bp, and representing all three genomic compartments (i.e., plastid: atpB, matK, ndhF, and rbcL; mitochondrial: ccmB, cob, matR, nad1B-C, nad6, and rps3; and nuclear: 18S rDNA, PHYC, and newly developed low-copy EMB2765). Our sampling of 190 taxa includes representatives from all families of Malpighiales. These data provide greatly increased support for the recent additions of Aneulophus, Bhesa, Centroplacus, Ploiarium, and Rafflesiaceae to Malpighiales; sister relations of Phyllanthaceae + Picrodendraceae, monophyly of Hypericaceae, and polyphyly of Clusiaceae. Oxalidales + Huaceae, followed by Celastrales are successive sisters to Malpighiales. Parasitic Rafflesiaceae, which produce the world's largest flowers, are confirmed as embedded within a paraphyletic Euphorbiaceae. Novel findings show a well-supported placement of Ctenolophonaceae with Erythroxylaceae + Rhizophoraceae, sister-group relationships of Bhesa + Centroplacus, and the exclusion of Medusandra from Malpighiales. New taxonomic circumscriptions include the addition of Bhesa to Centroplacaceae, Medusandra to Peridiscaceae (Saxifragales), Calophyllaceae applied to Clusiaceae subfamily Kielmeyeroideae, Peraceae applied to Euphorbiaceae subfamily Peroideae, and Huaceae included in Oxalidales.

301 citations

Journal ArticleDOI
TL;DR: Parsimony and Bayesian analyses of plastid rbcL and trnL-F DNA sequence data of the pantropical family Euphorbiaceae sensu stricto (s.s.) show that two subfamilies, 14 tribes, and 10 genera were found to be para- or polyphyletic.
Abstract: Parsimony and Bayesian analyses of plastid rbcL and trnL-F DNA sequence data of the pantropical family Euphorbiaceae sensu stricto (s.s.) are presented. Sampling includes representatives of all three subfamilies (Acalyphoideae, Crotonoideae, and Euphorbioideae), 35 of 37 tribes and 179 of the 247 genera of uniovulate Euphorbiaceae sensu lato (s.l.). Euphorbiaceae s.s. were recovered as a monophyletic group with no new adjustments in circumscription. Two clades containing taxa previously placed in Acalyphoideae are found to be successive sisters to all other Euphorbiaceae s.s. and are proposed here at subfamilial rank as Peroideae and Cheilosoideae. The remainder of the family fall into seven major lineages including Erismantheae and Acalyphoideae s.s. (parts of Acalyphoideae), Adenoclineae s.l., Gelonieae, articulated crotonoids and inaperturate crotonoids (parts of Crotonoideae), and Euphorbioideae. Potential synapomorphies and biogeographical trends are suggested for these clades. Acalyphoideae s.s., inaperturate crotonoids, and Euphorbioideae tribe Hippomaneae each have two major subclades that represent novel groupings without apparent morphological synapomorphies. Two subfamilies, 14 tribes, and 10 genera were found to be para- or polyphyletic. Noteworthy among these, Omphaleae are embedded in Adenoclineae, Hureae 1 Pachystromateae in Hippomaneae, Ditta in Tetrorchidium, and Sapium s.s. in Stillingia.

284 citations

References
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Journal ArticleDOI
TL;DR: Palynology is a rather heterogeneous subject, and the establishment of a separate section of palynology at the VIII International Botanical Congress can hardly be described as an unqualified success, but informal palynological meetings with a restricted membership have taken place more or less regularly.
Abstract: The term " palynology " was coined by Hyde and Williams 1 to cover all work with pollen grains and spores. The term is convenient and has been widely accepted, but it must not be taken to indicate that palynology should have a status as a science of its own. This it is not: pollen grains and spores are used in a wide variety of investigations in pure and applied botany, recent and fossil, which have practically nothing in common except the fact that pollen and spores are used as instruments of research. In that respect palynology resembles microscopy: the microscope is also used as an instrument in a great variety of unrelated investigations. There is a special science of the microscope, which is a branch of optics, and there is a special science of the pollen grain, viz., pollen morphology, which is a branch of plant morphology. The difference is that, whereas " microscopy " means the application of the microscope, " palynology " comprises both the science itself, i.e., pollen morphology, and its application. Palynology is a rather heterogeneous subject, and the establishment of a separate section of palynology at the VIII International Botanical Congress (Paris, 1954) can hardly be described as an unqualified success. This failure does not reflect unfavourably on the French organizing committee which had done very good preparatory work, nor was it due to the loss of time spent in discussions of administrative problems. The inherent weakness was, I think, the heterogeneity of the subject. The much smaller palynological symposium arranged by Dr. Erdtman in connection with the VII International Botanical Congress (Stockholm, 1950) was very successful. Similar international symposia ought to be arranged informally in the future for discussing technical problems. Both in Europe and in the United States informal palynological meetings with a restricted membership have taken place more or

93 citations


"Pollen morphology of the Euphorbiac..." refers background or methods in this paper

  • ...According to Faegri and Iversen they are called: baculae. clavae, echinae, gemmae, scabrae■ and verrucae (PI. I, F2 t/m 7) (for descriptions see glossary). Psilate pollen grains have no structure elements on the tectum (PI. I, FI). Structure elements on the top of the tectum may also be arranged in different structure types (reticulum, striae). If a tectum is present, corresponding structure types of the columellae are called intra-reticulum, intra-striae. Sometimes columellae can give an impression of a reticulum. This is, however, a “pseudo-reticulum” in which each columella represents a “ lumen ” and the space between the columellae, the “ muri”. A real reticulum is always formed by several structure elements. In the present study no difference is made between structure and sculpture. According to Potonié (1934), all elements outside the tectum form the sculpture of a pollen grain....

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  • ...According to the nomenclature of Faegri and Iversen the pollen grains of Neoscortechinia are scabrate. The author would like to call the small spines microechinate according to Erdtman (1952). Echinate pollen grains are rarely found in the subfamily of the Crotonoideae, only in the Croton configuration....

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  • ...According to Faegri and Iversen they are called: baculae. clavae, echinae, gemmae, scabrae■ and verrucae (PI. I, F2 t/m 7) (for descriptions see glossary). Psilate pollen grains have no structure elements on the tectum (PI. I, FI). Structure elements on the top of the tectum may also be arranged in different structure types (reticulum, striae). If a tectum is present, corresponding structure types of the columellae are called intra-reticulum, intra-striae. Sometimes columellae can give an impression of a reticulum. This is, however, a “pseudo-reticulum” in which each columella represents a “ lumen ” and the space between the columellae, the “ muri”. A real reticulum is always formed by several structure elements. In the present study no difference is made between structure and sculpture. According to Potonié (1934), all elements outside the tectum form the sculpture of a pollen grain. Potonié tried to give sharp definitions of these terms, but admitted at the same time, that structure and sculpture pass into each other. Faegri and Iversen (1950) also stated, that structure and sculpture are easy to confuse....

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  • ...Faegri and Iversen (1950) confuse this aperture with a real porus when the coipus transversalis has the shape of a circle....

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  • ...Faegri and Iversen (1950) confuse this aperture with a real porus when the coipus transversalis has the shape of a circle. Consequently, when using their key for the determination of European pollen types, it is sometimes difficult to decide if a “porus longitudinal elongated” or a “transversal furrow” is present. Erdtman calls coipi + coipi transversales “composite apertures”. For the term coipus transversalis he introduced the new term os (pi. ora). If this term is used in that sense the name will have to be rejected as being a synonym. It may, however, be maintained for that part of the coipus transversalis that crosses the colpus (PI. I, D3). Coipi transversales stand perpendicular on the colpi. Usually they are boat-shaped. Sometimes they fuse together into one single aperture along the equator of the pollen grain (colpus transversalis equatorialis), but it is also possible that the colpus transversalis becomes isodiametric (colpus transversalis circularis PI. I, D2). The medial dimension of the colpus transversalis is rarely larger than the equatorial one (Pleiostemon type, p. 30). Edges of colpi transversales can also have thickenings; according to the shape of the colpus transversalis they are called: costae circulares, costae transversales and costae equatoriales (PL I, D4, 5, 6). To express the proportions of the colpus transversalis in exact figures, the quotient m : e is added to the description of this character. In this formula m is the meridional axis and e the equatorial axis of the colpus transversalis (PI. I, Dl). Iversen and Troels-Smith (1950) introduced the term Polar Area Index (P....

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MonographDOI
01 Jan 1858

86 citations