A cladistic evaluation of the lower and higher green plants (Viridiplantae)

This paper presents a cladistic analysis and classification of the green plants (Viridiplantae). It is intended to be more balanced than previous treatments because more attention is paid to the lower green plants, or green algae. A major dichotomy is reflected by the structure of the flagellar root system of motile cells. Taxonomically, this justifies recognition of two divisions of green plants, viz.Chlorophyta sensu stricto, andAnthocerotophyta. The latter embraces a portion of the green algae plus all embryophytes. From a cladistic viewpoint it is doubtful whether land plants are strictly monophyletic.     

The phylogeny of land plants: A cladistic analysis based on male gametogenesis

A cladistic analysis was carried out to resolve phylogenetic pattern among bryophytes and other land plants. The analysis used 22 taxa of land plants and 90 characters relating to male gametogenesis.Coleochaete orChara/Nitella were the outgroups in various analyses using HENNIG86, PAUP, and MacClade, and the land plant phylogeny was unchanged regardless of outgroup utilized. The most parsimonious cladograms from HENNIG86 (7 trees) have treelengths of 243 (C.I. = 0.58, R.I. = 0.82). Bryophytes are monophyletic as are hornworts, liverworts, and mosses, with hornworts identified as the sister group of a liverwort/moss assemblage. In vascular plants, lycophytes are polyphyletic andSelaginella is close to the bryophytes.Lycopodium is the sister group of the remaining vascular plants (minusSelaginella). Longer treelengths (over 250) are required to produce tree topologies in which either lycophytes are monophyletic or to reconstruct the paraphyletic bryophyte phylogeny of recent authors. This analysis challenges existing concepts of bryophyte phylogeny based on more classical data and interpretations, and provides new insight into land plant evolution.     

A functional classification of wetland plants

Abstract. In this paper we review the search for guilds in plant communities, and provide a summary of the process, emphasizing five steps: (1) defining function, (2) selecting traits which reflect function, (3) screening for those traits, (4) constructing trait matrices, and (5) grouping species according to these traits. We illustrate this process for wetland plant species based upon a matrix of 27 traits and 43 species from across eastern North America. The 43 species were selected to represent the widest range of life history types possible as well as both common species and nationally rare or endangered species. We found three main functional groups: ruderals, matrix and interstitial species, which we subdivide into a total of seven guilds. The growing number of such studies in the literature suggest that this may be an expedient measure for conservation biology and a promising one for predictions.     

A cladistic analysis of the tribeAstereae (Asteraceae) with notes on their evolution and subtribal classification

TheAstereae were surveyed and the genera arranged in 23 informal groups. The generic groups were used to sample representative genera for a cladistic analysis based on morphological characters. The resulting cladogram was used for discussion of evolution and subtribal classification within the tribe. The lower basic chromosome numbers x = 4, 5, 6, and 8 are interpreted as reductions from a primitive x = 9. The subtribeGrangeinae occupies a phylogenetically basal position as sister group to the rest of the tribe. This may be divided into two large groups, largely corresponding to the homochromousSolidagininae and to the heterochromousAsterinae sensu lato, i.e. including theBellidinae, Hinterhuberinae, Conyzinae, andBaccharidinae. The latter four subtribes are derived within theAsterinae, and hence reduced to synonymy. Several intercontinental relationships indicate that a geographical subdivision of the tribe should be avoided, although in our analysis most of the groups proved to be restricted to one of five major regions.     

A cladistic analysis of interspecific relationships ofSaguinus

The dental and cranial morphologies of all species ofSaguinus, S. oedipus, S. geoffroyi, S. leucopus, S. nigricollis, S. fuscicollis, S. labiatus, S. mystax, S. imperator, S. bicolor, andS. midas are examined. The following hypotheses are developed by cladistic methodology, using only synapomorphic characters to assess the interspecific relationships ofSaguinus.Saguinus are divided into two main groups; one consists ofS. oedipus, S. geoffroyi, andS. leucopus, and the other includesS. inustus, S. nigricollis, S. fuscicollis, S. labiatus, S. mystax, S. imperator, S. bicolor, andS. midas. In the former group,S. oedipus is more closely related toS. geoffroyi than either is toS. leucopus. In the latter group,S. labiatus, S. mystax, andS. imperator are classified into one group, andS. bicolor andS. midas form one monophyletic group.     

安徽黄精属(Polygonatum)植物的分支分析

以形态学为依据 ,结合细胞分类学、叶表皮和花粉形态的研究成果 ,用分支分析的方法探讨了安徽产黄精属 11种植物的种间演化关系。在分支分析中 ,选择万寿竹属、舞鹤草属和竹根七属作为复合外类群。根据复合外类群比较原则和一般演化规律 ,确定性状极性。结果表明 :( 1)琅琊黄精与长苞黄精为姊妹群 ,并与其余 9种黄精明显分为 2大支 ;( 2 )另一支 9种黄精中 ,玉竹、长梗黄精和金塞黄精亲缘关系密切并与其余 6种再分为 2支 ;( 3)剩下 6种黄精中 ,距药黄精和多花黄精 2种互生叶黄精极为密切并与 4种轮生叶黄精分为 2组 ;( 4 ) 4种轮生叶黄精中 ,黄精、轮叶黄精和安徽黄精亲缘关系最为密切     

A cladistic analysis of Haemanthus and Scadoxus

Estimates, based on various cladistic methods, of the evolutionary relationship between the species of Haemanthus and Scadoxus are presented. The different methods are compared and discussed. On the data available the compatibility analysis gave a result easier to explain biologically compared to the parsimony analysis. In Haemanthus the results are ambiguous and more data needed. In Scadoxus the following sub–generic division is supported: Two subgenera, Scadoxus and Demeusea , the first with two sections, Scadoxus and Gyaxis , the second with three, Demeusea, Gamolepis and Choananthus.     

A cladistic analysis of the anomalocystitid mitrates

A cladistic analysis of the anomalocystitid mitrates is presented. A neutral terminology for the anomalocystitid skeleton is proposed, independent of the zoological interpretation of the fossils as echinoderms or as craniates. The anomalocystitid monophyly is supported by parsimony, although the instability of several basal taxa makes it difficult to ascertain the sequence in which characters were acquired or modified in the transition from the mi-trocystitids to the anomalocystitids. The genus Barrandeocarpus falls outside the anomalocystitids as traditionally defined in the literature, and is either polyphyletic or monophyletic. Diamphidiocystis drepanon is either a basal anomalocystitid or the sister taxon to the group ( Enoploura popei + Allanicytidiidae). Ateleocystites guttenbergensis is placed either at the base of the anomalocystitids or as the sister taxon to a group including mainly boreal forms, the only non-boreal members being the South African Bokkeveldia oosthuizeni and the Australian Victoriacystis wilkinsi.     

Light production by green plants

1. Green plants have been found to emit light of approximately the same color as their fluorescent light for several minutes following illumination. This light is about 10^–3 the intensity of the fluorescent light, about one-tenth second after illumination below saturation or 10^–6 of the intensity of the absorbed light. 2. The decay curve follows bimolecular kinetics at 6.5°C. and reaction order 1.6 at 28°C. 3. This light saturates as does photosynthesis at higher light intensities and in about the same intensity range as does photosynthesis. 4. An action spectrum for light emitted as a function of the wave length of exciting light has been determined. It parallels closely the photosynthetic action spectrum. 5. The intensity of light emission was studied as a function of temperature and found to be optimal at about 37°C. with an activation energy of approximately 19,500 calories. Two-temperature studies indicated that the energy may be trapped in the cold, but that temperatures characteristic for enzymatic reactions are necessary for light production. 6. Illumination after varying dark periods showed initial peaks of varying height depending on the preceding dark period. 7. 5 per cent CO₂ reversibly depresses the amount of light emitted by about 30 per cent. About 3 minutes are required for this effect to reach completion at room temperatures. 8. Various inhibitors of photosynthesis were tested for their effect on luminescence and were all inhibitory at appropriate concentrations. 9. Irradiation with ultraviolet light (2537A) inhibits light production at about the same rate as it inhibits photosynthesis. 10. This evidence suggests that early and perhaps later chemical reactions in photosynthesis may be partially reversible.     

Homoserine esterification in green plants

Extracts of phylogenetically diverse plans were surveyed for their ability to synthesize the following homoserine esters which are potential precursors for methionine and threonine synthesis in green plants: O-acetyl-, O-oxalyl-, O-succinyl-, O-malonyl-, and O-phosphohomoserine. Synthesis of O-acylhomoserine esters was detected only in Pisum sativum L. and Lathyrus sativus L. Extracts of P. sativum, a plant known to accumulate O-acetylhomoserine, catalyzed the specific synthesis of this ester from homoserine and acetyl-CoA. Extracts of L. sativus, a plant known to accumulate O-oxalylhomoserine, catalyzed the specific synthesis of this ester from homoserine and oxalyl-CoA. None of the other plants surveyed, including representatives of the green algae, horsetails, gymnosperms, and angiosperms, catalyzed the synthesis of any of the O-acylhomoserine esters studied. In contrast, synthesis of O-phosphohomoserine by the reaction catalyzed by homoserine kinase was demonstrated in extracts of all plants examined, including the two exceptional legumes.     

A simple classification of the complex parts of vascular plants

Four operational morphological units are defined to characterize 'typical' stems, leaves, roots and hairS. Any complex part can be classified among these OMUs by a graphical representation or by a quadruplet suitable for computer-aided analyses. Thirty-nine examples are given, suggesting a continuous view of plant morphology.