Chromosome numbers in the genus Mentha L.

One hundred and fifty-seven chromosome numbers of a range of taxa from both hemispheres are reported in the genus Mentha. Plants of both wild and cultivated origin have been sampled, including hybrids, some of which have been synthesized from known parents. Some of the causes of the great taxonomic complexity of the group are discussed and the need for accurate and unambiguous identification of the plant material is stressed. There is a critical review of the chromosome numbers in relation to their taxonomy, with a discussion on probable basic numbers. The most useful areas of future research are indicated.     

Chromosome evolution in the genus Ophioglossum L.

Cytological observations on eleven species of Ophioglossum revealed low gametic ( n ) chromosome numbers of 30, 34 and 60 in populations of O.eliminatum , contrasting with an earlier report of n = 90 in the same species. The rest of the species is based on n =120.Cytologically studied species of Ophioglossum exhibit a range of chromosome numbers from n = 30 in O.eliminatum to n =720 in O.reticulatum. The weighted highest common factor (HGF) from all the reported chromosome numbers in twelve species was found to be 30. This number is proposed as the palaeobasic chromosome number for the genuS. Reported chromosome numbers which are not multiples of 30 were subjected to sequential analysis, yielding three distinct ultimate base numbers, 4, 5 and 6, which can produce n = 30 in seven different ways. The neobasic number, n= 120, appears to have arisen through various combinations and permutations of these, theoretically 2401 routes; only a relatively few of these routes exist today, suggesting that extreme selection has been exerted against the majority, and further suggesting that Ophioglossum represents an evolutionary dead end through repeated cycles of polyploidy and is possibly at the verge of extinction. The stoichiometric model of evolution, which derives the various chromosome numbers possessed by the twelve species from the basic and ultimate basic chromosome numbers, is used to explain chromosomal evolution in the genus.     

Chromosome numbers in plant cytotaxonomy: concepts and implications

Chromosome number is the karyotype feature most commonly used in cytotaxonomical analyses. The chromosome number can be a plesiomorphic characteristic of a large clade or a recurrent trait which arose independently in two or more clades. Some concepts regarding chromosome number variation, such as base number, aneuploidy, paleopolyploidy, and neopolyploidy have been used by different authors in quite different ways. Therefore, its use in cytotaxonomy and karyotype evolution deserves much attention. In this paper, these terms are reappraised and their meaning and implication for plant cytotaxonomy are discussed.     

Chromosome numbers in the genus Lippia (Verbenaceae)

The genus Lippia (Verbenaceae) comprises about 200 taxa mainly distributed in Brazil, Mexico, Central America, Africa, Argentina and Paraguay. Some problems involving the number and delimitation of species have been reported. In order to contribute to the solving of these problems, the chromosome numbers of 14 Lippia species are documented. The following species were collected at Espinhaço Range, Southeast Brazil: Section Zapania (L. corymbosa, L. diamantinensis, L. hermannioides, L. lacunosa, L. rotundifolia, L. rubella), section Rhodolippia (L. florida, L. lupulina, L. pseudothea, L. rosella), section Goniostlachyum (L. glandulosa, L. pohliana, L. sidoides) and section Dioicolippia (L.filifolia). Immature inflorescences were collected and the ideal size for chromosome observation was determined. The majority of species have a haploid chromosome number from 10 to 14. Few species have a higher chromosome number, which suggests the occurrence of polyploidy. The relationships between chromosome numbers and the taxonomic sections are also discussed.     

Chromosome numbers and taxonomic notes in the genus Nama (Hydrophyllaceae)

Chromosome numbers are reported for 48 collections representing 15 species and three varieties ofNama. Counts for 10 taxa are initial reports, all being diploid withn = 7. Diploid counts forN. jamaicense (n = 7), previously known only as tetraploid, are also reported. Comments on the taxonomic relationships of selected taxa are included.     

Chromosome numbers and their taxonomic implications in the genusPoa of Japan

As part of the work leading to a taxonomic revision ofPoa of Japan, chromosome numbers of nearly all indigenous species of JapanesePoa, together with those of some putative interspecific hybrids, were examined. The following chromosome numbers were found:Poa annua, 2n=28;P. crassinervis, 2m=28;P. acroleuca, 2n=28;P. hisauchii, 2n=28;P. nipponica, 2n=28;P. crassinervis, 2n=28;P. acroleuca, 2n=35;P. tuberifera, 2n=28;P. fauriei, 2n=28;P. radula, 2n=42;P. hakusanensis, 2n=70;P. hayachinensis, 2n=42;P. malacantha var.shinanoana, 2n=63≈98;P. yatsugatakensis, 2n=ca. 71≈74, 77;P. sachalinensis, 2n=63, ca. 64, ca. 74;P. matsumurae, 2n=28;P. ogamontana, 2n=42;P. sphondylodes, 2n=28;P. viridula, 2n=42, 49, 56;P. nemoralis, 2n=70;P. glauca, 2n=42, 49, 56;P. eminens, 2n=42. It became clear that information obtained from chromosome counts is quite helpful in clarifying species boundaries in several species aggregates, such as thePoa acroleuca-hisauchii-nipponica aggregate. Results of the examination of morphological features of the voucher specimens in various species aggregates with taxonomic difficulties were reported, and the needs of some amendments for the species delimitation appearing in current floristic manuals were pointed out. A summary of chromosome counts so far made for JapanesePoa was tabulated. ThePoa flora of Japan characteristically lacked diploid plants.     

Chromosome numbers and their systematic implications in Australian marine angiosperms: ThePosidoniaceae

Somatic chromosome numbers of 2n = 20 are reported for all eight species of AustralianPosidonia: P. angustifolia, P. australis, P. coriacea, P. denhartogii, P. kirkmanii, P. ostenfeldii, P. robertsonae, andP. sinuosa. All species apparently have five larger and five smaller pairs of chromosomes. There is no evidence that speciation inPosidonia, which is relatively prolific in comparison to other seagrasses, is accompanied by change of chromosome number.     

Taxonomic and evolutionary relationships in the genus Vella L. (Cruciferae)

Thirty-two differential characters are numerically analysed for the six existing taxa of the genus Vella L. The closely related monotypic genus Boleum Desv. is also included for comparison. Most of the characters used are morphological, but cariological, ecological and biogeographical aspects have also been studied. The results indicate that four distinct species, one ( V. pseudocytisus L.) with three sub-species, should be distinguished. The new combination V. anremerica (Lit. et Maire) Gómez-Campo (basionym: V. pseudocytisus L. subsp. anremerica Lit. et Maire) and the new name V. pseudocytisus L. subsp. paui Gómez-Campo for V. pseudocytisus L. var. glabrescens Willk., nornen nudum are presented. A key is given to aid identification of these taxa. Their conservation status is also discussed.     

Chromosome numbers and taxonomic implications in the fern genusAzolla (Azollaceae)

Investigation of chromosome numbers of allAzolla species, and for the first time of hybrids, has been undertaken. Removal of wax from the leaf surface proved invaluable in achieving clear cytological preparations and providing unambiguous chromosome numbers. In contrast to previous records, the speciesA. pinnata, A. filiculoides, A. filiculoides var.rubra, A. caroliniana, A. microphylla, andA. mexicana were found to be 2n=44, andA. nilotica to be 2n=52. Several triploids (2n=66) and one tetraploid (2n=88) were identified. No geographical pattern could be observed in the distribution of triploids which probably derive from the function of unreduced gametes. The chromosome number of hybrids occasionally deviates from the diploid chromosome number (2n=44). The small chromosome size limits karyotypic analysis and only differences in overall chromosome size can be observed. Taxonomic implications of chromosome numbers and sizes are discussed.     

Chromosome studies in southern species of Mimosa (Fabaceae,Mimosoideae) and their taxonomic and evolutionary inferences

In this work, chromosome numbers and karyotype parameters of 36 taxa of the genus Mimosa were studied, especially from the southern South America center of diversification. Results support that x = 13 is the basic chromosome number in the genus. Polyploidy is very frequent, ca. 56 % of the total of the studied species here are polyploid, confirming that polyploids are more frequent at higher latitudes. The most common ploidy levels found are 2x and 4x, but some species studied exhibit 6x and 8x. In different groups, several ploidy levels were found. Parameters of chromosome size show statistically significant differences between close species, and asymmetry index A ₂ exhibited low variation between them. It is possible to infer variations of chromosome size between diploids and tetraploids and between basal and derived taxa. The present studies confirm or reveal polyploidy in several groups of South America which are highly diversified in the southernmost area of distribution of the genus, such as sect. Batocaulon ser. Stipellares and sect. Calothamnos. Our data are discussed in a taxonomic context, making inferences about the origin of some polyploid taxa. Polyploidy could be an important phenomenon that increases the morphologic diversity and specific richness in southern South America. On basis of our data, it is possible to hypothesize hybridization between same-ploidy level or different ploidy level taxa. As already shown in the literature, our results confirm the importance of the polyploidy in the speciation of the genus.     

Chromosome numbers in Compositae. XVIII.

Chromosome numbers and other cytogenetic data were determined from microsporocytes in 316 collections including 13 tribes of Compositae, mostly from Africa, Australia, Mexico, Central America, and South America. First reports are provided for 66 species and the genera Cassinia (2n ≈ 14_II), Feldstonia (2n = 11_II), Gochnatia (2n ≈ 23_II), and Pseudoconyza (n = 10). In addition, new chromosome numbers are established at the generic level in Acourtia, Calea, Craspedia, Gnaphalium, Helipterum, Liabum, Leucheria, Smallanthus, Trixis, and Viguiera and at the specific level in 13 additional species.     

On the Phloem of Mimosa pudica L.

The phloem of Mimosa pudica L. was examined in view of somereports that the sieve elements in this plant show featuresnot previously described for these cells in Leguminosae. Inthe present study only a usual dicotyledonous type of sieveelement was recognized. The sieve elements pass through stagesof differentiation involving development and dispersal of P-proteinbodies, disintegration of nuclei, and appearance of plastidsstoring a starch staining red with iodine. Callose occurs onthe transverse or moderately oblique sieve plates. The phloemcontains secretory cells. They are wide and long and have transverseor more or less inclined end walls. In younger cells the endwall bears in the centre a conspicuous pit to which the protoplastsof the superimposed cells are firmly attached. In many oldercells the pit region is replaced by a perforation so that thecontents of superimposed cells may be completely merged. Itremains to be determined whether the perforation is presentin an intact plant or results from a rupture during sampling.The secretory cells accumulate material that gives a positivetest for carbohydrates and a negative test for proteins.     

Chromosome numbers in the algae: Phaeophyta II

L-systems provide a method for modelling seaweed branching patterns in terms of simple rules. These rules can be used to generate computer graphics images of an alga's basic architecture, which, of course, is often obscured by adventiltious growth in living plants. L-systems provide a mathematical abstraction that allows us to compare species by focusing on essential differences in their substitution rules rather than relying entirely on the visual appearance of branching patterns. Two species of red algae from closely related genera in the Dasyaceae—Dasya rigidula and Dasysiphonia concinna—are virtually identical in pseudolateral branching detail and appear to diverge solely in terms of pseudolateral position. L-systems models and their graphical representations are presented to demonstrate that the two-dimensional, alternate-distichous pattern of pseudolateral position for Dasysiphonia concinna can be derived in a straightforward way from that of the three-dimensional, spiralled pattern of Dasya rigidula. These models illustrate a case in which generic distinction is based upon an easily observable but relatively trivial feature, differences other than branching pattern being quite subtle.