Chromosome numbers of Coleoptera from Argentina

A list is presented containing data on chromosome numbers and sex determining mechanisms of 90 species of Argentina beetles, belonging to the families Staphylinidae (2 spp.), Meloidae (3 spp.), Elateridae (1 sp.), Coccinellidae (5 spp.), Tenebrionidae (11 spp.), Scarabaeidae (30 spp.), Cerambycidae (3 spp.), Chrysomelidae (27 spp.), Curculionidae (7 spp.) and Lampyridae (1 sp.), Asphaera t-album (Chrysomelidae) had n=10+X+6y; in Epicauta atomaria (Meloidae) individuals with 2 n=22, 21 and 20 were found.This work was supported by grants of National Research Council of Argentina (CONICET) and SUBSYT.     

Chromosome numbers in Impatiens from Thailand

Chromosome numbers are given for Impatiens chiangdaoensis (2n = 12), I. violaeflora (2n = 10, 12) and I. mengtzeana (2n = 16). A survey of known chromosome numbers of Impatiens from Thailand is also given.     

Chromosome numbers of dominican compositae

Chromosome numbers of 34 species of Dominican Compositae in 26 genera and nine tribes are reported. First counts are given forCoreopsis buchii (2n = 64),Lagascea mollis (2n = 34),Spilanthes urens (n = 16),Liabum subacaule (n = 18),Eupatorium sciatraphes (2n = 40),Hieracium gronovii (2n = 18),Vernonia buxifolia (2n = 34),V. sprengeliana (2n = 34),V. racemosa (2n = 28), andChaptalia leiocarpa (2n = 48,ca. 58). Our report forNarvalina domingensis (2n = 120) is the first for any species of this genus.     

Chromosome numbers of Thai Rubiaceae

Chromosome numbers for 14 taxa of indigenous Thai Rubiaceae are presented. They include first counts for 3 genera: Aphaenandra (A. uniflora), Prismatomeris (P. tetrandra subsp. malayana) and Tarennoidea (T. wallichii) ; all show diploidy on x=11. The remaining counts are first counts for species: Argostemma diversifolium, A. neurocalyx and A. pictum, Coptosapelta flavenscens, Gardenia saxtilis, Ixora sp., Morinda sp., Mussaenda sanderiana, Oxyceros horridus, Rothmannia wittii (first count for an Asiatic species of the genus) (all diploid on x=11), and Canthium sp. (tetraploid on x=11). The poor state of karyological knowledge of indigenous Thai Rubiaceae is discussed, and a table including all relevant known chromosome counts is presented. Chromosome data are only known for 38 genera (ca. 41% of all Rubiaceae genera occurring in Thailand); chromosome numbers are often only available for one or few taxa of each genus [in sum, for only about 50 (or for roughly 10% of all) taxa]. Of only 14 genera (ca. 15%), chromosomes were counted from Thai material (for the others, counts originate from elsewhere, i.e. refer to more widely distributed taxa also extending into Thailand).     

Chromosome numbers of flowering plants from northern Norway and Svalbard

Chromosome numbers of 25 taxa of flowering plants from northern Norway and Svalbard are reported. Four species and one subspecies, Carex halophila F. Nyl. (2n = ca. 78), C. stenolepis Less. (2n = ca. 80), Salicorniapojarkovae N. Sem. (2n = 36), Alnus incano (L.) Moench ssp. kolaensis (Orlova) Love (2n = 28), and Saxifraga svalbardensis D. O. Øvstedal (2n = ca. 64), have not been studied karyologically before. Chromosome numbers of four additional species are reported for the first time from Norway; those of another six species for the first time from northern Norway. The hybrid Salix herbacea L. (2x) x 5. polaris Wahlenb. (6x) is proved tetraploid and may be fertile. A possible hybrid between Saxifraga hyperborea R. Br. and S. rivularis L. was revealed.     

Chromosome numbers in Nigerian Compositae

Chromosome counts are presented for 54 collections of Nigerian Compositae. The collections comprise 37 taxa belonging to 21 genera and 34 specieS. Most of the taxa studied are colonisers of disturbed habitats.     

Chromosome numbers of the Australian Zosteraceae

 Somatic chromosome numbers of 2n = 24 are reported for all three species of Australian Zostera: Z. capricorni Aschers., Z. muelleri Irmisch ex Aschers. and Z. mucronata den Hartog and 2n = 36 for Heterozostera tasmanica (Martens ex Aschers.) den Hartog. All Australian zosteroidean species apparently have similar chromosome morphology: dot-like or rod shaped. It is suggested that the chromosome number and its morphology can be used to distinguish genera and subgenera in the Zosteraceae but not for species identification, and that speciation is not accompanied by changes of chromosome numbers. Received December 1, 1999 Accepted September 6, 2000     

Chromosome numbers of fishes. I

The published chromosome numbers for 208 temperate and tropical freshwater fishes have been compiled in alphabetical order within the families. This facilitates the work for ichthyologists interested in the karyotype(s) of a particular species, genus or family as well as giving an overall account of the basic chromosome numbers and karyological trends in fishes.     

Chromosome numbers of the European seagrasses

The chromosome numbers of the five European seagrasses have been determined in material from several sites along the coasts of the Atlantic Ocean, the North Sea and the Mediterranean:Zostera marina L., 2n = 12;Z. noltii Hornem., 2n = 12;Posidonia oceanica (L.)Delile, 2n = 20;Cymodocea nodosa (Ucria)Aschers., 2n = 14, 2n = 28;Halophila stipulacea (Forsk.)Aschers., 2n = 18. The difference in chromosome morphology betweenZ. marina andZ. noltii supports the division of the genus into two subgenera.     

Chromosome numbers of miscellaneous Malagasy Acanthaceae

Meiotic chromosome numbers are reported for 12 species in eight genera of Acanthaceae from Madagascar. Chromosome numbers of 11 species are reported for the first time. Counts inMendoncia (n=19) andNeuracanthus (n=20) are the first for these genera. A new chromosome number (n=30) is reported inJusticia. Systematic implications of the chromosome counts are addressed and basic chromosome numbers for these eight genera of Malagasy Acanthaceae are discussed.     

Chromosome numbers of the Australian Cymodoceaceae

The somatic chromosome numbers of the eleven Australian seagrass species belonging to five genera in the Family Cymodoceaceae were determined. The chromosome numbers in Amphibolis and Thalassodendron are reported for the first time. Cymodocea and Halodule species have the following chromosome numbers: Cymodocea angustata Ostenf., 2n = 14, 28; C. rotundata Ehrenb. & Hempr. ex Asch., 2n = 14; C. serrulata (R. Br.) Asch. & Magnus, 2n = 14, 28; Halodule pinifolia (Miki) den Hartog, 2n = 32; H. uninervis (Forsk.) Asch., 2n = 32; H. tridentata (Steinh.) Endl. ex Unger, 2n = 14. Halodule has the highest chromosome numbers among the seagrasses and they are the largest in sizes with a distinct bimodal type in the family. Syringodium isoetifolium (Asch.) Dandy has 2n = 20. Both endemic Amphibolis antarctica (Labill.) Sonder ex Asch. and A. griffithii (J. Black) den Hartog have 2n = ca. 36 and have the smallest chromosomes in the family appearing as small dots. Thalassodendron pachyrhizum den Hartog has 2n = 28. Chromosome numbers appear to be identical or closely related among different species in the same genus but they vary in the five genera in the Cymodoceaceae suggesting that these five genera may have evolved independently in the past.     

Chromosome numbers of Costa Rican grasses

Chromosome counts are presented for 217 species of 103 genera of grasses from Costa Rica. Four of the genera and 90 of the species are reported for the first time. In addition, 26 counts differ from previous records for the same taxon. The generaGynerium, Lithachne, Luziola, andThrasya were heretofore unknown cytologically. First counts are also given for the following species:Agrostis bacillata, A. pittieri, A. sub patens, Andropogon angustatus, A. bicornis, A. virgatus, Aristida capillacea, A. jorullensis, Arundinella berteroniana, A. deppeana, Axonopus aureus, A. capillaris, A. chrysoblepharis, Bouteloua americana, B. disticha, Bromus exaltatus, Calamagrostis intermedia, C. nuda, C. pittieri, Chusquea lehmannii, C. tonduzii, Cinna poaeformis, Deschampsia pringlei, Digitaria panicea, Echinochloa polystachya, Echinolaena gracilis, Eragrostis simplicijlora, Eriochloa distachya, E. polystachya, Eriochrysis cayennensis, Festuca dolichophylla, Gymnopogon fastigiatus, Gynerium sagittatum, Hymenachne amplexicaulis, Imperata contracta, Isachne polygonoides, Ischaemum latijolium, Lithachne pauciflora, Luziola fragilis, Manisuris aurita, Panicum aquaticum, P. arundinariae, P. boliviense, P. cordovense, P. grande, P. haenkeanum, P. milleflorum, P. parviglume, P. pilosum, P. polygonatum, P. rudgei, P. stenodes, P. trichanthum, P. trichoides, P. viscidellum, Paspalum candidum, P. centrale, P. decumbens, P. fasciculatum, P. jimenezii, P. microstachyum, P. multicaule, P. nutans, P. parviflorum, P. pilosum, P. prostratum, P. pumilum, P. reclinatum, P. saccharoides, P. scabrum, P. serratum, P. squamulatum, P. standleyi, Pennisetum bambusiforme, P. distachyum, Pereilema beyrichianum, Pharus parvifolius, Sacciolepis myuros, Schizachyrium condensatum, Sorghastrum incompletum, Sporobolus ciliatus, S. purpurascens, Streptochaeta sodiroana, Thrasya gracilis, T. petrosa, T. robusta, Trisetum pringlei, T. tonduzii, Uniola pittieri, and Zeugites pittieri. In addition, the following counts are different from previous records for the same taxon:Aegopogon cenchroides, Axonopus poiophyllus, Bouteloua media, Brachiaria plantaginea, Chusquea subtessellata, Digitaria adscendens, Homolepis aturensis, Hymenachne donacifolia, Ichnanthus axillaris, I. pallens, I. tenuis, Ischaemum ciliare, Ixophorus unisetus, Oplismenus burmannii, O. hirtellus, Panicum geminatum, P. glutinosum, P. mertensii, P. parvifolium, P. sellowii, Paspalum convexum, Pennisetum nervosum, P. setosum, Polypogon elongalus, Raddia costaricensis, Schizachyrium hirtijlorum.