Molecular Cytogenetics of an Amphiploid Trigeneric Hybrid between Triticum durum, Thinopyrum distichum and Lophopyrum elongatum

In situ hybridization of total genomic DNA was used to analyselines derived from an amphiploid between tetraploid wheat,Triticumdurum Desf. (2n =4x =28), and the wheatgrassesThinopyrum distichum(Thunb.) A. Löve (2n =4x =28) andLophopyrum elongatum (Host)A. Löve (2n =2x =14). A range of chromosome numbers wasdetected, arising from loss or gain of chromosomes. Total genomicDNA probes fromThinopyrum species,L. elongatum andTriticum monococcumL. were able to discriminate chromosomes from the A and B genomesof tetraploid wheat and those of wheatgrass-origin. The methoddid not discriminate the two wheatgrass genomes, J and E, indicatingtheir close similarity. Chromosomal aberrations—includingtelocentric and ring chromosomes—were frequent. Distalinter-genomic translocations of parts of A and B genome chromosomearms, unusual in wheat itself, were more frequent than translocationsbetweenT. durum and wheatgrass.In situ hybridization of an rDNAprobe most frequently revealed four sites associated with secondaryconstrictions onT. durum chromosomes and four onTh. distichumorL. elongatum chromosomes, although there was variation inthe number of loci between and within plants. Within interphaseand prophase nuclei, the three genomes were not intermixed andoften lay in distinct sectors. Wheat; hybrids; Triticum ; Triticeae; evolution; introgression; nuclear architecture; rDNA; in situ hybridization     

Polyploidy and Evolution in Wild and CultivatedDahliaSpecies

Observations on the chromosomes of nine species ofDahliaCav.(Asteraceae, Heliantheae—Coreopsidinae) show that somehave 2n=32, others 2n=64, with a third group having both chromosomenumbers in the same taxon. Karyotype investigations showed thatthe chromosomes can be divided into groups of 14 metacentricsplus two submetacentrics per set of 16 chromosomes.In situhybridizationusing an rRNA gene probe indicated that the 2n=32 species haveeight hybridization sites whilst the 2n=64 species have 16 sites.Silver nitrate staining of these regions showed that not allof these nucleolar organizers are active. Meiotic analysis atmetaphase I and pachytene, by synaptonemal complex spreading,shows that the 2n=32 species have exclusive bivalent formationwhereas the 2n=64 species have small numbers of univalents plusquadrivalents in addition to bivalents. This study proposesthatDahliaspecies with 2n=32 are allotetraploids whereas thosespecies and chromosome races with 2n=64 are their autopolyploidderivatives. We suggest that a bivalent-promoting mechanismin the 2n=32 species may account for their meiotic behaviouras their component genomes appear so similar, and that thismechanism is also responsible for the low number of quadrivalentsin the 2n=64 taxa.Copyright 1998 Annals of Botany Comapny Chromosome pairing,Dahlia, in situhybridization, karyotype analysis, polyploidy, synaptonemal complex analysis     

Shoot Formation from Explant Cultures of Fourteen Potato Cultivars and Studies of the Cytology and Morphology of Regenerated Plants

Plants were regenerated in quantity from cultured excised stem,rachis or leaf pieces of 13 potato (Solarium tuberosum L.) cultivarsusing modifications of a two-step procedure. Pronounced differenceswere observed in the response of different cultivars and explantsources to medium formulations containing different auxins orcytokinins. A few plants were recovered from tuber pieces ofseven cultivars by a different two-step procedure. Morphologicaldifferences from control plants were observed in some of theprimary regenerants. Anthocyanin pigmentation of tubers wasscored and stable changes to red-splashed white or white tuberswere found in some plants regenerated from cv. Desiree. Regenerantsfrom the particoloured cultivars Cara and King Edward oftenlost this trait but it returned to varying extents in subsequentgenerations. Most of the regenerated plants (87 per cent) containedthe euploid number of chromosomes (2n = 4x = 48). The methodsare suitable for production of plants for assessment of somaclonalvariation in a range of genotypes. Potato breeding, somaclonal variation, chromosome variation, skin colour, explant culture, plant regeneration, solanum tuberosum L. potato     

The extent and position of homoeologous recombination in a distant hybrid of Alstroemeria: a molecular cytogenetic assessment of first generation backcross progenies

To estimate the extent and position of homoeologous recombination during meiosis in an interspecific hybrid between two distantly related Alstroemeria species, the chromosome constitution of six first generation backcross (BC₁) plants was analysed using sequential fluorescent in situ hybridization (FISH) and genomic in situ hybridization (GISH) analysis. Four different probes were used for the FISH analysis: two species-specific and two rDNA probes. The six BC₁ plants were obtained from crosses between the hybrid A. aurea×A. inodora with its parent A. inodora. GISH clearly identified all chromosomes of both parental genomes as well as recombinant chromosomes. The sequential GISH and FISH analysis enabled the accurate identification of all individual chromosomes in the BC₁ plants, resulting in the construction of detailed karyotypes of the plants. The identification of the recombinant chromosomes provided evidence which chromosomes of the two species are homoeologous. Two of the BC₁ plants were aneuploid (2n=2x+1=17) and four triploid (2n=3x=24), indicating that both n and 2n gametes were functional in the F₁ hybrid. Using GISH, it was possible to estimate homeologous recombination in two different types of gametes in the F₁ hyrid. The positions of the crossover points ranged from highly proximal to distal and the maximum number of crossover points per chromosome arm was three. Compared with the aneuploid plants, the triploid plants (which received 2n gametes) clearly possessed fewer crossovers per chromosome, indicating reduced chromosome pairing/recombination prior to the formation of the 2n gametes. Besides homeologous recombination, evidence was found for the presence of structural rearrangements (inversion and translocation) between the chromosomes of the parental species. The presence of the ancient translocation was confirmed through FISH analysis of mitotic and meiotic chromosomes. Received: 7 October 1998; in revised form: 4 December 1998 / Accepted: 10 December 1998     

Differential Accumulation of Heterochromatin as a Cause for Karyotype Variation in Phalaenopsis Orchids

Karyotypes of nine Phalaenopsis species and the closely relatedDoritis pulcherrima were compared based on Feulgen- and DAPI-stainedsomatic metaphase chromosomes prepared from root tips. All specieshad the same chromosome number (2n = 2x = 38), but their karyotypesdiffered markedly in absolute chromosome size, relative chromosomesize, and the position of the centromere. Both genome size andthe amount of constitutive heterochromatin (CH) varied widelyamong the species studied, and there was a positive correlationbetween these two parameters. The distribution of CH in thegenomes was non-random: one or both arms of long chromosomesusually possessed large blocks of CH, while the small chromosomescontained little or no CH. DAPI-staining revealed that mostCH regions are rich in AT base pairs. We suggest that differentialaccumulation of CH is a major cause for karyotype variationin Phalaenopsis orchids. Copyright 2001 Annals of Botany Company Phalaenopsis, Doritis pulcherrima, karyotype differentiation, constitutive heterochromatin, total chromosome volume, nuclear DNA content     

Spatial Separation of Ancestral Genomes in the Wild Grass Milium montianum Parl.

Previous work showed a strong tendency for genomes from twodifferent parents to be spatially separated in cell nuclei ofseveral man-made F₁ hybrids between grass species. An importantquestion therefore is whether similar nonrandom genome dispositionoccurs in wild species. Milium montianum Parl. (2n = 22) isa naturally occurring allopolyploid grass combining two geneticallydissimilar chromosome sets (V and M genomes), each originatingfrom a different ancestral species. These two ancestral genomeswere easily discriminated as all V genome chromosomes were largerthan all M genome chromosomes. In two-dimensional spread preparations,the V genome derived from M. vernale Bieb. (2n = 8), and theM genome (of different but uncertain origin) showed a highlysignificant tendency to lie apart. Generally, the V chromosomestended to surround the M chromosomes in both mitotic and meioticnuclei suggesting that this arrangement persists throughoutplant development. Such nuclear organization is probably undergenetic control and may facilitate some independent behaviourof ancestral genomes in allopolyploids. Indeed it may play asignificant role in plant evolution and speciation, especiallyif different intranuclear positions (e.g. central or peripheral)are correlated with preferential phenotypic expression of ancestralgenes. Milium montianum Parl., Gramineae, allopolyploid, spatial chromosome disposition, ancestral genome separation, plant speciation and evolution     

Nuclear DNA Content in Twelve Species of Alstroemeria L. and Some of their Hybrids

Nuclear DNA content (2C-value), estimated through flow cytometryusing propidium iodide (PI), was shown to vary from 36.5 pgto 78.9 pg among 29 accessions of 12Alstroemeria species (2n=2x =16). The extremes were found inA. magnifica ssp.magnificaand inA. ligtu ssp.simsii , both belonging to the Chilean speciesgroup. The four Brazilian species exhibited less variation innuclear DNA content (49.8–56.4 pg), than the eight Chileanspecies (36.5–78.9 pg). Nuclear DNA content was positivelycorrelated (r =0.92,n =7,P <0.01) with the total chromosomelength. It was also positively correlated (r =0.85,n =5,P <0.01)with the length of C-bands, when only the Chilean species wereconsidered. When both karyotype parameters, length of non-C-bandedchromosome regions (x) and length of C-bands (y) were determined,it was possible to predict the nuclear DNA content (z) withthe formula z=0.65x +1.31y-0.45 (R ²=0.97,P =0.004). The DAPI fluorescence of most accessions was proportional tothe PI fluorescence (r =0.98,P <0.001), except for one accessionofA. ligtu , that had a relatively high PI/DAPI ratio (1.88).The PI/DAPI ratios of the Brazilian species were lower (1.59–1.67)than those of the Chilean species (1.68–1.88), which mightreflect a difference in base pair composition. Four groups ofspecies could be distinguished on the basis of fluorescencevalues. Diploid interspecific hybrids were shown to have a DNAcontent intermediate to the values of the parents involved.Both the PI and the DAPI fluorescence values of these hybridsapproximated the mid parent values. Tetraploids, derived fromselfing of diploids, had PI and DAPI fluorescence values thatwere twice that of the diploid hybrids. It was possible to distinguishaneuploids from euploids based on fluorescence values. Alstroemeria ; aneuploidy; C-banding; DAPI; evolution; flow cytometry; genome size; geophytes; karyotypes; Inca Lily; nuclear DNA; propidium iodide     

Production and characterization of arboreous and fertile <Emphasis Type="Italic">Solanum melongena</Emphasis> + <Emphasis Type="Italic">Solanum marginatum </Emphasis>somatic hybrid plants

In crop plants the shift from being annuals to perennials may allow future agricultural systems requiring less energy inputs. The practicability of this was tested for Solanum melongena. Leaf protoplasts of S. melongena (2n = 2x = 24) and one of the related arborescent species Solanum marginatum (2n = 2x = 24) were electrofused and fertile somatic hybrids with arborescent habit regenerated. The magnetic cell sorter (MACS) technique was used for the selection of heterokaryons. The hybrid nature of 18 regenerated plants was assessed on the banding patterns generated by inter-simple sequence repeat PCR. When taken to maturity in the greenhouse, hybrids grew more vigorously compared to the parental species. Their morphological traits were intermediate between those of S. melongena and S. marginatum. Hybrids flowered and produced an average of 85% stainable viable pollen and fertile fruits. The somatic hybrids were maintained in the greenhouse for more than 3 years and continued to produce flowers developing into two types of fruits with plentiful seeds. Fruits were either striated green containing non-germinable seeds or yellow with fully germinable seeds. Their S₁ progenies showed common features with S₀ hybrids, including fertility and arborescent habit. Cytologically, somatic hybrids exhibited the expected chromosome number of 2n = 4x = 48, while chromosome pairing during microsporogenesis was associated with a low frequency of intergenomic pairing. It is concluded that an arborescent perennial species has been obtained by somatic hybridization. The usefulness of this species per se or in eggplant breeding will depend not only on the transmission of the arborescent habit to cultivated eggplant varieties, but also on the variability that should be created from backcrossing the S. melongena + S. marginatum hybrids to S. melongena.     

A Nicotiana Gametosomatic Hybrid and its Progenies

A Nicotiana gametosomatic hybrid between N. tabacum and N. glutinosawas studied. It was shown to have a stable somatic chromosomecomplement of 2n=5x=60. Karyotypes and measures of DNA contentshow that there have been no major changes in the parental chromosomenumbers or morphology accompanying hybridization. Forty-eightchromosomes are derived from N. tabacum (2n=4x=48); 12 fromN. glutinosa (2n=2x=24). Homologous pairs of N. tabacum chromosomesusually pair normally at meiosis. Trivalents incorporating aglutinosa chromosome do occur but usually these remain as univalents. The fertility of the hybrid is low but some products of self-pollinationwere obtained. These carry the complete N. tabacum genome witha few glutinosa chromosomes, some of which form supplementarybivalents at meiosis. All derivatives studied were mixoploidbut progressive selfing reduces the extent of abnormality ofmitotic divisions. The study of morphological and developmentaltraits indicates that the addition of even a few chromosomesof N. glutinosa to the N. tabacum complement can modify thetabacum phenotype substantially. There is considerable variationamong the derivatives and scope for fixing desirable qualitiesthrough selection. The presence of only a haploid set of glutinosachromosomes in the original hybrid makes the return to a desirablegenotype more efficient than that achieved through more conventionalbreeding methods. Key words: Nicotiana, gametosomatic hybrid, selfed progeny, cytology     

The cytology of Brachycome lineariloba

A study of approximately 300 plants in the taxonomic species B. lineariloba is reported. Five biological species differing in chromosome number exist in this species complex. The species with the lowest number (species A, n = 2) often carries B chromosomes, which may be large, or minute. It also exists in three racial forms which differ in karyotype. Observations on naturally occurring hybrids in zones of overlap show that two of the races differ by an unequal interchange. — The species with n = 8 (species C) is probably of amphidiploid origin from the cross A X B. Species B, E and D, with n = 6, 5 and 4 respectively, may represent a series of reductions in chromosome number. They show close karyotypic relationships. The relationship of species A with D, E and B is obscure.     

Production of 2n Gametes in Diploid Subspecies of Dactylis glomerata L. 2. Occurrence and Frequency of 2n Eggs

Whereas polyploidy has been found in more than half the Gramineae,the occurrence of 2n gametes, a potentially major mechanismof polyploid production, has been rarely studied. In the presentwork, the frequency of 2n egg production in nine diploid (n= 2x = 14) subspecies of the polyploid complex Dactylis glomeratahas been estimated by determining the ploidy level of the progenyin 98 2X-4X crosses. The 2n egg origin of the 4X offspring wasverified using enzyme markers. The frequency of 2n egg productionin each subspecies was estimated from the number of 4X offspring,the number of florets in the seed plant and the fertility ofthe subspecies. The ploidy level of the progeny was determinedby chromosome counts or nuclear DNA quantification using flowcytometry. Plants producing 2n eggs were detected in 47% ofthe fertile crosses, involving eight subspecies. Variabilitywas related to individuals and not to subspecies. Average 2negg frequency was 0·49% for all crosses, and 1·53%for crosses where 2n egg production was detected. Individualfrequencies did not exceed 3·5%, with the exception of26% in one plant. Triploid block was higher and fertility, frequencyof high 2n gamete producers and average 2n gamete frequencywere lower in the 2X-4X crosses than in the opposite 4X-2X crossesinvolving the same plants, previously studied. Diplogynous anddiplandrous gamete production were not correlated with eachother. However, the widespread occurrence of plants producingboth kinds of 2n gametes in almost all the studied subspecies,as well as the presence of several individuals able to producehigh rates of 2n eggs or 2n pollen, support the hypothesis thattetraploids can be formed anywhere and anytime by sexual polyploidizationin diploid populations of Dactylis glomerata L. 2n eggs, polyploidy, Dactylis glomerata L., flow cytometry, sexual polyploidization     

Giemsa C-banded Karyotypes of Eight Species of Alstroemeria L. and Some of Their Hybrids

Karyotype analysis of Alstroemeria angustifolia ssp. angustifolia,A. aurea, A. inodora, A. ligtu spp. ligtu, A. magnifica ssp.magnifica, A. pelegrina, A. philippii and A. psittacina usingFeulgen-staining and Giemsa C-banding techniques revealed foreach species a characteristic chromosome morphology and C-bandingpattern. These characteristics could be used to identify manyindividual chromosomes in diploid interspecific hybrids. Besidesinterspecific variation, some degree of intraspecific variationin C-banding pattern was observed within A. angustifolia ssp.angustifolia, A. aurea, A. ligtu ssp. ligtu, A. magnifica ssp.magnifica and A. philippii . All species had large chromosomes (2 n =2 x =16) and asymmetrickaryotypes. In many species the short arms of the acrocentricchromosomes were darkly stained upon Giemsa C-banding. Thesetelomeric bands seemed satellites. B-chromosomes were observedin one species, A. angustifolia ssp. angustifolia . A variablenumber of large intercalary and telomeric C-bands was presentin the Chilean species, whereas the Brazilian species showedonly small C-bands. The differences in karyotypes suggest anearly separation of the Chilean and Brazilian species, afterwhich speciation followed different evolutionary pathways. InAlstroemeria the Giemsa C-banding technique can be valuableto plant taxonomists for unravelling species relationships. Alstroemeria ; Inca lily; evolution; Giemsa C-banding; karyotype     

Karyotypic changes in potato plants regenerated from protoplasts

Over two hundred plants were regenerated from shoot-culture derived proto-plasts of potato (Solanum tuberosum L. cv. Majestic). Some had grossly aberrant phenotypes but the majority were similar to, or indistinguishable from normal control Majestic. Cytological examination showed that on average, 57% of the regenerants had the normal chromosome number (2n=4x=48). The remainder were aneuploids and fell into two classes in approximately equal numbers. The first class was limited at about the euploid level (ie, 2n=44–49). The second class contained plants with higher chromosome numbers ranging from 2n=73 to the octaploid level (2n=8x=96). The overall results represent an improvement over our earlier studies on chromosome variation in protoplast-derived potato plants. In addition, three cases of structural chromosome variation were observed.     

THE HORDEUM VIOLACEUM COMPLEX OF IRAN

Fifty-seven Iranian collections of Hordeum violaceum Boiss. & Huet, a perennial forage grass, contained diploid (2n = 14), tetraploid (2n = 28), and hexaploid (2n = 42) chromosome races. All collections came from moderate to high elevations in the Alborz and Zagros mountains and adjacent plateau areas of Iran. Each chromosome race had a discrete distribution, and the hexaploids were the most widespread. The diploids were cytologically regular, except for a chromosome interchange that occurred in about half of the plants. The tetraploids and hexaploids behaved cytologically as autopolyploids. The hexaploids were taller, coarser and later-flowering than the diploids and tetraploids, and they had fewer but thicker culms and larger seeds. The tetraploids were the leafiest and most productive, making them the most desirable from an agronomic standpoint. All races were more or less self-sterile, a characteristic that sets H. violaceum apart from most other Hordeum species. The taxonomic status of H. violaceum and its closest relatives, H. turkestanicum Nevski and H. brevisubulatum Link, is uncertain because of close morphological similarities and the occurrence of chromosome races in each taxon.     

Physical localization of rRNA genes by fluorescence in situ hybridization (FISH) and analysis of spacer length variants of 45S rRNA (slvs) genes in some species of genus Sesbania

The somatic chromosome numbers 2n = 12 in S. macrantha, S. coerulescens and 2n = 24 in S. simplicuscula were determined, additionally the contradictory chromosome numbers of S. bispinosa (2n = 12, 13, 14, 24) and S. pachycarpa (2n 12, 14) were determined as 2n = 24 and 2n = 14, respectively. The number of 5S rDNA sites in chromosome pair 1 was highly conserved in all the diploid and tetraploid species studied irrespective of their geographic distribution, suggesting that all diploid and tetraploid species/cytotypes of Sesbania analyzed in the present study are in close proximity. Cytogenetic mapping of the 45S multi-gene family was also carried out using fluorescence in situ hybridization. 45S rDNA was consistently located on short or long arms of two sub-metacentric chromosome pairs except on one chromosome pair in S. macrantha and on three chromosome pairs in S. bispinosa and S. cannabina. Out of these nine species, we observed the homogenization of intergenic spacer in six species and find only one spacer length variant (slv) located on one to three chromosome loci. However, three of the species were observed to have two slvs located on two different chromosomes. The species were grouped as per their evolutionary relationship on the basis of the results of the present study.     

In Vitro Micropropagation of Delphinium malabaricum (Huth) Munz.--a Rare Species

A micropropagation technique was developed for Delphinium malabaricumusing nodes from inflorescence stalks Maximum shoot proliferationwas obtained on Murashige and Skoog's medium supplemented with2-1P (10 mg l^–1) and inositol (100 mg l^–1) Fromthe sixth passage onwards, shoots could be multiplied by omissionof inositol and reduction of 2-1P (0.5 mg l^–1) concentrationBest rooting response was obtained with a 24-h pulse treatmentof shoots with 0.5 mg I^–1 IBA in the dark, transfer oftreated shoots to hormone-free half-strength MS medium and incubationunder 24-h light. Regenerated plants were established successfullyin the field Cytological examination of root tips of in vitroand control plants showed identical chromosome number (2n =16) Delphinium malabaricum (Huth) Munz, micropropagation, tissue culture, rare plant     

Mapping of ribosomal DNA and (TTAGGG)n telomeric sequence by FISH in the bivalve Patinopecten yessoensis (Jay, 1857)

The chromosome set of Patinopecten yessoensis (Jay, 1857) wascharacterized using Giemsa staining, DAPI staining and fluorescencein situ hybridization (FISH) with three repetitive DNA probes[18S–28S rDNA, 5S rDNA and telomeric (TTAGGG)_n]. DAPIstaining showed that AT-rich regions were located on the centromereof almost all chromosomes and interstitial banding was not observed.FISH showed that 18S–28S rDNA spread over the short armsof two subtelocentric chromosome pairs and 5S rDNA was locatedon the long arm of one subtelocentric chromosome pair. SequentialFISH demonstrated that 18S–28S and 5S rDNA were locatedon different chromosomes. FISH also showed that the vertebratetelomeric sequence (TTAGGG)_n was located on both ends of eachchromosome and no interstitial signals were detected. Sequential18S–28S rDNA and (TTAGGG)_n FISH indicated that repeatedunits of the two multicopy families were closely associatedon the same chromosome pair. (Received 4 January 2007; accepted 1 September 2007)     

Cytological Analysis of Seedling Roots, Transformed Root Cultures and Roots Regenerated from Callus of Swainsona galegifolia (Andr.) R. Br.

The stability of chromosome number was investigated in culturesof roots from Swainsona galegifolia. Roots from germinated seedsor plants grown in vitro when cultured in liquid medium howed90% or more cells with the diploid number of 2n = 32. The remainingcells showed aneuploidy mostly below 32. The stability of chromosomenumbers was not affected by transformation with Agrobacteriumrhizogenes although when roots were transformed with A. rhizogenesLB 9042 the range of chromosome numbers in the few aneuploidcells present was higher than in roots for which strain A4 wasused. In contrast, roots regenerated from callus had only 15%of cells with 2n = 32 and showed a modal number of 18. Six rootcultures established from individual roots regenerated fromcallus showed a wide variation in number (8–83). Fivecultures had a modal number around 18, the sixth, a modal numberof 39 which is above the diploid number. The implication ofthe results for the production of secondary metabolites fromroot culture is discussed. Key words: Agrobacterium rhizogenes, callus cultures, chromosome number, root cultures, Swainsona galegifolia     

Somatic Embryogenesis and Plant Regeneration from Freely-suspended Cells and Cell Groups of Panicum maximum Jacq

Embryogenic calluses derived from cultured immature embryosand young inflorescences of Panicum maximum Jacq. were placedin Murashige and Skoog's liquid medium supplemented with 1 mg1^–1 2, 4- dichlorophenoxyacetic acid (2, 4-D) and 2.5per cent coconut water, to initiate suspension cultures. Suspensionsconsisted of two types of cells: small, richly-cytoplasmic andoften starch-containing embryogenic cells, and large, vacuolatednon-embryogenic cells. A presumed sequence of developmentalstages from single embryogenic cells to globular and heart-shapedstages of embyrogenesis was observed in the suspension cultures.Plantlets were produced from the embryoids when the suspensionswere plated in an agar medium without any hormone or with only0.2 mg 1^–12, 4-D or naphthalene acetic acid. Embryogenicsuspension cultures derived from immature embryos as well asfrom inflorescence segments gave rise to plants which showedthe normal somatic chromosome number of 2n = 4x = 32. Panicum maximum Jacq., Guinea grass, embryogenesis, regeneration, suspension culture     

CHROMOSOME NUMBERS IN UMBELLIFERAE. III

Chromosome numbers are reported for 156 collections representing 100 taxa of Umbelliferae. Approximately two thirds of the collections are from Mexico, Central and South America and indicate a high percentage of polyploid species in certain genera found in this area. Chromosome numbers for plants belonging to 78 taxa are published here for the first time, previously published chromosome numbers are verified for 18 taxa and chromosome numbers differing from those previously published are reported in seven instances. No chromosome counts have been previously published for nine of the genera included here. Further aneuploidy and polyploidy were found in Eryngium, and Lomatium columbianum has been found to be a high polyploid with 2n = 14x. Every chromosome count is referable to a cited herbarium specimen.