Identification of the Genomic Constitution ofMusaL. Lines (Bananas, Plantains and Hybrids) Using Molecular Cytogenetics

The genomic constitutions of someMusaL. lines (bananas, plantainsand artificial hybrids) were identified using molecular cytogenetictechniques. Double targetin situDNA:DNA hybridization to chromosomespreads using as probes, total genomic DNA isolated from diploidMusalinesof known AA (labelled with biotin-11-dUTP) and BB (labelledwith digoxigenin-11-dUTP) genome constitution was carried out.The use of 60% acetic acid combined with heating over a flamegave high quality chromosome spreads free of cytoplasm forinsituhybridization. Total genomic A DNA labelled broad centromericregions of all 22 chromosomes of the diploid line, Calcutta4 (M. acuminataColla. ssp.burmanniccoides; A genome) with somechromosomes showing stronger hybridization. Labelled DNA fromthe B genome hybridized strongly to the centromeric regionsof all 22 chromosomes of Butohan 2 (M. balbisianaColla; B genome).The two satellited chromosomes of genome B labelled stronglywith genomic A DNA.In situhybridization of labelled A and Bgenomic DNA to metaphase chromosomes of triploid AAB and ABBcultivars discriminated between A and B genome chromosomes.The plantains Agbagba, Obino l'Ewai and Mbi Egome showed 22genome A and 11 genome B chromosomes while the cooking bananasBluggoe and Fougamou showed 11 genome A and 22 genome B chromosomes.Hybridization of labelled A and B genomic DNA to chromosomesof the hybrids showed that TMP2x 2829-62 has all 22 genome Achromosomes while TMPx 4698-1 has 33 genome A and 11 genomeB chromosomes.In situhybridization of labelled total genomicDNA to chromosomes has immense potential for identificationof chromosome origin and can be used to characterize cultivarsand hybrids produced inMusabreeding.Copyright 1997 Annals ofBotany Company Genomicin situhybridization; banana; plantain; hybrids; plant breeding; genome organization; biodiversity     

Chromosome identification and nuclear architecture in triticale tritordeum F1 hybrids

In situ hybridization with cloned, repetitive DNA probes andtotal genomic DNA enables the parental origin of all chromosomesto be established in metaphases of triticale tritordeum F¹hybrids (2n=6x=42). Nuclei contain seven chromosomes of Hordeumchilense origin, seven from Secale cereale and 28 of wheat origin.When used as a probe, total genomic rye DNA labelled the ryechromosomes strongly and uniformly along their lengths, withbrighter regions coincident with the terminal heterochromatin.The probe labelled the wheat-origin chromosomes weakly and wasalmost undetectable on the H. chilense-origin chromosomes. Incontrast, under the same conditions, H. chilense DNA hybridizedstrongly to the H. chilense- and, with intermediate strength,to the S. cereale-origin chromosomes, excluding the subtelomericheterochromatin: it hybridized only weakly to the wheat chromosomes,in some experiments revealing characteristic bands on wheatchromosomes. Cloned repetitive DNA probes from rye and H. chilensewere used as probes to identify the linkage groups of all oftheir own-species chromosomes. Analysis of hybridization patternsof various probes to prophase and interphase nuclei indicatedthat there are many non-random features in the localizationof both repetitive DNA and whole chromosomes, although generalpatterns of nuclear organization have yet to emerge. Both theparticular lines used and the techniques developed here arelikely to be valuable for production and characterization ofplant breeding material. Key words: In situ hybridization, triticale, cytogenetics, plant breeding, Hordeum chilense     

The importance of plankton to Cassin's auklets during breeding

The breeding chronology, food habits, growth and reproductivesuccess of Cassin's Auklets, Ptychoramphus aleuticus, were investigatedon Triangle Island, British Columbia. The breeding of Cassin'sAuklets coincides with the plankton bloom in the eastern NorthPacific. Cassin's Auklets in British Columbia feed their youngmostly large copepods, Calanus cristatus, and euphausiids, chieflyThysanoessa spinifera, but fish was an important food item inone summer. Chicks which hatched early, grew and survived betterthan late-hatched chicks and this may relate to food availability.Adults and chicks on Triangle Island were heavier than thoseon South Farallon Island, California. The heavier weight andgreater numbers of Cassin's Auklets in British Columbia as comparedwith regions to the south may relate to Calanus cristatus availabilityand abundance in northern areas.     

Physical Characterization of the Chromosomal DNA of the Yeast Saccharomyces exiguus

The number of chromosomes in the yeast Saccharomyces exiguuswas determined to be thirteen by two-dimensional pulsed-fieldgel electrophoresis. The thirteen chromosomes ranged in DNAsize from 520 to 2,600 kbp, with a total length of approximately14 Mbp. Numbers I to XIII were assigned to the chromosomes indecreasing order of DNA length. Southern hybridization analysisusing total DNAs from S. exiguus and S. cerevisiae as probesshowed that there was no significant homology between the chromosomalDNAs of the two species, except in the case of the chromosomalDNA that included rDNA. When rDNA and genes LEU2, TRP1, URA3and HO of S. cerevisiae were used as hybridization probes, itwas apparent that S. exiguus had DNA sequences homologous tothe rDNA and to the LEU2 and HO genes. In S. exiguus, rDNA-likeand LEU2-like DNAs were located on chromosomes I and IX, respectively,and HO-like DNA was located on chromosome VI or VII. (Received May 17, 1993; Accepted July 15, 1993)     

Cytological Studies in the Cycads: Sex Chromosomes in Cycas

The chromosomes of Cycas pectinata are studied from root tipand pollen mitoses. The male and female plants showed the samenumber of chromosomes (2n = 22) with almost identical chromosomemorphology. The only difference is that in the female planttwo chromosomes of the somatic complement (pair III) bear satellites,while in the male the same pair is heteromorphic with only oneof its members bearing a satellite. This becomes further clearwhen two types of haplid complements are noticed in pollen mitosis,one type possessing a satellited chromosome, and the other showingnone bearing a satellite. The pair of chromosomes which is heteromorphic in the male isassumed to be associated with sex determination in Cycas, themale being the heterogametic sex with XY type of sex chromosomes.     

The Hybrid Origin of Two Cultivars of Crocus (Iridaceae) Analysed by Molecular Cytogenetics including Genomic Southern and in situ Hybridization

The origin of the two common cultivars of Crocus, C. 'Stellaris'(2n = 2x = 10) and C. 'Golden Yellow' (2n = 3x = 14) was investigatedby fluorescent in situ hybridization using both total genomicDNA and cloned DNA sequences as probes. The clear differentiationbetween the chromosomes after genomic in situ hybridizationsupports the proposals of a hybrid origin of the cultivars andshows that they have the same parental genomes originating fromC. flavus (2n = 8) and C. angustifolius (2n = 12). C. 'Stellaris'has four chromosomes of C. flavus origin and six chromosomesof C. angustifolius origin. C. 'Golden Yellow' has eight chromosomesof C. flavus origin and six chromosomes of C. angustifoliusorigin. The number and location of 18S-5·8S-26S rRNAgenes on the chromosomes of the hybrids and of the parentalspecies agree with the results from the genomic probings. Hybridizationto Southern membranes also supports the hybrid origin of C.'Golden Yellow'.Copyright 1995, 1999 Academic Press Taxonomy, cytology, rDNA sites, in situ hybridization, Southern hybridization, Crocus     

In Situ Localization of Parental Genomes in a Wide Hybrid

In situ hybridization enabled DNA originating from the two parentalgenomes to be distinguished in plant hybrids. A probe of biotinylatedtotal genomic DNA from Secale africanum labelled the chromosomesof S. africanum origin but not those from Hordeum chilense inroot-tip chromosome spreads of the sexual hybrid between thetwo species. Hybridization of total genomic DNA from S. africanumto DNA on filters (dot blots) confirmed the distinction betweenDNA from Hordeum and Secale. The total genomic probe hybridizedto the whole length of the chromosomes from S. africanum remarkablyuniformly, labelling both euchromatin and heterochromatin, exceptat the centromeric region. The probe binding was visualizedas a yellow colour by the fluorescein-coupled detection systemwhich contrasted with the red fluorescing counterstain of theunlabelled chromatin. The chromosomes originating from bothparents could be seen and distinguished as red and yellow fluorescenceat all stages of the cell cycle. At interphase and prophase,the chromatin originating from the two parental genomes didnot mix. Chromosomes or groups of chromosomes occupied distinctdomains and also tended to be arranged in a Rabl configurationwith the centromeres clustered at one end of the nucleus. Wepropose calling the technique using total genomic DNA as a probe‘genomic in situ hybridization.’ Hordeum chilense, Secale africanum, hybrids, genomic in situ hybridization, DNA, repetitive sequences, chromosomes, chromosome disposition, nuclear order     

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     

Accessory Chromosomes in a tree--Ficus krishnae

Accessory chromosomes in a tree, Ficus krishnae are reportedfor the first time. Besides the normal complement of 2n = 26;1–2 small euchromatic accessory chromosomes were encountered.The frequency of accessory chromosomes in somatic cells was30 per cent. In meiotic cells one accessory chromosome was presentin 54 per cent of cells while two were observed in 9 per centof the pollen mother cells.     

Functional and Structural Chromosome Analyses in Autotetraploid Silene latifolia

Recent immunocytological and molecular data show that heterochromaticnuclear regions, both constitutive and facultative, are modifieddifferently (cytosine hypermethylation and histone hypoacetylation)and late replicating, when compared to euchromatin. Intrusiveand/or additive (supernumerary) DNA sequences are often functionallysilenced; this is accompanied by their heterochromatinization.In this work we present a number of karyological studies onautotetraploid female cells of Silene latifolia (syn. Melandriumalbum). Immunofluorescence analyses do not indicate any globaldifferences in DNA methylation, histone H4 acetylation, andchromosome replication patterns which could arise as a consequenceof the duplication of the whole chromosome set of the originaldiploid genome. Similarly, the number of silver-positive nucleoliroughly correlates to the ploidy level. Early replication andH4 hyperacetylation have been detected at all subterminal chromosomeregions. This, together with cDNA in situ hybridization patterns,indicates the localization of gene-rich regions. DNA methylationand chromosome replication patterns, but not histone H4 acetylation,show differences among the four X chromosomes present: one tothree X chromosomes were observed as hypermethylated and/orlate replicating. Taken together, the data demonstrate thatthere is no overall silencing of the additional two sets ofautosomes in the tetraploid cells, but the X chromosomes couldbe subject to an irregular dosage compensation. Copyright 1999Annals of Botany Company DNA methylation, histone acetylation, polyploidy, replication patterns, sex chromosomes, Silene latifolia (syn.Melandrium album ).     

Repetitive DNA, Genome and Species Relationships in Avena and Arrhenatherum(Poaceae)

Repetitive sequences have been widely used for examining genomeand species relationships by in situ and Southern hybridization.In the present study, double-stranded DNA sequences, from denaturedDNA reannealed to Cot = 1, from Avena strigosa(2 n = 2x = 14;A genome; referred to as CotA) and Avena sativa(2n = 6 x =42; ACD genome; referred to as CotACD) were isolated with ahydroxyapatite column, and were used for in situ hybridizationon hexaploid A. sativa chromosomes. Probe CotACD labelled allchromosomes evenly throughout their length at the same intensity.Probe CotA labelled the 28 A and D genome chromosomes stronglyand the 14 C genome chromosomes weakly. Three cloned repetitivesequences, pAvKB9 (126 bp), pAvKB26 (223 bp) and pAvKB32 (721bp) were characterized in the A, B, C and D Avena genomes andthe genus Arrhenatherum using molecular and cytological methods.Clones pAvKB9 and pAvKB26 were absent from the Avena C genome,while both could identify the presence of the D genome by Southernhybridization. In situ hybridization to diploid and tetraploidAvena species revealed that the probes showed a dispersed genomicorganization and that they are present on both arms of all chromosomes.These sequences were excluded from areas where tandem repeats,such as rRNA genes and telomeres, are present. These resultsindicate the close relationship between A and D genomes andthe presence of common DNA sequences between A and C Avena genomes.All three clones hybridized to Southern blots containingArrhenatherumdigested genomic DNA, indicating Arrhenatherum’s closeaffinity to A, B and D Avena genomes. Copyright 2000 Annalsof Botany Company Cereals, DNA, hydroxyapatite, in situ hybridization, oats, reassociation kinetics, repetitive DNA     

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     

Effects on Growth and Development of Individual Chromosomes from Slow-growing Lophopyrum elongatum Love when Incorporated into Bread Wheat (Triticum aestivum L.)

Aspects of growth and development were evaluated in the fast-developingannual Triticum aestivum L. ‘Chinese Spring’, theslow-developing perennial Lophopyrum elongatum Löve, theiramphiploid, and chromosome addition and substitution lines ofL. elongatum into ‘Chinese Spring’. Relative growthrates (RGR) of shoots of L. elongatum and the amphiploid werelower than those of ‘Chinese Spring’ (34 and 13%respectively) and main stem development was also slower. Therewas no difference in shoot RGR of any of the chromosome additionor substitution lines and that of ‘Chinese Spring’when assessed between Haun stages 2.0 and 5.0. In contrast,several aspects of plant development were observed to differin the chromosome addition and substitution lines. SubstitutingE genome chromosomes (with the exceptions of 3E and 4E) forD genome chromosomes, or adding E genome chromosomes, slowedthe rate of main stem development, at least up to Haun stage5.0. Despite these differences in the rate of main stem development,the appearance of adventitious roots commenced at approximatelyHaun stage 2.0 in all genotypes. However, the numbers of adventitiousroots and tillers at the 5.0 Haun stage differed between someof the lines when compared to ‘Chinese Spring’.Although incorporation of some L. elongatum chromosomes alteredaspects of plant development, all lines showed more similarityto bread wheat than to L. elongatum, reflecting, in part, thegreater genetic contribution made by bread wheat to these lines.Copyright 2001 Annals of Botany Company Adventitious roots, chromosome addition and substitution lines, Haun stage, Lophopyrum elongatum, relative growth rate (RGR), Triticum aestivum(wheat)     

Native or Exotic? Double or Single? Evaluating Plants for Pollinator-friendly Gardens

In a series of dawn-to-dusk studies, we examined the natureand accessibility of nectar rewards for pollinating insectsby monitoring insect visits and the secretion rate and standingcrop of nectar in the British native plant species Salvia pratensis,Stachys palustris, S. officinalis, Lythrum salicaria, Linariavulgaris, the non-native Calendula officinalis, Petunia x hybrida,Salvia splendens, and the possibly introduced Saponaria officinalis.We also compared single with double variants ofLotus corniculatus, Saponaria officinalis, Petunia x hybrida andCalendula officinalis. All the British species studied are nectar-rich and are recommendedfor pollinator-friendly gardens. They showed maximal secretionrates of about 10–90 µg sugar per flower h^-1, andmost had mean standing crops of about 5–60 µg sugarper flower. In all British species studied, the corolla wasdeep enough for the relatively long-tongued bumblebee Bombuspascuorum, but the shallower flowers of Lythrum salicaria werealso much visited by shorter-tongued bees and hoverflies, aswell as by butterflies. The exotic Salvia splendens, presumablycoevolved with hummingbirds in the Neotropics, has such deepflowers that British bees cannot reach the nectar except bycrawling down the corolla. With a secretion rate approaching300 µg sugar per flower h^-1and little depletion by insects,S. splendens accumulated high standing crops of nectar. S. splendens,and single and double flowers of the two probably moth-pollinatedspecies Petunia x hybrida and Saponaria officinalis, receivedfew daytime visits despite abundant nectar but Calendula waswell visited by hoverflies and bees. We compared single anddouble variants of Lotus corniculatus,Petunia x hybrida andCalendula officinalis, and also Saponaria officinalis, the lastbeing probably introduced in Britain (Stace, 1997 New floraof the British Isles. 2nd edn. Cambridge: Cambridge UniversityPress). In Petunia, Saponaria and Lotus, double flowers secretedlittle or no nectar. In Calendula, where doubling involved achange in the proportion of disc and ray florets rather thanmodification of individual flower structure, double and singlecapitula had similar standing crops of nectar. Except inCalendula, exotic or double flowers were little exploited by insect visitors.In the exotics, this was probably due to the absence or scarcityof coevolved pollinators, coupled, in double flowers, with theabsence of nectar. Copyright 2001 Annals of Botany Company Salvia pratensis, Salvia splendens, Stachys palustris, Stachys officinalis,Lythrum salicaria , Linaria vulgaris, Lotus corniculatus, Saponaria officinalis,Petunia x hybrida, Calendula officinalis, wild flowers, double flowers, gardens, nectar, secretion rate, standing crop, pollinators, bumblebees, Bombus, honeybees, Apis, hoverflies, butterflies,Anthidium manicatum     

Transformation of Vicia faba Cotyledon and Stem Tissues7Agrobacterium rhizogenes: Infectivity and Cytological Studies

Transformation of Vicia faba cotyledon and stem tissues by Agrobacteriumrhizogenes has been demonstrated. Hormone autotrophy and NPTIIdot blot assays were used to confirm the transgenic nature ofroot clones, and to show the co-transfer of the T-DNA from theRi plasmid and the NPTII gene from pBIN 19. An effect of plantgenotype on susceptibility to A. rhizogenes was observed. Theresponse to infection depended on tissue type in addition toplant genotype. Cytological analysis of transformed root clonesuncovered variation in ploidy up to the octoploid level andstructural rearrangements of chromosomes. The possible originsof these karyotype changes and their implications are discussed. Key words: Vicia faba, Agrobacterium rhizogenes, transformed roots, genotypic effects, chromosomes     

A COMPARATIVE STUDY OF CHROMOSOMES IN FOUR SPECIES OF THEODOXUS (GASTROPODA: NERITIDAE)

Karyological analysis was performed on Theodoxus baeticus (Lamarck,1822), T. valentina (Graells, 1846), T. velascoi (Graells, 1846)and T. fluviatilis (Linne, 1758), collected from freshwaterbodies of eastern Spain. Cells possessing diploid chromosomenumbers of 2n 5 25 were most common in the tissues of males,whilst 2n 5 26 was most prevalent in females. The sixth pairof chromosomes had only one homologue in mitotic cells of males,indicating the XO/XX sex-determining mechanism. The absolutelength of chromosomes ranged from 1.65 to 6.33 mm. The relativesizes of chromosomes varied from 3.92 to 13.33% of the totalhaploid set length. In all species chromosome pairs no. 1, 4,7-13 were composed of metacentric, pairs no. 5 and 6of submetacentricchromosomes. Pairs no. 2 and 3 were submetacentric, subtelocentricor submeta- subtelocentric according to the species studied.There were significant differences (P, 0.05) among the relativelength, as well as centromeric indices of different chromosomepairs across the species. Karyological differences were greatestbetween T. fluviatilis and three other Theodoxus species. (Received 6 March 2000; accepted 8 May 2000)     

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     

Investigations of Genome Relationships Between Leymus, Psathyrostachys and Hordeum Inferred by Genomic DNA:DNA in situ Hybridization

Genome relationships between the genera Leymus Hochst., PsathyrostachysNevski and Hordeum L. (Poaceae, Triticeae) were investigatedby fluorescent in situ hybridization using both total genomicDNA and cloned DNA sequences as probes. In hybrids between speciesof Hordeum and Leymus there was a clear differentiation betweenthe H genomes of Hordeum species and the genomes of Leymus speciesafter probing with genomic Hordeum or Leymus DNA. Chromosomesof species of Leymus and Psathyrostachys were also differentiatedby subtelomeric heterochromatic segments or by negative bandsalong their length. The number and location of 18S-5·8S-26SrRNA genes varied between the investigated genera. Unusually,L. angustus and P. stoloniformis rDNA sites were localized onboth ends of some chromosomes. Interphase nuclei of the Hordeumx Leymus hybrids had groups of chromosomes from both parentalgenomes in discrete, non-intermixed domains.Copyright 1994,1999 Academic Press Taxonomy, evolution, molecular evolution, repetitive DNA, rDNA sites, in situ hybridization, Triticeae, Leymus, Hordeum, Psathyrostachys     

The Structure and Development of the Thallus in the British Species of Gelidium and Pterocladia

The apical structure and the development of the thalli of allthe British species of Gelidium and Pterocladia have been investigated;the development of G. pulchellum is described in detail. Eachaxis is terminated by one or more apical cells, which by theirsegmentation form the tissues of the thallus. An axial filamentis distinct for a short distance behind each apical cell, butsecondary pit-connexions develop rapidly so that in sectionthe mature axis has the appearance of a multi-axial structure. Lateral branches of the frond develop by the segmentation ofthe lateral branch apical cells, which are formed by the transformationof superficial cortical cells, either in the meristematic ormature parts of the axes. The extreme variability of externalappearance is due principally to the indeterminate origin ofall lateral branches. The thallus in the British species of Gelidium and Pterocladiaconsists of erect fronds borne on creeping axes. The relativeproportions of the frond and creeping axes in various speciesand their survival through adverse conditions are discussed.