Sur une nouvelle applicaton de la theorie de P information a la description des series chronologiques planctoniques

Corrélations simples (r) et pondérées (r_p)entre S. setosa (trois stades cumulés), S. minima etS. inflata (stade 1), S. bipunctata, et les quatre paramétreshydrologiques retenus. ^aSeuil de signification 5%. ^bSeuil designification 1%     

Effects of cycloheximide and kinetin pretreatments on responses of susceptible and resistant Avena leaf protoplasts to the phytotoxin victorin

Avena leaf protoplasts from varieties susceptible (cv. Park)and resistant (cv. Victory) to victorin incorporate the labelfrom ³H-L-leucine, ³H-uridine and ³H-thymidine into trichloroaceticacid-insoluble materials at comparable rates. When incubatedin the presence of the toxin, susceptible protoplasts beginto lyse after a short period of time; the effect on resistantprotoplasts is minimal. Victorin also significantly reducesincorporation of label from leucine and to a lesser extent fromuridine and thymidine into susceptible protoplasts but has anegligible effect on resistant protoplasts. Pretreatment ofsusceptible leaves with cycloheximide but not kinetin protectsagainst the subsequent action of victorin on apparent proteinsynthesis and lysis of protoplasts. ¹Permanent address: Institut National de la Recherche Agronomique,Station de Physiologie et Biochemie Végétales,"La Grande Ferrade", Centre de Recherches de Bordeaux, 33 Pont-de-la-Maye,Bordeaux, France. ²School of Forestry and Environmental Studies, Yale University. ³Supported by grant GI-32958 of the RANN program of the NationalScience Foundation to A. W. Galston. We are indebted to WhitneyAdams, jr. for expert assistance. (Received April 10, 1976; )     

Genetic Variation and Population Structure of Oriental Migratory Locust, Locusta migratoria manilensis, in China by Allozyme, SSRP-PCR, and AFLP Markers

Allozyme analysis, microsatellite primer PCR (SSRP-PCR), and amplified fragment length polymorphism (AFLP) techniques were used to assess genetic diversity and population structure of the Chinese oriental migratory locust, Locusta migratoria manilensis. A total of 299 PCR markers (67 SSRPs and 232 AFLPs) were detected in eight populations, of which 98.7% were polymorphic markers. The proportion of polymorphic loci (95.5–98.8%) by SSRP+AFLP markers indicated no significant differences between populations, and all populations exhibited a similar level of variability; results of the allozyme analysis demonstrated that 19 loci gave rise to a lower level of polymorphism (55.6–66.7%). The genetic distances between the populations were relatively low. Shannon’s index and Nei’s gene diversity showed low differentiation among the populations. Allozyme analysis, however, reflected greater similarity and smaller differentiation between the populations than those shown by SSRP and AFLP markers. Neighbor-joining dendrograms derived from both the allozyme and SSRP+AFLP markers showed that the genetic distances among Chinese oriental migratory locust populations were not greatly influenced by geographic distance and breeding habitats.     

Ecologie alimentaire de Cyclothone braueri Jespersen et Taning, 1926 (Gonostomatidae) en mer Ligure, Mediterranee occidentale

Stomach contents of 4557 specimens of Cyclothone braueri wereanalyzed. Specimens were captured between 300 and 900 m depth,during November 1980 through December 1981. Results showed thatthis species is a carnivore that feeds mainly on zooplanktonorganisms, of wide vertical distribution, comprising about 38prey items. Most important preys were Copepods' (80%) and Ostracods(12%). Other minor items were euphausid larvae, amphipods anddecapod crustaceans. Dominant prey species was Pleuromamma gracilis,and in minor proportion, Euchaeta marina, Chiridius poppei,and Calanus helgolandicus. The emptiness coefficient was quitehigh (V = 72.6%), with significant differences (P < 0.05)between sexes: V(males) = 81%, V(females) = 71%; between depths:V(at 400 m) = 63%, V(at 900 m) = 79%, and between seasons: V(autumn)= 80%, V(winter) = 60%. Nous avons analysé les contenus stomacaux de 4557 spécimensde Cyclothone braueri capturés entre 300 et 900 m deprofondeur, pendant la période comprise entre novembre1980 et décembre 1981. Le contenu stomacal montre quele régime alimentaire de cette espéce est carnivoreconstitué par 38 sortes de proies, appartenant fondamentalementaux copépodes (80%) et ostracodes (12%). En mondre proportionon trouvait de larves d'euphausiacés, amphipodes et crustacésdécapodes. L'espèce-proie dominante fut Pleuromammagracilis, suivi de loin par Euchaeta marina, Chiridius poppeiet Calanus helgolandicus. La plupart des espèces proiessont des organismes zooplanctoniques d'une vaste distributionverticale. Le coefficient de vacuité est tres élevé(V = 72.6%), présentant des variations significatives(p << 0.05) en fonction du sexe (V mâles = 81% etV femelles = 71%), de la profondeur de pêche (V = 63%à 400 m et V = 79% à 900 m), et de la saison del'année (V = 80% en automne et V = 60% en hiver).     

Genetic diversity and phylogenetic relationships in alder,Alnus firma, revealed by AFLP

Molecular markers for alder,Alnus firma Sieb. et Zucc, have not been studied extensively. Here, we used amplified fragment length polymorphism (AFLP) to investigate genetic relationships among 15 natural populations. EcoRI-ACG + Msel-CTG combinations revealed the highest polymorphism (62.2%). A total of 171 DNA fragments were identified. On average, 58.1% of the AFLP markers that were generated using four primer pairs were polymorphic. Diversity was insignificant among the populations. The combination of a wind-pollinated, outcrossing breeding system along with large population sizes, and the ability to regenerate by stump sprouting may explain the high level of genetic diversity within this species. The majority (98%) of the genetic variance resided within populations. The average number of individuals that were exchanged between populations per generation was very high (N _em = 12.3). Gene dispersal in alder is apparently by seed dispersalvia water and human activity as well as through pollen. Five individuals per population were claded in the same cluster.     

Temporal Relationship between Action Potential and Ca2+ Transient in Characean Cells

Temporal relationship between the action potential and the changein cytosolic Ca²⁺ concentration was investigated in cells offour species of Characeae, Chara corallina, Nitellopsis obtusa,Nitella flexilis and Nitella axilliformis. The Ca²⁺ transientwas detected by light emission from Ca²⁺-sensitive photoproteinaequorin injected into the cytoplasm. Action potential was triggeredby an outward or sometimes inward electric current pulse of20–50 ms in most cases. In all species the action potentialstarted at almost the same time as the time at which the lightemission from aequorin began to increase. Also the peak of actionpotential almost coincided with that of light emission, whichis in contrast with the slower Ca²⁺ transient in Chara reportedby Thiel et al. [(1997) J. Exp. Bot. 48: 609]. A discussionwas made on the origin of Ca²⁺ transient and the ionic processesduring membrane excitation. (Received July 2, 1998; Accepted October 5, 1998)     

ALLOZYME VARIATION AMONG POPULATIONS OF BIOMPHALARIA PFEIFFERI (KRAUSS, 1848) (GASTROPODA: PLANORBIDAE) IN CAMEROON

Allozyme electrophoresis was used to study genetic diversityamong the freshwater, hermaphroditic snail Biomphalaria pfeifferiin Cameroon. Four of 19 loci studied were polymorphic. The allozymesfor two loci, aspartate aminotransferase-1 (AAT-1) and isocitratedehydrogenase (IDH), showed distribution patterns related toclimatic zones. AAT-1¹⁰⁰ and IDH¹⁰⁰ occurred predominantly inthe Tropical Climatic Zone, located in the northern half ofthe country. AAT-1¹⁴⁰ and IDH⁹⁰ were common in the EquatorialZone. Intrapopulation variations occurred in 5 of 19 populationsampled. Only one population, polymorphic for AAT-1 locus, waspanmictic. The other 4 populations were not in Hardy-Weinbergequilibrium. The deficiency of heterozygotes in those populationsis unusual for a member of the genus Biomphalaria and may bedue to a predominance of self-fertilization. Other explanationsinclude ecological factors or the presence of segregated sub-populationsthat do not outcross. This latter hypothesis is supported bythe total absence of heterozygotes for PGM alleles. (Received 24 August 1989; accepted 14 September 1989)     

FEEDING ACTIVITY OF LIMAX VALENTIANUS FERUSSAC: NOCTURNAL RHYTHM AND ALIMENTARY COMPETITION

Feeding activity of the slug Limax valentianus Férus-sacthroughout a 24-hour period began with the decrease in light.Feeding began 41 minutes after the start of locomotor activityand showed a maximum level in the beginning of the night L.valentianus had two to five meals each night, each meal lasting8.5 to 14 minutes. The overcrowding of the slugs induced a shorterduration of individual feeding periods and acts of aggressionduring meals. ^*Present address: Centre de Neurochimie, Laboratoire de neurobiologiemolécuiaire des interactions cellulaires. 5 rue BlaisePascal, 67084 Strasbourg, France (Received 7 July 1996; accepted 21 April 1997)     

Genetic variation and population structure of oriental migratory locust, Locusta migratoria manilensis, in China by allozyme, SSRP-PCR, and AFLP markers

Allozyme analysis, microsatellite primer PCR (SSRP-PCR), and amplified fragment length polymorphism (AFLP) techniques were used to assess genetic diversity and population structure of the Chinese oriental migratory locust, Locusta migratoria manilensis. A total of 299 PCR markers (67 SSRPs and 232 AFLPs) were detected in eight populations, of which 98.7% were polymorphic markers. The proportion of polymorphic loci (95.5-98.8%) by SSRP+AFLP markers indicated no significant differences between populations, and all populations exhibited a similar level of variability; results of the allozyme analysis demonstrated that 19 loci gave rise to a lower level of polymorphism (55.6-66.7%). The genetic distances between the populations were relatively low. Shannon's index and Nei's gene diversity showed low differentiation among the populations. Allozyme analysis, however, reflected greater similarity and smaller differentiation between the populations than those shown by SSRP and AFLP markers. Neighbor-joining dendrograms derived from both the allozyme and SSRP+AFLP markers showed that the genetic distances among Chinese oriental migratory locust populations were not greatly influenced by geographic distance and breeding habitats.     

Significance of Polyamines for Flowering in Spirodela punctata

Spirodela punctata strain O 5, a quantitative long-day plant,flowers only when ethylene-diamine-di-o-hydroxyphenylaceticacid (EDDHA) or salicylic acid was added to the nutrient medium[Scharfetter et al. (1978) Z. Pflanzenphysiol. 87: 445]. Undersuch conditions, cyclohexylamine and methylglyoxal-bis(guanylhydrazone)(both blockers of polyamine synthesis) inhibited flowering withoutsignificant effects on vegetative growth. Supply of spermidineabolished completely the inhibitor effects, but cannot replacethe EDDHA effect on flowering. ¹Dedicated to Prof. O. H. Volk, Wurzburg, on his 85th birthday. ²Present address: Facultad de Ciencias Forestales, UniversidadAutónoma de Nuevo León. Ap. Post. 41, 67700 Linares,Nuevo León, México. (Received October 19, 1988; Accepted February 3, 1989)     

Two-Dimensional Protein Patterns of Arabidopsis Wild-Type and Auxin Insensitive Mutants, axr1, axr2, Reveal Interactions between Drought and Hormonal Responses

In order to detect gene products involved in Arabidopsis droughtadaptive strategy, 2D-PAGE protein patterns of two auxin-insensitivemutants, axr1, axr2, differentially affected in specific droughtresponses, were compared to the wild-type Columbia ecotype,in well-watered and drought-stressed conditions. Coupled tocomputer analysis of polypeptide amounts, 2D-electrophoresisrevealed subtle changes in protein expression induced by progressivedrought stress and/or mutations affecting the auxin responsepathway. The differential protein patterns of axr1 and axr2 were consistentwith their contrasting drought responses. The specific leafand root protein patterns of axr1 showed that this mutationdisrupts drought responses related to auxin regulation. In particular,the near absence of drought rhizogenesis in axr1 was associatedwith a root protein pattern closer to the well-watered thanto the water-stressed axr2 and Columbia wild-type root proteinpatterns. Also, the largely different effects of axr1 and axr2mutations suggest that they affect different pathways in auxinresponse. Several sets of polypeptides, whose regulation wasaffected by drought and/or mutation, were thus detected. Thesepolypeptides could play a role both in the auxin and the droughtresponse pathways. Their identification, through microsequencing,should be most informative. ⁴Current address: Laboratoire de BioénergétiqueCellulaire, Département d'Ecophysiologie Végétaleet de Microbiologie, Centre d'Etudes de Cadarache, 13108 SaintPaul lez Durance, France     

Genetic Variation and Clonal Diversity of Psammochloa villosa(Poaceae) Detected by ISSR Markers

Genetic variation and clonal diversity of seven Psammochloavillosa(Poaceae) populations from northwest China were investigatedusing inter simple sequence repeat (ISSR) markers. Of the 84primers screened, 12 produced highly reproducible ISSR bands.Using these primers, 173 discernible DNA fragments were generatedwith 122 (70.5%) being polymorphic, indicating considerablegenetic variation at the species level. In contrast, there wererelatively low levels of polymorphism at the population levelwith the percentage of polymorphic bands (PPB) ranging from6.1 to 26.8. Analysis of molecular variance (AMOVA) showed thata large proportion of genetic variation (87.46%) resided amongpopulations, while only 12.54% resided among individuals withinpopulations. Clonal diversity was also high with 98 genets beingdetected from among 157 individuals using 12 ISSR primers. Theevenness of distribution of genotypes in P. villosa populationsvaried greatly, with all of the genotypes being local ones.No significant differences in genetic or clonal diversity werefound between populations in mobile or fixed dunes. The mainfactor responsible for the high level of differentiation amongpopulations and the low level of diversity within populationsis probably the clonal nature of this species, although selfingmay also affect the population genetic structure to some extent.The efficiency of ISSRs in identifying genetic individuals wasmuch higher than that of allozymes. An approximately asymptoticcorrelation was found between the number of genets detectedand the number of polymorphic loci used, suggesting that useof a high number of polymorphic bands is critical in genet identification.Copyright 2001 Annals of Botany Company Psammochloa villosa, ISSRs, genetic variation, clonal diversity     

REPRODUCTIVE CYCLE, MANAGEMENT AND CONSERVATION OF PAXYODON SYRMATOPHORUS (BIVALVIA: HYRIIDAE) FROM THE TOCANTINS RIVER, BRAZIL

The reproductive cycle of a population of Paxyodon syrmatophorus(Meuschen, 1781), a mussel exploited for its shells in the lowerTocantins River, Brazil, was studied between September 1997and August 1998. Monthly examination of gonad sections and inspectionof the demibranchs of females showed that gametogenesis takesplace all year round and that spawning occurs during the months ofthe dry season. Gravid females were found throughout the period betweenFebruary and September. Sexually mature mussels as small as 23mm in length were found and the smallest gravid female was 32mm in length. The implications of the findings are discussedin relation to the conservation and management of exploitedfreshwater mussel populations in the region. ³ Author for correspondence. Telefax: +55-91-8251209. Email: beasley{at}eletronet.com.br ⁴ Current address: UPIS, Sep/Sul EQ. 712/912 Conjunto "A" Brasília70390-125, DF Brazil (Received 20 September 1999; accepted 13 January 2000)     

Strategies d'adaptation photosynthetique chez des diatomees des I'Ocean Antarctique: variations du nombre et de la talile des unites photosynthetiques

Les diatomes Nitzschia turgiduloides et Chaetoceros deflandrei,rcoltes en fvrier–Mars 1980 dans le secteur indiende l'Ocan Antarctique, ont t maintenues en culture au laboratoire,sous des intensits himineuss variant de 140 2 µE m^–2s^–2. The production versus intensite lumineuse, tabliespar cellule et par unit de chlorophylle a, suggrent, selonla mthode de Richardson et al. (1983), une adaptation des espcesantarctiques la lumire par variation de la taille (estimepar la valeur I_k) et du nombre (volution de la pente initiale) des units photosynthtiques. Au plan ecologique, les valeursdes paramtres photosynthetiques en lumire Bmitante et en lumiresaturante sont faibles, caractristiques des algues ‘d'ombre’:concentration en chlorophylle a et productivit par celluleplus fortes quand les espces sont acclimates a des faiblesintensites lumineuses. Ce travail met ainsi en vidence I'importancedu facteur lumineux par rapport la basse temprature sur laproduction primaire de l'Ocan Antarctique.     

Development of microsatellite markers for Aquilegia buergeriana var. oxysepala (Ranunculaceae), a vulnerable Japanese herb

Aquilegia buergeriana var. oxysepala is a vulnerable herb, for which 20 microsatellite markers were developed. The applicability of these markers was confirmed by genotyping of 66 individuals collected from four natural populations in Japan. Of the 20 loci, 15 showed polymorphism. For the 15 polymorphic markers, the number of alleles per locus ranged from 2 to 12, and the expected and observed heterozygosities ranged from 0.13 to 0.77 and 0.02 to 0.65, respectively. The markers described here are sufficiently polymorphic and informative to investigate the genetic diversity and population genetic structure of A. buergeriana var. oxysepala.     

POPULATION GENETICS OF A SNAIL SPECIES COMPLEX IN THE BRITISH ISLES: LITTORINA SAXATILIS (OLIVI), L. NEGLECTA BEAN AND L. TENEBROSA (MONTAGU), USING SSCP ANALYSIS OF CYTOCHROME-B GENE FRAGMENTS

The intertidal snail Littorina saxatilis displays a range ofshell morphologies associated with a variety of habitats. Sincemorphology has an environmental and genetic basis, shell-basedtaxonomy may not accurately reflect genetic relationships. Weexplored genetic structure among adjacent populations of L.saxatilis (the robust open-shore type), L. neglecta (the tinybarnacle-dwelling type) and L. tenebrosa (the fragile brackish-watertype), at nine sites in Britain. Using single-strand conformationalpolymorphism analysis of a 375bp fragment of cytochrome-b wefound no evidence of species distinction. In AMOVA tests significantvariation was contained among populations (68%) and among individuals(32%, both P < 0.001), and insignificant variation was foundamong ecotypes. Genetic patterns suggested gene flow among ecotypesover small scales and a strong random input over larger scales. ^* To whom correspondence should be addressed. (Received 27 March 2000; accepted 10 July 2000)     

Genetic Diversity inBrassica oleraceaL. (Cruciferae) and Wild Relatives (2n=18) using RAPD Markers

This paper presents the evaluation of genetic diversity in 29populations of wild taxa of theBrassica oleraceaL. group (2n=18)and two cultivars, using RAPDs as molecular markers. In a previouspaper (Lázaro and Aguinagalde,Annals of Botany82: 000–000,1998), 11 isozymes were used for the same purpose. Results obtainedwith the two molecular markers (isozymes and RAPDs) are compared.DNA from ten individuals per population was analysed using sixdifferent primers; the 151 detected bands were polymorphic,11 were common to all species, six to all taxa, only one toevery population; and no bands were shared by every individual.The dendrogram obtained using genetic distances clustersB. oleraceapopulationswithB. bourgeaui, B. alboglabra, B. montanaandB. incana. B.insularis, B. macrocarpa, B. villosaandB. rupestrispopulationsform another cluster. Populations ofB. creticaandB. hilarionisformthe third cluster. Genetic diversity inB. oleraceapopulations,theB. rupestriscomplex andB. creticasubspecies was estimatedusing the AMOVA programme; the latter was the most diverse.Copyright1998 Annals of Botany Company. Brassica oleraceaL., wild relatives, genetic diversity, genetic resources, RAPD markers, AMOVA.     

Identification and characterization of a divalent cation-dependent glycosaminoglycan-binding protein from rat liver endothelium

Rat liver endothelial cells (LECs) express a membrane-associatedCa²⁺-dependent hyaluronan-binding activity (CaHA-BP) which isdistinct from the Ca²⁺-dependent, endocytic LEC HA receptor(Yannariello-Brown et al., J. Cell Biochem., 48, 73–80,1992). The CaHA-BP is specific for a subset of glycosaminoglycans,since Ca²⁺-dependent binding of ¹²⁵I-HA ({small tilde}80kDa)to LECs was competed with a 100-fold excess (w/w) of HA, chondroitinsulfate, and heparin, but not with chondroitin. The CaHA-BPactivity on intact LECs was pH-dependent. Optimal binding occurredat pH 6.0; no binding was detected at pH values 5 or 9. ¹²⁵I-HA,pre-bound in the presence of Ca²⁺ could also be dissociatedwith an acidic buffer (pH 5.0), as well as the divalent cationchelators EDTA and EGTA. ¹²⁵I-HA binding was stimulated by divalentcations other than Ca²⁺ such as Mg²⁺, Mn²⁺ and Ba²⁺; with theexception of Zn²⁺. A photoaffinity crosslinking reagent (¹²⁵I-ASD-HA)was used to identify specifically crosslinked polypeptides onLECs. In the absence of Ca²⁺ and in the presence of EGTA, onlybands at 175/166 kDa were consistently crosslinked. These bandshave been previously identified as the LEC Ca²⁺-independentendocytic HA receptor (Yannariello-Brown et al., J. Biol. Chem.,267, 20451/20455, 1992). In the presence of Ca²⁺, crosslinkingwas consistently seen to a 68 kDa polypeptide. Crosslinkingwas competed with a 100-fold excess (w/w) of HA. These and otherdata suggest that a 68 kDa protein is the most likely candidatefor the CaHA-BP in LECs. photoaffinity crosslinking hyaluronan calcium lectin     

穗花杉ISSR引物反应条件的优化与筛选

在研究穗花杉(Amentotaxus aragotaenia)的遗传多样性过程中,为了获得清晰、重复性好ISSR扩增结果,对影响ISSR-PCR的多个因素包括模板浓度、Taq酶的选择和用量、Mg²⁺和dNTPs浓度及退火温度等指标等进行了筛选和优化,确定了穗花杉ISSR-PCR分析的最适扩增条件： 20 μL PCR反应体系中,2 μL 10×Taq酶配套缓冲液,1.8 U Taq聚合酶（上海生工公司）,0.2 μmol·L^-1引物,0.18 mmol·L^-1 dNTP,1.5～2.5 mmol·L^-1 MgCl₂,10 ng·μL^-1模板DNA。用来自不同居群7个个体,以100个ISSR引物进行PCR扩增,筛选出扩增效果较好的10个引物。得到了92个位点,其中45个多态性位点,多态性位点比例为49%。