TRANSLOCATION OF IODINE IN LAMINARIA SACCHARINA(PHAEOPHYTA)1

Long-distance translocation of ¹²⁵I in Laminaria saccharina (L.) Lamour. followed a “source to sink” pattern. When the source of ¹²⁵I was placed on the distal mature part of the blade, the translocation was unidirectional, basipetal and directed towards the meristematic region at the blade-stipe junction. When the source was placed directly at the meristem there was no movement of label distal to the meristem. The velocity of¹²⁵I transport ranged from 2 to 3.5 cm · h^?1. The anion I^? seemed to be the only species of¹²⁵I transported. An assay of iodine content in different parts of L. saccharina plant showed much higher levels of iodine in the meristem, stipe and holdfast than in the blade. This distribution concurs well with the pattern of I^? translocation.     

THE OCCURRENCE OF FLAGELLATED EGGS IN LAMINARIA ANGUSTATA (PHAEOPHYTA,LAMINARIALES)1

Eggs of laminaria angustata Kjellman were shown to have two flagella. Compared with flagella of other phaeophycean swarmers, those of Laminaria eggs have several unique characters such as lack of mastigonemes, widely spaced basal bodies and no flagellar rootlets. The flagella abscise during egg liberation.     

IMMUNOFLUORESCENCE MICROSCOPY OF FERTILIZATION AND PARTHENOGENESIS IN LAMINARIA ANGUSTATA (PHAEOPHYTA)1

Normal fertilization and parthenogenesis of unfertilized eggs were observed in Laminaria angustata Kjellman by indirect immunofluorescence microscopy using a tubulin antibody. Sperm aster formation did not occur at plasmogamy. The centrosome of the egg gradually disappeared. Shortly after karyogamy, one centrosome reappeared near the zygote nucleus. During mitosis, the centrosome replicated and the daughter centrosomes migrated to opposite poles. The mitotic spindle was formed by microtubules that elongated from both poles. After the first cell division, each of the daughter cells received one centrosome that persisted throughout the development of the sporophyte. During parthenogenetic development, abnormal mono-, tri-, and multi-polar spindles were formed. These abnormal spindles caused abnormal nuclear and cytoplasmic division. Thus, cells were produced with 1) no nuclei, 2) multiple nuclei, 3) irregular numbers of chromosomes, and/or 4) no centrosomes. This is one of the reasons for the abortion and abnormal morphogenesis during parthenogenesis. Ultrastructural observations showed that, although cells of some parthogenetic sporophytes have centrioles, cells of almost all abnormally shaped parthenogenetic sporophytes lack centrioles. These results suggest that centrioles are required for normal centrosomal functions in Laminaria. Although centrioles are inherited paternally, some centrosomal material appears to be present or produced de novo in unfertilized eggs.     

BLUE LIGHT PHOTOREACTIVATION IN ULTRAVIOLET-IRRADIATED YOUNG SPOROPHYTES OF ALARIA ESCULENTA AND LAMINARIA SACCHARINA (PHAEOPHYTA)1

Exposure of ultraviolet (UV)-irradiated young sporophytes of Alaria esculenta (L.) Grev. and Laminaria saccharina (L.) Lamour. to visible light resulted in recovery from UV damage that would otherwise cause much higher mortality. For this photoreactivation, blue light was highly effective, whereas negligible reactivation was produced in green or red light. The blue quantum requirements for a 50% response were 1.9 mol·m^?2 in A. esculenta and 1.2 mol·m^?2 in L. saccharina, which were comparable to those reported for other blue light responses requiring high energy found in brown algae.     

ON THE TAXONOMY OF CALIFORNIA LAMINARIA (PHAEOPHYTA)1

It is suggested that Laminaria setchellii Silva be retained as a species separate from L. dentigera Kjellman as there is no evidence suggesting they are conspecific. Further, L. saccharina (L.) Lamouroux and L. groenlandica Rosenvinge should also continue to be recognized as valid components of the California flora.     

CIRCANNUAL GROWTH RHYTHM AND PHOTOPERIODIC SORUS INDUCTION IN THE KELP LAMINARIA SETCHELLII (PHAEOPHYTA)1

Growth and reproduction of laboratory-grown sporophytes of Laminaria setchellii Silva were investigated in a tank system with controlled conditions of daylength, temperature, and nutrients (N and P). A circannual growth rhythm of the frond was detected under constant laboratory conditions. In continuous long-day and night-break conditions the period τ of the free-running rhythm varied between 11.3 and 17.3 months; in short-day conditions the frond grew indefinitely. The growth rhythm of individual plants could be synchronized by a simulated annual cycle of day-length with a period of T = 12 months. The four seasons of the year were simultaneously simulated by phase shifting the annual cycle of daylength by 3, 6, or 9 months in three out of four tanks. The annual growth cycle followed these phase shifts, and initiation of the new blade always started just after the winter daylength minimum. The formation of sori was induced by a genuine photoperiodic short-day reaction in 1- to 2-year-old plants. Sori became, visible 9–14 weeks after transfer of individual plants from long-day to short-day conditions, whereas plants cultured in continuous long-day or night-break conditions remained sterile. Sporophytes with or without blades were able to continue growth or produce new blades in continuous darkness.     

A SEASONAL COMPARISON OF CARBON,NITROGEN, AND PIGMENT CONTENT IN LAMINARIA SOLIDUNGULA AND L. SACCHARINA (PHAEOPHYTA) IN THE ALASKAN ARCTIC1

Laminaria solidungula and L. saccharina inhabit the Beaufort Sea in the Alaskan High Arctic. Laminaria solidungula is an Arctic endemic, whereas L. saccharina extends from north temperate Pacific and Atlantic waters to the Arctic. Previous studies have shown that the two species have different seasonal timing of growth, but little comparative physiological information exists. As a first step in characterizing these two species from a mixed Arctic population, we measured variations in carbon, nitrogen, and photosynthetic pigment content in blade tissue from plants collected under the fast ice in April and during the open water Period in late July, Both species exhibited seasonal differences in many measured variables; seasonal differences in L. solidungula were most pronounced in growing basal blades. For example, the molar CIN ratio of basal blades averaged 11 in April and 21 in July for L. solidungula and 11.5 in April and 28 in July for L. saccharina. Basal and mature second blades differed in pigment content in April but not in July: chlorophyll a + c in L. solidungula basal and mature second blades averaged 19 and 27 nmol.cm^?2 in April and 30 and 29 nmol. cm^?2 in July, respectively. The corresponding values for L. saccharina were 17 and 29 nmol.cm^?2 in April and 16 and 16 nmol.cm^?2 in July (95% confidence intervals approximately 1–3 nmol. cm ^?2). Carotenoids exhibited similar patterns. Species differences in pigments, carbon, and nitrogen were minor and were probably effects rather than causes of the different seasonal patterns of growth and development. The primary difference between the two species may be the ability of L. solidungula to retain multiple metabolically active blades and to fuel areal growth with stored carbohydrates during winter near-darkness, whereas L. saccharina growth is more closely tied to active photosynthesis in the growing basal blade. The cause of old blade retention in L. solidungula and the possibility of other physiological differences between the two species, including gametophytes, remain to be determined.     

ULTRASTRUCTURE AND DNA RESTRICTION ENDONUCLEASE ANALYSIS OF CALLIPTAMUS ITALICUS ENTOMOPOXVIRUS

Abstract  Calliptamus italicus entomopoxvirus (CiEPV) was isolated from the grasshopper Calliptamus italicus . This virus mainly infects the host's fat body, and its development in the cytoplasm includes 4 steps: the appearance of viroplasm in the cytoplasm of fat body; the formation of immature virions by budding from viro-plasm; the differentiation of mature virions from immature virions and the accumulation of occlusion-body protein. The mature virions are oval with mulberry-like surface, measuring 190 nm X 350 nm in size. Most of the occlusion bodies are elliptical, some are square- round in shape. There are great differences in size ranging from 1.5 μm X 1.9 μm to 8.8 μm X 12.3 μm. CiEPV DNA, when cleaved with restriction endonuclease Eco R I Bg 1 II and Hin d III, produces 16–18 and 10 fragments respectively, and the molecular weight of this DNA was estimated to be 135.7 X 10⁶ daltons. Some characteristics of morphology and DNA were compared between CiEPV and Oedaleus asiaticus EPV (OaEPV) reported previously.     

ORIGINS OF GENOTYPIC VARIATION IN NORTH AMERICAN DANDELIONS INFERRED FROM RIBOSOMAL DNA AND CHLOROPLAST DNA RESTRICTION ENZYME ANALYSIS

Restriction enzyme analysis of ribosomal DNA (rDNA) and chloroplast DNA (cpDNA) is used to assess the relative contribution of hybridization and mutation as sources of genotypic variation in weedy asexual dandelions, with focus on the dandelion flora of North America. Of 318 North American dandelions surveyed, 145 rDNA-cpDNA clones are detected. The combined rDNA-cpDNA genotypes show that most of the polymorphic rDNA and cpDNA restriction sites or lengths in these plants are also present in weedy asexual dandelions collected from natural populations in Europe and in asexual and diploid taxa (microspecies) chosen to represent diverse Eurasian members of the genus. However, of 222 combined rDNA-cpDNA genotypes found in 427 asexual plants surveyed, only 9 genotypes are found in both North American and Eurasian dandelions. Two rDNA and three cpDNA characters are unique to individual plants in North America and are consistent with mutational origins of genotypic variation in asexual lineages. But the array of genotypic diversity, characterized by different combinations of the rDNA and cpDNA characters, show that multiple hybridization events are a more important source of genotypic variation than mutation in the asexual polyploids. The rDNA and cpDNA data also indicate polyphyletic origin of several asexual Taraxacum taxa.     

STIMULATION OF LIGHT-SATURATED PHOTOSYNTHESIS IN LAMINARIA (PHAEOPHYTA) BY BLUE LIGHT1

The light-saturated rate of photosynthesis in blue light was 50-100% higher than that in red light for young sporophytes of Laminaria digitata (Huds.) Lamour., although photosynthetic rates were slightly higher in red than in blue light at low irradiances. Short exposures to low irradiances (e.g. 2 min at 20 μmol · m^?2· s^?1) of blue light also stimulated the subsequent photosynthesis of Laminaria sporophytes in saturating irradiances of red light but had little effect on photosynthesis in low irradiances of red light. The full stimulatory effect of short exposures to blue light was observed within 5 min of the blue treatment and persisted for at least 15 min in red light or in darkness. Thereafter, the effect began to decline, but some stimulation was still detectable 45 min after the blue treatment. The degree of stimulation was proportional to the logarithm of the photon exposure to blue light over the range 0.15-2.4 mmol · m^?2, and the effectiveness of an exposure to 0.6 mmol · m^?2at different wavelengths was high at 402-475 nm (with a peak at 460-475 nm) but declined sharply at 475-497 nm and was minimal at 544-701 nm. Blue light appears, therefore, to exert a direct effect on the dark reaction of photosynthesis in brown algae, possibly by activating carbon-fixing enzymes or by stimulating the uptake or transport of inorganic carbon in the plants.     

CONSTRUCTION AND CHARACTERIZATION OF A TENTATIVE AMPLIFIED FRAGMENT LENGTH POLYMORPHISM–SIMPLE SEQUENCE REPEAT LINKAGE MAP OF LAMINARIA (LAMINARIALES,PHAEOPHYTA)1

A tentative amplified fragment length polymorphism–simple sequence repeat (AFLP–SSR) linkage map of Laminaria was constructed using a haploid population of 40 gametophyte clones isolated from an individual of Dongfang No. 2, the first commercially cultured hybrid of a female gametophyte clone of L. japonica Aresch. [=Saccharina japonica (Aresch.) C. E. Lane, C. Mayes et G. W. Saunders] and a male one of L. longissima Miyabe [=Saccharina longissima (Miyabe) C. E. Lane, C. Mayes et G. W. Saunders]. To the map, 263 markers (255 AFLP, seven SSR, and the gametophyte sex) were assigned. The map consisted of 25 linkage groups (LGs) with ≥ four markers, five triplets, and 15 doublets, which is 1,629.0 centiMorgans (cM) in length, covering 66% of Laminaria genome. The maximum space between loci is 24.63 cM. A putative sex‐determining region was identified in LG₂, which was characterized by a dense marker distribution around the gametophyte sex locus. The linkage map itself and the methodology associated with its construction will facilitate the genetic study and further trials of the linkage map construction of Laminaria.     

ADAPTATION OF PHOTOSYNTHESIS IN LAMINARIA SACCHARINA (PHAEOPHYTA) TO CHANGES IN GROWTH TEMPERATURE1

The effect of growth temperature on photosynthetic metabolism was studied in the kelp Laminaria saccharina (L.) Lamour. Photosynthesis was subject to phenotypic adaptation, with almost constant photosynthetic rates being achieved at growth temperatures between 0 and 20° C. This response involved: (1) an inverse relationship between growth temperature and photosynthetic capacity, (2) a reduction in the Q₁₀ value for photosynthesis of L. saccharina grown at 0 and 5° C compared with 10, 15 and 20° C grown sporophytes, and (3) an acquired tolerance of photosynthesis to temperatures between 15–25° C (which inhibited photosynthesis in 0 and 5° C grown L. saccharina) in sporophytes grown at 10, 15 and 20° C. The physiological basis of these adaptations is discussed in terms of observed changes in activities and kinetics of the Calvin cycle enzyme ribulose-1, 5-bisphosphate carboxylase (oxygenase) and efficiency of light harvesting-electron transport systems.     

烟夜蛾18S rDNA的克隆及序列分析

利用PCR方法克降得到了烟夜蛾18S rDNA全基因序列,基因全长1904bp;构建了其全长、保守区和非保守区的系统发育树,比较了与其他已知蛾类昆虫18S rDNA全序列的同源性.结果表明,蛾类之间该基因的同源性达到92%以上,利用其多变区构建的发育树更能反映蛾类昆虫的亲缘关系;比较烟夜蛾与棉铃虫的18S rDNA序列发现,两个近缘种之间仅有lO个核苷酸的差异.     

AXENIC TISSUE CULTURES FROM THE SPOROPHYTES OF LAMINARIA DIGITATA AND LAMINARIA HYPERBOREA (PHAEOPHYTA)

Starting material for the tissue cultures was the meristematic basal zone of the blade. Pieces treated 30–60 sec in hypochlorite solution were rinsed and placed on agar plates made from the artificial seawater ASP6 F2 solidified with 6 g agar l^?1. After 6 weeks colorless callus-like tissue grew out from some pieces. Treatment with activated charcoal removed some inhibiting substances from the agar medium as numbers of callus developing pieces increased on such plates. A combination of 10^?5 M NAA and 5 · 10^?7 M kinetin gave a yellow-brown tissue. A differentiation in the tissue from L. hyperborea was observed as well as the formation of meiospores, which grew out into male and female plants. Thalli of sporophytes were observed but they never reached a length of more than one mm before they died or changed to an irregular pattern of growth.     

NUCLEOTIDE SEQUENCES OF THE SMALL-SUBUNIT RIBOSOMAL RNA GENES FROM SELECTED LAMINARIALES (PHAEOPHYTA): IMPLICATIONS FOR KELP EVOLUTION1

The entire small-subunit (SSU) ribosomal ribonucleic acid sequence was inferred for kelp representing seven genera: Alaria marginata Postels and Ruprecht (1824 bp), Egregia menziesii (Turner) Areschoug (1825 bp), Lessoniopsis littoralis (Tilden) Reinke (1825 bp), Macrocystis integrifolia Bory (1825 bp), Nereocystis leutkeana (Mertens) Postels and Ruprecht (1824 bp), Postelsia palmaeformis Ruprecht (1826 bp), and Pterygophora californica Ruprecht (1825 bp). We obtained a partial sequence for Eisenia arborea Areschoug (1669 bp) from a single clone of polymerase chain reaction-amplified product. The SSU sequence was too conserved among these morphologically distinct taxa to permit phylogenetic analysis. The divergence between the most distant taxa was only 0.66%. This value was used in a SSU molecular clock to suggest that the most distantly related kelp investigated in this study diverged between 16 and 30 (more probably 16 and 20) million years ago.     

GENETIC MAPPING OF THE LAMINARIA JAPONICA (LAMINARALES,PHAEOPHYTA) USING AMPLIFIED FRAGMENT LENGTH POLYMORPHISM MARKERS1

To establish a molecular‐marker‐assisted system of breeding and genetic study for Laminaria japonica Aresch., amplified fragment length polymorphism (AFLP) was used to construct a genetic linkage map of L. japonica featuring 230 progeny of F₂ cross population. Eighteen primer combinations produced 370 polymorphic loci and 215 polymorphic loci segregated in a 3:1 Mendelian segregation ratio (P ≤ 0.05). Of the 215 segregated loci, 142 were ordered into 27 linkage groups. The length of the linkage groups ranged from 6.7 to 90.3 centimorgans (cM) with an average length of 49.6 cM, and the total length was 1,085.8 cM, which covered 68.4% of the estimated 1,586.9 cM genome. The number of mapped markers on each linkage group ranged from 2 to 12, averaging 5.3 markers per group. The average density of the markers was 1 per 9.4 cM. Based on the marker density and the resolution of the map, the constructed linkage map can satisfy the need for quantitative trait locus (QTL) location and molecular‐marker‐assisted breeding for Laminaria.     

VARIATION IN NITROGEN PHYSIOLOGY AND GROWTH AMONG GEOGRAPHICALLY ISOLATED POPULATIONS OF THE GIANT KELP,MACROCYSTIS PYRIFERA (PHAEOPHYTA)1

Three geographically isolated populations of the giant kelp, Macrocystis pyrifera (L.) C. Ag., were examined for responses to nitrate availability in batch culture experiments using juvenile sporophytes reared from spores in the laboratory. Although maximum rates of nitrate-saturated growth were similar among groups, there were significant quantitative differences in the response to nitrate limitation that can be related to natural patterns of nutrient availability at these sites. Plants from Santa Catalina Island (most oligotrophic) achieved maximum growth rates at ambient nitrate concentrations that were lower than those for plants from Monterey Bay, California (most eutrophic), or Refugio State Beach (near Santa Barbara, California). Tissue nitrogen and amino acid concentrations were highest in plants cultured from Santa Catalina Island populations at all external nitrate concentrations, suggesting that differences in nitrate requirements for growth may reflect the efficiency of nitrate uptake and assimilation at subsaturating nitrate concentrations. Given the different physical environments from which these plants came, the data suggest that geographically isolated populations of M. pyrifera have undergone genetic divergence that can be explained by ecotypic adaptation to unique habitat conditions at these sites.     

POPULATION STRUCTURE OF THE BOTTLENOSE DOLPHIN (TURSIOPS TRUNCATUS) AS DETERMINED BY RESTRICTION ENDONUCLEASE ANALYSIS OF MITOCHONDRIAL DNA

Abstract: Restriction fragment length polymorphisms of mitochondrial DNA (mtDNA) were used to test for population subdivision in the bottlenose dolphin (Tursiops truncatus). Atlantic and Pacific dolphin mtDNA samples exhibited distinctly different haplotypes (approximately 2.4% sequence divergence), indicating a lack of gene exchange. Within the Atlantic Ocean, mtDNA samples from the Gulf of Mexico and the Atlantic Coast were also found to be distinct, with a sequence divergence of approximately 0.6%. The Atlantic Coast–Gulf of Mexico dichotomy is consistent with patterns of genetic variation from other marine and coastal organisms from this region, and supports the hypothesized role of bio-geographic events in promoting the divergence of these and other forms. Regional differentiation was identified along the Atlantic Coast, whereas low sequence divergences among haplotypes and consistent haplotype frequencies across populations suggested considerable gene exchange among Gulf of Mexico populations. A highly divergent haplotype found in two individuals from two localities in the Gulf of Mexico is best explained by dispersal from either a distinct offshore Gulf stock or an unsampled Atlantic Coast stock. Additional samples are required to test for the existence of a distinct offshore race and, if it exists, to identify its distribution and contribution to population structure.     

SEQUENCE AND PHYLOGENY OF THE PSAB GENE OF PYLAIELLA LITTORALIS(PHAEOPHYTA)1

The psaB gene codes for one of two highly conserved P700 chlorophyll a apoproteins of photosystem I. This gene was cloned from the brown alga, Pylaiella littoralis (L.) Kjellm., and its primary sequence was determined. The inferred amino acid sequence of the P. littoralis protein was compared to homologous sequences from land plants, green algae, and a cyanobacterium. The psaB protein sequence is very conserved in all the examined taxa, and an unrooted phylogenetic tree, generated from a distance matrix, shows that the P. littoralis gene is closer to that of the cyanobacterium Synechocossus sp. PCC 7002 than are those of green algae, land plants, and Euglena gracilis.