Determining uptake of 'non-labile' soil cadmium by Thlaspi caerulescens using isotopic dilution techniques

We assessed the ability of several populations of the metal-hyperaccumulator species, Thlaspi caerulescens , to mobilize non-labile cadmium in soils historically contaminated by Pb/Zn mine spoil or sewage sludge. Radio- labile Cd was determined chemically as an ' E -value', [Cd _E ], and biologically as an ' L -value', [Cd _L ]. For comparison, chloride-extractable Cd, [Cd_chlor], was also determined using 1 M CaCl₂ as a single-step soil extractant. Values of [Cd _L ] were measured for six populations of T. caerulescens that varied substantially in their ability to assimilate soil Cd, and a non-accumulator species with a similar growth habit, Lepidium heterophyllum . Seeds were sown in soil spiked with ¹⁰⁹Cd and grown for 9–12 wk in a controlled environment room. Values of [Cd _L ] were determined from the specific activity of ¹⁰⁹Cd and concentration of Cd in the plant leaves. For the six soils studied, [Cd _E ] ranged from 4.9 to 49% of total soil Cd [Cd_T]. Values of [Cd _L ] were, in general, in close agreement with both [Cd _E ] and [Cd_chlor] and substantially less than [Cd_T]. However, [Cd _L ] showed no correlation with the concentration of Cd in plant tissue, [Cd_shoot]. This suggests that, in the soils studied, T. caerulescens did not mobilize non-labile soil Cd by producing root exudates or altering rhizosphere pH. The results imply that there may be significant restrictions to metal bioavailability, even to hyperaccumulator species, in heavily contaminated soils in which a large proportion of the metal may be present in 'non-labile' forms.     

松梢蚧

松梢蚧又称松针蚧,是同翅目珠蚧科松蚧属专寄生在松树针叶上的害虫。由于它发生起始于松树梢头的新针叶,有些地区的群众称它为松梢蚧,表达了它发生的特点。松树受害严重的可使枝梢上的针叶大部脱落,影响松树生长。 在我国浙江早已发现中华松梢蚧(Matsucoccus sinensis Chen)。Ferris(1950)重新描述了在昆明云南松上采到的所谓中华松梢蚧。我们研究了从昆明采集的标本,发现它不是中华松梢蚧,而是一个新种。Ferris的鉴定和重新描述,很容易引起对中华松梢蚧的误解。     

Effect of latitude on flavonoid biosynthesis in plants

The growth conditions in different latitudes vary markedly with season, day length, light quality and temperature. Many plant species have adapted well to the distinct environments through different strategies, one of which is the production of additional secondary metabolites. Flavonoids are a widely spread group of plant secondary metabolites that are involved in many crucial functions of plants. Our understanding of the biosynthesis, occurrence and function of flavonoids has increased rapidly in recent decades. Numerous studies have been published on the influence of environmental factors on the biosynthesis of flavonoids. However, extensive long‐term studies that examine the effect of the characteristics of northern climates on flavonoid biosynthesis are still scarce. This review focuses on the current knowledge about the effect of light intensity, photoperiod and temperature on the gene–environment interaction related to flavonoid biosynthesis in plants.     

Analysis of Chlamydomonas reinhardtii Histones and Chromatin

Chromatin spreads made from isolated nuclei of the unicellular green alga Chlamydomonas reinhardtii show the beaded fibers typical of eukaryotic polynucleosomes. Micrococcal nuclease digestions confirmed the presence of nucleosomes with a repeat length of 189 base pairs, essentially the same as typical mammalian cells. Basic nuclear proteins extracted from isolated nuclei or chromatin with 1 M calcium chloride and 0.3 M hydrochloric acid are resolved into seven major components by electrophoresis in the presence of sodium dodecyl sulfate (SDS). These seven components were subjected to qualitative peptide mapping with V8 protease on SDS gels for comparison with the major histone components of calf thymus. Finally, the C. reinhardtii basic nuclear proteins were fractionated by reversed phase high performance liquid chromatography and their amino acid composition determined. From these studies, we conclude that C. reinhardtii has a full complement of the five histones with properties very similar to those of both higher animals and higher plants.     

Effects of artificial ultraviolet-B radiation on growth and fatty acid composition of duckweed (Lemna minor)

1. Duckweed (Lemna minor), collected either in summer or early fall was exposed under laboratory conditions to control (photosynthetically active and UV‐A radiation) or experimental (control plus UV‐B radiation) conditions. 2. Growth and survival were determined by counting the number of green, and brown/white fronds following 1–5 or 11 days of irradiation. Growth of duckweed was impaired by exposure to UV‐B radiation in the fall experiment but not in the summer. 3. Fatty acid compositions were analysed following 5 or 11 days of irradiation and a recovery period of 0, 5, 29 or 40 h. Concentrations of the major fatty acids, palmitic, linoleic (LA) and α‐linolenic (ALA) acids were similar in the summer and fall duckweed collections, but the summer samples had higher concentrations of the desaturation products of LA and ALA. 4. UV‐B exposure had small, but significant, and contrasting effects on duckweed fatty acid concentrations. In the summer experiment, duckweed exposed to UV‐B had slightly lower concentrations of major fatty acids than control duckweed, while the reverse was true in the fall experiments. 5. These minor effects of UV‐B on concentrations of LA and ALA would be unlikely to have a major impact on the supply of these essential fatty acids from duckweed to freshwater food webs.     

Elevated CO2 stimulates cells to divide in grass meristems: a differential effect in two natural populations of Dactylis glomerata

In this study, we tested the hypothesis that elevated [CO₂] shortens the cell cycle in meristems of Dactylis glomerata, more in a Portuguese population (38°53′N) than in a Swedish population (63°09′N). In the shoot meristem, the cell cycle shortened to about the same extent (～ 26%) in both populations exposed to the elevated [CO₂] treatment. In the root meristem, the cell cycle shortened by 17% in the Portuguese and by 8% in the Swedish population. However, the proportion of rapidly cycling cells increased in the Portuguese much more than in the Swedish population in both meristems. In the root meristem, there was a 1.86-fold increase in the Portuguese compared with a 1.31-fold increase in the Swedish. In the shoot meristem, the increases were 1.5–3-fold for the Portuguese and 1.2-fold for the Swedish. The data are consistent in showing that a major response to the elevated [CO₂] treatment was an increase in the proportion of cells that were cycling and that this was more marked for the Portuguese population. A more general response to the elevated [CO₂] treatment was a shortening of the cell cycle regardless of population.     

Seismic Stress Responses of Soybean to Different Photosynthetic Photon Flux

Physical agitation applied as periodic seismic stress (shaking)reduced stem clongation, leaf expansion, and biomass accumulationby vegetative soybeans. Level of photon flux (PPF) influencedthe type and extent of plant response to mechanical stress.Plant parts responded differently as PPF varied between 135and 592 µmol m^–2 S^–1. Stem length was significantlyreduced by seismic stress at 135 µmol m^–2 s^–1but this effect was insignificant at higher PPFs. Reduced stemlength resulted from an inhibition of internode elongation.Stem diameter was unaffected by stress at the PPFs tested. Incontrast to effects on stem elongation, leaf area was insensitiveto stress treatments at 135 µmol m^–2 S^–1 butwas progressively inhibited by stress as PPF increased. Statisticallysignificant reductions in shoot f. wt and d. wt by seismic stressoccurred only at 295 µmol m^–2 S^–1. Root biomassaccumulation was not affected by seismic stress at any PPF usedin this study. Glycine max (L.) Merr. cv. Century 84, mechanical stress, photosynthetic photon flux, seismic stress, soybean     

Variability of DNA Content in Individual Cells of <Emphasis Type="Italic">Bacillus</Emphasis>

THE average content of DNA in Bacillus spores is unaffected by the growth medium and is constant for each species¹. Within the Bacillus group, however, the average amount of DNA per spore varies from species to species¹. A cell of B. cereus contains on average twice as much DNA as the spore and during sporulation this DNA is divided equally between the spore and the sporangium². Estimates^3–5 of genome size vary from 1.3 × 10⁹ to 10 × 10⁹ daltons and the number of genomes per cell from 2 to 4^4–8. Some of these variations may be associated with differences within the cells rather than differences of methodolqgy; spores within a population vary not only in size and shape, but also in their content of stainable chromatin⁹. Moreover, in ‘Renografm’ density gradients¹⁰, spores band within a range of densities. If spores are taken from a narrow part of this range, regrown and rebanded, the original pattern of dispersal occurs, suggesting that spores in the same population normally show variation in density as well as in size (A. I. Aronson, personal communication).