Regrowth and Nutrient Composition of Different Plant Organs in Grass-clover Canopies as Affected by Phosphorus and Potassium Availability

Regrowth after cutting and the distribution of nitrogen (N),phosphorus (P) and potassium (K) in different plant organs ofwhite clover and perennial ryegrass growing in pure or mixedswards were investigated under field conditions in a soil witha low-to-moderate availability of P and K. In all treatments,white clover constituted more than 70% of the above-ground biomassin the mixed swards. The petioles were the dominant pool ofdry matter throughout regrowth and contained the greatest amountsof N, P and K. Increased supply of P and K increased the growthof ryegrass, but not that of white clover in the mixed swards.The increased competition from ryegrass led to a decline inthe yield of white clover laminae as well as in the N contentper unit of dry matter in laminae, petioles and stolons. TheP content of all white clover organs also declined followingP application to the mixed swards, whereas K application increasedtheir K contents. In the pure swards of ryegrass and white clover,yields and contents of N, P and K in the dry matter were eithernot affected or increased following P and K application. Itwas concluded that commonly-used defoliation heights may remove80% or more of the nutrient and dry matter pools located inthe petioles but the remaining quantities of dry matter andnutrients in the petioles will normally exceed the correspondingquantities in the stolons. Copyright 2001 Annals of Botany Company Coexistence, competition, phosphorus, potassium, regrowth, ryegrass, white clover     

Urea production by Thiosphaera pantotropha and by anaerobic enrichment cultures from marine sediments

Abstract The production of urea by Thiosphaera pantotropha was studied. Batch cultures were grown on acetate as energy source and with NO₃⁻ or O₂ as terminal electron acceptor. Urea accumulated in the media during exponential growth in aerobic and anaerobic cultures of T. pantotropha . Urea production continued after the cells had entered the stationary growth phase. Bacterial ability to produce urea was supported by studies of cultures enriched for denitrifying, sulphate-reducing and fermenting bacteria. The results implied that urea production was common among bacteria normally considered to be important in marine sediments.     

Ecology and ethics: relation of religious belief to ecological practice in the Biblical tradition

The Bible, without which Western civilization is inexplicable, has powerful ecological teachings that support an ecological worldview. While these teachings are not widely practised in our time. continuing degradation of ecological systems by humanity requires their re-examination by ecologists and the church. Such re-examination can help develop the mutual understanding necessary for making ethical ecological judgements and putting these teachings into practice in an appropriate manner. Among these teachings are the expectation that people will serve and keep the Creation (earthkeeping principle), that creatures and ecosystems not be relentlessly pressed (sabbath principle), that provisions must be made for the flourishing of the biosphere (fruitfulness principle), that the Earth be filled with biologically diverse and abundant life (fulfilment principle), that pressing the biosphere's absolute limits must be avoided (buffer principle), that people should seek contentment and not selfish gain (contentment principle), that people should seek biospheric integrity rather than self-interest (priority principle) and that people should not fail to act on what they know is right (praxis principle). Ecologists need to recognize and respect these and other biblical ecological teachings and be ready to assist churches in their care and keeping of Creation. And churches must join ecologists in the work of assuring the continued integrity of the biosphere.     

Unsaturated Free Fatty Acids Increase Benzodiazepine Receptor Agonist Binding Depending on the Subunit Composition of the GABAA Receptor Complex

Abstract: It has been shown previously that unsaturated free fatty acids (FFAs) strongly enhance the binding of agonist benzodiazepine receptor ligands and GABA_A receptor ligands in the CNS in vitro. To investigate the selectivity of this effect, recombinant human GABA_A/benzodiazepine receptor complexes formed by different subunit compositions (α_xβ_yγ₂, x = 1, 2, 3, and 5; y = 1, 2, and 3) were expressed using the baculovirus-transfected Sf9 insect cell system. At 10^?4M, unsaturated FFAs, particularly arachidonic (20:4) and docosahexaenoic (22:6) acids, strongly stimulated (>200% of control values) the binding of [³H]flunitrazepam ([³H]FNM) to the α₃β₂γ₂ receptor combination in whole cell preparations. No effect or small increases in levels of unsaturated FFAs on [³H]FNM binding to α₁β_xγ₂ and α₂β_xγ₂ receptor combinations were observed, and weak effects (130% of control values) were detected using the α₅β₂γ₂ receptor combination. The saturated FFAs, stearic and palmitic acids, were without effect on [³H]FNM binding to any combination of receptor complexes. The hydroxylated unsaturated FFAs, ricinoleic and ricinelaidic acids, were shown to decrease the binding of [³H]FNM only if an α₁β₂γ₂ receptor combination was used. Given the heterogeneity of the GABA_A/benzodiazepine receptor subunit distribution in the CNS, the effects of FFAs on the benzodiazepine receptor can be assumed to vary at both cellular and regional levels.     

Detection of a nucleolar 7-2 ribonucleoprotein and a cytoplasmic 8-2 ribonucleoprotein with autoantibodies from patients with scleroderma

In studies on antinucleolar antibodies in sera from 24 patients with scleroderma, an autoimmune disease, one serum, designated "anti-To", contained antibodies against a nucleolar 7-2 ribonucleoprotein and a novel cytoplasmic 8-2 ribonucleoprotein. The 7-2 and 8-2 RNAs are distinct RNAs with a pppG terminus. They are partially conserved between rat and human species and are present in distinct ribonucleoprotein particles. Eight sera contained antibodies that precipitated particles containing nucleolar U3 RNA; these antibodies appear to be directed against preribosomal particles containing U3 ribonucleoprotein, rather than the U3 ribonucleoprotein particles alone. All these ribonucleoproteins required proteins for antigenicity. These antibodies will be of use in studies on the structure and function of these novel small ribonucleoproteins.     

Self-assembly of simian virus 40 large T antigen oligomers by divalent cations.

In simian virus 40-transformed cells, simian virus 40 large T antigen can be detected in different forms separable by sucrose density gradient centrifugation. In our experiments, light forms sedimented around 5 to 7S, oligomers such as tetramers were detected around 16S, and higher aggregates sedimented in a broad distribution reaching above 23S. The oligomers sedimenting at and above 16S could be disassembled into the slowly sedimenting 5 to 7S forms by chelating agents [EDTA or ethylene bis(oxonitrilo)tetraacetate]. After the addition of divalent cations (CaCl2 or MgCl2) in excess of chelating agents, oligomeric forms reassembled and appeared in a sedimentation pattern resembling that observed before treatment with chelating agents. Time course studies permitted the identification of the 5 to 7S forms as precursors upon pulse-labeling (15 min); the 16S and higher oligomers were identified as the successors after a 14-h chase. Treatment of extracts of pulse-chase-labeled cells with chelating agents again disassembled the oligomers, whereas pulse-labeled precursors did not change their 5 to 7S sedimentation pattern. Adding an excess of divalent cations reassembled the pulse-chase-labeled T antigen to oligomers but did not influence the sedimentation behavior of pulse-labeled 5 to 7S precursors. It is therefore reasonable to assume that a posttranslational modulation induces divalent cation binding, leading finally to the oligomerization of T antigen. Thus, some of the multifunctional activities of T antigen can be dictated by divalent cation binding properties.     

Functional mechanism of water splitting photosynthesis

A personal account is given on physico-chemical aspects of photosynthesis. The article starts with the way I entered the field of photosynthesis. Then, selected results from our research group are discussed. Three methods used for functional analysis in our laboratory are described: the repetitive flash spectroscopy; the electrochromic volt- and ammeter; and the membrane energization by a battery. Our subsequent studies deal with the two photoreaction centers, the primary charge separation, the plastoquinones as a transmembrane link between the two centers and the vectorial electron- and proton pathways. The results led to a picture of the elementary functional mechanism of the molecular machinery in the thylakoid membrane. The perspective then focuses on the coupling between the electric field, protons and phosphorylation. This section is followed by our observations and analysis of the mechanism of water cleavage and its coupling with the functioning of reaction center II. Finally, information is provided on structural aspects of the two reaction centers. The article ends with a retrospect.Abbreviations ADP(ATP) adenosine di(tri)phosphate - A₀, A₁ electron carriers - Car carotenoid - Chl-a ₁ (P700) chlorophyll-a ₁ - Chl-a _II (P680) chlorophyll-a _II - Cyt cytrochrome - Fd ferredoxin - FeS iron sulphur - Fe iron - F_X, F_A, F_B FeS clusters - HA hydroxylamine - Mn manganese - NADP⁺ (TPN) nictoinamide adenine dinucleotide phosphate - PC plastocyanin - Pheo pheophytin - PQ plastoquinone - P phosphate - Q_A (Q_B) primary (secondary) plastoquinone acceptor - RC I(II) reaction center I (II) - S_{0, 1, 2, 3, 4} different states of the water splitting enzyme S - Tyr tyrosine - X,Y,Z unknown redox components This article was written at the invitation of Govindjee.     

Structure of kinetochore fibers: Microtubule continuity and inter-microtubule bridges

To understand how microtubules interact in forming the mitotic apparatus and orienting and moving chromosomes, the precise arrangement of microtubules in kinetochore fibers in Chinese hamster ovary cells was examined. Individual microtubules were traced, using high voltage electron microscopy of serial 0.25 m sections, from the kinetochore toward the pole. Microtubule arrangement in kinetochore fibers in untreated mitotic cells and in cells recovering from Colcemid arrest were similar in two respects: the number of microtubules per kinetochore (mean 14 and 12, respectively) and the nearest neighbor intermicrotubule distance (mean90 nm). In Colcemid recovered cells, over 90% of the microtubules in kinetochore fibers were attached to the kinetochore (i.e. kinetochore microtubules) and extended most or all of the distance to the pole. Few free microtubules were present in the kinetochore fibers; most non-kinetochore microtubles terminated in the pole. Since kinetochores in this Colcemid-recovered system have been demonstrated to nucleate microtubules (Witt et al., 1980), it seems likely that most if not all of these kinetochore microtubules originated at the kinetochore. Some of the reconstructed kinetochore fibers were attached to chromosomes with bipolar orientation, suggesting that kinetochore microtubules need not interact with many polar microtubules for orientation to occur. In Colcemid recovered cells lysed to reduce cytoplasmic background, microtubules in kinetochore fibers were preferentially preserved. The parallel and near-hexagonal order typical of microtubules in kinetochore fibers was maintained, as was the number of kinetochore microtubules (mean, 13). The intermicrotubule distance was slightly reduced in lysed cells (mean, 60 nm). Crossbridges about 5 nm wide and 30–40 nm long were visible in kinetochore fibers of lysed cells. Such crossbridges probably contribute to the stabilization and parallel order of microtubules in kinetochore fibers, and may have a functional role as well.