Short-term changes in tree populations in a tropical evergreen forest at Varagalaiar, Western Ghats, India

Within a 30-ha permanent plot of a tropical evergreen forest in the Anamalais, Indian Western Ghats, all the 13415 trees 30cmgbh (belonging to 153 species) were identified and tagged during 1997–1998. This communication reports the results of tree population changes based on two annual censuses (1999 and 2000) of the plot after the initial census, and compares the results with other tropical forest sites. One species, Ficus beddomei, disappeared from the plot and there was no new addition of species. Of the 96 species that showed changes in their population density, for 12 species recruitment and mortality matched. Tree recruitment (5 treesha^–1year^–1) exceeded mortality (4 treesha^–1year^–1) during the two-year period. Four modes of tree deaths were recorded in our site. The per cent mortality of trees differed between tree size classes during each recensus. The plot tree density increased progressively in the two-year period, indicating that shifts in species composition and density in natural forests, without major catastrophic disturbance, occur slowly.     

Induction of the Synthesis of Endo-1,4-β-xylanase and β-Galactosidase in Original and Recombinant Strains of the Fungus Penicillium canescens

The induction of synthesis of the secreted enzymes endo-1,4--xylanase (EC 3.2.1.8) and -galactosidase (EC 3.2.1.23) in original and recombinant Penicillium canescens strains has been studied. In all producer strains, the synthesis of these enzymes was induced by arabinose and its metabolite arabitol. The two enzymes differed in the concentration of arabinose required for induction: the synthesis of -galactosidase was most pronounced at 1 mM, whereas maximum synthesis of endo-1,4--xylanase was observed at 5–10 mM. An increase in the number of endo-1,4--xylanase copies in the high-copy-number strain of the fungus suppressed the synthesis of -galactosidase; the synthesis of endo-1,4--xylanase in the high-copy-number recombinant producing -galactosidase was affected to a lesser extent. The amount of enzymes synthesized did not depend on the saccharide used as the sole source of carbon for growing the mycelium prior to its transfer to the inducer-containing medium.     

Acetyl-L-Carnitine Arginine Amide Prevents β 25–35-Induced Neurotoxicity in Cerebellar Granule Cells

Cerebellar granule cells (CGC) at different stages of maturation in vitro (1 or 6 DIV), were treated with 25–35 and acetyl-L-carnitine arginine amide (ST857) in presence of 25 mM KC1 in the culture medium, and neuronal viability was assessed. Three days of treatment slightly modified the survival of 1 DIV-treated cells, which degenerate and die five days later -amyloid matching. Similarly, a significative neurotoxic effect was observed on 6 DIV treated-cells after 5 days of exposure to the peptide, while the death occurred within 8 days. ST857 coincubated with 25–35 was able to rescue neurons from 25–35-induced neurotoxicity. We also studied the changes in Ca²⁺ homeostasis following glutamate stimulation, in control and -amyloid treated single cells, either in presence or in absence of ST857. 25–35 did not affect basal [Ca²⁺]_i, while modified glutamate-induced [Ca²⁺]_i increase, causing a sustained plateau phase of [Ca²⁺]_i, that persisted after the removal of the agonist. ST857 pretreatment completely reverted this effect suggesting that, in CGC chronically treated with 25–35, ST857 could protect the cells by neurotoxic insults of the peptide likely interfering with the cellular mechanisms involved in the control of Ca²⁺ homeostasis.     

Somatic embryogenesis in cultured mature zygotic embryos of Abies balsamea

Embryo suspensor masses (ESMs) were induced by culture of isolated mature zygotic embryos of balsam fir [Abies balsamea (Mill.)] on media containing 10 M cytokinin [6-(--dimethylallylamino)purine (2iP), 6-benzyladenine (BA), or thidiazuron (TDZ)]. Once induced, ESMs proliferated on media containing 2iP, BA or TDZ (10 M) or on 4.5 M BA in combination with 10 M naphthyl-1-acetic acid. When ESMs were transferred to media containing 5–80 M abscisic acid, cotyledonary-stage embryos were formed. Embryos were readily germinated on medium lacking growth regulators.Abbreviations ABA abscisic acid - BA 6-benzyladenine - ESM embryo-suspensor mass - 2iP 6-(--dimethylallylamino)purine - NAA naphthyl-1-acetic acid - TDZ N-phenyl-N-1,2,3-thiadiazol-5-yl urea (thidiazuron)     

The activity of CK2 in the extracts of COS-7 cells transfected with wild type and mutant subunits of protein kinase CK2

Protein kinase CK2 is ubiquitous in eukaryotes and is known to phosphorylate many protein substrates. The enzyme is normally a heterotetramer composed of catalytic ( and ) and regulatory () subunits. The physiological regulation of the enzyme is still unknown but one of the factors that may play an important role in this regulation is the ratio of the catalytic and regulatory subunits present in cells. The possible existence of free CK2 subunits, not forming part of the holoenzyme, may be relevant to the physiological function of the enzyme in substrate selection or in the interaction of the subunits with other partners. The objective of this work was to study in COS-7 cells the effects of transient expression of CK2 subunits and mutants of the catalytic subunit on the CK2 phosphorylating activity of the extracts of these cells. Using pCEFL vectors that introduce hemaggutinin (HA) or a heptapeptide (AU5) tags in the expressed proteins, COS-7 cells were transfected with and subunits of Xenopus CK2, with the subunit of D. rerio, and with Xl CK2A¹⁵⁶, which although inactive can bind tightly to CK2, and with Xl CK2E⁷⁵E⁷⁶, which is resistant to heparin and polyanion inhibition. The efficiency of transient transfection was of 10–20% of treated cells.Expression of CK2 or CK2E⁷⁵E⁷⁶ in COS-7 cells caused an increase of 5–7-fold of the CK2 activity in the soluble cell extracts. If these catalytic subunits were cotransfected with CK2, the activity increased further to 15–20-fold of the controls. Transfection of CK2 alone also increase the activity of the extracts about 2-fold. Transfection with the inactive CK2A¹⁵⁶ yielded extracts with CK2 activities not significantly different from those transfected with the empty vectors. However, cotransfection of CK2 or CK2E⁷⁵E⁷⁶ with CK2A¹⁵⁶ caused a 60–70% decrease in the CK2 activity as compared to those of cells transfected with only the active CK2 subunits. These results can be interpreted as meaning that CK2A¹⁵⁶ is a dominant negative mutant that can compete with the other catalytic subunits for the CK2 subunit. Addition of recombinant CK2 to the assay system of extracts of cells transfected with catalytic subunits causes a very significant increase in their CK2 activity, demonstrating that CK2 subunit is limiting in the extracts and that an excess of free CK2 has been produced in the transfected cells. Transfection of cells with CK2E⁷⁵E⁷⁶ results in a CK2 activity of extracts that is 90% resistant to heparin demonstrating that a very large proportion of the CK2 activity is derived from the expression of the exogenous mutant. In both the in vivo and in vitro systems, the sensitivity of CK2E⁷⁵E⁷⁶ to heparin increases considerably when it forms part of the holoenzyme CK2₂₂.     

The activity of certain enzymes in the liver of mice,selected for weight gain

Summary Examining the weight gains of mice in selected and nonselected lines maintained on a low (10%) and high (20%) protein diet, and of their crossbreds, it was ascertained that the highest values occurred in selected lines maintained on a high protein level and the lowest in crossbreds.Analysing the enzyme activity — aldolase, aminotransferase AspAT and AlAT — in the liver of these animals, it was observed that selected mice maintained on either of the protein levels demonstrated usually values significantly lower than for the nonselected ones.     

<Emphasis Type="Italic">Uncisudis posteropelvis</Emphasis>, a new species of barracudina (Aulopiformes: Paralepididae) from the western North Pacific Ocean

Six specimens (2 flexion larvae: 9.5–10.4mm in notochord length; 4 postflexion larvae: 12.3–18.2mm in standard length) collected from the western North Pacific are tentatively ascribed to the genus Uncisudis of the tribe Lestidiini of the subfamily Paralepidinae (Paralepididae) in sharing remarkably elongate and filamentous pelvic fin rays, their tips reaching the origin of the anal fin. They are described as Uncisudis posteropelvis sp. nov. in uniquely having the insertion of pelvic fins closer to the origin of anal fin than to the posterior end of dorsal fin base among lestidiine species. Addition to this character, the new species has remarkably elongate and filamentous dorsal fin rays, the short distance between anus and origin of anal fin (4.2–6.1% of standard length, SL), the posteriorly located pelvic fins (prepelvic length 69.4–71.5% SL), dorsal fin rays 10, anal fin rays 28–29, myomeres 41–42+38–40=80–81 (vertebrae 38+41=79), and peritoneal pigment spots 11–12. The occurrence of larvae differing in pigment pattern from the present new species suggests another undescribed species of Uncisudis in the western South Pacific.     

Sequential control of phytochrome-mediated synthesis de novo of β-amylase in the cotyledons of mustard (Sinapis alba L.) seedlings

In the cotyledons of mustard (Sinapis alba L.) seedlings irradiated from the time of sowing with continuous red light, the photoreversibility of the phytochrome-mediated increase in -amylase activity (EC 3.2.1.2) is lost 36 h after sowing (coupling point). However, the induced increase of -amylase activity cannot be detected before 46 h after sowing (starting point). Density labeling with deuterium oxide shows that the increase of enzyme activity in light and darkness coincides precisely with the synthesis of -amylase protein. Thus, phytochrome mediates an increase of -amylase synthesis de novo. Since there is no turnover detectable by density labeling, it is concluded that -amylase of mustard cotyledons is a physiologically stable enzyme (half-life >5 d). The 10-h time gap between loss of photoreversibility and onset of light-induced -amylase synthesis points to a relatively stable regulatory element within the signal chain (transmitter) which links -amylase synthesis to the primary action of phytochrome. A 12-h lag between the cessation of phytochrome action and the cessation of induced -amylase synthesis indicates a limited lifetime of the transmitter (about 12 h). The effect of this result on the interpretation of the coupling point is discussed.Abbreviations P_r, P_fr red and far-red absorbing forms of phytochrome     

A kinetic analysis of the facultative photoperiodic response in Amaranthus retroflexus L.

The ontogenetic change taking place in the facultative photoperiodic response of A. retroflexus to inductive short-day (SD) conditions was studied by exposing plants to continuous induction after different initial exposures to long-days (LD), and comparing the kinetics of their developmental responses (cumulative number of plants with reproductive apices, flowering stage, and height of the apical dome). As the plants progressed from emergence to autonomous flowering (i.e., in non-inductive conditions), their response to continuous induction became progressively more rapid. Reproductive development was initiated following a progressively shorter lag-phase after the start of induction, but its subsequent rate remained unchanged. Until the onset of reproductive development, the undifferentiated upper part of the shoot apex (apical dome) elongated much more rapidly in SD than in LD. However, in both cases reproductive development was initiated when the apex had elongated to about the same extent, after which its elongation accelerated considerably, but to similar rates in both photoperiods. The data indicate that progress towards reproductive development takes place in inductive (SD), as well as in non-inductive (LD) photoperiods, but one cycle of the latter is as effective as 0.20–0.25 of a cycle of the former. —Plants induced at different stages in ontogeny started to change their subsequent branching pattern (ratio of leafy to leafless branches) as soon as induction was delayed beyond autonomous flowering.Abbreviations LD long-days - SD short-days - RGR Relative Growth Rate     

Methodological problems in evolutionary biology VIII. Biology and culture

Biology cannot accommodate all aspects of culture. Aspects of culture that a biological approach can take into account can be covered by the biological categories of phenotype and environment. There is no need to treat culture as a separate category. Attempts to elaborate biological explanations of cultural variation will meet with success only if biologists expand theories of development, and integrate them in evolutionary biology. The alternative — elaborating the idea of so-called cultural inheritance — makes little sense from a biological point of view.     

Über das Zusammenwirken des erregenden und des hemmenden Neurons des M. abductor der Krebsschere beim Ablauf von Reflexen des myotatischen Typus

Zusammenfassung Eine speziell für die Verwendung in strömenden Körperflüssigkeiten konstruierte Caissonelektrode ermöglichte an dem zum Abduktor des Scherenfingers ziehenden Paar motorischer Axone die oszillographische Analyse der bei Reflexvorgängen eintretenden peripheren Interferenz von erregenden und hemmenden Impulsen. Werden mit dem Fingerglied der festgeklemmten Schere entsprechende kurze Bewegungen vorgenommen, so treten myotatische Reflexe auf, und die Aktionen der erwähnten 2 motorischen Ganglienzellen entsprechen dabei formell sehr weitgehend jenem Schema Sherringtons, durch welches für das spinale Säugerpräparat die — dortselbst intrazentral erfolgende — Umschaltung solcher Reflexvorgänge auf die gemeinsame Endstrecke aufgehellt wurde: Wir registrierten einerseits autogene, auf der Seite des gedehnten Muskels selbst eintretende Effekte (nämlich eine Streuentladung erregender Impulse, welche von einer kürzer dauernden, inversen Hemmeraktivierung begleitet ist) und anderseits die durch Dehnung des Antagonisten auszulösende reziproke Reaktion, welche aus einer Streuentladung von Hemmerimpulsen samt schwächerer inverser Aktivierung des Erregerneurons besteht. Für die am häufigsten auftretende Form der reflektorischen Antwort — die Streuentladung — darf als charakteristisch gelten, daß die Impulsfrequenz der im betreffenden Versuchstypus dominierenden, also eigentlich myotatischen Reaktion beinahe übergangslos auf durchschnittlieh 70 Hz emporstieg, um nach einem oder zwei entsprechend kurzen Intervallen (von z. B. 17 msec) zunächst auf mäßige Werte wie etwa 10–15 Hz abzusinken und dann früher oder später zu erlöschen.     

A novel cilia-based feature within the food grooves of the ctenophore Mnemiopsis mccradyi Mayer

We describe a novel compound ciliary structure (g-cilium) from the food groove of the lobate ctenophore Mnemiopsis mccradyi. G-cilia are small, flat compound ciliary organelles that are oriented with their tips pointing toward the mouth. Typically three to four rows of g-cilia line the inner surface of the tentacular groove, which together with the transport groove, make up the food groove. G-cilium cells are 11.4 m long and 4.2 m wide at the g-cilium base. The g-cilium itself is 3.4 m long and tapers to a flat, sharp tip. G-cilia are not motile but are surrounded by many hundreds of smaller, actively motile cilia that beat with orally-directed effective strokes. G-cilia contain 50 conventional `9+2' cilia embedded in a fibrous core that arises from the cell body. In addition, g-cilia contain mitochondria, thousands of small membrane-bounded vesicles and rod bacteria. G-cilia basal bodies are anchored by large, strongly-banded rootlets that extend approximately the entire length of the cell. G-cilia may have organizational, sensory and/or secretory function within the feeding apparatus. Their placement strongly suggests that they play critical roles in feeding. They may enhance the efficiency of prey capture and so contribute to M. mccradyi's well-known voracious appetite. By enhancing prey capture they probably play a critical role in the capacity of this organism to follow prey dynamics, so contributing to dense blooms in mid-late summer in coastal regions.     

Die Biologische Anstalt Helgoland Gegenwart und Zukunft

Ohne ZusammenfassungIn der Septemberausgabe des Der Helgoländer (offizielles Veröffentlichungsorgan des Vereins Helgoland e. V. — Geschichte und Kultur der Deutschen Bucht und zugleich Sonderausgabe der Cuxhavener Allgemeinen für die Insel Helgoland) erschienen anläßlich des 75 jährigen Bestehens der Biologischen Anstalt Helgoland insgesamt 19 Beiträge über unsere Anstalt. In etwas veränderter Form wird hier der Einleitungsaufsatz — mit freundlicher Genehmigung der Cuxhavener Allgemeine — abgedruckt.     

The molecular structure of “chromo proteinoids” — Amino acid thermolysates containing abiogenetically produced flavins and deazaflavins as prosthetic groups

Attempts are made to define chromo-proteinoids in their complete molecular structure, in order to study their functional properties in relation to prebiotically evolving systems. KAG — a thermolysate produced by copolycondensation of the amino acid lysine, alanine, and glycine (180°C/5h) — serves as a model archaic compund of low enough molecular mass (2000D) that can be analysed in all its molecular dimensions.     

The metachromasia of fluorescence of acridine dyes

Summary 1. Fluorescence- and absorption spectra of a number of acridine dyes were measured at several concentrations, in different solvents and at various pH and temperatures.2. In aqueous solutions metachromatic shifts are visible with all dyes — except acridine-yellow — with increasing concentrations, even when the dye is present as di- or trivalent ions in strongly acid solutions.3. Under conditions where reabsorption of the fluorescent light is excluded: completely separated fluorescence and absorption spectra, or measurement of fluorescence in capillaries with 0.8 mm internal bore, metachromatic effects are absent.4. Reasons are given to consider the hypothesis of specific aggregation (formation of dimeric dye-particles) as doubtful. In the case of the acridine dyes the optical properties of the monomeric dye ions are sufficient to explain the metachromatic shifts.With 10 Figures in the Text     

Analysis of the 5′ flanking sequence of the Gγ globin gene by denaturing gradient gel electrophoresis confirms the heterogeneity of the Bantu βs haplotype

Summary The GCTT polymorphism recently described at positions — 1106 and — 1105 in the 5 flanking region of the G globin gene for the Bantu ^S haplotype was analysed by denaturing gradient gel electrophoresis. We studied 108 ^S chromosome and 122 ^A chromosomes. The TT sequence was found as follows: in all of 80 chromosomes bearing the Bantu ^S haplotype with the 6-bp deletion -400 nt from the G gene in 3 out of 5 Bantu ^S chromosomes without the deletion, in 1 out of 122 ^A chromosomes from different ethnic origins but in none of 23 ^S chromosomes bearing the Senegal, Benin or Cameroon haplotypes. These results confirm the heterogeneity of the Bantu ^S haplotype and allow a tentative evolutionary sequence for the different alleles at this locus to be presented.     

Über Chromatin und DNS-Synthese im Nucleolus

Zusammenfassung Im Nucleolus der Leberzellen von Ratten ist elektronenmikroskopisch — mit Formalinfixierung — kontrastreiches Chromatin und autoradiographisch — mit H³-Thymidin — eine DNS-Synthese nachweisbar. Das Chromatin ist nicht in die netzigen Anteile der Nucleolarsubstanz (Nucleolonema), sondern in die dazwischen liegenden Aufhellungen eingelassen, doch sind nur einige dieser Räume und auch diese oft nur unvollständig von Karyoplasma (= Chromosomensubstanz) ausgefüllt. Die einzelnen Chromatin-Einschlüsse erreichen normalerweise die lichtmikroskopischesichtbarkeitsgrenzenicht. Lediglich in hepatozellulärenTumornucleolen sind bereits in gewöhnlichen Präparaten feulgenpositive Strukturen festzustellen.Aus den Befunden wird gefolgert: der Nucleolus der Somazellen ist generell von — meist sublichtmikroskopischen — Anteilen aufgelockerter und aufgesplitterter Chromosomen durchzogen. Dabei handelt es sich um die nucleolusorganizer-Region der Nucleolarchromosomen, denen der organisierte Nucleolus auch in der Intermitose verhaftet bleibt.     

Interaction of Topotecan,DNA Topoisomerase I Inhibitor,with Double-stranded Polydeoxyribonucleotides. 4. Topotecan Binds Preferably to the GC Base Pairs of DNA

Interaction of topotecan (TPT) with synthetic double-stranded polydeoxyribonucleotides has been studied in solutions of low ionic strength at pH 6.8 by linear flow dichroism (LD), circular dichroism (CD), UV-Vis absorption, and Raman spectroscopy. The complexes of TPT with poly(dG-dC)·poly(dG-dC), poly(dG)·poly(dC), poly(dA-dC)·poly(dG-dT), and poly(dA)·poly(dT), as well as complexes of TPT with calf thymus DNA and coliphage T4 DNA studied by us previously, have been shown to have negative LD in the long-wavelength absorption band of TPT, whereas the complex of TPT with poly(dA-dT)·poly(dA-dT) has positive LD in this absorption band of TPT. Thus, there are two different types of TPT complex with the polymers. TPT has been established to bind preferably to GC base pairs because its affinity to the polymers of different composition decreases in the following order: poly(dG-dC)·poly(dG-dC) > poly(dG)·poly(dC) > poly(dA-dC)·poly(dG-dT) > poly(dA)·poly(dT). The presence of DNA has been shown to shift the monomer–dimer equilibrium in TPT solutions toward dimer formation. Several duplexes of the synthetic polynucleotides bound together by bridges of TPT dimers may participate in the formation of the studied type of TPT–polynucleotide complex. Molecular models of TPT complex with linear and circular supercoiled DNAs and with deoxyguanosine have been considered. TPT (and presumably the whole camptothecin family) proved to represent a new class of DNA-specific ligands whose biological action is associated with formation of dimeric bridges between two DNA duplexes.     

Laboratory culture studies of Trichodesmium isolated from the Great Barrier Reef Lagoon, Australia

Cultures of Trichodesmium from the Northern and Southern Great Barrier Reef Lagoon (GBRL) have been established in enriched seawater and artificial seawater media. Some cultures have been maintained with active growth for over 6years. Actively growing cultures in an artificial seawater medium containing organic phosphorus (glycerophosphate) as the principal source of phosphorus have also been established. Key factors that contributed to the successful establishment of cultures were firstly, the seed samples were collected from depth, secondly, samples were thoroughly washed and thirdly, incubations were conducted under relatively low light intensities (PAR 40–50molquantam^–2s^–1). N₂ fixation rates of the cultured Trichodesmium were found to be similar to those measured in the GBRL. Specific growth rates of the cultures during the exponential growth phase in all enriched media were in the range 0.2–0.3day^–1 and growth during this phase was characterised by individual trichomes (filaments) or small aggregations of two to three trichomes. Characteristic bundle formation tended to occur following the exponential growth phase, which suggests that the bundle formation was induced by a lack of a necessary nutrient e.g. Fe. Results from some exploratory studies showed that filament-dominated cultures of Trichodesmium grew over a range of relatively low irradiances (PAR 5–120molquantam^–2s^–1) with the maximum growth occurring at 40–50molquantam^–2s^–1. These results suggest that filaments of the tested strain are well adapted for growth at depth in marine waters. Other studies showed that growth yields were dependent on salinity, with maximum growth occurring between 30 and 37psu. Also the cell yields decreased by an order of magnitude with the reduction of Fe additions from 450 to 45nM. No active growth was observed with the 4.5nM Fe addition.     

Localization of genes coding for biochemical traits on the second chromosome of Drosophila imeretensis Sokolov (D. littoralis Meigen)

We have investigated 13 alleles of four genes coding for acid phosphatase, -and -esterases, and malic enzyme. The genes were localized and their positions regarding the centromere are as follows: Acph-1—centromere—Me—cu—dt—-Est—[Inversion 2t]—-Est. The occurrence of crossing-over in Drosophila imeretensis males, as well as the tetrameric structure of malic enzyme, was confirmed.