Vermicomposting as an Added-Value Post-treatment for Livestock Waste Composts

The aim of this work was to study the effects of vermicomposting on selected properties of composts derived from animal and plant wastes. For this, two different worm beds were established and fed with two composts: C1, made from goat (Capra aegagrus hircus) manure and rosemary (Rosmarinus officinalis) pruning wastes, and C2, made from rabbit (Oryctolagus cuniculus) manure and grass clippings, to study the quality of the final vermicomposts. Physical and chemical properties were determined in the end products. Vermicomposting improved several properties of the composts, increasing their total water-holding capacity (in C1, from 333 to 451 mL/L, and in C2, from 371to 419 mL/L), reducing salinity (in C1, from 6.8 to 2.4 dS/m, and in C2, from 10.3 to 4.6 dS/m), and balancing pH in the final composts obtained, especially in C1 (from 8.57 to 8.02). The type of raw material used in the worm beds significantly influenced the final characteristics of the end products obtained and the development of the process, with more favorable results being obtained with the compost derived from rabbit manure and grass clippings (C2).     

Morphological characterisation and agronomic evaluation of transgenic broccoli (Brassica oleracea L. var. italica) containing an antisense ACC oxidase gene

Morphological characterisation and agronomic evaluation was conducted on 12 transgenic broccolilines containing a tomato antisense1-aminocyclopropane-1-carboxylic acid (ACC) oxidase gene. Plants of three cultivars: Shogun (Sh), Green Beauty (Gy) and Dominator (D), were regenerated from hairy root cultures after co-cultivation with Agrobacterium rhizogenes strain A4T harbouring the binary vector pLN35. The T-DNA of pLN35 contains genes encoding a tomato antisense ACC oxidase gene (35S-ACC-5′7′) and a neomycin phosphotransferase II gene (NOS-NPTII-NOS) for kanamycin resistance. The transgenic plants were transferred to a greenhouse and fertile plants obtained. Integration of the foreign DNA into the broccoli genome was confirmed by the polymerase chain reaction and Southern analyses. Transgenic plants showed evidence of hairy root (HR)-induced morphological changes to varying degrees. Of the 12 characterised transgenic lines, three lines(Gy/7, D/1 and D/2) performed within the limits of acceptability for all head quality parameters analysed (size, density, colour, shape and leafiness). The ethylene production from stalks of four field-grown transgenic lines of Green Beauty broccoli showed significant reductions in activity relative to the control 98 h after harvest. The Dominator transgenic lines D/1 and D/2 showed significant improvements in head colour relative to the control from 48 h after harvest. These results are consistent with the ethylene production patterns determined previously for these lines. The head colour results are consistent with previous results suggesting that two enzyme systems may be involved in broccoli senescence, giving two bursts of ethylene production, with only the second burst inhibited by the antisense ACC oxidase gene used. This revised version was published online in August 2006 with corrections to the Cover Date.     

The distribution and diversity of Collembola in saltmarsh habitats of the German North Sea – a preliminary study

The distribution pattern and diversity of Collembola communities in the soils of low and high intertidal saltmarshes were compared. The intertidal “mud” soils are colonized by Collembola to depth of 30 cm and at a distance of 10 m towards the sea from coastal edge. The communities of Collembola in low intertidal saltmarsh soils are dominated by a population of Archisotoma sp. The contents of organic matter in the intertidal saltmarsh soils influenced the distribution of Archisotoma sp.     

Control of Cyclohexane Atmospheric Emissions During Soil Remediation

Gaseous effluent from the treatment of contaminated soils must becontrolled to avoid atmospheric emissions of volatile organiccompounds during remediation. The combination of carbonadsorption with catalytic deep oxidation for control ofcyclohexane emissions is analysed in this paper. The activitiesof activated carbons prepared with almond shells and impregnatedwith CoO, Co₃O₄ and CrO₃ were compared, inrelation with carbon structure, catalyst content and catalystspecies. The microcatalytic-chromatographic technique developedwas very suitable for rapid comparison of the catalyticactivities. Carbons with a better development of surface areaand pore volumes showed higher catalytic activities. Theincreasing of catalyst content also increased catalyticactivity. Cobalt is better than chromium to catalyse the deepoxidation of cyclohexane, the oxidation state of cobalt inCo₃O₄ being better than in CoO.     

RFLP markers are an effective tool for the identification of creeping bentgrass (Agrostis stolonifera L.) cultivars

The potential use of RFLP molecular markers for the identification of four creeping bentgrass (Agrostis stolonifera L.) cultivars and one variety of A. tenuis Sibth. used as control, was investigated. Seven probes out of the total 44 screened were able to differentiate all five cultivars at once. On the basis of their genetic similarity the varieties bred at the Pennsylvania State University were grouped closely together, whereas the variety Prominent and the A. tenuis control were more distantly related.     

Some effects of light intensity and photoperiod on the sea bass larvae (Dicentrarchus labrax (L.)) reared at the Centre Oceanologique de Bretagne

Four experiments were performed to determine the effects of light intensity on the growth and survival of sea bass larvae; two experiments dealt with the photoperiod and two with the combined effects of light intensity and the photoperiod. Recently hatched larvae from the same spawning were used within each experiment.The light intensity experiments show that there is better growth but poorer survival at higher light intensities. The photoperiod experiments show a better growth at 18 h photoperiod and a better survival at 12 h exposure to light. The study of the combined effects of light intensity and photoperiod confirmed the hypothesis that strong light intensities are lethal to newly hatched larvae (with no pigmentation). If the light intensity is lowered during the first week, the best rearing conditions were found to be continuous lighting relative to survival rate, and 14–16 h photoperiod relative to growth.     

Fucose-Rich Sulfated Polysaccharides from Two Vietnamese Sea Cucumbers Bohadschia argus and Holothuria (Theelothuria) spinifera: Structures and Anticoagulant Activity

Fucosylated chondroitin sulfates (FCSs) FCS-BA and FCS-HS, as well as fucan sulfates (FSs) FS-BA-AT and FS-HS-AT were isolated from the sea cucumbers Bohadschia argus and Holothuria (Theelothuria) spinifera, respectively. Purification of the polysaccharides was carried out by anion-exchange chromatography on DEAE-Sephacel column. Structural characterization of polysaccharides was performed in terms of monosaccharide and sulfate content, as well as using a series of non-destructive NMR spectroscopic methods. Both FCSs were shown to contain a chondroitin core [→3)-β-d-GalNAc-(1→4)-β-d-GlcA-(1→]_n bearing sulfated fucosyl branches at O-3 of every GlcA residue in the chain. These fucosyl residues were different in pattern of sulfation: FCS-BA contained Fuc2S4S, Fuc3S4S and Fuc4S at a ratio of 1:8:2, while FCS-HS contained these residues at a ratio of 2:2:1. Polysaccharides differed also in content of GalNAc4S6S and GalNAc4S units, the ratios being 14:1 for FCS-BA and 4:1 for FCS-HS. Both FCSs demonstrated significant anticoagulant activity in clotting time assay and potentiated inhibition of thrombin, but not of factor Xa. FS-BA-AT was shown to be a regular linear polymer of 4-linked α-L-fucopyranose 3-sulfate, the structure being confirmed by NMR spectra of desulfated polysaccharide. In spite of considerable sulfate content, FS-BA-AT was practically devoid of anticoagulant activity. FS-HS-AT cannot be purified completely from contamination of some FCS. Its structure was tentatively represented as a mixture of chains identical with FS-BA-AT and other chains built up of randomly sulfated alternating 4- and 3-linked α-L-fucopyranose residues.     

Tissue distribution of Red Spotted Grouper Nervous Necrosis Virus (RGNNV) genome in experimentally infected juvenile European seabass (Dicentrarchus labrax)

The distribution of viral genome in the tissues of juvenile European seabass (Dicentrarchus labrax) during the course of a Red Spotted Grouper Nervous Necrosis Virus (RGNNV) infection has not yet been described. The present study addresses this and indicates which target organs may be involved in viral replication. This information should enable more accurate detection of virus in asymptomatic carriers, and in turn help to control the spread of the disease. The aim of this study was to examine the pattern of expression of viral genomic segments RNA1 and RNA2, using two absolute real-time PCRs (RT-qPCR), over the course of a RGNNV infection after administering the virus by intramuscular injection. In situ hybridization was also used to locate the RNA2 viral segment in different organs throughout the infection. The experimental challenge provoked an acute form of viral nervous necrosis (VNN), with a resulting cumulative mortality of 37%. The RT-qPCRs designed allowed the detection of both genomic segments in all the organs tested (nervous and non-nervous tissues) at all sampling times examined. The highest viral RNA copy number was found in eyes, although viral replication appeared to begin in the brain. Viral replication was also recorded in pooled internal organs and in caudal fin. However, the increase in the viral RNA copy number in these organs did not result in an increased viral titre, which may indicate that a productive infection does not take place in non-nervous tissues, possibly due to a failure in a viral post-replication step.     

Initial cooling time before freezing affects post‐thaw quality and reproductive performance of rabbit semen

The aim of this study was to investigate the effect of initial cooling time at 5°C during semen cryopreservation on post‐thaw quality and reproductive performance of rabbit semen. Pooled semen samples (n = 6) were divided into two subsamples and cooled at 5°C for 45 or 90 min. After cooling, the semen samples were diluted to a ratio of 1:1 (v:v) with a freezing extender composed of Tris‐citrate‐glucose (TCG) containing 16% of dimethylsulfoxide and 0.1 mol/L sucrose. The semen was subsequently loaded in 0.25 ml straws, equilibrated at 5°C and frozen in liquid nitrogen vapor. After thawing, sperm motility, viability, osmotic resistance, acrosome and DNA integrity were assessed. Our results indicate that the longer cooling time, that is, 90 min before cryopreservation significantly improves sperm post‐thaw viability, motility and fertility. In fact, reproductive performances obtained with semen frozen after a 90 min cooling time were similar to those produced by fresh semen insemination. Hence, the present research provides an effective freezing protocol for rabbit semen that will allow for the creation of a sperm cryobank for the conservation of Italian rabbit genetic resources, as well as the use of frozen semen doses in commercial farms.     

Pseudomonas fluorescens contamination of a feline packed red blood cell unit and studies of canine units

Background: While screening programs have reduced the risk of infectious disease transmission by donors in human and veterinary blood banking, bacterial contamination of blood products has emerged as a major complication in human medicine. Objectives: To describe a Pseudomonas fluorescens (Pf)‐contaminated feline packed RBC (pRBC) unit and experimentally investigate Pf‐contaminated canine pRBCs. Methods: Canine pRBCs were inoculated with Pf‐rich pRBCs from the sentinel feline unit and stored at 4°C or 20°C for 72 hours. Aliquots from the pRBCs were serially evaluated by microscopy, culture, and a eubacterial 16S rRNA real‐time PCR assay. Results: One Pf‐contaminated feline unit turned black after 22 days of storage and was removed from the blood bank; a source was not found, and no other contaminated units were identified. Canine pRBCs spiked with 5 or 25 μL of the sentinel unit became culture‐ and/or 16S PCR‐positive at ≥8 hours at 20°C and 48 hours at 4°C and developed a color change at ≥24 hours. Sensitivity studies indicated that without incubation, inoculation of ≥100 μL Pf‐rich pRBCs was necessary for a positive 16S PCR test result. Conclusions: P. fluorescens grows in stored pRBCs slowly at 4°C and rapidly at 20°C. Screening of blood products for color change, estimating bacterial concentration with microscopy, and 16S PCR testing are simple and fast ways to detect bacteria in stored blood. Aseptic collection, temperature‐controlled storage, and regular visual monitoring of stored units is recommended. Discolored units should not be transfused, but examined for bacterial contamination or other blood product quality problems.