Natural revegetation of indigenous roadside vegetation by propagules from topsoil

Road construction degrades large areas of indigenous vegetation. Better understanding of ecosystem restoration after degradation will require development and assessment of improved restoration techniques. The potential of natural revegetation based on propagules from topsoil as a restoration technique, to achieve succession towards indigenous vegetation, is not fully understood and accepted as an alternative method for vegetation establishment. The aim of this study was to evaluate this restoration technique by comparing different topsoils with respect to their potentials for revegetation and to describe the early succession on these topsoils by recording change in vegetation cover and the number of species.The study road RV23 is situated in south-east Norway and runs mainly through mixed, mostly coniferous forest. The topsoil (the upper 30 cm) was removed before road construction started, stockpiled during the construction period and then redistributed on the road verge afterwards. In 1999, 10 macroplots of 25 m² were placed randomly on selected topsoils of different qualities, to represent the soil variation in the study area. The soil quality varied from organic-rich to organic-poor soils. Each macro plot contained four 1-m² mesoplots in which the species composition was recorded in 2000 and 2001.Univariate statistical tests were applied to reveal change in vegetation cover between macroplots within 1 year and between years 2000 and 2001. Furthermore, statistical tests were used to reveal the change in single-species frequencies between the study years.Two years after deposition of topsoils, the vegetation cover was generally satisfactory from an aesthetical point of view. However, the variation in vegetation cover and species composition was considerable on different topsoils, reflecting both the local variation of the indigenous vegetation and the soil quality. A total of 121 species of vascular plants were recorded in all 10 macroplots, although not more than 59 species were found in one macroplot. Species composition and single-species frequencies changed considerably from the first year to the second. Among the 61 species that were recorded in more than five mesoplots, the frequency of 16 species increased and the frequency of 10 species decreased significantly (P<0.05). Most of the decreasing species can be considered as weed species and are not represented in the present indigenous vegetation, while most of the increasing species are. The vegetation change from 2000 to 2001 apparently represents the first steps in a succession towards an ecosystem dominated by species of the indigenous vegetation.     

Coagulase-negative, novobiocin-resistant staphylococci on the skin of animals and man, on meat and in milk.

The occurrence of coagulase-negative, novobiocin-resistant staphylococci, i.e. Staphylococcus cohnii, Staphylococcus saprophyticus, Staphylococcus sciuri and Staphylococcus xylosus, on the skin of animals and man has been studied. On cultures from cats, cows, dogs, guinea pigs, mice, rabbits and sheep studied, such organisms were predominant among the coagulase-negative staphylococci. From the skin of the hands of 21 of 38 persons whose professions brought them into contact with animals, e.g. inséminât ors, slaughterhouse workers and veterinarians, coagulase-negative, novobiocin-resistant staphylococci were isolated. This finding contrasted with that regarding 50 persons lacking such contacts, of whom only 1 harboured such bacteria. S. saprophyticus was isolated only from those slaughterers presenting with wounds on their hands. Coagulase-negative, novobiocin-resistant staphylococci were also isolated from every second specimen collected from the surface of meat at a slaughterhouse. No difference in the culture results could be demonstrated from specimens collected before and after cutting-up of the carcasses. Of 26 strains of coagulase-negative, DNase-negative staphylococci isolated from milk with pathological CMT, all but 5 were novobiocin-resistant. Fifteen were classified as S. xylosus, 4 as S. sciuri and 1 as S. cohnii. Of another 15 DNase-positive strains, 3 were resistant to novobiocin. Finally, clinical infections with coagulase-negative, novobiocin-resistant staphylococci in man, e.g. urinary tract infections caused by S. saprophyticus, are considered in relation to possible contagious reservoirs and modes of spread.     

Mixtures of crushed rock, forest soils, and sewage sludge used as soils for grassed green areas

In two container experiments, we evaluated mixtures of crushed rock, forest soil, and sewage sludge for use as growth media in green areas. We applied two types of crushed rock (0–2 mm fraction), two forest soils (sandy loam), and limed sewage sludge (pH 10), and studied the growth of ryegrass (Lolium multiflorum var. westervoldicum) during one growing season.Including ≥0.2 m³ m⁻³ sewage sludge in the soil mixtures initially inhibited growth, presumably due to toxic levels of ammonium-N. Up to 0.25 m³ m⁻³ sludge increased the total yield of ryegrass, but at a level as low as 0.1 m³ m⁻³, more nutrients were available than could be taken up by the crop. At present, up to 0.3 m³ m⁻³ sewage sludge is allowed in soil mixtures used in green areas in Norway, although that level should probably be lowered due to the risk of abnormal (enhanced or inhibited) plant growth, and leaching of nutrients. We recommend a maximum of 0.1 m³ m⁻³ when applying the kind of sludge used in our experiments.All mixtures containing acid forest soil gave better results than those comprising slightly alkaline forest soil. The best mixture for ryegrass was crushed rock and acid forest soil at a ratio of 1:2. Compared to pure acid forest soil ryegrass grew equally well or better on mixtures containing ≥0.50 m³ m⁻³ acid forest soil. The differences in growth between the various soil mixtures were due to texture and physical properties, and to dissimilarities in the effects of sewage sludge on mineralisation of nitrogen in the mixtures comprising acid and slightly alkaline forest soil.     

Gill amoebae from freshwater rainbow trout (Oncorhynchus mykiss): In vitro evaluation of antiparasitic compounds against Vannella sp.

Gill parasitic infections challenge farming of rainbow trout (Oncorhynchus mykiss, Walbaum) in freshwater facilities. Apart from flagellates (Ichthyobodo, (Pinto) and ciliates (Ichthyophthirius (Fouquet), Ambiphrya (Raabe), Apiosoma (Blanchard), Trichodinella (Sramek-Husek) and Trichodina (Ehrenberg)), we have shown that amoebae are prevalent in Danish trout farms. Gills were isolated from farmed rainbow trout in six fish farms (conventional and organic earth pond and recirculated systems) and placed on non-nutrient agar (NNA) moistened with modified Neff's amoeba saline (AS) (15°C). Gill amoebae from all examined fish colonized the agar and were identified based on morphological criteria showing species within the genera Trinema (Dujardin) (family Trinematidae), Vannella (Bovee) (family Vannellidae). In addition, hartmannellid amoebae were recorded. We established a monoculture of Vannella sp., confirmed the genus identity by PCR and sequencing and performed an in vitro determination of antiparasitic effects (dose–response studies) of various compounds including sodium chloride (NaCl), hydrogen peroxide, peracetic acid, formalin, aqueous garlic and oregano extracts and a Pseudomonas H6 surfactant. All amoebae were killed in concentrations of 16.90 mg/ml (garlic), 17.90 mg/ml (oregano), NaCl (7.5 mg/ml), hydrogen peroxide (100 µg/ml), peracetic acid (0.03 µg/ml), formaldehyde (25 µg/ml) and the Pseudomonas H6 surfactant (250 µg/ml).     

Testing the yield of a pilot‐scale bubble column photobioreactor for cultivation of the microalga Rhodomonas salina as feed for intensive calanoid copepod cultures

A dual column photobioreactor (PBR) (2 × 47 L) with mixed CO₂/air bubbling was tested for cultivation of the microalga Rhodomonas salina as food for live feed copepods. In the continuous growth phase, the cell density was relatively stable at 2.40 ± 0.13 × 10⁶ cells/ml at an average dilution rate of 0.46 ± 0.02 per day throughout the 30‐day experiment. The produced algae had a high content of both total fatty acids (TFA) and free amino acids (FAA). Especially, the harvested algae contained a high proportion of poly‐unsaturated fatty acids that made up 80% of the TFA and of essential amino acids (35% of all FAA), implicating desirable components as feed for copepods. The current PBR was sufficient to feed a culture of the calanoid copepod Acartia tonsa at a density of 2,500 adult/L in ca. 500 L culture with a daily yield of approximately 17 × 10⁶ eggs. To be able to sustain the integrated copepods production, the suggested volume of the algae cultures should be ca. 20% of the copepod culture volume.     

Fluoride retention of Atlantic salmon (Salmo salar) fed krill meal

The present experiment was performed to study how fluoride from krill meal enriched muscle, whole fish and bone of adult Atlantic salmon (Salmo salar) reared in sea water. Atlantic salmon (mean weight 0.5 kg) were divided into four triplicate groups and fed a commercial fish meal based diets with 0, 100, 200 and 300 g krill kg^?1 feed, respectively, for 12 weeks. The fluoride concentrations in the experimental feeds were analysed to be 18, 132, 235 and 358 mg kg^?1, respectively. Growth, mortality and feed efficiency were recorded through the experiment. Fluoride concentration was measured in muscle, whole‐body, and bone initially and after 12 weeks of feeding. The fluoride concentrations in the samples were determined by alkali fusion and fluoride ion‐selective electrode. Growth, mortality and feed efficiency ratio were not affected by the dietary treatments. The results showed that fluoride concentration in muscle, whole body and bone were not affected by the dietary fluoride level. The fluoride concentration in the tissues showed great variation among replicates of the group given the same diet. Fillets of the fish varied between 0.3 and 1.4 mg fluoride kg^?1 wet weight, whereas the whole‐body concentration of fluoride varied between 3.3 and 6.1 mg kg^?1 wet weight and the fluoride bone concentration varied between 5.8 and 7.2 mg kg^?1 fresh weight. These results suggest that Atlantic salmon are highly tolerant of dietary fluoride given as krill meal with concentration of fluoride up to 350 mg kg^?1 diet, and that accumulation of fluoride from feeding diets containing krill meal does not lead to tissue accumulation in the fish, at least over a short period of time.     

Peracetic acid degradation and effects on nitrification in recirculating aquaculture systems

Peracetic acid (PAA) is a powerful disinfectant with a wide spectrum of antimicrobial activity. PAA and hydrogen peroxide (HP) degrade easily to oxygen and water and have potential to replace formalin in aquaculture applications to control fish pathogens, for example the ectoparasite, Ichthyophthirius multifiliis.We studied water phase PAA and HP decay in three aquaculture situations, i) batch experiments with two types of system waters, ii) PAA decay at different fish densities, and iii) degradation of PAA in submerged biofilters of recirculating aquaculture systems (RAS). Furthermore, effect of PAA on the nitrification activity and the composition of the nitrifying population were investigated.PAA and HP decay showed first order kinetics. High dosage PAA/HP in water with low COD inhibited HP removal, which was not observed in water having a higher COD content. PAA decay was significantly related to fish stocking density, with half life constants for PAA of 4.6 and 1.7 h at 12 and 63 kg m^− 3, respectively.PAA application to RAS biofilter showed rapid exponentially decay with half life constants of less than 1 h, three to five times faster than the water phase decay rates.Biofilter surface specific PAA removal rates ranged from 4.6 to 13.9 mg PAA m^− 2 h^− 1 and was positively correlated to the nominal dosage. Low PAA additions (1.0 mg L^− 1) caused only minor impaired nitrification, in contrast to PAA application of 2.0 and 3.0 mg L^− 1, where nitrite levels were significantly increased over a prolonged period, albeit without fish mortality. The dominant ammonium oxidizer was Nitrosomonas oligotropha and the dominant nitrite oxidizer was Nitrospira. Based on the present findings and other recent results from field and in vitro studies, application perspectives of PAA are discussed.     

Carotenoids in diets for salmonids: I. Pigmentation of rainbow trout with the individual optical isomers of astaxanthin in comparison with canthaxanthin

Visual and chemical determinations revealed that the individual optical isomers of astaxanthin were more efficacious than canthaxanthin in pigmenting the flesh of rainbow trout (Salmo gairdneri, Richardson). The visual assessment of the astaxanthin pigmentation by means of a colour scale correlated well with the chemical determination. The same utilization was found for all three astaxanthin isomers, (3S, 3′S)-, (3R, 3′S)-, (3R, 3′R)-astaxanthin and a 1 : 2 : 1 mixture of the three isomers.No epimerization took place at the chiral centres of C-3 and C-3′ in astaxanthin. Astaxanthin and canthaxanthin were not interconverted. No metabolites were detected in the flesh.     

光温条件对新热带干旱树种种子萌发和苗木建成的影响

测定了香红椿（Cedrela odorata）、神圣愈疮木（Guaiacum sanctum）和柠檬树（Calycophyllum candidissimum）种子萌发所需要的条件、并对光强对在尼加拉瓜开阔地、半开阔地和干旱森林林冠下所营造的香红椿和神圣愈疮木的苗存活率和生长的影响进行了研究。结果表明,在20-35℃常温条件下,柠檬树在有光照条件下种子萌发率显著高于黑暗条件的种子萌发率;香红椿和神圣愈疮木的种子在光照和黑暗条件下都有一定程度的萌发,最适萌发温度均为20-25℃。研究还表明,变温条件培养并没有提高3个树种的种子萌发率。在林冠层下和开阔地上神圣愈疮木苗木的存活率分别为70％和80％,两种条件下的周径相对生长速率分别为1．42mm／月和1．88mm／月。总的来说,在3个树种中,香红椿幼苗存活率较低,特别是在冠层内生长的幼苗。以上结果说明：柠檬树种子萌发需要光照;而香红椿和神圣愈疮木种子萌发对温度条件较为敏感。神圣愈疮木幼苗在裸地条件下存活率较高,可以作为退化土地造林备选树种。图2表2参43。     

Temporal distribution of porcine circovirus 2 genogroups recovered from postweaning multisystemic wasting syndrome affected and nonaffected farms in Ireland and Northern Ireland.

Porcine circovirus type 2 (PCV2) is now recognized as the essential infectious component of porcine postweaning multisystemic wasting syndrome (PMWS). PMWS was first recognized in high-status, specific pathogen-free pigs in Canada in 1991 and is now an economically important disease that affects the swine industry around the world. Recently, reports of genomic studies on PCV2 viruses indicated that 2 distinctive genogroups of PCV2 exist.4,10 This report involves the results of a study on the distribution of predominant PCV2 genogroups recovered from samples taken from PMWS-affected and PMWS-nonaffected farms on the island of Ireland over a 9-year period and the results of a study on PCV2 genogroup recovery from fecal samples taken from a farm in Northern Ireland from 2003 to 2005 that was first diagnosed as PMWS positive in August 2005. The results indicate that, although at least 2 distinct genogroups of PCV2 have been circulating on pig farms on the island of Ireland, there does not appear to be a direct relationship between infection with these different genogroups of PCV2 and the development of PMWS.