Using movements and diet analyses to assess effects of introduced muskellunge (Esox masquinongy) on Atlantic salmon (Salmo salar) in the Saint John River, New Brunswick

The muskellunge was introduced in the Saint John River system from stockings in a headwater lake in the 1970s. They have migrated down the system as far as the river’s first dam, Mactaquac Hydroelectric Facility, at Fredericton and appear to have established several reproducing populations along the river. This exotic invader represents a potential threat to the severely depleted Atlantic salmon stocks in the river. We radio-tracked muskellunge over a 2-year period in the middle reaches. Home ranges extended to ∼100 km in both riverine and lacustrine areas, including 78% of individuals trans-located upstream of the dam making their way back through the dam successfully. Downstream of the dam, home ranges were <25 km. No spawning areas were detected. An isotope analyses of diet indicated that the large sub-adults and adults had established the greatest proportion of their biomass in a more ¹⁵N depleted environment typical of areas farther upstream. Isotope mixing models could not accurately determine the proportion of Atlantic salmon smolts that may have been consumed by muskellunge, but anadromous salmon had ≤7% probabilities of being in the diet. A bioenergetics model suggested ≤5% of the annual food intake by muskellunge occurs during the smolt out-migration period. For the Saint John River, the impacts of growing numbers of muskellunge are multi-faceted creating a complex management challenge. Muskellunge appear to minimally increase predation risk for Atlantic salmon smolts while their increasing numbers are creating a growing recreational fishery and potential threat to the native fish community and ecosystem.     

Electron ionization mass spectra of reduced and permethylated urinary oligosaccharides from patients with mannosidosis

The electron ionization mass spectra of reduced and permethylated isomeric mixtures of the major urinary tri- to deca-oligosaccharides of patients with mannosidosis are reported. Many of the oligosaccharide isomers can be differentiated in the mixtures on the basis of their distinct fragmentation patterns.     

5-Chloropicolinic acid is produced by specific degradation of 4-chlorobenzoic acid by Sphingomonas paucimobilis BPSI-3

We have previously shown that the bacterium Sphingomonas paucimobilis BPSI-3, isolated from PCB-contaminated soil, can degrade halogenated biphenyls, naphthalenes, catechols and benzoic acids. However, before such an organism can be used in bioremediation, it is important to characterise the degradation products and determine the degradation pathways to ensure that compounds more toxic or mobile than the original contaminants are not produced. In the degradation of 4-chlorobiphenyl, S. paucimobilis BPSI-3 produces a novel chlorinated picolinic acid. In this paper, we show that 4-chlorobenzoate is an intermediate in this degradation and, through ¹⁵N-labelling, that 5-chloropicolinate is the only nitrogenous metabolite isolated under the extraction conditions used. The position of the chlorine indicates that degradation of 4-chlorocatechol occurs exclusively via a 2,3-extradiol cleavage. These data allow us to postulate a more definitive catabolic pathway for the biodegradation of 4-chlorobiphenyl to 5-chloro-2-hydroxymuconic acid semialdehyde via 4-chlorobenzoate in S. paucimobilis BPSI-3. Received 19 April 1999/ Accepted in revised form 23 July 1999     

Isolation of chromatin fragments rich in non-histone protein after endonuclease digestion of rat liver nuclei

Detergent-washed rat liver nuclei, prepared in the presence of a protease inhibitor, were incubated for up to 60 min at 37 °C. The action of endonucleases produced chromatin fragments which could be removed from the nuclei by extraction with 8 M urea 50 mM phosphate, pH 7.6, 15% of the total nuclear DNA being extracted. No DNA could be detected in this extract after incubation of nuclei at 4 °C. The chromatin fragments were sedimented by centrifugation at 90000 g or by chromatography on Sepharose 4B. The DNA fragment sizes were similar to those found in nucleosome particles but the protein/DNA ratio was approx. 5.3:1. The nuclei were prelabelled with [³H]tryptophan and 60% of the label present in the 8 M urea extract was found to sediment with the chromatin fraction. SDS polyacrylamide gel electrophoresis of the latter showed the presence, in addition to histones, of at least 25 polypeptide species of tightly bound non-histone proteins with molecular weights in excess of 30000.     

Traits explain sorting of C4 grasses along a global precipitation gradient

1. Species distributions are closely associated with moisture availability, but the underlying mechanisms remain unresolved. Drought relations are especially important for plants such as C₄ grasses that dominate seasonally dry ecosystems. Here, we test the hypothesis that C₄ grass species sampled across global precipitation gradients show variation in survival under drought that can be explained by their traits.
2. Our experiment subjected 18 C₄ grass species to a lethal drought under controlled environmental conditions. The number of days until death was measured, along with root traits, senescence, and aspects of hydraulic function.
3. We identified two strategies: Drought‐avoiding species that stayed green as the water potential declined and drought‐tolerating species that senesced more quickly but could extend survival via drought‐tolerant meristems.
4. Plants that stay‐green for longer occupied drier habitats and had the longest survival under drought, facilitated by narrow root diameter and isohydric stomatal behavior. Plants that senesced quickly had thicker roots, an anisohydric strategy, and occupied wetter habitats.
5. Global distributions of C₄ grasses can be predicted by variation in rates of senescence, meristem survival, root traits, and stomatal strategy, showing the value of these traits for understanding plant distributions in relation to climate.

     

Modified Methodology to Improve Flow Cytometric Dna Histograms from Paraffin-Embedded Material

Flow Cytometric (FCM) DNA content analysis of paraffin-embedded tissues has become a widely accepted procedure in assessing the biologic course in some tumors from archival material. Difficulty in interpreting histograms is frequently due to high levels of debris, and wide coefficients of variation (CV). These may lead to underestimating near-diploid abnormality. Although the clinical significance of low-degree aneuploidy has yet to be established, the procedure reported here improved our endeavor to detect DNA Indices (DI) of at least 1.1%. Experience has shown that careful technique can result in overall improvement of DNA histograms by lowering levels of debris and % CV, dramatically so in some cases. Archival histograms can be generated that rival in quality fresh tissue results. Archival material is currently employed for diagnostic and research purposes.