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Variations in sulphur and nitrogen foliar concentration of deciduous and conifers vegetation in Slovakia
1997
Maňkovská, Blanka
The foliage contents of Sₜₒₜₐₗ and Nₜₒₜₐₗ were determined in 405 Permanent monitoring plots in four National Parks and sixteen Landscape Protection Areas and were compared with 1483 Permanent monitoring plots on Slovakia. The foliage content of S ranged from 0.72 to 6.77 g kg⁻¹ in hardwoods and from 0.98 to 4.3 g kg⁻¹ in softwoods. A critical increase was determined in one National Park and in four Landscape Protection Areas. The foliage content of N ranged from 9.7 to 48.7 g kg⁻¹ in softwoods, and from 7.8 to 51.4 g kg⁻¹ in hardwoods. An insufficient level of N was determined in one Landscape Protection Area and a critical increase in four Landscape Protection Areas. The sulphur to nitrogen ratio ranged from 0.08 to 0.176 in softwoods, and from 0.078 to 0.253 in hardwoods. The foliage surface on hitherto explored four National Parks and sixteen Landscape Protection Areas in network 4×4 km was covered by all categories of rigid fallout particles. Fly-ash from coal combustion were observed each of National Parks and Landscape Protection Areas by scanning electron microscopy. Mycelia and spore, mineral matters, sand and soil particles were present on all National Parks and Landscape Protection Areas. Particles derived from aluminium production were observed at three Landscape Protection Areas. Particles derived from cement production and from lime works were observed at two National Parks and six Landscape Protection Areas. Particles derived from ferrous metals industry were observed at each of National Parks and Landscape Protection Areas and particles typical for other technologies were present in three of National Parks and twelve Landscape Protection Areas.
Show more [+] Less [-]Sulphur isotope composition of stream water, moss and humus from eight arctic catchments in the Kola Peninsula region (NW Russia, N Finland, NE Norway)
1997
de Caritat, P. | Krouse, H. R. | Hutcheon, I.
In summer 1994, stream water, moss and humus samples were collected for sulphur isotopic analysis from eight catchments located in the western Kola Peninsula region, where several industrial centres emit high loads of SO₂ and other elements to the atmosphere. Three potential sources of sulphur and their isotopic signatures were identified: (1) marine (δ ³⁴S+20 to +21‰ CDT), (2) anthropogenic emissions (<+10‰), and (3) geogenic (variableδ ³⁴S, mostly <+10‰). Averaged per catchment, the sulphur isotopic composition varies between +6.0 and +16.3‰ for stream water sulphate, +6.0 and +8.4‰ for moss sulphur, and +5.2 and +12.2‰ for humus sulphur. Theδ ³⁴S composition of stream water from the more remote catchments is quite variable, reflecting several natural (geogenic) sources, but it becomes restricted to the range +8 to +10‰ near the pollution sources. A plot ofδ ³⁴S vs. 1:SO₄ in stream water suggests that sulphate originating from the smelters has aδ ³⁴S value ≈+9.5‰, and is a dominant source. Sulphur isotope values for moss and humus are consistent with the deduced composition for the emitted sulphur, though for humus a component of geogenic sulphur incorporated via vegetation uptake may play a role. Further isotopic characterisation of atmospheric emissions, together with environmental samples, is needed to better understand sulphur sources and sinks in the area.
Show more [+] Less [-]Bleached kraft pulp mill discharged organic matter in recipient lake sediment : Environmental and molecular properties
1997
Saski, Eija K. | Mikkola, Raimo | Kukkonen, Jussi V. K. | Salkinoja-Salonen, Mirja S.
Environmental properties of organic matter contained halogen and sulfur were studied in sediments of bleached kraft pulp mill effluent (BKME) recipient lakes and 2 m³ outdoor enclosures (mesocosms). The BKME contributed to 1% (v/v) of the total water flow in the lake downstream of the pulp mill where the sediments contained 1.7 to 4 mg of tetrahydrofuran extractable organic halogen (EOX-Cl) and 0.6 to 0.8 mg of tetrahydrofuran extractable organic sulfur (EOS-S) g⁻¹ of organic matter. Upstream sediment contained 0.03 mg of EOXCl and 0.7 mg of EOS-S g⁻¹ of organic matter. EOX was a better indicator for the influence of BKME in the recipient sediment than EOS. The polarity of BKME contained EOX corresponded to log Kᵒʷ of < 1, and that of the downstream sediment contained EOX to > 4.5. HP-SEC analysis of the molecular weight distribution (MWD) of the EOX showed a peak between 300 to 600 g mol⁻¹ for the BKME and between 1000 to 2000 g mol⁻¹ for the downstream sediment. The MWD of the BKME contained EOS peaked at 300 to 1000 g mol⁻¹, and that of the downstream sediment contained EOS at 1000 to 5000 g mol⁻¹. These results indicate that BKME contained organic halogen and sulfur undergo major structural transformations when incorporated into sediment. The biota-to-sediment accumulation factor (BSAF) of EOX from sediments formed downstream of the mill and in the mesocosms to the lipids ofLumbriculus variegatus was 0.4 to 0.7. This is of a similar order of magnitude to the BSAF reported for 2,3,7,8-tetrachlorodibenzop-dioxin and 2,3,7,8-tetrachlorodibenzofuran.
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