brechignac_f_desmet_g_eds_equidosimetry_ecological_standardi
.pdfTOTAL |
|
– |
– |
121,269 |
100,00 |
|
|
PEAT TOGETHER WITH MYCELIUM OF FUNGI |
|
||
0-5 cm |
20000 |
4270 |
85,400 |
51,34 |
|
5-10 cm |
50000 |
527 |
26,350 |
15,84 |
|
10-15 cm |
60000 |
500 |
30,000 |
18,04 |
|
15-20 cm |
60000 |
218 |
13,080 |
7,86 |
|
20-25 cm |
70000 |
100 |
7,000 |
4,21 |
|
25-30 cm |
75000 |
60 |
4,500 |
2,71 |
|
including mycelium (in all peat |
70 |
800000 |
56,000 |
33,67 |
|
layers) |
|
|
|
|
|
TOTAL |
335000 |
– |
166,330 |
100,00 |
|
(peat with fungi mycelium) |
|
|
|
|
263
Table 2. Distribution of 137Cs activity in ecosystem of Cladonio-Pinetum, density of ground deposition of 137Cs – 46,4 kBq·m-2 (1,25 Ci·km-2 )
|
|
|
Mass, kg·ha-1 |
137Cs specific |
137Cs activity, |
Part of 137Cs total activity, % |
Ecosystem component |
|
activity, Bq·kg-1 |
MBq·ha-1 |
|
||
Tree canopy |
|
|
23402 |
– |
9,791 |
50,56 |
Wood |
|
|
8547 |
126 |
1,077 |
5,56 |
Bark |
|
|
1155 |
700 |
0,809 |
4,18 |
Branches |
|
|
4774 |
350 |
1,671 |
8,63 |
Annual shoots |
|
150 |
1210 |
0,182 |
0,94 |
|
Needles |
|
|
2079 |
385 |
0,800 |
4,13 |
Roots thick |
|
|
6110 |
730 |
4,460 |
23,03 |
Roots thin |
|
|
587 |
1350 |
0,792 |
4,09 |
Juvenile tree layer |
|
5,9 |
800 |
0,004 |
0,026 |
|
Undergrowth layer |
|
22 |
290 |
0,006 |
0,031 |
|
Grass–dwarf-shrub layer* |
*288 |
*418 |
0,120 |
0,62 |
||
Lichen layer |
|
|
1995,8 |
– |
8,197 |
43,586 |
Sublayer of epigeous lichens |
1995 |
– |
8,192 |
43,56 |
||
Cladina arbuscula ssp. mitis |
1400 |
4180 |
5,852 |
30,22 |
||
Cladonia uncialis |
|
360 |
4300 |
1,548 |
7,99 |
|
Cladonia gracilis |
|
180 |
4400 |
0,792 |
4,09 |
|
Cladonia subulata |
|
55 |
4440 |
0,244 |
1,26 |
|
Sublayer of epiphytic lichens |
0,8 |
5800 |
0,005 |
0,026 |
||
(Hypogymnia physodes) |
|
|
|
|
||
Moss layer |
|
|
70,5 |
6800 |
0,479 |
2,48 |
(Polytrichum piliferum) |
|
|
|
|
||
Layer |
of |
Macromycetes |
4,76 |
– |
0,524 |
2,708 |
(fruitbodies) |
|
|
|
|
|
|
Cortinarius sanguineus |
0,84 |
160000 |
0,134 |
0.69 |
264
Lactarius rufus |
0,96 |
100000 |
0,096 |
0,50 |
|
Cantharellus cibarius |
0,14 |
11120 |
0,002 |
0,008 |
|
Siullus variegatus |
0,87 |
79200 |
0,07 |
0,36 |
|
Siullus bovinus |
0,66 |
58700 |
0,04 |
0,20 |
|
Boletus badius |
0,41 |
75700 |
0,03 |
0,16 |
|
Paxillus involutus |
0,88 |
174000 |
0,153 |
0,79 |
|
TOTAL |
– |
– |
19,367 |
100,00 |
|
|
SOIL TOGETHER WITH MYCELIUM OF FUNGI |
|
|
||
Forest litter |
16400 |
– |
76,310 |
14,44 |
|
Forest litter semi-decomposed |
3200 |
293 |
0,938 |
0,18 |
|
Forest litter decomposed |
13200 |
5710 |
75,372 |
14,26 |
|
Mineral soil layers |
4935600 |
– |
452,274 |
85,57 |
|
ÍŲ 0-2 cm |
228000 |
1250 |
285,000 |
53,92 |
|
ÍŲ 2-4 cm |
290800 |
330 |
95,964 |
18,16 |
|
ÍŲ 4-6 cm |
288400 |
110 |
31,724 |
6,00 |
|
ÍŲ 6-8 cm |
338000 |
35 |
11,830 |
2,24 |
|
ÍŲ 8-10 cm |
289600 |
20 |
5,792 |
1,10 |
|
ÍŲ 10-12 cm |
317200 |
14 |
4,444 |
0,84 |
|
г 12-14 cm |
332400 |
6 |
1,994 |
0,38 |
|
г 14-16 cm |
363200 |
5 |
1,816 |
0,34 |
|
г 16-18 cm |
343200 |
6 |
2,059 |
0,39 |
|
г 18-20 cm |
335200 |
6 |
2,011 |
0,38 |
|
г 20-22 cm |
315200 |
9 |
2,837 |
0,54 |
|
г 22-24 cm |
366000 |
5 |
1,830 |
0,35 |
|
г 24-26 cm |
392000 |
6 |
2,352 |
0,44 |
|
г 26-28 cm |
362800 |
3 |
1,088 |
0,21 |
|
г 28-30 cm |
373600 |
4 |
1,494 |
0,28 |
265 |
|
|
|
|
|
266
including mycelium |
1200 |
– |
132,035 |
|
(in all soil layers) |
|
|
|
|
TOTAL |
4012800 |
– |
528,543 |
100,00 |
(soil with fungi mycelium) |
|
|
|
|
*Note: average-weighted data on whole layer.
Table 3. Distribution of 137Cs activity in ecosystem of Molinio-Pinetum, density of ground deposition of 137Cs – 580,0 kBq·m-2 (15,68 Ci·km-2)
Ecosystem component |
Mass, kg·ha-1 |
137Cs specific |
137Cs activity, |
Part of 137Cs total activity, % |
|
|
activity, Bq·kg-1 |
MBq·ha-1 |
|
TREE CANOPY (total) |
252552 |
– |
1073,8 |
49,93 |
² layer (Pinus sylvestris) |
248151 |
– |
1057,5 |
49,17 |
Wood |
185539 |
2690 |
499,1 |
23,21 |
Bark |
9416 |
13860 |
130,5 |
6,07 |
Branches alive |
15213 |
10090 |
153,5 |
7,14 |
Branches dried up³ |
8075 |
3678 |
29,7 |
1,38 |
Needles |
7879 |
21550 |
169,8 |
7,90 |
Roots |
22029 |
3400 |
74,9 |
3,48 |
²² layer (Betula pubescens) |
4401 |
– |
16,3 |
0,76 |
Wood |
1875 |
1760 |
3,3 |
0,15 |
Bark |
230 |
5645 |
1,3 |
0,06 |
Branches |
1020 |
6470 |
6,6 |
0,31 |
Leaves |
235 |
11060 |
2,6 |
0,12 |
Roots |
1041 |
2400 |
2,5 |
0,12 |
Moss layer |
20802 |
48120 |
1001,0 |
46,55 |
(Pleurozium schreberi) |
|
|
|
|
Layer of epiphytic lichens |
32,8 |
57920 |
1,9 |
0,09 |
(Hypogymnia physodes) |
|
|
|
|
Grass–dwarf-shrub layer |
1518 |
– |
66,7 |
3,10 |
Vaccinium myrtillus |
1270 |
40860 |
51,9 |
2,41 |
aboveground phytomass |
|
|
|
|
underground phytomass |
217 |
44300 |
9,6 |
0,45 |
Dryopteris carthusiana |
20 |
162670 |
3,2 |
0,15 |
aboveground phytomass |
|
|
|
|
underground phytomass |
11 |
180000 |
2,0 |
0,09 |
Layer of Macromycetes |
2,67 |
– |
7,1 |
0,33 |
(fruitbodies) |
|
|
|
|
Suillus variegatus |
0,4 |
2258400 |
0,9 |
0,04 |
Paxillus involutus |
1,1 |
3500000 |
3,9 |
0,18 |
Russula paludosa |
0,3 |
1240000 |
0,4 |
0,02 |
Xerocomus badius |
0,35 |
2800000 |
1,0 |
0,05 |
Lactarius rufus |
0,3 |
2900000 |
0,9 |
0,04 |
Cantharellus cibarius |
0,22 |
160000 |
0,04 |
0,00 |
TOTAL |
– |
– |
2150,5 |
100,00 |
|
SOIL TOGETHER WITH MYCELIUM OF FUNGI |
|
||
Forest litter |
56911 |
– |
2282,1 |
49,68 |
267
268
Ferest litter noncomposed |
2544 |
14036 |
35,7 |
0,78 |
Forest litter semi-decomposed |
21745 |
50500 |
1098,1 |
23,90 |
Forest litter decomposed |
32622 |
35200 |
1148,3 |
25,00 |
Mineral soil layers |
3438022 |
– |
2311,8 |
50,32 |
ÍÅ 0-2 cm |
133138 |
6660 |
886,7 |
19,30 |
ÍÅ 2-4 cm |
172018 |
3270 |
562,5 |
12,24 |
ÍÅ 4-6 cm |
211026 |
1433 |
302,4 |
6,58 |
ÍÅ 6-8 cm |
243158 |
760 |
184,8 |
4,02 |
ÍÅ 8-10 cm |
220323 |
310 |
68,3 |
1,49 |
ÍÅ 10-12 cm |
253241 |
216 |
54,7 |
1,19 |
Å 12-14 cm |
272143 |
140 |
38,1 |
0,83 |
Å 14-16 cm |
276190 |
126 |
34,8 |
0,76 |
Å 16-18 cm |
241667 |
120 |
29,0 |
0,63 |
Å 18-20 cm |
234545 |
110 |
25,8 |
0,56 |
²1 20-22 cm |
248182 |
110 |
27,3 |
0,59 |
²1 22-24 cm |
242500 |
120 |
29,1 |
0,63 |
²1 24-26 cm |
240000 |
100 |
24,0 |
0,52 |
²2Ð 26-28 cm |
237391 |
115 |
27,3 |
0,59 |
²2Ð 28-30 cm |
212500 |
80 |
17,0 |
0,37 |
including mycelium |
1200 |
2258000* |
2710,08 |
58,99 |
(in all soil layers) |
|
|
|
|
TOTAL |
3494933 |
– |
4593,9 |
100,00 |
(soil with fungi mycelium) |
|
|
|
|
269
The analysis of distribution of the total stock of 137Cs on the components of ecosystem as a whole (with allowance of radionuclide activity in soil and mycelium of mushrooms) also demonstrates the specific geochemical regularities. In particular, the part of 137Cs activity retained by the main forest layer, the tree canopy, in forest ecosystems of Ukrainian Polessye varies in a wide range , from 1,8 % up to 16 % of a total stock of radionuclide in forest ecosystem as a whole. Due to the growth of phytomass of this vegetation layer increase of part of the radionuclide activity retained
by the tree canopy is observed. In ecosystem Molinio-Pinetum the tree canopy contained: for the age to 10 years, 3 % of the total stock of 137Cs of ecosystem, for 30
years 7 %, for 55 years - 15 % [19]. In the Pinus sylvestris tree canopy in automorphic landscapes the observed increase is mainly due to the biomass of trunk wood and bark (40-60 % of a 137Cs sum activity of tree canopy). In hydromorphic landscapes of ombrotrophic bogs in cenosis Ledo-Sphagnetum magellanici the tree canopy of pine retains only 2,03 % of a total stock of 137Cs of ecosystem as a whole, and due to trunk
less than 30 %. In 60-year old forests of cenosis Serratulo-Pinetum pine the tree canopy contained 2-3 % of a total stock of 137Cs of ecosystem and in the oak canopies
of similar age, 6-9 % is due to the greater intensity of radionuclide accumulation [2, 12, 16, 19].
It is necessary to underline that in deciduous forests the intensity of biological migration of 137Cs also increases due to the intensive annual cycling of significant radionuclide activity with litter-fall and its relatively fast decomposition [12].
The layer of undergrowth (living form – shrubs) of the average crown closeness (0,3-0,5) independently from species composition, in forests of Polessye retained only 0,01-0,05 % of a total stock of 137Cs of forest ecosystem; the close indexes are also characteristic for the layer of juvenile trees (up to 0,01 % of the total 137Cs activity of ecosystem) because their insignificant phytomass per unit area.
Grass–dwarf-shrub layer is characterized by various phytomass in forest cenosis in Ukrainian Polessye – from very rarefied (with the sum projective cover 5- 15%) in cenosis Cladonio-Pinetum and Peucedano-Pinetum up to 60 % of projective cover in forested bogs of cenosis Ledo-Sphagnetum magellanici and 95 % in cenosis Molinio-Pinetum. Accordingly a part of the sum of 137Cs activity retained by this layer of vegetation in forests of automorphic landscapes varies from 0,01-0,02 % in cenoses
Cladonio-Pinetum and Peucedano-Pinetum up to 1,0 % in cenosis Molinio-Pinetum sharply increasing up to 2,5-4,0 % in the forests of hydromorphic landscapes as a result of more intensive 137Cs accumulation by all plant species of the layer as well as because essentially smaller relative part of tree canopy in retaining of 137Cs.
Lichen layer consists of two sublayers – epiphytic (on trunks of trees) which part independently from species composition does not exceed 0,01-0,03 % of a sum activity of 137Cs of forest ecosystem, however this sublayer of lichens plays the main role in the interception of 137Cs stemflow. The sublayer of epigeous lichens plays an important role in the formation of phytomass in cenosis Cladonio-Pinetum, where lichens are dominants of undergrowth vegetation of forests, the part of this sublayer reaches 1,5-3 % of a total stock of 137Cs contained in the ecosystem as a whole.
The role of moss layer, the majority of phytocenosis of boreal forests, in retaining of 137Cs by biota is extremely important. As it was shown earlier the part of the sum 137Cs activity circulating in forest ecosystem and retained by layer of
270
green mosses in forests of automorphic landscapes in cenosis Peucedano Pinetum varied from 1% in 10-year's pine forests up to 15% in 50-year's cenosis [19]. In forests of the analyzed automorphic landscapes the part of green moss layer changed from 0,1% in cenosis Cladonio-Pinetum up to 15 % in cenosis Molinio-Pinetum. In hydromorphic landscapes in cenosis Ledo-Sphagnetum magellanici the role of moss layer (from sphagnum mosses) increased up to 35-40% in relation to the total stock of 137Cs content in the forest ecosystem.
Also it should be noted that the role of moss layer is determining, as a biogeochemical barrier, the path of vertical 137Cs migration in all types of forest landscapes – from forest litter to mineral soil layers in automorphic landscapes and from peat litter to peat in hydromorphic ones.
Special attention was paid to studying the role of the mushroom complex in retaining of 137Cs activity in forest ecosystems. During mushroom fruitbodies sampling period the productivity of mushrooms on our experimental plots was low – 6-8 times smaller in comparison with average long-term data on the region [12; 13], therefore in spite of significant 137Cs specific activity in mushrooms fruitbodies, their contribution to retaining of the total 137Cs activity of ecosystem was not so large – 0,1-0,2%. However the part of sum 137Cs activity in mushrooms mycelium deducted from macroblock of soil with forest litter changed from 20 % in forested bog ecosystem of cenosis LedoSphagnetum magellanici up to 40 % in cenosis Molinio-Pinetum.
Thus our calculation has allowed to draw the conclusion that soil (in automorphic landscapes – together with forest litter) contained from 28% of a total stock of radionuclide of ecosystem in cenosis Molinio-Pinetum up to 38 % in cenosis
Ledo-Sphagnetum magellanici and 72% in cenosis Cladonio-Pinetum. The results obtained visibly demonstrate that in conditions when the biological circulation of radionuclide is slow because of unfavorable ecological conditions, as for example in cenosis Cladonio-Pinetum a large part of total stock of radionuclide remains in the soil and is not taken up by vegetation.
It is necessary to underline that the results obtained in this research are in good agreement with data published earlier [5; 19] in which the relative part of soil with forest litter in retaining of 137Cs varied in the limits 60-65 %, including mycelium of mushrooms in this value.
Our research of 137Cs distribution in three forest ecosystems allowed us to draw a conclusion that key components in distribution of this radionuclide in analyzed biogeocenoses were:
in Cladonio-Pinetum – pine tree canopy and epigeous lichen layer;
in Ledo-Sphagnetum magellanici – Sphagnum layer;
in Molinio-Pinetum – pine tree canopy and green moss layer.
So according to the above proposed methodology the heavy metal content was studied in salient key components of ecosystems (table 4).
Analysis of above mentioned data shows that not only 137Cs but also heavy metal content were higher in peak key component. So the distribution of total stock of investigated pollutants should be approximately analogue too. But in other cases essential differences of distribution both in concentrations of pollutants and in its total stock can be observed. Nevertheless, in our mind these regularities of distribution of pollutants are specific and approximately constant in each ecosystem.
Table 4. Average content of 137Cs and heavy metals in some components of different forest ecosystems.
Component |
137Cs cont., |
|
Heavy metal content, mg·kg-1 d.w. |
||
|
Bq·kg-1 d.w. |
Cu |
Zn |
Pb |
Co |
Cladonio-Pinetum |
|
|
|
|
|
*Pine tree canopy |
385±45 |
1,17±0,22 |
9,85±1,12 |
0,51±0,07 |
0,03±0,004 |
(needles) |
|
|
|
|
|
*Epigeous lichen layer |
4180±50 |
3,12±0,38 |
13,54±1,50 |
1,48±0,17 |
0,26±0,03 |
Soil (mineral 0-2 cm) |
1250±140 |
1,54±0,20 |
3,00±0,44 |
1,09±0,21 |
0,028±0,00 |
Ledo-Sphagnetum magellanici |
|
|
|
|
|
*Sphagnum layer (alive |
16100±1900 |
3,40±0,42 |
21,3±2,75 |
4,67±0,55 |
0,52±0,06 |
part) |
|
|
|
|
|
*Sphagnum layer (dead |
11700±2000 |
2,45±0,29 |
28,00±3,42 |
13,65±1,54 |
0,83±0,11 |
part) |
|
|
|
|
|
Cranberry berries |
8600±900 |
17,75±2,01 |
12,30±1,23 |
0,02±0,003 |
0,01±0,00 |
Pine tree canopy (needles)2720±300 |
2,08±0,22 |
12,04±1,24 |
0,30±0,05 |
0,03±0,00 |
|
Molinio-Pinetum |
|
|
|
|
|
*Pine tree canopy |
21550±2300 |
4,52±0,47 |
8,04±0,95 |
0,17±0,02 |
0,003±0,00 |
(needles) |
|
|
|
|
|
*Green moss layer |
48120±5000 |
30,14±3,21 |
19,24±2,22 |
0,94±0,10 |
0,17±0,02 |
Bilberry (shoots) |
40860±4000 |
8,50±1,00 |
13,92±1,44 |
0,02±0,003 |
0,013±0,00 |
Bilberry (berries) |
41000±4200 |
27,08±3,12 |
28,84±3,24 |
0,002±0,00 |
0,012±0,00 |
Soil (mineral 0-2 cm) |
6660±700 |
2,08±0,31 |
4,00±0,43 |
1,09±0,20 |
0,03±0,003 |
Note: key components were marked *.
271
272
4. References
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13.A. Shcheglov et al. To the problem of role of higher macromycetes in biogeochemical migration of 137Cs in forest ecosystems. in: Proceedings Chernobyl-94, vol. 1, 1996. pp. 460-472 (in Russian).
14.A. Yunatov. Foundation of ecological profiles and experimental plots. in: Field geobotany, vol. 3, Moscow-Leningrad, Nauka, 1964. pp. 9-35 (in Russian).
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16.S. Mamikhin, A. Shcheglov. Dynamics of Cs-137 in the forests of the 30-km zone around the Chernobyl nuclear power station. in: Proc. Seminar on the dynamic behaviour of radionuclides in forests, Stockholm, 1992. p. 10.
17.T. Nylén. Uptake, turnover and transport of radiocaesium in boreal forest ecosystem. Dissertation. Uppsala, 1996.
18.R. Olsen, E. Joner and L. Bakken. Soil fungi and the fate of radiocaesium in a soil ecosystem – a discussion of possible mechanisms involved in the radiocaesium accumulation in fungi and the role of fungi as a Cs-sink in the soil. in: Transfer of radionuclides in natural and semi-natural environment. Eds. G.Desmet et al., London-New York, Elsevier Applied Science, 1990. pp. 657-663.
19.A. Orlov, V. Turko, S. Irklienko, V. Krasnov, A. Kalish. The distribution of the total 137Cs activity in biogeocenoses of pine forest of Ukrainian Polessye. in: Proc. of the VI Symposium, vol. 1, Szarvas, 1999. pp. 79-84.