Volume 9
Issue 2
Biology
JOURNAL OF
POLISH
AGRICULTURAL
UNIVERSITIES
Available Online: http://www.ejpau.media.pl/volume9/issue2/art-32.html
GRASSES (POACEAE) OF THE GRAVEL-PITS OF THE SIEDLECKA UPLAND (E POLAND)
Grzegorz Bzdon1, Janusz Krechowski2
1 Department of Botany,
Institute of Biology, University of Podlasie in Siedlce, Poland
2 Department of Botany, Institute of Biology,
University of Podlasie, Siedlce, Poland
Data on share of grasses in the flora of selected 65 gravel-pits of the Siedlecka Upland as well as their ecological characterisation are presented in the paper. The Poaceae is one of the most species-rich families found in these localities. Among 60 grass species the most frequent include Arrhenatherum elatius, Dactylis glomerata subsp. glomerata and Elymus repens. The domination of meadow species from classes Molinio-Arrhenatheretea and Trifolio fragiferae-Agrostietalia stoloniferae as well as synanthropic grasses from classes Stellarietea mediae and Agropyretea intermedio-repentis was observed. The dominant life form of grasses are hemicryptophytes. Native species prevail over anthropophytes in the studied objects. This paper also presents the results of analysis of the flora based on ecological indicator values [21].
Key words: Poaceae, gravel-pits, ecological indicator values, Siedlecka Upland.
INTRODUCTION
Excavations, formed as a result of mineral extraction, belong to the most poorly investigated ecological margins. More accurate floristic and phytosociological studies regarding the flora of excavations formed as a result of sand exploitation were carried out in the Silesian [7; 5; 9] and Western Pomeranian regions [17]. The data on the occurrence of Lycopodiela inundata in oligotrophic gravel-pits of the Małe Mazowsze region and Łęczyńsko-Włodawskie Lake District were reported by Cieszko & Kucharczyk [4]. The studies carried out by Czarnecka [3] in the gravel-pits of the Middle Vistula Valley mesoregion also focused on Lycopodiela inundata populations. The results of studies on the participation of grasses in selected 12 gravel-pits of the Siedlecka Upland were published by Bzdon [2]. The investigation on participation of the Poaceae flora in plant communities of gravel-pits of the Silesian Upland were carried out by Baba et al. [1].
Siedlecka Upland mesoregion is situated in the central-eastern Poland. It occupies the area of 2502 km2 and expands from Podlaski Przełom Bugu mesoregion in the north to Łuków Plain mesoregion in the south. Present morphology of the earth’s surface of the Poludniowopodlaska Lowland, including Siedlecka Upland is a result of evolution of land-forms since Middle Polish Glaciation and denudation processes characteristic for Baltic Glaciation [10].
In the geobotanical division of Poland [19] the area of studies is situated in the Łukowsko-Siedlecka Upland, which is a part of Podlasie Province. Pine forests, multispecies mixed forests and well preserved hygrophilous meadow, shrub and peat bog communities are characteristic for the investigation area.
Poaceae belongs to the most numerous families (the second family after Asteraceae as regards its richness) and constitutes 7.3% of the Polish flora [12]. In the Polish lowlands there are 298 species of grasses which belong to 86 genera [6]. A large number of plant species (including the Poaceae family) are good indicators of habitat conditions. The list of ecological indicator values for native and naturalized species was published by Zarzycki [20] and Zarzycki et al. [21].
The paper was prepared within the limits of grant number 2 PO4G 105 28.
The aim of this paper is to present the distribution of grass species in the gravel-pits of the Siedlecka Upland and their ecological characterisation.
MATERIAL AND METHODS
Field investigations were carried out between 2001 and 2002 in the area of the Siedlecka Upland. The composition of flora of selected 65 gravel-pits was investigated on the basis of floristic-ecological lists prepared in optimal vegetation period. The list of species was completed in other phenological seasons, which was followed by analysis of floristic-ecological data.
For the nomenclature of the taxa Mirek et al. [16] was followed, whereas for the syntaxonomic units Matuszkiewicz [14].
Historical-geographic groups of species were distinguished according to Kornas & Medwecka-Kornas [11] division, modified by Mirek [15] and Jackowiak [8]. The status of species was accepted after Korniak [13]. For life forms as well as ecological indicator values Zarzycki et al. [21] was followed.
RESULTS AND DISCUSSION
Among 598 plant species present in 65 gravel-pits of the Siedlecka Upland, 60 species of Poaceae were recorded (Table 1), which constitutes 22.6% of the total number of grasses found in the Polish lowlands [18]. The share of grasses in the flora of the Siedlecka Upland gravel-pits reaches 10.0% and is slightly lower, compared with data obtained by Baba et al. [1] from gravel-pits of the Silesian Upland (12.7%). Młynkowiak & Kutyna [17] reported the similar share of Poaceae in the flora of the studied gravel-pits.
The most frequent grass species in the investigated objects include Arrhenatherum elatius (95.4%), Dactylis glomerata subsp. glomerata (92.3%), Elymus repens (80.0%), Festuca rubra (69.2%) and Phleum pratese (60.0%) (Table 1). All these species belong to apophytes. However Baba et al. [1] reported other grass species which play the most significant role in the composition of plant communities of the Silesian Upland. They include Calamagrostis epigejos, Corynephorus canescens, Digitaria ischaemum, Agrostis capillaris, Phragmites australis, Molinia caerulea, Danthonia decumbens, Koeleria glauca, Poa compressa and Holcus lanatus.
Table 1. Grass species of the sandpits of the Siedlecka Upland |
Grass species |
I |
II |
III |
IV |
L |
T |
K |
W |
Tr |
R |
H |
Agrostis capillaris |
34 |
Ap |
2 |
h |
4 |
4-3 |
3 |
2-3 |
3-4 |
3-4 |
2 |
Agrostis stolonifera |
11 |
Ap |
6 |
h |
4 |
4-3 |
3 |
4 |
3-4 |
3-5 |
1-2 |
Alopecurus geniculatus |
16 |
Ap |
6 |
h |
4 |
4-3 |
3 |
5 |
4 |
3-4 |
2 |
Alopecurus pratensis |
18 |
Ap |
6 |
h |
4 |
4-3 |
3 |
4 |
4 |
4 |
2 |
Anthoxanthum odoratum |
19 |
Ap |
6 |
h |
4 |
4-3 |
3 |
3 |
3 |
3 |
2 |
*Apera spica-venti |
20 |
Ar |
7 |
t |
4 |
4-3 |
3 |
3 |
3 |
2-3 |
2 |
Arrhenatherum elatius |
62 |
Ap |
6 |
h |
4 |
4 |
3 |
3 |
4 |
4-5 |
2 |
*Avena fatua |
1 |
Ar |
7 |
t |
5 |
5-4 |
3 |
2-3 |
3 |
4-5 |
2 |
Avena sativa |
19 |
Df |
8 |
t |
. |
. |
. |
. |
. |
. |
. |
*Avenella flexuosa |
11 |
Sn |
2 |
h |
3-4 |
4-1 |
2 |
3 |
2 |
1-3 |
1-2 |
Avenula pubescens |
2 |
Ap |
6 |
h |
4 |
4 |
3 |
3-4 |
3 |
4-5 |
2 |
Briza media |
1 |
Ap |
6 |
h |
4 |
4-2 |
3 |
3 |
3 |
2-4 |
2 |
Bromus hordeaceus |
20 |
Ap |
6 |
t |
4 |
4 |
3 |
3 |
4 |
4 |
2 |
Bromus inermis |
13 |
Ap |
7 |
h |
5 |
4-5 |
3 |
2-3 |
3 |
4-5 |
1-2 |
*Bromus tectorum |
10 |
Ar |
7 |
t |
5 |
4-5 |
3 |
2 |
2 |
3 |
1 |
Calamagrostis arundinacea |
2 |
Ap |
2 |
h |
3 |
4-2 |
3 |
3 |
3 |
2-3 |
2 |
Calamagrostis epigejos |
32 |
Ap |
2 |
g |
4 |
4-3 |
3 |
3 |
3 |
3 |
1 |
Corynephorus canescens |
35 |
Ap |
4 |
h |
4 |
4 |
3 |
2 |
2 |
3-5 |
1 |
Cynosurus cristatus |
3 |
Ap |
6 |
h |
4 |
4-2 |
3 |
3 |
4 |
4 |
2 |
Dactylis glomerata |
60 |
Ap |
6 |
h |
4 |
4-2 |
3 |
3 |
4-5 |
4-5 |
2 |
Danthonia decumbens |
7 |
Sn |
2 |
h |
4-3 |
4-3 |
3 |
3-4 |
2 |
2-3 |
2 |
Deschampsia caespitosa |
19 |
Ap |
6 |
h |
3-5 |
4-1 |
3 |
4 |
3-4 |
3-4 |
2-3 |
*Digitaria ischaemum |
2 |
Ar |
7 |
t |
5 |
4 |
3 |
2 |
1-2 |
3 |
1-2 |
*Digitaria sanguinalis |
3 |
Ar |
7 |
t |
4 |
4 |
3 |
3 |
2 |
2 |
2 |
*Echinochloa crus-galli |
32 |
Ar |
7 |
t |
5 |
4 |
3 |
3-4 |
4-5 |
3-4 |
2 |
Elymus caninus |
23 |
Ap |
1 |
h |
3 |
4-3 |
3 |
4 |
4-5 |
4 |
2 |
Elymus hispidus |
4 |
Ap |
3 |
g |
5 |
5 |
3 |
2 |
3 |
5 |
2 |
Elymus repens |
52 |
Ap |
7 |
g |
4 |
3-4 |
3 |
3 |
3-4 |
3-5 |
1-2 |
*Eragrostis minor |
3 |
Kn |
7 |
t |
5 |
4 |
3 |
2 |
2-3 |
4 |
2 |
Festuca gigantea |
4 |
Ap |
1 |
h |
2-3 |
4-3 |
3 |
4 |
4 |
4 |
2 |
Festuca ovina |
24 |
Ap |
4 |
h |
4 |
4-3 |
3 |
2 |
2 |
3-5 |
2 |
Festuca pratensis |
13 |
Ap |
6 |
h |
4 |
4-3 |
3 |
3 |
4 |
4 |
2 |
Festuca rubra |
45 |
Ap |
6 |
h |
4 |
4-3 |
3 |
2-4 |
3 |
4 |
3 |
Glyceria fluitans |
6 |
Ap |
5 |
hy |
4 |
4-3 |
3 |
5-6 |
4 |
4 |
3 |
Glyceria maxima |
2 |
Ap |
5 |
hy |
4 |
4-3 |
3 |
6 |
4-5 |
4 |
3 |
Holcus lanatus |
6 |
Ap |
6 |
h |
4 |
4-3 |
3 |
4 |
3-4 |
4 |
2 |
Holcus mollis |
5 |
Ap |
2 |
g(h) |
3-4 |
4-3 |
3 |
3-4 |
3 |
3 |
2 |
*Hordeum vulgare |
9 |
Df |
8 |
t |
. |
. |
. |
. |
. |
. |
. |
Koeleria glauca |
3 |
Ap |
4 |
h |
5 |
4 |
3 |
2 |
1-2 |
4-5 |
1 |
*Lolium multiflorum |
5 |
Kn |
7 |
h(t) |
5 |
4-3 |
3 |
3 |
4 |
4 |
2 |
Lolium perenne |
28 |
Ap |
6 |
h |
4 |
4-3 |
3 |
3 |
4 |
4 |
2 |
Melica nutans |
1 |
Sn |
1 |
g |
2-3 |
4-3 |
3 |
3 |
3 |
4 |
2 |
Molinia caerulea |
3 |
Sn |
6 |
h |
4 |
4 |
3 |
4-5 |
2-3 |
1-5 |
2-3 |
*Panicum miliaceum |
2 |
Df |
8 |
t |
. |
. |
. |
. |
. |
. |
. |
Phalaris arundinacea |
8 |
Ap |
5 |
g(h) |
4 |
4-3 |
3 |
5 |
4 |
4-5 |
2 |
*Phalaris arundinacea |
1 |
Df |
8 |
h |
. |
. |
. |
. |
. |
. |
. |
Phleum phleoides |
2 |
Ap |
3 |
h |
5 |
5 |
3 |
2 |
2-3 |
5 |
2-3 |
Phleum pratense |
39 |
Ap |
6 |
h |
4 |
4-3 |
3 |
2-3 |
3-4 |
4-5 |
2 |
Phragmites australis |
13 |
Ap |
5 |
g(hy) |
4-5 |
4-3 |
3 |
5-6 |
3-4 |
4 |
2-3 |
Poa angustifolia |
2 |
Ap |
7 |
h |
4 |
5-4 |
3 |
2-3 |
3 |
4-5 |
2-3 |
Poa annua |
10 |
Ap |
6 |
t(h) |
5-3 |
4-1 |
3 |
3 |
4 |
4 |
2 |
Poa compressa |
5 |
Ap |
7 |
h |
5 |
5-4 |
2 |
2 |
3 |
5 |
2 |
Poa palustris |
10 |
Ap |
6 |
h |
4 |
4-3 |
3 |
4-5 |
4 |
4-5 |
2 |
Poa pratensis |
32 |
Ap |
6 |
h |
4 |
4-3 |
3 |
3 |
4 |
4 |
2 |
Poa trivialis |
12 |
Ap |
6 |
h |
4 |
4-3 |
3 |
4 |
4 |
4 |
2 |
*Secale cereale |
23 |
Df |
8 |
t |
. |
. |
. |
. |
. |
. |
. |
*Setaria pumila |
18 |
Ar |
7 |
t |
5 |
4 |
3 |
2-3 |
3 |
3-4 |
2 |
*Setaria viridis |
29 |
Ar |
7 |
t |
5 |
4 |
3 |
3 |
3 |
3-4 |
2 |
*Triticum aestivum |
6 |
Df |
8 |
t |
. |
. |
. |
. |
. |
. |
. |
*Zea mays |
3 |
Df |
8 |
t |
. |
. |
. |
. |
. |
. |
. |
The distinct domination of the synanthropic species (93.3%) in the flora of grasses in the investigated objects was observed (Fig. 2). Among them there were only 4 species (6.7%) considered to be spontaneophytes in Poland [13]. In the group of synanthropic grasses apophytes (39 species – 69.6%) prevail over anthropophytes (17 species – 30.4%), which differentiates the studied flora from the geographic-historical composition of synanthropic grasses in Poland (27.6% of apophytes and 72.4% of anthropophytes, according to Korniak [13]. The difference mainly results from the low percentage of diaphytes observed in the gravel-pits in the area of Siedlce. The whole group of diaphytes consists of ergasiophygophytes. Among antropophytes 8 species of archaeophytes (14.3% of synanthropic flora of grasses), 7 species of diaphytes (12.5%) and 2 species of kenophytes (3.6%) were noted. The participation of particular groups of anthropophytes in the synanthropic flora of Polish grasses is different (archaeophytes – 11.1%, diaphytes – 50.8%, kenophytes – 10.5%, according to Korniak [13].
Meadow species from classes Molinio-Arrhenatheretea and Trifolio fragiferae-Agrostietalia stoloniferae (21 taxa – 35.0 % of Poaceae flora) and synanthropic grass species from classes Stellarietea mediae and Agropyretea intermedio-repentis (14 taxa – 23.3 %) prevail in the studied objects (Fig. 3), which is similar to the data obtained from the Silesian Upland [1].
The dominant life form of grasses (56.7%) are hemicryptophytes (Fig. 4). The significant percentage of terophytes (28.3%) and geophytes (11.7%) was also observed. Much higher participation of terophytes in the grass flora of gravel-pits in the Siedlce region compared with the data obtained from the Silesian Upland (16.0%) [1] may be a result of close proximity of the studies objects to agrophytocoenoses (a source of annual plants).
Fig. 1. Localization of the gravel-pits in the Siedlecka Upland |
![]() |
Fig. 2. Geographic-historical spectrum of grass species in the flora of selected sandpits of the Siedlecka Upland |
![]() |
Fig. 3. Phytosociological spectrum of grass species in the flora of selected sandpits of the Siedlecka Upland |
![]() |
Fig. 4. Life forms of grass species in the sandpits of the Siedlecka Upland |
![]() |
The data on the percentage of grass species of various ecological indicator values [21] are presented in Table 2. The major results are as follows:
The largest group of Poaceae prefer moderate (50.0%) and full (21.7%) light.
45.0% of grass species prefer moderately cool and moderately warm climatic conditions (group 3/4). Less numerous group (20.0%) comprises stenotype species adjusted to moderately warm climatic conditions (group 4).
In the studied gravel-pits species of grasses with no continental preferences dominate (group 3 – 51 species). Only 2 species, Deschampsia flexuosa and Poa compressa, belong to the group of subatlantic species present mainly in western Poland.
Poaceae found in the gravel-pits of the Siedlecka Upland represents the wide spectrum of soil moisture values, from “dry” to “water”, with the visible domination of species which prefer fresh soils (group 3 – 31.7%). The results presented by Baba et al. [1] from the Silesian gravel-pits (37.8%) are similar. Excavations formed as a result of sand exploitation in the area of the Siedlecka Upland are smaller and shallower. They usually do not reach the level of ground waters. Consequently, the increase in the participation of grasses of dry habitats (group 2) – 15.0% and decrease in the percentage of grasses which prefer wet (group 3 – 3.3%) and water conditions (group 4 – 1.7%) in comparison with the data from the Silesian Upland [1] are noted.
The analysis of the composition of grass flora indicates the domination of species of mesotrophic (group 3 – 26.7%) and eutrophic soils (group 4 – 25.0%). The studied objects are distinguished by minor participation of grasses of fertile habitats, which dominate in the gravel-pits of the Silesian Upland (33.3%) [1].
The largest participation of grass species adjusted to neutral soils (group 4 – 30.0%), as well as neutral and alkaline soils (group 4/5 – 16.6%), was noted in the Siedlecka Upland. The gravel-pits of the Silesian Upland are characterised by the presence of grass species which prefer more acidic habitats.
Grasses adjusted to mineral-humic soil (group 2) prevail in the investigated area (60.0%). Their participation in flora is higher than in the studied gravel-pits of the Silesian region (42.0%).
Table 2. Share of grasses characterised by various ecological indicator values in the sandpits of the Siedlecka Upland |
Value of index |
Percentage of species |
||||||
L |
T |
K |
W |
Tr |
R |
H |
|
1 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
6.7 |
1–2 |
0.0 |
0.0 |
0.0 |
0.0 |
3.3 |
0.0 |
8.3 |
2 |
0.0 |
0.0 |
3.3 |
15.0 |
10.0 |
1.7 |
60.0 |
2–3 |
3.3 |
0.0 |
0.0 |
10.0 |
5.0 |
5.0 |
8.3 |
3 |
3.3 |
0.0 |
85.0 |
31.7 |
26.7 |
8.3 |
5.0 |
3–4 |
5.0 |
45.0 |
0.0 |
6.6 |
11.7 |
10.0 |
– |
4 |
50.0 |
20.0 |
0.0 |
11.7 |
25.0 |
30.0 |
– |
4–5 |
1.7 |
8.3 |
0.0 |
3.3 |
6.6 |
16.6 |
– |
5 |
21.7 |
3.3 |
0.0 |
3.3 |
0.0 |
5.0 |
– |
5-6 |
– |
– |
– |
3.3 |
– |
– |
– |
6 |
– |
– |
– |
1.7 |
– |
– |
– |
Eurybionts |
3.3 |
11.7 |
0.0 |
1.7 |
0.0 |
11.7 |
0.0 |
Undefined |
11.7 |
11.7 |
11.7 |
11.7 |
11.7 |
11.7 |
11.7 |
Total |
100.0 |
100.0 |
100.0 |
100.0 |
100.0 |
100.0 |
100.0 |
CONCLUSIONS
The floristic composition of gravel-pits is varied and relates to the numerous factors: surrounding communities, origin of soil and its sort, excavation depth, level of ground water and human activity.
Gravel-pits represent the large diversity of habitats – from dry, acidic, oligotrophic to wet, alkaline and fertile.
The domination of the synanthropic grass species and the high percentage of terophytes due to anthropogenic character of the objects are observed.
REFERENCES
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Accepted for print: 09.06.2006
Grzegorz Bzdon
Department of Botany,
Institute of Biology, University of Podlasie in Siedlce, Poland
B. Prusa 12, 08-110 Siedlce, Poland
email: botanika@ap.siedlce.pl
Janusz Krechowski
Department of Botany, Institute of Biology,
University of Podlasie, Siedlce, Poland
B. Prusa 12, 08-110 Siedlce, Poland
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