Abstract
The distributional patterns and ecology of the ponto-mediterranean species Poecilimon schmidtii were only insufficiently known until now, despite assumed to be one of the northernmost distributed species of the genus. Based on the review of all available published and own field data, we improved the distribution map of the species and recorded it for the first time from Poland. The distribution survey was carried at 1,208 sites in Slovakia, 39 sites in SE Poland and 26 sites in W Ukraine between 1994 and 2015. P. schmidtii was found at 59 sites and the habitat requirements were analysed. The results show a clear preference of the species for broadleaved forest ecotones with hazel and Rubus spp. shrubs being the main host plants. The species was present in grid cells with a lower mean altitude, a higher annual mean temperature and a lower annual precipitation compared to those available within the northern species’ range. Its altitudinal distribution was between 105 and 950 m a.s.l. Altogether, 70 Orthoptera and one mantid species were recorded and assemblages of Orthoptera and Mantodea were described for 49 sites with P. schmidtii in Slovakia and Poland. On average 18.9 ± 7.5 (SD) species were found per site, ranging from 7 to 37. Using detrended correspondence analysis it was not possible to distinguish between the orthopteran assemblages with and without (n = 94) P.schmidtii. In the assemblages, P. schmidtii was more often present with mountainous species.
Acknowledgements
We would like to appreciate the assistance with fieldwork provided by P. Kaňuch, P. Tuček, M. Mikuš, A. Sliacka from IFE SAS Zvolen and M. Balla and A. Macková from State Nature Conservancy of the Slovak Republic (Protected Landscape Area Latorica and Východné Karpaty, respectively). This study was supported by grants of Slovak scientific grant agency VEGA No. 2/0061/15 and 2/0097/16.
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Appendix 1. Records of Poecilimon schmidtii in Slovakia and Poland (PL). For published data: site No. in Appendix 2, (site name, geographic coordinates); for unpublished data in the form: DFS grid cells, site name (altitude, geographic coordinates) (site No. in Appendix 2.), abundance, M – males, F – females, n – nymph, date (day.month.year).
Published data:
6900, 6901, 6997 (Čejchan 1963; Chládek & Gavlas 2004); 7000 (Čejchan 1958, 1963; Chládek & Gavlas 2004); 7295, 7394, 7395 (Nagy et al. 1998), 7596, 7698, 7699 (Krištín et al. 2011). Sites No. 14 (Nová Sedlica, 49.05583 N, 22.50806 E), 17 (Hankovce, 49.02447 N, 21.94027 E), 29 (Senderov, 48.816 N, 21.99499 E), 33 (Ruskov Bogota 1, 48.69065 N, 21.51916 E), 39 (Slanec castle, 48.63797 N, 21.46797), 41 (Ruskov Bogota 2, 48.69019 N 21.51875 E), 47 (Ladmovce, 48.42638 N, 21.78403 E), 49 (Tisa, Malé Trakany, 48.40009 N, 22.14614 E) in Appendix 2.
Unpublished data:
6695 – Korejovce (350 m a.s.l., 49.38319 N, 21.64354 E) (site 1 in Appendix 2), 1 F, 05.08.2010; 6696 – Driečna (440 m a.s.l., 49.3251 N, 21.79855 E) (site 2), 1 M, 23.07.2015; 6696 – Nižný Komárnik (420 m a.s.l., 49.37613 N, 21.72373 E), 1 F, 12.08.2014; 6697 – Čertižné (415 m a.s.l., 49.343 N, 21.83876 E), 1 M, 31.07.2015; 6793 – Hervartov (480 m a.s.l., 49.24769 N, 21.19887 E) (site 3), 1 F, 31.07.2013; 6798 (PL) – Laborec sadle on Polish side between Medzilaborce (SK) and Radoszyce (660 m a.s.l., 49.2904 N, 22.01862 E) (site 4), 1 Mn, 22.07.2015; 6800 – Zálom saddle, Ruské (590 m a.s.l., 49.09797 N, 22.37658 E) (site 5), 1M, 1 F, 22.07.2015; 6800 – Ruské – East (580 m a.s.l., 49.11314 N, 22.36766 E) (site 6), 1 Fn, 22.07.2015; 6800 –Ruské (500 m a.s.l., 49.1155 N, 22.34483 E) (site 7), 1Mn, 22.07.2015; 6800 –Ruské – North (690 m a.s.l., 49.13241 N, 22.33281 E) (site 8), 1Mn, 22.07.2015; 6800 (PL) – Ruské sadle – East, Polish side N of border point No. 32/7 (910 m a.s.l., 49.14613 N, 22.34255 E) (site 9), 1 Fn, 22.07.2015; 6800 (PL) – Okrąglik – West, Polish side, N of border point No. I/30 (950 m a.s.l., 49.14498 N, 22.35702 E) (site10), 1M, 1 F, 22.07.2015; 6900 – Topoľa – Ruské (510 m a.s.l., 49.08487 N, 22.38285 E) (site 11), 2 Fn, 22.07.2015; 6900 – Zálom saddle – South, Ruské (604 m a.s.l., 49.09769 N, 22.3783 E) (site 12), 1 Mn, 22.07.2015; 6900 – Ruský Potok (490 m a.s.l., 49.03241 N, 22.41455 E) (site 13), 1 M, 22.07.2015; 6901 – Pod Stinskou, Zboj (580 m a.s.l., 49.00382 N, 22.48286 E) (site 15), 1 M, 07.07. 2015; 6995 – Domaša Dobrá – West (345 m a.s.l., 49.01437 N, 21.66472 E) (site 16), 1 M, 16.07.2015; 6996 – Domaša Dobrá – East (310 m a.s.l., 49.01645 N, 21,66841 E), 1 F, 1M, 16.07.2015; 7000 – Ruská Volová – North (305 m a.s.l., 48.95857 N, 22,3747 E) (site 18), 1 F, 3 M, 21.07.2015; 7000 – Ruská Volová – East (380 m a.s.l., 48.96071 N, 22.38714 E) (site 19), 1 F, 21.07.2015; 7000 – Brezovec saddle (380 m a.s.l., 48.94825 N, 22.39873 E) (site 20),1 F, 21.07.2015; 7095 – Kvakovce (305 m a.s.l., 48.99712 N, 21.65145 E) (site 21), 1 F, 04.08.2010; 7096 – Malá Domaša (200 m a.s.l., 48.9965 N, 21.69737 E) (site 22), 1 F, 04.08.2010; 7096 – Brekov – West (240 m a.s.l., 48.90129 N, 21.82902 E) (site 23), 1 Fn, 01.06.2014; 7097 – Brekov – East (230 m a.s.l., 48.90244 N, 21.83507 E) (site 24), 1 Fn, 01.06.2014; 7097 – Humenský Sokol (213 m a.s.l., 48.89274 N, 21.9362 E) (site 25), 2 M, 1 F, 03.07.2015; 7099 – Morské oko (660 m a.s.l., 48.91127 N, 22.20952 E) (site 26), 2 M, 2 F, 31.07.2015; 7197 – Humenský Sokol – South, Chlmec (250 m a.s.l., 48.877046 N, 21.947664 E) (site 27), 1 Fn, 01.06.2014; 7197 – Viniansky hrad castle – quarry (155 m a.s.l., 48.81794 N, 21.94242 E) (site 28), 1 M, 03.08.2010; 7197 – Trnava pri Laborci (230 m a.s.l., 48.82676 N, 21.92649 E) (site 30), 3 M, 4 F, 03. 08. 2010; 7198 – Senderov – Kaluža (187 m a.s.l., 48.81608 N, 22.00409 E) (site 31), 2 F, 03.08.2010; 7199 – Podhoroď castle (380 m a.s.l., 48.8219 N, 22.30375 E) (site 32), 3 F, 1 M, 1 Fn, 21.07.2015; 7295 – Bačkov, Dargov (277 m a.s.l., 48.75183 N, 21.60616 E) (site 34), 2 F, 1 M, 03.08.2010; 7295 – Bačkovská dolina valley (360 m a.s.l., 48.74733 N, 21.55921 E) (site 35), 6 F, 2 M, 03.08.2010; 7299 – Kolibabovce (184 m a.s.l., 48.71698 N, 22.26003 E) (site 36), 2 F, 04.08.2010; 7299 – Priekopa (349 m a.s.l., 48.75665 N, 22.28022 E) (site 37), 1 F, 03.09.2015; 7394 – Rákoš – East (415 m a.s.l., 48.64029 N, 21.43771 E) (site 38), 10 n, 26.05.2013; 7394 – Strahuľka, Slanec (415 m a.s.l., 48.62822 N, 21.4765 E) (site 40), 2 F, 2 M, 16.07.2015; 7399 – Krčava (145 m a.s.l., 48.67901 N, 22.25626 E) (site 42), 1 F, 04.08.2010; 7493 – Perín (240 m a.s.l., 48,52688 N, 21,19079 E) (site 43), 6 n, 26.05.2013; 7493 – Gyňov (178 m a.s.l., 48.58827 N, 21.32187 E) (site 44), 8 n 26.05.2013; 7494 – Skároš, Marovka creek valley (360 m a.s.l., 48.57913 N, 21.40448 E) (site 45), 6 n, 26.05.2013; 7596 – Cejkov (205 m a.s.l., 48.4515 N, 21.76325 E) (site 46), 2 F, 2 M, 16.07.2015; 7598 – Tisa river, Malé Trakany (105 m a.s.l., 48.39502 N, 22.14562 E) (site 48), 1 F, 26.07.2013; Willemse F. & Willemse L. 2008. An annotated checklist of the Orthoptera-Saltatoria from Greece including an updated bibliography. Articulata Beiheft 13: 1–91.
Orthoptera assemblages with species relative abundance and frequency (F%) in 49 sites of P. schmidtii occurrence in SE Poland and E Slovakia (relative abundance: 1 = < 3 ind., 2 = 3–10 ind., 3 = 11–100 ind., 4 = > 100 ind.; for sites’s numbers – see Appendix 1).
| Species/Site No. | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 | 16 | 17 | 18 | 19 | 20 | 21 | 22 | 23 | 24 | 25 | 26 | 27 | 28 | 29 | 30 | 31 | 32 | 33 | 34 | 35 | 36 | 37 | 38 | 39 | 40 | 41 | 42 | 43 | 44 | 45 | 46 | 47 | 48 | 49 | F% |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Barbitistes constrictus Brunner von Wattenwyl, 1878 | 1 | 1 | 1 | 1 | 2 | 1 | 12.2 | |||||||||||||||||||||||||||||||||||||||||||
| Conocephalus dorsalis (Latreille, 1804) | 1 | 2 | 2 | 6.1 | ||||||||||||||||||||||||||||||||||||||||||||||
| Conocephalus fuscus (F., 1793) | 2 | 3 | 3 | 2 | 3 | 2 | 2 | 2 | 3 | 2 | 1 | 1 | 3 | 3 | 28.6 | |||||||||||||||||||||||||||||||||||
| Decticus verrucivorus (L., 1958) | 3 | 3 | 2 | 1 | 1 | 2 | 2 | 3 | 3 | 2 | 1 | 1 | 2 | 2 | 4 | 2 | 2 | 2 | 1 | 2 | 1 | 2 | 1 | 1 | 2 | 3 | 3 | 2 | 1 | 1 | 61.2 | |||||||||||||||||||
| Ephippiger ephippiger (Serville, 1831) | 2 | 3 | 4.1 | |||||||||||||||||||||||||||||||||||||||||||||||
| Isophya kraussii Brunner von Wattenwyl, 1878 | 1 | 1 | 1 | 2 | 1 | 1 | 3 | 2 | 1 | 1 | 2 | 1 | 24.5 | |||||||||||||||||||||||||||||||||||||
| Isophya modesta (Frivaldsky, 1867) | 2 | 2.0 | ||||||||||||||||||||||||||||||||||||||||||||||||
| Isophya pienensis Mařan, 1954 | 2 | 2.0 | ||||||||||||||||||||||||||||||||||||||||||||||||
| Isophya posthumoidalis Bazyluk, 1971 | 1 | 2 | 1 | 2 | 3 | 2 | 1 | 2 | 16.3 | |||||||||||||||||||||||||||||||||||||||||
| Isophya stysi Čejchan, 1957 | 1 | 1 | 2 | 2 | 1 | 2 | 1 | 2 | 3 | 1 | 3 | 1 | 2 | 2 | 1 | 2 | 1 | 2 | 2 | 38.8 | ||||||||||||||||||||||||||||||
| Leptophyes albovittata (Kollar, 1833) | 2 | 4 | 4 | 3 | 3 | 3 | 3 | 3 | 2 | 4 | 3 | 3 | 3 | 3 | 3 | 3 | 3 | 4 | 2 | 4 | 3 | 3 | 3 | 4 | 3 | 2 | 3 | 2 | 3 | 3 | 2 | 3 | 2 | 4 | 3 | 4 | 3 | 3 | 3 | 2 | 2 | 83.7 | ||||||||
| Leptophyes discoidalis (Frivaldsky, 1867) | 2 | 1 | 1 | 2 | 2 | 2 | 12.2 | |||||||||||||||||||||||||||||||||||||||||||
| Meconema thalassinum (Degeer, 1773) | 1 | 1 | 1 | 1 | 2 | 1 | 1 | 1 | 1 | 1 | 1 | 2 | 1 | 2 | 1 | 1 | 1 | 1 | 2 | 1 | 1 | 42.9 | ||||||||||||||||||||||||||||
| Metrioptera bicolor (Philippi, 1830) | 1 | 2 | 1 | 1 | 4 | 2 | 4 | 1 | 2 | 2 | 1 | 2 | 3 | 2 | 2 | 3 | 2 | 34.7 | ||||||||||||||||||||||||||||||||
| Metrioptera brachyptera (L., 1758) | 3 | 4 | 4.1 | |||||||||||||||||||||||||||||||||||||||||||||||
| Metrioptera roeselii (Hagenbach, 1822) | 3 | 3 | 4 | 2 | 2 | 3 | 3 | 3 | 2 | 3 | 3 | 2 | 2 | 2 | 3 | 4 | 3 | 3 | 3 | 3 | 3 | 2 | 2 | 3 | 1 | 3 | 2 | 3 | 2 | 4 | 1 | 2 | 3 | 3 | 2 | 2 | 3 | 4 | 3 | 2 | 2 | 1 | 85.7 | |||||||
| Phaneroptera falcata (Poda, 1761) | 3 | 2 | 4 | 3 | 3 | 3 | 1 | 1 | 3 | 3 | 4 | 1 | 3 | 3 | 2 | 2 | 2 | 2 | 2 | 2 | 3 | 3 | 3 | 3 | 1 | 4 | 3 | 4 | 3 | 3 | 1 | 3 | 2 | 3 | 2 | 3 | 3 | 75.5 | ||||||||||||
| Phaneroptera nana Fieber, 1853 | 1 | 1 | 2 | 1 | 1 | 2 | 12.2 | |||||||||||||||||||||||||||||||||||||||||||
| Pholidoptera aptera (F., 1793) | 2 | 3 | 2 | 2 | 2 | 3 | 2 | 3 | 2 | 18.4 | ||||||||||||||||||||||||||||||||||||||||
| Pholidoptera griseoaptera (Degeer, 1773) | 1 | 2 | 4 | 1 | 3 | 3 | 3 | 3 | 2 | 3 | 3 | 3 | 2 | 2 | 4 | 3 | 3 | 3 | 3 | 3 | 3 | 3 | 2 | 3 | 3 | 3 | 3 | 3 | 3 | 3 | 3 | 3 | 3 | 3 | 3 | 3 | 3 | 4 | 1 | 3 | 3 | 2 | 3 | 4 | 3 | 3 | 1 | 3 | 3 | 100 |
| Pholidoptera transsylvanica (Fischer, 1853) | 2 | 3 | 2 | 2 | 2 | 2 | 2 | 14.3 | ||||||||||||||||||||||||||||||||||||||||||
| Platycleis grisea (F., 1781) | 4 | 4 | 4 | 4 | 1 | 1 | 3 | 2 | 1 | 3 | 3 | 4 | 24.5 | |||||||||||||||||||||||||||||||||||||
| Poecilimon fussii Brunner von Wattenwyl, 1878 | 3 | 2.0 | ||||||||||||||||||||||||||||||||||||||||||||||||
| Poecilimon schmidtii (Fieber, 1853) | 1 | 1 | 1 | 1 | 2 | 1 | 1 | 1 | 1 | 1 | 2 | 2 | 1 | 2 | 1 | 2 | 1 | 2 | 1 | 1 | 1 | 2 | 1 | 1 | 1 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 1 | 2 | 2 | 2 | 1 | 3 | 2 | 2 | 1 | 1 | 3 | 4 | 2 | 1 | 2 | 2 | 2 | 100 |
| Ruspolia nitidula (Scopoli, 1786) | 1 | 1 | 1 | 1 | 2 | 1 | 1 | 2 | 2 | 3 | 2 | 2 | 2 | 26.5 | ||||||||||||||||||||||||||||||||||||
| Tettigonia cantans (Fussli, 1775) | 3 | 3 | 3 | 2 | 3 | 3 | 3 | 2 | 3 | 3 | 2 | 2 | 2 | 3 | 2 | 3 | 3 | 1 | 2 | 3 | 3 | 1 | 2 | 2 | 49.0 | |||||||||||||||||||||||||
| Tettigonia caudata (Charpentier, 1842) | 2 | 2.0 | ||||||||||||||||||||||||||||||||||||||||||||||||
| Tettigonia viridissima L., 1758 | 2 | 1 | 1 | 1 | 3 | 2 | 1 | 1 | 3 | 4 | 4 | 4 | 2 | 1 | 2 | 2 | 2 | 2 | 3 | 2 | 2 | 2 | 3 | 1 | 1 | 1 | 53.1 | |||||||||||||||||||||||
| Gryllotalpa gryllotalpa (L., 1758) | 1 | 2 | 2 | 6.1 | ||||||||||||||||||||||||||||||||||||||||||||||
| Myrmecophilus acervorum (Panzer, 1799) | 2 | 2.0 | ||||||||||||||||||||||||||||||||||||||||||||||||
| Eumodicogryllus bordigalensis (Latreille, 1804) | 1 | 1 | 1 | 6.1 | ||||||||||||||||||||||||||||||||||||||||||||||
| Gryllus campestris L., 1758 | 2 | 2 | 2 | 2 | 2 | 1 | 3 | 3 | 3 | 2 | 1 | 2 | 3 | 3 | 2 | 2 | 32.7 | |||||||||||||||||||||||||||||||||
| Melanogryllus desertus (Pallas, 1771) | 1 | 2.0 | ||||||||||||||||||||||||||||||||||||||||||||||||
| Modicogryllus frontalis (Fieber, 1844) | 1 | 2.0 | ||||||||||||||||||||||||||||||||||||||||||||||||
| Oecanthus pellucens (Scopoli, 1763) | 3 | 2 | 2 | 2 | 1 | 2 | 3 | 4 | 4 | 4 | 4 | 4 | 4 | 4 | 3 | 4 | 3 | 3 | 36.7 | |||||||||||||||||||||||||||||||
| Xya pfaendleri (Harz, 1970) | 3 | 3 | 4.1 | |||||||||||||||||||||||||||||||||||||||||||||||
| Xya variegata Latreille, 1809 | 4 | 4 | 4.1 | |||||||||||||||||||||||||||||||||||||||||||||||
| Tetrix bipunctata (L., 1758) | 1 | 1 | 1 | 1 | 1 | 1 | 12.2 | |||||||||||||||||||||||||||||||||||||||||||
| Tetrix subulata (L., 1758) | 2 | 1 | 2 | 2 | 2 | 1 | 1 | 1 | 16.3 | |||||||||||||||||||||||||||||||||||||||||
| Tetrix tenuicornis Sahlberg, 1893 | 1 | 2 | 1 | 1 | 1 | 3 | 2 | 1 | 1 | 1 | 1 | 22.4 | ||||||||||||||||||||||||||||||||||||||
| Tetrix undulata (Sowerby, 1806) | 1 | 1 | 4.1 | |||||||||||||||||||||||||||||||||||||||||||||||
| Calliptamus italicus (L., 1758) | 3 | 2 | 3 | 3 | 4 | 2 | 2 | 2 | 2 | 2 | 3 | 2 | 2 | 4.1 | ||||||||||||||||||||||||||||||||||||
| Aiolopus thalassinus (F., 1781) | 1 | 1 | 26.5 | |||||||||||||||||||||||||||||||||||||||||||||||
| Odontopodisma rubripes Ramme, 1931 | 2 | 1 | 3 | 3 | 2.0 | |||||||||||||||||||||||||||||||||||||||||||||
| Mecostethus parapleurus (Hagenbach, 1822) | 2 | 1 | 3 | 2 | 3 | 2 | 2 | 28.6 | ||||||||||||||||||||||||||||||||||||||||||
| Oedipoda caerulescens (L., 1758) | 2 | 3 | 3 | 4 | 3 | 3 | 2 | 69.4 | ||||||||||||||||||||||||||||||||||||||||||
| Psophus stridulus (L., 1758) | 2 | 1 | 63.3 | |||||||||||||||||||||||||||||||||||||||||||||||
| Stethophyma grossum (L., 1758) | 3 | 4.1 | ||||||||||||||||||||||||||||||||||||||||||||||||
| Chorthippus albomarginatus (Degeer, 1773) | 3 | 42.9 | ||||||||||||||||||||||||||||||||||||||||||||||||
| Chorthippus apricarius (L., 1758) | 3 | 3 | 2 | 2 | 4 | 2 | 2 | 1 | 1 | 1 | 1 | 3 | 2 | 2 | 4.1 | |||||||||||||||||||||||||||||||||||
| Chorthippus biguttulus (L., 1758) | 2 | 2 | 2 | 2 | 1 | 3 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 3 | 2 | 2 | 2 | 3 | 2 | 2 | 3 | 2 | 2 | 3 | 2 | 3 | 2 | 3 | 3 | 2 | 2 | 2 | 20.4 | |||||||||||||||
| Chorthippus brunneus (Thunberg, 1815) | 1 | 3 | 1 | 2 | 1 | 2 | 1 | 1 | 1 | 2 | 3 | 2 | 2 | 2 | 3 | 3 | 3 | 3 | 2 | 2 | 3 | 2 | 2 | 3 | 3 | 3 | 2 | 3 | 3 | 2 | 2 | 10.2 | ||||||||||||||||||
| Chorthippus dichrous (Eversmann, 1859) | 3 | 3 | 93.9 | |||||||||||||||||||||||||||||||||||||||||||||||
| Chorthippus dorsatus (Zetterstedt, 1821) | 2 | 1 | 2 | 2 | 3 | 3 | 2 | 2 | 1 | 1 | 2 | 3 | 2 | 1 | 3 | 4 | 2 | 3 | 3 | 2 | 2 | 6.1 | ||||||||||||||||||||||||||||
| Chorthippus mollis (Charpentier, 1825) | 3 | 1 | 89.8 | |||||||||||||||||||||||||||||||||||||||||||||||
| Chorthippus montanus (Charpentier, 1825) | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 3 | 3 | 6.1 | |||||||||||||||||||||||||||||||||||||||
| Chorthippus oschei Helversen, 1985 | 1 | 2 | 2 | 3 | 3 | 2.0 | ||||||||||||||||||||||||||||||||||||||||||||
| Chorthippus parallelus (Zetterstedt, 1821) | 3 | 3 | 3 | 3 | 3 | 3 | 3 | 3 | 3 | 4 | 3 | 3 | 4 | 4 | 4 | 4 | 3 | 4 | 3 | 3 | 3 | 4 | 4 | 4 | 4 | 4 | 3 | 2 | 2 | 2 | 4 | 4 | 3 | 3 | 3 | 4 | 2 | 4 | 4 | 3 | 2 | 4 | 4 | 2 | 3 | 3 | 89.8 | |||
| Chorthippus vagans (Eversmann, 1848) | 1 | 1 | 1 | 36.7 | ||||||||||||||||||||||||||||||||||||||||||||||
| Chrysochraon dispar (Germar, 1834) | 2 | 1 | 4 | 1 | 3 | 2 | 2 | 1 | 3 | 3 | 1 | 2 | 3 | 3 | 3 | 2 | 2 | 2 | 1 | 1 | 2 | 1 | 2 | 2 | 2 | 2 | 1 | 1 | 2 | 2 | 3 | 3 | 2 | 2 | 2 | 3 | 3 | 2 | 1 | 1 | 2 | 1 | 2 | 2 | 14.3 | |||||
| Euchorthippus declivus (Brisout de Barneville, 1849) | 1 | 3 | 3 | 8.2 | ||||||||||||||||||||||||||||||||||||||||||||||
| Euchorthippus pulvinatus (F. de Waldheim, 1846) | 1 | 14.3 | ||||||||||||||||||||||||||||||||||||||||||||||||
| Euthystira brachyptera (Ocskay, 1826) | 2 | 2 | 4 | 3 | 3 | 4 | 3 | 3 | 3 | 4 | 3 | 3 | 3 | 1 | 4 | 4 | 4 | 1 | 4 | 3 | 2 | 2 | 3 | 3 | 4 | 4 | 4 | 1 | 1 | 1 | 3 | 3 | 4 | 4 | 1 | 2 | 2 | 4 | 4 | 2 | 4 | 3 | 3 | 2 | 22.4 | |||||
| Gomphocerippus rufus (L., 1758) | 3 | 4 | 2 | 1 | 3 | 2 | 1 | 1 | 2 | 2 | 2 | 2 | 1 | 2 | 4 | 1 | 2 | 3 | 16.3 | |||||||||||||||||||||||||||||||
| Omocestus haemorrhoidalis (Charpentier, 1825) | 3 | 1 | 2 | 2 | 3 | 3 | 2 | 2 | 1 | 3 | 3 | 24.5 | ||||||||||||||||||||||||||||||||||||||
| Omocestus rufipes (Zetterstedt, 1821) | 1 | 2 | 2 | 3 | 2 | 1 | 2 | 2 | 4.1 | |||||||||||||||||||||||||||||||||||||||||
| Omocestus viridulus (L., 1758) | 2 | 2 | 3 | 3 | 3 | 2 | 4 | 2 | 2 | 2 | 2 | 1 | 6.1 | |||||||||||||||||||||||||||||||||||||
| Stenobothrus crassipes (Charpentier, 1825) | 4 | 1 | 1 | 46.9 | ||||||||||||||||||||||||||||||||||||||||||||||
| Stenobothrus lineatus (Panzer, 1796) | 3 | 1 | 2 | 2 | 2 | 2 | 1 | 2 | 3 | 3 | 2 | 2 | 2 | 2 | 2 | 2 | 3 | 1 | 3 | 1 | 2 | 3 | 3 | 8.2 | ||||||||||||||||||||||||||
| Stenobothrus nigromaculatus (Herrich-Schaffer, 1840) | 2 | 2 | 2 | 2 | 2.0 | |||||||||||||||||||||||||||||||||||||||||||||
| Mantis religiosa (L., 1758) | 2 | 1 | 2 | 1 | 1 | 2 | 1 | 2 | 3 | 4 | 2 | 2 | 3 | 2 | 1 | 1 | 2 | 1 | ||||||||||||||||||||||||||||||||
| No. of species | 14 | 26 | 16 | 10 | 11 | 17 | 19 | 19 | 12 | 17 | 15 | 11 | 24 | 14 | 19 | 19 | 17 | 7 | 18 | 19 | 17 | 13 | 24 | 26 | 30 | 16 | 31 | 23 | 20 | 20 | 23 | 25 | 16 | 21 | 13 | 30 | 31 | 5 | 8 | 13 | 16 | 25 | 11 | 11 | 10 | 22 | 37 | 33 | 33 |
©2016 Institute of Zoology, Slovak Academy of Sciences
Artikel in diesem Heft
- Synthesis of multifunctional γ-PGA-based superparamagnetic iron oxide nanoparticles for magnetic resonance imaging and controlled drug release
- Organic solvent stable protease isolation and characterization from organic solvent tolerant strain of Lysinibacillus sphaericus PAP02
- The impact of grazing absence in inland saline vegetation – a case study from Slovakia
- How dose of biochar and biochar with nitrogen can improve the parameters of soil organic matter and soil structure?
- Water repellent effects of manure amended soils on organic matter decomposition, C retention, and respired CO2-C
- Rainfall interception in a disturbed montane spruce (Picea abies) stand in the West Tatra Mountains
- ASL16 gene, a member of AS2/LOB family, is essential for lateral root formation in Arabidopsis
- Meiobenthic Assemblages from the Southwestern Coast of the Black Sea, İğneada (Turkey)
- Oviposition by selected water mite (Hydrachnidia) species from Lake Skadar and its catchment
- Parasitic mesostigmatid mites (Acari) – common inhabitants of the nest boxes of starlings (Sturnus vulgaris) in a Polish urban habitat
- Mayfly (Insecta: Ephemeroptera) assemblages of a regulated perennial Mediterranean river system in the Western Balkans
- Distribution and ecology of the flightless bush-cricket Poecilimon schmidtii at its northern range margin
- Sexual size monomorphism and body variation in the fat dormouse Glis glis in Slovakia
Artikel in diesem Heft
- Synthesis of multifunctional γ-PGA-based superparamagnetic iron oxide nanoparticles for magnetic resonance imaging and controlled drug release
- Organic solvent stable protease isolation and characterization from organic solvent tolerant strain of Lysinibacillus sphaericus PAP02
- The impact of grazing absence in inland saline vegetation – a case study from Slovakia
- How dose of biochar and biochar with nitrogen can improve the parameters of soil organic matter and soil structure?
- Water repellent effects of manure amended soils on organic matter decomposition, C retention, and respired CO2-C
- Rainfall interception in a disturbed montane spruce (Picea abies) stand in the West Tatra Mountains
- ASL16 gene, a member of AS2/LOB family, is essential for lateral root formation in Arabidopsis
- Meiobenthic Assemblages from the Southwestern Coast of the Black Sea, İğneada (Turkey)
- Oviposition by selected water mite (Hydrachnidia) species from Lake Skadar and its catchment
- Parasitic mesostigmatid mites (Acari) – common inhabitants of the nest boxes of starlings (Sturnus vulgaris) in a Polish urban habitat
- Mayfly (Insecta: Ephemeroptera) assemblages of a regulated perennial Mediterranean river system in the Western Balkans
- Distribution and ecology of the flightless bush-cricket Poecilimon schmidtii at its northern range margin
- Sexual size monomorphism and body variation in the fat dormouse Glis glis in Slovakia