| Nálezy podle období | |||||
|---|---|---|---|---|---|
| Dictynidae | 0-1900 | 1901-1950 | 1951-2000 | 2001+ | ∑ |
| Dictyna arundinacea (Linnaeus, 1758) Není ohrožený | 5× | 8× | 249× | 92× | 354× |
| České jméno | cedivečka obecná |
|---|---|
| Stupeň ohrožení | Není ohrožený |
| Nálezy | 354 nálezů, 154 kvadrátů |
| První nález |
1859, F. Prach, Prach 1866 |
| Poslední nález | 2025 , Aleš Prágr |
| Areál rozšíření | Holarctic |
| Fytogeografická oblast |
|
| Původnost stanovišť |
|
| Vlhkost stanovišť |
|
| Stratum |
|
| Osvětlení stanovišť |
|
| Hojnost výskytu |
|
| Nadm. výška | 150-1100 |
The spatial distribution of parasitoids is closely linked to the distribution and ecological requirements of their hosts. Several studies have documented changes in the fauna composition of parasitoids in response to elevation, but data on parasitoids associated with spiders are missing. The koinobiont ichneumonid wasp Zatypota anomala is strictly specialised on spiders of the genus Dictyna (Dictynidae) in Europe. We examined the distribution of spiders of the family Dictynidae in forest ecotones in central Europe across a broad elevation gradient (110–1466 m a.s.l.). We checked the spiders for parasitism by Z. anomala. It was most abundant at the mid-elevations (median 712 m a.s.l., range 179–870 m a.s.l.). We identified four dictynid spider species as Z. anomala hosts. These were Dictyna arundinacea, Dictyna uncinata, Nigma flavescens, and Nigma walckenaeri. All four species and the genus Nigma were recorded as hosts for the first time. The parasitoids strongly preferred juvenile instars of their hosts. The body length differed between parasitised Dictyna and Nigma spiders (medians: 1.95 mm and 2.55 mm, respectively). The distribution of Dictyna and Nigma spiders overlapped along the elevation gradient, but parasitism incidence significantly differed between spider genera along the elevation gradient. Nigma was parasitized at lower elevations between 179–254 m a.s.l. and Dictyna at higher elevations between 361–870 m a.s.l. The phenology of Z. anomala is closely tied to the univoltine life strategy of its host spiders. The parasitoid female oviposits in autumn, and its offspring overwinter as larvae on the host, reach adulthood during spring, and pass the summer as an adult.
| Dictyna arundinacea (Linnaeus, 1758) ES | Samci | Samice | Mláďata | Nálezy |
|---|---|---|---|---|
| Individuální sběr | 29 | 102 | 1 | 53 |
| Smyk | 105 | 208 | 44 | 123 |
| Sklepávání | 4 | 24 | 1 | 19 |
| Prosev | 5 | 10 | 0 | 12 |
| Zemní past | 13 | 35 | 0 | 21 |
| Neurčeno | 64 | 131 | 21 | 125 |
| Samci | Samice | Mláďata | Nálezy |
| Dictyna arundinacea (Linnaeus, 1758) ES | Samci | Samice | Mláďata | Nálezy |
|---|---|---|---|---|
| Rákosiny a orobincové porosty stojatých vod | 3 | 4 | 0 | 4 |
| Louky | 1 | 10 | 0 | 7 |
| Paseky | 1 | 9 | 0 | 6 |
| Travnaté stepi | 3 | 2 | 0 | 3 |
| Ruderály | 5 | 9 | 0 | 7 |
| Těžebny písku a jiných nezpevněných hornin | 9 | 5 | 0 | 8 |
| Lesostepní doubravy | 2 | 3 | 0 | 4 |
| Písčiny | 4 | 67 | 1 | 14 |
| Rašeliniště | 6 | 14 | 0 | 10 |
| Písčité břehy | 1 | 2 | 0 | 1 |
| Mezofilní louky | 1 | 1 | 0 | 2 |
| Vřesoviště nižších poloh | 3 | 1 | 0 | 2 |
| Kamenolomy | 4 | 8 | 1 | 6 |
| Neurčeno | 84 | 121 | 51 | 136 |
| Mokré louky | 4 | 20 | 0 | 12 |
| Bylinné porosty břehů | 1 | 6 | 2 | 6 |
| Lesní okraje | 2 | 9 | 0 | 4 |
| Suché louky | 27 | 70 | 10 | 16 |
| Vrbové křoviny - vlhké (vrbové) křoviny | 0 | 1 | 0 | 1 |
| Stepi, vřesoviště, písčiny | 2 | 2 | 0 | 1 |
| Suché křoviny | 2 | 6 | 0 | 3 |
| Slaniska | 0 | 1 | 0 | 1 |
| Dubohabřiny | 0 | 1 | 0 | 1 |
| Ovocné sady s luční vegetací | 3 | 5 | 0 | 8 |
| Ostřicové porosty stojatých vod | 1 | 2 | 0 | 3 |
| Porosty borůvek | 3 | 2 | 0 | 3 |
| Výsadby jehličnanů | 0 | 2 | 1 | 3 |
| Močály | 6 | 20 | 0 | 11 |
| Úhory | 17 | 13 | 0 | 9 |
| Skalní stepi na vápenci | 2 | 3 | 0 | 3 |
| Xerotermní travinobylinná společenstva | 1 | 13 | 1 | 9 |
| Reliktní bory na skalách | 10 | 11 | 0 | 5 |
| Suťové a roklinové lesy | 0 | 1 | 0 | 1 |
| Louky | 1 | 4 | 0 | 6 |
| Louky a pastviny | 0 | 2 | 0 | 2 |
| Pastviny | 1 | 1 | 0 | 2 |
| Suché doubravy | 0 | 9 | 0 | 5 |
| Vlhké lesní lemy | 1 | 2 | 0 | 3 |
| Stojaté a pomalu tekoucí vody | 0 | 3 | 0 | 3 |
| Ostatní pole | 0 | 1 | 0 | 1 |
| Haldy a výsypky | 3 | 5 | 0 | 4 |
| Lužní lesy nížin | 0 | 2 | 0 | 2 |
| Lesní cesta | 1 | 1 | 0 | 2 |
| Polní biotopy | 0 | 1 | 0 | 1 |
| Stinné skály nižších poloh | 0 | 1 | 0 | 1 |
| Luční ostřicové mokřady | 0 | 10 | 0 | 5 |
| Acidofilní bory | 0 | 1 | 0 | 1 |
| Okraje silnic | 0 | 1 | 0 | 1 |
| Mokřady | 0 | 1 | 0 | 1 |
| alpínské trávníky | 1 | 2 | 0 | 1 |
| Výsadby listnáčů | 5 | 18 | 0 | 2 |
| Břehy tekoucích vod | 0 | 1 | 0 | 1 |
| Samci | Samice | Mláďata | Nálezy |