Anna KRÓL, İzabela HAJDAMOWICZ, Cezary TKACZUK

Diel and seasonal activity of ground dwelling spiders (Araneae) in a sandy grassland habitat

The paper concerns the diel and seasonal activity of ground dwelling spiders on a sandy grassland in the Bug River Valley in East-Central Poland. The spiders were captured using pitfall traps in 2009 and 2010 from May to July. The material was collected one day a week, day and night. Traps were checked every 3 h, eight times a day. It was found that for spiders with larger bodies, from the families Lycosidae and Philodromidae, the peak of their activity was in the afternoon, and smaller spiders belonging to the families Linyphiidae and Tetragnathidae showed the greatest activity in the morning. Species Pardosa palustris and Xerolycosa miniata were dominant spiders of the studied grassland. The time of their highest diel activity was different by several hours. It was observed that P. palustris individuals were more numerous in that habitat in early June and X. miniata spiders from mid-June. Spiders of the dominant family Lycosidae were in the highest numbers in the second half of May and in early June, while most of the spiders of other families were captured before or after the period of prevailing presence of dominant spiders.

Keywords:

Species competition cooccurrence, Xerolycosa miniata, Pardosa palustris,

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Alderweireldt M (1994). Day/night activity rhythms of spiders occurring in crop-rotated fields. Eur J Soil Biol 30: 55-61.
Bayram A (1996). A study on the diel activity of Pardosa spiders (Araneae, Lycosidae) sampled by the time sorting pitfall trap in different habitats. Turk J Zool 20: 381-387.
Bell-Pedersen D, Cassone VM, Earnest DJ, Golden S, Hardin PE, Thomas TL, Zoran MJ (2005). Circadian rhythms from multiple oscillators: lessons from diverse organisms. Nat Rev Genet 6: 554-556.
Bel’skaya EA, Esyunin SL (2003). Arachnids (Arachnidae) in a spring wheat agrocenosis in southern Sverdlovsk oblast and the effect of treatment with Decis, a pyretroid insecticide, on their populations. Russ J Ecol+ 5: 395-398.
Birkhofer K, Fließbach A, Wise DH, Scheu S (2008). Generalist predators in organically and conventionally managed grass- clover fields: implications for conservation biological control. Ann Appl Biol 153: 271-280.
Chapman EG, Schmidt JM, Welch KD, Harwood JD (2013). Molecular evidence for dietary selectivity and pest suppression potential in an epigeal spider community in winter wheat. Biol Control 65: 72-86.
Chatterjee S, Isaia M, Venturino E (2009). Spiders as biological controllers in the agroecosystem. J Theor Biol 258: 352-362.
Foelix RF (1996). Biology of Spiders. 2nd ed. New York, NY, USA: Oxford University Press.
Frampton GK, Van Den Brink PJ, Wratten SD (2001). Diel activity patterns in arable collembolan community. Appl Soil Ecol 17: 63-80.
Hajdamowicz I, Pilacka L, Meissner W (2015). Spider assemblages and dynamics on seasonal island in the Pripyat River, Belarus. Turk J Zool 39:1-11.
Harwood JD, Obrycki JJ (2005). Web-construction behavior of linyphiid spiders (Araneae, Linyphiidae): competition and co- existence within a generalist predator guild. J Insect Behav18: 593-607.
Harwood JD, Sunderland KD, Symodson WO (2004). Prey selection by linyphiid spiders: molecular tracking of the effects of alternative prey on rates of aphid consumption in the field. Mol Ecol 13: 3549-3560.
Harwood JD, Sunderland KD, Symodson WO (2005). Monoclonal antibodies reveal the potential of the tetragnathid spider Pachygnatha degeeri (Araneae: Tetragnathidae) as an aphid predator. B Entomol Res 95: 161-167.
Honek A (1988). The effect of crop density and microclimate on pitfall trap catches of Carabidae, Staphylinidae (Coleoptera) and Lycosidae (Araneae) in cereal fields. Pedobiologia 32: 233- 242.
Jõgar K, Metspalu L, Hiiesaar K (2004). Abundance and dynamics of spiders (Lycosidae) in different plant communities. Agronomy Research 2: 145-152
Krumpalova Z, Tuf IH (2013). Circadian rhythms of ground living spiders: mechanisms of coexistence strategy based on the body size. Pol J Ecol 61: 575-586.
Lundgren JG, Nichols S, Prischmann DA, Elsbury M (2009). Seasonal and diel activity patterns of generalist predators associated with Diabrotica virgifera (Coleoptera: Chrysomelide). Biocontrol Sci Techn 19: 327-333.
Matuszkiewicz W (2006). Przewodnik Do Oznaczania Zbiorowisk Roślinnych Polski. Warsaw, Poland: Wydawnictwo Naukowe PWN (in Polish).
Mestre L, Garcia N, Barrientos JA, Espadaler X, Pinol J (2013). Bird predation affects diurnal and nocturnal web-building spiders in a Mediterranean citrus grove. Acta Oecol 47: 74-80.
Nyffeler M, Benz G (1988). Feeding ecology and predatory importance of wolf spiders ( Pardosa spp.) (Araneae, Lycosidae) in winter wheat fields. J Appl Ecol 106: 123-134.
Nyffeler M, Sunderland KD (2003). Composition, abundance and pest control potential of spider communities in agroecosystems: a comparison of European and US studies. Agr Ecosyst Environ 95: 579-612
Pfiffner L, Luca H (2003). Effects of low-input farming systems on carabids and epigeal spiders - a paired farm approach. Basic Appl Ecol 4: 117-127.
Roberts MJ (1996). Collins Field Guide. Spiders of Britain and Northern Europe. London, UK: Harper Collins Publishers.
Romero SA, Harwood JD (2010). Diel and seasonal patterns of prey available to epigeal predators: evidence for food limitation in a linyphiid spider community. Biol Control 52: 84-90.
Samiayyan K (2014). Spiders - The Generalist Super Predators in Agro-ecosystems. In: Abrol DP, editor. Integrated Pest Management. Current Concepts and Ecological Perspective. San Diego, CA, USA: Academic Press, pp. 283-310.
Samu F, Szinetar C (2002). On the nature of agrobiont spiders. J Arachnol 30: 389-402.
Schmidt JM, Harwood JD, Rypstra AL (2012). Foraging activity of a dominant epigeal predator: molecular evidence for the effect of prey density on consumption. Oikos 121: 1715-1724.
Symodson WOC, Sunderland KD, Greenstone MH (2002). Can generalist predators be effective biocontrol agents? Annu Rev Entomol 47: 561-594.
Szymkowiak P, Woźny M (1998). Dominance structure and seasonal changes in the abundance of dominant epigeic spiders in pastures of Northern Greater Poland. In: Selden PA, editor. Proceedings of the 17th Colloquium of Arachnology; 14–18 July 1997. Edinburgh, UK: British Arachnological Society, pp. 245-252.
Thomas CFG, Brown NJ, Kendall DA (2006). Carabid movement and vegetation density: Implications for interpreting pitfall trap data from split-field trials. Agr Ecosyst Environ 113: 51-61.
Tuf IH, Tufova J, Jerabkova E, Dedek P (2006). Diurnal epigeic activity of myriapods (Chilopoda, Diplopoda). Norwegian Journal of Entomology 53: 335-344.
Uetz GW, Halaj J, Cady AB (1999). Guild structure of spiders in major crops. J Arachnol 27: 270-280.
Van Berkum FH (1982). Natural history of a tropical, shrimp-eating spider (Pisauridae). J Arachnol 10: 117-121.
Watts JC, Ross CR, Jones TC (2015). Diel life-history characteristics of personality: consistency versus flexibility in relation to ecological change. Anim Behav 101: 43-49.
Welch KD, Harwood JD (2014). Temporal dynamics of natural enemy-pest interactions in a changing environment. Biol Control 75: 18-27.
Ximenez-Embun MG, Zaviezo T, Grez A (2014). Seasonal, spatial and diel partitioning of Acyrthosiphon pisum (Hemiptera: Aphididae) predators and predation in alfalfa fields. Biol Control 69: 1-7.