Cereal leaf beetles (Oulema spp., Coleoptera: Chrysomelidae) control following various dates of wheat sowing and insecticidal treatments

In this paper, we report the sowing date and intensity of chemical control on presence of the cereal leaf beetles (CLB) on spring wheat. The CLB monitoring (Oulema melanopus L. and Oulema gallaeciana Voet.) was conducted in May–June of each year, following the announcement of the IOR-PiB in Poznań (Institute of Plant Protection, National Research Institute), that economic threshold levels in Poland of this pest is observed. For the spring sowing dates between (20 March–20 April) and late autumn sowings (21 November–7 December) larger amounts of CLB adults (1.6–1.1) in comparison to early autumn sowings (25 October–02 November) were noticed (0.4). Following the insecticidal seed treatment with imidacloprid, the occurrence of adults was 0.2–0.7 individual per stem, while the use of fungicidal treatment with triadimenol–imazalil–fuberidazol resulted in average 1.1–2.2 individual per stem. The reduction in the number of larvae per stem was 7–10 fold larger following the foliar application (pirimicarb + dimethoate + cypermethrin) compared to the seed treatment with imidacloprid. The lowest grain yield (3.83 t ha^?1) from the spring crop without any insecticide was obtained. Foliar application with blend of pirimicarb + dimethoate + cypermethrin increased the yield crop by 0.41 t ha^?1 (10.7%) and additionally by 0.78 t ha^?1 (20.4%) to compare to the fungicidal control when imidacloprid was used. Wheat seed treatment with imidacloprid and sowing date in autumn showed to be suitable and economically efficient preventive strategies for controlling the pest population.     

Influence of Integrated Membrane Treatment on the Phytotoxicity of Wastewater from the Coke Industry

In this paper, coke wastewater that had passed through biological and integrated membrane processes (filtration on sand bed—reverse osmosis) was chosen to assess the phytotoxicity of selected industrial wastewater with regard to the test plant—Vicia faba. An innovative research technique in vitro test was conducted in a large scale phytothrone chamber on two matrices: cotton and Murashige and Skoog Basal Medium (MSBM). The toxicity of wastewater was evaluated for samples: (1) treated in the treatment plant by biological processes, (2) filtrated through a sand bed and filtrated (3) reverse osmosis (RO) membrane. The results showed that there is a noticeable correlation between increasing concentrations of wastewater and seed germination of the test plant. Although the wastewater collected from the coke plant was treated biologically, it showed very high levels of germination inhibition (90–98% for cotton matrix and 92–100% for MSBM matrix) and strong toxic effects. The wastewater collected from the coke plant showed a significantly greater phytotoxic effect compared with those obtained from the effluent treated on a sand bed and in RO. However, wastewater, even after treatment on a sand bed (reduction of COD—39%, TN—46%, TOC—42%, TC—47%, SS—50%, 16PAHs—53%), was still toxic and germination inhibition was in the range of 24–48% for the cotton matrix and 14–54% for the MSBM matrix. The toxicity of wastewater treated in the membrane process was the lowest (reduction of COD—85%, TN—95%, TOC—85%, TC—86%, SS—98%, 16PAHs—67%). The germination inhibition was in the range of 4–10% for the cotton matrix and 2–12% for the MSBM matrix. These samples are classified as non-toxic or slightly toxic to the model plant. The present study highlights the necessity of monitoring not only the basic physical and chemical indicators (including the level of toxic substances as PAHs), but also their effect on the test organisms in wastewater samples.     

Influence of stocking density and type of feed on the rearing of crucian carp, <Emphasis Type="Italic">Carassius carassius</Emphasis> (L.), larvae under controlled conditions

Two experiments were conducted into the rearing of crucian carp larvae under controlled conditions in an experimental closed water system. In both cases, the rearing lasted 21 days. The first experiment concerned the initial stocking density (from 50 to 600 individuals per l), whilst the second one studied the first food offered (two types of Artemia nauplii, decapsulated Artemia cysts and three types of commercial feeds) which were applied at the moment of exogenous feeding commencement. The best results were obtained using 50 larvae per l, whilst there were no significant differences within the range 200–600 larvae per l. The application of dry feed had a negative influence on the survival and other parameters. The highest survival rate was found in the groups fed with freshly hatched Artemia naupli. The results obtained indicate that the rearing of crucian carp larvae may be successfully conducted in very high stocking densities. However, the very high sensitivity of crucian carp larvae to the type of food offered during the initial days of life should be taken into account. The data presented in this article could be very useful in crucian carp larviculture.     

Food selection of burbot (Lota lota L.) larvae reared in illuminated net cages in mesotrophic Lake Maróz (north-eastern Poland)

Feeding and food selection of burbot (Lota lota L.) larvae reared in illuminated cages were studied. The experiment was carried out in mesotrophic Lake Maróz, in north-eastern Poland, for 6 weeks in two successive years. The initial stocking density was 1,250 larvae (20 DPH) per cage. Food selection according to the zooplankton groups (Rotifera, Cladocera and Copepoda) and length classes was expressed by the Strauss linear selectivity index (L). Zooplankton species composition in the lake was similar in the two seasons of the study and organisms shorter than 0.5 mm prevailed in the plankton. The mean number of prey found in burbot alimentary tracts increased from about 40 up to over 200 during the course of the study. A very large inter-individual variation in the amount of food organisms consumed by fish was noted. Analysis of the values of the Strauss food selectivity index shows that at the beginning of the first year of the experiment, burbot larvae preferred copepods, most numerous in the environment at that time; later, fish tended to select cladocerans. In the second year of the study, fish more often ate copepods, irrespective of their quantities in the environment. During the whole study, reared burbot larvae did not eat rotifers, even when they were numerous in cages. Similarly to the rotifers, the smallest planktonic organisms, measuring up to 0.5 mm in length, were typically neglected by fish, while the 0.6–1.0 mm group was most frequently selected. There were also considerable individual differences between particular burbot specimens in their food preferences.     

A passage and storage system for isolated bovine endometrial epithelial and stromal cells

To establish a storage system for isolated endometrial cells, we investigated the basal, oxytocin (OT)- and tumor necrosis factor (TNF) alpha-stimulated production of prostaglandin (PG) F(2alpha) in bovine-passaged and frozen-thawed endometrial cells. Stromal and epithelial cells obtained from cows in the early stage of the estrous cycle (Days 2-5) were frozen at -80 C or further cultured and/or passaged until passage 4 in DMEM/Ham's F-12 supplemented with 10% calf serum. A fresh-unfrozen primary culture and one-time passaged fresh-unfrozen cells were used as the control. When both unfrozen and frozen cells reached confluence, the culture medium was replaced with fresh medium with 0.1% BSA and the cells were stimulated with OT (100 ng/ml) or TNFalpha (1 ng/ml) for 4 h. The passage and freezing of the endometrial cells did not affect their morphology. In primary culture of frozen and unfrozen endometrial cells, OT strongly stimulated PGF(2alpha) production in epithelial cells, and TNFalpha strongly stimulated PGF(2alpha) production in stromal cells (P<0.05). The basal output of PGF(2alpha) in frozen stromal cells was similar to that in unfrozen stromal cells. However, the basal output of PGF(2alpha) in frozen epithelial cells was significantly lower than that unfrozen cells (P<0.05). On the other hand, in passaged cells, the basal level of PGF(2alpha) production was retained until passage 1 in epithelial cells, whereas it was retained until passage 4 in stromal cells. Although epithelial cells responded to OT in PGF(2alpha) production until passage 2 (P<0.05), the stromal cells showed a significant response to TNFalpha until passage 4 (P<0.05). These results suggest that stored cells could be used for studying the physiology of bovine endometrium in vitro until passage 1 in endometrial epithelial cells, and until passage 4 in stromal cells.     

Changes in the physical and the sensorial properties of wheat bread caused by interruption and slowing of the fermentation of yeast-based leaven

Here we propose an original study on the effect of an interruption and slowing of the fermentation of yeast-based leaven on the physical properties of bread.     

Phyto- and endogenous estrogens differently activate intracellular calcium ion mobilization in bovine endometrial cells

The main purpose of this study was to check whether phyto- and endogenous estrogens influence calcium ion mobilization [Ca(2+)](i) in bovine endometrial cells and whether this action is connected with biological effects i.e. prostaglandin (PG)F(2alpha) production. In our study we used two calcium measurement methods by comparing the microscopic method with widely used quantitative - spectrofluorometric method of [Ca(2+)](i) measurement. We also wanted to confirm whether visualization of calcium ion [Ca(2+)](i) in cells using microscopic method supported by micro image analysis (Micro Image Olympus system) reflects real, qualitative changes in the ion concentration. In both methods a cell-permeable form of fluorescent [Ca(2+)](i) indicator Fura-2 was used. Cultured bovine endometrial epithelial and stromal cells influenced by phorbol-2-myristate-13-acetate (PMA; positive control), estradiol 17-beta (E(2); endogenous estrogen) and active metabolites of phytoestrogens (environmental estrogens) were used as a model to study PGF(2alpha) secretion and [Ca(2+)](i) mobilization in the cells. Equol and para-ethyl-phenol in doses of 10(-8)-10(-6) M increased PGF(2alpha) concentration both in epithelial and stromal cells (P<0.05). In both methods, equol and para-ethyl-phenol did not cause intracellular [Ca(2+)](i) mobilization in epithelial and stromal cells (P>0.05). Both methods revealed that only E(2) and PMA induced intracellular [Ca(2+)](i) mobilization in epithelial and stromal cells (P<0.05). The results of both methods were highly correlated (P<0.001; r=0.82 for epithelial cells and r=0.89 for stromal cells). In conclusion, both methods gave approximately the same results and showed that phytoestrogens, in contrast to PMA and E(2), did not cause intracellular [Ca(2+)](i) mobilization in endometrial cells. The obtained results proved that the [Ca(2+)](i) visualization method supported by micro image analysis can produce similar results to the spectrofluorometric method.