Overwintering insects must avoid injury and death from the freezing of tissues and from metabolic disruptions associated with exposure to low, non-freezing temperatures. The winter climates of the world are classified in relation to insect overwintering on the basis of their minimum temperatures and the duration of the winter (when temperatures are below the thermal range for activity and development). Outside the Tropical Wet zone, the severity of exposure to cold (temperature, snowfall, duration of exposure, predictability, variability) can vary from a few days at 0°C to months below -20°C with extremes as low as -60°C. The severity of the temperature exposure may be ameliorated by the selection by insects of overwintering sites (exposed, partly-exposed, protected). The relationships among overwintering habitats, the minimum winter temperature in climatic zones, and the supercooling points (SCP) of over 350 terrestrial insects from published reports were examined. Variability in the SCP among insects within each climatic zone and habitat was wide. Among the freeze-susceptible species that overwintered in exposed or partly-protected habitats the SCP and the cold severity of climate were correlated. This was not the case for insects that overwintered in protected habitats. The SCP's of freeze-tolerant insects were generally higher than the freeze-susceptible insects, and the SCP's were not tightly linked with the cold severity of climatic zone. Insects, both freeze-susceptible and freeze-tolerant, overwintering in exposed habitats had lower SCP's than insects from habitats that offered some protection from ambient temperatures. Thirty-eight species had reports of SCP's for different geographical locations. Although there were occasionally differences in the SCP's, there was no consistent pattern of insects having lower SCP's when overwintering in colder habitats. The incidence of freeze-tolerance was higher in boreal and polar climatic zones than in climatic zones with warmer winters. Holometabola insects had a higher incidence of freeze-tolerance than hemimetabola insects. Suggestions for future research directions are outlined.
The winter diet of the great cormorant (Phalacrocorax carbo) was studied by means of examining regurgitated pellets, individual fish bones and fish remains collected from below the roosting trees in two sites on the River Vltava in Vyšší Brod and at Slapy Reservoir, Czech Republic, and by analysis of stomach contents of birds shot on the River Vltava in Prague. Using diagnostic bones (os pharyngeum, dentale, maxillare, praeoperculare) and own linear regression equations between measured dimension of the diagnostic bone and fish total length (LT), a total of 1152 fish of 22 species and 6 families were identified in the diet of great cormorants and their sizes were reconstructed. At all three localities on the main stream of the River Vltava, roach (Rutilus rutilus), bream (Abramis brama), bleak (Alburnus alburnus), European chub (Squalius cephalus), European perch (Perca fluviatilis) and ruffe (Gymnocephalus cernuus) made up at least 74.2 % of the cormorants’ diet. A great potential for fish stock losses was identified for the River Vltava at Vyšší Brod and in Prague where the loss of fish due to overwintering great cormorants was estimated to be 22 kg ha–1 and up to 79 kg ha–1 respectively, i.e. belonging among the highest ever published figures for fish withdrawal caused by great cormorants from any inland waters (carp fishponds excluded). Most probably, both great cormorants and anglers are responsible for the decrease in catches of brown trout (Salmo trutta m. fario) and grayling (Thymallus thymallus) from the River Vltava in Vyšší Brod.
The food composition of noctule bats (Nyctalus noctula) was investigated using droppings analyses methods (29 samples/ 322 pellets) over two winters (2001/2002 and 2002/2003) in ten urban and rural localities in Central Europe (Slovakia, Czech Republic). Two orders of arachnids (Araneida, Acarina) and nine orders of insects (Homoptera, Heteroptera, Psocoptera, Neuroptera, Coleoptera, Hymenoptera, Lepidoptera, Diptera, Siphonaptera) were identified in the droppings. The most important order in all samples was Lepidoptera (mean F = 53 %, mean V = 35 %), followed by Diptera (F = 38 %, V = 12 %), Coleoptera (F = 21 %, V = 9 %) and Araneida (F = 15 %, V = 3 %). Differences were found in the composition of the most important food components among two urban and one rural locality as well as in the portion of secondary components (hair, slime). Regarding seasonal changes in the food composition, three periods were identified in winter – the beginning (November – January), the middle (February) and the end of the season (March). Some seasonal trends could be identified in the Diptera and Coleoptera, with a decrease in frequency and volume in the middle of the winter. The most important food component (Lepidoptera) showed no seasonal trend over winter. The bats could hunt insects outside or collect them also very probably directly in the shelters.
Winter habitat use, niche breadth and overlap between the native and invasive species of medium sized predators, the red fox, pine marten and raccoon dog in particular, were studied in three landscapes with different habitat structure in Lithuania. Meadows were preferred by foxes but avoided by raccoon dogs and pine martens. Pine martens intensively used various forest habitats, whilst raccoon dogs tended to prefer swamps. The habitat niche breadth (Hurlbert’s standardized niche breadth) varied with respect to both the species and the study site. The habitat niche overlap was larger between raccoon dog and pine marten than that between raccoon dog and red fox. Our results suggest a low impact of the invasive raccoon dog on red fox and pine marten in studied landscapes.
Seasonal variability of maximum quantum yield of PSII photochemistry (Fv/Fm) was studied in needles of Taxus baccata seedlings acclimated to full light (HL, 100% solar irradiance), medium light (ML, 18% irradiance) or low light (LL, 5% irradiance). In HL plants, Fv/Fm was below 0.8 (i.e. state of photoinhibition) throughout the whole experimental period from November to May, with the greatest decline in January and February (when Fv/Fm value reached 0.37). In ML seedlings, significant declines of Fv/Fm occurred in January (with the lowest level at 0.666), whereas the decline in LL seedlings (down to 0.750) was not significant. Full recovery of Fv/Fm in HL seedlings was delayed until the end of May, in contrast to ML and LL seedlings. Fv/Fm was significantly correlated with daily mean (T mean), maximal (T max) and minimal (T min) temperature and T min was consistently the best predictor of Fv/Fm in HL and ML needles. Temperature averages obtained over 3 or 5 days prior to measurement were better predictors of Fv/Fm than 1- or 30-day averages. Thus our results indicate a strong light-dependent seasonal photoinhibition in needles of T. baccata as well as suggest a coupling of Fv/Fm to cumulative temperature from several preceding days. The dependence of sustained winter photoinhibition on light level to which the plants are acclimated was further demonstrated when plants from the three light environments were exposed to full daylight over single days in December, February and April and Fv/Fm was followed throughout the day to determine residual sensitivity of electron transport to ambient irradiance. In February, the treatment revealed a considerable midday increase in photoinhibition in ML plants, much less in HL (already downregulated) and none in LL plants. This suggested a greater capacity for photosynthetic utilization of electrons in LL plants and a readiness for rapid induction of photoinhibition in ML plants. Further differences between plants acclimated to contrasting light regimes were revealed during springtime de-acclimation, when short term regeneration dynamics of Fv/Fm and the relaxation of nonphotochemical quenching (NPQ) indicated a stronger persistent thermal mechanism for energy dissipation in HL plants. The ability of Taxus baccata to sustain winter photoinhibition from autumn until late spring can be beneficial for protection against an excessive light occurring together with frosts but may also restrict photosynthetic carbon gain by this shade-tolerant species when growing in well illuminated sites. and P. Robakowski, T. Wyka.
Otter (Lutra lutra) diet was studied by analysing of 180 spraints and 29 partly consumed fish remains found in winter around fishponds in South Bohemia (Czech Republic). The proportion of fish found in spraints was 95.6% of all prey items, roach (Rutilus rutilus), topmouth gudgeon (Pseudorasbora parva) and common carp (Cyprinus carpio) being the most numerically abundant species with 37.3, 21.3 and 19.0% respectively. Carp dominated the diet bymass (47.8%), whilst roach and “other commercial fish species” (predatory and herbivorous fish, tench, Tinca tinca) formed 21.8 and 15.3% of total biomass, respectively. Small fish (< 200 mm) predominated in the diet and only 4.0% of all fish found in spraints exceeded 300 mm TL. Large fish remains were very scarce in spraints and were best recorded from uneaten prey remains. The partially eaten remains of carp, pike (Esox lucius) and common bream (Abramis brama) were found on banks or ice, but most (86%) were carp. The original length of carp corpses ranged between 283 and 530 mm TL, and the proportion of body mass consumed varied between 5.0 – 90.1%. The length of pike remains ranged from 386 to 754 mm TL, of which 84.0% of body mass on average was consumed by otters. The otter diet apparently reflects food availability in fishponds and supply channels. Small water basins with a high stock density can be vulnerable to serious damage especially during the winter period and at such places, where no better accessible source of food is available to otters. However, in many such places simple mitigation measures may be able to reduce otter predation.