Respiration rates of two species of Gnathostomulids

Summary Respiration rates for two species of Gnathostomulida from poorly oxygenated subtidal sands of Bermuda were measured using Cartesian diver respirometers.ForHaplognathia cf.ruberrima a respiration-body weight regression gaveR=0.790·W ^0,649 (in l·10^-3O₂/h and g wet weight). Respiration rates for adult animals ofGnathostomula sp. of a mean weight of 1.3 g ranged between 0.25 and 0.63 l·10^-3 O₂/h. These rates are low when compared with literature data on meiobenthic species from a wider habitat range but similar to respiration rates of marine and limnic nematodes living in sediments with strongly reducing capacity.     

Proposed standard weight (Ws) equation for European perch (Perca fluviatilis Linnaeus, 1758)

Relative weight (W_r) is an important and commonly used condition index that provides a measure of the well‐being of a fish population by comparing the actual weight of a specimen with the ideal weight of a specimen of the same species and of the same length in good physiological condition, i.e. the standard weight (W_s). Two methods of calculating the standard weight are proposed in the literature: the RLP method and the EmP method. The aim of this study was to develop a standard weight equation for European perch by means of both methods, using length–weight data from 64 913 fish from 18 countries (across Europe and Oceania). The resulting equations were: log₁₀ (W_s) = ?3.1483 + 1.2663 log₁₀ (TL) + 0.4291 [log₁₀ (TL)]² for the EmP method and log₁₀ (W_s) = ?5.3493 + 3.2152 log₁₀ (TL) for the RLP method. The applicable length‐range of the two W_s equations was restricted to 80–460 mm. A further research aim was to compare the performances of RLP and EmP. The resulting quadratic EmP W_s equation did not exhibit length‐related biases, which suggests that it can be used to compute relative weight for European perch.     

Growth and respiration of Cyprideis torosa Jones 1850 (Crustacea Ostracoda)

Summary The ostracod Cyprideis torosa Jones 1850 is a dominant species in brackish water habitats. To assess its importance, growth and respiration were measured. The shells form an increasing part of total weight as the animals grow but there is no correlation between shell weight and soft parts weight in the adults, indicating that tissue growth is a continuous process in these ostracods.Respiration was measured at 20° C. The slope of the log-log regression of respiration on dry weight was 0.746, showing that Cyprideis torosa follows the general rule for this relationship. The respiration rate per unit biomass was 0.246 nl O₂ g^-1 h^-1, which is low but well within the range of observed meiobenthic respiration rates.The Q₁₀, expressing the temperature dependence of respiration, was 2.15. The general validity of Price and Warwick's (1980) hypothesis relating Q₁₀ to stability of food supply is questioned.     

Adrenergic receptors and the regulation of vascular resistance in bullfrog tadpoles (Rana catesbeiana)

Summary Vascular adrenergic sensitivity to exogenous catecholamines was examined in tadpoles of the American bullfrog (Rana catesbeiana), ranging from stage III to XIV. Central arterial blood pressure was measured in decerebrate bullfrog tadpoles to determine a reasonable initial infusion pressure. Solutions of epinephrine and phenylephrine were infused into the vasculature of pithed tadpoles, and the resulting changes in vascular resistance (R _v) were used to construct log dose-response relationships. Epinephrine infusion produced a dose-dependent increase in R _v (EC₅₀=5.3·10^-7 M), which could be reversed by sodium nitroprusside (a smooth muscle relaxant) and blocked by phenoxybenzamine (an -adrenergic antagonist). Larval R _v also increased with infusion of the -agonist phenylephrine (EC₅₀=7.4·10⁸ M). Infusion of 10^-6 M isoproterenol (a -agonist) largely reversed the phenylephrine-induced increase in R _v. These results indicate that the capacity exists for both -mediated vasoconstriction and -mediated vasodilation early in bullfrog ontogeny. Neither initial R _v nor the responses to infused epinephrine or phenylephrine were significantly correlated to development over the range of larval stages used in this study.Abbreviations ECG electrocardiogram - EPI epinephrine - ISO isoproterenol - PHE phenylephrine - POB phenoxybenzamine - R _v vascular resistance - SNP sodium nitroprusside     

On the water balance ofPhytoseiulus persimilis A.-H. and its ecological significance

The net water vapour exchange ofPhytoseiulus persimilis A.-H. is described. Water loss by transpiration increases progressively with ambient temperature. The transpiration rate is directly proportional to the saturation deficit of the air (15 to 30° C) and at constant temperature linearly dependent on the water vapour activity: m_T=–0.81 a_v+0.91 (for a_v 0.0 to 0.85 at 20°C). Phytoseiulus persimilis is able to absorb water vapour from the unsaturated atmosphere. This occurs above a certain threshold (critical equilibrium activity, CEA), which is a_v=0.9 at 15 to 25°C and increases to a_v=0.935 at 30°C.The environmental humidity conditions influencingP. persimilis on the leaf surface are described. The diurnal water vapour profile within the laminar layer at the leaf surface includes periods with water vapour values high enough for these mites to utilize their water vapour sorption capability and to restore a previously-suffered water deficit. In addition,P. persimilis shows a positive hygrotactic behaviour when in a state of water deficit.The survival time of starvingP. persimilis is at least doubled when a possibility to absorb water vapour is available. The water balance at limited food resources is discussed. With a food supply (one prey mite, containing about 5.5 g water) every 3 days and a water vapour activity of a_v=0.76 (20°C), water balance is achieved and the survival time is maximal (approximately 120 days).     

Oxygen consumption and flight muscle activity during heating in workers and drones of Apis mellifera

Summary Instantaneous oxygen consumption, muscle potential frequency, thoracic and ambient temperature were simultaneously measured during heating in individual workers and drones of honey bees. Relationships between these parameters and effects of thoracic temperature on power input and temperature elevation were studied. Oxygen consumption increased above basal levels only when flight muscles became active. Increasing muscle potential frequencies correlated with elevated oxygen consumption and raised thoracic temperature. The difference between thoracic and ambient temperature and oxygen consumption were linearly related. Oxygen consumption per muscle potential (l O₂ · g _–1 ^thorax · MP^–1) was two-fold higher in drones than in workers. However, oxygen consumption for heating the thorax (l O₂ · g _–1 ^thorax · (T_th-T_a) · °C^–1) was nearly the same in workers and drones. Thoracic temperature affected the amount of oxygen consumed per muscle potential (R₁₀=1.5). Achieved temperature elevation per 100 MP was more temperature sensitive in drones (R₁₀=6–10) than in workers (R₁₀=3.6). Q₁₀ values for oxygen consumption were 3 in workers and 4.5–6 in drones. Muscle potential frequency decreased with a Q₁₀=1.8 in workers and 2.7 in drones. Heating behaviour of workers and drones was different. Drones generated heat less continuously than workers, and showed greater interindividual variability in predilection to heat. However, the maximal difference between ambient and thoracic temperature observed was 22 °C in drones and 14 °C in workers, indicating greater potential for drones.Abbreviations DL dorsal-longitudinal muscle - DV dorsoventral muscle - MP muscle potential - T _a ambient temperature - T _th thoracic temperature     

Changes in body weight of two species of predatory mites (Acarina: Phytoseiidae) as a consequence of feeding in an interactive system

Changes in body weight of two species of predatory mites,Phytoseiulus persimilis Athias-Henriot andAmblyseius degenerans (Berlese), when each species was feeding alone on the prey miteTetranychus pacificus McGregor, were determined in the laboratory. The body weight of a starved adult femaleP. persimilis could increase 105.6% (13.05 g) to full satiation, whereasA. degenerans increased 43.2% (7.6 g). A simple model is used to describe the weight changes of each species. Changes in body weight also were determined when each of the two species fed with conspecifics at a high and low predator density. WithP. persimilis there was a reduction in body weight as well as in reproduction and in the number of prey killed when feeding at a high density of conspecifics. These reductions were not observed withA. degenerans. WhenP. persimilis fed with heterospecifics (A. degenerans), reductions in these three variables were less marked. The reductions are attributed primarily to the effect of sharing prey meals with conspecifics. Possible mechanisms for these reductions through meal-sharing are discussed.     

Respiration rates of Chiloplacus sp. and other arctic nematodes at low and high temperatures

Summary Respiration of an undescribed species of soil nematode of the genus Chiloplacus from the Canadian High Arctic was measured at 2°, 5°, 10°, 15°, 20° and 25°C. The corresponding metabolic rates were 0.2697×10^-3 l, 0.3406×10^-3 l, 0.8408×10^-3 l, 0.8539×10^-3 l, 1.8420×10^-3 l and 2.9360×10^-3 l O₂ ind^-1 h^-1, respectively, for a nematode of 1.0 g dry weight. The relationship between respiration and dry weight for Chiloplacus sp. at 10°C is described by the function log R=-3.0693+0.8844 log W. Q₁₀ values for the 2°–5°, 5°–10°, 10°–15°, 15°–20° and 20°–25°C temperature intervals were 2.18, 6.09, 1.03, 4.65 and 2.54, respectively. Chiloplacus sp. showed raised metabolic rates at low tempetatures compared with species from warmer environments. Metabolic rates of representative samples of the soil, nematode fauna (dominated by individuals of the genus Plectus) from the same location were 0.1593×10^-3 l, 0.3603×10^-3 l and 0.5332×10^-3 l O₂ ind^-1 h^-1 at 5°, 10° and 15°C for an average nematode of 0.4297 g dry weight.     

The intrinsic electrophysiological characteristics of fly lobula plate tangential cells: I. Passive membrane properties

The passive membrane properties of the tangential cells in the fly lobula plate (CH, HS, and VS cells, Fig. 1) were determined by combining compartmental modeling and current injection experiments. As a prerequisite, we built a digital base of the cells by 3D-reconstructing individual tangential cells from cobalt-stained material including both CH cells (VCH and DCH cells), all three HS cells (HSN, HSE, and HSS cells) and most members of the VS cell family (Figs. 2, 3). In a first series of experiments, hyperpolarizing and depolarizing currents were injected to determine steady-state I-V curves (Fig. 4). At potentials more negative than resting, a linear relationship holds, whereas at potentials more positive than resting, an outward rectification is observed. Therefore, in all subsequent experiments, when a sinusoidal current of variable frequency was injected, a negative DC current was superimposed to keep the neurons in a hyperpolarized state. The resulting amplitude and phase spectra revealed an average steady-state input resistance of 4 to 5 M and a cut-off frequency between 40 and 80 Hz (Fig. 5). To determine the passive membrane parameters R _m (specific membrane resistance), R _i (specific internal resistivity), and C _m (specific membrane capacitance), the experiments were repeated in computer simulations on compartmental models of the cells (Fig. 6). Good fits between experimental and simulation data were obtained for the following values: R _m = 2.5 kcm², R _i = 60 cm, and C _m = 1.5 F/cm² for CH cells; R _m = 2.0 kcm², R _i = 40 cm, and C _m = 0.9 F/cm² for HS cells; R _m = 2.0 kcm², R _i = 40 cm, and C _m = 0.8 F/cm² for VS cells. An error analysis of the fitting procedure revealed an area of confidence in the R _m -R _i plane within which the R _m -R _i value pairs are still compatible with the experimental data given the statistical fluctuations inherent in the experiments (Figs. 7, 8). We also investigated whether there exist characteristic differences between different members of the same cell class and how much the exact placement of the electrode (within ±100 m along the axon) influences the result of the simulation (Fig. 9). The membrane parameters were further examined by injection of a hyperpolarizing current pulse (Fig. 10). The resulting compartmental models (Fig. 11) based on the passive membrane parameters determined in this way form the basis of forthcoming studies on dendritic integration and signal propagation in the fly tangential cells (Haag et al., 1997; Haag and Borst, 1997).     

Bimetallic copper(II) and zinc(II) complexes of acyclic Schiff base ligands derived from amino acids

The acyclic Schiff-base ligands (2-(OH)-5-(R³)C₆H₂-1,3-(HCNC(R¹)(R²)CO₂H), derived from the dialdehyde 2-hydroxy-5-R-1,3-benzenedicarboxaldehyde (R = Me or t-Bu) and two equivalents of the amino acids glycine, 2,2-diphenylglycine or phenylalanine, have been reacted with the metal acetates M(OAc)₂ (M = Cu, Zn) in the presence of triethylamine, affording the complexes [HNEt₃][M₂(CH₃CO₂)₂(2-(O)-5-(t-Bu)C₆H₂-1,3-(HCNC(R¹)(R²)CO₂)₂] (M = Cu, R¹ = R² = C₆H₅, R³ = Me (1); M = Zn, R¹ = R² = H, R³ = t-Bu (2); M = Zn, R¹ = R² = C₆H₅, R³ = t-Bu (3); M = Zn, R¹ = H, R² = CH₂C₆H₅, R³ = t-Bu (4)) in good yields. The crystal structures of 1·MeCN, 2·, 3·2MeOH, and 4·3MeOH have been determined.     

Filtering impacts of larval and sessile zebra mussels (Dreissena polymorpha) in western Lake Erie

Summary We assessed the feeding biology of veliger larvae of the introduced zebra mussel (Dreissena polymorpha Pallas) in laboratory experiments using inert microspheres as food analogues. Mean clearance rate on 2.87-m beads ranged between 247 and 420 L veliger^–1 day^–1. Clearance rate was unrelated to bead concentration up to 100 beads L^–1, but was positively correlated with veliger shell length. Clearance rates of Dreissena veligers are within the range of those reported for marine bivalve veligers of similar size and for herbivorous Great Lakes microzooplankton, but are orders of magnitude lower than those of settled, conspecific adults. The impact of settled zebra mussel grazing activities on phytoplankton stocks may be up to 1162 times greater than that exerted by veliger populations in western Lake Erie. Based on 1990 size-frequency distributions and associated literature-derived clearance rates, reef-associated Dreissena populations in western Lake Erie (mean depth 7 m) possess a tremendous potential to filter the water column (up to 132 m³ m^–2 day^–1) and redirect energy from pelagic to benthic foodwebs. Preliminary analyses indicate that chlorophyll a concentration is strongly depleted (<1 g L^–1) above Dreissena beds in western Lake Erie.     

The effect of temperature on the respiration rate of meiofauna

Summary The effect of temperature on respiration rate has been established, using Cartesian divers, for the meiofaunal sabellid polychaeteManayunkia aestuarina, the free-living nematodeSphaerolaimus hirsutus and the harpacticoid copepodTachidius discipes from a mudflat in the Lynher estuary, Cornwall, U.K. Over the temperature range normally experienced in the field, i.e. 5–20° C the size-compensated respiration rate (R _c) was related to the temperature (T) in °C by the equation Log₁₀ R _c=-0.635+0.0339T forManayunkia, Log₁₀ R _c=0.180+0.0069T forSphaerolaimus and Log₁₀ R _c=-0.428+0.0337T forTachidius, being equivalent toQ ₁₀ values of 2.19, 1.17 and 2.17 respectively. In order to derive the temperature response forManayunkia a relationship was first established between respiration rate and body size: Log₁₀ R=0.05+0.75 Log₁₀ V whereR=respiration in nl·O₂·ind^-1·h^-1 andV=body volume in nl.TheQ ₁₀ values are compared with values for other species derived from the literature. From these limited data a dichotomy emerges: species with aQ ₁₀2 which apparently feed on diatoms and bacteria, the abundance of which are subject to large short term variability, and species withQ ₁₀1 apparently dependent on more stable food sources.     

Flight of the honey bee VI: energetics of wind tunnel exhaustion flights at defined fuel content,speed adaptation and aerodynamics

To gain information on extended flight energetics, quasi-natural flight conditions imitating steady horizontal flight were set by combining the tetheredflight wind-tunnel method with the exhaustion-flight method. The bees were suspended from a two-component aerodynamic balance at different, near optimum body angle of attack and were allowed to choose their own speed: their body mass and body weight was determined before and after a flight; their speed, lift, wingbeat frequency and total flight time were measured throughout a flight. These values were used to determine thrust, resultant aerodynamic force (magnitude and tilting angle), Reynolds number, total flight distance and total flight impulse. Flights in which lift was body weight were mostly obtained. Bees, flown to complete exhausion, were refed with 5, 10, 15 or 20 l of a 1.28-mol·l^-1 glucose solution (energy content w=18.5, 37.0, 55.5 or 74.0 J) and again flown to complete exhaustion at an ambient temperature of 25±1.5°C by a flight of known duration such that the calculation of absolute and relative metabolic power was possible. Mean body mass after exhaustion was 76.49±3.52 mg. During long term flights of 7.47–31.30 min similar changes in flight velocity, lift, thrust, aerodynamic force, wingbeat frequency and tilting angle took place, independent of the volume of feeding solution. After increasing rapidly within 15 s a more or less steady phase of 60–80% of total flight time, showing only a slight decrease, was followed by a steeper, more irregular decrease, finally reaching 0 within 20–30 s. In steady phases lift was nearly equal to resultant aerodynamic force; tilting angle was 79.8±4.0°, thrust to lift radio did not vary, thrust was 18.0±7.4% of lift, lift was somewhat higher/equal/lower than body mass in 61.3%, 16.1%, 22.6% of all totally analysable flights (n=31). The following parameters were varied as functions of volume of feeding solution (5–20 l in steps of 5 l) and energy content. (18.5–74.0 J in steps of 18.5 J): total flight time, velocity, total flight distance, mean lift, thrust, mean resultant aerodynamic force, tilting angle, total flight impulse, wingbeat frequency, metabolic power and metabolic power related to body mass, the latter related to empty, full and mean (=100 mg) body mass. The following positive correlations were found: L=1.069·10^-9 f ^2.538; R=1.629·10^-9 f ^2.464; P _m=7.079·10^-8 f ^2.456; P _m=0.008v+0.008; P _m=18.996L+0.022; P _m=19.782R+0.021; P _m=82.143T+0.028; P _m=1.245·bm _f ^1.424 ; P _{mrel e}=6.471·bm _f ^1.040 ; =83.248+0.385. The following negative correlations were found: V=3.939–0.032; T=1.324·10^-4–0.038·10^-4. Statistically significant correlations were not found in T(f), L(), R(), f(), P _m(bm _e), P _{m rel e}(bm _e), P _{m rel f}(bm _e), P _{m rel f}(bm _f).Abbreviations A(m²) frontal area - bl(m) body length - bm(mg) body mass - c(mol·1^-1) glucose concentration of feeding solution - c _D (dimensionless) drag coefficient, related to A - D(N) drag - F _w(N) body weight - F _wp weight of paper fragment lost at flight start - f wingbeat frequency (s^-1) - g(=9.81 m·s^-2) gravitational acceleration - I(Ns)=R(t) dt total impulse of a flight - L(N) lift vertical sustaining force component - P _m(J·s^-1=W) metabolic power - P_{m ret} (W·g^-1) metabolic power, related to body mass - R(N) resultant aerodynamic force - Re v·bl·v ^-1 (dimensionless) Reynolds number, related to body length - s(m) v(t) dt virtual flight distance of a flight - s(km) total virtual flight distance - T (N) thrust horizontal force component of horizontal flight - T _a (°C) ambient temperature - t(s) time - t _tot (s or min) total flight time - v(m·s^-1) flight velocity - v(l) volume of feeding solution - W (J) energy and energy content of V - ( °) body angle of attack between body longitudinal axis and flow direction - ( °) tilting angle ( 90°) between R and the horizont in horizontal flight v(=1.53·10^-5m²·s^-1 for air at 25°) kinematic viscosity - (=1.2 kg·m^-3 at 25°C) air density     

The effect of in vitro pretreatments on subsequent shoot organogenesis from excised Rubus and Malus leaves

Shoot regeneration from Rubus leaves was obtained on a medium containing MS salts, vitamins and sugars, Staba vitamins, casein hydrolysate (100 mg l^–1) and 10 M thidiazuron. Shoot regeneration from Malus leaves was obtained on N⁶ rice anther medium with 5 M thidiazuron. In vitro pretreatment of source shoots with either colchicine or thidiazuron enhanced the organogenic potential of detached leaves of two Rubus hybrids. The response to colchicine was quadratic and occurred at non-mutagenic concentrations (75–250 M). The response to thidiazuron was exponential between 0 and 5 M. When applied as a pretreatment, the effectiveness of several different cytokinins (benzyladenine, thidiazuron, zeatin) at enhancing Malus and Rubus organogenesis was related to the shoot proliferation activity of the cytokinin and to treatment-induced variation in leaf and petiole size.Abbreviations BA benzyladenine - 2,4-D 2,4-dichlorophenoxyacetic acid - IBA indolebutyric acid - MS Murashige & Skoog basal medium devoid of plant growth regulators - OI organogenesis-initiating subculture - PTI colchicine pretreatment subculture - PTII cytokinin pretreatment subculture - NAA naphthaleneacetic acid - TDZ thidiazuron - zeatin trans-zeatin     

Do light intensity,temperature and photoperiod affect the entrapment of mites on glandular hairs of cultivated tomatoes?

The effects of plant growth conditions (light intensity, temperature and photoperiod) on the proportion of spider mites (Tetranychus urticae) and predatory mites (Phytoseiulus persimilis) entrapped by type VI trichomes were investigated in the cultivated tomato Lycopersicon esculentum. Trichomes released sticky substances showing rapid hardening when the trichome head was ruptured by contact with mites. Adult individuals of both species of mites were immobilized by exudates in a higher percentage on leaf stalks from plants grown in the light (160 einsteins cm^-2s^-1) than on leaf stalks from plants grown in the shade (50 einsteins cm^-2 s^-1). Leaf stalks from plants grown in the light showed bigger trichome heads. More predatory mites were also entrapped on the leaf stalks from plants grown at 18°C (65% RH) as compared to the ones grown at 24°C (60% RH), whereas trichome heads were bigger under the former conditions. Contrary to leaf stalks, leaflet areas, through differences in trichome density and size, showed no diffences in predator and spider mite entrapment. Trichome head size was probably related to mite entrapment. It is also hypothesised that temperature increase might influence predator entrapment through effects on trichome quality.     

Photoinhibition of photosynthesis in intact kiwifruit (Actinidia deliciosa) leaves: Effect of light during growth on photoinhibition and recovery

Photoinhibition of photosynthesis was induced in intact kiwifruit (Actinidia deliciosa (A. Chev.) C. F. Liang et A. R. Ferguson) leaves grown at two photon flux densities (PFDs) of 700 and 1300 mol·m^-2·s^-1 in a controlled environment, by exposing the leaves to PFD between 1000 and 2000 mol·m^-2·s^-1 at temperatures between 10 and 25°C; recovery from photoinhibition was followed at the same range of temperatures and at a PFD between 0 and 500 mol·m^-2·s^-1. In either case the time-courses of photoinhibition and recovery were followed by measuring chlorophyll fluorescence at 692 nm and 77K and by measuring the photon yield of photosynthetic O₂ evolution. The initial rate of photoinhibition was lower in the high-light-grown plants but the long-term extent of photoinhibition was not different from that in low-light-grown plants. The rate constants for recovery after photoinhibition for the plants grown at 700 and 1300 mol·m^-2·s^-1 or for those grown in shade were similar, indicating that differences between sun and shade leaves in their susceptibility to photoinhibition could not be accounted for by differences in capacity for recovery during photoinhibition. Recovery following photoinhibition was increasingly suppressed by an increasing PFD above 20 mol·m^-2·s^-1, indicating that recovery in photoinhibitory conditions would, in any case, be very slow. Differences in photosynthetic capacity and in the capacity for dissipation of non-radiative energy seemed more likely to contribute to differences in susceptibility to photoinhibition between sun and shade leaves of kiwifruit.Abbreviations and symbols F _o , F _m , F _v instantaneous, maximum, variable fluorescence - F _v /F _m fluorescence ratio - F _i =F _v at t=0 - F F _v at t= - K _D rate constant for photochemistry - k(F _p ) first-order rate constant for photoinhibition - k(F _r ) first-order rate constant for recovery - PFD photon flux density - PSII photosystem II - _i photon yield of O₂ evolution (incident light)     

Length–weight relationships and growth parameters of two endemic fish species (Floridichthys polyommus Hubbs, 1936 and Fundulus persimilis Miller, 1955) from the Yucatan Peninsula,Mexico

This study reports length‐weight relationships and growth parameters for Floridichthys polyommus Hubbs, 1936 and Fundulus persimilis Miller, 1955 from La Carbonera, a karstic tropical coastal lagoon on the northwestern coast of the Yucatan Peninsula, Mexico. Specimens were collected between April 2009 and March 2010. The resulting length‐weight relationship for F. polyommus was: W = 0.0180 Lt^3.37 and W = 0.0142 Lt^3.35 for F. persimilis. This study presents the first estimation for both species of the von Bertalanffy growth model parameters, the growth performance index, the L₅₀, and is the first report of the length‐weight relationship for F. persimilis.     

Interactions of two natural enemies of Tetranychus urticae,the fungal entomopathogen Beauveria bassiana and the predatory mite,Phytoseiulus persimilis

The effect of either untreated or treated adults of the spider mite, Tetranychus urticae Koch (Acari: Tetranychidae) by Beauveria bassiana (Bals.) Vuillemin (Ascomycota: Hypocreales) DEBI008 at 1×10⁶ (conidia/ml) was investigated on developmental stages and life table parameters of Phytoseiulus persimilis Athias-Henriot (Acari: Phytoseiidae) under laboratory conditions. Four time intervals (0, 24, 48 and 72 h post-inoculation of spider mites) were considered for studying the predator characteristics as different treatments. Duration of each life stage, longevity, reproduction rate, intrinsic rate of natural increase (r _m ), net reproductive rate (R ₀), mean generation time (T) and finite rate of increase (λ) of the P. persimilis were calculated on both untreated and B. bassiana treated spider mite adults. Data analysis showed that longevity and fecundity of predatory mites fed on untreated and treated mites (time interval 0) were higher in comparison with other time intervals after inoculation. The entomopathogenic fungus adversely affected longevity and fecundity of the predatory mite. Fertility life table parameters of predatory mites fed on T. urticae treated by B. bassiana at different time intervals showed that T, R ₀, λ and r _m are strongly affected by the fungus presence and these parameters had significant differences among time treatments. The least r _m value was observed in the time interval of 72 h post-inoculation. The fitness of T. urticae was affected by B. bassiana 24, 48 and 72 h post-inoculation of mite adults, and consequently it caused decreased longevity of P. persimilis and accordingly a decrease in the intrinsic rate of natural increase of the predator.     

Growth characteristics of Uranoscopus scaber Linnaeus 1758, inhabiting the Iskenderun Bay (Northeastern Mediterranean)

This study aimed to determine the age and some growth characteristics of Atlantic stargazer (Uranoscopus scaber) from Iskenderun Bay (Northeastern Mediterranean). For this purpose, a total of 150 Atlantic stargazer ranging in size from 9.1 to 28.0 cm in total length (weight: 11.7–345.7 g) were collected as by-catch from a commercial trawl fishing boat at a depth of 80–100 m between May 2015 and January 2016. The bottom trawl gear used was equipped with a 44 mm stretched mesh size net at the cod-end. The percentage of females and males were 46.7% and 53.3% respectively. The total length–weight relationships equation with coefficient of determination (R²) were found as W = 0.011*TL^3.131, R² = .9728, for all individuals, W = 0.015*TL^3.021, R² = .9512 for females and W = 0.0102*TL^3.136, R² = .9553 for males. By using the von Bertalanffy equation, the growth parameters of Atlantic stargazer were estimated to be L_∞ = 42.35 cm, k = 0.098, t₀ = −1.8474 for all individuals; L_∞ = 36.92 cm, k = 0.138, t₀ = −1.2693 for females and L_∞ = 38.77 cm, k = 0.1, t₀ = −2.334 for males. In this study, age reading was done by two independent readers and index of average percentage error (IAPE) was calculated as 6.1%. The highest condition factor value calculated as 1.81 in the age group 6 and the lowest condition factor value was calculated as 1.48 in the age group 1.     

Seasonal and spatial variation of woody tissue respiration in a <Emphasis Type="Italic">Pinus cembra</Emphasis> tree at the alpine timberline in the central Austrian Alps

Total stem, branch, twig, and coarse root respiration (R_t) of an adult Pinus cembra tree at the alpine timberline was measured continuously at ten positions from 7 October 2001 to 21 January 2003 with an automated multiplexing gas exchange system. There was a significant spatial variability in woody tissue respiration when expressed per unit surface area or per unit sapwood volume. Surface area related maintenance (R_m) respiration at 0°C ranged between 0.109 and 0.643 mol m^–2 s^–1 and there was no clear trend with respect to tissue type and diameter. Sapwood volume based R_m at 0°C by contrast, varied between 2.5 mol m^–3 s^–1 in the stem and 193.2 mol m^–3 s^–1 in thin twigs in the upper crown. Estimated Q₁₀ values ranged from 1.7 to 3.1. These Q₁₀ values were used along with R_m at 0°C and annual woody tissue temperature records to predict annual total R_m. Annual total R_m accounted for 73±6% of annual R_t in 2002.