Effects of ingested ivermectin on body mass

Abstract. Adults of Neomyia cornicina (F.) given continuous access to cow dung containing ivermectin at concentrations of 0.5.0.25 and 0.125 μg g^-1, the range found in the dung of injected cattle (Sommer et al. , 1992), were monitored every 12 h for changes in mass and excretory rates over a period of 3–5 days. Compared with the control insects, adult females that had ingested ivermectin showed disrupted patterns of daily mass change, an increase in dawn mass, and greatly reduced rates of excretion. Flies fed continuously with dung containing ivermectin at 0.25 μg g^-1 and 0.125 μg g^-1 in a regime identical to the above showed significantly increased abdominal mass compared with the controls. The observations are discussed in relation to other known effects of ivermectin on insect physiology.     

Determination of the toxicity of faeces of cattle treated with an ivermectin sustained-release bolus and preference trials using a dung fly, Neomyia cornicina

The toxicity of dung from cattle treated with an ivermectin sustained-release bolus was estimated in terms of ivermectin or ivermectin equivalents, using a laboratory bioassay with the dung fly Neomyia cornicina Fabricius (Diptera, Muscidae). The mortalities of flies measured 7 days after feeding for 24 h on dung containing known concentrations of ivermectin (between 0.125 and 1 g ivermectin per gram fresh dung) were compared with the mortalities of insects fed for 24 h on dung from cattle treated 21 days previously with an ivermectin sustained-release bolus. The toxicity of the bolus dung was equivalent to dung containing 0.66 g ivermectin per gram fresh dung. To determine whether insects could differentiate between control dung and dung from bolus-treated cattle, choice-chamber tests were carried out. There was no significant difference in the percentage of females that chose either dung type, suggesting that they were unable to distinguish the dung of bolus-treated cattle from control dung. Results are discussed in relation to the impact that bolus use can have on the insect fauna of cattle dung.     

Occurrence of aflatoxin in some liver curative herbal medicines

Fifty herbal medicine samples of seven different taxa known to cure liver disorders were analysed for aflatoxin contamination. Twenty-three samples, out of 50, were contaminated with various levels of aflatoxins. Amongst the 23 contaminated samples the maximum level of aflatoxin B¹ recorded was 2.23 μg g^-1 in Asparagus racemosus and the minimum 0.28 μg g^-1 in Emblica officinalis . Aflatoxin G¹ was only found in one species, Terminalia belarica . Aflatoxin production of the isolates of Aspergillus flavus was also examined and the highest levels were produced by isolates from A. racemosus (1.07-2.47 μg ml^-1). Aflatoxin contamination of herbal drugs may be a risk for patients because the level of aflatoxins is much higher than the tolerance level fixed by the WHO for foods.     

Feeding responses of the horsefly, Tabanus nigrovittatus, to phagostimulants

ABSTRACT. Wild caught horseflies, Tabanus nigrovittatus Macq. (Diptera, Tabanidae), were presented solutions of 0.15 MNaCl at 37°C containing various concentrations of ATP, ADP, AMP, adenosine, phytic acid or 2,3-diphosphoglycerate in an artificial feeding apparatus. The insects fed upward through a Para-film M® membrane. ADP (ED₅₀ 35 μM) was more potent than ATP (ED₅₀ 112 μM) and AMP (ED₅₀ 382 mUM). All of these diets were deposited in the midgut, an indication that the flies were in the 'blood feeding' mode. Adenosine caused only 23% gorging at 1 mM. Phytic acid caused only 10% gorging at 1 mM and 2,3-diphosphoglyceric acid had no activity at 0.6 mM. Flies would feed only in highly reflective cages under high levels of light intensity (1200–1500 lux) at the membrane surface.     

Pathogenicity of different isolates of Vibrio harveyi in tiger prawn, Penaeus monodon

P.-C. LIU, K.-K. LEE AND S.-N. CHEN. 1996. The pathogenicity of six Vibrio harveyi strains in tiger prawn, Penaeus monodon , was studied, using both live bacteria and extracellular products (ECP). The organisms originally isolated from diseased penaeids were more virulent using both live bacteria and ECP (LD₅₀, 4.87–8.65 times 10⁴colony-forming units (cfu) and 1.20–1.51 μg protein g^-1body weight) than the two reference strains originally isolated from either sea water (ATCC 25919; LD₅₀, 3.18 times 10⁶cfu and 2.70 μg protein g^-1body weight) or diseased Talorchestia sp. (ATCC 14126, 0.418 times 10⁶cfu and 2.34 μg protein g^-1body weight). Each strain was reisolated from the haemolymph and the hepatopancreas of moribund prawns following each bacterial challenge. Both the live bacteria and the ECPs of the penaeid isolates exhibited stronger proteolytic (caseinase), phospholipase and haemolytic activities than those of the reference strains. These results indicate that there are differences between penaeid and non-penaeid isolates of V. harveyi in pathogenicity and reveal that proteases, phospholipases, haemolysins or exotoxins might play leading roles in the pathogenicity of V. harveyi in the tiger prawn, Penaeus monodon .     

STUDIES ON THE FEEDING OF MYZUS PERSICAE (SULZ.) ON RADIOACTIVE PLANTS

Adult apterae of Myzus persicae (Sulz.), were fed, after a period of fasting, on leaves containing radioactive phosphorus. The weight of sap imbibed by the aphids after varying feeding times was estimated by relating their radioactivity, at the end of each feeding period, to the activity per unit fresh weight of the leaf lamina on which they fed. The calculations were made on the assumption that ³²P is uniformly distributed in the leaf tissues.
The mean rates of uptake so estimated were about 10 μg. of sap for the first hour of feeding; 40 μg/hr. between 1 and 4 hr. feeding, and 17 μg./hr. between 6 and 24 hr. feeding. The decrease in apparent rate of uptake with the longer feeding times is attributed to loss of ³²P in nymphs born during the feeding period.
When aphids were fed on seedlings raised in water culture solution containing ³²P no activity was detected after 5 min. feeding and an insignificant fraction after 15 min., but when the isotope was introduced by immersing the leaves for several days in the culture solution, aphids fed for 5 and 15 min. became appreciably active.
The increase in rate of uptake after 1 hr. of feeding indicates that aphids do not start to feed normally until they reach the phloem, but the activity after short feeding times suggests that previously starved aphids feed to some extent on other tissues, possibly only on the epidermis.     

Hydrogen Production by Rumen Holotrich Protozoa: Effects of Oxygen and Implications for Metabolic Control by In Situ Conditions

Experiments with washed suspensions of holotrich protozoa (Isotricha spp. and Dasytricha ruminantium ) showed that both organisms have an efficient 0,-scavenging capability (apparent K_m values 2.3 and 0.3 μM, respectively). Reversible inhibition of H₂, production increased almost linearly with increasing O₂ up to 1.5 μM; higher levels of O₂ gave irreversible inhibition. In situ determinations of H, CH₄, O₂, and CO₂, in ovine rumen liquor, using a membrane inlet mass spectrometer probe, indicated that O₂, was present before feeding at 1-1.5 μM and decreased to undetectable levels (<0.25 μM) within 25 min after feeding. A transient increase in O₂. concentration after feeding occurred only in defaunated animals and resulted in suppression of CH₄ and CO₂ production. The presence of washed holotrich protozoa decreases the O₂ sensitivity of CH₄ production by suspensions of a cultured methanogenic bacterium Methanosarcina barkeri . It is concluded that holotrich protozoa play a role in ruminal O₂ utilization as well as in the production of fermentation end products (especially short-chain volatile fatty acids) utilized by the ruminant and H, utilized by methanogenic bacteria. These hydrogenosome-containing protozoa thus both control patterns of fermentation by influencing O₂ levels, and are themselves regulated by the low ambient O₂ concentrations they experience in the rumen.     

Effects of mammalian gonadotropin-releasing hormone analogue, pimozide, and the combination on plasma gonadotropin levels in different seasons and induction of ovulation in female catfish

In the catfish Heteropneustes fossilis , 0.5μg g-¹ B.W. mGnRH-A alone or the low dose of 0.05 μg g^-1 B.W. in combination with pimozide [a dopamine (DA)-receptor antagonist, 5 or l0μg g^-1 B.W.], caused a preovulatory surge in plasma gonadotropin (GTH) and induced a high rate of ovulation. The ovulatory response of the catfish to the low dose of mGnRH-A when given alone was not effective in the early (July) but was effective in the late spawning season (August). Plasma GTH response to these treatments showed seasonal variations. Pimozide administration potentiated the response to mGnRH-A in a season-dependent manner, being effective only in the prespawning and spawning phases. Pimozide treatment alone did not affect plasma GTH. These observations suggest that the release of GTH from the pituitary is subject to seasonal differences in the sensitivity of the GnRH system and the degree of its modulation by dopamine.     

Development of bile salt-dependent lipase in larval turbot

Pancreatic bile salt-dependent lipase (BSDL) was present with 0·5 μg BSDL larva⁻¹ from hatching in turbot larvae. The enzyme content increased during the yolk sac phase to 1·1 μg BSDL larva⁻¹. This suggests that larval turbot are able to digest lipids from the start of exogenous feeding. The BSDL synthesis was stimulated first by food about 5 days after the onset of first feeding. The content per larva increased exponentially in fed larvae to 20 μg BSDL larva⁻¹ on day 23 after hatching and decreased in starved larvae. In contrast, the specific content decreased during the first feeding phase, meaning that smaller larvae had a higher content of enzyme related to their biomass than did bigger larvae.     

The nectar of the Strelitzia reginae flower

The nectar of Strelitzia reginae Ait. was analysed using enzymatic methods and found to contain glucose, fructose and sucrose. Sugar composition changed considerably over the nectar producing period: there was an increase in the amount of glucose (41%) and fructose (32%) between the early and middle stage of secretion and thereafter a decrease of 13 and 24%, respectively, towards the end of secretion. Although the amount of sucrose secreted was initially as much as the glucose and fructose combined, it subsequently decreased, first by 14% and then by 70% at the end of the secretory period so that, whereas in the initial stages of secretion sucrose was quantitatively the dominant sugar, glucose and fructose made up the major part of the nectar as secretion reached its conclusion.
The amounts of potassium and sodium remained at the same low level (around 150 and 30 μg g^-1 [w/v) respectively) throughout secretion, while calcium (initially 18 μg g^-1) and magnesium (initially 8.0 μg g^-1) increased by 47 and 56% respectively, between the early and late stages of secretion. No free amino acids, inorganic phosphate or iron could be detected. Enzymatic analysis revealed only a trace amount of starch. Transmission electron micrographs from both immature and mature plants, however, showed starch grains among other cytoplasmic remnants in the nectary lumen. Mitochondria, vesicles, lipid droplets and ribosomes could also be identified among the luminal cytoplasmic remnants.     

Acid-induced acute toxicity of aluminium to three species of filter feeding caddis larvae (Trichoptera, Arctopsychidae and Hydropsychidae)

1. Arctopsyche ladogensis , Hydropsyche angustipennis and Hydropsyche siltalai larvae were exposed to nominal aluminium concentrations of 0, 625, 1250, 2500 and 5000 μg Al l^–1 at pH 5.0 for 96 h. Larvae reared at pH 6.4 and without any aluminium treatment were used as controls. Morphological abnormalities in the anal papillae of the larvae were used as the response variable in estimating the median effective concentrations (EC₅₀) of aluminium.
2. No morphological abnormalities were observed in the control larvae. Only a few individuals of A. ladogensis had darkened anal papillae at pH 5.0 without additional aluminium treatment, whereas increasing aluminium concentrations significantly increased the number of individuals in all species displaying darkening and reduction of the papillae.
3. A. ladogensis appeared to be the most sensitive species to increasing aluminium concentrations, as reflected by the significantly lower mean EC₅₀ value for this species compared with those of H. siltalai and H. angustipennis . H. angustipennis larvae were the most tolerant to aluminium.
4. The results indicate that interspecific differences in sensitivity to aluminium may be a key factor influencing the guild structure of filter feeding caddis flies in acidified streams. The results also imply that toxic effects of aluminium on filter feeding caddis larvae occur due to the impairment of normal osmoregulation processes via damage to the ion-regulatory organs.     

Acid-induced acute toxicity of aluminium to three species of filter feeding caddis larvae (Trichoptera, Arctopsychidae and Hydropsychidae)

1. Arctopsyche ladogensis , Hydropsyche angustipennis and Hydropsyche siltalai larvae were exposed to nominal aluminium concentrations of 0, 625, 1250, 2500 and 5000 μg Al l^–1 at pH 5.0 for 96 h. Larvae reared at pH 6.4 and without any aluminium treatment were used as controls. Morphological abnormalities in the anal papillae of the larvae were used as the response variable in estimating the median effective concentrations (EC₅₀) of aluminium.
2. No morphological abnormalities were observed in the control larvae. Only a few individuals of A. ladogensis had darkened anal papillae at pH 5.0 without additional aluminium treatment, whereas increasing aluminium concentrations significantly increased the number of individuals in all species displaying darkening and reduction of the papillae.
3. A. ladogensis appeared to be the most sensitive species to increasing aluminium concentrations, as reflected by the significantly lower mean EC₅₀ value for this species compared with those of H. siltalai and H. angustipennis . H. angustipennis larvae were the most tolerant to aluminium.
4. The results indicate that interspecific differences in sensitivity to aluminium may be a key factor influencing the guild structure of filter feeding caddis flies in acidified streams. The results also imply that toxic effects of aluminium on filter feeding caddis larvae occur due to the impairment of normal osmoregulation processes via damage to the ion-regulatory organs.     

Defecation, apparent absorption efficiency, and the importance of water obtained in the food for water balance in captive brown long-eared (Plecotus auritus) and Daubenton's (Myotis daubentoni) bats

Mean apparent dry mass absorption efficiency by P. auritus fed on mealworms was 0.853 (S.D.=0.4, n=43). Mean apparent energy absorption efficiency by P. auritus and M. daubentoni fed on mealworms was 0.90 (S.D.=0.007, n=8). The mean energy content of mealworms was 28.6 kJ.g^-1 dry mass (S.D.=1.1, n=8), and that of faeces was 19.5 kJ.g^-1 (S.D.=0.7, n=8) in P. auritus and 19.9 kJ.g^-1 (S.D.=1.3, n=8) in M. daubentoni . Water content of mealworms was 61.1% wet mass (S.D.=1.4, n=173); water content of faeces was 73.3% in P. auritus (S.D.=6.8, n=76) and 72.3% (S.D.=7.0, n=42) in M. daubentoni . Oven-dried mealworms consisted of <1% ash, <1% carbohydrate, 31% lipid and 39% protein. We suggest that the dry mass unaccounted for (28%) represented chitin, of which 59% was apparently absorbed during digestion. Apparent absorption by mass of both lipid and protein by P. auritus fed on mealworms was greater than 90%. Cumulative post-prandial defecation was sigmoidal in both bat species with 50% (by mass) of faeces being voided within 4 h and 95% within 12 h of feeding. On the basis of previous measurements, using doubly-labelled water, of daily energy expenditure and water flux in free-living P. auritus , we predict that water intake via the food, as free water and as potential metabolic water, represents 20 to 40% of total daily water flux for P. auritus during lactation in the wild.     

The magnetic immuno-polymerase chain reaction assay for the detection of Campylobacter in milk and poultry

L. DOCHERTY, M.R. ADAMS, P. PATEL AND J. McFADDEN. 1996. A rapid and sensitive technique, based on the magnetic immuno-polymerase chain reaction assay (MIPA), was developed for the detection of Campylobacter jejuni in milk and chicken products. Target bacteria are captured from the food sample by magnetic particles coated with a specific antibody and the bound bacteria then lysed and subjected to PCR. The MIPA could detect 420 cfu g^-1of chicken after 18 h, 42 cfu g^-1after 24 h, and 4.2 cfu g^-1after 36 h enrichment. For artificially contaminated milk 63 cfu ml^-1could be detected after 18 and 24 h and 6.3 cfu ml^-1after 36 h enrichment.     

The response to capture and confinement stress of plasma cortisol, plasma sex steroids and vitellogenic oocytes in the marine teleost, red gurnard

Reproductively active female red gurnard Chelidonichthys kumu were captured on long-lines, and placed in confinement tanks for 24, 48, 72 and 96 h to examine the effect of capture and confinement on reproductive parameters (experiment I). Plasma cortisol at the time of capture was elevated to levels typical of stressed fish in other species (53–125 ng ml⁻¹). Final plasma cortisol levels in red gurnard confined for any length of time were not significantly different from one another (ranging from 17 to 43 ng ml⁻¹), indicating that fish were chronically stressed when held in captivity for up to 96 h after capture. When initial and final plasma cortisol levels were compared within confinement groups, cortisol decreased significantly after 24 and 96 h of confinement indicating that some acclimation to captivity may have occurred. In contrast, plasma 17β-estradiol (E₂) and testosterone (T) levels decreased significantly to levels comparable to those in post-spawned fish, after any period of confinement, and remained low throughout the experiment. Another group of fish was captured and confined in the same manner as experiment I but subjected to repeated blood sampling every 24 h, until 96 h post-capture. In these fish, plasma cortisol levels decreased significantly from 127 ng ml⁻¹ after 24 h confinement and thereafter showed no change (25–45 ng ml⁻¹). Plasma E₂ decreased significantly after 72 h of confinement while plasma T showed no change from levels at capture. Increased amounts of follicular atresia were found in vitellogenic oocytes of fish confined for longer periods of time in experiment I, indicating that capture and confinement stress affect reproduction negatively in captive wild fish.     

Influence of bicarbonate and metal ions on the development of root Fe(III) reducing capacity by Fe-deficient cucumber (Cucumis sativus) plants

The effect of bicarbonate and selected metal ions on the development of enhanced root Fe(III) reducing capacity (a response to Fe deficiency of dicotyledons) was studied in young plants of cucumber ( Cucumis sativus L. cv. Ashley) grown in nutrient solution. Pretreatment of 11-day-old Fe-deficient cucumber plants with 20 m M NaHCO₃, for at least 23 h prior to determination of root Fe(III) reducing capacity, markedly inhibited this response. The inhibitory effect of bicarbonate could be partly reversed by a 4- to 8-h treatment with either 10 μ M MnSO₄, 10 μ M FeEDDHA, 2 μ M ZnSO₄, 0.5 μ M NiCl₂, or 0.25 μ M , or CoSO₄ (final concentrations), added to the nutrient solution. By contrast, the addition of other salts of metal ions, like CuSO₄ and Cd(NO₃)₂, at 0.25, 0.5 or 1 μ M , or MgSO₄, at 0.5, 1 or 2 m M (final concentrations), had no beneficial effect. The results suggest that bicarbonate may inhibit the development of root Fe(III) reducing capacity by diminishing the availability of certain metal ions required for this response.     

The effect of light intensity and spectrum on the incidence of first feeding by larval haddock

Under full–spectrum white light, feeding success of haddock Melanogrammus aeglefinus first feeding larvae, as measured both by proportion of larvae feeding and mean prey consumed, peaked at 1·7-18 μmol s^-1 m^-2. Feeding was significantly reduced at lower and higher intensities. A similar result was observed for larvae feeding under blue (470 nm) light, with significantly greater feeding success at intermediate light intensity (1·8 μmol s^-1 m^-2). When different light qualities were compared, larvae had significantly greater feeding success when exposed to blue (470 nm) light than either full-spectrum white or green (530 nm) light. Haddock larvae were capable of prey capture under all light treatments tested, indicating a necessary degree of adaptive flexibility in feeding response. The results are consistent with predisposition of haddock larvae to optimal feeding in a visual environment comparable with open ocean nursery grounds. Information on the impact of light on haddock first feeding can be incorporated into models of larval growth, survival, year-class strength and recruitment, and assist in developing husbandry protocols to maximize larval survival in aquaculture.     

Ascorbic acid and α-tocopherol levels in larvae of Atlantic halibut before and after exogenous feeding

Ascorbic acid (AA) and α-tocopherol (α-TOH) levels in whole Atlantic halibut larvae were constant during the yolk sac stage at 170 and 131 ng individual⁻¹, respectively. At hatching c . 80% of the AA and 97% of the α-TOH were contained within the yolk-sac compartment. With development, AA and α-TOH levels in the yolk decreased, at different rates. At first feeding (at 200 day degrees post hatch, D°PH)>95% of AA but <30% of α-TOH in the yolk at hatching had been transferred to the larval body. Transfer of α-TOH was completed at 360 D°PH, when the yolk was completely absorbed. The plankton offered to the larvae at first feeding (chiefly Temora longicornis ) contained 756 μg g⁻¹ AA and 120 μg g⁻¹α-TOH (dry weight). The AA content increased to 472 ng individual⁻¹ within one week after first feeding, while it declined slightly in unfed larvae. In fed larvae the AA content reached c . 3500 ng individual⁻¹ at 580 D)PH. The α-TOH content increased only slightly in the first week of feeding (206 to 431 D°PH), but then increased to > 800 ng individual⁻¹ at 483 D°PH.     

Increase in respiratory rate during feeding in larvae of the cinnabar moth Tyria jacobaeae

ABSTRACT. This study tested the effect of diet and phase of the feeding cycle on oxygen consumption by fifth-instar larvae of the cinnabar moth Tyria jacobaeae (L.) (Lepidoptera: Arctiidae). There was no significant variation in respiratory rates among larvae fed different diets, which were floral parts, upper, middle and lower leaves of the host plant tansy ragwort, Senecio jacobaea. The respiratory rates ( x ± 95% Cl μlO₂h^-1) of feeding larvae (279.5 ± 30.9) were higher than those of larvae at rest (179.7 ± 12.2), but were not significantly different from those of larvae in the post-ingestive phase (272.8 ± 35.8).
The respiratory rates of feeding larvae increased linearly with the ingestion rate, such that an additional 21.1 μl O₂ were consumed for every mg dry mass of plant material eaten per hour.     

Dietary ascorbic acid requirements during the hatchery production of turbot larvae

The effect of high ascorbic acid (AA) levels transferred through enriched live food was evaluated for turbot Scophthalmus maximus larvae in two consecutive feeding experiments. The same feeding strategy was applied to all treatments, except for the AA content of the live food which was manipulated through bioencapsulation with ascorbyl palmitate. This resulted finally in a low, medium and high-AA treatment. The AA incorporation levels in the turbot larvae (up to 1400 μg AA g DW⁻¹) were correlated with the AA content of the live food administered. However, feeding the high AA concentration resulted in the same values as for the medium treatment, indicating a saturation of the body AA reserves. Under standard culture conditions, no differences in growth nor overall survival could be detected among the different groups, illustrating that the dietary AA requirements of larval turbot are met by non-enriched live food containing already 500 μg AA g DW⁻¹. The larvae of the high-AA treatment, however, showed a better pigmentation rate (47 and 32% for experiments 1 and 2, respectively) compared to the other groups (35 and 25%, respectively). Evaluation of the physiological condition applying a salinity stress test revealed an improvement by feeding extra AA, significantly in the medium-AA treatment. Though not significantly different, cumulative mortalities after challenge with Vibrio anguillarum amounted to 50% for the control v. 40% for the fish fed medium and high-AA diets, respectively. Moreover, the onset of mortalities in this study was slower (not significantly) for the fish fed the extra AA.