Characterization of Colorado potato beetle lipophorin: A hydrocarbon-rich diacylgycerol-poor lipophorin

• 1.1. The lipid composition of lipophorin from the Colorado potato beetle, Leptinotarsa decemlineata Say, was analyzed.
• 2.2. This insect lipophorin contains 44% lipid and is characterized by large amounts of hydrocarbons and small amounts of diacylglycerol.
• 3.3. This is the first observation of a diacylglycerol-poor insect lipophorin in haemolymph.
• 4.4. Since the main energy source for flight in the Colorado potato beetle is proline, the low diacylglycerol content in lipophorin must be related to its peculiar flight metabolism.
• 5.5. This lipophorin, however, can still take up appreciable amounts of diacylglycerol from the locust fat body. Hydrocarbon uptake by this lipophorin was also demonstrated.
• 6.6. The main function of this lipophorin therefore seems to be transport of hydrocarbons from oenocytes to the cuticle.

     

Environmental and genetic influences on the thermal physiology of Rana sylvatica

• 1.1.|Intraspecific variation in the thermal physiology of Rana sylvatica was examined.
• 2.2.|Heat and cold tolerances of both adult and larval representatives were determined for animals representing populations from New York, Maryland, Kentucky, Ohio, Michigan and Canada.
• 3.3.|In general, frogs from more northern localities exhibited lower heat tolerances.
• 4.4.|There was no evidence of interpopulational differences in cold tolerance. Similar trends were revealed by larval testing.
• 5.5.|Interpopulational differences among laboratory-reared tadpoles suggests a strong genetic component to Rana sylvatica thermal physiology.

     

Contribution of aerobic and anaerobic scope to the total metabolic scope of the desert skink,Chalcides ocellatus (Forskal)

• 1.1. Measurements of aerobic scope (resting and active oxygen consumption rates) and anaerobic scope (resting and active production of lactate rates in the whole body homogenates) were carried out on the desert skink, Chalcides ocellatus at temperatures between 10 and 40°C.
• 2.2. The aerobic scope was maximal around the preferred body temperature with a low thermal temperature dependence above the preferred levels.
• 3.3. During initial stages of forced activity, C. ocellatus employed anaerobic metabolism as its major energy source.

     

Ventilatory rate in the butterfish (Pholis gunnellus) as a consequence of temperature and previous emersion

• 1.1. Observation of ventilation in immersed Pholis gunnellus showed a linear relationship between ventilatory rate and temperature between 8 and 20°C.
• 2.2. At 13°C and after 30 min emersion, ventilatory rate was initially lower than prior to emersion, providing evidence of adequate uptake of O₂ for standard metabolism during the emersion period.
• 3.3. This species has a laterally elongate body form with reduced scales and extensive mucus secretion.
• 4.4. During emersion, gaping behaviour probably exposes the gills and extensively vascularised oesophageal regions to air.
• 5.5. These are considered to be morphological and behavioural adaptations by P. gunnellus, to aerial respiration in the intertidal habitats occupied by this species.

     

Investigation of phycocyanin-membrane interaction: Promotion of membrane interactions

• 1.1. In a continuing investigation of phycocyanin-membrane surface interaction, fluorescence quenching experiments were performed with a mixture of two populations of fluorescence probe-encapsulated phospholipid bilayer vesicles in the presence and absence of phycocyanin.
• 2.2. These membrane vesicles were prepared with 1,2-dimyristoyl phosphatidylcholine (DMPC), cholesterol and a probe molecule.
• 3.3. A fluorophore was encapsulated in one population of membrane vesicles, while a quencher was encapsulated in another population of membrane vesicles.
• 4.4. The result was compared with those of experiments in the presence of other biomolecules, including albumin, cytochrome c, hemoglobin, myoglobin or RNA.
• 5.5. Interestingly, a one-third reduction of the fluorescence intensity was observed in the mixture of these two populations of membrane vesicles in phycocyanin's presence.
• 6.6. In contrast, the other biomolecules caused no significant reduction in the fluorescence intensity.
• 7.7. These findings were evidence of a phycocyanin-induced membrane perturbation.
• 8.8. This was further demonstrated by a phycocyanin-induced change in the thermotropic behavior of DMPC vesicles, as measured by differential scanning microcalorimetry.
• 9.9. Such a unique property of phycocyanin is believed to be associated with its known membrane surface-interacting character.
• 10.10. A possible phycocyanin-modulated membrane-membrane interaction was discussed.

     

Allozyme variation in a dimeric esterase of the oriental fruit fly,Dacus dorsalis (insecta: tephritidae), from peninsular malaysia

• 1.1. Seven natural populations of Dacus dorsalis were analyzed for a dimeric esterase by means of horizontal starch-gel electrophoresis.
• 2.2. The electrophoretic phenotypes were governed by nine codominant Est-D alleles.
• 3.3. The commonest allele in all seven population samples was Est-D¹⁰⁰ which encoded an electrophoretic band with intermediate mobility.
• 4.4. The distribution of EST-D phenotypes were in accordance with Hardy-Weinberg expectations.
• 5.5. There was no geographic variation in the distribution of Est-D alleles.

     

The energy costs of temperature regulation in birds: The influence of quick sinusoidal temperature fluctuations on the gaseous metabolism of the japanese quail (Coturnix coturnix japonica)

• 1.1. Quick sinusoidal temperature fluctuations (constant average 10°C) cause an increase in metabolism in comparison to an invariable constant ambient temperature of the same dimension.
• 2.2. At the observed mean value of 10°C metabolism is increased by 0.8% per 1 K/hr based on the values of resting metabolic rate (correlation: M = 53.5 + 0.445 T_a, M in J/K g hr, T_a = ambient temperature change in K/hr) and 0.6% based on the values of activity metabolism (M = 70.4 + 0.425 T_a).
• 3.3. The absolute augmentation of metabolism per 1 K/hr is, by comparison, the same for day and night. Its amount is 0.42 and 0.43 J/K g hr respectively.
• 4.4. In the response of metabolism to temperature fluctuations no differences could be found with respect to the amplitude and frequency modifications of temperature.
• 5.5. The increase of energy consumption is probably caused to a greater extent by “overshoot” of the feedback control system in the course of adjusting metabolism to new levels according to the ambient temperature conditions.
• 6.6. Short term ambient temperature changes (i.e. measuring different temperature levels in one night to test basic metabolism vs ambient temperature) cannot produce reasonable values for basic metabolic rate, since these artificially high values reflect the testing procedure.

     

Comparative study of hemoglobins from different Artemia populations. The influence of temperature on the oxygen equilibria

• 1.1. The P50 values of extracellular hemoglobin (Hb) of five Artemia populations from different geographical origin are affected by temperature.
• 2.2. The free oxygen binding energy is high for all the populations (ΔH between −34.7 and −56.2kj/mol).
• 3.3. A possible correlation between thermal sensitivity of Hb and the ambient temperature of the habitat must be considered very carefully.
• 4.4. The occurence of different quantities of Hb1 (αα chains) Hb2 (αβ chains) and Hb3 (ββ chains) in the different populations possibly influences thermal sensitivity.

     

The energetics of shedding: Energy content of snake skin

• 1.1. The weight and energy content of sloughed skins of 92 individual snakes of 22 different species in three families were measured.
• 2.2. Weight and total energy content of shed skins were highly correlated with body weight.
• 3.3. The heat of combustion (kJ/g) of sloughed skins varied significantly among families and was higher in species having unkeeled scales than in those with keeled scales.
• 4.4. The presence of keels significantly affected weight of skins, even when skin weight is adjusted for covariance with body weight.
• 5.5. Neither body weight nor ambient temperature significantly affected the heat of combustion of sloughed skins.
• 6.6. The energy content of shed skin, expressed as a proportion of daily metabolism, decreased with ambient temperature, but the effect is minimized in large snakes.
• 7.7. Small snakes expended relatively less energy in sloughed skins than large snakes when the expenditure is expressed in terms of total daily metabolized energy.

     

The effects of acclimatization on body weight and oxygen consumption in Dipodomys panamintinus

• 1.1. Seasonal acclimatization effects on oxygen consumption, body temperature, and body weight were evaluated in three different experimental groups of Dipodomys panamintinus.
• 2.2. Body weights of wild field as well as captive animals housed in outdoor sand cages were maximum in winter and lowest in summer for both sexes.
• 3.3. Mean oxygen consumption was maximum in winter and lowest during spring in both sexes of the wild field and captive exposed groups.
• 4.4. Neither weight nor oxygen consumption of indoor control animals varied with the seasons.
• 5.5. No significant differences in body temperatures were observed during either the fall or winter seasons.

     

Genetic variability in south african blue wildebeest (Connochaetes taurinus)

• 1.1. We used protein gel-electrophoresis to investigate genetic heterogeneity at 33 protein coding loci in a total of 46 blue wildebeest (C. taurinus) kept under different management regimes.
• 2.2. Average heterozygosity ranged from 2.14 to 4.3% and within-population differences accounted for 97.2% of total relative gene diversity.
• 3.3. Comparatively little divergence was found between animals sampled from populations with very diverse population sizes and management histories, with the largest genetic distance estimated between any two populations being only 0.0021.
• 4.4. We discuss our results with particular emphasis on the influence of management history on genetic diversity and divergence in C. taurinus.

     

Genetic diversity in horses inferred from distribution of hemotypes—II. Genetic structure of mixed breed population

• 1.1. Fifteen populations of 10 horse breeds ranging from 110 to 2232 individuals yielded 61 phenotypes of electrophoretic variants at six blood loci.
• 2.2. The numbers of different hemotypes varied from 79 to 239, and the ratios of number of individuals to number of hemotypes varied from 1.38 to 9.34.
• 3.3. The genetic structure of the pooled mixed breed population comprising 11,393 individuals disclosed features similar to those of the least diversified component breeds.
• 4.4. The mean ratio of n individuals to n hemotypes was 11.33.
• 5.5. This figure represents a first direct attempt to estimate the individual genetic diversity in horses.

     

Allozyme variation in a wild african elephant (Loxodonta africana) population from the Kruger National Park,South Africa

• 1.1. Blood, liver, heart, testis, skin, eye, muscle and kidney samples were obtained from elephants (Loxodonta africana) in the Kruger National Park during a culling programme in April 1992.
• 2.2. Gene products of 25 protein coding loci in L. africana were examined by horizontal starch-gel electrophoresis.
• 3.3. Eighteen protein coding loci (72%) displayed monomorphic gel banding patterns whereas only seven (28%) displayed polymorphic gel banding patterns.
• 4.4. Average heterozygosity values for adults, youngsters and the total population are respectively 0.058, 0.024 and 0.047.
• 5.5. Relative gene diversities within and between populations are 84% and 16% respectively.
• 6.6. Two population simulation programmes were utilized to predict the duration of the current variability present in this species, based on current genetic variation and gene transfer from one generation to the next.

     

Breast,hips, and buttocks revisited: Honest fatness for honest fitness

This paper comments on: Low, B. S., Alexander, R. D., and Noonan, K.M. Human hips, breast, and buttocks: Is fat deceptive? Ethology and Sociobiology 8: 249-247, 1987. In it I argue that:

• 1.1. Sexual selection has probably not been the most important selection pressure on
• 2.female human body shape.
• 3.2. Male humans in different cultures find different aspects of the female body attractive
• 4.and therefore are unlikely to have exerted consistent directional sexual selection on
• 5.the female body.
• 6.3. Breast size is not correlated with lactation success.
• 7.4. Visible hip width is not correlated with parturition success.
• 8.5. Women would lower their fitness if they tried to deceive men about their internal
• 9.pelvic dimensions.
• 10.6. There are many alternative hypothesis to explain the existence of fat onwomen's
• 11.breast, hips, and buttocks.

     

Changes in high-energy phosphate metabolism in the water scorpion,Ranatra chinensis,under cold water-warm water stress

• 1.1. To evaluate changes in high-energy phosphate metabolism in the water scorpion (Ranatra chinensis) under restraint and cold water-warm water stresses, in vivo [³¹P]NMR spectra were obtained.
• 2.2. Under restraint stress, arginine phosphate (Arg-P) decreased by 10% after 1 hr and remained at that level thereafter, while β-ATP showed negligible changes over 6 hr.
• 3.3. As the water temperature gradually increased or decreased, the relative concentration of Arg-P decreased due to enzyme regulation.
• 4.4. Repeated cold water-warm water stress, which consisted of repeated 15 min exposures to cold water (5°C) followed by 15 min exposures to warm water (30°C) caused distinct decreases in Arg-P and β-ATP concentration. These decreases were dependent on the frequency of exposure.
• 5.5. Phosphomonoesters (PME) increased not only with restraint stress but also with cold water-warm water stress.
• 6.6. The effect of cold water-warm water stress on high-energy phosphate metabolism was greater than that of restraint stress.

     

Metabolic rates of Calathus melanocephalus (L.) (coleoptera,carabidae) from alpine and lowland habitats (jeløy and finse,norway and drenthe,the netherlands)

• 1.1. Metabolic rates (ml O₂/mg/hr) of three geographically separated populations of the carabid beetle Calathus melanocephalus L. (Finse and Je 10y, Norway and Drenthe, The Netherlands) were measured and compared by ANCOVA.
• 2.2. No significant relationship (P > 0.05) between metabolic rates and body weight or sex of the animals were found.
• 3.3. Individuals mostly acclimated to low temperatures by increased metabolic rates and in the opposite direction to higher temperatures. Individuals collected in early summer also showed higher metabolic rates than those caught later in the autumn.
• 4.4. Contradicting the theory of metabolic cold adaptation, beetles from The Netherlands had the highest metabolic rates, beetles from Finse intermediate rates and beetles from Jeløy the lowest rates.
• 5.5. No significant relation were found between geographical origin of the beetles and their respective chill-coma temperature.

     

The thyroid gland and temperature regulation in the prairie vole,Microtus ochrogaster and the chipmunk Tamias striatus

Absract

• 1.1. The basal metabolism of the vole, Microtus ochrogaster, a non-hibernator is about 80% below that expected for microtine rodents, while the basal metabolism of the chipmunk, Tamias striatus, is about 20% below that expected for small mammals.
• 2.2. Blocking thyroid secretion results in a 3°C improvement in the vole. and a 2°C improvement in the chipmunk, to the highest air temperature tolerated.
• 3.3. Blood levels of thyroxine in both species did not change as a function of ambient temperatures, whereas rates of radioiodine release were reciprocally related to ambient temperature.
• 4.4. There was no indication that the thyroid gland of the chipmunk was ever inactive either preceding, or during, hibernation.

     

A test of the thermal coadaptation hypothesis with black rat snakes (Elaphe obsoleta) and northern water snakes (Nerodia sipedon)

• 1.The thermal coadaptation hypothesis predicts that (1) ectotherms experiencing a narrow range of body temperatures in the wild will evolve to perform well over a narrow range of body temperatures and that (2) the optimal temperature for performance will be equal to the preferred body temperature of the species.
• 2.We tested the predictions of the thermal coadaptation hypothesis with black rat snakes (Elaphe obsoleta) and northern water snakes (Nerodia sipedon) because black rat snakes experience lower and more variable body temperatures than northern water snakes at our study site.
• 3.We measured swimming speed, tongue-flicking speed, and striking speed in black rat snakes, and swimming speed and tongue-flicking speed in northern water snakes.
• 4.Adult water snakes generally had narrower performance breadths and higher optimum performance temperatures than adult black rat snakes.
• 5.Performance breadths were the same for swimming, tongue flicking, and striking within adult black rat snakes, but performance optima for these behaviours differed significantly. Performance breadths differed and performance optima were the same for swimming and tongue flicking within adult northern water snakes.
• 6.The relative swimming performance of neonates of the two species was similar in breadth to that of adults, but the thermal optimum for neonate black rat snakes was higher than that of adults.
• 7.Overall, our results provided support for the thermal coadaptation hypothesis.

     

Effects of temperature and metabolic inhibitors on contraction of anterior byssus retractor muscle of Mytilus

• 1.1. Anterior byssus retractor muscle of Mytilus (ABRM) was stimulated to contract by ACh (acetylcholine) and effects of temperature (5–30°C), FDNB (1-fluoro 2,4 dinitro-benzene) and IAA (iodoacetic acid) on tension response were examined.
• 2.2. Isometric tension was highest at the temperature range of 10–20°C and decreased at higher and lower temperature than that range.
• 3.3. The rate of tension decay after washing of ACh was accelerated by the increase of temperature.
• 4.4. Tension redevelopment after release of 1 % during contraction was much smaller at 5°C than at 20°C.
• 5.5. Tension development by ACh and the rate of tension decay after washing of ACh were remarkably decreased by the treatment of FDNB or IAA.
• 6.6. The above results were discussed from the viewpoint that energy metabolism might be related to catch.

     

Metabolic and behavioral responses of American kestrels to food deprivation

• 1.1. The effect of short-term (79 hr) food deprivation at 27°C on body mass, locomotor activity, body temperature (T_b), and resting oxygen consumption was determined in eleven American kestrels (Falco sparverius).
• 2.2. The change in body mass during resting followed the relation, % mass remaining = 99 e^{0.07(days fasting)}. There was no significant difference in the rate of relative mass loss between males and females.
• 3.3. Locomotor activity, measured as perch hopping, was highly variable in both control and fasted birds and showed no correlation with stage of the fast, basal metabolic rate (BMR), or rate of mass loss during food deprivation.
• 4.4. Body temperatures of fasted birds declined continuously by 0.2–0.4°C per day from 39.3 to 38.3°C.
• 5.5. Both males and females responded to food deprivation with a decrease in metabolism. By the third night of fasting, BMR had declined 23.4% from 0.845 W (bird day)⁻¹ to 0.647 W (bird day)⁻¹. The observed reduction in BMR is 2.4 times that expected from a 1°C decline in T_b (assuming Q₁₀ = 2.5) indicating active suppression of metabolism.