The growth analysis of water hyacinth,Eichhornia crasipes solms,in different water temperature conditions

A 40-day culture experiment of water hyacinth was made in 4 different water temperatures, 15, 20, 25 and 30°C, which were combined with 4 levels of concentration of culture solution, 1/3, 1, 3 and 9-fold of the standard solution containing 28 ppm of totalN and 7.7 ppm of totalP. The optimum condition for obtaining the maximum plant growth shifted from 30°C: 3-fold condition in the early stage to 20–25°C: 3-fold condition in the later stages of the experiment. The relation between the fresh weight biomass per 100-l tank,w, and the concentration of culture solution,f, was expressed successfully by a reciprocal equation,1/w=A F/f+A F ^′f/(1-f/C F)+B F, in whichA f,A f′, andB f are time dependent coefficients andC f is the upper limit of the concentration to permit plant growth which can change with time. The relation betweenw and water temperature,T, was expressed by another reciprocal equation,1/w=A T/e ^aT+A T^′e^bT+B T, in whicha andb are constants andAt At′ andB t are time dependent coefficients. The latter formulation shows that the temperature can be breated as an exponential factor, and it suggests the possibility of the growth coefficient of the logistic growth equation, ψ, being affected by temperature.     

Interactive effects of elevated temperature and drought on plant carbon metabolism: A meta-analysis

Elevated temperature (T_e) and drought often co-occur and interactively affect plant carbon (C) metabolism and thus the ecosystem C cycling; however, the magnitude of their interaction is unclear, making the projection of global change impacts challenging. Here, we compiled 107 journal articles in which temperature and water availability were jointly manipulated, and we performed a meta-analysis of interactive effects of T_e and drought on leaf photosynthesis (A_growth) and respiration (R_growth) at growth temperature, nonstructural carbohydrates and biomass of plants, and their dependencies on experimental and biological moderators (e.g., treatment intensity, plant functional type). Our results showed that, overall, there was no significant interaction of T_e and drought on A_growth. T_e accelerated R_growth under well-watered conditions rather than under drought conditions. The T_e × drought interaction on leaf soluble sugar and starch concentrations were neutral and negative, respectively. The effect of T_e and drought on plant biomass displayed a negative interaction, with T_e deteriorating the drought impacts. Drought induced an increase in root to shoot ratio at ambient temperature but not at T_e. The magnitudes of T_e and drought negatively modulated the T_e × drought interactions on A_growth. Root biomass of woody plants was more vulnerable to drought than that of herbaceous plants at ambient temperature, but this difference diminished at T_e. Perennial herbs exhibited a stronger amplifying effect of T_e on plant biomass in response to drought than did annual herbs. T_e exacerbated the responses of A_growth and stomatal conductance to drought for evergreen broadleaf trees rather than for deciduous broadleaf and evergreen coniferous trees. A negative T_e × drought interaction on plant biomass was observed on species-level rather than on community-level. Collectively, our findings provide a mechanistic understanding of the interactive effects of T_e and drought on plant C metabolism, which would improve the prediction of climate change impacts.     

Thermoregulatory responses to egg cooling in incubating bantam hens

Summary O₂ consumption, electromyographic activity (EMG), heart rate (HR), cloacal temperature (T _b) and broodpatch temperature (T _sb) were measured in bantam hens incubating eggs of different temperatures (T _e). For comparison, the metabolic response to low ambient temperature (T _a) was measured in non-incubating hens.O₂ consumption increased nearly linearly with decreasingT _e down to 30°C. At this temperature O₂ consumption was about 3.5 x the resting level. Below 30°C O₂ consumption increased non-linearly, and reached 4.6 x the resting consumption at 15°C. Eggs of 10 and 0°C gave no further increase. Pectoral muscle EMG and HR also increased in response to egg cooling. The onset of egg cooling was associated with a decrease inT _b andT _sb. Hens exposed to lowT _a showed a lower critical temperature of about 24°C.It is concluded that heat loss from the brood-patch during incubation of cold eggs is compensated by shivering thermogenesis. AtT _e below 15°C heat production is at a maximum level, corresponding to the expected O₂ consumption at exposure to an ambient temperature of –65°C.Abbrevations EMG electromyography - T _a ambient temperature - T _b cloacal temperature - T _e egg temperature - T _sb brood-patch skin temperature     

Effect of incubation temperature and androgens on dopaminergic activity in the leopard gecko, Eublepharis macularius

Male leopard geckos that hatch from eggs incubated at a female‐biased temperature (T_f) behave differently when compared with males hatching at a temperature which produces a male‐biased sex ratio (T_m). We investigated the effect of incubation temperature and androgen implantation on aspects of the dopaminergic system of T_f and T_m males. Our data suggest that more dopamine (DA) is stored in the nucleus accumbens of naive T_f males compared with naïve T_m males when they encounter a receptive female conspecific across a barrier. No difference was measured in the preoptic area and the ventral tegmental area (VTA). This difference in intracellular DA levels in a motivation‐related brain nucleus might be correlated with differences in sociosexual behavior observed between the two morphs. There were no differences in tyrosine hydroxylase (TH) expressing cell numbers in the VTA of cholesterol (CH)‐implanted naive castrated T_f and T_m males. Only T_f males implanted with testosterone had significantly higher TH immunopositive cell numbers in the VTA compared with CH‐ and dihydrotestosterone‐implanted T_f males. These data indicate that both the embryonic environment as well as the circulating hormonal milieu can modulate neurochemistry, which might in turn be a basis for individual variation in behavior. © 2007 Wiley Periodicals, Inc. Develop Neurobiol, 2007     

The effect of exogenous catecholamines on the ventilatory and cardiac responses of normoxic and hyperoxic rainbow trout,Oncorhynchus mykiss

Ventilation frequency, opercular pressure amplitude, heart rate, dorsal aortic pressure, arterial pH, arterial O₂ tension, and plasma catecholamine levels were recorded in rainbow trout, Oncorhynchus mykiss, during normoxia (19.7 kPa, 148 mmHg) or hyperoxia (51.2 kPa, 384 mmHg) after injection of various concentrations of catecholamines. In normoxic fish, adrenaline injection resulted in a depression of arterial O₂ tension, hypoventilation due to a drop in ventilation frequency, and a drop in heart rate, while dorsal aortic pressure increased. Noradrenaline depressed ventilation frequency, but opercular pressure amplitude increased to a far greater extent, and dorsal aortic pressure increased. During hyperoxia, adrenaline injection lowered ventilation frequency, opercular amplitude and heart rate, but dorsal aortic pressure increased. The stimulatory effects of noradrenaline on ventilation were abolished during hyperoxia, but the cardiac responses were similar to those seen during normoxia. These results indicate that catecholamines can modify the ventilatory output from the respiratory centre, and modification of ventilation frequency can occur independently of opercular pressure amplitude.Abbreviations f _g ventilation frequency - HPLC high performance liquid chromatography - P _op opercular pressure amplitude - f _h heart rate - P _DA dorsal aortic pressure - pH_a arterial pH - P _aO₂ arterial oxygen tension - PO₂ oxygen tension     

THE INFLUENCE OF MATING SYSTEM AND OVERLAPPING GENERATIONS ON EFFECTIVE POPULATION SIZE

The effective population size (N_e) depends strongly on mating system and generation time. These two factors interact such that, under many circumstances, N_e is close to N/2, where N is the number of adults. This is shown to be the case for both simple and highly polygynous mating systems. The random union of gametes (RUG) and monogamy are two simple systems previously used in estimating N_e, and here a third, lottery polygyny, is added. Lottery polygyny, in which all males compete equally for females, results in a lower N_e than either RUG or monogamy! Given nonoverlapping generations the reduction is 33% for autosomal loci and 25% for sex-linked loci. The highly polygynous mating systems, harem polygyny and dominance polygyny, can give very low values of N_e/N when the generation time (T) is short. However, as T is lengthened, N_e approaches N/2. The influence of a biased sex ratio depends on the mating system and, in general, is not symmetrical. Biases can occur because of sex differences in either survival or recruitment of adults, and the potential for a sex-ratio bias to change N_e is much reduced given a survival bias. The number of juveniles present also has some influence: as the maturation time is lengthened, N_e increases.     

Theoretical studies on the role of food exploitation for the competition of scaamble type

A model was made to clarify the basic processes of competition to occur among larvae by the exploitation as defined byBakker (1969). It was found that this model is applicable to the experimental results on the food exploitation among Droshophila larvae obtained byBakker (1961). In the model the preimaginal stage is divided into two periods;T_f which is the time that a group of larvae spends in exhausting the food after hatching, and T_s which is the duration of the starvation period after T_f.T_f and then W_l (larval body weight) just after the end of T_f are decided by F_s (amount of food supplied per larva at larval hatching) and F_c (amount of food consumed per larva).T_f affects on the onset of T_s as well as R_l (rate of decrease in the individual body weight during T_s).W_a (weight of emerging adults) is gotten by a subtraction of R_l from W_l just after the end of T_f,R_e is affected directly by these components of W_l and R_l. As a result, W_a and R_e are expressed by functions of F_s. This model confirmed that the food exploitation lead to the competition of scramble type. Finally it was suggested that there exist some strategies which prevent ill-effects owing to the food exploitation.     

Thermal clamping of temperature-regulating flowers reveals the precision and limits of the biochemical regulatory mechanism

The flowers of several families of seed plants warm themselves when they bloom. In some species, thermogenesis is regulated, increasing the rate of respiration at lower ambient temperature (T _a) to maintain a somewhat stable floral temperature (T _f). The precision of this regulation is usually measured by plotting T _f over T _a. However, such measurements are influenced by environmental conditions, including wind speed, humidity, radiation, etc. This study eliminates environmental effects by experimentally ‘clamping’ T _f at constant, selected levels and then measuring stabilized respiration rate. Regulating flowers show decreasing respiration with rising T _f (Q ₁₀ < 1). Q ₁₀ therefore becomes a measure of the biochemical ‘precision’ of temperature regulation: lower Q ₁₀ values indicate greater sensitivity of respiration to T _f and a narrower range of regulated temperatures. At the lower end of the regulated range, respiration is maximal, and further decreases in floral temperature cause heat production to diminish. Below a certain tissue temperature (‘switching temperature’), heat loss always exceeds heat production, so thermoregulation becomes impossible. This study compared three species of thermoregulatory flowers with distinct values of precision and switching temperature. Precision was highest in Nelumbo nucifera (Q ₁₀ = 0.16) moderate in Symplocarpus renifolius (Q ₁₀ = 0.48) and low in Dracunculus vulgaris (Q ₁₀ = 0.74). Switching temperatures were approximately 30, 15 and 20°C, respectively. There were no relationships between precision, switching temperature or maximum respiration rate. High precision reveals a powerful inhibitory mechanism that overwhelms the tendency of temperature to increase respiration. Variability in the shape and position of the respiration–temperature curves must be accounted for in any explanation of the control of respiration in thermoregulatory flowers.     

Thermoregulation as a limit to habitat use in alpine marmots (Marmota marmota)

Summary The body temperature (T _b) of free-living alpine marmots rose with activity; the higher the effective environmental temperature (T _e), the higher the rise. Maximum T _bof 40° C was reached at the time of greatest activity in late afternoon or evening. The activity pattern was strongly influenced by the microclimate. Up to an T _eof 25° C the animals spent more time above ground and were more active the higher T _ewas, but above 25° C this trend was reversed, and the animals withdrew increasingly into their burrows. On warm days the activity pattern was therefore bimodal and above ground presence was reduced, in contrast to cool days. Hence behavioural thermoregulation limits the available time for above ground activity on days with high T _ein this strictly diurnal species. We suggest that the alpine marmots' preference for south oriented slopes is due to the better conditions for hibernation there, the microclimate during summer is more favourable on northerly slopes. Thermoregulatory constraints could also keep alpine marmots away from lower elevations.     

Temperature regulation and microhabitat choice by free-ranging Galapagos fur seal pups (Arctocephalus galapagoensis)

Summary Behavioural activity, and core and surface temperatures of 4 unrestrained Galapagos fur seals were recorded in the natural habitat during their first weeks of life. Climatic variables were registered simultaneously. Pup behaviours were divided into bouts of resting (55% of total time), sucking (23%) and other activities (22%). Pups maintained a constant body temperature from their first day. Core temperature (T _e ) was 37.7° C±0.3° C (x ± SD) over 39 pup-days and 8 pup-nights. Skin temperature was correlated with T _c , but flipper temperature was not. No daily T _c rhythm was detected. Microclimate data were used to calculate operative temperature T _e . Environmental temperatures can be very high, with T _e above T _c 6–9 h a day for animals exposed to the sun, but below it in the shade. T _c is about 22° C at night. Pups avoid overheating mainly by withdrawing into the shade and reducing activity to a minimum during the hot hours of the day. Sun-exposed pups could be active at any time during the day if they had access to water, which was usually around high tide.     

In vitro synthesis and characterization of bacteriochlorophyll-<Emphasis Type="Italic">f</Emphasis> and its absence in bacteriochlorophyll-<Emphasis Type="Italic">e</Emphasis> producing organisms

Bacteriochlorophyll(BChl)-f which has not yet been found in natural phototrophs was prepared by chemically modifying chlorophyll-b. The retention time of reverse-phase high-performance liquid chromatography of the synthetic monomeric BChl-f as well as its visible absorption and fluorescence emission spectra in a solution were identified and compared with other naturally occurring chlorophyll pigments obtained from the main light-harvesting antenna systems of green sulfur bacteria, BChls-c/d/e. Based on the above data, BChl-f was below the level of detection in three strains of green photosynthetic bacteria producing BChl-e.     

Characterization of a signal peptide sequence in the cell-free translation product of sheep elastin mRNA

In vitro explant cultures of near-term sheep nuchal ligament secrete tropoelastin of approximate M_r 70,000–72,000 while the elastin cell-free product of sheep nuchal ligament RNA is 2000 to 3000 M_r larger. Automated Edman degradation of immunoprecipitates of radiolabeled cell-free elastin precursor demonstrated the presence of a 26-residue signal sequence which was absent from sheep tropoelastin secreted from explant cultures. In addition, a 20-residue overlap was established between the cell-free product and the secreted protein. This overlap region, representing the N-terminal sequence of ovine tropoelastin, demonstrated complete homology with the N-terminal sequence of porcine tropoelastin and near complete homology with chick tropoelastin. These findings suggest that cotranslational removal of this hydrophobic peptide extension is likely a correlate of vectorial transport of elastin into the secretory apparatus.     

Use of operative temperature and standard operative temperature models in thermal biology

Operative temperature (T_e) and standard operative temperature (T_es) models have been used to address ecological questions about the thermal biology of ectotherms and endotherms for over 25 years. This review focuses on the accuracy and use of T_e and T_es models in ecological and physiological studies. The utility of T_e and T_es models lie in the fact that they take a multivariate problem involving inputs of air temperature, ground temperature, solar radiation, and wind speed and map them into a single thermal metric on a spatial scale appropriate for the animal. The most reliable T_e models are copper casts that mimic the morphology and absorptivity of an animal. Simplified T_e models such as cylinders and spheres have been shown to produce errors in T_e as large as 12 °C under certain conditions and should only be used after careful calibration against a live animal. The accuracy of heated T_es models has been addressed in much less detail then that of T_e models. When calibrated and used under conditions of low solar radiation, heated taxidermic mounts and simplified T_es models produce errors in net heat production on the order of 5% or less. In order to provide reliable data, all types of models must be calibrated over an ecologically realistic range of environmental conditions experienced by the animal. This advice has been largely ignored in the literature, where 61% of the of studies examined failed to properly calibrate the models prior to use. Additionally, studies using these models tend to lack experimental rigor, using only one or two models to make measurements on 1 or 2 days of the active season. When used correctly, T_e and T_es models can be powerful tools for integrating the thermal environment experienced by an animal into a single metric that can address questions regarding the ecology, physiology, and behavior of endotherms and ectotherms. However, until investigators make the effort to use these models in a scientifically valid manner with proper calibration and experimental design their value to thermal biologists will be limited.     

Long-term acid-induced wall extension in an in-vitro system

When frozen-thawed Avena sativa L. coleoptile and Cucumis sativa L. hypocotyl sections, under tension, are acid-treated, they undergo rapid elongation (acid-extension). The acid-extension response consists of two concurrent phases: a burst of extension which decays exponentially over 1–2 h (ExE), and a constant rate of extension (CE) which can persist for at least 6 h. The extension (AL) is closely represented by the equation: L = a – a · e ^kt + c · t where a is the total extension of the exponential phase, k is the rate constant for ExE, and c is the rate of linear extension (CE). Low pH and high tension increased a and c, whereas temperature influenced k. The magnitude of the CE (over 50% extension/10 h), the similarity in its time course to auxin-induced growth, and the apparent yield threshold for CE indicate that CE is more likely than ExE to be the type of extension which cell walls undergo during normal auxin-induced growth.Abbreviations and symbols CAWL capacity for acid-induced wall extension - CE linear phase of acid-extension - ExE exponential phase of acid-extension - IAA indole-3-acetic acid     

Monte Carlo simulation of denaturation of adsorbed proteins

Denaturation of model proteinlike molecules at the liquid–solid interface is simulated over a wide temperature range by employing the lattice Monte Carlo technique. Initially, the molecule containing 27 monomers of two types (A and B) is assumed to be adsorbed in the native folded state (a 3 × 3 × 3 cube) so that one of its sides is in contact with the surface. The details of the denaturation kinetics are found to be slightly dependent on the choice of the side, but the main qualitative conclusions hold for all the sides. In particular, the kinetics obey approximately the conventional first-order law at T > T_c (T_c is the collapse temperature for solution). With decreasing temperature, below T_c but above T_f (T_f is the folding temperature for solution), deviations appear from the first-order kinetics. For the most interesting temperatures, that is, below T_f, the denaturation kinetics are shown to be qualitatively different from the conventional ones. In particular, the denaturation process occurs via several intermediate steps due to trapping in metastable states. Mathematically, this means that (i) the transition to the denatured state of a given molecule is nonexponential, and (ii) the denaturation process cannot be described by a single rate constant k_r. One should rather introduce a distribution of values of this rate constant (different values of k_r correspond to the transitions to the altered state via different metastable states). Proteins 30:168–176, 1998. © 1998 Wiley-Liss, Inc.     

Solubilized elastin substrate for continuous fluorimetric assay of kinetics of elastases

Elastolysis is central to progression of emphysema and aortic aneurysms. Characterization of steady-state enzyme kinetics of elastolysis is fettered by the insolubility of mature elastin and the polydispersity of solubilized elastin. We prepared a fluor-tagged, 100-kDa fraction (fEln-100) from commercial α-elastin. It is soluble, less heterogeneous in mass, cross-linked like mature elastin, and likely to retain the capacity of α-elastin to self-assemble. fEln-100 has introduced the ability to compare quantitatively the apparentk_cat and K_m of elastases. For example, metalloelastase (MMP-12) displays higher apparent affinity for fEln-100, while MMP-2 displays faster catalytic turnover.     

Adaptation of homeostatic thermoregulation: comparison of incubating and non-incubating Bantam hens

Summary Incubating and non-incubating Bantam hens were exposed to identical thoracic skin cooling to study the difference between their physiological responses with regard to thermoregulatory adaptation to incubation. Under resting conditions thoracic skin temperature (T _ths) and metabolic heat production (M) were significantly higher in broody than in non-broody hens, indicating a permanently increased conductance of the brood patch. Thoracic skin cooling from 35 to 25 °C decreased T _ths less in broody than in non-broody hens. In broody hens, these coolings induced a large, immediate increase in M, no constriction of brood patch vasculature, and a decrease in colonic temperature (T _c). This decrease in T _c triggered no further increase in M, but induced vasoconstriction in the feet. The coolings induced a smaller increase in M in the non-broody hens, accompanied by pronounced vasoconstriction, and did not affect T _c and foot temperature, T _f. The effects of more severe thoracic skin cooling (between 25 and 15°C) differed much less between non-broody and broody hens. Vasoconstriction of the brood patch also occurred in the latter. It is concluded that in adaptation to incubation the thoracic skin becomes more sensitive, and its input signal becomes stronger for the control of certain effector systems of thermoregulation, allowing a controlled heat transfer to the eggs.Abbreviations BM body mass - M metabolic heat production - T _c colon temperature - T _ths thoracic skin temperature - T _f foot temperature - T _bs back skin temperature - T _stim stimulation temperature - VO₂ oxygen consumption     

Thermal time and ecological strategies - a unifying hypothesis

Rates of embryogenesis and of development and growth in several nematodes are linearly related to temperature over a considerable range. On this basis, published data on the thermal time requirements are compared for a tropical and a temperate species of plant parasitic nematode Meloidogyne javanica and M. hapla respectively, the two being closely related and morphologically and biologically similar. M. hapla has a lower base temperature (T_b) and a higher thermal constant (S) than M. javanica with the relative values being almost inversed. Consequently, above their respective T_b values the slope of the relationship between rate of development and temperature was greater for the tropical species than that for the temperate species. A mathematical exploration of the relationship between T_b and S was made assuming that, over a narrow range, T_b×S was a constant. With this assumption, for any given average environmental temperature (T_e) the optimum base temperature for minimum developmental duration was T_e/2, and the temperature at which the duration of development was equal for the otherwise identical species was shown to be the sum of their base temperatures. The practical effect of the differences in T_b and S was to give M. hapla, the temperate species, a shorter life cycle and hence a competitive advantage at temperatures below 21ÅC and M. javanica, the tropical species, the advantage above that temperature. It is argued that a negative correlation between T_b and S is likely to be widespread, and provides a mechanism for regulating the distributions of related, competing organisms. Support for the hypothesis that the value of S tends to decrease as T_b increases is derived from data on the embryogenesis of an animal parasitic nematode Haemonchus contortus and from seed germination studies. Contrary results and exceptions are also briefly discussed. The observed interaction between T_b and S may be fundamental to many poikilothermic organisms and plants and provides an explanation for tropical species generally having higher T_b values than temperate ones. The ecological implications of different values of T_b and of S, including their relationship with organisms which are “r” or “K” strategists are briefly discussed.     

Upper thermal limits of cardiac function for Arctic cod Boreogadus saida,a key food web fish species in the Arctic Ocean

The objective of this study was to determine the upper thermal limits of Arctic cod Boreogadus saida by measuring the response of maximum heart rate (f_Hmax) to acute warming. One set of fish were tested in a field laboratory in Cambridge Bay (CB), Nunavut (north of the Arctic Circle), and a second set were tested after air transport to and 6 month temperature acclimation at the Vancouver Aquarium (VA) laboratory. In both sets of tests, with B. saida acclimated to 0° C, f_Hmax increased during acute warming up to temperatures considerably higher than the acclimation temperature and the near‐freezing Arctic temperatures in which they are routinely found. Indeed, f_Hmax increased steadily between 0·5 and 5·5° C, with no significant difference between the CB and VA tests (P > 0·05) and with an overall mean ± s.e. Q₁₀ of 2·4 ± 0·5. The first Arrhenius breakpoint temperature (T_AB) for f_Hmax was also statistically indistinguishable for the two sets of tests (mean ± s.e. 3·2 ± 0·3 and 3·6 ± 0·3° C), suggesting that the temperature optimum for B. saida could be reliably measured after live transport to a more southerly laboratory location. Continued warming above 5·5° C revealed a large variability among individuals in the upper thermal limits that triggered cardiac arrhythmia (T_arr), ranging from 10·2 to 15·2° C with mean ± s.e. 12·4 ± 0·4° C (n = 11) for the field study. A difference did exist between the CB and VA breakpoint temperatures when the Q₁₀ value decreased below 2 (the Q₁₀ breakpoint temperature; T_QB) at 8·0 and 5·5° C, respectively. These results suggest that factors, other than thermal tolerance and associated cardiac performance, may influence the realized distribution of B. saida within the Arctic Circle.