Effects of temperature on metabolic rate and lower dissolved oxygen tolerance of juvenile speckled peacock bass Cichla temensis

The speckled peacock bass Cichla temensis is a popular sport and food fish that generates substantial angling tourism and utilitarian harvest within its range. Its popularity and value make this species important for management and a potential aquaculture candidate for both fisheries enhancement and food fish production. However, little is known of optimal physiochemical conditions in natural habitats, which also are important for the development of hatchery protocols for handling, spawning and grow-out. Speckled peacock bass have been documented to have high sensitivity to extreme temperatures, but the metabolic underpinnings have not been evaluated. In this study, the effects of temperature (25, 30 and 35°C) on the standard metabolic rate (SMR) and lower dissolved oxygen tolerance (LDOT) of juvenile speckled peacock bass (mean ± standard error total length 153 ± 2 mm and wet weight 39.09 ± 1.37 g) were evaluated using intermittent respirometers after an acclimation period of 2 weeks. Speckled peacock bass had the highest SMR at 35°C (345.56 ± 19.89 mgO₂ kg⁻¹ h⁻¹), followed by 30°C (208.16 ± 12.45 mgO₂ kg⁻¹ h⁻¹) and 25°C (144.09 ± 10.43 mgO₂ kg⁻¹ h⁻¹). Correspondingly, the Q₁₀, or rate of increase in aerobic metabolic rate (MO₂) relative to 10°C, for 30–35°C was also greater (2.76) than from 25 to 30°C (2.08). Similarly, speckled peacock bass were the most sensitive to hypoxia at the warmest temperature, with an LDOT at pO₂ of 90 mmHg (4.13 mg l⁻¹) at 35°C compared to pO₂ values of 45 mmHg (2.22 mg l⁻¹) and 30 mmHg (1.61 mg l⁻¹) at 30 and 25°C, respectively. These results indicate that speckled peacock bass are sensitive to temperatures near 35°C, therefore we recommend managing and rearing this species at 25–30°C.     

Physiological ecology of frillneck lizards in a seasonal tropical environment

The frillneck lizard, Chlamydosaurus kingii, is a conspicuous component of the fauna of the wetdry tropics of northern Australia during the wet season, but it is rarely seen in the dry season. Previous studies have demonstrated that during the dry season the field metabolic rate (FMR) is only about one-quarter of the wet-season rate, and one factor involved in this seasonal drop is a change in the behavioural thermoregulation of the species such that lower body temperatures (T _bs) are selected during dry-season days. Here we examine other factors that could be responsible for the seasonal change in FMR: standard metabolic rates (SMR) and activity. Samples from stomach flushing revealed that the lizards in the dry season continued to feed, but the volume of food was half as much as in the wet season. SMR in the laboratory was 30% less in the dry season. During the dry season, the energy expended by the lizards is 60.4 kJ kg^-1 day^-1 less than during the wet season. Combining laboratory and field data, we determined the relative contribution of the factors involved in this energy savings: 10% can be attributed to lower nighttime T _b, 12% is attributable to lower daytime T _b, 12% is attributable to decreased metabolism, and the remaining 66% is attributable to other activities (including e.g. locomotion, reproductive costs, digestion). Calculations indicate that if FMR did not drop in the dry season the lizards would not survive on the observed food intake during this season. Seasonal analysis of blood plasma and urine indicated an accumulation of some electrolytes during the dry season suggesting modest levels of water stress.     

Standard metabolic rate models for Carmine Shiner (Notropis percobromus) and Common Shiner (Luxilus cornutus) across different temperature regimes

Standard metabolic rates (SMR) were measured empirically for carmine shiner Notropis percobromus and common shiner Luxilus cornutus to develop SMR models that predict metabolic responses of each species under thermal conditions observed in the wild. SMR increased significantly with body mass and rising water temperature, ranging from 0.05 mg O₂ h⁻¹ at 10°C to 0.89 mg O₂ h⁻¹ at 20°C for N. percobromus weighing 0.6–2.5 g and from 0.11 mg O₂ h⁻¹ at 10°C to 0.98 mg O₂ h⁻¹ at 20°C for L. cornutus weighing 0.8–6.6 g. SMR models significantly differed between sympatric species on account of differences in model intercepts (RA) and temperature coefficients (RQ), however, the allometric relationships between mass and SMR did not significantly differ between species. Known distribution of N. percobromus and L. cornutus includes the Birch River located in Manitoba, Canada, where N. percobromus is listed as Endangered. Little is known about the physiology of N. percobromus or the species' ability to acclimate or adapt to different environmental conditions. While size differences between species contributed, in part, to differences in SMR predictions for Birch River populations, SMR trends (< 2 mg O₂ h⁻¹) for individuals weighing 1 g were similar for both species across daily temperatures. Respirometry experiments contributed to developing species-specific SMR models and inform on the effect of natural and anthropogenic stressors, namely water temperature, on the conservation of N. percobromus in this ecosystem.     

Reflex bradycardia does not influence oxygen consumption during hypoxia in the European eel (Anguilla anguilla)

Most teleost fish reduce heart rate when exposed to acute hypoxia. This hypoxic bradycardia has been characterised for many fish species, but it remains uncertain whether this reflex contributes to the maintenance of oxygen uptake in hypoxia. Here we describe the effects of inhibiting the bradycardia on oxygen consumption (MO₂), standard metabolic rate (SMR) and the critical oxygen partial pressure for regulation of SMR in hypoxia (Pcrit) in European eels Anguilla anguilla (mean ± SEM mass 528 ± 36 g; n = 14). Eels were instrumented with a Transonic flow probe around the ventral aorta to measure cardiac output (Q) and heart rate (f _H). MO₂ was then measured by intermittent closed respirometry during sequential exposure to various levels of increasing hypoxia, to determine Pcrit. Each fish was studied before and after abolition of reflex bradycardia by intraperitoneal injection of the muscarinic antagonist atropine (5 mg kg⁻¹). In the untreated eels, f _H fell from 39.0 ± 4.3 min⁻¹ in normoxia to 14.8 ± 5.2 min⁻¹ at the deepest level of hypoxia (2 kPa), and this was associated with a decline in Q, from 7.5 ± 0.8 mL min⁻¹ kg⁻¹ to 3.3 ± 0.7 mL min⁻¹ kg⁻¹ in normoxia versus deepest hypoxia, respectively. Atropine had no effect on SMR, which was 16.0 ± 1.8 μmol O₂ kg⁻¹ min⁻¹ in control versus 16.8 ± 0.8 μmol O₂ kg⁻¹ min⁻¹ following treatment with atropine. Atropine also had no significant effect on normoxic f _H or Q in the eel, but completely abolished the bradycardia and associated decline in Q during progressive hypoxia. This pharmacological inhibition of the cardiac responses to hypoxia was, however, without affect on Pcrit, which was 11.7 ± 1.3 versus 12.5 ± 1.5 kPa in control versus atropinised eels, respectively. These results indicate, therefore, that reflex bradycardia does not contribute to maintenance of MO₂ and regulation of SMR by the European eel in hypoxia.     

Physiological ecology of a tropical dragon,Lophognathus temporalis

Lophognathus temporalis is an arboreal lizard from the wet–dry tropics of Australia. During the wet season the field metabolic rate (FMR) of the lizards was 209 kJ kg^?1 d^?1, but during the dry season FMR was only 62 kJ kg^?1 d^?1. Similarly, water flux decreased from 73.6 mL kg^?1 d^?1 in the wet season to 18.5 mL kg^?1 d^?1 in the dry season. Body temperatures (T_b) were significantly lower in the dry season, and operative temperatures, calculated by incorporating microclimatic data with characteristics of the lizards, indicated that the seasonal shift was due to changes in thermoregulatory behaviour rather than limitations of the thermal environment. By combining field measurements of T_b and FMR with laboratory measurements of standard metabolic rate over a range of T_b, we were able to subdivide the FMR into its components and to determine which factors contributed to the seasonal reduction in energy expenditure. During the dry season, lizards used 147 kJ kg^?1 d^?1 less energy than during the wet season, and 24% of this decrease was estimated to be due to the passive effects of lower nighttime T_b, 14% was due to the active selection of lower daytime T_b, 27% was due to the physiological shift to lower standard metabolic rates, and 35% was due to reduced activity in the dry season. Although the population size remained relatively constant (107 lizards ha^?1 during the wet season and 125 lizards ha^?1 during the dry season), the population structure changed, reflecting the seasonal patterns of recruitment and mortality. The number of lizards active at any one time was much lower in the dry season, reflecting the lower levels of activity in this season. The energy expenditure of the population of L. temporalis was 612 kJ ha^?1 d^?1 during the wet season and 113 kJ ha^?1 d^?1 during the dry season.     

Influence of experimental set-up and methodology for measurements of metabolic rates and critical swimming speed in Atlantic salmon Salmo salar

In this study, swim-tunnel respirometry was performed on Atlantic salmon Salmo salar post-smolts in a 90 l respirometer on individuals and compared with groups or individuals of similar sizes tested in a 1905 l respirometer, to determine if differences between set-ups and protocols exist. Standard metabolic rate (SMR) derived from the lowest oxygen uptake rate cycles over a 20 h period was statistically similar to SMR derived from back extrapolating to zero swim speed. However, maximum metabolic rate (MMR) estimates varied significantly between swimming at maximum speed, following an exhaustive chase protocol and during confinement stress. Most notably, the mean (±SE) MMR was 511 ± 15 mg O₂ kg⁻¹ h⁻¹ in the swim test which was 52% higher compared with 337 ± 9 mg O₂ kg⁻¹ in the chase protocol, showing that the latter approach causes a substantial underestimation. Performing group respirometry in the larger swim tunnel provided statistically similar estimates of SMR and MMR as for individual fish tested in the smaller tunnel. While we hypothesised a larger swim section and swimming in groups would improve swimming performance, U_crit was statistically similar between both set-ups and statistically similar between swimming alone v. swimming in groups in the larger set-up, suggesting that this species does not benefit hydrodynamically from swimming in a school in these conditions. Different methods and set-ups have their own respective limitations and advantages depending on the questions being addressed, the time available, the number of replicates required and if supplementary samplings such as blood or gill tissues are needed. Hence, method choice should be carefully considered when planning experiments and when comparing previous studies.     

Effects of acute temperature changes on the swimming abilities and oxygen consumption of Ptychobarbus kaznakovi from the Lancang River

Water temperature is known to be a particularly important environmental factor that affects fish swimming performance, but it is unknow how acute temperature changes affect the fish performance of Ptychobarbus kaznakovi. P. kaznakovi in the Lancang River have declined quickly in recent years, and this species was used to examine the effects of acute temperature changes on swimming abilities and oxygen consumption in a Brett‐type swimming tunnel respirometer. The standard metabolic rate (SMR) and routine metabolic rate (RMR) showed 216% and 134% increases, respectively, at 22°C (an acute increase from 17 to 22°C) compared to those at 12°C (an acute decrease from 17 to 12°C). Moreover, the RMR was approximately 1.7, 1.6 and 1.3 times the value of the SMR at 12°C, 17°C and 22°C, respectively. The critical swimming speed (U_crit) of P. kaznakovi at 22°C was 5.45 ± 0.45BL/S, which was 45% higher than that at 12°C (3.77 ± 0.92BL/S). The oxygen consumption rates (MO₂) reached their maximum values at swimming speeds near the U_crit for all the temperature treatments. The maximum metabolic rate (MMR) values at 12°C, 17°C and 22°C were 274.53 ± 142.60 (mgO₂ kg^?1 hr^?1), 412.85 ± 216.34 (mgO₂ kg^?1 hr^?1) and 1,095.73 ± 52.50 (mgO₂ kg^?1 hr^?1), respectively. Moreover, there was a narrow aerobic scope at 12°C compared to that at 17°C and 22°C. The effect of acute temperature changes on the swimming abilities and oxygen consumption of P. kaznakovi indicated that water temperature changes caused by dam construction could directly affect energy consumption during the upstream migration of fish.     

Metabolic rates in an anadromous clupeid, the American shad (Alosa sapidissima)

To assess the energetics of migration in an anadromous fish, adult American shad (Alosa sapidissima) were swum in a large respirometer at a range of speeds (1.0–2.3 body lengths (BL) s⁻¹, 13–24 °C). Metabolic rate (M_O2) was logarithmically related to swimming speed (Bl s⁻¹; r ² = 0.41, slope = 0.23 ± 0.037) and tailbeat frequency (beats × min⁻¹; r ² = 0.52, slope = 0.003 ± 0.0003). Temperature had a significant effect on metabolic rate (r ² = 0.41) with a Q₁₀ of 2.2. Standard metabolic rate (SMR), determined directly after immobilization with the neuroblocker gallamine triethiodide, ranged from 2.2–6.2 mmolO₂ kg⁻¹ h⁻¹ and scaled with mass (W) such that SMR = 4.0 (±0.03)W^{0.695(±0.15)}. Comparison of directly determined and extrapolated SMR suggests that swimming respirometry provides a good estimate of SMR in this species, given the differences in basal activity monitored by the two methods. Overall, American shad metabolic rates (M_O2 and SMR) were intermediate between salmonids and fast-swimming perciforms, including tunas, and may be a result of evolutionary adaptation to their active pelagic, schooling life history. This study demonstrates variability in metabolic strategy among anadromous fishes that may be important to understanding the relative success of different migratory species under varying environmental conditions. Accepted: 3 March 1999     

Aerobic swimming performance of juvenile Schizothorax chongi (Pisces, Cyprinidae) in the Yalong River, southwestern China

Schizothorax chongi (locally known as Xilian Yu), a fish species commonly found in Yalong River, has been declining quickly in recent years. One of the important factors, among many, is the interruption of the free flowing river by dams. To obtain data that can be applied to the design of a fishway for S. chongi and other species in the community, a laboratory study of juvenile S. chongi’s swimming energetics and kinematics was conducted in a flume-type respirometer equipped with a high speed video camera system to record swimming behavior. The aerobic metabolic rate, tail beat frequency (TBF) and tail beat amplitude (TBA) were measured during steady swimming at varying flow rates for fish of similar mass. A power function accurately describes the relationship between oxygen consumption rate (MO₂) and swimming speed (U). The estimated standard metabolic rate (SMR) calculated from the power function was 445.34 mg O₂ kg⁻¹ h⁻¹, similar to the experimental result of 431.5 mg O₂ kg⁻¹ h⁻¹. The relationship between cost of transport (COT) and U was, characteristically, inverse bell-shaped, with COT_min = 44.6 J kg⁻¹ m⁻¹ at U _opt = 5.5 body lengths per second (bl s⁻¹). There was a significant positive linear correlation between TBF and U. The slope of the correlation (0.33) was lower than for many other species, implying that S. chongi swim efficiently. The TBA, ranging from 0.15 to 0.2 bl, was found to be independent of U. Kinematic analyses indicates that S. chongi primarily depends on the caudal fin to generate forward thrust and employs three velocity-dependent swimming gaits. This investigation provides data on the swimming ability of S. chongi that will add to the basic science required for fishway design.     

Growth and maintenance respiration in leaves of northern red oak seedlings and mature trees after 3 years of ozone exposure

A two-component model of growth and maintenance respiration is used to study the response of northern red oak (Quercus rubra L.) seedlings and 32-year-old trees to sub-ambient (10 μmol h; cumulative dose based on 7 h daily mean), ambient (43 μmol h), and twice-ambient (85 μmolh) ozone. The relative growth rates (RGR) of leaves sampled from seedlings and trees were similar across treatments, as were specific leaf respiration rates (SRR). Growth coefficients estimated from the SRR versus RGR relationship averaged 25-3 mol CO2 kg^?1 leaf dry mass produced for seedlings and 21-5 mol kg^?1 for trees. Maintenance coefficients ranged from 0-89 to 1-07 mol CO₂ kg^?1 leaf dry mass d^?1 for seedlings and from 0-64 to 0-84 mol kg-1 d^?1 for trees. Neither coefficient was affected by ozone. Leaves sampled throughout the growing season also showed little response of respiration to ozone. This occurred despite a 30% reduction in net photosynthesis for trees grown at twice-ambient ozone. These results suggest that growth and maintenance respiration in young northern red oak leaves are not affected by ozone and that in older leaves injury can occur without a parallel increase in so-called ‘maintenance’ respiration.     

蚂蚁筑巢对西双版纳热带森林土壤有机氮矿化的影响

蚂蚁作为生态系统工程师能够调节土壤微生物及理化环境,进而对热带森林土壤有机氮矿化速率及其时间动态产生显著影响。以西双版纳白背桐热带森林群落为研究对象,采用室内需氧培养法测定土壤有机氮矿化速率,比较蚁巢和非蚁巢土壤有机氮矿化速率的时间动态,揭示蚂蚁筑巢活动引起土壤无机氮库、微生物生物量碳及化学性质改变对有机氮矿化速率时间动态的影响。结果表明：（1）蚂蚁筑巢显著影响土壤有机氮矿化速率（P<0.01）,相较于非蚁巢,蚁巢土壤有机氮矿化速率提高了261%;（2）土壤有机氮矿化速率随月份推移呈明显的单峰型变化趋势,即6月最大（蚁巢1.22 mg kg^-1 d^-1、非蚁巢0.41 mg kg^-1 d^-1）,12月最小（蚁巢0.82 mg kg^-1 d^-1、非蚁巢0.18 mg kg^-1 d^-1）;（3）两因素方差分析表明,不同月份及不同处理对土壤有机氮矿化速率、NH₄-N及NO₃-N产生显著影响（P<0.05）,但对NO₃-N的交互作用不显著;（4）蚂蚁筑巢显著提高了无机氮库（NH₄-N与NO₃-N）、微生物生物量碳、有机质、水解氮、全氮及易氧化有机碳等土壤养分含量,而降低了土壤pH值;（5）回归分析表明,铵态氮和硝态氮对土壤有机氮矿化速率产生显著影响,分别解释87.89%、61.84%的有机氮矿化速率变化;（6）主成份分析表明NH₄-N、微生物生物量碳及有机质是影响有机氮矿化速率时间动态的主要因素,而全氮、NO₃-N、易氧化有机碳、水解氮及pH对土壤有机氮矿化速率的影响次之,且pH与土壤有机氮矿化速率呈显著负相关。总之,蚂蚁筑巢活动主要通过影响土壤NH₄-N、微生物生物量碳及有机质的状况,进而调控西双版纳热带森林土壤有机氮矿化速率的时间动态。研究结果将有助于进一步提高对土壤氮矿化生物调控机制的认识。     

The cost of living slowly: metabolism,Q10 and repeatability in a South American harvestman

Abstract Resources are usually considered to be limited in caves and underground habitats. Therefore, lower metabolic rates of ectotherms in these environments should be advantageous. The standard metabolic rate (SMR) of the common harvestman Pachylus paessleri Roewer, 1913 (Arachnida, Opiliones) is determined at two ambient temperatures. Repeatability of SMR is estimated by two methods: (i) product–moment correlation on residuals of body mass and (ii) variance components. Estimations of the thermal sensitivity of metabolic rate (individual Q₁₀). SMR of P. paessleri at 20 °C show a mean of 19.01 ± 6.04 and 14.99 ± 3.64 μL CO₂ h^?1 for males and females, respectively. Thermal sensitivity of SMR is 2.11 ± 0.23 with a substantial coefficient of variation of 26.7%. In males, residuals of CO₂ release are significantly repeatable (r_p = 0.61) between measurements realized 5 months apart, which reflects the consistency of this trait over time. As typical soil inhabitants, the harvestman P. paessleri present a lower metabolic rate in comparison with arthropods of similar body mass (e.g. arachnids). Although the coefficient of thermal sensitivity is within of the range reported for arthropods inhabiting Mediterranean zones, it is lower than expected for an organism with such a low SMR. This appears to be the first report of repeatability of metabolic rate in a harvestman species.     

大兴安岭北部天然针叶林土壤氮矿化特征

采用顶盖埋管法对大兴安岭地区天然针叶林(樟子松林、樟子松-兴安落叶松混交林和兴安落叶松林)土壤铵态氮(NH~+_4-N)、硝态氮(NO~-_3-N)、净氮矿化速率进行研究,并探索土壤理化性质与氮矿化之间的相关性,为大兴安岭地区森林生态系统土壤养分管理及森林经营提供帮助。结果表明:观测期内(5—10月)3种林型土壤无机氮变化范围为31.51—70.42 mg/kg,以NH~+_4-N形式存在为主,占比达90%以上,且与纯林相比混交林土壤无机氮含量较高。3种林型土壤净氮矿化、净氨化、净硝化速率月变化趋势呈V型,7、8月表现为负值,其他月份为正值。净氮矿化速率变化范围樟子松林为-0.54—1.28 mg kg~(-1) d~(-1)、樟子松-兴安落叶松混交林为-0.13—0.55 mg kg~(-1) d~(-1)、兴安落叶松林为-0.80—1.05 mg kg~(-1) d~(-1)。土壤净氨化过程在土壤氮矿化中占主要地位,占比达60%以上。3种林型土壤净氮矿化、净氨化及净硝化速率垂直差异显著,0—10 cm土层矿化作用明显高于10—20 cm土层(P0.05)。土壤氮矿化速率与土壤含水量、土壤有机碳含量、土壤C/N、枯落物全氮含量和枯落物C/N均存在显著相关性。不同类型的森林土壤及枯落物的质量也存在差异,进而影响土壤氮矿化特征。     

A three‐phase excess post‐exercise oxygen consumption in Atlantic salmon Salmo salar and its response to exercise training

The recovery of oxygen uptake to the standard metabolic rate (SMR) following exhaustive chasing exercise in Atlantic salmon Salmo salar parr occurred in three phases (rapid, plateau and slow). The initial recovery phase lasted 0·7 h and contributed 16% to the total excess post‐exercise oxygen consumption (EPOC). It was followed by a longer plateau phase that contributed 53% to the total EPOC. The slow recovery phase that completed recovery of SMR, which has not been reported previously, made a 31% contribution to the total EPOC. The plasticity of EPOC was demonstrated in exercise‐trained fish. Exercise training increased EPOC by 39% when compared with control fish (mean ± S.E., 877·7 ± 73·1 v . 629·2 ± 53·4 mg O₂ kg^?1, d.f. = 9, P <  0·05), with the duration of the plateau phase increasing by 38% (4·7 ± 0·58 v . 3·4 ± 0·16 h, d.f. = 9, P <  0·05) and the contribution of the slow phase to the total EPOC increasing by 80% (173·9 ± 23·9 v . 312·5 ± 50·4 mg O₂ kg^?1, d.f. = 9, P  < 0·05). As a result, the combination of the plateau and slow phases of exercise‐trained fish increased by 47% compared with control fish (756·6 ± 71·4 v . 513·6 ± 43·1 mg O₂ kg^?1; d.f. = 9, P  = 0·01). To substantiate the hypothesis that the plateau and slow recovery phase of EPOC was related to general metabolic recovery following exhaustive exercise, the time‐course for recovery of SMR was compared with previously published metabolite recovery profiles. The final phase of metabolic recovery was temporally associated with the final phases of gluconeogenesis, lactate oxidation and muscle intracellular pH regulation. Therefore, the plasticity of the latter phase of EPOC agreed with the known effects of exercise training in fishes.     

Energetic limitation of avian parental effort: Field experiments in the kestrel (Falco tinnunculus)

We studied the limiting factors for brood size in the kestrel, Falco tinnunculus, by measuring parental effort in natural broods of different size and parental response to manipulation of food satiation of the brood. Parental effort was quantified as total daily time spent in flight, and total daily energy expenditure, from all-day observations. During nestling care males with different natural brood sizes (4 to 7 chicks), spent an average of 4.75 h · d^?1 in flight independent of brood size, and expended an average total daily energy of 382 kJ · d^?1. Due to a higher flight-hunting yield (mammal-prey caught per hour hunting), males with larger natural broods were able to provision their broods with the same amount of food (mainly Microtus arvalis) per chick (62.6 g · d^?1), with the same effort as males with smaller broods. This provisioning rate was close to the mean feeding rate of hand-raised chicks in the laboratory, that were fed ad libitum, (66.8 g · d^?1 · chick^?1). Our food deprivation experiments revealed that male kestrels strongly respond to food shortage in the nest. In the older nestling phase males on average increased their daily rate of food delivery to the nest as a response to experimental food deprivation by almost three times to 646.4 g · d^?1, by increasing their flight activity level from 4.46 to 8.41 h · d^?1. This increased energy expenditure was sustained, for as long as eleven days, by increasing the metabolizable energy intake up to what is presumed to be the maximum rate. Even under considerable experimental food stress (chicks not being satiated due to continuous removal of delivered food by the observers) about half of the available daylight time remained unused for foraging. We conclude 1) that the mean daily energy expenditure of males during nestling care — to which clutch size is apparently initially adjusted — is well below the maximum they are able to sustain and 2) that the energy expenditure they can sustain under extremely high nestling demand is not set by the available time for foraging or the available energy in the environment. Thus the birds normally operate well below their presumed maximum, and only during food shortage, e.g., as caused by our experiments, do they increase activity up to this maximum. Therefore we conclude that the kestrels have costs other than energy expenditure, such as parental survival, that are involved in the increased “cost” of parental effort. We discuss possible generalisations about existing energetic limitations during parental care in altricial birds. From published estimates of daily energy expenditure during parental care (DEE_par) in 30 different bird species we derived the equation: DEE_par = 14.26 kg^0.65 Watt. This relationship differs significantly in slope (T = 2.49; p > 0.02) from the allometric equation for the maximum rate of energy assimilation (DME_max) as provided by Kirkwood (1983): DME_max = 19.82 kg^0.72 Watt. In smaller species (ca. 25 g) DEE_par about equals DME_max, while in the larger species (ca. 10 kg) DEE_par represents only about 60% of the predicted DME_max. This suggests that limitations in parental effort are more frequently set by the maximum sustainable energy intake in the smaller species than in larger species. Our allometric equations for DEE_par suggests that the relation between BMR, estimated using the equations of Aschoff and Pohl (1970), and the observed parental energy expenditure, is such that on average bird parents work at a daily level somewhere between 3 and 4 times BMR.     

甘肃中东部地区9种薹草属植物分布区群落特征和土壤养分状况

为探究薹草属(Carex L.)植物在不同植被类型中的分布状况,该研究对甘肃中东部地区9种薹草属(Carex L.)植物分布区的群落特征进行调查,并对土壤养分状况进行比较分析,以揭示野生薹草群落物种多样性和分布特征与土壤环境因子间的关系。结果表明：(1) 9种薹草群落物种多样性差异性较大,Shannon-Wiener多样性指数(H)、Simpson优势度指数(D_si)均以青绿薹草群落最高,亚柄薹草最低;Patrick丰富度指数(R)以异穗薹草群落最高,细叶薹草群落最低;Pielou均匀度指数(J_sw)以凹脉薹草群落最高,亚柄薹草最低。(2) 9种野生薹草属植物适宜生长的土壤pH呈中性或弱碱性,且有机质、氮素、钾素含量较丰富,磷含量偏低;土壤有机质、pH、全氮、全磷、全钾、碱解氮、速效磷、速效钾含量的平均值分别为41.07 g·kg^-1、8.35、1.16 g·kg^-1、0.65 g·kg^-1、5.60 g·kg^-1、47.94 mg·kg^-1、5.82 mg·kg^-1和100.60 mg·kg^-1。(3) 9种薹草属植物群落物种多样性与全氮、全磷、全钾、碱解氮、有机质、降雨量和海拔呈正相关关系,而与土壤pH、速效磷、速效钾呈负相关关系,且降雨量、土壤pH、速效磷和有机质对9种野生薹草属植物群落物种多样性影响较大。     

Accumulation of selenium by different plant species grown under increasing sodium and calcium chloride salinity

High levels of naturally occurring selenium (Se) are often found in conjunction with different forms of salinity in central California. Plants considered for use in phytoremediation of high Se levels must therefore be salt tolerant. Selenium accumulation was evaluated for the following species under increasing salt (NaCl and CaCl) conditions:Brassica napus L. (canola),Hibiscus cannibinus L. (kenaf),Festuca arundinacea L. (tall fescue), andLotus tenuis L. (birdsfoot trefoil). The experimental design was a complete randomized block with four salt treatments of <1, 5, 10, and 20 dS m^-1, four plant species, three blocks, and six replicates per treatment. Ninety days after growing in the respective salt treated soil with a Se concentration of 2 mg Se kg^-1 soil, added as Na₂SeO₄, all plant species were completely harvested. Among the species tested, shoot and root dry matter yield of kenaf was most significantly (p<0.001) affected by the highest salt treatment and tall fescue and canola were the least affected species. Generally there was a decrease in tissue accumulation of Se with increasing salt levels, except that low levels of salinity stimulated Se accumulation in canola. Canola leaf and root tissue accumulated the highest concentrations of Se (315 and 80 mg Se kg^-1 DM) and tall fescue the least (35 and 7 mg Se kg^-1 DM). Total soil Se concentrations all harvest were significantly (p<0.05) lower for all species at all salt treatments. Removal of Se from soil was greatest by canola followed by birdsfoot trefoil, kenaf and tall fescue. Among the four species, canola was the best candidate for removing Se under the tested salinity conditions. Kenaf may be effective because of its large biomass production, while tall fescue and birdsfoot trefoil may be effective because they can be repeatedly clipped as perennial crops.     

Sorption of Methyl tert -Butyl Ether (MTBE) and tert -Butyl Alcohol (TBA) to Hyporheic Zone Soils

Soil water distribution coefficients (K _d ) for methyl tert-butyl ether (MTBE) and its primary biodegradation intermediate tert-butyl alcohol (TBA) were determined for seven hyporheic zone soils ranging from 1 to 7% in organic carbon. Samples were collected in the area of the Spring Creek hyporheic zone in Ronan, Montana. Values for K _d ranged from 1.5 to 8.7 L kg^?1 for MTBE and from 0.15 to 0.41 L kg^?1 for TBA, and were highly correlated to the organic carbon content of the solids. However, for TBA the use of non-linear K _F values is more appropriate based on the results obtained, and the value of K _OC is calculated based on linear K _d transformation of the data. Distribution coefficients normalized to the fraction of organic carbon (log K _OC ) for MTBE and TBA were determined to be 2.13 ± 0.060 and 0.762 ± 0.088, respectively.     

Steady-state nutrition and growth responses of Betula pendula to different relative supply rates of copper

In a series of experiments on the growth and nutrition of copper-limited birch (Betula pendula Roth) plants, growth was controlled by the relative addition rate of copper, R_Cu (d^–1). This was 0·05, 0·10, 0·15 or 0·20 d^–1 with free access to all other nutrients. An additional treatment provided free access to all nutrients. The pH in the nutrient solution was ≈ 4·5 and conductivity was 100 μS cm^–1. At steady-state growth, there was a linear relationship between the relative growth rate, R_G, and R_Cu. The [Cu] of the plants ranged from 2·4 to 2·7 μg g^–1 dry mass (DM) in all treatments with limiting R_Cu and was ≈ 28 μg g^–1 in the free access treatment. The plants showed specific copper deficiency symptoms at limitation. Total non-structural carbohydrate concentrations and the fraction of plant DM partitioned to roots was much less at copper limitation than at free access. The uptake rate of copper per unit root growth rate, dCu/dW_r (μmol g^–1 root DM) was unaffected by the copper supply. Low rates of plant growth at copper limitation were associated with high values of specific leaf area (SLA; 47 m² kg^–1) and leaf area ratio (LAR; 28 m² kg^–1 plant DM) but lower values of net assimilation rate (NAR; 2·5 kg m^–2 leaf DM d^–1) than were found at free access, 28 m² kg^–1 (SLA), 17 m² kg^–1 DM (LAR) and 14 kg m^–2 leaf DM d^–1 (NAR), respectively. It is not obvious from the present data how the growth response can help alleviate copper limitation in the field.     

Digestion and energy metabolism in a small arboreal marsupial,the Greater Glider (Petauroides volans), fed high-terpeneEucalyptus foliage

Summary The digestion and metabolism ofEucalyptus radiata foliage was studied in a small (1–1.5 kg) arboreal marsupial, the greater glider (Petauroides volans). Mean dry matter intake was 44 g·kg^–0.75·d^–1 and mean cell wall digestibility was 34%; these values fall within the range of other marsupials fedEucalyptus foliage. Digestible energy content ofE. radiata was high compared to other eucalypts because of the high content and digestibility of essential oils. However, excretion of essential oils and their metabolites in the urine meant that greater gliders retained only 55% of their digestible energy intakes (0.61 MJ · kg^–0.75· d^–1) as metabolizable energy (ME). Low ME intakes were not offset by low standard metabolic rates (2.39 W · kg^–0.75), but the efficiency with which ME substituted for tissue energy was high (94%), so that greater gliders were able to maintain energy balance and body mass onE. radiata foliage.Abbreviations ME metabolizable energy - DE digestible energy - RQ respiratory quotient - FHP fasting heat production