黑线仓鼠繁殖输出与基础代谢率的关系

为了解黑线仓鼠繁殖输出与基础代谢率(BMR)的关系,阐明最大持续能量收支(SusMR)的限制水平, 揭示哺乳期能量收支对策,本文测定了哺乳期黑线仓鼠的体重、摄食量、BMR 和身体组成,以及哺乳期的胎仔数、胎仔重和泌乳能量支出(MEO)。结果显示,黑线仓鼠哺乳期体重降低了15.0 ± 0.8% , 摄食量显著增加, 哺乳高峰期平均摄食量为13.9 ± 0.3 g /d, 摄入能为222.1 ± 5.3 kJ/ d, 比哺乳初期增加121% , 比对照组高288% ;哺乳高峰期MEO 为62.4 ± 2.3 kJ/ d, 哺乳末期BMR 为49.7 ± 1.1 kJ/ d; 断乳时平均胎仔数4.7 ± 0.2、窝胎仔重50.5 ±1.6 g; 哺乳末期BMR 比对照组增加48% ,BMR 与消化系统各器官的相关性高于对照组; BMR 与胎仔数、胎仔重、乳腺重量和MEO 显著正相关。结果表明:初次繁殖的黑线仓鼠哺乳期SusMR 限制为4.47 ×BMR, 在自身维持和繁殖输出之间采取了“权衡分配”的原则,通过体重降低以减少BMR 的增加幅度, 从而有利于繁殖输出。     

Performance and carcass characteristics of steers fed with two levels of metabolizable energy intake during summer and winter season

Climate change is producing an increase on extreme weather events around the world such as flooding, drought and extreme ambient temperatures impacting animal production and animal welfare. At present, there is a lack of studies addressing the effects of climatic conditions associated with energy intake in finishing cattle in South American feed yards. Therefore, two experiments were conducted to assess the effects of environmental variables and level of metabolizable energy intake above maintenance requirements (MEI) on performance and carcass quality of steers. In each experiment (winter and summer), steers were fed with 1.85 or 2.72 times of their requirements of metabolizable energy of maintenance. A total of 24 crossbred steers per experiment were used and located in four pens (26.25 m²/head) equipped with a Calan Broadbent Feeding System. Animals were fed with the same diet within each season, varying the amount offered to adjust the MEI treatments. Mud depth, mud scores, tympanic temperature (TT), environmental variables, average daily gain, respiration rates and carcass characteristics plus three thermal comfort indices were collected. Data analysis considered a factorial arrangement (Season and MEI). In addition, a repeated measures analysis was performed for TT and respiration rate. Mean values of ambient temperature, solar radiation and comfort thermal indices were greater in the summer experiment as expected (P<0.005). The mean values of TT were higher in steers fed with higher MEI and also in the summer season. The average daily gain was greater during summer v. winter (1.10±0.11 v. 0.36±0.06) kg/day, also when steers were fed 2.72 v. 1.85 MEI level (0.89±0.12 v. 0.57±0.10) kg/day. In summer, respiration rate increased in 41.2% in the afternoon. In winter, muddy conditions increased with time of feeding, whereas wind speed and rainfall had significant effects on TT and average daily gain. We conclude that MEI and environmental variables have direct effects on the physiology and performance of steers, including TT and average daily gain, particularly during the winter. In addition, carcass characteristics were affected by season but not by the level of MEI. Finally, due to the high variability of data as well as the small number of animals assessed in these experiments, more studies on carcass characteristics under similar conditions are required.     

Energy turnover in European hares is centrally limited during early,but not during peak lactation

We investigated metabolizable energy intake (MEI) and milk energy output in European hares throughout gestation and lactation in females raising three young, i.e., close to maximum litter size in this precocial species. We hypothesized that herbivorous hares may face a central limitation of energy turnover during lactation, imposed by maximum capacity of the gastrointestinal tract. Females were provided with low-energy or high-energy diets, either continually, or during lactation only. Unexpectedly, females on either diet reached identical peak MEIs (>6 times BMR) during late lactation, with females on low-energy diet increasing food intake proportionally. Thus, we reject our hypothesis that in lactating hares, peak MEI is centrally limited. During early lactation, MEI and milk transfer was, however, significantly impaired in females on the low-energy diet, indicating a temporal central limitation due to a time-lag caused by the readjustment of energy intake capacity. Importantly, irrespective of the diet, females significantly increased peak MEI late in the breeding season. Consequently, earlier in the season, when energy reserves are still high, energy throughput was not limited by physiological constraints at all. We conclude that extreme MEI may have fitness costs, and that females maximize lifetime reproductive success by actively down-regulating MEI whenever possible.     

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.     

防御性攻击行为对黑线仓鼠能量收支的影响

攻击行为是增强个体生存能力和提高繁殖成功机会的最有效竞争方式之一。为理解攻击行为对小型哺乳动物能量学收支策略的影响,以具有独居且好斗习性的黑线仓鼠为研究对象,基于居留者-入侵者（resident-intruder）争斗方式将入侵鼠放入居留鼠笼中（10min / d）,21d后测定能量摄入、基础代谢率（BMR）,分析BMR和内脏器官重量的相关性。结果显示,攻击行为使居留组BMR增加了26.2%,使摄入能和消化能显著增加。居留组体重、胴体重,以及某些代谢活性器官（肝脏、肺脏、肾脏、胃、小肠和盲肠）重量显著增加,且这些器官重量与BMR显著正相关。结果表明,增加能量摄入和BMR是黑线仓鼠应对攻击行为的主要能量学收支策略;在种内个体之间强烈的攻击行为可能是该鼠维持较高水平BMR的原因之一。     

冷驯化条件下高山姬鼠能量对策的初步研究

为进一步了解横断山区小型哺乳动物的能量代谢对策,本文主要研究了横断山的外来物种——高山姬鼠(Apodemus chevrieri)持续冷暴露28d的能量变化。结果表明,随着冷驯化时间延长,体重和体温降低;摄入能、消化能和可代谢能增加,至21d后这3项指标又下降;BMR和NST增加,并且28d后它们分别是对照组的187.19%和155.97%;(NST-BMR)/BMR比值7d时增加到1.02,21d后下降至0.53,并保持稳定。因此,在持续冷暴露下,高山姬鼠采取适当降低体重和体温、增加能量摄入、增加BMR和NST产热等途径来维持能量代谢平衡,但是NST在产热中的作用逐渐降低。这种能量模式很可能代表了一种外来小型啮齿动物对于在横断山生存独特的能量适应策略。     

Partitioning of late gestation energy expenditure in ewes using indirect calorimetry and a linear regression approach

Abstract

Late gestation energy expenditure (EE_gest) originates from energy expenditure (EE) of development of conceptus (EE_conceptus) and EE of homeorhetic adaptation of metabolism (EE_homeorhetic). Even though EE_gest is relatively easy to quantify, its partitioning is problematic. In the present study metabolizable energy (ME) intake ranges for twin-bearing ewes were 220 – 440, 350 – 700, 350 – 900 kJ per metabolic body weight (W^0.75) at week seven, five, two pre-partum respectively. Indirect calorimetry and a linear regression approach were used to quantify EE_gest and then partition to EE_conceptus and EE_homeorhetic. Energy expenditure of basal metabolism of the non-gravid tissues (EE_bmng), derived from the intercept of the linear regression equation of retained energy [kJ/W^0.75] and ME intake [kJ/W^0.75], was 298 [kJ/W^0.75]. Values of the intercepts of the regression equations at week seven, five, and two pre-partum were 311, 398, and 451 [kJ/W^0.75], respectively. The difference between the intercepts for different weeks was used to calculate EE_homeorhetic. The remaining part of EE_gest was considered to be EE_conceptus. In conclusion, the good agreement between our values of EE_conceptus and those in the literature indicates the method's validity.     

黑线仓鼠的BMR个体差异及其应对高脂食物的能量学对策

为探讨高脂食物对小型哺乳动物能量代谢的影响及其与基础代谢率(Basal metabolic rate, BMR)的关系,将成年雌性黑线仓鼠(Cricetulus barabensis)分为高、低BMR组,每组再随机分为低脂、高脂食物组,驯化6周后,测定体重、摄入能和代谢率,以及消化酶活力、褐色脂肪组织(Brown adipose tissue, BAT)和主要内脏器官与肌肉的细胞色素c氧化酶(Cytochrome c oxidase, COX)活性、解偶联蛋白(Uncoupling protein, UCP) mRNA表达等。结果显示,高脂食物对高、低BMR组动物体重均无显著影响。与低脂食物组相比,高脂食物组的摄食量、摄入能和消化能显著下降,小肠脂肪酶活力显著增强,消化率明显增加,但高、低BMR组的组间差异不显著。夜间代谢水平显著高于昼间,高脂食物使高BMR组的夜间代谢率显著升高。BAT、肌肉和内脏器官COX活性不受高脂食物的影响,高、低BMR组的组间差异也不显著。高脂食物组仅肝脏UCP2表达显著上调。结果表明,能量摄入和消化系统形态及功能的可塑性调节是黑线仓鼠应对高脂食物的主要策略;黑线仓鼠的代谢率具有显著的昼夜节律,既受高脂食物的影响,也与动物自身的BMR水平有关,但UCP表达具有组织特异性,这可能不是导致BMR个体差异的因素。     

Why water birds forage at night: a test using black‐tailed godwits Limosa limosa during migratory periods

Many migratory water birds are known to feed both during day and night outside the breeding season, but the underlying factors and mechanisms determining this foraging pattern are poorly understood. We addressed this topic by comparing both diurnal and nocturnal foraging activity (FA) and metabolizable energy intake rate (MEIR) in migrating black‐tailed godwits Limosa limosa staging in two different habitats, rice fields and coastal salt pans. Black‐tailed godwits staging in rice fields during pre‐breeding migration fed on rice seeds, and only foraged during the daylight period (FA: 81.89 ± 3.03%; MEIR: 1.15 ± 0.03 kJ · min^?1). Daily energy consumption (DEC) of godwits relying on seeds was enough to meet the theoretical daily energy expenditure (DEE). In contrast, black‐tailed godwits staging in salt pans during post‐breeding migration fed on chironomid larvae, and they foraged during both daylight (FA: 67.36 ± 4.30%; MEIR: 0.27 ± 0.01 kJ · min^?1) and darkness (FA: 69.89 ± 6.89%; MEIR: 0.26 ± 0.00 kJ · min^?1). Nocturnal energy intake contributed 31.7% to DEC, the latter being insufficient to fully meet DEE. Our findings give empirical support to the view that diurnal foraging is the norm in many migratory water birds outside the breeding season, and nocturnal foraging occurs when the daily energy requirements are not met during the daylight period, supporting the supplementary food hypothesis.     

Thermal energetics of the New-Guinean moss-forest rat (Rattus niobe) in comparison with other tropical murid rodents

The thermal energetics of rodents from cool, wet tropical highlands are poorly known. Metabolic rate, body temperature and thermal conductance were measured in the moss-forest rat, Rattus niobe (Rodentia), a small murid endemic to the highlands of New Guinea. These data were evaluated in the context of the variation observed in the genus Rattus and among tropical murids. In 7 adult R. niobe, basal metabolic rate (BMR) averaged 53.6±6.6 mL O₂ h⁻¹, or 103% of the value predicted for a body mass of 42.3±5.8 g. Compared to other species of Rattus, R. niobe combines a low body temperature (35.5±0.6 °C) and a moderately low minimal wet thermal conductance c_min (5.88±0.7 mL O₂ h⁻¹ °C⁻¹, 95% of predicted) with a small size, all of which lead to reduced energy expenditure in a constantly cool environment. The correlations of mean annual rainfall and temperature, altitude and body mass with BMR, body temperature and c_min were analyzed comparatively among tropical Muridae. Neither BMR, nor c_min or body temperature correlated with ambient temperature or altitude. Some of the factors which promote high BMR in higher latitude habitats, such as seasonal exposure to very low temperature and short reproductive season, are lacking in wet montane tropical forests. BMR increased with rainfall, confirming a pattern observed among other assemblages of mammals. This correlation was due to the low BMR of several desert adapted murids, while R. niobe and other species from wet habitats had a moderate BMR.     

食物限制对黑线仓鼠能量代谢和产热的影响

为阐明动物应对食物短缺的能量学对策与其自身的代谢水平的关系,测定了不同限食程度下黑线仓鼠的体重、基础代谢率和非颤抖性产热。结果发现,限食使基础代谢率、非颤抖性产热、褐色脂肪组织细胞色素c氧化酶活性降低。90% 限食驯化4 周后,存活率为80% ,60% 限食驯化4 周后,存活率为30% 。低温驯化使黑线仓鼠基础代谢率和非颤抖性产热显著增加,使80% 限食动物的体重和存活率显著降低。高基础代谢率组的摄食量比低基础代谢率组多23.8% ,80% 限食后两组体重降低的幅度和存活率差异不显著。结果表明:高水平的代谢率使黑线仓鼠对食物资源短缺的敏感性增加;支持“代谢率转换假说”,符合“具有储食习性的动物对食物短缺的生理耐受性较低” 的预测。     

Energy metabolism by splanchnic tissues of mature sheep fed varying levels of lucerne hay cubes

The objective of this study was to determine the pattern of energy metabolites net flux across the portal-drained viscera (PDV) and total splanchnic tissues (TSP) in mature sheep fed varying levels of lucerne hay cubes. Four Suffolk mature sheep (61.4 ± 3.6 kg BW) surgically fitted with multi-catheters were fed four levels of dry matter intake (DMI) of lucerne hay cubes ranging from 0.4- to 1.6-fold the metabolizable energy (ME) requirements for maintenance. Six sets of blood samples were simultaneously collected from arterial and venous catheters at 30-min intervals. With increasing DMI, apparent total tract digestibility increased linearly and quadratically for dry matter (P < 0.05), quadratically (P < 0.05) with a linear tendency (P < 0.1) for organic matter and tended to increase quadratically (P < 0.1) for NDF. PDV release of volatile fatty acids (VFA) and β-hydroxybutyric acid was relatively low at 0.4 M and then linearly increased (P < 0.05) with increasing DMI. Net PDV flux of non-esterified fatty acids showed curvilinear decrease from 0.4 to 1.2 M and then increased at 1.6 M. The respective proportions of each VFA appearing in the portal blood differed (P < 0.05) with DMI and this difference was more obvious from 0.4 to 0.8 M than from 0.8 to 1.6 M. Heat production, as a percentage of ME intake (MEI), decreased linearly (P < 0.05) with increasing DMI accounting for 37%, 21%, 16% and 13% for PDV and 62%, 49%, 33% and 27% for TSP at 0.4, 0.8, 1.2 and 1.6 M, respectively. As a proportion of MEI, total energy recovery including heat production, decreased linearly with increasing DMI (P < 0.05) accounting for 113%, 83%, 62% and 57% for PDV and 140%, 129%, 86% and 83% for TSP at 0.4, 0.8, 1.2 and 1.6 M, respectively. Regression analysis revealed a linear response between MEI (MJ/day per kg BW) and total energy release (MJ/day per kg BW) across the PDV and TSP, respectively. However, respective contributions of energy metabolites to net energy release across the PDV and TSP were highly variable among treatments and did not follow the same pattern of changes in DMI.     

Effects of temperature on microbial ethanol production I. The temperature profile curve of ethanol production of the yeast strain saccharomyces cerevisiae Sc 5

The temperature-profile curve of ethanol production of the yeast Saccharomyces cerevisiae Sc 5 is shown. Accordingly the biokinetic sphere of ethanol formation consists of 5 ranges. The maximum specific ethanol formation rate v₀ is reached within the temperature limits of 32°C ≦ T ≦ 36°C, and the maximum temperature for ethanol formation amounts to T″_max = 57°C. Within the first suboptimum temperature range ethanol formation is not retarded thermally. Using a modified ARRHENIUS equation the activation energy of ethanol formation was calculated to be ΔH_ÊtOH = (78.5 ± 2.2) kJ/mol.     

黑线仓鼠自身生存和繁殖输出间的权衡不受温度影响

  为阐明野生小型哺乳动物哺乳期能量收支对策,深入理解最大持续能量摄入（SusEI）限制的因素和机理,测定了不同环境温度下（21℃、30℃和5℃）与哺育不同胎仔数（自然胎仔数Con、减少Minus和增加胎仔数Plus）的黑线仓鼠哺乳期体重、摄食量、基础代谢率（BMR）、非颤抖性产热（NST）,以及褐色脂肪组织（BAT）细胞色素C氧化酶（COX）活性、血清T₃、T₄和催乳素水平。结果显示,哺乳期体重显著降低,摄食量显著增加,21℃和30℃组间差异不显著。最大持续摄食量约为14g/d,Minus组比Con和Plus组低20.3%和18.6%。温度对摄食量的影响显著,5℃下摄食量达16g/d,比21℃和30℃组高14%（P<0.05）。Con和Minus组胎仔数维持稳定,而Plus组胎仔数显著降低,断乳时Con和Plus组胎仔数差异不显著。Minus组胎仔重显著低于Con和Plus组。断乳时Minus组平均幼体体重比Con和Plus组分别高17.9%和24.9%（P<0.05）。5℃下BMR、NST、COX活性、血清T₃、T₄和催乳素水平显著高于21℃和30℃,而21℃和30℃组间差异不显著。结果表明：黑线仓鼠SusEI水平为5×BMR,低温下可通过增加能量摄入应对代谢产热的能量支出,在自身维持和繁殖输出之间采取了“权衡分配”的能量学策略,研究结果支持热耗散限制假说,也符合外周限制假说的预测。     

Isolation and characterisation of two chymotrypsins from the midgut of Locusta migratoria

Two chymotrypsin isozymes (CTR 1 and CTR 2) from the midgut lumen of Locusta migratoria have been identified and purified. MALDI-TOF mass spectrometry revealed an M_r of 22 679 (±30) for CTR 1 and 22 592 (±30) for CTR 2. Both chymotrypsins hydrolysed S-(Ala)₂ProPhe-pNA (CTR 1: K_m=0.29±0.01 mM, V_max=83.0±1.4 U/mg; CTR 2: K_m=0.42±0.01 mM, V_max=48.9±1.1 U/mg) and S-(Ala)₂ProLeu-pNA (CTR 1: K_m=0.50±0.04 mM, V_max=1.7±0.1 U/mg; CTR 2: K_m=1.12±0.08 mM, V_max=11.4±0.6 U/mg), but neither enzyme hydrolysed BTpNA, S-Phe-pNA, Ac-Leu-pNA or S-(Ala)₃-pNA. CTR 1 and CTR 2 activities were effectively inhibited by AEBSF, PMSF, TPCK, chymostatin, SBTI and BPTI. Using S-(Ala)₂ProPhe-pNA as the substrate, CTR 1 gave optimal activity between pH 8.0 and 10.0, while CTR 2 was optimally active over the range pH 8.0–11.0. The N-terminal 15 amino acids of the purified chymotrypsins were determined, revealing their unique sequences which are also different from another, previously characterised Locusta chymotrypsin.     

高山姬鼠冷驯化过程中的能量收支

为探讨栖息于横断山地区高山姬鼠的能量代谢特征,采用食物平衡法,在冷驯化条件下,对其能量收支进行了测定。分别测定了冷驯化(5 ± 1℃ ,42 d)过程中,高山姬鼠体重、体温、每日摄入能、消化能、消化率、粪便能及可代谢能、可代谢率的变化。结果表明:随着冷驯化时间的延长,高山姬鼠的体重和体温降低,28 d 时达到最低值后保持稳定,其中体重在冷驯化14 d 时即与对照组有显著差异,28 d 时平均比对照组降低了15.5% ,体温在14 d 后和对照组有显著差异。每日摄入能、消化能、可代谢能升高,三者均在冷驯化14 d 后与对照组有极显著差异,21 d 时达到最高后保持稳定。粪便能、消化率和可代谢率在冷驯化过程中没有显著变化。高山姬鼠在冷暴露过程中,通过降低体重减少绝对能量需求;通过降低体温减少用于维持体温恒定所消耗的能量;通过增加能量摄入维持正常的生理机能。高山姬鼠在冷驯化过程中表现出的变化模式,与其低纬度、高海拔、年平均温度较低的生存环境有关,这在一定程度上反映了横断山区小型哺乳动物在低温胁迫下的生存机制和适应对策。     

Effects of amantadine on the dynamics of membrane-bound influenza A M2 transmembrane peptide studied by NMR relaxation

The molecular motions of membrane proteins in liquid-crystalline lipid bilayers lie at the interface between motions in isotropic liquids and in solids. Specifically, membrane proteins can undergo whole-body uniaxial diffusion on the microsecond time scale. In this work, we investigate the ¹H rotating-frame spin-lattice relaxation (T _1ρ) caused by the uniaxial diffusion of the influenza A M2 transmembrane peptide (M2TMP), which forms a tetrameric proton channel in lipid bilayers. This uniaxial diffusion was proved before by ²H, ¹⁵N and ¹³C NMR lineshapes of M2TMP in DLPC bilayers. When bound to an inhibitor, amantadine, the protein exhibits significantly narrower linewidths at physiological temperature. We now investigate the origin of this line narrowing through temperature-dependent ¹H T _1ρ relaxation times in the absence and presence of amantadine. Analysis of the temperature dependence indicates that amantadine decreases the correlation time of motion from 2.8 ± 0.9 μs for the apo peptide to 0.89 ± 0.41 μs for the bound peptide at 313 K. Thus the line narrowing of the bound peptide is due to better avoidance of the NMR time scale and suppression of intermediate time scale broadening. The faster diffusion of the bound peptide is due to the higher attempt rate of motion, suggesting that amantadine creates better-packed and more cohesive helical bundles. Analysis of the temperature dependence of $ { \ln }\left( {T_{1\rho }^{ - 1} } \right) $ indicates that the activation energy of motion increased from 14.0 ± 4.0 kJ/mol for the apo peptide to 23.3 ± 6.2 kJ/mol for the bound peptide. This higher activation energy indicates that excess amantadine outside the protein channel in the lipid bilayer increases the membrane viscosity. Thus, the protein-bound amantadine speeds up the diffusion of the helical bundles while the excess amantadine in the bilayer increases the membrane viscosity.     

Time energy budgets and food use of Atlantic brant across their wintering range

We conducted extensive behavioral and food sampling of Atlantic brant (Branta bernicla hrota) across their winter range and used time–activity budgets for brant to determine daily energy expenditure (DEE). Sampling occurred 1 December–31 May 2006–2008 in 11,225-km² sites between Rhode Island and Virginia containing important estuarine and upland habitat. To calculate DEE we used instantaneous scan sampling to estimate time–activity budgets. We also determined foods eaten by brant and energy density of food plants. Last, we quantified body condition of brant, which differed among years, months, regions, and ages, and sexes. Overall DEE for brant was 1,530 ± 64 kJ/day. There was considerable variation in time–activity budgets among years, months, regions, habitat, tide, temperature, and time-of-day, but we detected no significant difference in DEE of brant between years or among regions. However, DEE in January (2,018 ± 173 kJ/day) was nearly double the DEE of brant in May (1,048 ± 137 kJ/day). Brant spent their time feeding (32.3%), swimming (26.2%), resting (16.2%), and flying (14.5%). The percent of brant foreguts sampled contained macroalgae (53%) eelgrass (Zostera marina; 18%), salt marsh cordgrass (Spartina alterniflora; 17%), and terrestrial grass (Poa. sp.) and clover (Trifollium sp.; 9%). Energy density differed by vegetation type: macroalgae (12.6 ± 0.1 kJ/g), eelgrass (14.1 ± 0.1 kJ/g), new-growth salt marsh cordgrass (16.9 ± 0.2 kJ/g), and terrestrial grass and clover (17.7 ± 0.1 kJ/g). Atlantic brant exhibited behavioral plasticity thereby allowing modification of daily activity budgets to meet seasonally varying energetic requirements associated with wintering and spring staging. Recognizing a variable DEE can be used along with eventual estimates of food biomass and total metabolizable energy on the landscape to calculate carrying capacity (goose use days) on state, region, or range-wide scales. © 2011 The Wildlife Society.     

Weekly changes in basal metabolic rate with eight weeks of overfeeding

Objective : The contribution of basal metabolic rate (BMR) to weight gain susceptibility has long been debated. We wanted to examine whether BMR changes in a linear fashion with overfeeding. Our hypothesis was that BMR does not increase linearly with 1000‐kcal/d overfeeding in lean healthy subjects over 8 weeks. The null hypothesis states that BMR increases linearly with 1000‐kcal/d overfeeding in lean healthy subjects. Research Methods and Procedures : Initially, 16 lean healthy sedentary subjects completed 2 weeks of weight maintenance feeding at the General Clinical Research Center. The subjects were then overfed by 1000 kcal/d over 8 weeks. BMR was measured under standard conditions each week using indirect calorimetry. Results : Baseline BMR was 1693 ± 154.5 kcal/d. BMR increased from 1711 ± 201.3 kcal/d at week 1 of overfeeding to 1781 ± 171.65 kcal/d at the second week of overfeeding (p = 0.05). BMR fell during the third week of overfeeding to 1729 ± 179.5 kcal/d (p = 0.05). After 5 weeks of overfeeding, BMR reached a plateau. Thereafter, there was no further change. Comparison of BMR with weeks of overfeeding was significantly different compared with the linear model (p < 0.05). Discussion : Increases in BMR in lean sedentary healthy subjects with 1000‐kcal/d overfeeding are not linear over 8 weeks. There seems to be a short‐term increase in BMR in the first 2 weeks of overfeeding that is not representative of longer‐term changes.     

Temperature response of parameters of a biochemically based model of photosynthesis. I. Seasonal changes in mature maritime pine (Pinus pinaster Ait.)

Responses of plant processes to temperature may vary according to the time scale on which they are measured. In this study, both short‐term and seasonal responses of photosynthesis to temperature were examined. A field study of seasonal changes in the temperature response of photosynthesis was conducted on two provenances, French and Moroccan, of mature maritime pine (Pinus pinaster Ait.). Measurements were made every 2 months over a 1‐year period and used to parameterize a mechanistic model of photosynthesis. Temperature responses of maximum Rubisco activity, V_cmax, and potential electron transport rate, J_max, were obtained for each measurement period, as was the response of stomatal conductance, g_s, to water vapour pressure deficit (VPD). Absolute values of V_cmax and J_max at 25 °C were related to needle nitrogen content, N_area.N_area, and thus V_cmax and J_max, were negatively correlated with the mean minimum temperature in the month preceding measurements. The ratio of J_max : V_cmax at 25 °C varied between 1 and 1·7 but did not show any seasonal trend. Nor was there any seasonal trend in the relative temperature response of V_cmax, which had an activation energy H_a of approximately 57 kJ mol^?1 throughout the experiment. The activation energy of J_max was also close to constant throughout the experiment, averaging 39 kJ mol^?1. For the French provenance, the optimal temperature of J_max was positively correlated with the maximum temperature of the previous day, but no such correlation was found for the Moroccan provenance. The response of g_s to VPD also varied seasonally, with much stronger stomatal closure in winter months. Taken together, these results implied a translational shift downwards of the photosynthetic temperature response curve with increasing T_prev, and a shift in the temperature optimum of photosynthesis of 5–10 °C between summer and winter. These results illustrate that the short‐term temperature response of photosynthesis varies significantly on a seasonal basis.