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We measured the following variables to investigate the effects of fasting and temperature on swimming performance in juvenile qingbo (Spinibarbus sinensis): the critical swimming speed (Ucrit), resting metabolic rate (ṀO2rest) and active metabolic rate (ṀO2active) of fish fasting for 0 (control), 1, 2 and 4 weeks at low and high acclimation temperatures (15 and 25 °C). Both fasting treatment and temperature acclimation had significant effects on all parameters measured (P<0.05). Fasting at the higher temperature had a negative effect on all measured parameters after 1 week (P<0.05). However, when acclimated to the lower temperature, fasting had a negative effect on Ucrit until week 2 and on (ṀO2rest), (ṀO2active) and metabolic scope (MS, (ṀO2active)(ṀO2rest)) until week 4 (P<0.05). The values of all parameters at the lower temperature were significantly lower than those at the higher temperature in the identical fasting period groups except for (ṀO2rest) of the fish that fasted for 2 weeks. The relationship between fasting time (T) and Ucrit was described as Ucrit(15)=−0.302T2−0.800T+35.877 (r=0.781, n=32, P<0.001) and Ucrit(25)=0.471T2−3.781T+50.097 (r=0.766, n=32, P<0.001) at 15 and 25 °C, respectively. The swimming performance showed less decrease in the early stage of fasting but more decrease in the later stage at the low temperature compared to the high temperature, which might be related to thermal acclimation time, resting metabolism, respiratory capacity, energy stores, enzyme activity in muscle tissue and energy substrate utilization changes with fasting between low and high temperatures. The divergent response of the swimming performance to fasting in qingbo at different temperatures might be an adaptive strategy to seasonal temperature and food resource variation in their habitat.  相似文献   

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Arctic Grayling (Thymallus arcticus) are among the most widely distributed and abundant freshwater fish in the Yukon Territory of Canada, yet little information exists regarding their broad and fine‐scale population structures or the number and size of these populations. The estimation of population abundance is fundamental for robust management and conservation, yet estimating abundance in the wild is often difficult. Here, we estimated abundance of an Arctic Grayling population using multiple genetic markers and the close‐kin mark‐recapture (CKMR) method. A total of N = 1,104 Arctic Grayling collected from two systems in Yukon were genotyped at 38 sequenced microsatellites. We first identified structure and assessed genetic diversity (effective population size, N^e). Collections from one of the systems (Lubbock River) comprised adults and young‐of‐the‐year sampled independently allowing the identification of parent–offspring pairs (POPs), and thus, the estimation of abundance using CKMR. We used COLONY and CKMRsim to identify POPs and both provided similar results leading to indistinguishable estimates (95% CI) of census size, that is, N^c(COLONY) = 1858 (1259–2457) and N^c(CKMRsim)=1812 (1229–2389). The accuracy of the population abundance estimates can in the future be improved with temporal sampling and more precise age or size‐specific fecundity estimates for Arctic Grayling. Our study demonstrates that the method can be used to inform management and conservation policy for Arctic Grayling and likely also for other fish species for which the assumption of random and independent sampling of adults and offspring can be assured.  相似文献   

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《Biophysical journal》2022,121(13):2503-2513
It is generally assumed that volume exclusion by macromolecular crowders universally stabilizes the native states of proteins and destabilization suggests soft attractions between crowders and protein. Here we show that proteins can be destabilized even by crowders that are purely repulsive. With a coarse-grained sequence-based model, we study the folding thermodynamics of two sequences with different native folds, a helical hairpin and a β-barrel, in a range of crowder volume fractions, φc. We find that the native state, N, remains structurally unchanged under crowded conditions, while the size of the unfolded state, U, decreases monotonically with φc. Hence, for all φc>0, U is entropically disfavored relative to N. This entropy-centric view holds for the helical hairpin protein, which is stabilized under all crowded conditions as quantified by changes in either the folding midpoint temperature, Tm, or the free energy of folding. We find, however, that the β-barrel protein is destabilized under low-T, low-φc conditions. This destabilization can be understood from two characteristics of its folding: 1) a relatively compact U at T<Tm, such that U is only weakly disfavored entropically by the crowders; and 2) a transient, compact, and relatively low-energy nonnative state that has a maximum population of only a few percent at φc=0, but increasing monotonically with φc. Overall, protein destabilization driven by hard-core effects appears possible when a compaction of U leads to even a modest population of compact nonnative states that are energetically competitive with N.  相似文献   

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Diurnal changes in physiological and psychological responses to consistent relative humidity (RH) conditions were investigated in the present study. Lightly clothed six male and six female subjects participated in the first experiment at 40% and 50% RH, and seven male and seven female subjects participated in the second experiment at 60%, 70%, and 80% RH. Both experiments were conducted at 28 °C air temperature (Ta) from 9:00–18:30. Skin temperatures, local heat flux rates and tympanic temperature (Tty) were monitored at 2-min intervals throughout the experimental period. Body weight loss and oxygen consumption rate were measured during the 9:30–10:30, 13:30–14:30, and 17:30–18:30 periods. Thermal sensation and thermal comfort responses were recorded at the same periods. The amount of heat loss was greater than metabolic heat production (M) in the male subjects but was well balanced with M in the female subjects. A morning increase in Tty at 50%–80% RH was observed, and mean skin temperature (Tsk) at 70% and 80% RH was significantly higher (p < 0.05) than Tsk at 40% and 50% RH in both subject groups. Although difference in the relationship between thermal sensation and Tsk based on sex was confirmed, diurnal changes in thermal sensation were observed in both subject groups based on the responses of “warm” in the morning but “neutral” or “slightly warm” in the evening at 70% and 80% RH. This result demonstrates that high RH may be acceptable in the late afternoon and evening at 28 °C and indicates that dynamic control of RH during the daytime (e.g., low RH in the morning and high RH in late afternoon) may be beneficial to save energy when using air-conditioning.  相似文献   

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Studies are reported on the chemical reduction of the homobinuclear bis(μ-phosphido) metal complexes (CO)3Fe(μ-PR2)2Fe(CO)3 (R = Ph or Me), (NO)2-Fe(μ-PPh2)2Fe(NO)2 and (CO)4M(μ-PPh2)2M(CO)4 (M = Mo or W). Two reduction pathways have been observed which result in different two-electron transformations: (1) with Na or LiAlH4, electron transfer to yield the corresponding symmetric dianions of the type LnM(μ-PR2)2MLn2? without metalmetal bond and (2) with M′BR′3H(M′ = Li, Na, or K; R′ = Et or sec-Bu), hydride transfer to give monoanionic complexes of the type LnM(μ-PR2)(μ-L)MLn?1(PR2H)? or LnM(μ-PR2)MLn(PR2H)? (M = Fe, Mo, or W; L = CO or NO; R = Ph or Me). The monoanionic complexes can be deprotonated with n-BuLi at ?78 °C to the corresponding unsymmetric dianions LnM(μ-PR2)(μ-L)MLn?1(PR2)2? (M = Fe; L = CO or NO; R = Ph) or symmetric dianions LnM(μ-PR2)2MLn2? (M = Mo or W; L = CO; R = Ph). The unsymmetric dianions isomerize on slight warming to the symmetric dianions, which undergo protonation by CF3COOH to yield the aforementioned monoanions. Reactions of several members of these three classes of binuclear anions with CF3COOH, alkylating reagents, 1,1-diiodohydrocarbons and metal diiodo complexes have resulted in the synthesis of new binuclear and trinuclear compounds. Examples include (CO)3(H)Fe(μ-PPh2)Fe(CO)3(PPH2H), (CO)3Fe(μ-PPh2)(μ-C(R)O)Fe(CO)2(PPh2R) (R = Me, Et, n-Pr, or i-Pr), (CO)4M(μ-PPh2)2M(CO)3(C(R)Ome) (M = Mo or W; R = Me or Ph), (CO)2(η3?C3H5)Fe(μ?PPh2)?Fe(CO)3(PPh2C3H5), (CO)4M(μ?PPh2)2M(CO)3(C(R)Ome), (NO)2Fe(μ?CH2)(μ?Ph2PPPh2)Fe(NO)2, and Fe2Co(η5-C5H5)(CO)(NO)4(μ-PPh2)2. Synthetic and mechanistic studies on these reactions are presented.  相似文献   

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