ライフサイエンスコーパス: energy gain

1 push by the laser further increases the ion energy gain.

2 f ITER, a fusion reactor that promises a net energy gain.

3 optimize foraging strategies to maximize net energy gain.

4 y, which should be optimised to maximise net energy gain.

5 ibution of a particular membrane to the free energy gain.

6 on reaction with methane yields the greatest energy gain.

7 nd edibility and has been argued to increase energy gain.

8 mpared to fibrils, results in a smaller free energy gain.

9 substantial length to achieve a significant energy gain.

10 pesticide pollutants, respectively, per net energy gain.

11 ustain and propagate the burn, enabling high energy gain.

12 forage fishes but did not show the greatest energy gains.

13 behaviour of an animal that maximizes total energy gained.

14 plasma with more than a gigaelectronvolt of energy gain, accelerating a trailing positron bunch in a

15 inding could benefit from the potential free energy gain accompanying the release of these water mole

16 g strategy by which blue whales may maximize energy gain amid ephemeral foraging opportunities.

17 the coefficient of variation of the rate of energy gain among patches, and the ratio of the expected

18 >100 MV m(-1) accelerating gradient, >50 MeV energy gain and excellent output beam quality.

19 High gradients of energy gain and high energy efficiency are necessary par

20 Our simulations reproduced the energy gain and showed that ions were accelerated mainly

21 results for below-gap optical pumping reveal energy-gain and -loss Floquet replica valence bands that

22 plasma wakefield accelerators have imparted energy gain approaching 10 gigaelectronvolts to single n

23 days HRT, shifted from neutral to positive (energy gain around 2.7 GJ/d) after thermal pretreatment.

24 nce of the boundary energy, we show that the energy gain associated with boundary curvature relaxatio

25 he in-plane lattice constants diminishes the energy gain associated with the tetragonal distortion, a

26 Despite a focusing energy gain below unity, the unprecedented power gain is

27 Tooling increased the net energy gain by 50% and decreased the proportion of fiber

28 We report the demonstration of the energy gain by a distinct trailing positron bunch in a p

29 HP pathway enables M. concilii dominance and energy gain by carbon fixation and methanogenesis, respe

30 iation friction can dramatically enhance the energy gain by electrons from a laser pulse in a strong

31 ink the observed electrochemical currents to energy gain by individual cells, thus overlooking the po

32 Resource tracking, where animals increase energy gain by moving to track phenological variation in

33 conclusion, obstruction of electron flow and energy gain by sulfate limitation offers an explanation

34 he electron density is lowered, the exchange energy gained by aligning the electron spins should exce

35 which case the distance of acceleration and energy gain can be strongly limited by head erosion.

36 nfirmed by both the high negative Gibbs free energy gain, DeltaG = -115.95 kJ/mol, calculated using t

37 f possible dimer conformations, and that the energy gain depends on the interplay between structural

38 Prey profitability (energy gained divided by prey handling time) is an essen

39 sly during the synthesis cycle, allowing the energy gain due to spontaneous binding of ADP to one cat

40 rgy-dissipation via phonon emission outpaces energy gains due to standard Auger-type energy transfer

41 routes shape animal movement and presumably, energy gains during migration.

42 Density functional theory showed that the energy gain from CO binding to low-coordinated Cu atoms

43 of mammalian mastication will affect the net energy gain from foods.

44 The large energy gain from oxygen redox reactions is often connect

45 ase) is a transmembrane enzyme that utilizes energy gained from ATP hydrolysis to transport sodium an

46 The energy gained from intercalation is slightly greater tha

47 how that cooking substantially increases the energy gained from meat, leading to elevations in body m

48 ng not on molasses in reactor feed but using energy gained from oxidation of sulfur compounds produce

49 Within 18-h test, the energy gained from the MPPC was 76.8 J, 76 times higher

50 e oxygen minimum zones (OMZs) where they use energy gained from the oxidation of reduced sulfur to fu

51 The docking energy gained from this induced fit is 0.7 kcal/mol for

52 al bonding driven by the competition between energy gains from covalency and delocalization, and ener

53 foods, the idea that cooking meat increases energy gain has never been tested.

54 alternative, a biofuel should provide a net energy gain, have environmental benefits, be economicall

55 However, the energy gain in a single-stage LPA can be limited by lase

56 The maximum energy gain in a single-stage LWFA is limited by dephasi

57 a non-local relaxation process, in which an energy gain in one domain of the moire lattice is paid f

58 uction and biotransformation of arsenate for energy gain in sediments that present a two-fold greater

59 goal of achieving burning fusion plasmas and energy gain in the laboratory.

60 ein between the two GET phases by leveraging energy gained in ATP binding and hydrolysis to undergo s

61 -bound functional potencies are derived from energy gains in the transition from a precoupled complex

62 nition (FI) is a promising approach for high-energy-gain inertial confinement fusion in the laborator

63 ws the optical pulse, is primarily due to an energy gain involving the photoexcited charge carriers t

64 throttles reconnection so that the electron energy gain is a large fraction of the released magnetic

65 Although energy gain is a well-known effect from cooking starch-r

66 al/mol to the helix stability, while no free energy gain is detected if the two residues have the rev

67 Later in the photocycle, the free energy gain is transferred from the chromophore to the p

68 Based on the energy gain/loss balance under external field and electr

69 A highly favourable energy gain/loss rate ratio realized in magnetically dop

70 in terms of raw material, solvent, time and energy gained more importance to provide a sustainable l

71 The energy gain must reside in or near the photoisomerized r

72 A high-potency agonist had an energy gain of -11.1 kcal mol(-1).

73 ding 2000 angstrom(2) with a total solvation energy gain of -35.4 kcal/mol.

74 left from 22 angstrom to 31 angstrom with an energy gain of -4.8 kcal mol(-1), making GDP water-expos

75 their bandgaps, exhibiting a large apparent energy gain of 0.6-1.4 eV per photon.

76 cle-tracking simulations, we infer a maximum energy gain of 0.915 kilo-electron volts over 30 microme

77 field of the second stage is detected via an energy gain of 100 megaelectronvolts for a subset of the

78 uccessful predation, we estimate a daily net energy gain of 2.4 MJ (5.1 MJ acquired, 2.7 MJ expended)

79 -95% recovery efficiency, resulting in a net energy gain of 57-62 kJ/mol-CO2 captured.

80 ed barrier of 116 kJ mol(-1) and the overall energy gain of 72 kJ mol(-1).

81 application of the model to examine the net energy gain of a typical pause-travel predator (the Atla

82 dscape of fibril growth and reduces the free energy gain of Abeta peptide binding to the fibril by ap

83 mW/m(2) in 2011, which represents an annual energy gain of around 1.0 x 10(15) J.

84 The energy gain of electrons happens during their interactio

85 piratory pathways, describing the respective energy gain of host-cell and PMP resulting from varying

86 on demonstrate that half of the binding free energy gain of m(7)GTP with respect to GTP can be attrib

87 Here we show that an energy gain of more than 42 GeV is achieved in a plasma

88 o exothermic for Galpha opening, but with an energy gain of only -1.4 kcal mol(-1).

89 ectively doubles their energy, producing the energy gain of the 3-km-long SLAC accelerator in less th

90 improves beam quality and leads to projected energy gains of 125 GeV in a single, sub-meter stage dri

91 photocathode wakefield acceleration combines energy gains of tens of GeV m(-1) with generation of ult

92 cene gives rise to a substantial anti-Stokes energy gain (PDI, 0.70 eV; tetracene, 0.86 eV).

93 charged particle beams at high gradients of energy gain per unit length is necessary to achieve an a

94 We show how energy gain, predation and damage can be combined in a s

95 indicate that the fundamental limitation to energy gain presented by laser depletion can be overcome

96 mediated DNA strand displacement (DSD) using energy gains provided in DNA toeholds.

97 t allow for 'uphill' energy transfer with an energy-gain rate that greatly exceeds the intraband cool

98 However, the microbial carbon allocation to energy gain relative to biosynthesis was unchanged, sign

99 ical processes create tipping points between energy gain, reproduction or survival.

100 ELS), cathodoluminescence (CL), and electron energy gain spectroscopy (EEGS); (ii) four-dimensional s

101 el also releases less air pollutants per net energy gain than ethanol.

102 se counteracting effects result in a maximum energy gain through a complete removal of water molecule

103 cificity (i.e. the result of greater binding energy gained through interactions with major histocompa

104 omplex suggests that there is a considerable energy gain upon binding of maltotriose in comparison to

105 te linear acceleration of electrons with keV energy gain using optically generated terahertz pulses.

106 ions illustrate that substantial anti-Stokes energy gains via a TTA process can be effortlessly reali

107 Large digestive organs increase rates of energy gain when food is plentiful but are costly to mai

108 urgy due to their good recyclability and 95% energy gain when made from scrap.

109 self-assembly reflects a balance between the energy gain when particle cores approach and the entropy

110 nergyscape reflects spatial variation in net energy gains, while the optimal movement landscape inclu