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1 also show reduced feeding in the morning and midday.
2 ine circadian rhythmicity with a peak around midday.
3 ours, with complete sulfide depletion around midday.
4 emained at a sunny beach for 3(1/2) hours at midday.
5 y appearing as a burst of new particles near midday.
6 ission rates of up to 35.4 mg m(-2) h(-1) at midday.
7 n modulating anthocyanin biosynthesis around midday.
8 nder the high irradiance of full sunlight at midday.
9 a decrease in water potential to -1.8 MPa at midday.
10 a pattern suggesting maximum axial length at midday.
11  the maximum axial length tended to occur at midday.
12 mol guard cell pair(-1) between daybreak and midday.
13 in implicit time), reaching a peak at around midday.
14   Maximum rates of carboxylation (V(c,max)), midday A and g(s) rates at the middle canopy, and decrea
15 e scaling law in light-dark cycles, tracking midday across conditions with variable day length.
16 ) regression slope < 1 or T(c) < T(a) around midday) across global extratropics, including temporal a
17 ,2,3,4-tetrahydro-naphthalene (8-OH-DPAT) at midday advanced the phase of the free-running circadian
18  hours, we segmented movements into morning, midday, afternoon, and evening.
19 rse particles at four time periods (morning, midday, afternoon, and overnight) in summer 2009 and win
20      Higher ROS activity was observed in the midday/afternoon during summertime, while the peak activ
21 ate afternoon, a reduced green preference at midday and a robust avoidance of blue throughout the day
22 adients, with drylands exhibiting widespread midday and afternoon depression in photosynthesis.
23 n plant water potential (Psi) at predawn and midday and describe a method that predicts Psi at stomat
24                                              Midday and evening breath CIRs correlated strongly with
25                                         When midday and evening MPAH were analyzed separately, HRs co
26 neurons peak in clock gene expression around midday and in calcium activity about three hours later.
27 Multiple cognitive domains were evaluated at midday and late afternoon following complete abstention
28 n the symbiosome membrane was highest around midday and lowest around midnight.
29 that sucrose concentrations are > 1100 mM at midday and midnight.
30  markers of degradation, particularly during midday and nighttime hours, which are not typically samp
31  high-humidity conditions (up to 80%) during midday and nighttime, respectively.
32 isuospatial performance better at subjective midday and olfactory performance better at subjective mi
33 line during phase II (moderate drought), and midday and predawn Psi reached similar values during pha
34 dicating that all three groups seek shade at midday and that light activation of the suprachiasmatic
35  during long days with the peak occurring at midday and the low point midway through the dark period.
36 ighest level of the O2 message is present at midday and the lowest level at midnight.
37 oral ataluren (10 mg/kg in morning, 10 mg/kg midday, and 20 mg/kg in evening) or matching placebo for
38               Three breath samples (fasting, midday, and evening) were collected on each of 3 noncons
39 round illumination is most intense, e.g., at midday, and that the surround is minimal following maint
40 ation down to avoid photoinhibitory light at midday; as the attenuation of light increased with bioma
41 ut time spent outdoors in direct sunlight at midday at 3 life periods: high school to age 24 years, a
42 ality, particularly as this clustered around midday at weekends.
43  BC response; these peaks are shifted toward midday because most diesel truck traffic occurs during o
44 obust evidence that supports the efficacy of midday bright light therapy for bipolar depression.
45  12-, and 14-h photoperiods) were shifted to midday by noninductive (18- and 20-h) photoperiods, and
46 ximately 1/3 of the total emissions detected midday by the aircraft and approximately 2/3 of the west
47             The up-regulation is overcome at midday by the repressing activity of LNK proteins, as in
48               The highest VPD site had lower midday canopy water potentials, canopy conductance (g(c)
49 cal stimulation of the DRN during subjective midday caused a 1.3-h advance in the free-running circad
50                                          The midday concentration of chloroplastic DMAPP in cottonwoo
51 d a temperature drop of 5.4 degrees C during midday conditions with a solar intensity of 850 watts pe
52 leaf rolling 1 (psl1) mutant with 'napping' (midday depression of photosynthesis) phenotype and reduc
53              Compared with directly measured midday embolism levels, the PAD and AI methods substanti
54  enhancement ratio is clearly observed, with midday enhancement ratios approximately four times great
55 ator reported hourly activity data show that midday episodic emissions from manual liquid unloadings
56 ficacy of adjunctive bright light therapy at midday for bipolar depression.
57                              Baboons avoided midday heat but increased dawn and night activity under
58 a mean 2.9 +/- 0.01 degrees C warming during midday hours in summer, and shifts with warming were unr
59 rly in the day during May, August and around midday in September, leading to sustained reductions in
60 th an increasing non-nitrate fraction around midday, in close agreement with aircraft observations.
61  from the warmest locations maintained lower midday leaf temperatures, a higher midday stomatal condu
62 eep) , the seasonal plasticity of WA(deep) , midday leaf water potential (Psi(md) ), species abundanc
63       While isohydric species maintain their midday leaf water potential (PsiM) under soil water defi
64 ots is the most likely driver of declines in midday leaf water potential needed for ABA biosynthesis
65 nitored the seasonal dynamics of predawn and midday leaf water potentials and leaf phenology for bran
66 s among C4 plants were linked with declining midday leaf water potentials.
67 s and had slightly less negative predawn and midday leaf water potentials.
68 ow-fiber/low-residue diets for the early and midday meals.
69 dian fluctuation (P < .05) and was lowest at midday (mean +/- SD, 10.14 +/- 2.62 mm(3)) and highest a
70 at episodic sources can substantially impact midday methane emissions and that aircraft may detect da
71 .93 (95% CI: 0.89-0.97, p-trend = 0.003) for midday MPAH and 0.76 (95% CI: 0.70-0.83; p-trend < 0.001
72                      Participants eating 5-7 midday MPAH had 9% lower T2D risk than those with 0-2 mi
73 AH had 9% lower T2D risk than those with 0-2 midday MPAH, and participants having 5-7 evening MPAH ha
74 ay-active and sleep at night, they exhibit a midday nap, or "siesta," that can vary in intensity and
75                        Despite the fact that midday naps are characteristic of early childhood, very
76 ucrose and starch in leaves, and morning and midday net carbon assimilation rates were significantly
77  GA1 levels in 90M and 100M was shifted from midday, observed earlier with 12-h photoperiods, to an e
78 imately 65% to 70% of the DMAPP recovered at midday occurred in the chloroplasts, indicating that mos
79  winds from the north-northwest at the time (midday) of the abrasion operations.
80 imate an atmospheric lifetime for CH(2)OO at midday on the order of approximately 1 s with respect to
81                     Frequencies of consuming midday or evening MPAH were assessed at baseline and dur
82  at one of two predominant circadian phases, midday or mid-night, times of behavioral quiescence; mRN
83 r rarely affects photosynthesis at TROPOMI's midday overpass, a time when the forest canopy is most o
84 eometers and remote sensing (ECOSTRESS) have midday peak temperatures of approximately 34 degrees C d
85  Rubisco transcripts were highest during the midday period, decreased at later times during the light
86 e, including inhibition lowered estimates of midday productivity around 20% for the modeled region of
87                             For all species, midday Psi was much more negative than predawn Psi durin
88 during phase I (mild drought), reductions in midday Psi were minor while predawn Psi continued to dec
89 24 in situ measurements of daily predawn and midday Psi, the temporal variability of hydraulic behavi
90  total, root and nodule biomass, predawn and midday quantum yields, maximum electron transport rates,
91 t is commonly observed in animals during the midday, raising the possibility of shared mechanisms.
92                                          The midday reduction in green preference in favour of dim li
93 ystems have slopes >=1 or T(c) > T(a) around midday, rejecting the above hypothesis.
94 e in C57BL/6J mice is consistently better at midday relative to midnight.
95  this species exhibits seasonality such that midday rest expands on long warm days, possibly to avoid
96 nts were acquired at Jezero Crater, Mars, at midday, retrieving an average ozone column abundance of
97 easing light intensity leads to an increased midday siesta in Drosophila behavior.
98 gaster, enabling this species to prolong its midday "siesta," a mechanism that likely diminishes the
99 ned lower midday leaf temperatures, a higher midday stomatal conductance, and maintained turgor press
100 al regulation, with increased closure during midday stress periods but normal aperture under benign c
101 f sun protection, time spent outdoors in the midday sun (days and hours), and the number of sunburns
102 ime spent outdoors (days and minutes) in the midday sun and number of sunburns in the past 3 months w
103 g adolescents, computer support can decrease midday sun exposure and increase sunscreen use.
104 warmed plants was as well-matched with prior midday temperatures as Topt of plants in the ambient tre
105 ce, in plants that were shifted to 90% RH at midday, the guard cell apoplast Suc content declined to
106                    These cones generate diel midday thermogenic temperature increases as large as 12
107             Serum and urine sampling at late midday time points may be the optimal approach for OA st
108 2) and Cl(2) ranged from detection limits at midday to campaign maximum values at night reaching 2100
109 amounts of beta-carotene and fat were fed at midday to children 3-6 y of age for 3 wk.
110 increasing temperatures by moving labor from midday to cooler hours.
111 increase in release from a nadir during late midday to peak levels at the light/dark transition.
112 his diurnal osmotic adjustment, estimates of midday turgor were always >0.7 MPa.
113          We conclude that the extremely weak midday twilight experienced by krill at high latitudes d
114 n below the horizon at midday; we term this "midday twilight." Here, we characterize light across a l
115 evels of nitrous acid and nitrogen oxides at midday under typical marine boundary layer conditions.
116                                     Assuming midday UVB levels, sufficient but suboptimal vitamin D s
117 =.7), or in the evening/night versus morning/midday versus varying times (218.8 +/- 119.7 v 195.5 +/-
118                              Measurements of midday vertical atmospheric CO2 distributions reveal ann
119 hase-advancing sleep deprivation stimulus at midday was prevented by intra-DRN injection of metergoli
120 ed were substantially more negative than the midday water potentials for five grass species monitored
121          The models were applied to estimate midday, water column photosynthesis based on an atmosphe
122  by the sun's elevation below the horizon at midday; we term this "midday twilight." Here, we charact
123 ance shifts induced by novel wheel access at midday were suppressed, but not blocked, by intra-DRN in
124  between aircraft studies (basin total for a midday window) and emissions inventories (annualized reg
125  for fibrinogen and von Willebrand factor at midday, with overall diurnal variations of 3% and 10%, r
126 riation in growth, water stress (predawn and midday xylem tension), drought avoidance traits (branch

 
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