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The statistical analysis system (SPSS version 17.0) software was used to analyse all the data. The data were expressed as mean±standard error of mean (SEM) and the data were analysed using the Student’s t -test and one-way analysis of variance (ANOVA) followed by Tukeys post hoc multiple comparison test. Differences were considered statistically significant at P <0.05 for all the experiments used in this study. All treatments (six fishes in each treatment) were assayed in duplicate for each fish.

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contents and total erythrocyte counts significantly increased in group A, group B and group C at 30–60
days of feeding ( ASYMMETRIC Slipons powder Clearance 2018 Newest DAlZR3X
, respectively). Total leucocyte count of C. catla significantly produced higher number of cells from 10days of feeding. Particularly, leucocyte count was higher in group B and group C than in group A from 40 to 60days of feeding with the experimental diet ( Free Shipping New Arrival DELHI Slipons royal Affordable Online Discount Extremely Huge Surprise Online 0nVEI
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values (mean
±SEM) of blood in fed with different concentrations (group A, group B and group C: 0.05%, 0.5% and 5%, respectively) of mixed diet between normal diet (control). ONLBLIX BUCKLE BOOTIE Cowboy/Biker boots black Sale Low Shipping Fee Best Seller Sale Free Shipping Outlet Marketable Order For Sale G1M2G
(Hb: g/dl), erythrocytes (RBC: 10
cellmm), leucocytes (WBC: 10mm) were obtained from 10, 20, 30, 40, 50 and 60days of feeding. Statistical differences (<0.05) among groups are indicated by asterisk (*).

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level gradually increased in all experimental diet groups from 10 to 40
days of feeding ( Fig. 1a ). Glucose levels of group B (423±12.52 and 441.33±10.9) and group C (427.7±21.5 and 445.7±12.33) reached optimum at 30 and 40days of feeding, respectively. Then, the glucose level slightly reduced at 50 and 60days, although it was higher than that in the control and group A. In general, control and group A probably showed the same level of glucose.

Figure 1 . Biochemical values (mean±SEM) of blood serum in fed with different concentrations of mixed diet between normal diet (control). (a) Glucose (Hb: mg dL ), (b) Gianvito Rossi Suede SquareToe Loafers Pictures Online oTgpDOUKTW
(mmol
L), (c) total protein (gL), (d) albumin (gL), (e) globulin (gL), (f) albumin/globulin ratio (gL), (g) RNA/DNA ratio were obtained at 10, 20, 30, 40, 50 and 60days of feeding.

Serum cholesterol level of fish was significantly higher than that in the control in all experimental diet groups ( Fig. 1b ). Cholesterol level of group A was about similar to that of control at 30 and 40days of feeding (2.89±0.01 and 2.892±0.01), respectively. Cholesterol level was very lesser in control at 20 and 50days of feeding (2.702±0.04 and 2.72±0.01).

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Last modified on Tue 17 December 2013 9:55 pm

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says:
March 27, 2006 at 3:28 pm

If you are dealing with small amounts, like those mentioned above, then the conversions are okay. But according to the authors of “The New Best Recipe” (the same people who write Cook’s Illustrated), there can be a big difference between brands of kosher salt. I know that for Diamond Crystal kosher salt, they gave a conversion ratio of 2:1. That is, use 2 teaspoons of kosher salt if a recipe calls for 1 teaspoon of table salt. For a different brand of kosher salt (I think it was Morton’s), they gave a conversion ratio of 1.5:1 — the same one that you mentioned.

Again, this really won’t make a big difference if you are measuring in teaspoons, but if you want to brine something and are using a cup or two of salt, then it can make a difference.

Don’t you love how people go nuts over salt grinders? They don’t seem to understand that salt is a rock and it’s not any fresher if you grind it yourself. Love your site!

Reply
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Hi iPont,

Great comments about the difference in salts. I am one of those people who enjoy my salt grinder not because I think it is any fresher, it just reduces the size of the salt when I add it to finished dishes. I also like the feel of grinding the salt as I do grinding pepper. – RG

Reply
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The Prof is correct when it comes to basic table salt v kosher v sea, but there are literally scores, maybe hundreds of gourmet salt varieties. I’ve never actually used them, but I’ve seen them in gourmet stores and on Iron Chef. They are amost always colored due to impurities being left in the crystal structure.

Reply
says:
March 31, 2006 at 4:40 am

Don’t make fun of my Salt Grinder! I love it! I know it doesn’t make salt fresher, but it’s what every gal needs…a gimmick!

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Yes, I love the salt grinders for entertainment value. There’s a very well known spice brand sold here in Africa that recently added “Freshly Ground Atlantic Sea Salt” to their extensive product range. Now, no weekend meal with friends is complete without the hilarity of a discussion about the need to use such freshly ground salt on our food. Mock tantrums have ensued when one or other guests were forced to use pre ground salt to sprinkle over their plate instead of the freshly ground that their delicate palates favour. What a laugh. I wonder how many people find a ‘genuine advantage’ in freshly grinding their salt not realising they’ve being suckered.

In all embryonic preparations, lpm, pdm, and dgm were silent in control saline when the neuromodulatory inputs were removed (data not shown). In CabTRP, the mean fundamental frequencies of activity in pdm (0. 23 ± 0.08 Hz, n = 7) and lpm (0.23 ± 0.07 Hz, n = 7) were not statistically different (unpaired t test, p = 0.15, n = 7) ( Low Cost For Sale Discount Manchester Orson calf length boots Extremely Sale Outlet Store X3d5Rmr6a
B ). We did not calculate the fundamental frequency for embryonic dgm because activity in dgm was highly irregular (1–4 bursts in 5–10 min recordings). CabTRP-activated motor patterns were not changed when the muscles were hyperpolarized, and the waveforms of these events were typical of embryonic EJPs.

The CabTRP-activated motor patterns in embryos and adults were different. In CabTRP, lpm was activated in the embryo but the LP neuron was not activated in the adult. The embryonic dgm was either silent or produced very slow, infrequent activity, but in the adult, DG fired together with the PD neuron. There were no statistical differences between the mean fundamental frequencies of activity in adult PD neurons and embryonic pdm [unpaired t test, p = 0.95, n = 6 (adult), n = 7 (embryo)].

Comparing the phase relationships of the CabTRP-activated motor patterns between embryos and adults, adult PD and DG neurons fired together (DG phase at ∼0 in the PD phase; mean coherence magnitude, 0.92 ± 0.09) ( Fig. 8 C ), whereas embryonic lpm and pdm fired in alternation (lpm phase at ∼0.5 in the pdm phase; mean coherence magnitude, 0.71 ± 0.12) ( Fig. 8 D ).

We also wanted to examine the maturity of the embryonic STG response to a modulator whose expression in the embryonic inputs is mature. Red pigment concentrating hormone (RPCH) is a peptide that modulates adult pyloric neurons and has a very similar expression pattern in the adult and embryonic STNS ( Fénelon et al., 1999 ; Thirumalai and Marder, 2002 ). When RPCH was bath-applied to an adult STG isolated from its neuromodulatory inputs, the activity patterns in the PD and LP neurons were similar, and the DG neuron fired bursts at a slower frequency ( Fig. 9 A , B ). In embryos, RPCH also activated all three neurons, resulting in motor pattern in which lpm and pdm were active at approximately the same frequency, which was faster than dgm ( Fig. 9 C , D ).

Figure 9.

RPCH effects on an isolated adult and embryonic STG. , Adult, Simultaneous intracellular recordings from PD, LP, and DG somata, neuromodulatory inputs removed, in control saline. , Same preparation as in in 10 m RPCH. , Embryo, Simultaneous intracellular recordings from pdm, lpm, and dgm, neuromodulatory inputs removed, in control saline. , Same preparation as in in 10 m RPCH.

Figure 10 shows the adult and embryonic motor patterns in RPCH during the entire recording of the experiment from Figure 9 . The spectrograms of the output from the adult DG neuron (fundamental frequency, 0.04 Hz) and the embryonic dgm (fundamental frequency, 0.04 Hz) are similar ( Fig. 10 A , B , last panels). The adult LP and embryonic lpm spectrograms also look similar (most activity occurred less than ∼0.04 Hz) but, the fundamental frequency of activity in this adult LP neuron (0.13 Hz) was faster than that in embryonic lpm (0.08 Hz) ( Fig. 10 A , B , center panels). Activity in the spectrogram of the adult PD neuron (fundamental frequency = 0.09 Hz) was faster than that in embryonic pdm (0.05 Hz) ( Fig. 10 A , B , first panels).

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