54 PRACTICAL PHYSIOLOGY. [VI. 



(d.) The spectrum shows four absorption-bands ; a faint band midway be- 

 tween C and D, another similar one between D and E, but close to D ; a third 

 band near E ; and a fourth one, darkest of all, occupying the greater part of 

 the space between b and F, but nearer the former. 



In all cases make drawings of what you see, and compare them with the 

 table of characteristic spectra suspended in the laboratory. 



18. Picro-Carmine. Its spectrum closely resembles that of 

 Hb0 2 , but the two bands are much nearer the violet end, one 

 being midway between D and E, and the other to the violet side of 

 E. The bands are unchanged on addition of Am 2 S or Stokes's 

 fluid. The solution does not give proteid reactions. 



ADDITIONAL EXERCISES. 



19. Prolonged Action of Methaemoglobin-forming Reagents. Allow 

 KMn0 4 , K 3 FeCy 6 , iodine, amyl or potassium nitrite or glycerine to act on Hb0. 2 

 for some days at 40 C. Methaemoglobin is first formed, then hsematin. The 

 latter is partially precipitated. Precipitate may be washed with water and 

 dissolved in dilute acid or alkali. In the case of K 3 FeCy 6 the solution becomes 

 cherry-red, and contains cyan-hsematin. Its spectrum shows one broad band, 

 like that of Hb, between D and K, unchanged on shaking with air. In the case 

 of amyl nitrite the final product in solution has a spectrum like that of Hb0 2 , 

 unchanged on treatment with Am. 2 S (? HbNO). 



HbO 2 solution or dilute blood left on the water-bath at 40 C. for some days 

 shows first a partial formation of methsemoglobin and later becomes Hb. It 

 does not become converted into hsematin (/. A. Menzies}. 



20. Effect of Sodium Fluoride. To Hb0 2 solution or diluted blood, add a 

 few drops of i per cent. NaFl solution, and keep at 40 C. until the colour 

 changes from scarlet to a rich crimson. Examine the spectrum. In addition 

 to traces of the Hb0. 2 bands, there will be seen two bands, one very distinct to 

 the red side of D, slightly nearer the red than the band of alkali-haematin, the 

 other, not easily seen, to the violet side of E. On addition of Am 2 S, the spec- 

 trum changes first to that of Hb0 2 , then Hb. 



21. Effect of Acids. (a.) To 15 cc. dilute blood which gives a well-marked 

 spectrum of Hb0. 2 , add 5 drops of i per cent. HC1 (or other acid). The colour 

 changes to brown, and the spectrum to that of acid haematin. Add ammonia, 

 the spectrum becomes that of alkaline methsemoglobin, and, on addition of 

 Am 2 S, the solution changes to HbO, then Hb. But, if Am 2 S be added with- 

 out previous addition of ammonia, the spectrum becomes that of htsmo- 

 chromogen first becoming Hb on standing, and then Hb0 2 appears on shaking 

 the solution with air. 



(b.) Place 15 cc. of solution of pure Hb0 2 with well-marked spectrum in 

 each of five test-tubes. To these add i, 2, 5, 10, and 15 drops of i per cent. 

 HC1 respectively. Place all on a water-bath at 40 C. for 24 hours, or longer 

 if necessarj 7 . In some of the tubes a precipitate of hfiematin will be found, and 

 in one of these the supernatant fluid will be colourless, and will give proteid 

 reactions. Decant the colourless fluid, and collect arid wash with water the 



