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Effect on formation of bone trabeculee

W . B a u e r a n d A . M a r b l e . IV. Hyperpara*- thyroidism. W . B a u e r , A . M a r b l e , a n d D.

C l a e l i n ( J . C lin. I n v e s t., 1932, 1 1 , 1— 19, 21— 35, 37— 45, 47— 62).— I . S m a ll d o se s p r o d u c e d n o const, c h a n g e in C a o r P m e ta b o l is m ; 30 m g. p e r d a y caused a n in c re a se in faecal a n d a d e c re a s e in u r in a r y Ca and P , t h e q u a n titie s b e in g re v e rs e d la te r . T h e Ca and P b a la n c e s a n d th e se ru m -C a , -P , a n d -N w ere only s lig h tly affec ted .

I I . W h e n th e re is a d e fic ien c y of C a in th e serum o r b o n es, e rg o ste ro l th e r a p y p ro d u c e s C a re te n tio n .

I V . T h e b en e ficia l r e s u lts a r e d ir e c tly re la te d to t h e C a in ta k e . O n a h ig h C a in ta k e , w ith ergosterol, th e r e w ere : d e c re a s e d faecal C a, in c re a se d urinary C a, p o s itiv e C a b a la n c e , se ru m -C a , faecal a n d urinary P ; a fa ll i n p o s itiv e P b a la n c e a n d s e r u m - P ; and a r ise in th e p r o d u c t of se ru m -C a a n d -P .

Ch em ical Abstracts.

Photochemistry of ergosterol. E . H . R e e r in k a n d A . v a n W i j k .— See th is v o l., 480.

Hormones and ergosterol intoxication. M.

H a e n d e l a n d J . M a l e t (R e v . asoc. m dd. A rgentina, 1929, 4 2 , 295— 324).— T h e to x ic effects o n ra b b its of la rg e doses of ir r a d ia te d e rg o ste ro l a r e dim inished by c o n c u r re n t a d m in is tr a tio n of in s u lin o r sexual h o r­

m o n e , a n d in c re a s e d b y t h a t of a d re n a lin e , th y ro id in , o r h y p o p h y s in . C h e m ic a l A b s t r a c t s .

Vitamin-D content of red palm oil. W . J .

D a n n (B io ch em . J . , 1932, 2 6 , 1 5 11 5 4).— F o u r sa m p le s of r e d p a lm o il sh o w ed v e r y l i t t l e a n tira c h itic

B IO C H E M IS T R Y . 6 5 9

a c tiv ity , 100 m g. d a ily of th e ric h e s t (n a tiv e ) oil b ein g in su fficien t t o p r o te c t r a t s fro m ric k e ts . T h e o il is re c o m m e n d e d a s a so u rc e of v ita m in-A fre e fro m

v ita m in -D . A . C o h e n .

Determination of vitamin-D. K. M. Key a n d B. G. E . M o r g a n (B io ch em . J . , 1932, 2 6 , 196— 207).

— T h e c u r a tiv e effect o n r a t s of g r a d e d d o se s of v ita m in - ! ) h a s b e e n d e te r m in e d b y re fe re n c e to D y e r ’s scale o f h e a lin g (cf. th is v o l., 97). C u rv es re la tin g d eg ree of h e a lin g t o d o sa g e a r e sim ila r to th o s e of D y e r, g iv e s im ila r r e s u lts f o r t h e v ita m in - D v a l. of u n k n o w n s u b s ta n c e s , a n d a g re e w ith r e s u lts of p ro p h y la c tic te s ts in w h ic h a s h c o n te n t of fa t-fre e bone is d e te rm in e d . A c h a n g e in t h e C a : P r a ti o in S te e n b o c k ’s ra c liito g e n ic d ie t fro m 4 : 1 to 2 : 1 is eq u iv . to t h e a n tir a c h itic effect o f a d a ily d o se of 0-7 u n i t of v ita m in - D . A . C o h e n .

Determination of vitamin-D. I. Relation­

ship between graded doses of a standard solution of vitamin-D, administered to young rats on a rachitogenic diet, and the ash content of their bones. E. M. Hu m e, M. Pi c k e r s g i l l, a n d M. M.

G a f f i k in (B io ch em . J . , 1932, 2 6 , 488— 505).— W ith g ro u p s o f a n im a ls of t h e sa m e l i t t e r c o m p o sitio n on d iffe re n t d o se s w ith 10— 20 a n im a ls p e r dose, s m o o th c u rv e s a r e o b ta in e d . W h e n t h e v a ls . fo r th e p e r c e n t­

ag e a s h a r e p l o tt e d a g a in s t t h e lo g a rith m s of th e doses (w ith t h e e x c e p tio n of t h e lo w e s t a n d t h e h ig h e st) a lin e a r r e la tio n s h ip b e tw e e n t h e tw o v a ria b le s is re v e a le d . F o r a s s a y in g p u rp o s e s tw o g ro u p s o f 8— 10 y o u n g r a t s re c e iv e s u ita b le d o se s of ir r a d ia te d ergo- ste ro l, w h ils t tw o o th e r g ro u p s of a n im a ls sim ila rly c o n s titu te d a s re g a rd s l i t t e r a n d sex re c e iv e tw o doses of t h e u n k n o w n su b s ta n c e . T h e a v e ra g e r e s u lt of th e g ro u p s re c e iv in g t h e u n k n o w n d o se is th e n r e a d fro m c u rv e s w h ic h h a v e b e e n c o n s tr u c te d t o c o rre la te doses of a s ta n d a r d so lu tio n of ir r a d ia te d e rg o ste ro l a d m in iste re d p r o p h y la c tic a lly w ith t h e p e rc e n ta g e of ash in t h e b o n e s o f y o u n g r a t s o n a ra c h ito g e n ic d ie t.

I f th e r e s u ltin g v a ls . fo r t h e d o se s of t h e s ta n d a r d d o n o t fa ll d ir e c tly o n o n e of t h e c u rv e s, t h e e x p e rim e n t is r e p e a te d . I f t h e y d o n o t f a ll on a n y of t h e c u rv e s, a g r a p h i n w h ic h t h e a s h v a ls. a re p l o tt e d a g a in s t lo g a rith m s o f th e doses is e m p lo y e d , sin ce th e s e g ra p h s a r e s tr a i g h t lin e s, a n d a k n o w le d g e of tw o p o in ts is su fficie n t to c o n s tr u c t t h e w h o le g ra p h .

S. S. Z lL V A .

Determination of vitamin-D. II. Compari­

son of radiography and bone analysis in the estimation of vitamin-D. III. Stability of pre­

parations of vitamin-D. R . B . B o u e d i l l o n , H . M. B r u c e , a n d T . A . W e b s t e r (B io ch em . J . , 1932, 2 6 , 506— 521, 522— 530).— I I . A ra d io g ra p h ic scale is d esc rib e d sh o w in g v a rio u s d eg re es of d e v e lo p m e n t of r ic k e ts fo r u se i n d e te r m in a tio n of v ita m in - D b y m e a su re m e n t of i t s p r o p h y la c tic effec t. T h e e rro r in th e d e te r m in a tio n of t h e r e s u lt a n t effect is c o n ­ sid e ra b ly g r e a te r w ith t h e ra d io g ra p h ic sc ale th a n w ith bone a n a ly sis. T h e ch ief v a r ia tio n s i n t h e s e n s itiv ity of a sto c k of r a t s f e d o n a su p p o s e d ly c o n s t, d ie t a re p ro b a b ly d u e t o so m e f a c to r o th e r t h a n v ita m in - D . T he p ro p h y la c tic r a d io g r a p h ic sc ale is less s a tis fa c ­ to ry th a n t h e c u r a tiv e scale.

I I I . V ita m in - D in so lu tio n in o liv e oil m a y d e ­

t e r i o r a te se rio u sly if k e p t a t ro o m te m p , fo r p e rio d s of a y e a r o r m o re. D e te r io ra tio n a t 0° h a s n o t b e e n d e te c te d in th e tim e a v a ila b le . E x tr a p o la tio n fro m r e s u lts a t h ig h e r te m p , su g g e sts t h a t p re p s , a t 0°

m a y lose h a lf th e n ’ a c tiv i ty in a b o u t 3 y e a rs , b u t th e r e is som e re a so n t o t h in k t h a t th e so lid ific a tio n of th e o il h a s a p r e s e rv a tiv e effect a n d t h a t t h e s ta b ili ty a t 0° m a y b e g re a te r t h a n t h e e x p e rim e n ts su g g e st.

T h e a d d itio n of v a rio u s co m m o n s u b s ta n c e s lik e ly t o b e p r e s e n t a s im p u ritie s h a s n o v e ry g r e a t effect w ith t h e e x c e p tio n o f S w h ic h ca u ses d e te rio ra tio n .

S. S. Z f lv a .

Apparatus for determination of carbon dioxide and oxygen of respiration [of fruit]. M . H . H a l l e r a n d D . H . R o s e (Science, 1932, 7 5 , 439—

440). L . S. T h e o b a ld .

Biological effect of associated water mole­

cules. H . T. B a r n e s a n d T . C. B a r n e s ( N a tu r e , 1 9 3 2 ,1 2 9 , 691).— H 20 f ro m r e c e n tly c o n d e n se d s te a m , c o n ta in in g less tr ih y d r o l, ca u se s f ila m e n ts of Spirogyra

to a s su m e a co lo u rless m a ss o c c u p y in g less v o l. t h a n t h e fila m e n ts in tr ih y d r o l H , 0 w h ic h m a in ta in s th e r ig id ity a n d tu r g o r of th e cells. L . S. T h e o b a ld .

Biological degradation of chlorophyll. I I .

Phyllobombycin and probophorbide. H . F i s c h e r a n d A . H e n d s c h e l (Z. p h y sio l. C hem ., 1932, 2 0 6 , 255— 2 7 8 ; cf. A ., 1931, 966).— H y d ro ly s is of p h y llo ­ b o m b y c in w ith K O H in M eO H o r P r O H g iv e s a m ix tu re of u n c r y s ta llis a b le c h lo rin s, in c lu d in g c h lo rin e. T r e a t m e n t w ith H B r in A c O H a t 170°

o r w ith H C 0 2H a t 140° gives sm a ll a m o u n ts of de- o x y p h y llo e r y th rin a n d r h o d o p o rp h y r in e s te r. W ith H B r - A c O H a t 50° p h y llo e r y th rin w a s p ro d u c e d a n d id e n tifie d sp e c tro sc o p ic a lly . R e d u c tio n w ith H I a f te r tr e a t m e n t w ith 0 2 le d t o th e is o la tio n of phaeo- p o r p h y r in a 5 e s te r. P h y llo b o m b y c in , t r e a t e d w ith d ia z o m e th a n o w ith o u t c ry s ta llis a tio n , g a v e t h e c ry s t.

Me3 e s te r (I), m . p . 264° (Fe, Zn, a n d Gu sa lts), id e n tic a l w ith p h a s o p u rp u rin 18 M e3 e s te r. R e d u c ­ tio n of (I) w ith H I in A c O H g a v e a n e s te r, m . p . 224°, s p e c tro sc o p ic a lly re se m b lin g e h lo ro p o rp h y rin ei

e s te r. H B r a n d A cO H a t 170° p r o d u c e d fsophaeo- p o r p h y rin ct4. A t 50°, tr a c e s of p h y llo e r y th rin to g e th e r w ith e h lo ro p o rp h y rin e6 w ere o b ta in e d . W h e n t r e a te d w ith p y rid in e a n d N a 2C 0 3, (I) g a v e p s e u d o v e rd o p o rp h y rin . P h y llo b o m b y c in m u s t c o n ­ ta i n a n u c le u s w ith a p ro p io n ic a c id , a n u c le a r C 0 2H , a n d a n OA c r a d ic a l (th e tw o l a s t fro m t h e re d u c tiv e h y d r o ly tic fission of th e isocyclic rin g of c h lo ro p h y ll).

P h y llo e r y th r in w as o b ta in e d fro m sh e e p fceces.

C o p ro p o rp h y rin w as also d e te c te d a n d fo u r probo- phorbides w ere iso la te d a s t h e e s te rs : a ( J l e e s te r, m . p . 2 2 6 °; oxime; Fe s a l t ) ; b (Me e s te r, m . p . 207°) ; c (Me e s te r, m . p . 2 3 3 °); d (Me e s te r, m . p . 230°).

T h e se p ro b o p h o rb id e s a re d iv id e d s p e c tro sc o p ic a lly in to tw o g ro u p s : (i) a, c, d a n d (ii) b. T h e a n a ly s is of b g iv e s th e c o n s titu tio n C3GH 40O 6N 4 ; w ith H I b

y ie ld s e h lo ro p o rp h y rin e6 a n d tr a c e s of p h y llo e r y th rin . I t is clo sely r e la te d t o p h y llo b o m b y c in . P ro b o p h o r ­ b id e a rese m b le s p h y llo e r y th rin a n d is c o n v e rte d in to th e l a t t e r b y H I in A cO H . P ro b o p h o rb id e s c a n d d

c o n ta in m o re H a n d OM e t h a n a b u t a r e e a sily c o n ­ v e r te d in to p h y llo e r y th rin .

W in te r faeces of r a b b it s c o n ta in e d p h y llo e r y th rin

6 6 0 B R IT IS H C H E M IC A L A B S T R A C T S .— A .

a n d a c h lo rin , is o la te d a s th e Me e s te r (d ia z o m e th a n e ), m . p . 221°. T h e c ru d e E t 20 e x t r a c t a f te r 3 m in . w ith H I in A c O H a t 65° g a v e rh o d o p o rp h y rin . T r e a t ­ m e n t of p h æ o p h y tin w ith H I in A c O H fo r 2 m in . g a v e p h æ o p o r p h y r in a5, w h ic h w h e n h e a te d fo r 24 h r.

w ith H B r in A c O H a t 50— 55° g a v e p h y llo e r y th rin . J . H . B ir k in s h a w .

Formation of chlorophyll in roots exposed to light, especially in the roots of barley. R . J . G a u t h e r e t (C o m p t. r e n d ., 1932, 1 9 4 , 1510— 1513).—

T h e ro o ts of b a r le y m a y d e v e lo p a g re e n c o lo u r d u e to c h lo ro p h y ll w h e n p la c e d in lig h t, th e m o s t m a rk e d r e s u lts b e in g o b ta in e d w ith is o la te d r o o ts d e ta c h e d fro m th e p la n t. G lucose o r fru c to s e a d d e d to th e m e d iu m h a s a fa v o u ra b le effect.

W . 0 . Kerm ack.

Absorption and migration of nitrogen in the leaves of Salix fraç/ilis, L. N . T . D e l e a n o a n d M. A n d r e s c o (B u i. Soc. S tiin te C lu j, 1931, 6 , 209—

2 2 0 ; C hem . Z e n tr., 1932, i, 537).— T h re e s ta g e s in t h e life cyclo a r e : g ro w th (2 5 % ), a s s im ila tio n p e rio d (5 0 % ), N -m ig ra tio n (2 5 % ). I n th e l a s t p e r io d th e N is p r e s e n t ch iefly a s N H 3 a n d N H 2-a c id s ; th e q u a n t ity of a lb u m in - N fa lls. A . A . Ë l d r i d g e .

Stimulation of growth and metabolism in wheat tissue. A . R a d o ë f e (C o m p t. r e n d ., 1932, 1 9 4 , 1527— 1529).— T h e s tim u la tio n of th e g ro w th of w h e a t e m b ry o s w h ic h is p r o d u c e d b y M g a n d M n a n d t o o n ly a v e r y s lig h t e x t e n t b y Z n , F e , a n d Cu, is n o t a c c o m p a n ie d b y a n y sig n ific a n t in c re a s e in th e m e ta b o lic r a t e m e a s u re d b y th e 0 2 a n d C 0 2 e x c h a n g e .

W . 0 . Kerm ack.

Wax metabolism i n t h e leaves of Brussels sprout. P . N . S a h a i a n d A . C. C h i b n a l l (B io c h em . J . , 1931, 2 6 , 403—4 1 2 ).— T h e follo w in g c o n s titu e n ts w ere id e n tifie d in th e le a f-w a x : w -n o n aco san e, 15-n o 15-n a c o s a 15-n o 15-n e , 1 5 -15-n o 15-n ae o sa15-n o l, c e ry l alco h o l, c e ro tic a c id , a n d p r o b a b ly n - lie n tria c o n ta n e . O lefines w ere a b s e n t. T h e se ed s c o n ta in n o w a x , b u t s y n th e s is ta k e s p la c e r a p id ly in a ll p a r t s of t h e e m b ry o a n d p ro c e e d s c o n tin u o u s ly in th e le a f th r o u g h o u t t h e life- h is to ry of t h e p la n t. T h e c o m p o sitio n o f t h e w a x d o es n o t a l te r th r o u g h o u t th is p e rio d a n d th e r e is n o e v id e n c e t h a t th e p a ra ffin is fo rm e d b y r e d u c tio n of t h e k e to n e . A ll th e c o m p o n e n ts of th e w a x a re p r o b a b ly e n d - p r o d u c ts o f m e ta b o lism .

S . S. Z ilv a .

Synthesis and metabolism in cultivated plants.

S. O d é n a n d K . S j ô b e r g (M edd. C e n tr. F ô rs o k s v a s . J o r d b r u k ., 1931, N o . 386, 3— 56 ; C hem . Z e n tr., 1931, ii, 3109).—T h e in c re a se in N a n d m in e ra l c o n s titu e n ts is m o s t m a r k e d d u r in g th e f irs t h a lf of th e v e g e ­ t a t i v e p e rio d . T h e c a r b o h y d r a te c o n t e n t u n d e rg o e s la rg e v a r ia tio n s . A . A . E l d r i d g e .

Utilisation of excess mineral matter in the leaf in relation to growth of the plant. H . L e g a t u a n d L . M aum e (C o m p t. re n d ., 1932, 1 9 4 , 933— 935).

—A n in c re a se d K c o n te n t of th e le a v e s o f th e p o ta to is n o c r ite r io n o f th e w t. of fre s h tu b e r s o b ta in e d .

P . G. M a r s h a l l .

Rôle of plastids and of the cytoplasm in amyl- ogenic condensation. A . M a ig e (C o m p t. r e n d ., 1932, 1 9 4 , 1376— 1378).— A d isc u ssio n of th e fo r m ­ a tio n of s ta r c h in p la n t cells. T h e p la s tid s a r e p ro b

-a b ly c o n c e rn e d w ith t h e c o n v e rsio n of th e p ro ­ e n z y m e in to t h e a c tiv e a m y lo g e n e se w h ic h effects c o n ­

d e n s a tio n . W . 0 . K e r m a c k .

Absorption of salts by plant tissues. G. E . B r ig g s (A m i. B o t., 1932, 4 6 , 301— 322).— R e c e n t w o rk is d isc u sse d a n d ev id e n c e a d v a n c e d to sh o w th a t th e m e c h a n ism of s a l t in ta k e b y p la n ts f ro m dil.

so lu tio n s is b y a n e x c h a n g e of a n io n s b e tw e e n so lu tio n a n d e e ll-sa p a n d of c a tio n s b e tw e e n s o lu tio n a n d c y to p la s m . F r o m m o re cone, s o lu tio n s of single sa lts b o th a n io n s a n d c a tio n s p a s s in to th e sa p . I n v ery d il. s o lu tio n s le a c h in g o f io n s fro m c y to p la s m a n d sap

is sig n ific a n t. A . G. P o l l a r d .

Plant nutrition. III. Effect of potash de­

ficiency on the rate and respiration in leaves of barley. F . J . R i c h a r d s (A n n . B o t., 1932, 4 6 , 367—

388).— D ifferences in th e r a ti o o f d r y w t. t o le a f area in b a r le y p la n ts g ro w n w ith v a r y in g p ro p o rtio n s of K a re a lm o s t e n tir e ly a t t r i b u t a b l e to d ifferen ces in H 20 c o n te n t. L e a f-to -le a f v a ria tio n s in t h e sa m e p la n t r e s u lt fro m d ifferen ces in a n a to m ic a l s tr u c t u r e . W ith d e c re a sin g p ro p o rtio n s o f K in t h e n u tr ie n t, re sp ir­

a tio n r a te s in c re a se u p t o a m a x ., s u b s e q u e n tly falling w ith f u r th e r d ilu tio n of t h e n u tr ie n t. T h e se facts a r e d isc u sse d in r e la tio n t o th e c a r b o h y d ra te a n d N H 2- a c id c o n te n t of th e le av e s. T h e K c o n te n t of leaves v a rie s w ith t h a t o f t h e n u tr ie n t, b u t th e r e la tio n s h ip is n o t lin e a r. F ro m le a v e s ric h in K le a c h in g of the e le m e n t b y r a in is p r o b a b le , b u t n o le a c h in g occurs f ro m K -d e fic ie n t p la n ts . A . G. P o l l a r d .

Reserve polysaccharide of the seeds of fenu­

greek. Digestibility and fate during germin­

ation. K . M . D a o u d (B io c h em . J . , 1932, 2 6 , 255—

263).— A cid h y d ro ly sis of t h e p o ly s a c c h a rid e yields e q u iv . a m o u n ts of m a m io se a n d g a la c to s e . T h e poly­

s a c c h a rid e , w h ic h is a s a l t of a silic o p h o sp h o ric ester of m a n n o g a la c ta n , is n o t h y d r o ly s e d b y sa liv a or p a n c r e a tic e x t r a c t, a n d d o es n o t a lte r th e blood-sugar a f t e r in g e stio n . D u rin g g e r m in a tio n o f t h e seeds the m a n n o se a n d g a la c to s e a r e c o n v e rte d in to glucose,

fru c to s e , a n d su c ro se . A . C ohen.

Determination of glutamine in presence of asparagine. A . C. C h i b n a l l a n d R . G . W e s t a l l (B io ch em . J . , 1932, 2 6 , 122— 132).— I n th e reaction w ith H N O , in t h e V a n S ly k e d e te r m in a tio n 92% of t h e t o t a l N of g lu ta m in e a p p e a rs a s N H 2-N. After h e a tin g g lu ta m in e 3 h r . a t 100° a t p H 8, th e am ide-N a n d N H 2-N a re 35 -5 % a n d 8 -5 % o f th e to ta l N, respectively". A s p a ra g in e is s ta b le a n d g iv es normal v a ls. T h e r e s u lts a re e m p lo y e d t o d e te rm in e the g lu ta m in e a n d a s p a ra g in e c o n te n ts o f m ix tu re s of th e s e s u b s ta n c e s a n d of p la n t e x tr a c ts , se v e ra l cases of

w h ic h a re q u o te d . A . C ohen.

Relations between the physiological and geo­

logical characters of a forest of C'ryptonieria japónicaand soil conditions. K . M o r ik a w a (Bull.

Coll. A g rie. K y u s h u F u k u o k a , 1931, 4 , N o . 4 ; _ P roc.

I n t e r n a t . Soc. S oil Sei., 1932, 7 , 31).— T ra n sp ira tio n r a te s a n d th e H 20 a n d a s h c o n te n ts of le a v e s v a rie d in p a r a lle l w ith g ro w th r a te s . A . G. P o l l a r d .

Fat, lecithin, and protein of the soya bean.

I I . K ü h l ( P h a rm . Z e n tr ., 1932, 7 3 , 2 4 3— 248).—A rev ie w .

B IO C H E M IS T R Y . 6 6 1

Separation of growth-promoting substances.

N . N i e l s e n a n d V . H a b t e l h i s (C o m p t. re n d . L a b . C arlsb erg , 1932, 1 9 , N o . 8, 17 p p . ; cf. A ., 1931, 1091, 1334).— R h iz o p u s s u in u sf o rm s tw o g r o w th -p ro m o tin g s u b s ta n c e s w h e n g ro w n in a N H 4 ta r t r a te - g lu c o s e m e d iu m . O ne, s u b s ta n c e A ,is sol. in E t 20 , is readily- d e s tro y e d o n o x id a tio n b y H 20 2, a n d p r o m o te s th e g ro w th of A v e n a co leo p tiles a s sh o w n b y t h e b e n d in g re a c tio n . T h e o th e r, s u b s ta n c e B , is in so l. in E t 20 , is n o t o x id is e d b y H 20 2, a n d p r o m o te s th e g r o w t h of A s p e r g illu s n ig er. B o th s u b s ta n c e s a re s ta b le t o h e a t.

E . 0 . H o w i t t .

Chemistry of the plant growth-promoting substance. F . K o g l a n d R . J . H a a g e n - S m it (P ro c.

K . A k a d . W e te n s c h . A m s te rd a m , 1931, 3 4 , 1411—

1416).— A u n i t is d e fin e d a s t h e le a s t q u a n t i t y of a c tiv e s u b s ta n c e w h ich , u n d e r s t a n d a r d c o n d itio n s, w ill ca u se a b e n d in g of 10° in t h e d e c a p ita te co le o p tile of A v c n a s a tiv a w ith in 2 h r . T h e a c tiv ity of p r o d u c ts fro m v a rio u s so u rce s is g iv e n . T h e a c tiv e p rin c ip le is o b ­ ta in e d a s a b y - p ro d u c t in th e p r e p , o f ce strin fro m p r e g n a n c y u rin e . A N a H C 0 3 e x t r a c t of t h e u r in e is acidified a n d e x t r a c te d w ith E t 20 . I n a c tiv e im ­ p u r ity is re m o v e d b y b o ilin g lig h t p e tro le u m , th e insol. re s id u e h a v in g a n a c tiv i ty o f 130,000 u n its p e r m g. I t is d iss o lv e d in a q . E tO H a n d t h e s o lu tio n e x tr a c te d w ith C cH c, t h e h o rm o n e re m a in in g in t h e fo rm e r. F u r t h e r p u rific a tio n v ia t h e P b s a lt y ie ld s a p r o d u c t o f 10 G u n its p e r m g . T h e a c tiv e p r in c ip le a f te r d is tilla tio n a t 125— 1 3 0 °/0 -l m m . h a s a n a c tiv i ty of 5 x l 0 6 u n its p e r m g. T w o c r y s ta llis a tio n s f ro m a q . C 0 M e2 y ie ld a p r o d u c t, m . p . 172° (u n c o rr.) (C 68-62, H 10-18% ), w ith a n a c tiv i ty of 3 0 x 1 0 ® u n its p e r m g . T h e n a m e a u x in is su g g e ste d . T h e e lin (P a rk e D a v is , 50 R .U . p e r c.c.) is in a c tiv e as re g a rd s g ro w th effect in c o n t r a s t t o so m e p re p s , of

p ro g y n o n . P . G. M a r s h a l l .

Flow of sap in plants. B . H u b e r (B er. d eu t.

b o t. G es., 1932, 5 0 , 89— 109).— T h e r a t e of flow of s a p is d e te r m in e d b y t h e r a t e of tra n s m is s io n of h e a t fro m a lo c a lly w a rm e d s te m a r e a t o a th e rm o c o u p le . R a d io a c tiv e s u b s ta n c e s {e.g., T h -B ) a re su c ce ssfu l in d ic a to rs of s a p flow . A . G. P o l l a r d .

Relations between the growth of various parts of the melon seedling and the quantity of reserves left for the embryo. P . C h o u a r d a n d G. T e i s s i e r (C om pt. r e n d ., 1932, 1 9 4 , 1513— 1515).— R e m o v a l of p a r t of t h e fo o d r e s e rv e s fro m t h e se ed s of C u cu m is melor e s u lts in a g e n e ra l d e c re a s e in size of t h e r e s u lt­

ing e m b ry o , b u t t h e r e la tiv e size of th e p a r t s is n o t sig n ific an tly a lte r e d . W . O. K e r m a c k .

Stomatal movement and hydrogen-ion con­

centration. E . P . Sm i t h a n d M . S . Jo l l y ( N a tu r e , 1932, 1 2 9 , 544).T h e p Hv a ls. a t w h ic h th e s to m a ta of th e g u a rd -c e lls o f T u lip a , S c illa , I r i s , a n d T ra d es- cantia a r e o p e n in s o lu tio n s of C 0 2, a n d in B .D .H .

“ u n iv e rsa l b u ffe r m ix t u r e ,” a r e re c o rd e d .

L . S. T h e o b a ld .

Radioactivity and the germination of bulbs.

D. M o n t e t (C o m p t. r e n d ., 1932, 1 9 4 , 1093— 1095).—

W ith th e h y a c in th a n d t u l i p a m o re f u lly d e v e lo p e d foliage is o b ta in e d u n d e r t h e in flu e n ce of r a d io ­ a c tiv ity , w h e th e r s u p p lie d in t h e fo rm of R a e m a n a tio n

o r U 20 6. T h e o p tim u m q u a n t i t y of th e l a t t e r fo r in c re a s e d g ro w th of t h e tu li p is 0-5 g. p e r 1500 g.

o f soil. P . G . M a r s h a l l .

Action of Italian radioactive soils on germin­

ation of seeds and on growth of plants. G.

M e z z a d r o li a n d E . V a r e t o n ( A tti R . A cc a d . L in c e i, 1931, [v i], 1 4 , 443— 447).— W i th p la n ts g ro w n in K n o p p ’s n u tr ie n t so lu tio n , a d d itio n o f fin e ly g ro u n d r a d io a c tiv e soil sho w in g 4-2 x l O -9 g. o f R a p e r g.

c a u se s m a rk e d in c re a se s in t h e r o o t a n d p l a n t g ro w th . I n field e x p e rim e n ts , th e u se of t h e so il a s fe r tilis e r r e s u lts in g re e n e r a n d s tro n g e r p la n ts a n d in in c re a se of th e c ro p b y a t le a s t 2 0 % . T . H . P o f e .

Direct versus indirect effects on potato- amylase by chemicals which induce sprouting of dormant tubers. F . E . D e n n y (C o n tr. B o y c e T h o m p s o n I n s t . , 1932, 4 , 53— 63).— T h e effect of c e r ta in c h e m ic a ls {e.g.,e th y le n e c h lo ro h y d rin , N aC N S , a n d K C N S ) o n t h e a m y la s e a c tiv i ty of e x p re sse d p o t a t o ju ic e (d ire c t effect) w a s n o t r e la te d to t h e ir a c tio n in s tim u la tin g t h e s p r o u tin g of th e tu b e r s , n o r t o c h a n g e s in a m y la s e a c tiv i ty p ro d u c e d s u b ­ s e q u e n t t o tr e a t m e n t of th e w h o le tis s u e w ith th e s e s u b s ta n c e s (in d ir e c t effect). S p ro u tin g re sp o n se w as m o re n e a r ly r e la te d to th e in d ir e c t a m y la s e effect.

K N 0 3 a n d K O I w ere n o t m a rk e d ly a c tiv e in in d u c in g s p r o u tin g a n d h a d l i t t l e effec t o n a m y la s e a c tiv ity . T h e s p r o u tin g re sp o n se t o c h e m ic a l tr e a t m e n t is in d ir e c t a n d is n o t d e p e n d e n t o n th e d e v e lo p m e n t of h ig h a m y la s e a c tiv i ty in tr e a te d tu b e rs .

A . G. P o l l a r d .

Development and ripening of peaches as correlated with physical characteristics, chemi­

cal composition, and histological structure of the fruit flesh. I. Physical measurements of growth and flesh texture in relation to the market and edible qualities of the fruit. M . A . B l a k e , O. W . D a v id s o n , R . M. A d d om s, a n d G. T . N i g h t i n ­ g a l e (N ew J e r s e y A g ric. E x p . S ta . B u ll., 1931, N o . 525, 35 p p . ; cf. A ., 1931, 273).— T h e in c re a se d v e g e ta tiv e a c tiv i ty a n d p r o d u c tio n o f te n d e r g ro w th re s u ltin g f ro m h ig h N fe e d in g o ccu rs in d e p e n d e n tly of t h e n a t u r e of t h e N so u rce . R e p e a te d t r e a tm e n t w ith N fe rtilis e rs o r c e r ta in s y s te m s of c u ltu r a l o p e ra tio n s p ro d u c e a h ig h N -lo w c a r b o h y d ra te ty p e of tre e . T r e a tm e n ts of a n o p p o site c h a ra c te r p ro d u c e a low N - h i g h c a r b o h y d ra te ty p e . A . G. P o l l a r d .

Origin o f the uronic acids in the humus o f soil, peat, and composts. S. A . W a k sm a n a n d H . W . R e u s z e r (Soil S ci., 1932, 3 3 , 135— 151).— D u rin g th e b io lo g ic a l d ec o m p , of p la n t re sid u e s, tr u e p e n to s a n s a re a tta c k e d m o re re a d ily t h a n u ro n ic a c id co m p lex e s.

I n d iffe re n t p la n t m a te ria ls th e r e la tiv e p r o p o rtio n s of v a rio u s h em ice llu lo ses a n d t h e r e la tiv e e a se of d ec o m p , v a rie s c o n s id e ra b ly . M a n u rin g of so il c a u se s a n in c re a se in p e n to s a n c o n te n t. P ro lo n g e d c u l tiv ­ a t io n w ith o u t t h e a d d itio n of org. m a t t e r r e s u lts i n a d e c re a s e d h u m u s c o n te n t a n d a r e la tiv e in c re a s e i n u ro n ic a c id s. A . G. P o l l a r d .

Apparatus for continuous extraction of plant materials with ether under tropical conditions.

W . J . B l a c k i e (J.S .C .I., 1932, 5 1 , 129— 1 3 0 t).— T h e a p p a r a tu s is d esig n e d t o e x t r a c t 100 g. of m a te r ia l.

662 B R IT IS H C H E M IC A L A B S T R A C T S .— A .

V a p o u r a n d s ip h o n tu b e s a r e c a rrie d b y a g la ss c o n ­ n e c tin g p ie c e w h ic h is a t ta c h e d a t e a c h e n d b y lo n g g ro u n d -g la ss jo in ts t o b o ilin g fla sk (1500 c.c.) a n d e x ­ t r a c t o r ( 7 x 3 0 cm .). T h e l a t t e r is c o n n e c te d b y a g ro u n d -g la s s j o in t w ith H g s e a l t o a w o rm c o n d e n se r.

C. W . D a v ie s .

Lignin-like complexes in fungi. C. T h om a n d M. P h i l l i p s (J . W a sh . A ca d . S c i, 1932, 2 2 , 237—

239).— B ro w n -w a lle d m o u ld s su c h a s Cladosporium

a n d Alternaria c o n ta in 17— 2 9 % of lig n in -lik e s u b ­ s ta n c e s , a n d b ro w n -w a lle d b r a c k e t fu n g i su c h a s

Trametes pini a n d Fomes igniarius la rg e r p ro p o rtio n s . L ig h t-c o lo u re d b r a c k e t fu n g i c o n ta in v e r y little .

C. W . G ib b y.

Composition of the cell membrane of the alder ( A l n u s q l u t i n o s a ) . K . N e v r o s ( P r a k ti k a , 1931, 6, 2 7 0 - 2 7 - 1 ; C hem . Z e n tr., 1932, i, 536).—

S c h m id t’s im p r o v e d C102 m e th o d w a s e m p lo y e d in th e d e te r m in a tio n o f t h e c e llu lo s e : x y la n r a tio . 0-01— 0 -2 % N a O H re m o v e d th e c a r b o x y l s u b s ta n c e s c o n s is tin g of 2 a c id s a n d x y l a n ; w ith > 0 - 2 % th e p e n to s a n b e g in s t o d isso lv e, a n d w ith 9 % m a x . s o lu b ility o cc u rs, w ith d is s o lu tio n o f cellu lo se c o n ­ s t i tu e n t s . A t t a c k b y 5— 7 % N a O H o n th e cellulose is d im in is h e d b y a d d itio n o f 3 % N a C l w ith o u t d im in ­ u tio n of t h e s o lu b ility of t h e sk e le ta l su b s ta n c e . T h e a c id -fre e s u b s ta n c e re m a in in g a f te r t r e a t m e n t o f th e l a t t e r w ith O-OSN-NaOH c o n ta in s 3C6H 10O 5 : 1C5H 80 4.

H e n c e t h e ce llu lo se a n d t h e H ,0 - s o l. x y la n a re c h e m ic a lly c o m b in e d . A . A . E ld r id c .e .

Juice of the Maguey plant (Manso f i n o ) . I.

H . D . J o n e s (J . A m e r. P h a r m . A ssoc., 1932, 2 1 , 35 4 — 356).— T h e c o m p o sitio n , p r o p e r tie s , a n d re a c tio n s of

“ a g u a m ie l,” th e fre s h ju ic e of Agave atrovirens, K a rw , a n d o f t h e s y r u p a r e g iv e n . E . H . S h a r p le s .

New vegetable constituent: uric acid. R.

F o s s e , P . d e G r a e v e , a n d P . E . T h om as (C o m p t. r e n d ., 1932, 1 9 4 , 1408— 1413).— U ric a c id e x is ts in m a n y p la n ts a n d e sp e c ia lly in g ra in s , a n d h a s b e e n is o la te d in a p u r e fo rm f ro m t h e se ed s of Melilotus officinalis.

W . 0 . Iv e rm a ck .

Non-alkaloidal fraction of ergot. H . L a n g - ECKER (A rch. e x p . P a th . P h a r m ., 1932, 1 6 5 , 29 9 — 3 2 4 ).— T h e s e p a r a tio n of t h e a lk a lo id s fro m th e a m in e s i n e x t r a c ts of e r g o t a n d t h e s ta n d a r d is a tio n of t h e l a t t e r b y c o m p a ris o n w ith h is ta m in e in th e ir a c tio n o n t h e s m a ll in te s tin e a n d u te r u s of t h e g u in e a -p ig w e re in v e s tig a te d . T h e “ in te s tin e v a l .” is less t h a n t h e “ u te r u s v a l .,” b u t w ith in c re a sin g p u r i t y th e v a ls.

t e n d to ag re e, in d ic a tin g t h a t t h e in te s tin e m e th o d is sp . fo r t h e a m in e f ra c tio n . I n e r g o t p re p s , th e a v e ra g e a m in e c o n te n t is lo w er t h a n th e a lk a lo id c o n te n t, b u t t h e fo rm e r e x h ib its a g r e a te r s ta b ility . E rg o ta m in e (1 : 40,000) su p p re s s e s t h e to n u s a c tio n o f h is ta m in e in t h e s u rv iv in g g u in e a -p ig in te s tin e . C 0 2, H ,S , o r in c re a se d a c id ity g r e a tly d im in ish e s th is a c tio n to a n e x t e n t w h ic h is n o t in flu e n c e d b y th e ag e o f th e e x t r a c t. B a c te r ia l in f e c tio n of t h e e x t r a c ts o c c a s io n a lly le a d s t o in c re a s e d a c tio n o n th e in te s tin e a n d u te r u s . T h u s fo llo w in g b a c te ria l f e r m e n ta tio n a m a te r ia l c a n b e s e p a r a te d w h ic h clo sely rese m b le s, b u t is n o t id e n tic a l w ith , h is ta m in e , a lth o u g h tr a c e s of th e l a t t e r a r e p r e s e n t. F . O. H o w i t t .

Glucoside fractions of Digitalis leaves. M.

G u g g e n h e im , K . F r o m h e r z , a n d W . K a r r e r (Arch, e x p . P a t h . P h a r m ., 1932, 1 6 5 , 41 2 — 415).— T h e w o rk of H o e k s tra (A., 1931, 1453) is c ritic is e d o n th e

G u g g e n h e im , K . F r o m h e r z , a n d W . K a r r e r (Arch, e x p . P a t h . P h a r m ., 1932, 1 6 5 , 41 2 — 415).— T h e w o rk of H o e k s tra (A., 1931, 1453) is c ritic is e d o n th e

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