ROCZNIKI GLEBOZNAWCZE T. XXXVI, NR 2, S. 5-20, WARSZAWA 1985
FRANCISZEK MACIAK, HORST SÖCHTIG
INFLUENCE OF PEAT-FORMING PROCESS ON THE CHANGES
OF NITROGEN AND PHENOLIC COMPOUNDS IN PEATS
W arsaw A gricultural U niversity,
Institut of Plant N utrition and Soil Science
Braunschweig — Volkenrode, RFG
INTRODUCTION
The form ation of peat involves the biochemical process of plant m ate
rial, in which both lesses and increase of certain substances in peat occur,
substances w hich had been previously in peat-form ing plants. Diuring
the process of decomposition of the plan t residues, large quantities of
new chemical compound are synthesized by various groups of m icro
organisms and therefore in peat a distinction betw een microbial and
plant residue is largely difficult [2, 3, 11, 24].
In the process of peat form ation and hum ification of plant residues
m any factors, especially environm ental conditions, play an im portant
role.
Among the factors of peat formation, the most im portant is the com
position of plans, because only specific species of plants are able to form
a certain kind of peat. The com parative chemical analyses of peats and
peat-form ing plants [1, 12, 21, 22] show th a t there is an increase in the
content of nitrogen, lignin fraction and humic substances, but a decrease
of cellulose and hemicellulose content in the course of the decomposition
of plan t m aterial. These changes are distinctly evident in the analysis
of nitrogen compounds (II). According to previous investigations [12]
the process of peat form ation involves a decrease in the amine nitrogen
content and an increase in hydrolysis-resistant nitrogen content. The
increase in amide nitrogen content is characteristic, especially in case
of low peats [11, 12]. Also the lignins or its degradation products of
different species of peat-form ing plants are chiefly concentrated in the
nonhydrolysable fraction of peat and humic acids [3, A, 6, 7, 14, 18,
19, 20].
6
F. Maciak, H. Söchtig
In the present work various kinds of low and high peats as well
as different species of peat-form ing plants were analysed for nitrogen
and phenolic compounds, with the aim to determ ine
a relationship
betw een individual plant species and the kind of peat formed.
MATERIAL AND METHODS
The low-peat samples were taken from upper 0— 20 cm and from
the layer below 50 cm from the deposits peatbog of the area of Biebrza
(Poland), which has been under cultivation since long time.
The high-peat samples w ere taken from the profile of the unculti
vated highmoor at Ramsloh (Fed. Rep. of. Germany). The peat-form ing
p lants were collected from low and high-m oor in the province of Warsaw.
Botanical compostion and the degree of peat decomposition was de
term ined w ith microscopic method: pH value of peat (in H20) — w ith
potentiom etric method using a glass electrode; ash — by ignition of peats
or plant at the tem perature of 550°. Acid hydrolysis of peat-form ing
plants and peats was in the solution of 6 N HC1 at the tem perature
of 120°C for 18 hours. Analyses of particu lar nitrogen forms were accom
plished by B r e m n e r ’ s [5] method. The am ount of lignin fraction
in peats and plants was estim ated by hydrolysis of the air-dry samples
in 72ю/о H2S 0 4 — R i 11 e r et al. [23] w ithout p retreatm ent w ith organic
solvents.
The phenolic substances w ere determ ined in the hydrolysates and
residues obtained in hydrolysis of peat w ith 6 N HC1. The acid hydro
lysates were extracted three tim es w ith peroxide free ether and the
residues were reducted w ith sodium amalgam under nitrogen atm osphere
as an in ert gas according to the m ethod of B u r g e s et al. [7]. The
raction m ixture was acidified and extracted w ith peroxide-free ether.
The phenols w ere identified in the concentrated ether extracts from
both by two demensional thin layer chrom atography (Silician gel CF
254 F. Merck, Darmstad) chloroform — acetic acid (8:2) and dibuty-
lether-acetic acid (10:1) as selvents. Well separated phenol-spots were
isolated by scraping the support-areas from the glass plate, after elution
w ith methanol, the absorbance was m easured for registering ultraviolet
absorbtion spectra (190—350
/Lira).
S tandard samples of phenols were
utilised for identification. The am ount of phenols was calculated in
mg per 100 g of dry m atter.
INVESTIGATIONS RESULTS
1.
G e o b o t a n i c a l c h a r a c t e r i s t i c s o f t h e p e a t - f o r -
m i n g p l a n t s a n d t h e p e a t s a m p l e s . It follows from the
data presented in Table 1 th a t peat samples represent almost all im
por-Zmiany w składnikach azotowych i fenolowych w torfach
7
ta n t kinds, of low and high peats. The proportion of peat-form ing plant
residues in the peat samples determ ines the kind of peats. The residues
of Phragmites communis in the reed peat am ount to 90%. The sedge
peat consists in 75% of residues of sedges. The woody peats are built in
25-65°/o from rem nants of Alnus glutinosa wood. The sphagnum peat
consists m ainly of Sphagnum sec. Pałustria w ith a large proportion of
Sphagnum sec. Palustria w ith a large proportion of Sphagnum sec. Cus-
pidata.
Ta b l e 1
G o o b o t a n i c a l c h a r a c t e r i s t i c o f p e a t s S a m p l e No. D e p t h o f b o x i n g a cm S i t e b o t a n i c a l c o m p o s i t i o n K i n d o f p e a t Decompo s i t i o n Ash i n % o f d . r a . pH d e c r e e c r u d e p u r e 1 2 3 4 5 6 7 3 9 1 a 0 - 2 0 Wi zn a С а г е х з р . 75 B r y a l e a 15 J a l i x з р . 7 M e n y u n t h e s t r i f o l i a t a 3 s o d g e - p e a t 40 1 3 , 7 4 1 6 , 3 3 6 , В 1 b b e l o w 50 A' izna С а г е х з р . <35 B r j r a l e s 25 Morg an t h o u t r i f o ï i a t a 3 A r i o p h o r u m a n ^ u p t i f o l i u m 2 a e d ę e - m o s s P ^ a t 20 7 , 1 5 3 , 16 - , 4 2 a 0 - 1 7 Ko-:;i?y Garez" p . JO nryult -T. 15 i r i o p h o r u r i a n r n r . t i f o l i u m ’ 5 .•jedre-.-noss 45 15, 5 1 1 , 5 5 •:, о 2 b bo l ow 50 K o u i ł y С а г е х з р . 65 Br у и l e s У- M c n y a n t h o s t r i f o l i a t a 3 J r i o p h o r u m a n ' r u s t i f o l i u m 2 p e a t 15 1 ^ 20 5 , Л9 - , 4 3 a - 1 7 B i e b r z a f i o l d 44 P h r a g r n i t e s comrruinir: 50 А1пиз f j l u t i n o s a 15 С а г е х з р . 5 5r a m i n e a s 30 m ; c k d e v e l o pe d f r o m r e e d po a t Э7 0 Г d , 51 5 , 5 3 b 1.10 low 50 Bio Ьг'^а f i _ - I d \Ą P h r a ^ m i t e n c oi .- .- un is 65 A l n u o r i - j l i n o o ^ 25 C a r o x з р . 10 r e e d p o a t 45 1 3 , : : ^ 1 1 , 4 2 0 , 1 4 a 0 - 1 9 B i e b r : : a f i e l d 9 A l n u s g l u t i n o j a 15 P h r a g m i t ô 3 com: nuni 3 25 C i r t x s p . 10 G r a m i n e a e 50 .т.'.: с к do vo l o pe d f Г 0 !Л г е е d р оa t o v e r 15, ~ 1 10, . H 5 , i 4 b bo l ow 50 B i e b r z a f i a I d 9 P h r a ^ n i t e o c o mm u ni s 30 G a r e x з р . 2 A l n u s . ; l u t i n o 3 a 3 5С 7 , 0 5 ^ , 2 5 a 0 - 1 7 '.„od :;o 1 j .\ . A l : : r a g i t e s c o mm u ni s 5 A l n u s g l u t i r . o s a 10 C a r e x s p . 10 J r < m i n e a e 7 5 70 r , > ; 5 b b e l o w 50 M o d z el ó w k a Phrui.7r»it0 3 c o a : » u n i » 75 C a r e : : : p . 20 A l n u s ~ ' : u t i n c 3 a 5 r e e d p e a t 70 K V ; : , ■■',37 ••-,38
F. Maciak, H. Söchtig
1 2 3 4 5 6 7 8 ? 6 a 0 - 1 7 K o s i ł y f i e l d 2 A l n u s g l u t i n o s a . 50 C a r e x s p . 10 G r a m i n e a e 40 muck d e v e l o p e d f r o m wood p e a t o v e r 60 1 8 , 1 2 1 0 , 7 1 6 , 6 6 b b e l o w 50 K o s i ł y f i e l d 2 A l n u s g l u t i n o s a 60 S a l i x s p . 10 C a r e x s p . 15 P h r a g m i t e s c o n m u r . i s 15 a l d e r p e a t 50 1 4 , 6 7 8 , 5 4 6 , 1 7 a 0 - 1 7 Łamane G r a d y A l n u s G l u t i n o s a 25 P h r a g n i t e s c o m n u n i s 10 G r a m i n e a e 65 muck d e v e l o p e d f r o n wood p e a t 50 l 6 , 7 4 1 0 , 4 2 6 , 2 7 b b e l o w 50 Łamane G r a d y A l n u s g l u t i n o s a 65 S a l i x s p . 17 C a r e x s p . 3 P h r a g m i t e s c o mm u ni s 15 a l d e r p e a t 60 1 5 , 3 0 1 3 , 2 4 5 , 9 8 0 - 1 5 R e r a z l oh S p h a gn um s e c . P a l u s t r i a 3 5 S ph a gn um s e c . C u s p i d a t a 10 E r i c a c e a e 2 E r i o p h o r u m v a g i n a t u m 3 s p h a g n u m p e a t 5 . 1, 4 С - 3 , 7 9 1 5 - 3 0 Rumz lo li Sph a gn um s e c . P a l u s t x i a 53 Sp ha g nu m s e c . C u s p i d a t a 30 E r i c a c e a e 7 E r i o p h o r u m v a g i n a t u m 4 P i c e a e x c e l s a 1 s ph a g n u m p e a t 5 1*24 - 3 , 7 10 1 5 0 - 1 6 5 R a m z l o h S ph a gn um s e c . P a l u s t r i a 65 S ph a gn um s e c . C u s p i d a t a 15 Sp ha g nu m s e c . A c u t i f o l i a 5 E r i c a c e a e 8 E r i o p h o r u m v a g i n a t u m 10 s p h a g n u m p e a t 13 1 , 1 4 - 4 , 6 11 1 6 5 - 1 5 0 R a m z l c h S ph agn um s e c . P a l u s t r i a 42 Sp ha g nu m s e c . C u s p i d a t a 20 S ph a gn um s e c . A c u t i f o l i a 10 E r i c a c e a e 12 E r i o p h o r u m v a g i n a t u m 1б s p h a g n u m p e a t 26 1» 12 - 4 , 2 12 3 0 0 - 3 1 5 R a n z 1 oh S pha gnum 3 e c . P a l u s ü r i a 5 S ph a gn um s e c . C u s p i d a t a 15 E r i c a c e a e 10 E r i o p h o r u m v a g i n a t u m Ю E r i o p h o r u m p e a t 50 C - . « - 4 , 1 13 3 1 5 - 3 30 S ph agn um з е с . F a l u s t r i a 5 S ph a gn um y e c . C u c p i d a t a 20 S ph agn um s e c . A c u t i f o l i a 3 E r i c a c e a e 15 E r i o p h o r u m v a g i n a t u m 55 E r i o p h o r u m p e a t 55 o , -jC - 4» 1<jec . F a ] u 3 t r i a : S pha gnum im or:, c a t n a , S . c y t n b i f o l i u r a , 5 . p a p i l l o s u m G e c . C u G p i a a t a : S ph a gn um c u s p i d a t u r . i , S e r e c u r v u m
G e e . A c u t i f o l i a ; Sph a gn um a c u t i f o l i a m , S . r u b e l l u r n
E r i c a c e a e : l e d u m p a l u s t r e , C x y c o c c u s q u a d r i p -э t a l u 3 , G a l l u n - , v u l g a r i s
Cottongrass peat in built mainly from Eriophorum vaginatum (65—70).
D ifferent kinds of low or high peats contain very often notable ad
m ixtures of other plant residues.
The degree of decomposition in low peats ranges w ithin the limits from
15 to over 70%, w hile in high peats — from 5 to 55%.
Zmiany w składnikach azotowych i fenolowych w torfach
9
The ash content of low peats is in 7,15 to 18,7% of d ry m atter. The
ash content in high peats ranges from 0,91 to 1,64% of dry m atter.
The pH value of low peats ranges from 5,9 to 6,8, while in high
peats — from 3,7 to 4,6. In the respective peat-form ing plants the ash
content ranges from 3,10% to 21,35% of dry m atter. Among plants
investigated only Phragnites communis (13,15%), Carex pilosa (15,32%)
Equisetum plaustre (21,35%) show very high content of ash, in others
it lies below 10% of dry m atter.
2.
C o n t e n t o f n i t r o g e n f o r m s i n p e a t s a n d p e a t -
- f o r m i n g p l a n t s . It is clear from the data presented in Tables 2
Ta b l e 2
N i t r o g e n f o r m s i n p e a t a D e p t h o f b o r i n g s cm De co mpo I n % o f t o t a l N' T o t a l w S a m p l e No. s i t i o n d e g r e e % nh4 -n N03- N a m i d e N a m i n e N h e x o s e a m i n e К i n s o l u b l e h u r ai n e N n o n i d e n t i f N i n % o f d . m . 1 a 0 - 2 0 40 1 , 1 0 3 , 7 8 1 6 , 7 8 2 7 , 3 2 6 , 0 2 2 3 , 3 7 2 0 , 3 2 3 , 8 3 2 1 b > 5 0 20 1 , 3 8 2 , 7 1 1 3 , 3 2 2 4 , 5 4 9 , 0 0 2 6 , 2 2 2 2 , 8 2 3 , 5 2 1 2 a 0 - 1 7 45 1 , 5 3 6 , 3 6 1 9 , 9 5 2 2 , 1 0 3 , 6 6 2 3 , 2 1 2 3 , 0 0 3 , 5 9 4 2 b > 50 15 1 , 2 5 2 , 4 9 1 4 , 8 1 2 4 , 6 3 4 , 2 4 2 7 , 1 6 2 5 , 4 1 3 , 6 8 1 3 a 0 - 1 7 > 6 0 1 , 0 0 4 , 0 5 1 8 , 6 1 2 9 , 6 3 5 , 9 4 2 2 , 8 4 1 7 , 9 4 4 , 1 6 5 3 b > 5C 45 1 , 5 0 2 , 0 4 1 4 , 3 7 2 7 , 5 5 5 , 3 8 3 1 , 7 0 1 4 , 4 5 3 , 4 2 2 4 a 0 - 1 9 > 7 0 1 , 2 6 4 , 4 3 1 8 , 5 5 ;-:*3,47 7 , 5 6 2 1 , 7 5 1 ; 193 4 , 2 3 3 4 b > 5 0 50 1 , 2 3 3 , 0 0 1 4 , 4 5 2 6 , 11 6 , 1 9 2 9 , 5 5 1 9 , 4 5 3 , 9 3 5 5 a 0 - 1 7 70 1 , 1 5 3 , 5 1 2 0 , 6 9 2 2 , 6 0 7 , 9 7 2 5 , 6 9 1 b, 19 3 , 7 8 6 5 b > 50 70 1 , 9 6 2 , 2 6 1 6 , 2 4 2 4 , 1 5 •‘ , 2 4 3 4 , 7 8 1 6 , 3 7 3 , 4 0 4 6 a 0 - 1 7 > 6 0 0 , 8 5 3 , 5 7 1 8 , 1 1 2 3 , 6 3 5 , 5 2 2 4 , 5 3 2 3 , 7 9 3,е71 6 b > 50 50 1 , 0 5 3 , 1 0 1 6 , 6 7 1 9 , 8 3 1 , 7 0 3 2 , 3 5 2 5 , 2 9 3 , 4 5 3 7 a 0 - 1 7 5C 1 , 5 1 4 , 0 3 1 7 , 4 9 2 0 , 6 3 3 , 5 4 2 5 , 3 5 2 7 , 3 9 3 , 5 6 9 7 b ? 50 60 2 , 0 2 3 , 9 8 1 6 , 3 0 2 1 , 0 2 3 , 9 6 3 0 , 4 4 2 2 , 2 6 3 , 5 5 8 5 0 - 1 5 5 2 , 4 2 1 , 1 5 1 4 , 4 5 3 7 , 4 0 1 , 8 9 1 9 , 7 1 2 2 , 9 8 0 , 9 0 6 9 1 5 - 3 0 5 3 , 6 9 1 , 0 7 1 3 , 1 9 3 3 , 5 9 1 , 1 8 2 1 , 9 1 2 5 , 3 7 0 , 7 8 6 10 1 5 0 - 1 6 5 18 3 , 4 9 1 , 1 0 1 4 , 0 0 3 0 , 9 1 3 , 9 3 2 4 , 8 8 2 1 , 6 9 1 , 2 2 2 11 1 6 5 - 1 8 0 28 3 , 2 2 0 , 8 6 9 , 9 1 2 4 , 6 0 5 , 9 7 3 9 , 3 2 1 5 , 6 2 1 , 1 8 0 12 3 0 0 - 3 1 5 50 4 , 8 3 1 , 0 1 1 3 , 2 5 1 6 , 5 4 4 , 6 5 3 7 , 9 8 2 1 , 7 4 0 , 8 7 1 13 3 1 5 - 3 3 0 55 5 , 9 4 1 , 4 8 1 9 , 1 9 2 2 , 7 5 3 , 1 6 3 9 , 4 7 S , C 1 0 , 7 6 3and 3 th a t all kinds of low peat contain much higher am ounts of total
nitrogen, th a n peat-form ing plants from lowmoors. The situation is
reverse in the case of high peats, i.e. peat-form ing plants of highmoor
have higher content of total nitrogen as compared to their high peats.
W ith regard to m ineral nitrogen content, both peat-form ing plants
and peats are sim ilar, only th ere are differences in the content of
ammonium and n itra te nitrogen. The higher values of am m onium and
" i t r * o r ? r . Глгшп i n p o n t - f o r m i n * p l a n t s i n ,ù o f t o t a l N T o t a l Samn i e No. P l a n t a ?;o, -n a m i d e rimine M h e x o n e -- a m i n e i n s o - l u b ] h u n i r . o N r.cn i ' i e n t i f ÎI i n % o f d , n . 1 C a r o x r o o t r a t ' : - - - 2 , 2 4 1 2 C' -.roz e r r n c i l i . i 1, ¥ i 4 , ? 5 ' - , 5 3 4 0 , 1 9 2 , 0 7 1 4 , 7 1 2 7 , 2 6 1 , 5 1 5 3 С'•.rex p -. eu ' .i o cy p er ' uз 3 , 2 2 5 , 4 3 1 0 , 1 4 4 2 , 9 6 3 , 3 4 1 4 , 4 4 2 0 , 4 6 1 , 2 7 6 4 С -'.ro.c p i l o s a - - - 3 , 9 0 1 5 ù l y c o r i a a q u a t i c . a - - - 3 , 3 3 5 6 i v ir i 1 tC‘3 с OMÎT, un i .1 2 , 2 7 1, i>d 7 , 3 5 3 7 , 3 2 2 ■■ 6 1 5 , 6 4 3 1 , 6 7 3 , 3 5 4 7 1*32 1, 7o 3 , 1 4 4 4 , 4 7 2 , 3 3 1 1 , - 3 2 о , 2 , 7 3 3 - IS l".a p - i l ’;:: ï r o 2 , :ij 2 , 2 3 1 0 , 4 0 4 4 , 0.- 3 , 4 5 10, 40 2 0 , 5 0 2 , 3 7 7 9 . *.i 1 : r i dr. i o i ' - ' i c i r : * ; Ils 2 , 0 4 2 , jO 1 2 , 5 1 4 4 , 1 5 2 , 7 - 1 4 , 7 1 2 0 , 3 9 1 , 3 7 3 10 . i : i p o r . i u l . i u i l n u r i a 2 , 5 2 2 , 2 J 3 , 5 5 4 3 , 2 k 2 , 2 3 1 1 , 2 3 2 9 , 3 7 2 , 9 0 1 11 J oma rui a i r e - - - 1 , 6 4 4 12 2 1 bu 2 , 7 4 1 1 , 1 4 1 , ^ ô 1 3 , 3 3 2 4 , 1 4 1 , 8 6 9 13 З р Ь а . т . ш p a l u s t r i s - - - 1 , 3 2 4 14 JphKtT-un! c :3 ; ' / i d at u i : ; 3 , 3 2 3 , 9 6 1 1 , 3 7 4 2 , 3 7 / . 3 1 4 , 0 2 1 7 , 3 3 1 , 4 7 3 15 C a l l u n a v u l g a r : . - 1, ^3 3 , 8 3 9 , 7 4 4 0 , 5 5 5 , 2 7 1 5 , 7 1 2 3 , 0 0 1 , 5 1 5 l 6 : i n u s G i l v c : ; ü r i 3 2 , 11 3 , 2 2 o , 4 3 4 0 , 7 2 5 , 1 7 , 3 0 2 3 , 16 1 , 4 3 0 17 Latium p: iAun;r-> 2 , 72 3 , ^ 7 , 3 0 3 5 , 6 9 5 , 7 ô 1 4, > 0 , 7 5 1, 320 13 0:c>-c o c c uj q u ' i i r i p - ï î n l u s 2 , - 3 5 , 0 ; ; ; , 3 3 4 1 , 4 5 1, 3ô 1 5 , 3 4 2 j , 5 * 1 , 4 0 1 19 » • ^c cl ni um u l i ^ ' i n o . ï u m 3 , 4 2 6 , 2 7 3 3 , 2 3 2 , 3 1 1 5 , 0 4 3£.,-.i5 1 , 7 0 2 2 0 a r Jr i o p i i o r u m v ^ i n a u u a - - - 1 , 4 7 6 2 1b o r i o p : : o r u m v a g i n a : . ici 2 , 2 o 3 , - 4 3 , 0 5 4 2 , 1 1 4 , 4 0 11, j ô 2 7 , . v ; i , 22 ^ r i o p h o r u m a n g u s t i r ' o l i u . u 2 , 3 , 5 3 1 0 , 9 3 4 4 , 6 2 3 , 4 7 1 3 , » 7 1 , 3 5 3 - n o t a n a l j - j - - - a , b - c o l l e c t e d f r o i a • j r e n t h i s - . M O o rj
lower of n itrate nitrogen than in plants occur in high peats. On the
other hand, both peat-form ing plants from lowmoor and from highmoor
contain a high am ount of nitrate nitrogen.
The plants contain about 40% of amine nitrogen in relation to the
total nitrogen. The highest values (40-44%) of amine nitrogen occur both
in peat-form ing plants of lowmoors and in peat-form ing plants of high-
moors. In all cases individual kinds of peat contain sm aller (20-50%)
am ounts of amine nitrogen than compared species of peat-form ing plants.
In particular, it is tru e for a low peats and for very strongly decompo
sed high peats. However it is different w ith other nitrogen fractions.
Both low and high peats contain much more amide and insoluble humine
nitrogen as the plants compared.
W ith regard to the hexozam ine-nitrogen, particular kinds of peat
have m ostly more of this fraction than respective plants. As the
peat-form ing process goes on, th ere takes place a large increase in peat
Zmiany w składnikach azotowych i fenolowych w torfach
11
of insoluble hum ine nitrogen (non hydrolysable in 6 N HCl) w hich is
often twice as high as in plants.
Investigated peats and plants have a very high content of lignin
(Tables 4, 5); however, individual kinds of peats contain evidently higher
T -a 1 о 4 C o n t e n t and c h a r a c t a r o f ? . ig ni n f r a c t i o n i n peat?» заг. р1ел : Sa mo l» : ; o p t h o f b o r i n g С 21 D'.‘с 0:1 p o s i t i o n C o r t o n t o f l i r n i n f r a c t i o n s i n a o f i . ? . . T c t ' i l M i n l i p r . i n f r a c t i o n s i n л. o f d . a . ■I i n l i a ^ i n f r a c t i o n s i n % o f t o t - i l Я t o t a l a c h f r e e V---0 - 2 2 /10 со 09 5 0 , 7 5 . ? 3 6 ? , 98 1 b > 50 20 6 1 , 9 4 6 1 , 35 1- 7 3 , 0 2 с - 1 7 45 3 7 , 8 3 5 1 , 2 1 : , 9 9 6-1,35 ' b > 5 0 6 5 , 9 2 6 5 , 3 3 4, 7 3 , 3 2 3 П 0 - 1 7 > : o 6 0 , 9 2 5 7 , 1 3 4 , 9 6 7 2 , 6 0 3 ь > :-o 45 6 9 , 6 1 6 9 , 3 2 4 , 3 3 9 2 , 1 1 4 :i 0 - 1 9 >70 5 3 , 1 4 5 2 , 0 8 4 , 9 3 C 7 , 46 £ b > 5 0 50 6 9 , 0 0 6 8 , 5 5 4 , 6 8 8 1 , 7 3 5 i 0 - 1 7 70 6 1 , 5 5 5 7 , 2 6 3 , 9 9 6 4 , 9 9 5 b > 5 0 70 7 5 , 6 1 7- , 9 4 3 , 9 6 8 7 , 9 5 6 a 0 - 1 7 > 6 0 6 3 , 1 5 5 3 , 7 7 2 , 9 7 4 8 , 32 6 b > 50 50 6 7 , 9 6 6 6 , 7 4 2 , 8 3 5 5 , 6 6 7 a 0 - 1 7 50 4 9 , 9 0 4 5 , 4 1 4 , 0 9 5 7 , 1 5 7 b >5 0 60 7 3 , 2 1 7 1 , 0 2 4 , 3 5 8 9 , 6 1 8 C - 15 5 3 7 , 30 3 5 , 8 4 2 , 0 4 8 3 , 5 2 9 1 5 - 3 0 5 3 8 , 0 2 3 6 , 7 3 1 , 9 9 3 9 , 8 8 10 1 5 0 - 1 6 5 13 4 1 , 4 4 4 0 , 7 0 2 , 8 3 9 7 , 5 4 11 1 6 5 - 1 8 0 28 6 5 , 2 2 6 3 , 0 6 1 , 7 6 9 7 , 4 6 12 3 0 0 - 315 50 6 7 , 6 9 6 7 , 3 5 1 , 3 3 9 9 , 4 7 13 3 1 5 - 3 3 0 55 6 9 , 0 0 6 3 , 7 6 1 , 1 2 1 0 0 , 0 0
am ounts of these compounds than comparable species of peat-form ing
plants. From the data presented (Tables 4 and 5) it results th a t a larger
p a rt of the total nitrogen in peats and peat-form ing plants is bound w ith
lignin. P articularly high values (83-100%) of total nitrogen occur in
peat-form ing plants of highmoors and in high peats. Amoung individual
species of plants from lowmoor: Carex pseudocyperus and Salix cinerea,
contain the largest am ounts of nitrogen bound w ith lignin. Decomposed
low peats, from deeper layers of peat profiles, as for example reed, woody
or carex-moss peats contain also a very large p art of nitrogen bound
w ith lignin.
3. C o n t e n t of p h e n o l i c c o m p o u n d s in p e a t s a n d
p e a t - f o r m i n g p l a n t s . As already mentioned, the peat form ation
conducts to increase in peats of such substances as lignin and humic
12
F. Maciak, H. Söchtig
Ta b l e 5
C o n t e n t a n d c h a r a c t e r o f l i g n i n i n p e a t - f o r m i n g p l a n t e S a m p l e No. P l a n t C o n t e n t o f l i g n i n f r a c t i o n s i n % o f d . m . T o t a l N i n l i g n i n f r a c t i o n s i n % o f d . m . N i n l i g n i n f r a c t i o n s i n % o f t o t a l 17 t o t a l a o h f r e e 1 C a r e x r c s t r a t a 2 4 , 1 7 2 3 , 4 9 5 , 6 0 6 0 , 2 4 2 C a r e x g r a c i l i s 2 7 , 6 3 2 6 , 9 6 3 , 8 0 6 5 , 0 2 3 C a r e x p s c u d o c y p e r u 3 2 7 , 9 3 2 5 , 4 3 3 , 9 9 8 8 , 3 8 4 C a r e x p i l o s a 2 5 , 3 0 2 2 , 0 2 6 , 6 8 4 3 , 3 4 5 G l y c e r i a a q u a t i c a 1 9 , 9 9 1 3 , 7 4 4 , 8 2 2 8 , 7 9 6 P h r a g m i t e o c o mm u ni s 3 7 , 6 6 3 1 , 3 9 5 , 9 8 6 7 , 0 9 7 S a l i x c i n e r e a 5 9 , 5 6 5 9 , 1 5 4 , 3 4 9 4 , 2 3 8 E q u i o e t u a p a l u s t r e 3 0 , 8 8 2 4 , 4 2 5 , 1 3 6 6 , £7 9 V a l e r i a n a o f f i c i n a l i s 2 3 , 1 6 2 2 , 5 7 4 , 4 5 5 5 , 0 0 10 P i l i p e n d u l a u l i n a r i a 3 6 , 5 8 3 4 , 8 5 5 , 4 5 6 0 , 6 0 11 C om a r u n p a l u s t r e 3 7 , 6 6 3 6 , 6 1 2 , 7 0 6 2 , 2 0 12 T y p h a l a t i f o l i a 2 2 , 2 2 2 2 , 0 1 4 , 1 9 4 9 , 8 2 13 S ph ag nu m p a l u s t r i a 1 4 , 9 3 1 4 , 5 5 3 , 1 7 3 5 , 6 1 14 Sp ha g nu m c u s p i d a t u m 2 1 , 1 3 1 8 , 6 2 4 , 9 6 7C, 74 15 C a l l u n a v u l g a r i s 4 8 , 5 7 4 3 , 3 0 1 , 6 9 5 1 , 7 5 16 P i n u e s i l v e s t r i 3 3 5 , 32 3 0 , 0 6 3 , 4 3 9 3 , 0 7 17 Ledum p a l u e t r e 4 8 , 7 3 4 7 , 1 4 3 , 2 3 8 1 , 7 7 13 O x y c o c c u a q u a d r i p e t a l u s 5 1 , 6 3 5 1 , 0 2 2 , 4 1 3 0 , 5 1 19 V a c c i n i u m u l i g i n o s u m 5 1 , 0 0 5 0 , 4 0 2 , 5 1 7 5 , 2 1 2 0 a E r i o p h o r u m v a g i n a t u m 32 ,6 8 3 0 , 6 5 2 , 9 3 6 4 , 8 7 21b E r i o p h o r u m v a g i n a t u m 2 3 , 3 3 2 8 , 1 6 5 , 0 1 7 1 , 2 2 22 E r i o p h o r u m a n g u s t i f o l i u m 2 9 , 9 3 2 8 , 4 1 3 , 7 9 8 3 , 1 5compounds because it is w ell-proved th at these substances are very
resistant to microbes. The high meolecular weight of lignin and hum ic
compounds constitute a source of low m olecular w eight phenolic sub
stances, which were form ed during degradation of lignin in peats
[9, 10].
In the present investigation the five phenolic compounds were isola
ted. From the data presented (Table 6) it follows th a t different kinds
of peats give variable values of phenolic compounds. Among the phenolic
substances isolated from peats p-hydroxybenzoic acid have been found
in a higher amount. However vanillic and protocatechuic acid were in
lesser amounts. It is interesting th a t other phenols, as syringic acid,
appeared only in well-decomposed low peats, contrary to p-hydroxyben
zoic aldehyde, w hich appears only in high peats. Considering individual
differences in the content of phenolic substances in soil form ations of
different kind of peat one can prove th a t the higher yields of p-hydroxy
benzoic, vanillic and protocatechuic acid are mostly in stronger decom
posed surface layers of low peats. Strongly decomposed high peats are
T a b l e 6
C o n t e n t o f p h e n o l i c c o m p o u n d s I n p e a t a Di g/ 1 0 0 g o f d . m . Sample D e p t h o f b o r i n g s D e c o m p o -a i t i o n p r o t o c a t e c h u i c a c i d p - h y d r o x y b e n z o i c a c i d v a n i l l i c a c i d I х1 Ï O . cm K i n d o f p e a t d e g r e e % h y d r o l y s i s h y d r o l y s i a h y d r o l y s i s h y d r o l y e e b N ::C1 *Ia a m a l ga m t o t a l 6 N HC1 Im a m a l gam t o t a l 6 N HC1 Ha a m a l g am t o t a l 6 If HC1 1 a 0 - 2 0 s e d g e p e a t 40 1 , 2 1 - / X 1 , 2 1 4 4 , 7 2 3 3 , 16 8 2 , 8 3 1 5 , 8 2 1 0 , 3 7 3 4 , 1 9 -1 b > 5 0 s e d g â - т о з з p e a t 20 0 , 8 4 - 0 , 8 4 1 7 , 0 0 - 1 7 , 0 0 1 2 , 1 3 - 1 2 , 1 8 -2 a 0 - 1 7 e e d g e - r a o a a p e a t 45 5 , 8 4 4 , 2 0 1 . , 0 4 5 0 , 6 8 2 3 , 2 5 7 3 , 9 3 3 5 , 3 0 1 9 , 9 9 5 5 , 2 9 traoe 2 b > 5 0 s e d g e - m o s a p e a t 15 0 , 6 9 7 , 2 0 1 , 3 9 3 5 , 7 9 4 3 ; 65 7 9 , 4 3 1 2 , 1 3 2 9 , 7 2 4 1 , 8 5 -3 a 0 - 1 7 m u ck d e v e l o p e d f r o m r e e d p e a t > GO 2 1 , 12 - 2 1 , U 5 7 , 2 3 1 3 , 1 1 7 0 , 3 9 3 9 , 2 4 - 3 9 , 2 4 1 2 , 3 7 3 b > 5 0 r e e d p e a t 4 5 3 , 0 9 - ; 4 , 0 3 1 5 , 7 5 3 9 , 0 3 2 5 , 1 3 3 2 , 4 3 5 7 , 6 1 4 . 5 1 4 a 0 - 1 9 m u c k d e v e l o p e d f r o m r e e d p e a t > 7 0 2 , 6 9 3 , 0 0 5 , - 9 4 1 , 5 1 1 3 , 9 0 5 5 , 4 1 2 2 , 5 3 - 2 2 , 5 3 traoe 4 b > 5 0 r e e d p e a t 5 0 0 , 7 1 1 6 , 2 0 l G , 9 1 1 2 , 4 6 2 5 , 6 8 3 3 , 1 4 1 1 , 3 3 4 6 , 4 3 5 7 , 8 1 -5 a 0 - 1 7 m u c k d e v e l o p e d f r o m r e e d p e a t 7 0 0 , 7 3 2 , 4 0 3 , 1 3 3 4 , 6 1 1 6 , 6 3 5 1 , 2 9 2 2 , 3 7 - 2 2 , 3 7 -5 b > 5 0 r e e d p e a t 70 2 , 3 5 - 2 , 35 4 3 , 6 9 - 4 3 , 6 9 2 4 , 55 - 2 4 , 5 5 tra o e 6 a 0 - 1 7 m u c k d e v e l o p e d f r o m w o o d p e a t > Co 3 , c 6 - 3 , 0 6 3 0 , 6 5 1 1 , 0 0 4 1 , 6 5 2 1 , 2 3 - 2 1 , 2 3 7 , 7 0 6 b > 5 0 a l d e r p e a t 5 0 1 1 , 4 3 - 1 1 , 4 3 1 0 , 3 7 - 1 0 , 3 7 2 2 , 0 2 - 2 2 , 0 2 8 , 2 2 7 a 0 - 1 7 m u ck d e v e l o p e d f r o m w o o d p e a t 5C 1 5 , 0 2 3 , 0 0 1 8 , 0 2 1 2 , 6 0 - 1 2 , 6 0 1 3 , 5 0 - 1 3 , 5 0 5 , 6 9 7 b > 5 0 a l d e r p e a t 68 6 , 5 1 “ 6 , 5 1 5 , 9 6 3 , 0 0 1 3 , 9 6 1 1 , 9 3 1 5 , 1 3 2 7 , 1 1 2 , 1 9 * N o t d e t e c t a b l e 3 3 S y s i n g i c a c i d14
F- Maciak, H. Söchtig
also richer in the content of the phenols m entioned contrary to
p-hydroxybenzoic aldehyde, the content of which is the highest in weakly
decomposed high peats (sphagnum peat).
As compared to peats, the peat-form ing plants (Table 7) are richer
in protocatechuic and p-hydroxybenzoic acid, however the level of
vanillic acid in peat-form ing plants is low. W ith regard to the syringic
acid and p-hydroxybenzoic aldehyde both phenols are found only in
some species of plants. Syringic acid content is in Comarum palustre
much less than in compared plants. The p-hydroxybenzoic aldehyde
appeared only in four plants. It is very interesting th a t p-hydroxybenzoic
aldehyde w ith a large am ount was isolated, first of all, in sphagnum
plants as well as in weakly decomposed sphagnum peats.
Among the plants investigated the highest content (over 10 mg/100 g)
of protocatechuic acid was in lowmoor plants (Salix cinerea, Filipendula
ulmaria, Comarum palustre and Hypha latifolia). However, the highmoor
plants: L edum palustre, Oxycoccus quadripetalus and Eriophorum vagi-
natum were also rich in protocatechuic acid. The highest value (about
300 mg/100 g) of p-hydroxybenzoic acid was obtained in Pinus silvestris.
The large amount of p-hydroxybenzoic acid (30-55 mg) was in p articular
in al species of Carex and in plants: Salix cinerea, Typha vatifolia, L {e-
dum palustre, Eriophorum vaginatum and Eriophorum angustifolium.
The highest value (over 10 mg/100 g) of vanillic acid occured in Salix
cinerea, Valeriana officinalis and Eriophorum august of olium.
DISCUSION OF RESULTS
From the data obtained for peat-form ing plants and peats, it follows
th at peat-form ing process leads to some quantative changes in nitrogen
and phenolic components.
As affected by peat form ation the content of total nitrogen increases
in the low peats m entioned in comparison to corresponding species of
low peat-form ing plants.
The increase presents probably an effect of a decrease of carbon
in organic m atter, w hich in the total bulk leads to relative increase in
the am ount of nitrogen [11, 16]. In case of high peat the situation is
reverse: peat-form ing plants of highmoors show somewhat higher content
of the total nitrogen then the samples of high peats. May be th a t in
peat-form ing processes occuring in highmoors the loss of carbon is not
significant because of a small activity of microbes. Some losses of the
nitrogen may occur also due to leaching [12].
There are also some quantitative differences w hen the corresponding
nitrogen fractions are taken into consideration. Individual kinds of peat
contain in all cases sm aller amounts (20-50%) of amine nitrogen than
T a b l e 7 C o n t e n t o f p h e n o l i c c o n i p o u r d s i r , p e n t —f o r m i n g p l a n t a a n d p e a t mg/ Ю О g o f d*im. 3 a n p l e P l a n t e p r o t o c a t e c h u i c a c i d p - h y d r o x y b o n z o i c a c i d v a n i l l i c a c i d i x x I ц Х Х Х N o. h y d r o l y s i s h y d r o l y s i s h y d r o l y s i s h y d r o l y s i s 6 IT I I Cl Na a m a l g a m t o t a l 6 N HC1 Na a n a l ^ a m t o t a l 6 N HC1 Na a m a l g a m t o t a l 6 N HC1 6 N H C l 1 2 3 4 5 6 7 8 9 10 11 12 1 3 1 C a r e x r o s t r a t a 4 , 2 7 - / X 4 , 2 7 3 2 , 7 0 5 , 5 0 4 5 , 2 8 6 , 0 7 6 , 0 7 -2 C a r e x g r a c i l i o 4 , 6 2 - 4 , 6 2 5 0 , 3 9 4 , 4 0 5 4 , 7 9 7 , 7 1 - 7 , 7 1 - -3 C a r e x p c c u d o c y p e r u e 9 , 3 2 - 9 , 3 2 5 3 , 2 7 - 5 3 , 2 7 9 , 6 3 - 9 , 6 3 - 8 , 4 8 4 C a r e x p i l o s a 2 , 8 2 - 2 , 8 2 2 9 , 9 3 - 2 9 , 9 3 7 , 3 4 - 7 , 3 4 - -5 G l y c e r i a a q u a t i o a 5 , 5 4 - 5 , 5 4 9 , 3 3 - 9 , 3 3 5 , 1 4 - 5 , 1 4 t r a c e -6 P h r a g m i t e e o o n n u n i s - - - 9 , 1 0 - 9 , 1 0 4 , 5 0 - 4 , 5 0 - -7 3 a l i x c i n e r e a 9 , 3 6 1 1 , 4 2 2 0 , 7 8 2 3 , 6 3 7 , 3 3 3 0 , 9 6 3 , 8 2 1 4 , 0 5 1 7 , 8 7 t r a c e -a E q u i s e t u m p a l u s t r e 1 , 4 6 5 , 4 0 6 , 8 6 6 , 0 7 6 , 2 4 1 2 , 3 1 4 , 0 0 - 4 , 0 0 t r u c e -9 V a l e r i a n a o f f i c i n a l i s 1 , 3 9 3 , 0 0 4 , 3 9 1 2 , 7 1 4 , 4 0 1 7 , 1 1 3 , 7 7 8 , 6 4 1 2 , 4 1 t r a c e -10 F i l i p e n d u l a u l i n a r i a 5 , 5 8 1 8 , 0 4 2 3 , 6 2 1 5 , 3 4 6 , 6 0 2 1 , 9 4 6 , 5 7 - 6 , 5 7 - -11 C o a a r u m p a l u s t r e 1 8 , 6 1 ‘ - 1 8 , 6 1 1 2 , 7 6 9 , 9 0 2 2 , 6 6 3 , 8 4 - 3 , 8 4 2 , 2 1 -12 T y p h a l a t i f o l i a 4 , 5 5 6 , 3 1 1 0 , 8 6 3 9 , 7 4 8 , 0 0 4 7 , 7 4 1 , 5 9 - 1 , 5 9 t r a c e -1 3 S p h a g n u m p a l u s t r i s 2 , 0 6 - 2 , 0 6 1 6 , 0 3 - 1 6 , 0 3 8 , 1 3 - 8 , 1 3 - 3 6 , 4 6 14 S p h a g n u m c u s p i d a t u m - - - 1 6 , 2 0 - 1 6 , 2 0 6 , 9 3 - 6 , 9 3 - 3 3 , 2 9 15 C a l l u n a v u l g a r i s 1 , 7 8 - 1 , 7 8 1 4 , 6 7 - 1 4 , 6 7 6 , 5 4 - 6 , 5 4 - -16 P i n u s s i l v e s t r i o 7 , 5 9 - 7 , 5 9 2 7 8 , 0 7 1 7 , 9 8 2 9 6 , 0 5 5 , 3 5 - 5 , 3 5 - -17 Le d um p a l u s t r e 1 5 , 9 5 1 1 , 4 2 2 7 , 3 7 3 0 , 3 0 - 3 0 , 3 0 5 , 1 2 - 5 , 1 2 - -18 O x y c o c c u s q u a d r i p e t a l u s 9 , 2 2 1 8 , 0 4 2 7 , 2 6 1 1 , 8 7 - 1 1 , 8 7 8 , 5 1 - 8 , 5 1 - -19 V a c c i n i u m u l i g i n o a u m 0 , 7 9 - 9 , 7 9 1 8 , 3 4 - 1 8 , 3 4 9 , 0 4 - 9 , 0 4 t r a o e -2 0 a E r i o p h o r u m v a g i n a turn 1 0 , 9 8 - 1 0 , 9 6 1 3 , 2 5 - 1 3 , 2 5 1 , 5 0 - 1 , 5 0 - -2 1 b E r i o p h o r u m v a g i n a t u m 7 , 0 5 1 0 , 8 2 1 7 , 8 7 3 4 , 0 0 5 , 1 3 3 5 , 1 3 6 , 9 1 - 6 , 9 1 - -2 -2 E r i o p h o r u m a n g u s t i f o l l u m 6 , 0 3 - 6 , 0 3 Z S , 0 1 4 , 7 7 3 0 , 7 3 7 , 2 7 8 , 1 0 1 5 , 3 7 - 1 . 1 1
■J 2 3 4 5 6 7 8 9 10 11 12 1 3 _ _ 8 S p h a g n u m p e a t 3 , 5 4 3 , 5 4 2 0 , 6 3 - 2 0 , 6 3 1 2 , 0 2 - 1 2 , 0 2 - 1 4 , 1 9 S p h a g n u m p e a t - 6 , 3 1 6 , 0 1 1 9 , 3 5 1 0 , 6 4 2 9 , 9 9 1 0 , 8 2 - 1 0 , 8 2 “ 1 4 , 9 10 S p h a g n u m p e a t 6 , 6 6 - 6 , 6 6 2 0 , 6 6 3 , 0 0 2 8 , 6 6 1 1 , 0 2 - 1 1 , 0 2 - 1 8 , 5 11 S p h a g n u m p e a t - 1 3 , 4 7 1 3 , 4 7 2 1 , 0 4 1 5 , 0 4 3 6 , 8 0 9 , 5 6 - 9 , 5 6 - 7 , 5 12 E r i o p h o r u m p e a t 2 7 , 4 6 1 8 , 6 4 4 6 , 1 0 3 , 1 7 7 , 3 3 1 5 , 5 0 4 , 4 4 1 6 , 7 5 2 1 , 1 9 “ 2 , 2 13 r J r i o p h o r u m p e a t 8 , 6 2 6 , 0 1 1 4 , 6 3 6 , 32 7 , 7 0 1 4 , 0 2 4 , 7 3 1 4 , 5 9 1 9 , 3 7 1 . 0 x - / N o t d e t e c t a b l e * * I 3 y s i n g l e a c i d XXX p - h y d r o x y b e n z o i c a l d e h y d e