assessment of seafood processing wastes as alternative sources of selenium in plant production
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Assessment of seafood processing wastes asalternative sources of Selenium in plant productionTrine A. Sogn a , Espen Govasmark b , Susanne Eich-Greatorex a , Anne Falk-Øgaard a &John A. MacLeod ca Department of Plant and Environmental Sciences , Norwegian University of LifeSciences , Aas, Norwayb The Norwegian Centre for Ecological Agriculture , Tingvoll, Norwayc Agriculture and Agri-Food Canada , Charlottetown, PEI, CanadaPublished online: 12 Apr 2007.
To cite this article: Trine A. Sogn , Espen Govasmark , Susanne Eich-Greatorex , Anne Falk-Øgaard & John A. MacLeod(2007) Assessment of seafood processing wastes as alternative sources of Selenium in plant production, Acta AgriculturaeScandinavica, Section B — Soil & Plant Science, 57:2, 173-181, DOI: 10.1080/09064710600768277
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ORIGINAL ARTICLE
Assessment of seafood processing wastes as alternative sources ofSelenium in plant production
TRINE A. SOGN1, ESPEN GOVASMARK2, SUSANNE EICH-GREATOREX1,
ANNE FALK-ØGAARD1 & JOHN A. MACLEOD3
1Department of Plant and Environmental Sciences, Norwegian University of Life Sciences, Aas, 2The Norwegian Centre for
Ecological Agriculture, Tingvoll, Norway and 3Agriculture and Agri-Food Canada, Charlottetown, PEI, Canada
AbstractIn some parts of the world, the soil selenium (Se) content is too low to ensure the Se level recommended for human oranimal consumption in the crops produced. In order to secure a desired concentration of Se in crops, Se has been applied asmineral fertilizer to agricultural fields. Since only a minor part of the inorganic Se applied is utilized by plants and smallincreases in Se concentrations in, e.g., drinking water, may be toxic, the method is somewhat controversial. As an alternativeto Se-enriched mineral fertilizer, different seafood-processing wastes have been examined as a source for Se in cropproduction. Both in greenhouse pot experiments and field trials the Se in seafood waste was not plant-available during thefirst growing season. There was no significant difference between the Se concentration in wheat growing in soil withoutadded Se and in soil receiving Se from seafood waste in amounts ranging from 0.9 to 9 g ha�1. Neither was any residualeffect of Se in seafood waste seen during a second year growth period. Thus, seafood-processing waste cannot be regarded asa potential source of Se in crop production. Possible mobilization of formerly applied Se, as seafood-processing waste or Seenriched mineral fertilizer due to changes in soil redox conditions were examined in a leaching experiment. The mobility offormerly applied Se was generally very low, but the results indicated that under permanently wet soil conditions leaching ofSe may occur in plant dormant periods in soils with low organic matter content and high pH.
Keywords: Plant-available selenium, seafood waste, selenium leaching, soil selenium, wheat.
Introduction
The trace element selenium (Se) is of fundamental
significance for human and animal health, foremost
as an important constituent of the antioxidant
enzyme gluthatione peroxidase. In parts of the
world, particularly in large areas of Scandinavia
(Wu & Lag, 1988; Gissel-Nielsen et al., 1984), in
Finland (Varo et al., 1988), in New Zealand (Gupta
& Watkinson, 1985) and in eastern Canada (Gupta
& Winter, 1975) plant availability of Se in soils is
very low. Thus, crops produced in these areas have a
very low Se concentration (Gupta & Winter, 1975;
Gissel-Nielsen et al., 1984; Gupta & Watkinson,
1985; Varo et al., 1988; Govasmark et al., 2005). In
order to ensure that the Se concentration in plants
reaches recommended levels of 0.1 to 0.2 mg kg�1
dry matter for humans and 0.2 to 0.3 mg kg�1 for
livestock, Se-enriched mineral fertilizers have been
used in crop production (Varo et al., 1988; Eurola
et al., 1989; Ekholm, 1997). However, results from
different trials show that only a limited part of the
added Se is utilized by plants (Mikkelsen et al.,
1989; Ylaranta, 1990; Ekholm et al., 1995; Bakken
& Ruud, 2000). Also, the residual effect has shown
to be very small (Singh, 1991). Between 70 and 90%
of the inorganic Se applied seemed to accumulate in
soil in forms not available for plants. It is still not
fully understood whether the applied Se will remain
immobile in the soil, or if changes in soil environ-
mental factors may cause mobilization. If mobilized,
the excess of the applied Se represents a potential
environmental problem since relatively small in-
creases in Se may result in toxic concentrations. A
Se concentration of 10 mg l�1 is usually regarded as
Correspondence: T. A. Sogn, Department of Plant and Environmental Sciences, Norwegian University of Life Sciences, P.O. Box 5003, N-1432 Aas, Norway.
Tel: �/47 64965565. E-mail: [email protected]
Acta Agriculturae Scandinavica Section B-Soil and Plant Science, 2007; 57: 173�181
(Received 12 January 2006; accepted 18 April 2006)
ISSN 0906-4710 print/ISSN 1651-1913 online # 2007 Taylor & Francis
DOI: 10.1080/09064710600768277
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the maximum acceptable for drinking water. For
instance, elevated Se concentrations in ground water
have been associated with leaching from agricultural
land in California (White et al., 1991), and thus Se
contamination of drinking water is of concern
(Hudak, 2004). It would evidently be safer to find
a Se source that is more bioavailable than inorganic
fertilizer enriched with Se. In organic farming, where
use of such fertilizer is restricted, alternative Se
sources must be found. Plants have been shown to
take up organic Se compounds, such as the amino
acid Se methionine (SeMet), in nutrient solution
experiments (Lauchli, 1993). In animal feeding
experiments, organic Se sources, such as SeMet or
selenoyeast, proved to be more bioavailable than
inorganic Se sources (Pehrson et al., 1989; Wang &
Lovell, 1997; Ortman, 1999). Organic Se sources
may therefore be an alternative to the inorganic Se
additives also in plant production. Fish and crusta-
ceans generally have a high Se content. Fish Se
concentration normally ranges between 0.10 and
1.90 mg kg�1 and crustacean Se concentration
between 0.20 and 2 mg kg�1. In addition, feed for
fish farming is usually enriched with Se in order to
ensure optimal mineral supplement and thereby
good fish health. In order to recycle a waste product
and thus utilize Se that already exists in the food
chain, seafood-processing waste may be evaluated as
a Se source in plant production. If positive results are
gained, the waste may be used as an ultimate Se
source within organic farming and as a desirable
alternative to the Se-enriched manufactured mineral
fertilizer within traditional plant production.
In this study, three different seafood-processing
wastes were assessed as Se sources in wheat produc-
tion both in greenhouse and field studies. Addition-
ally, the mobility of the Se not taken up by plants was
investigated in a leaching experiment with different
redox conditions prior to leaching. The hypotheses
to be tested were that: 1) Se-rich seafood-processing
waste, applied as an organic fertilizer, increases
wheat grain Se concentration; 2) oxidizing soil
conditions followed by reducing soil conditions
(heavy irrigation) may induce leaching of formerly
applied Se from soil.
Material and methods
The field experiment in Canada
A field study with wheat (Belvedere) cultivation and
organic Se fertilizer treatments consisting of two
different lobster wastes was established at the
Harrington research farm, Prince Edward Island,
Canada (6389?W, 46820?N). The site is situated
about 40 m above sea level with an annual precipita-
tion ranging from 800 to 1100 mm. The soil is a fine
sandy loam classified as a Typic Haplorthod in Soil
Taxonomy. The soil contained 3.1% (w/w) organic
matter in the plough layer and the pH was 6.5
(H2O, 1:1). The natural soil Se content was about
0.22 mg kg�1 (Gupta & Winter, 1975), and the
grain yields produced in this area have an average Se
concentration of 0.05 mg kg�1 (MacLeod et al.,
1998). The treatments were laid out in a randomized
block design with four replicates. The plot size was
20 m2 (5 m�/4 m) with a 2 m border around, and a
harvested area of only 0.36 m2. The levels of Se
applied with lobster waste ranged from 0.9 to 9 g
ha�1 (Table II). No mineral fertilizer was applied in
addition to the lobster waste, or to the control plots.
The grain crop was harvested at maturity, dried at
608C, and analysed for Se by a method described
below.
As Se fertilizer, fresh and composted waste was
applied to the soil. Chemical characteristics of the
two wastes are presented in Table I. For analysis of
most elements, except Se, samples of the lobster
waste (1 g) were digested in 12 ml HNO3 in a
microwave. The sample solution which evaporated
to 5 ml in the process, was diluted to 50 ml with
H2O and then centrifuged (3500 r.p.m. for 10 min)
before an aliquot was transferred to an 8-ml tube
and analysed by ICP optical emission spectroscopy
(ICP-OES). The lobster and grain samples were
analysed for total Se concentration by the recently
developed method of Govasmark and Grimmet
(2006). Briefly, 1 g of sample was digested in closed
Teflon vessels in the microwave using ultra-pure
HNO3 and 30% H2O2. Se in the digested solution
was reduced by concentrated HCl, derivatized with
2,3-diaminonaphthalene, and then extracted into
Table I. Chemical characteristics of the fish silage and the fresh and composted lobster waste.
Macronutrients (g kg�1 DM) Trace elements (mg kg�1 DM)
C:N N P K S Ca Mg Na Fe Zn Mn Cu B Co Se Al
Fish silage 3.8 11.4 20.5 11.5 10.4 23.7 2.6 16.3 530 590 10 40 nd1 nd1 0.90 30
Fresh lob. waste 6.2 42.3 16.1 3.0 3.3 158 8.7 6.6 336 45 259 24 29 0.26 0.45 382
Composted lob. waste 22.5 13.2 8.0 3.0 1.7 113 5.7 3.4 4437 37 301 23 15 1.94 0.34 8439
1nd�/not determined.
174 T.A. Sogn et al.
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cyclohexane. This solution was analysed for Se on a
high performance liquid chromatograph (HPLC)
equipped with a fluorescence detector. The method
was validated with a suite of reference materials.
The field experiment in Norway
A field experiment with cultivation of spring wheat
(Triticum aestivum L.) and different Se fertilizer treat-
ments was carried out at As, Norway (10845?E,
59840?N). The annual precipitation in this area is on
average about 800 mm. The experimental site is
situated about 70 m a.s.l. on a marine clay deposit.
The soil is a loam, classified as a Typic cryaquept in
Soil Taxonomy. The soil pH is about 5.8 (H2O,
1:2.5), and the organic matter content in the plough
layer about 5.3% (w/w). The natural soil Se content
is 0.29 mg kg�1 (Ruud, 1997). Plants growing in
this soil usually have a Se concentration B/0.02 mg
kg�1 (Ruud, 1997). Thus, a very small fraction of
the total soil Se pool is plant-available. As Se
supplement, the soil was applied Se-rich fish silage
(Table I) or Se-enriched NPK fertilizer ((21:3:8)
with 12 mg Se kg�1 as Na2SeO4). The Se concen-
tration in the fish silage was analysed by hydrid
generation atomic absorption spectrophotometry
(Perkin Elmer 1100-B) after digestion in HNO3
and Mg(NO3)2, ashed at 4508C and resolved in
HCl. The N concentration was determined by using
a CHN analyser (LECO EC-12) and the concen-
trations of other elements were analysed by use
of inductively-coupled plasma mass spectrometry
(ICP-MS) after microwave digestion.
The treatments were laid out in a randomized
block design with four replicates. The plot size was
21 m2 (3 m�/7 m), with a harvested area of 10 m2.
Each Se treatment plot received a total amount of Se
corresponding to 9 g ha�1, divided into 8 g Se ha�1
at the start of the experiment and 1 g Se ha�1 at
Zadoks stage 21 (Zadoks et al., 1974), i.e., at
tillering. The Se-treated plots were compared to
control plots without any added Se. In the control
treatment, a basic dose of NPK fertilizer (21:4:10)
corresponding to 140 kg N ha�1 was applied prior
to sowing. At Zadoks stage 21, a top dressing with
NPK corresponding to 18 kg N ha�1 was applied.
The Se-enriched (as NaSeO4) NPK fertilizer was
applied in an amount corresponding to the same
amount of N as in the control. In order to adjust for
the imbalance in P and K, the amounts of these
elements were adjusted with superphosphate and
KCl. To achieve the same amount of Se as in the
NPK�/Se (as Na2SeO4) treatment, 9514 kg fish
silage was applied per ha. To adjust for the N in the
fish silage (Table I), the amount of NPK fertilizer
(21:4:10) was reduced by 10 kg N ha�1 compared to
the amount used in the other treatments. The crop
was harvested at maturity. Grain samples were dried
and ground before digestion with strong acid
(HNO3) in an autoclave. The plant material was
analysed for Se by a high-resolution inductively-
coupled plasma mass spectrometry (HR-ICP-MS).
The pot experiment in Norway
A greenhouse pot experiment with wheat (Triticum
aestivum L.) growing in two different soil types was
conducted. The soil types were a commercial growth
peat and a loam soil taken close to where the field
experiment was carried out. In order to establish two
different pH levels, approximately 5.5 (pHlev 1) and
6.5 (pHlev 2), the soil was limed with different
amounts of CaCO3, depending on initial and in-
tended pH. The pH values found after the growth
period were, however, somewhat different from the
intended ones; pHlev 1 represented pH values
ranging from 4.8 to 5.5 in the peat, and from 4.5
to 5.4 in the loam, while pHlev 2 represented values
from 6.1 to 6.8 in the peat, and values from 5.8 to
6.3 in the loam.
The Se treatments were equivalent to those
conducted in the field experiment described above,
given as fish silage or Se-enriched NPK fertilizer.
There were seven replicates per treatment, three of
which were used for analysis at the end of the
experiment. Four pots were used in the leaching
experiment. The pot volume was 6.7 l. Moisture
content in the soil was maintained at 60% of field
capacity by regular irrigation with deionized water.
The crop was harvested at maturity. Grain and straw
Se concentrations were measured by use of HR-ICP-
MS after digestion with strong acid (HNO3) in an
autoclave.
In order to examine a possible residual effect,
three pots from the fish silage treatment were kept
for a second year growth experiment. All the pots
received NPK fertilizer as in the control, and no new
fish silage was added � otherwise the experiment ran
exactly similar to the first year.
Table II. Fresh and composted lobster waste and the correspond-
ing Se applied per m2 in the Canadian field experiment.
Se mg m�2
Applied kg plot�1 Fresh Silageed
0
5 0.113 0.085
10 0.225 0.170
20 0.450 0.340
40 0.900 0.680
Selenium in seafood processing wastes 175
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Four pots within each treatment from the first year
growth experiment were used in a leaching study in
order to examine if some of the Se that accumulated
in the soil from Se fertilization could be mobilized
due to changes in soil redox conditions. The leaching
experiment was divided, and in two replicates per
treatment, the soil was homogenized after harvest,
dried and remoistened to field capacity after 20 days,
while the soil in the two other replicates was kept
undisturbed and constantly moist at 60% of field
capacity. After 20 days also these pots were mois-
tened to field capacity. To simulate a heavy rainfall,
1 l distilled H2O was added to the pots in four doses
of 250 ml each, and the leachate was collected after
24 h. Se concentration in the leachate was analysed
by HR-ICP-MS.
Statistics
Treatment effects on plant Se concentration and
uptake, as well as soil pH and Se concentrations in
leachate were tested by analysis of variance and
multiple testing using the General Linear Model
(GLM) procedure and the Student- Neuman-Keul’s
(SNK) test of SAS (SAS Institute Inc. statistical
software). The differences were considered signifi-
cant at the p B/0.05 level.
Results and discussion
Experiment in Canada
In the Canadian field experiment, fresh and com-
posted lobster waste, in amounts ranging from 0.25
to 2 kg m�2, were used as Se source. Neither the
grain yield nor the grain Se concentration was
significantly affected by the Se-rich lobster waste
application (Figure 1). The grain yield was on
average 459, 517, and 497 g m�2 for the control,
fresh lobster waste, and composted lobster waste
treatments, respectively, and the average grain Se
concentrations were 0.13, 0.15, and 0.13 mg kg�1 in
the same treatments. The soil pH was not altered by
the lobster waste application. The lobster waste
decomposition process had led to a higher C:N ratio
and to somewhat lower concentrations of most
elements except for Fe, Al, Co, and Mn in the
composted waste relative to the fresh (Table I). The
higher C:N ratio in the decomposed waste (Table
III) could have influenced enhanced microbial im-
mobilization of Se. However, the Se in lobster waste,
independent of waste decomposition degree and
C:N ratio seems to be little plant-available, and
cannot be regarded as a potential source of Se in
crop production, at least not in the same growing
season as the application.
Experiments in Norway
Average grain yield in the field experiment in Nor-
way was 338 g m�2 and there were no significant
differences in grain yield between the treatments. As
expected, according to the low C:N ratio (Table I),
the fish silage represented a source of plant avai-
lable N during the growing season. There was no
significant difference in grain Se concentration ob-
served between the fish silage treatment (0.0119/
0.008 mg kg�1 DM) and the control (0.0139/
0
0.1
0.2
0 5 10 20 40 0 5 10 20 40
Fresh lobster waste Composted lobster waste
Se
mg
kg-1
DM
kg lobster waste applied per plot (20 m2)
Figure 1. Grain Se concentration in control (0) and after application of increasing amounts (5�40 kg per 20 m2) of fresh and silaged lobster
waste in the Canadian field experiment.9/St. dev. of the average is indicated by the bars, n�/ 4.
176 T.A. Sogn et al.
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0.008 mg kg�1 DM). Thus, the Se in fish silage was
not plant-available in the first growing season. On
the other hand, Se application via the NPK fertilizer
resulted in significantly higher Se concentration in
grain (0.2109/0.023 mg kg�1 DM) compared to
grain from fish silage and control plots. The Se
concentration in the wheat grain produced in soil
fertilized with NPK-Se reached the recommended
Se level in grain for animal feed and human bread
flour (0.1�0.2 mg kg�1). As percent of Se added,
the amount of Se found in the grain was, however,
only 7.2%.
In general, the results from the pot experiment
supported the finding from the field experiment in
that the Se from fish silage was not plant-available
during the first growing season, whereas application
of Se-enriched NPK fertilizer significantly increased
the plant concentration of Se (Figure 2). The straw
and grain Se concentrations in plants grown in soil
supplied with fish silage were not significantly
different from the control. Neither soil pH nor the
varying content of soil organic matter had any
significant impact on this result. Neither was there
any significant effect of Se treatment on plant growth
in the pot experiment. As seen in the field experi-
ment, and also as expected according to the low C:N
ratio (Table I), the fish silage represented a source of
plant available N during the growing season. How-
ever, reduced plant growth was observed in the loam
soil at the lowest pH level (pH 4.5). Estimated plant
Se uptake (straw Se concentration*straw weight�/
grain Se concentration*grain weight) (Table III)
revealed that in the case of wheat plants grown in
loam at pHlev 1 (i.e., pH 4.5), the higher plant Se
concentration was apparently a result of this reduced
growth. Up to almost 32% of the applied Se was
taken up by plants in the greenhouse experiment
(Table III). This figure is higher than the Se
utilization usually reported from field experiments
(Mikkelsen et al., 1989; Ylaranta, 1990; Ekholm
et al., 1995; Bakken & Ruud, 2000). The higher
plant and root density in the pot experiment has
apparently led to a better utilization of the applied Se
than in field.
The residual effect of inorganic Se fertilization has
shown to be of little importance in plant production
(Singh, 1991). The decomposition of fish silage in
soil is most probably not completed during the first
growing season and release of Se from seafood waste
decomposition in soil may partly occur in the plant-
dormant periods and coming growth seasons. In our
study the amount of residual Se from the fish silage
taken up by plants in the second growth season was
almost negligible (Figure 2; Fish_2 yr). Results from
a ten-year study with Se-rich sewage sludge applica-
tion, published by Edelbauer and Eder (2001)
showed no significant residual effect of added Se
via sludge. The application of sewage sludge induced
increased Se content in the upper 0�5 cm of soil,
while no significant increase in plant Se concentra-
tion was found. Thus, the residual effect of Se added
via organic waste products seemed to be as limited as
for Se enriched mineral fertilizer. The Se released in
the plant dormant period has, probably, quite
rapidly been transformed to forms strongly adsorbed
in soil. Perhaps the addition of organic matter has
induced enhanced binding of Se as well. The plant
concentration (Figure 2) and plant uptake of Se
(Table III) is often lower when fish silage is applied
than in the control treatment (not significant). pH
measurements in soil after harvest show a slightly
lower pH (not significant) in the pots applied fish
silage compared to the control. As plant availability
of Se generally decreases with decreasing soil pH,
this pH reduction may explain the lower plant
uptake of Se when fish silage is applied. Additionally,
Lee (1997) demonstrated excellent binding proper-
ties of sea food processing waste for phosphate,
which is an anion like selenate and selenite. Johnsson
(1991) and Gustafsson and Johnsson (1992) found
added mineral Se to be strongly bound to soil
organic matter. When the process was further
investigated, the Se retention seemed to be primarily
due to microbially mediated reductive incorporation,
whereby the Se anions are reduced to low valence
states and then incorporated into low-molecular-
weight humic substance fractions (Gustafsson &
Johnsson, 1994). They claimed further abiotic sorp-
tion of Se in organic matter to be important only as a
‘trapping’ mechanism for dissolved Se, but quanti-
tatively unimportant in the storage process. How-
ever, the effect of organic matter on Se availability in
soil is somewhat inconsistent. Winja and Schulthess
(2000) found that presence of organic acids as
oxalate and citrate inhibited adsorption of Se by
competition for the anion binding sites and thus in-
duced more labile and plant-available Se in the soil.
Leaching experiment
More information on the environmental fate of Se
applied to crops in Se-deficient areas has been
requested (e.g., MacLeod et al., 1998). At low pH
and reducing conditions, Se occurs mainly in the
form of selenite, whereas in oxidizing soil conditions
combined with higher pH the more mobile selenate
prevails. By studying distribution of Se in paddy soils
(rice fields) where oxidation and reduction occur
repeatedly, Kang et al. (1991) detected Se enrich-
ment in the lower soil horizons. In a similar way, but
to a lesser extent, we assume that ploughing com-
bined with a dry weather period may induce oxida-
Selenium in seafood processing wastes 177
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tion and remobilization of the soil-bound Se. If the
dry period is suddenly ended by heavy rainfall,
leaching of the remobilized Se may occur. Owing
to these assumptions, the leaching experiment in-
cluded physical disturbance and drying before the
actual leaching event. In the loam at pHlev 2,
significantly higher leaching of Se was found from
pots with soils being permanently wet than those
being dried before the leaching event. For all the
others, no significant differences were found be-
tween the pots exposed to physical disturbance and
drying and those kept permanently wet with regard
to Se leaching (Figure 3), independent of Se treat-
ment. Our hypothesis that oxidizing soil conditions
followed by reducing soil conditions (heavy irriga-
tion) may induce leaching of formerly applied Se
from soil was not verified. Rather, the results
indicated that leaching of applied Se may occur in
plant dormant periods, under permanently wet soil
conditions, in soil with low organic matter content
and high pH. Similar to the results regarding plant
availability, the Se applied to the soil as Se-enriched
NPK fertilizer showed significantly higher mobility
than the Se applied via fish silage (Figure 3), whereas
the latter did not differ from the control treatment.
Although significantly higher than the leaching
of Se from the control and fish silage treatments,
the leaching of Se from the pots with Se enriched
NPK was not alarming. The maximum Se concen-
tration measured in the leachate was 5.1 mg l�1.
Table III. Se applied, plant Se uptake and calculated plant Se utilization (%) during the first growth season in the greenhouse pot
experiment. Means (n�/ 3) followed by the same letter are not significantly different (p B/0.05).
Soil pHlev Treatment
Se applied
(mg pot�1)
Plant Se uptake
(mg pot�1)
Plant Se utilization
(%)*
Peat 1 Control 0 1.39a
NPK-Se 30 10.86b 31.56a
Fish silage 30 0.57a �/2.71b
2 Control 0 2.95a
NPK-Se 30 6.89b 13.11a
Fish silage 30 1.36a �/5.32b
Loam 1 Control 0 0.41a
NPK-Se 30 2.64b 7.46a
Fish silage 30 1.19a 2.61b
2 Control 0 1.32a
NPK-Se 30 9.31b 26.64a
Fish silage 30 0.91a �/1.37b
*((Plant Se uptake treatment � Plant Se uptake control)/Se applied in treatment) *100.
0
0.1
0.2
0.3
0.4
0.5
0.6
0.7
Con
trol
Fis
h
Fis
h_2y
r
NP
K_S
e
Con
trol
Fis
h
Fis
h_2y
r
NP
K_S
e
Con
trol
Fis
h
Fis
h_2y
r
NP
K_S
e
Con
trol
Fis
h
Fis
h_2y
r
NP
K_S
e
Peat, pHlev 1 Peat, pHlev 2 Loam, pHlev 1 Loam, pHlev 2
Se
mg/
kg D
M
Straw Grain
Figure 2. Grain and straw Se concentration [mg kg�1] in the greenhouse pot experiment. Fish_2yr denotes the second year residual effect
study of the fish silage treatment.9/St. dev. of the average is indicated by the bars, n�/ 3. The treatment abbreviation used along the
horizontal axis mean: ‘Fish’�/Fish silage, ‘Fish_2yr’�/ residual Fish silage (second yr) and ‘NPK_Se’�/Se enriched NPK fertilizer.
178 T.A. Sogn et al.
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This concentration is below 10 mg l�1, which is
generally regarded as the maximum acceptable Se
concentration for drinking water.
As mentioned above, there was a trend (not
significant) towards lower plant uptake of Se when
Se-rich fish silage was added compared with the
control treatment. In the leaching experiment there
was also a trend (not significant) towards lower
concentrations of Se in leachate from the pots
receiving fish silage than in the control treatment.
This may indicate that addition of organic matter has
reduced soil Se mobility. However, the effect of
organic matter application on soil Se mobility or
availability of applied mineral Se must be verified by
batch or column experiments.
Although the plant utilization of the applied Se
(organic or inorganic) varied in our experiments, the
general low plant uptake and the low leaching found
leave no doubt that application of Se (organic or
inorganic) will increase the soil total Se pool. Never-
theless, it is difficult to trace the additional Se in soil.
Within Scandinavia, Finland is the country practis-
ing the most liberal Se fertilization policy, and Se has
been applied to agricultural soils since 1985. This
fertilization practice has been accompanied by stu-
dies on long-term effects of the Se fertilization.
Usually less then 10% of the applied Se is found to
be taken up by the crop (Yli-Halla, 2005), and no
sign of increased Se concentration in surface waters
has been found (Wang et al., 1994). Comparison
of water-extractable Se in soil before the start of
application (Sippola, 1979) and after 14 years of
application gave no significant increases (Makela-
Kurtto & Sippola, 2002). In soil samples from 48
fields at ten different research stations in Finland,
sampled in 1994 and 2004, no significant changes
were found in aqua regia-extractable Se (Yli-Halla,
2005). No obvious environmental effects connected
to the Se-fertilization practices have been detected to
date (Alfthan & Aro, 2005). However, the interval
between deficiency and toxicity for Se is very tight.
For instance, elevated Se concentrations in ground-
water have been associated with leaching from
agricultural land in California (White et al., 1991),
and thus Se contamination of drinking water is of
concern (Hudak, 2004). Although the leaching of Se
from the pots with Se-enriched NPK in our experi-
ment was lower than the maximum acceptable Se
concentration for drinking water, the fact that it was
significantly higher than in the control treatment
should support use of a precautionary principle. As
important as establishing agronomic practice secur-
ing recommended levels of Se in food plants, is the
search for practices improving the plants’ utilization
of applied mineral Se, as well as Se sources which
have a higher utilization degree than Se enriched
mineral fertilizer.
Conclusions
The hypothesis that Se-rich seafood processing
waste increases wheat grain Se concentration when
Figure 3. Se concentration [mg l�1] in the leachate in the greenhouse experiment.9/St. dev. of the average is indicated by the bars, n�/ 2.
Each of the four groups of bars is linked to the soils loam or peat, each at different pH levels (pH lev). The abbreviations used on the bars
mean: ‘Contr.-ox’�/Control treatment, with drying. ‘Contr.-red’�/Control treatment, with constant wet soil conditions. ‘Fish-ox’ and
‘Fish-red’�/Fish silage treatment, with respectively drying or constant wet conditions. ‘NPK-Se-ox’ and ‘NPK-Se-red’�/Treatment with Se
enriched NPK fertilizer, with drying or constant wet conditions, respectively.
Selenium in seafood processing wastes 179
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applied to soil as a fertilizer, was not verified. There
was no significant difference between the Se con-
centration in wheat growing in soil without added
Se and in soil receiving Se in amounts from 0.9 to
9 g ha�1 as seafood waste. Nor was any residual
effect of the Se added as seafood waste found during
a second growth season. The hypothesis that oxidiz-
ing soil conditions followed by reducing soil condi-
tions (heavy irrigation) may induce leaching of
formerly applied Se from soil was not verified.
Rather the results indicated that leaching of applied
Se may occur under permanently wet soil conditions
in plant dormant periods, in soil with low organic
matter content and high pH.
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