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Sustainable Fertilization in Medicinal and Aromatic Plants: January 2015
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Chapter 10
Sustainable Fertilization in Medicinal
and Aromatic Plants
Alessandra Carrubba
Abstract The nutrient level in the soil is one of the most investigated aspects of
agricultural research, also including research into Medicinal and Aromatic plants.
The effect of fertilization has been studied in detail for many species, with
contrasting results as concerns above all the qualitative aspects of production.
Generally speaking, an increased level of nutrients induces an enhancement of
plant biomass, but when the goal of cultivation is different from herbage yield,
i.e. when a special plant part (seeds, or roots, or flowers) is of interest, or when the
quality features are especially important, the outcome of fertilization may be
dramatically different. A fine-tuned fertilization practice is therefore necessary,
and forms, rates and times of distribution of fertilizers must be accurately planned
and managed.
1 Introduction
A. Carrubba (*)
Department of Agricultural and Forest Sciences, Universita degli Studi di Palermo,
Palermo, Italy
e-mail: alessandra.carrubba@unipa.it
alessandra.carrubba@unipa.it
188 A. Carrubba
decreases, what usually causes chlorosis and retards development of certain plants
(arnica) (Catizone et al. 1986). Oppositely, in strong acid soils, the availability of
mineral elements increases, what can cause harmful accumulation of heavy metals
(Cd, Ni, etc.), especially in certain plant species that are prone to such phenomenon
(St. John’s wort, yarrow, and others) (Radanović et al. 2004).
Moisture plays a determinant role as well. Most crops have shown significant
interactions between nutrients and water, in that water deficiency conditions are
often claimed to influence negatively plant’s use of nutrients. As a consequence, in
the arid and semi-arid areas of the world, more fertilizer is used when water for
irrigation is available, and under rainfed Mediterranean conditions, fertilizer rec-
ommendations are tuned to the average rainfall incidence (Sivakumar and Huda
1984). A close interaction between nutrients and water availability was stated for
nitrogen (a highly soluble element), and e.g. in coriander, Nitrogen Use Efficiency
was found to increase with enhancing irrigation rate (Singh and Rao 1994).
Nevertheless, some evidence exists that a moderate N-P supply may mitigate the
detrimental effect of drought on biomass yield in some MAPs such as Bupleurum
chinense DC (Zhu et al. 2009).
Decisions concerning fertilization, actually, involve many consequences. An
improper nutrients supply may provoke a number of disadvantages on plants,
including lodging, pest attacks, cycle delay and so on. A few elements may exert
a negative effect on the quality features of product (quantity and quality of active
compounds) (Radanović et al. 2004). Finally, environmental issues linked to
fertilization practice are of concern. Indeed, for fertilization efficiency, elements
must be in a soluble form, that plants may easily recover from soil, and when
soluble elements are not picked up by plants, their excess in soil may generate
pollution problems.
Many aspects of fertilization technique have been deepened in MAPs manage-
ment. In most cases, the advised fertilizer amounts are tuned to obtaining high
herbage yields, and the quality features are of concern only in few very evident
occurrences. Table 10.1 summarizes a few information obtained from literature on
this topic. The so-called “three elements of fertility”, namely nitrogen (N), phos-
phor (P) and potassium (K) are taken into account, since they are usually the most
used in agricultural practice. Of course, the high variability of environments
involved in the various trials carried out worldwide makes somehow difficult to
generalize the outcomes of experimental results. The available information allows
however some general consideration. A first differentiation comes out between
annuals and perennials: many perennials, such as sage, gentian or lavender, have
reduced fertilizer needs in the first cropping year due to their small initial size, but
higher amounts are required in following years (Catizone et al. 1986; Karamanos
2000). This is especially true for nitrogen, that in most cases is top-dressed in 2 or
3 fractions, allowing plants to extract it from soil in concordance with their needs
along the growth cycle. Otherwise, P and K, claimed to have a scarce mobility
throughout soil profile, are usually supplied before transplant (at the time of soil
preparation) and distributed deeply enough to be absorbed by the roots during their
elongation. Of course, in decision-making concerning fertilization, factors related
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10 Sustainable Fertilization in Medicinal and Aromatic Plants 189
Table 10.1 Fertilizer amounts required by some selected MAPs (Data from Catizone et al. 1986;
Singh and Rao 1994; Rangappa and Bhardwaj 1998; Karamanos 2000; Joy et al. 2001, 2001a;
Rajamani 2001; Beyaert 2006; Basso 2009; Karkanis et al. 2011; Verma et al. 2011)
P2O5 K2O
Species N (kg ha-1) (kg ha–1) (kg ha–1)
Achillea millefolium 100 80–100 100–120
L. (Yarrow)
Althaea officinalis L. (Marsh
mallow)
1st year 100 (in 2 splits) 70 120
2nd year and following 100 (in 2 splits) 0 0
Anethum graveolens L. (Dill) 90–120 (50% at sowing, 50% 50–70 50–70
20–40 dd after emergence)
Angelica archangelica
L. (Angelica)
1st year 50–70 100–120 100–120
2nd year and following 50–70 (in spring) 0 0
Apium graveolens L. (Celery) 200 40 40
Artemisia spp. (Wormwood)
Annual (Artemisia annua L.) 50 50 50
Absinthe (A. absinthium L.) 150, in 2–3 splits 100 150
Roman wormwood 120–160 (50 % at sowing, 50 % 100–120 100–120
(A. pontica L.) after emergence)
Tarragon (A. dracunculus L.)
1st year 40–50 60–70 120–150
2nd year and following 40–50 0 0
Atropa bella-donna L. (Deadly
nightshade)
1st year 100 (at transplant) 100–120 0 (only if
needed)
2nd year and following 100 (before vegetative 0
regrowing)
Calendula officinalis 40–50 70–80 to 70–80 to
L. (Marigold) 100 50–100
Carum carvi L. (Carvi ) 100–120 (50 % at sowing, 50 % 60–80 60–80
before vegetative regrowing of
2nd year)
Colchicum autumnale
L. (Meadow saffron)
1st year 0 80–100 80–100
2nd year and following 40–50 (spring) 0 0
Coriandrum sativum 40–50 to 80–90 40 to 80– 40
L. (Coriander) 100
Crocus sativus L. (Saffron) Only if needed 60–70 60–70
Cuminum cyminum L. (Cumin) 30–40 30–40 30–40
Cymbopogon spp. (Lemongrass) 90 (1/3 at sowing, 2/3 after har- 30 30
vest of each year)
(continued)
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190 A. Carrubba
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10 Sustainable Fertilization in Medicinal and Aromatic Plants 191
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192 A. Carrubba
to environment, plant genotype, goals of cultivation, and farm, must be kept into
account. Total fertilizer rate is expected to be generally less important to plants than
distribution method and timing, in that the availability of elements along the
development of crops, above all in the physiological stages when it is especially
important for them, is more important than their overall amount (Arnon 1992).
Moreover, it must be stressed that the commercial and industrial interest of
MAPs is mainly due to their ability to produce and accumulate some special
secondary metabolites; hence, besides the bare aspect of yield enhancement, the
planning and management of fertilization must pay attention to all aspects related to
their quality features, and the nutrients supply must be carefully tuned to the goal of
cultivation (Franz 1983; Carrubba and Catalano 2009).
2 N Fertilization
As a matter of fact, N is the element that exerts the greatest and most evident effect
on crops, in this explaining the farmers’ tendency to spread high, and sometimes
excessive, doses (Arnon 1992; Neeteson et al. 1999). In this case, the fate of this
highly soluble element, and the consequent risks for health and environment, are of
major concern (Yadav et al. 1997). Of course, many possibilities are available to
minimize those risks, and N fertilization may be supplied to plants in various
moments, rates, and forms, with different effects on health and environment.
The specific effects of N fertilization have been studied in detail on many MAPs,
including peppermint (Dellacecca 1994), sage (Bezzi et al. 1992), fennel
(Omidbaigi and Hornok 1992), Origanum majorana (Trivino and Johnson 2000),
coriander (Carrubba 2009). Generally speaking, the primary effect of N fertilization
is to promote plant development. Literature shows many examples of this: herbage
yield was found to increase with increased N applications in coriander (Lenardis
et al. 2000), Scotch spearmint (Mentha gracilis Sole) (Kothari and Singh 1995),
peppermint (Piccaglia et al. 1993), Java citronella (Cymbopogon winterianus
Jowitt) (Singh et al. 1996b), Salvia fruticosa (Karamanos 2000), St. John’s Wort
(Hypericum perforatum L.) (Berti et al. 2000), geranium (Pelargonium sp.) (Singh
et al. 1996a), lavender (Biesiada et al. 2008), basil (Ocimum basilicum L.)
(Rangappa and Bhardwaj 1998), and many others. This effect is striking at low
fertilizer rates but becomes less and less evident with increasing N doses, until a
ceiling value that may be considered the optimal N supply for a given crop and
condition (Arnon 1992). The relationship between root and shoot dry matter
accumulation per year and the N fertilization rate often takes the shape of a
quadratic curve, as e.g. shown in ginseng (Beyaert 2006), where plant dry weight
increases to a maximum and then decreases with increasing N application rate with
a maximum at about 40 kg N ha 1. In coriander, N fertilization enhanced seed
yields by 10.7 % in comparison with the untreated plots, and generally speaking,
every 10 kg ha 1 of N-fertilizer supply (until the optimal rate is reached) is able to
generate an increase in seed yield ranging from about 20 to 70 kg ha 1, depending
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10 Sustainable Fertilization in Medicinal and Aromatic Plants 193
3 P-K Fertilization
Recommendations for phosphor (P) and potassium (K) supplies as found in the
literature for several MAPs are reported in Table 10.1. It is worth however to
underline that, when making decisions regarding fertilizers application, to account
for their availability in the soil is especially important. Moreover, the dosage of P-K
fertilization is also determined by the uptake of plants from soil, which on its turn is
dependent upon the expected yields (Pank 1993). Hence, soil testing is always to
recommend, and the opportunity to add fertilizers should be carefully evaluated
based on the goals of farmers.
In the field practice, as P and K are scarcely mobile along soil’s profile, they are
generally applied to perennials with the first soil works, allowing roots to find them
as long as they grow (Arnon 1992). Very often, a local distribution of these
elements at sowing time (“band” fertilization) is suggested (Kothari et al. 1987)
but a great care is needed in the regulation of width and depth of the band, since in
sensitive plants (e.g. anise), crop emergence may be injured (Catizone et al. 1986).
Phosphor was proven to have a positive influence on development of generative
organs and stimulation of flowering (Radanović et al. 2004), and it was
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194 A. Carrubba
demonstrated that it has the capability to anticipate maturity in grain crops, con-
ferring to them an important “drought escape” mechanism (Cooper 1984). A good P
availability in soil was claimed to be important for glycosides production in
foxglove (Catizone et al. 1986), and in sage, moderate P supplies led to significant
increment of plant height, number of branches, fresh and dry weights (Naguib
2011). In this last species, the peak in phosphor demand was observed at the seed
formation stage, i.e. later than that detected for nitrogen (Karamanos 2000).
Several studies have been devoted to study the effects of an excess in P, that
generally was found to be detrimental for various aspects of MAPs performance.
For example, in sage it causes a suppression in growth and development
(Karamanos 2000), whereas in opium poppy it has been suspected to favor fungal
infections on capsules (Catizone et al. 1986). Plants sensitivity is of course of
relevance, and species as vetiver have shown an overall noticeable sensitivity to
excess P. However, it should be noted that the optimal P concentration in the vetiver
foliage was only slightly lower than the toxic levels (Edelstein et al. 2009). Differ-
ent responses were finally observed about the effect of P supplies on essential oil
yield in MAPs, since an enhancement in lemon balm (Sharafzadeh et al. 2011) and
Japanese mint (Kothari et al. 1987), a decrease in lavender (Catizone et al. 1986)
and no effect in sage (Karamanos 2000) were respectively detected.
Potassium is claimed to exert a positive effect on roots development and
elongation, that is useful for several MAPs such as valerian or Echinacea
angustifolia (Radanović et al. 2004; Basso 2009). In the field cultivation, K
applications were found to exert a positive effect on stem differentiation in thyme
(Basso 2009) and remarkable effects on the mass of roots and on the content of
phenolic acids of Salvia miltiorrhiza Bunge (Buchwald 2004). A few negative
effects of excess K have been however pointed out in many MAPs: in lavender,
excess K promotes the formation of camphor, an unwelcome oil component
(Catizone et al. 1986); in Java citronella it shows a depressive effect on oil yields
(Malwatkar et al. 1984); in deadly nightshade, its availability is inversely correlated
with alkaloids content (Catizone et al. 1986).
Nevertheless, many evidences exist that a balanced ratio between nutrients may
be more important in determining several yield traits, than the absolute quantities of
the elements themselves. In chamazulene-yielding species (chamomile), when N:K
ratio is too low (unbalanced towards K), flowers are bigger but oil quality is reduced
due to an increase in bisabololoxide; otherwise, proportionally high N and low K
lead to a high content in bisabolole (Catizone et al. 1986). Similarly, the mutual
interference of nutrients is probably the reason why P fertilization was found to
have the maximum effect when P was applied with N, as seen e.g. in lemon balm
(Melissa officinalis L.) (Sharafzadeh et al. 2011).
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10 Sustainable Fertilization in Medicinal and Aromatic Plants 195
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196 A. Carrubba
yield rather than an enhancement of essential oil yield in plants. Otherwise, in other
species contrasting results were evidenced: N fertilization was found to interfere
with the production of essential oil in Lavandula spica and in anise (Catizone
et al. 1986), whereas no effect at all was found in small-seeded coriander (Carrubba
et al. 2010), Salvia fruticosa (Karamanos 2000) or Salvia officinalis (Bezzi
et al. 1992).
Besides the bare quantitative effect, a deeper detail of volatiles profile of plants
offers some interesting outcomes as well: in some Chinese aromatic rice ecotypes
total soil nitrogen was one of the key factors in producing the aroma of traditional
regional strains (Yang et al. 2012), whereas N supply was found to increase content
of menthol and menthone in mint essential oil (Catizone et al. 1986), and to
decrease carvone and increase limonene in Scotch spearmint (Kothari and Singh
1995). Oppositely, no fertilizer effects were detected on essential oil composition in
basil (Morakis et al. 2008) and sage (Piccaglia and Marotti 1993). Also in secondary
compounds different from essential oils, such as alkaloids in Papaveraceae or
Solanaceae (but others as well), nutrient supply is just one in many different
environmental factors involved in biosynthesis and storage processes, and to
make general statements it is a bit difficult (Bernáth 1992). In liquorice, N fertil-
ization was supposed to lead to the formation of roots and rhizomes scarcely
endowed in glycyrrhizin (Catizone et al. 1986), whereas no effect was detected
on ginsenoside content in ginseng roots (Beyaert 2006). Evidences exist, otherwise,
of a direct and positive correlation of the alkaloids content with N content in plant in
lupines, barley, Datura, Atropa, Papaver, periwinkle and deadly nightshade
(Sreevalli et al. 2004; Basso 2009). In the last species, this occurrence was found
to be more striking under water stress conditions (Baričevič et al. 1999; Baričevič
and Zupančič 2002). The authors suggest the hypothesis that under stress conditions
alkaloid plants shift their metabolism towards accelerated synthesis of nontoxic
secondary products (alkaloids), which might therefore represent the form of nitro-
gen storage in suffering plants.
Finally, the effect of nutrients on quality parameters of MAPs was proven to
interact with environmental and genetic factors. Among environmental factors,
growth conditions may be mentioned: increasing the amount of fertilizer caused a
significant concentration-dependent increase in antioxidant activity of cultivated
Teucrium polium compared with wild type. In contrast, increasing the amount of
fertilizer caused a significant concentration-dependent reduction in the antioxidant
activity of powders prepared from cultivated Eryngium creticum when compared
with wild plants (Azaizeh et al. 2005). The role of genetic factors was otherwise
recalled by Sangwan et al. (2001) when quoting the differentiated response of Java
citronella to nitrogen application, accounting for a variability in essential oil yield
up to 36 % among cultivars, at the same N levels.
Actually, it seems possible to conclude that plant responses may vary according
to the active principle, or group of active principles, that are of interest, and
depending upon cases, there are at least three factors that may modify the response
of plant. They are: (1) a change in dry matter production; (2) a change in the
proportions of organs; (3) a modification in the accumulation level (Bernáth 1992).
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10 Sustainable Fertilization in Medicinal and Aromatic Plants 197
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198 A. Carrubba
In some species, additionally, the possibility was stated that they act as
hyperaccumulators of heavy metals, as found in Clary sage that concentrated Pb,
Cu, Zn and Cd in all parts of plant, above all leaves (Angelova et al. 2005).
6 Organic Fertilization
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10 Sustainable Fertilization in Medicinal and Aromatic Plants 199
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