The fertilization guidelines on this website are based on
results from studies carried out predominantly in
California. However, for an optimal fertilization program, growers need
to make field-specific adjustments, which depend on expected
yield, soil properties, local weather conditions and crop management
(see Fig. 1). These factors affect crop nitrogen (N) uptake,
non-fertilizer N inputs and potential N losses. The major factors affecting soil N availability are discussed in the following sections.
Fig. 1: Overview of the most important site-specific
factors affecting crop N availability.
When determining the amount on N required, other
sources of N need to be taken into account. These sources
include soil residual nitrate, nitrate in the irrigation
water, and N mineralized during the growing season from
organic material, such as soil organic matter, plant residues,
manure and compost. Furthermore, a small amount of N is added to fields through
atmospheric deposition.
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Soil residual nitrate can be a significant source of crop available N. Nitrate concentrations can be expressed in units of nitrate or nitrate-N. One molecule of nitrate (chemical notation NO3-) is composed of three atoms of oxygen and one atom of N. Therefore, only 22.6% of the nitrate is actually N, which means that, 45 lbs of nitrate contain 10 lbs N. In reports of soil and water analyses, the nitrate or nitrate-N concentration is generally reported in mg/kg or ppm (parts per million).
A nitrate-N concentration of 10 ppm in one foot of the soil
profile corresponds to roughly 35 lbs N/acre. Not all the
nitrate present in the top foot or two of the profile in
spring may be available for plant uptake. Nitrate is very
mobile in the soil and can move with the irrigation water
below the root zone when water applications exceed evapotranspiration (ET).
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Irrigation water, especially well water, may contain N in the form of nitrate. When irrigation water with a high nitrate concentration is used, agronomically significant amounts of N can be added to a field. With one acre-inch of water with a nitrate-N concentration of 10 ppm, 2.27 lbs N/acre are applied to the field. With one acre-foot of the same water, 27.2 lbs N/acre are applied.
As is the case with soil residual nitrate, irrigation water nitrate can move with the infiltrating water below the root
zone when water applications exceed ET. This can occur in any type of irrigation system. To
account for leaching losses, only the nitrate in the water
taken up by crops is generally taken into account. Plant
uptake is closely related to ET. Estimates of ET
values for different crops, regions and irrigation system and
can be found here
and here.
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Microorganisms associated with roots of legumes can fix
atmospheric N through a process called biological N fixation. Several methods that do not require a
laboratory analysis have been proposed to estimate the N
that legume cover crops can add to soil. Both methods calculate the amount of N added through
biological N fixation. However, not the entire amount will become available to the next crop.
Method 1:
In the handbook "Cover Cropping for Vegetable Production", van
Horn and coauthors (2011) recommend the following procedure:
Table 1: Conversion factors for different legume cover
crops to calculate N content.
Method 2:
The handbook "Managing Cover Crops Profitably" (Sustainable
Agriculture Network, 2007) suggests calculating the dry yield
by harvesting a known area and drying the cover crops in the
sun for a few consecutive days or in the oven at 140 °F for 24
to 48 hours.
The yield can then be calculated using the following
equation:
Alternatively, the yield can be estimated by measuring the average height (in inches) of the crop. A 6-inch tall non-woody legume crop that covers the ground completely will contain roughly 2,000 lbs/acre dry matter. For each additional inch, add 150 lbs.
The dry yield can then be multiplied with the N content of annual legumes which is
about 3.5-4% N prior to flowering and
3-3.5% N at flowering. As an example, the dry yield of a
10-inch tall crop which does not flower yet yields
approximately 2,600 lbs/acre (2,000 lbs for the first six
inches and 4 × 150 lbs for the additional inches). With an N
content of 3.5-4%, this crop contains between 90 and
105 lbs N/acre.
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Alfalfa can fix large amounts of N. However, most of the fixed N is removed in the harvested forage. Based on an informal survey, Pettygrove and Putnam (2009) recommended that under Central Valley and desert conditions in California, the legume credit should be no more than 60-80 lbs N/acre.
Preliminary result from an ongoing study carried out at three
locations across the state indicated that the N credit of
alfalfa to wheat harvested as forage may be higher, ranging
from 80-150 lbs N/acre (Putnam et al., 2014).
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The N content of crop residues strongly affects the amount and timing of N released during the next growing season. The N content is often expressed as the carbon (C) to N ratio of the residues. Generally, residues with a C to N ratio of 20 or less result in net N mineralization. As the C content of most crop residues is between 40 and 45% of the dry mass, a C to N ratio of 20 corresponds roughly to an N content of 2%. Examples are legume residues and residues from vegetables such as lettuce and broccoli. These residues decompose quickly and the N is made plant available by the decomposer community.
In contrast, grain straw (e.g. wheat, barley or rice) and corn stover have a wide C to N ratio and N is released only slowly. When the C to N ratio is wider than approximately 30, soil mineral N may be immobilized by soil microorganisms, temporarily reducing the amount of N available to crops.
Crop residue decomposition is highly influenced by soil moisture, the greatest activity occurring in moist soils during the first two to three months following soil incorporation. Crop residues left on the soil surface decomposes more slowly.
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The decomposition and mineralization of soil organic matter can provide significant amounts of plant available N in the form of ammonium, which may be further converted to nitrate, both of which are readily plant available forms of N. However, the timing and amount of N mineralization may not coincide with crop N demand (Gaskell et al., 2006).
Soil organic matter and soil organic N contents are highest in the top foot of the soil profile. As an example, a soil with a soil organic matter content of 2% contains about 3500 lbs N/acre in the top foot of the profile. This value is based on the assumption that pores make up roughly 45% of the soil volume, and an N content of the organic matter of about 5%. Generally 1-3% of soil organic N is mineralized during the growing season (Bremner, 1965). Therefore, as a rough estimate, between 35 and 105 lbs N/acre will become available during the growing season in this soil with 2% soil organic matter. Many other factors also affect N mineralization, most importantly soil temperature, which varies considerably during the year (Figure 2).
Figure 3 illustrates the seasonal differences in N
mineralization from soil organic matter, but also the
uncertainty of the estimates.
Fig. 2: Annual changes in soil temperature at selected
locations in California at a depth of 6 inches (Data source: CIMIS).
Fig. 3: Estimated monthly N mineralization rates from
soil organic matter based on monthly average temperature in a
soil with an organic matter content of 2% in the top foot of the profile.
As mentioned above, soil moisture also affects N mineralization. In dry soil, N
mineralization is much slower. Therefore, in drip irrigated
fields, the amount of N mineralized per acre is reduced, as
only part of the soil volume is kept moist.
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Nitrogen in manure occurs mainly in organic forms and as ammonium (Pettygrove et al., 2009). The ammonium is directly available to plants provided it is not lost to the atmosphere in the form of ammonia (see below). Manure ammonium content varies widely depending on the source and its handling. Samples of corral scrapings, composted manure, lagoon sludge and mechanical screen solids taken from dairies in the San Joaquin Valley were found to have an ammonium-N proportion ranging from 0-6% of the total N (Pettygrove, 2009). In poultry manure, ammonium-N may comprise 14-17% of the total N (Gale et al., 2006; Hartz et al., 2000). Ammonium makes up a much higher proportion of lagoon water; Pettygrove (2009) found on average two thirds of the total N was in ammonium form. Lagoon water that is drawn from the bottom of lagoons where more solids are present may have a higher total N content but only about one third of it is in ammonium form (Campbell-Mathews et al., 2001).
The organic forms of N are not directly available to plants,
but must be mineralized by soil microorganisms. How
quickly organic N is mineralized depends on many factors, such
as manure properties, temperature, moisture, placement of the
manure and soil related factors. For these reasons it is
difficult to predict the amount and time N becomes available
to crops (Table 2). Some of the N is integrated into soil
organic matter and does not become available during the
growing season following its application.
Table 2: Estimated availability of organic N in manures (Pettygrove et al.,
2009).
From 40-70% of the expected mineralization will occur within the first two months after application, probably closer to 40% for material applied in late fall or winter (Pettygrove et al., 2009; Gale et al., 2006; Andrews and Foster, 2007). Expected lagoon water N mineralization will be slowed if solid particles do not infiltrate into the soil and remain on the surface, which may happen when lagoon water is not sufficiently diluted (Pettygrove, 2009).
Manure applications may contribute to N mineralization for
many years. In fields that have been manured continuously for
many years, the annual amount of N mineralized from recent and
past manure applications may roughly equal the total amount of
N added with manure the present year. Therefore, in fields
with at least 3-7 years of regular manure additions, the
manure application rates can be reduced to the point that
total manure N applied is approximately equal to projected
crop demand (Chang et al., 2007; Crohn, 2006). However, during
periods of high crop N demand, mineral fertilizers or manures
with high ammonium concentrations may be added to supplement N
mineralization (Pettygrove et al., 2009).
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Nitrogen is also added to fields through atmospheric deposition. In the Central Valley, total annual N deposition may reach 20 lbs/acre or more. However, this source of N is often not considered for N budget purposes and depends highly on location.
A map for total atmospheric deposition can be found here, which is located on the website of
the National
Atmospheric Deposition Program.
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Mineral fertilizers contain N in the form of urea, ammonium,
nitrate or a mixture of these. These N forms behave
differently in soil. Nitrate is very mobile and can easily be leached below the root zone with
irrigation water or rain. Time and amount of irrigation water
applications, as well as its uniformity across the field strongly
affect the risk of nitrate leaching during irrigation events.
Urea is relatively mobile in the soil, but is rapidly
converted to ammonium. Ammonium is less mobile, but is
generally quickly converted to nitrate by soil microorganisms
in warm and moist soils.
Minimizing leaching losses
When left on the soil surface, urea and ammonia based fertilizers, and to a lesser degree ammonium fertilizers, are prone to volatilization (Bremner, 1995). The losses may exceed one third of the N applied (Connell et al., 1979; Rochette et al., 2013). The most significant losses occur during the first week or two after application. This is due to the fact that the hydrolysis of urea to ammonium temporarily increases soil pH (Bremner, 1995). Anhydrous ammonia, aqua ammonia and UAN can similarly increase soil pH near the applied fertilizer and result in volatilization.
High soil pH, soil moisture levels below field capacity, high
application rates and high temperature increase the risk of
ammonia volatilization (Connell et al., 1979; Jones et al.,
2007). In contrast, the risk of volatilization is reduced in
soils with high clay and organic matter contents. These soils
generally have an increased pH buffer capacity and cation
exchange capacity.
Minimizing ammonia volatilization losses
Denitrification is the reduction of nitrate to nitrous oxide (N2O) or dinitrogen (N2) by soil microorganisms. Nitrous oxide and dinitrogen are gases and are lost to the atmosphere. The denitrification rate depends on soil water saturation, soil nitrate concentration, soluble organic C availability and temperature (Rolston et al., 1982). The denitrification rate is increased in wet or compacted soil when the proportion of soil pores filled with water increases above 60-70% and aeration is reduced (Dalal et al., 2003). High nitrate concentrations, high temperatures and the availability of C from manure, crop residues, or root exudates also increase denitrification rates.
Rolston and coworkers (1982) studied the influence of
irrigation frequency and incorporation of crop residue on
denitrification losses in a Yolo loam at Davis. Total
denitrification losses ranged from 0.7 to 5% of the nitrate
fertilizer applied (Rolston et al., 1978). More frequent
low-volume irrigations tended to lower losses, while the
availability of carbon from incorporated straw increased
losses. However, when the soil moisture was constantly above
field capacity, denitrification losses from plots cropped with
ryegrass reached 14% during the summer. Under the same
conditions, losses exceeded 70% of the applied nitrate-N in a
manure amended plot (Rolston et al., 1978). In contrast, very
little denitrification occurred in the same soils during the
cooler winter months and when soil moisture was below field
capacity.
Minimizing denitrification losses
* Daniel Geisseler is an Extension Specialist in the Department of Land, Air and Water Resources at the University of California, Davis. Patricia Lazicki is an Assistant Specialist in the Department of Land, Air and Water Resources at the University of California, Davis. William R. Horwath is professor of Soils and Biogeochemistry in the Department of Land, Air and Water Resources and the James G. Boswell Endowed Chair in Soil Science at the University of California, Davis.