Crop Evapotranspiration and Irrigation Scheduling in Blueberry
Crop Evapotranspiration and Irrigation Scheduling in Blueberry
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1. Introduction
There are currently 139,000 ha of blueberry worldwide, including 66,000 ha of highbush
[comprises northern highbush (Vaccinium corymbosum), southern highbush (Vaccinium sp.),
and rabbiteye (V. virgatum formerly V. asheii) cultivars] and 73,000 ha of lowbush blueberry (V.
angustifolium) (Strik & Yarborough, 2005; USHBC, 2009). The majority of the fruit is produced
in North and South America and Europe, although production is increasing in Asia and
Africa. No matter where blueberry is grown, proper irrigation management is critical for
producing high yields and good fruit quality. Even within a few days without rain or
irrigation, water stress develops quickly in blueberry, reducing photosynthesis and leading to
less growth and fruit production. Over irrigation, however, reduces blueberry root function,
increases soil erosion and nutrient leaching, and enhances the probability of developing crown
and root rot infection by soil pathogens such as Phytophthora. Developing accurate irrigation
regimes requires knowledge of both the timing and amount of water needed to replenish any
lost by crop transpiration and soil evaporation.
In this chapter, I discuss the importance of irrigation on growth and development in
blueberry and examine its relationship to plant water relations. Identified are symptoms of
water stress, the most critical stages of water limitations, and various techniques used to
monitor plant water status throughout the growing season. I then discuss irrigation
scheduling for blueberry, including procedures used to calculate crop evapotranspiration
and estimate total irrigation requirements, and finally present recent data on the best
methods to apply irrigation. Information is provided on the response of blueberry to not
only different irrigation systems and configurations but also of when and where to apply
the water. Throughout the chapter, irrigation methods and practices are related to other
factors essential to consider when growing blueberries, including interactions with field
establishment, planting bed management, nitrogen nutrition, and root disease.
first peak occurs in late-spring and the second, the largest, occurs after harvest.
Interestingly, both peaks occur when soil temperatures are at 14 to 18 ˚C, strongly
suggesting that root growth is regulated, at least in part, by soil temperature in blueberry.
Similar soil temperature optimums for root growth were found in other temperate fruit
species such as apple (Nightingale, 1935; Rogers, 1939) and peach (Nightingale, 1935). Shoot
growth, by comparison, appears less controlled by temperature and more controlled by
availability of plant resources. Shoot growth first peaks after the initial peak in root growth
but then declines when fruit maturation begins. During fruit maturation in mid-summer,
fruit provide a highly competitive sink for carbohydrates and nutrients, considerably
reducing the availability of resources to other parts of the plant. Because of the decline in
vegetative growth during this period, fruit removal is often recommended during the first 2
years of orchard establishment in order to increase growth of new plantings and improve
yields during following years (Strik & Buller, 2005). Aside from the beginning and end of
the growing season, shoot and root growth are lowest just prior to fruit harvest (Fig. 1).
Once harvest is complete, a second flush of new shoots and roots occur. Often, more than
Bud swell Full bloom Fruit set Immature Blue/ Harvest Flower bud Dormancy
green blue-pink formation
24
Soil temperature
21
at 15 cm ( C)a
18
o
15
12
9
6
25 60
Shoot 50
Mean shoot growth (mm)
20
unsuberized roots (mm)
Mean length of white
Roots
40
15
30
10
20
5
10
0 0
Apr May June July Aug Sept Oct
. Date
Fig. 1. Elongation of white unsuberized roots in relation to shoot growth, soil temperature,
and stage of development of highbush blueberry plants. Adapted from Abbott and Gough
(1987).
Crop Evapotranspiration and Irrigation Scheduling in Blueberry 169
one flush of shoots can happen after harvest, although the number of flushes varies
depending on cultivar and cultural practices. Flower bud induction overlaps with fruit
harvest and coincides with the second peak in root growth. Shoot and most root growth
finally ceases in late-autumn as the plant enters dormancy and does not resume until the
following spring.
Stage III
Rapid cell expansion
2.00 & ripening
1.75
1.50
Individual fruit weight (g)
1.25
Stage II
1.00 Slow growth
0.75 Stage I
Rapid cell
0.50 division
Jersey
Woodard
0.25 Tifblue
0.00
20 30 40 50 60 70 80 90 100 110 120
Time after full bloom (days)
Fig. 2. Individual fruit weight of ‘Jersey’ highbush blueberry and ‘Woodard’ and Tifblue’
rabitteye blueberries. Adapted from Tamada (2002).
(Fig. 2). Numerous studies on grape and tree fruit crops, which display similar double
sigmoidal patterns of fruit growth as blueberry, indicate that effects of moderate water
stress during this middle lag phase period has little effect on the size of the fruit at harvest.
Theoretically, water stress at this stage should also have minimal effects on fruit size in
blueberry. Abbott & Gough (1987), however, indicate that it is precisely at this stage of berry
development that vegetative growth is at its maximum peak (Fig. 1). Blueberry is dependent
170 Evapotranspiration – From Measurements to Agricultural and Environmental Applications
on new wood for production of fruit the following year. Conceivably, any water stress
occurring during this peak in shoot production could limit production of new canes for next
year’s crop.
Irrigation during Stage III is also critical and is perhaps the most sensitive period to water
stress, as any water limitations at this point will reduce cell expansion and berry size and
therefore have a large impact on yield. Mingeau et al. (2001) examined the effects of water
deficits at various phenological stages in ‘Bluecrop’ blueberry and found that even moderate
water stress (i.e., enough to reduce transpiration by 35%) during the final stage of fruit
growth and ripening strongly influenced yield by reducing both mean fruit weight and fruit
diameter. They also found that water stress after harvest reduced the number of flower
buds. Flower bud induction occurs in mid- to late-summer in most cultivars and overlaps
with late fruit development (Fig. 1). Thus, in addition to reducing yield of the current year’s
crop, water stress during the final stage of berry development will also reduce the number
of flowers and fruit produced the following year.
Nutrient requirements also vary over the growing season but do not necessarily correlate
with water demands. This difference is an important consideration when using irrigation to
fertigate (Bryla et al., 2010). Unlike water, the largest demands for many nutrients, including
nitrogen (N), typically occur early in the season during canopy development and at the
beginning of fruit production (Throop & Hanson, 1997).
ignored (which is often the case as it’s usually near zero in most plants), xylem pressure is
equal to xylem water potential, which can be the same as the water potential of the other
tissues in the chamber (if water equilibration has been achieved) (for details, see
Scholander et al., 1964).
Marked daily changes in the water potentials occur in the soil-plant-atmosphere continuum
(Fig. 3). In most plants, leaf stomata close at night and as a result, transpiration essentially
ceases, allowing root and leaf water to equilibrate with the soil water. The equilibration
process may take hours to occur but generally happens before dawn. When the soil is wet
and near field capacity, e.g., shortly after a rain or irrigation event, water potentials in the
soil, root, and leaf approach zero at night. The stomata then open at dawn and transpiration
begins, resulting in a decline in leaf water potential. Root and soil water potentials also
decline shortly thereafter. If there is no additional rain or irrigation, leaf, root, and soil water
potential becomes more and more negative. As the soil dries, the difference between root
and soil water potential must become larger each day in order to sustain water movement
from soil to the roots. In contrast, the difference between leaf and root water potential
remains constant until the plant is no longer able to sustain a water potential gradient
sufficient to absorb enough water to maintain leaf turgor, e.g., when leaf water potential
reaches -1.5 MPa. The leaf thus wilts at this point but recovers at night. If drought persists,
the leaf may wilt permanently and tissue damage will result.
0.0
Root
Soil
-0.5
Water potential (MPa)
-1.0
Leaf
-1.5
Onset of leaf wilting
1 2 3 4 5 6 7
Time, days without water
Fig. 3. Daily changes in soil, root, and leaf water potential following irrigation or a rain
event. The shaded regions on the x-axis represent night and the white regions represent
daytime. The figure is adapted from Slayter (1967).
172 Evapotranspiration – From Measurements to Agricultural and Environmental Applications
Predawn
0.0 A 70 B
Irrigated
-0.5 60
Water potential (MPa)
Transpiration (ml·h-1)
50
-1.0
Midday
40 Non-irrigated
-1.5
30
-2.0
Onset of leaf wilting
20
-2.5
0 1 2 3 4 5 6 7 8 0 1 2 3 4 5 6 7 8
Time, days without water Time, days without water
Fig. 4. A) Daily changes in predawn (0500 h) and midday (1400 h) leaf water potential and
B) evapotranspiration of 3-year-old ‘Elliott’ blueberry plants grown in 23 L pots filled with
sandy soil. Plants were either irrigated daily (B only) or exposed to drought for 7 days (A
and B). Each symbol represents the mean of six plants and error bars represent one standard
error.
300
Duke
Stomatal conductance (mmol·m ·s )
-1
Bluecrop
250
Elliott
-2
200
150
100
50
0
-1.4 -1.2 -1.0 -0.8 -0.6 -0.4 -0.2 0.0
Water potential (MPa)
Fig. 5. Relationship between leaf stomatal conductance and midday (1400 h) leaf water
potential in mature ‘Duke’, ‘Bluecrop’, and ‘Elliott’ blueberry plants grown under field
conditions. Adapted from Bryla & Strik (2006).
Under field conditions, water stress often develops in blueberry within 3 to 7 days without
rain or irrigation during summer, varying depending on plant age, cultural practices,
phenological development, soil texture, and weather conditions (Hess et al., 1997). Stress
symptoms include reduced shoot growth, increased root growth, lower water use, and less
photosynthesis. Young, succulent shoots and leaves wilt readily under dry conditions, and if
drought persists, leaf margins and tips may become necrotic and scorched. This scorching is
similar in appearance to salt injury often associated with over-fertilization (Caruso &
Ramsdell, 1995). Internode length is shortened by water deficits, as is the duration of shoot
growth when these deficits occur early in the growing season (B. Strik, personal
communication). Susceptibility to water deficits may increase after the initiation of fruit
ripening. Berries of small fruit crops, including blueberry, however, have few stomata. The
majority of the water lost by the plant occurs through the leaf surfaces with fruit playing a
minor direct role in plant water losses. Resistance to water deficits may be enhanced by
osmotic adjustment (e.g., Zhang & Archbold, 1993) or by increased root to shoot ratios (e.g.,
Renquist et al., 1982), leaf thickness and waxiness (Anderson et al., 1979), and cell wall
elasticity (e.g., Savé et al., 1993).
In France, mature ‘Bluecrop’ blueberries exposed to drought closed their stomates and
reduced transpiration gradually within 9 days after withholding irrigation (Améglio et al.,
2000). Upon rewatering, recovery was slow,with stomatal conductance and transpiration
returning to normal after 7 to 9 days. A vulnerability curve presented in the same study
indicated that embolism in the xylem vessels was negligible when leaf water potential was -1.2
MPa or higher but increased rapidly at lower water potentials. To develop the curve, hydraulic
conductance was measured at different applied pressures on 2 to 3 cm-long stem segments
excised under water (Sperry et al., 1988). Percent loss of hydraulic conductance was 50% at -1.4
MPa and 100% at -2.1 MPa. However, in situ embolism measured during actual water stress
174 Evapotranspiration – From Measurements to Agricultural and Environmental Applications
was usually less than 30%. Apparently, rapid reduction in stomatal conductance reduced
water loss and maintained water potential at the threshold of cavitation in ‘Bluecrop’,
protecting it from total xylem cavitation and enhancing its ability to recover from drought.
Bryla & Strik (2007) examined the onset of water stress in three cultivars of 5-year-old
highbush blueberry plants in Oregon, USA, including ‘Duke’, an early-season cultivar that
ripens in late June to mid July, ‘Bluecrop’, a mid-season cultivar that ripens in mid July to
early August, and ‘Elliott’, a late-season cultivar that ripens in early August to early
September. Plants were exposed to water stress during each ripening period. During each
period, stem water potential dropped only slightly within the first 3 to 4 days after irrigation
was withheld but declined substantially, in many cases, after 5 to 7 days without irrigation
(Fig. 6A-C). This later decline was associated with reduced rates of root water uptake,
indicated by smaller changes in soil water content in each treatment. Within each cultivar,
the most apparent decline in water potential occurred when fruit were in their final stages of
ripening, just prior to harvest. The differences in water potential were attributed to seasonal
variation in water use among the cultivars (Fig. 6D-F). ‘Duke’ acquired the most water,
using 5 to 10 mm per day from mid-May to mid-August, while ‘Elliott’ acquired the least,
using only 3 to 5 mm per day. Water use by ‘Bluecrop’ was intermediate. Water use was
highest during fruit filling and ripening but declined markedly after harvest, especially in
‘Duke’, which ripened earliest. A sharp decline in water use was less apparent in ‘Elliott’,
which had the latest and most extended fruit ripening period. Mingeau et al. (2001) reported
that almost 55% of the total seasonal water requirements of ‘Bluecrop’ occurred in June and
July during fruit ripening; once fruit were picked, plant water requirements decreased to
nearly half. Higher rates of stomatal conductance and water use have been associated with
increased photosynthetic activity during fruit ripening in lowbush blueberry (Hicklenton et
al., 2000). Thus, as ripening periods differ among cultivars, water requirements at any given
time of the year will also differ.
Duke Bluecrop Elliott
0.0
A B C
Water potential (MPa)
-0.3
-0.6
-0.9
-1.2
Harvest Harvest
-1.5
-1.8
Harvest
-2.1
Evapotranspiration (mm·d )
-1
10
D E F
8
4 Harvest
Harvest
2 Harvest
0
June July Aug Sept June July Aug Sept June July Aug Sept
Fig. 6. Seasonal changes in (A-C) leaf water potential and (D-F) evapotranspiration in
mature (A, D) ‘Duke’, (B, E) ‘Bluecrop’, and (C, F) ‘Elliott’ blueberry plants. Adapted from
Bryla & Strik (2007).
Crop Evapotranspiration and Irrigation Scheduling in Blueberry 175
1.4
A 1.4
B
Kc = Kcb + Ke
1.2 First blue fruit 100% blue fruit 1.2 Ke
1.0 1.0
Crop coefficent, Kc
Crop coefficent, Kc
0.8 0.8
0.4 0.4 K
cb
0.2 0.2
Crop
Bud break Initial
development
Mid season Late season
0.0 0.0
0 20 40 60 80 100 Apr. Jun. Aug. Oct. Dec.
Growth stage (% of full season) Month
Fig. 7. Crop coefficient curves for highbush blueberry from (A) AgriMet and (B) FAO-56.
Blueberry ET is calculated at various stages of crop development by multiplying Kc by ETr
or ETo, respectively.
The FAO-56 guidelines for calculating crop ET recommends using a simplified segmented
Kc curve approach whereby the growing season is divided into four distinct stages: initial,
crop development, mid season, and late season (Allen et al., 1998; Fig. 7B). In perennial
crops, the initial stage begins at bud break or the green-up date when new leaves are
initiated and continues to about 10% ground cover. The Kc during the initial stage (Kc ini) is
predominated by soil evaporation and therefore is large when the soil is wet from rain or
irrigation and small when the soil is dry. The crop development stage runs from 10%
ground cover to effective full cover. Again, full cover in blueberry occurs about when the
fruit just begin to turn blue but may be prior to fruit ripening in later season cultivars. The
mid-season stage runs from full cover to the beginning of leaf yellowing, i.e., the start of
senescence. It is the longest stage during the growing season and is the period in which Kc
reaches its maximum value (Kc mid). The late-season stage runs from leaf yellowing to
complete leaf senescence (Kc end). The Kc values increase linearly from Kc ini to Kc mid and
decrease from Kc mid to Kc end; however, the slopes will vary depending on the length of each
stage. Crop transpiration and soil evaporation may be combined into a single coefficient, Kc,
(single crop coefficient approach) or separated into two coefficients: a basal crop coefficient
(Kcb), which represents primarily the transpiration component of ET, and a soil evaporation
component (Ke) (dual crop coefficient approach). In this later case, Kc is replaced by Kcb + Ke.
The Kc values listed for berries (bushes) in FAO-56 are 0.30 (Kc ini), 1.05 (Kc mid), and 0.50 (Kc
end); the Kcb values are 0.20 (Kcb ini), 1.00 (Kcb mid), and 0.40 (Kcb end). Blueberry ET in this case is
calculated at each stage of development by multiplying Kc or Kcb+Ke by ETo. See Allen et al.
(1998) for procedures on calculating Ke.
To adjust for smaller plant size in new plantings, Fereres et al. (1982) developed a correction
factor, Fc, by correlating crop ET to canopy development using data from young almond
trees. The relationship was modified by Holzapfel et al. (2004) to estimate ET for young
blueberries using the following equation:
Fc K 1Sh K 2 (2)
and
As
Sh (3)
HL
Sh is percent shade (10 ≤ Sh ≤ 70), K1 and K2 are constants of the shadow factor adjusted for
irrigation method (equal to 0.0118 and 0.25, respectively, for drip and 0.0127 and 0.1125,
respectively, for microsprays), As is the area of the soil surface shaded by the crop canopy at
1200 h (m2), H is the distance between rows (m), and L is the distance between plants within
the row (m). The correction factor, Fc, is a function of cultural practices, the type of irrigation
system used, planting density, and climatic conditions of the area. Once a planting has 70%
cover or larger, it reaches an adult condition where crop ET is no longer a function of plant
size (Bryla & Strik, 2007). However, because blueberry is a relatively short crop (<2.0 m tall
and <1.5 m wide) with a fairly wide rows (3.0-3.6 m apart), Fc can also be used to adjust for
lack of canopy cover between rows in mature plantings.
Normally, irrigation should be scheduled to replace any water lost by crop ET. Keep in
mind, however, that these are ET estimates for mature, healthy, well-irrigated blueberry
plants. Adjustments to these values are needed when plants are young or stressed (e.g.,
nutrient deficient). Under these circumstances, irrigators should reduce the amount of
irrigation water applied but pay close attention to soil moisture conditions to avoid under-
or over-irrigating their crop. There are numerous devices available for monitoring soil
moisture, although some are more accurate and reliable than others. Many of these
monitoring devices need to be calibrated to a particular site so that gathered data can be
related to actual soil moisture conditions. Soil moisture monitors should be installed within
the root zone (usually 0.15-0.30 m deep) of a representative plant and should not be located
directly beneath an irrigation emitter.
In northwest Oregon, USA, average irrigation requirements throughout the growing season
are estimated to range from 4-16 mm of water per day with sprinklers and 1-4 mm of water
per day by drip (Table 1). The highest irrigation requirements typically occur in July,
although actual peak irrigation demands will vary throughout the summer depending on
weather and stage of fruit development. A well-maintained drip system generally requires
only about 25% of the water needed with sprinklers due to the higher efficiency associated
with drip irrigation. It should be noted, however, that the actual crop water use by sprinkler
and drip-irrigated blueberries is theoretically identical. Irrigation requirements will also
vary of course with location but are easily adjusted when calculating crop ET.
0.1
0.2
Soil depth (m)
0.3
Duke
0.4 Bluecrop
Elliott
0.5
0.6
0 10 20 30 40 50 60
-3
Root length density (cm roots cm soil)
Fig. 8. Root length density of mature ‘Duke’, ‘Bluecrop’, and ‘Elliott’ blueberry plants. Roots
were collected at 0.1-m depth increments. Adapted from Bryla & Strik (2007).
Frequent water applications are especially important when using drip, which tends to restrict
soil wetting and thus produces a smaller root system. When done properly, frequent
irrigations are beneficial and often increase growth and yield in many horticultural crops. For
example, frequent irrigation by drip in peach increased fruit size and yield compared to other
irrigation methods by maintaining higher tree water status between irrigations (Bryla et al.,
2005). It may also be important to apply water to both sides of the plant. Abbott & Gough
180 Evapotranspiration – From Measurements to Agricultural and Environmental Applications
(1986) found that when water was applied to only one side of the blueberry bush, growth and
production was severely restricted on the other side. Irrigators, however, particularly those
using drip, should be careful to avoid the temptation to over-irrigate. Over-irrigation depletes
the root zone of much-needed oxygen, thus reducing both root growth and nutrient uptake
and leading to a host of potential root disease problems. Davies & Flore (1986) observed, in
both highbush and rabbiteye blueberry, that stomatal conductance declined within 5 days and
photosynthesis declined within 9 days when plants were grown in flooded soil, and 18 days or
more were required for each process to recover to pre-flood conditions.
High-frequency irrigation may be especially beneficial and perhaps even required when
organic matter is incorporated into the planting bed. Organic matter often reduces water
holding capacity of the soil and can lead to problems with hydrophobicity. Soil
hydrophobicity is the lack of affinity of soil to water and is thought to be caused primarily
by a coating of long-chained hydrophobic organic molecules, such as those released from
decaying organic matter, on individual soil particles (DeBano, 2000). Hydrophobic soils
often become very difficult to rewet once they dry out. White (2006) found that even with
drip irrigation, sawdust incorporated into raised planting beds made it difficult to retain
adequate moisture in the upper portions of the soil where many of the blueberry roots were
located. To compensate, much longer and more frequent irrigation was required in beds
with incorporated sawdust than without. Personal observations indicate that, even after 50
mm of rainfall, dry beds with incorporated sawdust tend to remain dry and do not become
fully saturated until the following season. Krewer et al. (2002) found that water infiltrated
much more readily through sandy soil amended with pine post and pole peelings (2-45 mm
long pieces of bark and wood) than soil amended with milled pine bark, although plant
growth was slightly less in the soil with the larger-sized product.
fall below reference values, irrigation is increased. Typically, irrigation is increased by 5-10%
above the previous week’s rate when mean weekly stem water potentials are lower than
reference values, and decreased by 5-10% when actual and reference values are equal for two
consecutive weeks. To ensure plants are not over or under irrigated, soil water content should
also be monitored at least monthly. Soil water content measurements may also provide
information to help determine initial irrigation rates based on root-zone changes in the soil
water profile during the first few weeks of the growing season.
Fruit were first harvested beginning the third year after planting in ‘Elliott’ and fourth year
after planting in ‘Duke’ (Fig. 9). During the first 4 years of production, yields were similar in
‘Duke’ whether plants were irrigated by sprinklers or microsprays but lower when irrigated
by drip due again to higher incidence of root rot. Root rot does not usually result in plant
death in blueberry, although it will reduce growth and production even when plants are
treated with fungicide, as we did each year beginning the third year after planting. In
‘Elliott’, yields were slightly higher with drip than with sprinklers and microsprays during
the first year of production and still higher than sprinklers the second year. However, by the
third year, yield was similar between drip and sprinklers but higher when plants were
irrigated by microsprays. This latter result agrees with that of Holzapfel et al. (2004), who
compared drip and microsprays in ‘Bluecrop’. They positioned the microsprays under the
canopy on each side of the plants whereas we hung the microsprays above the canopy
between every other plant. Hanging the microsprays reduced the number of microsprays
needed and reduced problems with plants interfering with the microsprays.
16 Duke 28 Elliott
14 24
Sprinkler
12 Microspray 20
Drip
Yield (t·ha-1)
Yield (t·ha-1)
10 16
8 12
6 8
4 4
2 0
3 4 5 6 7 3 4 5 6 7
Years after planting Years after planting
Fig. 9. Marketable fruit yield of ’Duke’ and ‘Elliott’ blueberry irrigated by sprinklers,
microsprays, or drip. Each symbol represents the mean of five plots with six plants each,
and error bars represent one standard error.
After 2 years, plants irrigated by buried drip were larger and healthier than those irrigated
by surface drip, particularly when the laterals were placed near the base of the plants. Signs
of water stress, including marginal leaf necrosis, were evident in plants irrigated by surface
drip, even after 3 years. In comparison, there was no evidence of water stress in plants
irrigated by subsurface drip. The use of subsurface drip maintained lower soil water content
near the plants, which reduced root rot and encouraged more lateral root development.
Subsurface drip also eliminated water runoff and soil erosion observed with both the
surface drip configurations.
7. References
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Davies, F.S. & Johnson, C.R. (1982) Water stress, growth, and critical water potentials of
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