Carrot
seeds vigor on plant performance and crop yield
Vigor
de sementes de cenoura sobre o desempenho das plantas e rendimento da cultura
Vigor de semillas de zanahoria
sobre el desempeño de las plantas y rendimiento del cultivo
Gisela Hélnia Nunes Chipenete1,
Denise Cunha Fernandes dos Santos Dias2,
Daniel Teixeira Pinheiro3*,
Laércio Junio da Silva2, Dalcionei Pazzin3,
Aparecida Leonir da Silva3
1Master in Crop Science at Agronomy
Department, Universidade Federal de Viçosa. Av. PH Rolfs,
s/n, Viçosa, Minas Gerais, Brazil. ghnchipenete@gmail.com. 2Professor at Agronomy Department, Universidade
Federal de Viçosa. Av. PH Rolfs, s/n, Viçosa, Minas Gerais, Brazil.
dcdias@ufv.br. ; laercio.silva@ufv.br. 3PhD in Crop Science at Agronomy
Department, Universidade Federal de Viçosa. Av. PH Rolfs,
s/n, Viçosa, Minas Gerais, Brazil. pinheiroagroufv@gmail.com*; dalcionei@hotmail.com ; aparecidaleonir@gmail.com
Recebido:
17/07/2020; Aprovado: 26/12/2020
Abstract: Rapid emergence
and uniform seedling growth are essential attributes in the production of
vegetables such as carrots, whose sowing is direct in the field. The experiment
was conducted to evaluate the effect of carrot seed vigor on seedling
emergence, plant development, and yield. Four seed lots of carrot, cv. Brasília
were characterized for their physiological potential by germination and vigor
tests. A field experiment was conducted, where the seeds of each lot were sown
in in the field to evaluate seedling emergence at 10 and 14 days, the length of
the shoot and root at 30, 45 and 60 days after sowing, the crop growth rate,
commercial, non-commercial and commercial roots yield.
Seed vigor significantly affected the seedling emergence and development of
carrot plants in the field. The less vigorous lot showed lower final emergence
than the most vigorous lots and these negative vigor effects extended to the
most advanced stages of plant development. Carrot seed vigor affects seedling
emergence and plant growth in the field. Vigorous seeds causes
greater emergence, plant height and plant dry matter during the vegetative
phase. The use of less vigorous seeds causes yield losses of up to 27%.
Key
words: Daucus carota L.; Germination;
Productivity; Quality.
Palavras-chave: Daucus carota L.; Germinação;
Produtividade; Qualidade.
Palabras Clave: Daucus carota L.; Germinación; Productividad; Calidad.
INTRODUCTION
Successful crop
production depends on adequate seedling establishment in the field, which is
directly related to seed germination and vigor. Seed vigor comprises the sum of
seed properties that determine the potential for rapid and uniform seedling
emergence under environmental conditions, determining the development, yield,
and quality of the harvested product (FINCH-SAVAGE; BASSEL, 2016). Under field
conditions, vigorous seeds tend to produce seedlings with higher growth rates,
uniform emergence, and greater competition and survival. However, low-quality
seeds tend to lead to irregular stands, with emergence failures that compromise
the quality and yield (NASCIMENTO et al., 2011; LING et al., 2015).
The direct relation
between vigorous seeds and satisfactory yield has been reported in crops such
as wheat (ABATI et al., 2018), soybean (CAVERZAN et al., 2018) and others. In
vegetables, these characteristics are also related (RODO et al., 2003;
NASCIMENTO et al., 2011). In squash seeds at different maturity stages, which was
observed that seedling vigor is an effective parameter for composing quality
control in this species (SILVA et al., 2017). In cucumber, the seed vigor index
is directly related to yield (SHARMA et al., 2018). However, in some cases, the
effect of seed vigor on plant growth and final yield when there is no reduction
in field plant population can be controversial (MONDO et al., 2012).
Carrot (Daucus carota L.) is a vegetable of
great importance, with a global production that exceeds 40 million tons per
year (SHARMA, 2018). In Brazil, carrot production is around 700,000 tons per
year, being a very important activity for the family farm (EMBRAPA, 2020). In
this way, it is an extremely important vegetable, since has a good source of
nutritional substances such as vitamins, minerals, and dietary fibers (QUE et
al., 2019). Moreover, recent studies have shown other benefits of carrots, such
as pectin production (JAFARI et al., 2017), carotenoids production (ELLISON et
al., 2018), antioxidant properties (DONG et al., 2021), and others. Carrot
seeds are small, with few reserves, and are sown directly in the field.
According to Nascimento et al. (2011), the vigor in vegetable seeds is
important especially for species with these characteristics (small and few
reserves), once they are very sensitive to adverse environmental conditions,
affecting the uniform seedling establishment and compromising yield and final
product quality.
There is not much information about the
relation between seed vigor and carrot yield. Therefore, the experiment was
conducted to evaluate the effect of carrot seed vigor on seedling emergence,
plant development, and final crop yield.
MATERIAL AND METHODS
The research was conducted in the Agronomy Department at the Universidade Federal de Viçosa, Brazil.
Four commercial seed lots of carrot, cultivar “Brasília”, were used. Initially,
the seeds were evaluated by the following tests to characterize their initial
quality:
Moisture content (MC)
It was determined
by the oven method at 105 ± 3 °C for 24 hours (BRASIL, 2009). Two replications
of 5 g of seeds were used and the results were expressed as a percentage (%).
Germination (G)
The seeds were arranged
on two sheets of paper towel, moistened with distilled water (2.5 times the
weight of dry paper), in “gerbox” boxes. The boxes
were kept in a germinator at 20 °C and the evaluation was performed at 14 days
after sowing (BRASIL, 2009). Four replicates of 50 seeds from each lot were
used and the results were expressed as a percentage (%) of normal seedlings.
It was performed together with the germination test,
with the evaluation of normal seedlings performed seven days after sowing (BRASIL,
2009).
Seedling emergence (SE) and seedling emergence speed
index (ESI)
It was carried out in a greenhouse with four
replications of 50 seeds sowed in polystyrene trays containing moistened sand
up to 2/3 of the retention capacity. Daily evaluations were made of the number
of emerged seedlings with a size equal to or greater than 1.0 cm until the counts stabilization. The results were expressed as a
percentage (%) of normal seedlings. For the emergence speed index (ESI), the Equation
1 proposed by Maguire (1962) was used:
(1)
Where: ESI = Emergence speed
index (seedlings.day-1); E1, E2, En = Number of normal seedlings computed in the
first count, in the second count and last count; N1, N2, Nn = Number of days after sowing from the first
count to the second count and the last count.
Controlled
Deterioration (CD)
Initially, the
moisture content of the seeds was adjusted to 24% by the moist atmosphere
method at 20 oC. The moisture content of
the seeds was monitored by successive weighing at one-hour intervals until the
desired values were obtained. The seeds were placed in aluminized paper bags,
which were hermetically sealed and kept in a refrigerator at 10 ºC for 24 h.
After this period, they were kept in a water bath at 45 oC for
24 h (KRZYZANOWSKI; MARCOS-FILHO, 2020). Then the seeds were placed to
germinate as described for the germination test (BRASIL, 2009). Four replicates
of 50 seeds from each lot were used and the results were expressed as the
percentage of normal seedlings obtained seven days after sowing.
Germination
at sub (G15o) and supra optimum (G30o) temperatures
Four replications
of 50 seeds were placed to germinate according to the germination test, but at
temperatures of 30 °C (supra-optimum) and 15 °C (sub-optimal) in a BOD
incubator. The results were expressed as a percentage (%) of normal seedlings
obtained at seven days after sowing for supra-optimal temperature and at 10
days for sub-optimal temperature.
After the initial
characterization of the lots, a field experiment was conducted. Two rows of 20
m long and 1 m wide each were prepared, with four blocks of 5 m each. Four
replicates of 100 seeds from each lot were sown in longitudinal grooves 1 m
long and 2 cm deep, 0.20 m apart. The lateral grooves were considered as
borders and the useful area only the two central grooves (MATOS et al., 2011).
The soil chemical analysis was performed (Table 1). Before sowing, fertilization
with 40, 180, and 60 kg ha-1 of N, P2O5, and K2O
respectively was performed, defined on the basis of
soil analysis results and fertilizer recommendations for carrot cultivation (AQUINO
et al., 2016).
Table
1.
Chemcical analysis of the soil.
pH |
P |
K |
Ca2+ |
Mg2+ |
Al3+ |
|||||
H2O |
mg.dm3-1 |
cmol.dm3-1 |
||||||||
6.3 |
58.3 |
220 |
2.7 |
1.0 |
0 |
|||||
H + AL |
SB |
CTC (t) |
CTC (T) |
V |
m |
|||||
cmol.dm3-1 |
% |
|||||||||
3.0 |
4.2 |
4.2 |
7.2 |
59 |
0 |
|
||||
pH in water, KCl and CaCl - Relation 1:2,5. P
- K – Mehlich exctrator 1. Ca
- Mg - Al - Extractor: KCl - 1 mol/L. H + Al –
Calcium acetate extractor 0.5 mol/L - pH 7,0. SB = Sum of exchangeable bases CTC
(t) - Effective cation exchange capacity. CTC (T) - Cation exchange capacity. pH
7,0. V = Base saturation index. m = Aluminum saturation index.
In the first two
weeks, two irrigations were performed per day, lasting two hours each, keeping
the surface of the bed always moist. From then on, only daily irrigation
lasting 2 h was performed. The crop treatments were performed whenever
necessary. Topdressing fertilization was performed at 28 and 45 days after
sowing, using 60 kg ha-1 of N and K, respectively. At 28 days after
sowing, thinning was done leaving a spacing of about 5 cm between plants. One
of the rows was used to evaluate seedling emergence in the field and the other
to evaluate vegetative development and final crop production. In this, the
harvest was performed at 90 days after sowing.
The maximum, average and
minimum temperatures and relative humidity recorded during the experimental
period, as well as monthly cumulative rainfall are shown in Figure 1.
Figure
1. Minimum
(Min.), average (Aver.), and maximum (Max.) temperatures (oC);
relative air humidity (%) (A) and cumulative rainfall (B) during carrot development
in the field
Field seedling emergence was represented by percentage
of normal seedlings emerged (at least 1.0 cm height) at 10 and 14 days after
sowing.
Shoot
and root growth rate
With shoot and root
dry matter values, shoot and root growth rate (GR) (Equation 2) were
determined, according to Kolchinski et al.
(2006).
(2)
Where: DM1: Value
of dry mass obtained on the first day of the period to be considered (T1);
DM2: Value of dry mass obtained on the last day of the period to be
considered (T2); GR values are given in g.plant-1.day-1.
Evaluation of crop production and yield
Harvesting was performed by collecting plants from all
useful areas (25 m2 per block). The roots were separated from the
shoots and weighed to determine the total roots yield in kg. Then they were
classified into: commercial (length greater than 12
cm) and non-commercial (length less than 12 cm and / or roots with defects such
as purple / green shoulder, bifurcation and crack) (CEAGESP, 2015).
Statistical
analysis and experimental design
The seed quality
tests were conducted in a completely randomized design with four replications.
The data were submitted to analysis of variance and the means obtained for each
lot were compared by Tukey test at 5% probability.
RESULTS AND DISCUSSION
The
seed moisture content was similar for all analyzed lots, being around 7%. This
value is adequate for the packaging of vegetable seeds stored in hermetically
sealed aluminum containers. The germination of the lot 3 was inferior to the
others, which did not differ significantly from each other. Similar results
were obtained in the seedling emergence, emergence speed index, controlled
deterioration, and germination at supra-optimal temperature (Table 2).
Table
2.
Seed moisture content (MC), germination (G), first germination count (FGC),
seedling emergence (SE), emergence speed index (ESI), controlled
deterioration (CD), temperature germination sub (G15 °) and supra-optimal
(G30 º) obtained for the four seed lots of carrot. |
||||||||
Lots |
MC |
G |
FGC |
SE |
ESI |
CD |
G15º |
G30º |
(%) |
|
(%) |
||||||
1 |
7.2 |
83.5 a |
77.0 a |
69 a |
18 a |
51 a |
77.0 a |
76.5 a |
2 |
7.7 |
81.5 a |
72.5 ab |
67 a |
20 a |
51 a |
79.5 ab |
71.0 a |
3 |
7.2 |
68.7 b |
62.5 b |
47 b |
12 b |
39 b |
64.0 b |
53.0 b |
4 |
7.3 |
82.5 a |
74.0 ab |
68 a |
20 a |
53 a |
75.5 ab |
72.0 a |
CV (%) |
- |
6.24 |
8.01 |
9.97 |
13.34 |
10.91 |
8.64 |
7.23 |
Means followed by
the same letter in the column do not differ from each other by the Tukey test
at 5% probability. CV: Coefficient of variation
In
general, all of these tests are important for
assessing seed performance under adverse conditions, defining seed vigor
(FINCH-SAVAGE; BASSEL, 2016). In this context, the first germination count and
sub-optimal temperature germination tests allowed to classify the seed lots
into three vigor levels, being lot 1 as the most vigorous, lot 3 the less
vigorous, and lots 2 and 4 as intermediate. In all tests performed, we found
worse performance for seed lot 3 compared to the others (Table 2).
Through
the correlation analysis between the physiological quality evaluation and the
emergence of the field, it is observed that the first germination count and
sub-optimal germination temperature were significantly correlated with the
seedling emergence at 10 and 14 days (Table 3).
Table
3.
Pearson correlation coefficients obtained between germination (G), first
germination count (FGC), seedling emergence (SE), controlled deterioration
(CD), emergence speed index (ESI), germination at optimum sub (G15º) and
supra (G30º) temperature and emergence results at 10 (EM10) and 14 (EM14)
days for four carrot lots. |
|||||||||
|
G |
FGC |
SE |
CD |
ESI |
G15 ° |
G30 ° |
EM10 |
EM14 |
G |
|
0.629** |
0.827** |
0.564* |
0.729** |
0.529* |
0.724** |
0.350 |
0.235 |
FGC |
|
|
0.602* |
0.712** |
0.577* |
0.777** |
0.628* |
0.644* |
0.748** |
SE |
|
|
|
0.509* |
0.895** |
0.689** |
0.776** |
0.457 |
0.284 |
CD |
|
|
|
|
0.528* |
0.569* |
0.659** |
0.250 |
0.578* |
ESI |
|
|
|
|
|
0.523* |
0.702** |
0.270 |
0.276 |
G15 ° |
|
|
|
|
|
|
0.598* |
0.637* |
0.606* |
G30 ° |
|
|
|
|
|
|
|
0.472 |
0.500* |
EM10 |
|
|
|
|
|
|
|
|
0.649* |
EM14 |
|
|
|
|
|
|
|
|
|
*;**: Significant
correlation at 5 and 1% probability, respectively. |
It was also
observed that there was a significant correlation among the data obtained from
controlled deterioration, germination at supra-optimal temperature, and
emergence at 14 days (Table 3). These results indicate an association between
laboratory vigor test results and the emergence of carrot seedlings in the
field. Thus, the first germination count, controlled deterioration, and
germination tests at the sub and supra-optimal temperatures provided an
estimate of field seed performance. Among these tests, the first germination
count test is recommended to evaluate the physiological quality of carrot seeds
due to its simplicity of conduction and efficiency in ranking lots.
The germination at
sub or supra-optimal temperatures has been successfully used to classify seed
lots of carrot (SINGH et al., 2014),
cucumber (BALABUSTA et al., 2016), and melon
(PINHEIRO et al., 2017). As observed, the
germination at sub-optimal temperature was directly related to the carrot
emergence. It’s also related that temperatures above
30 °C caused decreases in seed germination of both “Brasília” and “Alvorada” cultivars. Dias et al. (2015) observed that the
germination of cultivar “Brasília” was reduced by the temperature of
35 °C. In general, these effects can be related to many cellular
alterations such as hormonal imbalance, genetic alterations, and others, the
reduce seed germination and vigor (WANG et al., 2018).
Lots 1 and 3
presented higher and lower emergence in the field at 10 (Figure 2A) and 14 days
(Figure 2B) after sowing, respectively.
Figure 2. Field seedling emergence (%) of four carrot seed lots at 10 (A) and 14 (B) days after sowing
Means followed by the same letters do not differ among lots within each period by the Tukey test at 5% probability. CV: Coefficient of Variation
The poor
performance of lot 3 (less vigor) was also observed in laboratory tests for
physiological potential evaluation (Table 2). It's probably related to the
lower amount of energetic reserves in these seeds,
which is important for embryonic nutrition and seedling development (NONOGAKI
et al., 2020).
The field seedling
emergence was less than 60% for all analyzed lots (Figure 2). Singh et al. (2014) evaluated the emergence of
eight commercial carrot lots and observed field emergence of between 33.2 to
56.5%, similar results to those observed. Marchi and
Cicero (2017) evaluated seven carrot lots and observed that seedling emergence
was directly related to vigor, reinforcing the importance of this test.
It was observed
that there was no significant difference between plots regarding plant height
at 30 days after sowing and root length at 30, 45, and 60 days. However, at 45
and 60 days, there was a lower height of plants from lot 3 compared to the
other lots (Figure 3A).
Figure
3. Plant
height (A), root length (B), shoot (C), and root (D) dry matter at 30, 45, and
60 days after sowing of four carrot seed lots.
Means followed by the same
letters do not differ among lots within each period by the Tukey test at 5%
probability. CV: Coefficient of Variation
Lot 3 showed lower
physiological potential through vigor tests (Table 2). Therefore, it is
confirmed that the less vigorous seeds originated in smaller plants (Figure
3A). The shoot and root dry matter presented similar results at 45 and 60 days
(Figure 3 C and 4 C).
The effects of
vigor on plant shoot height were observed later, at 45 and 60 days after sowing
(Figure 3 A). This fact is understandable due in longer cycle crops, the effect
of genotype x environment interaction assumes greater relevance and may nullify
the effects of seed vigor (TEKRONY; EGLI, 1991; NASCIMENTO et al., 2011). Moreover,
vigorous seeds allowed plants with higher initial growth, but these effects did
not persist until later evaluation periods (MONDO et al., 2012).
According to
Finch-Savage and Bassel (2016), temperature is one of
the main factors that affect the emergence and plant growth. These authors also
mention that solar radiation with water content can cause the soil surface to
heat to the point of affecting the microbial activity and reducing seed vigor.
In this context, no drastic changes in temperatures were observed, with maximum
values of approximately 30 ºC and average around 25 ºC (Figure 1A).
Precipitation data during the experimental period are shown in Figure 1B, and
it should be noted that the experiment was conducted under irrigation,
maintaining the availability of water in the soil at an appropriate level for
plant development until harvest. Thus, it was avoided that environmental factors
could negatively affect plant development so that the observed results could be
due to seed vigor.
Considering the
field development, lot 3 presented the lowest shoot and root growth rate, with
differences of up to 50% when compared to the highest vigor (lots 1 and 4)
(Figure 4).
Figure
4. Shoot
(A) and root (B) growth rate of plants at 30, 45, and 60 days after sowing
(DAS) of four carrot seed lots
Means followed by the same
letters do not differ among lots within each period by the Tukey test at 5%
probability. CV: Coefficient of Variation
Considering
the shoot growth (Figure 4A), lot 3 was inferior to the others in all seasons.
For the root growth (Figure 4B), this lot had less performance than the others
only at 60 days. The vigor effects on plant growth have been observed in crops
such as pea (STOLÁRIK et al., 2015), and wheat (ZAHORANOVÁ et al., 2016),
wherein general, plants originating from lower vigor seeds had lower growth
rate. The results observed for dry matter and growth rate are expected since
more deteriorated seeds will have greater degradation of energy reserves such
as lipids, proteins, and soluble sugars that are directed to the embryonic axis
for seedling formation (OLIVEIRA et al., 2017).
As
observed, seed vigor affected carrot field performance. For short-cycle
vegetables, such as carrots, the effects of seed vigor can directly affect
plant growth and dry matter accumulation in the field. TeKrony
and Egli (1991) attest that seed vigor has the most
significant effect on the yield of crops whose commercial product is harvest in
the vegetative phase or in the early reproductive phase. These authors point
out that the effects of seed vigor at the final stand may be especially critical
for crops that require adequate spatial distribution of plants to maximize yield, and delaying or decreasing seedling emergence may
reduce yield at harvest.
Considering the
four analyzed lots, no significant differences were observed in commercial/non-commercial
root yield, and in the total carrot root yield (Table 4).
Table 4. Commercial, non-commercial and total carrot
root yield and average productivity at 90 days after sowing of four seed lots. |
||||
Lots |
Roots yield (kg) |
Yield |
||
Commercial |
Non- |
Total |
Productivity (t ha-1) |
|
1 |
2.72 a |
0.866 a |
3.59 a |
68.0 a |
2 |
2.94 a |
0.5999 a |
3.54 a |
73.6 a |
3 |
2.15 a |
0.835 a |
2.99 a |
53.9 a |
4 |
2.68 a |
0.780 a |
3.46 a |
67.0 a |
CV (%) |
15.92 |
19.59 |
14.34 |
15.92 |
Means followed by the same letter in the column do
not differ by the Tukey test at 5% probability. CV: Coefficient of Variation |
Moreover, the yield
of 53.9 t ha-1 obtained for lot 3 was 27% lower than the highest
yield obtained (73.6 t ha-1), which in economic terms is not
negligible. In current studies, the direct relation between seed vigor and
field yield is confirmed in different crops. In wheat, the seed vigor was
associated with the higher seedling establishment, growth, and development of
plants at the initial phenological stages (ABATI et al., 2018). These authors
cite the possibly contributed to the increased light use efficiency, and
greater interception of the photosynthetically active radiation by the canopy,
influencing the grain yield. In soybean, plants originated from the high-vigor
seeds presented more efficiency on nitrogen fixation (CAVERZAN et al., 2018).
Therefore, these and other effects may have influenced the results observed in
the carrot.
In the present study,
it was observed that the use of low vigor seed can negatively affect the final
yield of carrot roots, causing losses of up to 27% in the average yield in
relation to the use of higher vigor seeds.
According to
Nascimento et al. (2011), the effect of seed vigor on seedling emergence and
initial stand are relevant and may interfere with plant development and
uniformity of the harvested product, making it difficult to standardize. These
authors consider that seed vigor is important for crops whose commercial
product is the shoot of the plant. In this context are leafy of vegetables, or
certain organs obtained from the plant that was harvested, usually an
underground structure like carrot, beets, onions, radishes, and turnips.
It
is important to emphasize that failures in the final stand are crucial for the
production and the final quality of the harvested product. Proper spacing
between carrot plants in the field is critical for proper root growth, as stand
failures can favor thicker roots, which are not well accepted in many consumer
markets.
CONCLUSIONS
Carrot seed vigor
affects seedling emergence and plant growth in the field. Vigorous seeds cause higher
emergence, plant height, and dry matter during the vegetative phase. The use of
less vigorous seeds causes yield losses of up to 27%.
ACKNOWLEDGMENTS
The authors are grateful to Claudio Chipenete
(for assisting the statistical analysis) and the Universidade Federal de Viçosa (UFV). This study
was funded in part by the
Coordenação de Aperfeiçoamento de Pessoal
de Nível Superior - Brasil (CAPES) – (Funding Code: 001), Conselho
Nacional de Desenvolvimento Científico e Tecnológico (CNPq), and Fundação de
Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG).
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