African Journal of
Agricultural Research

  • Abbreviation: Afr. J. Agric. Res.
  • Language: English
  • ISSN: 1991-637X
  • DOI: 10.5897/AJAR
  • Start Year: 2006
  • Published Articles: 6589

Full Length Research Paper

Physiological and agronomic characteristics of cassava genotypes

Douglas Goncalves Guimaraes
  • Douglas Goncalves Guimaraes
  • Graduate Program in Agronomy, State University of Southwest Bahia, Vitória da Conquista, Bahia, Brazil.
  • Google Scholar
Caio Jander Nogueira Prates
  • Caio Jander Nogueira Prates
  • Graduate Program in Agronomy, State University of Southwest Bahia, Vitória da Conquista, Bahia, Brazil.
  • Google Scholar
Anselmo Eloy Silveira Viana
  • Anselmo Eloy Silveira Viana
  • Department of Plant and Animal Science, State University of Southwest Bahia, Vitória da Conquista, Bahia, Brazil.
  • Google Scholar
Adriana Dias Cardoso
  • Adriana Dias Cardoso
  • CAPES/FAPESP, State University of Southwest Bahia, Vitória da Conquista, Bahia, Brazil.
  • Google Scholar
Vanderlei da Silva Santos
  • Vanderlei da Silva Santos
  • Embrapa Cassava and Fruticulture, Cruz das Almas, Bahia, Brazil.
  • Google Scholar
Sylvana Naomi Matsumoto
  • Sylvana Naomi Matsumoto
  • Department of Plant and Animal Science, State University of Southwest Bahia, Vitória da Conquista, Bahia, Brazil.
  • Google Scholar
Quelmo Silva de Novaes
  • Quelmo Silva de Novaes
  • Department of Plant and Animal Science, State University of Southwest Bahia, Vitória da Conquista, Bahia, Brazil.
  • Google Scholar
Nelson dos Santos Cardoso Junior2
  • Nelson dos Santos Cardoso Junior2
  • Department of Plant and Animal Science, State University of Southwest Bahia, Vitória da Conquista, Bahia, Brazil.
  • Google Scholar
Sandro Correia Lopes
  • Sandro Correia Lopes
  • Department of Plant and Animal Science, State University of Southwest Bahia, Vitória da Conquista, Bahia, Brazil.
  • Google Scholar

  •  Received: 21 October 2016
  •  Accepted: 19 January 2017
  •  Published: 02 February 2017


This experiment was conducted with the objective of evaluating physiological and agronomic characteristics of cassava genotypes in the municipality of Cândido Sales, State of Bahia, Brazil, between October 2010 and August 2012. Complete randomized block design was used, with three replications and 28 treatments formed by genotypes Amansa Burro, Aramaris, Bom Jardim, Bromadeira, Caipira, Caitité, Caravela, Kiriris, Lagoão, Lavra Velha, Malacacheta, Mulatinha, Parazinha, Peru, Poti Branca, Salangor, Sergipe, Sergipe, Simbé, Tapioqueira, Tussuma, Verdinha, 2006-4, 2006-5, 2006-8, 2006-10 and 2006-12, coming from UESB, EMBRAPA and farmers in the region. Sergipe genotype is present in two treatments, one planted with cuttings collected from local farmers only called Sergipe, and another called Sergipe MR planted with cuttings originated from the rapid multiplication method. The crop spacing used was 1.0 x 0.6 m and each plot composed by 60 plants, being 26 plants considered useful. The evaluations were performed at the end of the first crop cycle, in July 2011, and the harvest in August 2012, twenty-two months after planting. The higher total leaf area and the high photosynthetically active radiation absorbed by the plants canopy at the end of the first crop cycle were correlated to an increase of productivity of shoot and dry weight of root. There was no change in leaf water potential among the genotypes. The genotypes Caipira, Poti Branca, Verdinha and Sergipe from cuttings obtained by the rapid multiplication method showed high productivity for tuberous roots associated to a higher dry matter values. A greater starch yield was observed in genotypes 2006-5, Verdinha, Malacacheta, Poti Branca, Caipira, 2006-10, Sergipe MR, Parazinha and Mulatinha, thus, they might be future alternatives for regional cultivation for industrial production.

Key words: Manihot esculenta Crantz, water potential, leaf area, varieties, tuberous root, starch.


Cassava (Manihot esculenta Crantz) is a shrubby plant in Euphorbiaceae family that grows continuously having two alternating periods, one for growing and another for storing  carbohydrates  in  its  tuberous  roots,  and  these periods are followed by an interval of dormancy (Alves, 2002). Brazil is considered the possible center of origin for this species (Allem, 1994), which is one of the most important crop in the tropics and the basic  food  for  over 800 million people (Nassar et al., 2009), being cultivated on 16 million hectares worldwide (El-Sharkawy et al., 2008).
Cassava is mostly cultivated on tropical countries situated in equatorial region, between 30º North and 30º South to equator with an altitude variation from sea level to 2.000 m, and annual rainfall between 500 mm up to 2,000 mm, which shows cassava capacity to adapt to a great number of environments and ecosystems (El-Sharkawy, 2012).
In 2015, Brazil produced 23.06 million tons of roots (IBGE, 2016). According to FAO (2016), Brazil is the fourth biggest producer of cassava; behind of Nigeria, Thailand, and Indonesia. The Bahia State has the third biggest yield of cassava in Brazil, in 2015 the state had produced 2.09 million tons of roots; however, the yield has been dropped by low average of productivity, only 11.05 t ha-1. In the same year, the municipality of Cândido Sales was the biggest producer of cassava in the state of Bahia (IBGE, 2016).
The city of Cândido Sales is situated in the Southwest Bahia, and presents a semi-arid climate with hydric restriction in most part of the year, and cassava is one of the few alternatives for farmers. Being tolerant to low rainfall, cassava is a crop recognized by its social importance in areas characterized by erratic rainfall and an limited water resources systematization (El-Sharkawy and Tafur, 2010).
According to Lopes et al. (2010), among the causes that contribute to the low yield of cassava in Brazil, there is a lack of varieties adapted to different conditions, inadequate cultural practices or lack of it, and the use of low quality planting material, as well as growing in regions with annual precipitation lower than 1000-1500 mm, values considered adequate to the crop (Oliveira et al., 2006).
Selection of cassava varieties is important in many parts of the world. Acquah et al. (2011) identified that there is an immediate need for new cassava varieties in Africa to replace varieties that are losing desirable traits. In this context, Tumuhimbise et al. (2014), studying the effect of genotype and environment interaction on fresh root yield and cassava related traits in Uganda, observed a high degree of genetic variation among genotypes in three different environments. Demonstrating that cassava genotypes may have different behaviors in different environments, and may have a superior variety at each site.
The cassava is cultivated in all Brazilian regions with a diversity of varieties adapted to each of these different biomes giving to the species a large genetic diversity (Galera  and  Valle,  2007).  This  diversity  represents   a large base for breeding programs in tropics, concentrating genes for resistance to the major pests and diseases, also adaptation for different edaphoclimatic conditions (Fukuda et al. 1999).
According to Fukuda and Silva (2003), a way to improve the yield and the production system is the use of better varieties adapted to edaphoclimatic conditions for each region, due to the high genotype x environment interaction, a genotype rarely behave in a similar manner in different ecological regions.
In addition, according to Casaroli et al. (2007), the energy emitted by the sun, which affects the surface of the leaves, together with adequate supplies of water and nutrients, can be indicators of plant productivity. These factors are part of the physiological processes responsible for capturing solar energy and its subsequent biochemical transformation into organic compounds that result in food, fiber, cellulose and energy. Even for plants of one species, the rate of photosynthesis varies with genotypes (Pereira, 1987). Therefore, physiological studies among genotypes may indicate the most efficient in the conversion of photoassimilates to the production of tuberous roots and shoots of cassava plants.
However, many of created and selected varieties had not been used by farmers, and the most common cassava varieties used are still the same that have been planted in most regions during consecutive years (Fukuda et al., 1997), as it happens in the Southwest region of Bahia.
In this region, the variety Sergipe is the most cultivated among the cassava farmers for flour production and starch extraction, and the rusticity and the high productivity attributes justified the preference of producers in the region (Carvalho et al., 2009). However, in the last ten years, this variety has been suffering gradual drop in yield, and the introduction of new varieties may result in an improvement of living conditions for local farmers.
Given the above, this work was developed to evaluate physiological and agronomic characteristics of cassava genotypes, identifying the most promising genotypes for cultivation.


The experiment was conducted at the locality Bomba, coordinates 15º18’13’’ S and 41º17’32’’ W, municioality of Cândido Sales in southwest of Bahia state, Brazil. The city altitude in average is 627 m, and the semi-arid climate according to Köppen is classified as Aw type, tropical climate and dry season. The annual average temperature is 20.4ºC, and annual rainfall of 767.4 mm, being the rainy season between October  and  March  (SEI,  2013).  Figure  1 shows the rainfall data obtained during the trial period.
The soil in the experimental area was classified as Yellow Oxisol dystrophic clayey, which presented the following results for chemistry analysis in 0-20 cm depth: pH in water (1: 2.5): 4.5; P: 2.0 mg dm-3 (Mehlich-1); K +: 0.11 cmolc dm-3 (Mehlich-1); Ca2 +: 0.4 cmolc dm-3 (KCl extractor 1 mol L-1); Mg 2+: 0.4 cmolcdm-3 (KCl extractor 1 mol L-1); Al3+: 1.0 cmolc dm-3 (KCl extractor 1 mol L-1); H+: 5.4 cmolcdm-3 (SMP extractor solution, pH 7.5 at 7.6); Sum of Bases: 0.9 cmolc dm-3; CEC effective: 1.9 cmolc dm-3; CEC at pH 7.0: 7.3 cmolc dm-3; Base saturation: 12%; Aluminum saturation: 52%.
The area was tilled and plowed mechanically. The planting has occurred in October 2010 and it was done with cuttings 20 cm long and 2 to 3 cm in diameter, making an average of eight gems. The spacing between rows was 1.0 m and 0.60 m between plants, totaling 26 plants per plot, in 15.6 m².
Randomized block design with 28 treatments and three replications was utilized. The harvest was performed in August 2012, 22 months after planting.
Were evaluated 28 treatments, using 27 genotypes. The genotype Sergipe, the most cultivated in the region, was planted with cuttings collected with local farmers, called by Sergipe, and also planted with originated from the rapid multiplication method, called Sergipe MR, developed by the International Center of Tropical Agriculture (CIAT) in Colombia, and later adapted to Brazilian conditions (Santos et al., 2009).
Genotypes Amansa Burro, Aramaris, Caipira, Caravela, Kiriris, Lagoão, Mulatinha, Poti Branca, Tapioqueira and Verdinha were obtained from the Cassava Active Germplasm Bank in the National Research Center of Cassava and Fruticulture of EMBRAPA (Brazilian Agricultural Research Corporation), located in Cruz das Almas, Bahia, Brazil. In this sense, for developing this bank, these genotypes were collected from different regions of the country.
Genotypes Bom Jardim, Bromadeira, Caitite, Lavra Velha, Malacacheta, Parazinha, Peru, Salangor, Sergipana, Simbé and Tussuma were obtained from the Germplasm Collection of Cassava of  UESB  (Southwest  Bahia  State  University),  campus  of  Vitória  da Conquista, Bahia, Brazil. It was also utilized botanical seeds genotypes deriving from open pollination: 2006-4, 2006-5, 2006-8, 2006-10 and 2006-12.
At the end of the first growing season, in July 2011, nine months after planting, period characterized by mild temperatures and lower rainfall index, the foliar area was evaluated measuring all leaves of one plant in each spot, using Area Meter model LI-3100; the photosynthetically active radiation (PAR) absorbed by the canopy, between plants (RBP), and between rows (RBR), in the period from 11:00 to 12:30 h, between rows and between plants at 0.20 m by the soil level and full sun, was evaluated using ceptometer Decagon, model AccuPAR LP-80. The values were obtained from the equations: % of RBP = 100 – [(PAR between plants / PAR under full sun) x 100] and %RBR = 100 – [(PAR between rows / PAR under full sun) x 100]; The leaf water potential was determined by measuring the middle third leaves of two plants per plot, collected at 5:00 AM (predawn) and 12:00 PM (noon) using a pressure chamber (Model 1000, PMS) according to methodology proposed by Scholander et al. (1964).
At harvest, in August 2012, 22 months after planting, it was evaluated the shoot yield, the tuberous roots yield, the dry matter percentage in tuberous roots, by the hydrostatic balance method based on the equation: DM = 15.75 + 0.0564 R, being R the weight of 3 kg of roots in water (Grossmann and Freitas, 1950), and the percentage of starch in tuberous roots, calculated by subtracting from the dry matter content the constant 4.65 (Conceição, 1983).
The statistical analyzes were performed using SAEG program (System for Statistical Analysis and Genetic) version 9.1 (Ribeiro Júnior, 2001). Data were submitted to analysis of variance and average treatments grouped by the procedure proposed by Scott-Knott at 5% probability.
Data was analyzed for normality using the Lilliefors test and the variances homogeneity by Cochran's test. When necessary, data transformation was performed. The Pearson correlation was analyzed using the t-test, at 5% probability to assess the relation between dependent characteristics.


The agronomic characteristics evaluation of 22 months after planting (Table 1) showed that the genotypes Mulatinha and Poti Branca produced more shoot than the others, with yield of 20.29 t ha-1 and 16.52 t ha-1, respectively, being an alternative to animal feed or to increase production for planting cuttings in the region studied.
The shoot average yield obtained in this study was 9.80 t ha-1, relatively low compared to those found in the literature, as cited by Alves et al. (2011), whom reported for genotype Poti Branca and shoot yield of 43.00 t h-1. Such differences can be attributed to environmental conditions, particularly rainfall and temperature. According to Sagrilo et al., (2002), the production of aerial part depends mainly on climate factors, since high temperatures with heavy rainfall not only favor the growth of stems, but as also the leaves production.
There was a positive correlation between shoot yield and the tuberous roots yield (r = 0.39 *), and between shoot yield and starch yield (r = 0.44 *), indicating that plants with more developed aerial part produce more tuberous roots and more starch, due to the higher photoassimilates production. According to Mulualem and Ayenew (2012), increments of vegetative parts have significant effect on the dry matter production of cassava.
Observing the tuberous roots yield (Table 1), a variation from 8.12 t ha-1 (Lavra Velha) to 29.27 t ha-1 (2006-5) is noticed, indicating variability for this trait. Among the 28 genotypes studied, nine were considered to be more productive with values ranging from 17.50 t ha-1 to 29.27 t ha-1, being higher than the national average, which according to IBGE (2016), it was 15.24 t ha-1 in 2015.
The genotypes obtained from botanical seeds  selected in UESB showed higher values for tuberous roots yield, except genotype 2006-12.
The genotype Sergipe, when propagated through the traditional method, produced less tuberous roots than when planted with cuttings obtained by the rapid multiplication method (Santos et al., 2009). In this method, the selection and the care with the cuttings lead to obtain more vigorous plants, contrasting the plants development from cuttings collected from the producers. Due the continuous cultivation for about 25 years in low natural soil fertility, without the use of fertilizer and the accumulation of pests and diseases have caused a "degeneracy" for the propagation material of Sergipe genotype, which has led to reduced productivity and the consequent reduction of area cultivated with this material. The drought experienced in the region in recent years has helped to accentuate this problem.
The harvest of cassava roots must be performed in the physiological resting period of the plant, when the roots has higher content of dry matter, differently from the growth season, when the dry matter content in the roots is reduced (Sagrilo et al., 2006; Keating et al., 1982; Guimarães et al., 2009). These conditions are found in the study area during August, a period characterized by milder temperatures and low rainfall, when the majority of local farmers harvest the roots. This leads, however, the need for storage of planting material for three to four months until the beginning of the rainy season, usually in October or November, reducing their quality.
For the characteristic of dry mass for tuberous roots, it was possible to separate the genotypes into three groups, highlighting the genotype Lagoão into the group that showed higher values (Table 1). In this group the dry matter content ranged from 29.44 to 34.13%, values that can be considered high, according to Teye et al. (2011).
The satisfactory results presented by genotypes obtained from free pollination for tuberous roots yield did not occur to dry mass of roots. Despite these genotypes forming considerable number of roots, they had higher moisture, which is not suitable for the industrialization of cassava.
It is desirable that the varieties responsible for higher productions of tuberous roots be also those which have higher dry matter content, maximizing the yield of the final product by cultivated area unit (Vidigal Filho et al., 2000). In this study, the genotypes Caipira, Poti Branca, and Sergipe from cuttings obtained by the rapid multiplication method and Verdinha stood out in both characteristics.
The cassava starch and its derivatives have been used in products for human consumption or as input from various industries such as: canned food, packaging, glues, paper, mining, textile and pharmaceutical (Cardoso and Gameiro, 2006). Genotypes that have high yield of starch may be recommended for industrial use in the region.
Nine  genotypes  stood  out  for  starch  yield  (Table 1), showing values between 4.44 to 7.11 t ha-1. The overall average of the experiment was 3.98 t ha-1 of starch, considering the 28 treatments. Introducing genotypes can lead to increase yield of roots by improving the income of farmers in the region. However, this work is still recent in the studied region, and further studies in different locations and years are necessary to evaluate the yield stability and subsequent recommendation for cultivation.
Separation of two genotypes groups in relation to total leaf area is observed in Table 2. The group with the lowest total leaf area was formed basically by genotypes 2006-4, 2006-5, 2006-8, 2006-10 and 2006-12,  obtained from botanical seeds, deriving from open pollination selected in UESB, except the genotypes Bromadeira and Malacacheta traditionally farmed in the region.
Low temperatures and poor soil moisture change the pattern of leaf longevity, increasing the senescence process, abscission and restricting the expansion of the leaf blade (Calatayud et al., 2000). For El-Sharkawy (2006), larger leaf longevity may be important to achieve higher yields in crops such as cassava. In this crop, the development of the shoot and roots occur simultaneously, enabling the selection of cassava varieties for both traits simultaneously (Lenis et al., 2006). In this study, a correlation was found between total leaf area (TLA) and root dry weight (r = 0.43*), indicating that genotypes which maintained high leaf retention had higher starch accumulation in tuberous roots.
Table 2 indicates that the RBP and RBR were similar between genotypes. The study of correlations showed that higher value of these characteristics are associated to higher starch accumulation in the tuberous root (r = 0.34* and r = 0.50*, respectively).
The efficiency of genotypes for leaf area maintenance makes the plants to absorb more light energy producing more photoassimilates, accumulating it in the shoot and in the roots, as dry matter. The results corroborate with Lenis et al., (2006), which state that the increased longevity of the leaves or better leaf retention is a way to increase the cassava yield. These authors also highlight the importance for incorporating the leaf retention as an important feature to be target in breeding and selection programs to increase roots yield.
The genotypes showed similar leaf water potential (Ψw) in both the predawn period and the noon period (Table 3). This feature reflects the dynamic conditions of the water transport process in the soil-plant-atmosphere system, constituting the main component responsible for the water flow in the plant (Pereira, 2006).
Water stress usually occurs gradually in nature, and the tolerant plants have developed mechanisms to adapt to conditions of low water availability in the soil (Chaves Filho and Stacciarini-Seraphin, 2001). This study had showed no significant difference in leaf water potential between genotypes at extreme periods of day, therefore, it is concluded that the plant  defense  mechanisms  were similar between the different genotypes, such as osmotic adjustment to better coexist with drought, and they did not show considerable variation among them.


Therefore, regarding edaphoclimatic conditions of the experiment, it is concluded that:
i) Higher total leaf area and high photosynthetically active radiation absorbed by the canopy of plants, observed at the end of the first cycle, were correlated to the increase of shoot yield and root dry weight.
ii) There was no change in leaf water potential among the genotypes.
iii) The genotypes Caipira, Poti Branca, Verdinha and Sergipe from cuttings  obtained  by  the  method  of  rapid multiplication showed high productivity of tuberous roots associated with higher dry matter values.
iv) Greater starch yield was observed in genotypes 2006-5, Verdinha, Malacacheta, Poti Branca, Caipira, 2006-10, Sergipe MR, Parazinha and Mulatinha and they might be future alternatives for regional cultivation for industrial production.


The authors have not declared any conflict of interests.


Acquah WE, Marian Quain D, Twumasi P (2011). Genetic relationships between some released and elite Ghanaian cassava cultivars based on distance matrices. Afr. J. Biotechnol. 10(6):913-921.


Allem AC (1994). The origins Manihot esculenta Crantz (Euphorbiaceae). Genet. Resour. Crop Evol. 41:133-150.


Alves MCS, Carvalho HWL, Rangel MAS, Santos VS, Silva J, Rodrigues CS (2011). Comportamento de Cultivares de mandioca no Rio Grande do Norte. In: Congresso brasileiro de mandioca, 14, Maceió. Anais... Maceió.


Alves AAC (2002). Cassava botany and physiology, In. Cassava: Biology, Production and Utilization. Eds. Hillocks RJ, Thresh JM, Bellotti AC. Oxon, UK: CABI Publishing. pp. 67-89.


Calatayud PA, Llovera E, Bois JF, Lamaze T (2000). Photosynthesis in drought-adapted cassava. Photosynthetica 38(1):97-104.


Carvalho FM de, Viana AES, Cardoso CEL, Matsumoto SN, Gomes IR (2009). Sistemas de produção de mandioca em treze municípios da região Sudoeste da Bahia. Bragantia 68(3):699-702.


Cardoso CEL, Gameiro AH (2006). Caracterização da cadeia agroindustrial. In. Aspectos Socioeconômicos e Agronômicos da Mandioca. Editor: Luciano da Silva Souza... [et al.]. Cruz das Almas, Cruz das Almas, Bahia. pp. 19-40.


Casaroli D, Fagan EB, Simon J, Medeiros SP, Manfron PA, Dourado Neto D, Lier Q de J van, Müller L, Martin TN (2007). Radiação solar e aspectos fisiológicos na cultura de soja - uma revisão . Rev. da FZVA 14(2):102-120.


Chaves Filho JT, Stacciarini-Seraphin E (2001). Alteração no potencial osmótico e teor de carboidratos solúveis em plantas jovens de lobeira (Solanum lycocarpum St.-Hil.) em resposta ao estresse hídrico. Rev. Bras. Bot. 24(2):199-204.


Conceição AJ (1983). A Mandioca. São Paulo: Ed. Nobel, 382p.


El-Sharkawy MA (2012). Stress-tolerant cassava: the role of integrative ecophysiology-breeding research in crop improvement. Sci. Res. 2(2):162-186.


El-Sharkawy MA, Tafur SM (2010). Comparative photosynthesis, growth, productivity, and nutrient use efficiency among tall- and short-stemmed rain-fed cassava cultivars. Photosynthetica 48(2):173-188.


El-Sharkawy MA, Lopez Y, Bernal LM (2008). Genotypic variations in Activities of PEPC and correlations with leaf photosynthetic characteristics and crop productivity of cassava grown in low-land seasonally-dry tropics. Photosynthetica 46(2):238-247.


El-Sharkawy MA (2006). International research on cassava photosynthesis, productivity, eco-physiology, and responses to environmental stresses in the tropics. Photosynthetica 44(4):481-512.


FAO (Food and Agriculture Organization) (2016). Faostat Database Gateway. Disponível em. 



Fukuda WMG, Magalhães JA, Calvacanti J, Pina PR, Tavares JA, Iglesias C, Romero LAH, Montenegro EE (1997). Pesquisa participativa em melhoramento de mandioca: Uma experiência no Semi-árido do Nordeste do Brasil. Cruz das Almas, BA: EMBRAPA – CNPMF, ago. 1997. P 46.


Fukuda WMG, Silva S de O (2003). Melhoramento de mandioca no Brasil. In: Culturas Tuberosas Amiláceas Latino Americanas. Fundação Cargill. 2:242-255.


Fukuda WMG, Cavalcante J, Fukuda C, Costa IRS (1999). Variabilidade genética e melhoramento da mandioca (Manihot esculenta Crantz). Recursos genéticos e melhoramento de plantas para o Nordeste Brasileiro. Disponível em.


Galera JMSV, Valle TL (2007). Estruturação genética do germoplasma de mandioca através de informação comparativas entre estudos biológicos e antropológicos – resultados preliminares. Rev. raízes e amidos Trop. 3(1):363-366.


Grossmann J, Freitas AC (1950). Determinação do teor de matéria seca pelo peso específico em raízes de mandioca. Rev. Agron. 160/162(4):75-80.


Guimarães DG, Muniz WF, Moreira E de S, Viana AES, Cardoso CEL, Cardoso AD, Gomes IR, Fernandes ET, Anjos DN dos (2009). Avaliação da qualidade de raízes de mandioca na região Sudoeste da Bahia. Rev. raízes e amidos trop. 5:224-229.


IBGE (Instituto Brasileiro de Geografia e Estatística) (2016). Sistema IBGE de Recuperação Automática – SIDRA. 2016 Disponível em.


Keating BA, Evenson JP, Fukai S (1982). Environmental effects on growth and development of cassava (Manihot esculenta Crantz). III. Assimilate distribution and storage organ yield. Field Crops Res. 5:293-303.


Lopes AC, Viana AES, Matsomoto SN, Cardoso Júnior N dos S, São José AR (2010). Complementação da irrigação e épocas de colheita de mandioca cv. coqueiro no Planalto de Conquista, BA. Ciência e agrotecnologia 34(3):579-587.


Lenis JI, Calle F, Jaramilo G, Perez JC, Veballos H, Cock JH (2006). Leaf retention and cassava productivity. Field Crops Res. 95:126-134.


Mulualem T, Ayenew B (2012). Correlation and path coefficient analysis of Cassava (Manihot esculentaCrantz) at Jimma, Southwestern, Ethiopia. J. Nat. Sci. Res. 2(9):1-7.


Nassar NMA, Júnior OP, Souza MV, Ortiz R (2009). Potential of patents in cassava carotenoids and amino-acids. Recent Patents Food Nutr. Agric. 1(1):32-38.


Oliveira SL de, Coelho EF, Nogueira CCP (2006). Irrigação. In: Aspectos Socioeconômicos e Agronômicos da Mandioca. Editor: Luciano da Silva Souza... [et al.]. Cruz das Almas: Embrapa mandioca e fruticultura tropical. pp. 292-300.


Pereira AR (1987). Aspectos fisiológicos da produtividade vegetal. Rev. Bras. Fisiol. Vegetal 1(2):139-142.


Pereira MRR (2006). Comportamento fisiológico e morfológico de clones de Eucalyptussp. w. (hill ex. maiden) submetidos a diferentes níveis de água no solo. Dissertação (Mestrado em Irrigação e Drenagem), Faculdade de Ciências Agronômicas, Botucatu - SP, Brasil. 69 p.


Ribeiro Junior JI (2001). Análises Estatísticas no SAEG. Viçosa, Universidade Federal de Viçosa. 250 p.


Sagrilo E, Vidigal Filho PS, Pequeno MG, Vidigal MCG, Scapim CA, Kvitschal MV, Maia RR, Rimoldi F (2006). Effect of harvest period on foliage production and dry matter distribution in five cassava cultivars during the second plant cycle. Braz. Arch. Biol. Technol. 49(6):1007-1018.


Sagrilo E, Vidigal Filho PS, Pequeno MG, Scapim CA, Gonçalves-Vidigal MC, Maia RR, Kvitschal MV (2002). Efeito da época de colheita no crescimento vegetativo, na produtividade e na qualidade de raízes de três cultivares de mandioca. Bragantia 61(2):115-125.


Santos V da S, Souza A da S, Viana AES, Fereira Filho JR, Souza KA de, Menezes MC (2009). Multiplicação rápida, método simples e de baixo custo na produção de material propagativo de mandioca. Embrapa Mandioca e Fruticultura Tropical, Cruz das Almas. (Boletim de pesquisa e desenvolvimento, 44). 23 p


SEI (Superintendência de Estudos Econômicos e Sociais da Bahia) (2013). Estatística dos municípios Baianos. v. 4, 450 p. Disponível em. 



Scholander PF, Hammel HT, Hemingsen EA, Bradstreet ED (1964). Hydrostatic pressure and osmotic potencial in leaves of mangroves and some other plants. Proc. Nat. Acad. Sci. 52:119-125.


Teye E, Asare AP, Amoah RS, Tetteh JP (2011). Determination of the dry matter content of cassava (Manihot esculenta Crantz) tubers using specific gravity method. ARPN J. Agric. Biol. Sci. 6(11):23-28.


Tumuhimbisea R, Melisa R, Shanahana P, Kawukib R (2014). Genotype × environment interaction effects on early fresh storage root yield and related traits in cassava. Crop J. 2(5):329-337.


Vidigal Filho PS, Pequeno MG, Scapim CA, Vidigal MCG, Maia RR, Sagrilo E, Simon GA, Lima RS (2000). Avaliação de cultivares de mandioca na Região Noroeste do Paraná. Bragantia 59:69-75.