Is the basal area of maize internodes involved in borer resistance?
© Santiago et al; licensee BioMed Central Ltd. 2011
Received: 20 May 2011
Accepted: 14 October 2011
Published: 14 October 2011
To elucidate the role of the length of the internode basal ring (LIBR) in resistance to the Mediterranean corn borer (MCB), we carried out a divergent selection program to modify the LIBR using two maize synthetic varieties (EPS20 and EPS21), each with a different genetic background. We investigated the biochemical mechanisms underlying the relationship between the LIBR and borer resistance. Selection to lengthen or shorten the LIBR was achieved for each synthetic variety. The resulting plants were analyzed to determine their LIBR response, growth, yield, and borer resistance.
In the synthetic variety EPS20 (Reid germplasm), reduction of the LIBR improved resistance against the MCB. The LIBR selection was also effective in the synthetic variety EPS21 (non-Reid germplasm), although there was no relationship detected between the LIBR and MCB resistance. The LIBR did not show correlations with agronomic traits such as plant height and yield. Compared with upper sections, the internode basal ring area contained lower concentrations of cell wall components such as acid detergent fiber (ADF), acid detergent lignin (ADL), and diferulates. In addition, some residual 2,4-dihydroxy-7-methoxy-(2H)-1,4-benzoxazin-3-(4H)-one (DIMBOA), a natural antibiotic compound, was detected in the basal area at 30 days after silking.
We analyzed maize selections to determine whether the basal area of maize internodes is involved in borer resistance. The structural reinforcement of the cell walls was the most significant trait in the relationship between the LIBR and borer resistance. Lower contents of ADF and ADL in the rind of the basal section facilitated the entry of larvae in this area in both synthetic varieties, while lower concentrations of diferulates in the pith basal section of EPS20 facilitated larval feeding inside the stem. The higher concentrations of DIMBOA may have contributed to the lack of correlation between the LIBR and borer resistance in EPS21. This novel trait could be useful in maize breeding programs to improve borer resistance.
There is a large body of evidence that the morphological characteristics and structural defenses of plants affect normal feeding and establishment of corn borers on maize plants [6, 7]. Several plant characteristics are associated with resistance, including general plant traits such as plant age and plant and ear height [8–11]; leaf traits such as leaf age, timing of vegetative phase transition [12, 13], presence or density of trichomes , and leaf toughness [15–17]; stem traits such as the rind and pith toughness and thickness [5, 18]; and ear traits such as husk tightness and dimension of the silk-channels [19, 20]. There have been several studies on the structural characteristics of stems as mechanisms of resistance to MBC [5, 18]. The rind-puncture resistance evaluated by Butrón et al.  was a useful indicator of resistance in some materials, but the length of the meristematic area, an area located at the base of the internode, was a more promising trait .
To describe that trait in more detail, the internodes in corn are formed by intercalary meristems located at the base of the internode on the upper side of a node. Within a growing internode, the younger, undifferentiated tissues are near the intercalary meristem at the base of the internode and become progressively more developed and mature higher up the internode . During development, internodal cells undergo rapid elongation and the pulvinus line develops from the remains of the intercalary meristem at the base of the internode . The trait recorded in previous studies as 'length of meristematic area' corresponds to the area at the base of the internode where the rind tissue is light green or white in contrast to the darker green color of the rest of the internode . For accuracy, we have renamed this trait in the present study, because the relationship between the external measurement made at the end of vegetative development and the internal localization of intercalary meristem is unknown. The correct term for this measurement is 'length of the internode basal ring' (LIBR), and refers to the area located between the node and the pulvinus line (Figure 1b).
Taking into consideration this change in nomenclature, a remarkable difference in LIBR was found between inbred lines that were susceptible and resistant to MCB . The susceptible inbreds showed the largest LIBR, suggesting that the size and properties of this area could be related to the ability of the larvae to enter the plant. Furthermore, this character was strongly related to stem damage, measured as tunnel length. However, as the authors pointed out, the diverse genotypes evaluated could also have other resistance mechanisms, and the correlation between the LIBR and borer resistance could be due to some other reason. Therefore, it is necessary to further examine this relationship in the same genetic background.
In the Misión Biológica de Galicia [Spanish National Research Council (CSIC)] we have developed two maize synthetic varieties with different genetic backgrounds. EPS20 belongs to the "Reid" germplasm, which is used extensively for maize breeding in temperate areas. EPS21 has a diverse "non-Reid" background. In agronomic and molecular contexts, EPS20 is more uniform than EPS21 [24, 25]. After checking the variability of the LIBR in these two synthetic varieties, we carried out a divergent selection program to lengthen or shorten this area in both synthetics. Three cycles of divergent selection were carried out for each synthetic variety.
We investigated the biochemical mechanisms underlying the relationship between the LIBR and borer resistance. One of the major factors in the resistance of maize to several insects is a hydroxamic acid, 2,4-dihydroxy-7-methoxy-(2H)-1,4-benzoxazin-3-(4H)-one (DIMBOA) . When present at high levels during early stages of maize development, this acid inhibits feeding by the European corn borer (ECB) Ostrinia nubilalis (Hübner) (Lepidoptera: Pyralidae) , and is also effective against the MCB [28, 29]. However, DIMBOA concentrations decrease as the plant grows, and so this mechanism cannot protect plants against the second generation of both insect species . Because the LIBR includes an area with the remains of meristematic activity and cells in a primary physiological state, it is possibly that some DIMBOA remains in this area at advanced developmental stages.
We quantified diverse cell wall compounds previously related with borer resistance in the LIBR and surrounding areas. Cell wall composition may affect insect feeding for both nutritional and physical reasons . In grasses, hydroxycinnamic acids, namely p-coumaric (PCA) and ferulic acid (FA), are ester and/or ether-linked to cell-wall polymers [32, 33]. Formation of diferulates (DFAs) and higher oligomers of FA can cross-link arabinoxylan chains . These cell wall hydroxycinnamic acids in assorted tissues (kernel, leaf, pith, rind, and nodes) are related to resistance to borers including the ECB , the MCB [35, 36], Southwestern corn borer (Diatraea grandiosella Dyar) (Lepidoptera: Pyralidae), and sugarcane borer (Diatraea saccharalis Fabricius) (Lepidoptera: Pyralidae) . In addition, acid detergent fiber and lignin in maize leaf-sheaths and stalks are associated with resistance to stalk-tunneling by the ECB [38, 39].
In summary, the specific objectives of the current study were as follows: (1) to determine whether the LIBR could be modified via a selection program in two genetic backgrounds; (2) to evaluate the efficacy of a selection program in terms of resistance to MCB and other agronomic traits; and (3) to elucidate the biochemical mechanisms underlying the relationship between the LIBR and borer resistance.
Base materials (inbred lines) for the synthetic varieties EPS20 and EPS21, and their pedigrees
Group of germplasmb
(V3 × B14) B14
(V3 ×B14) B14
(Mt42 × WF9) WF9
(Mt42 × B14) B143
A158 × B14
A90 × WF9
(ND203 × A636) A6362
WF9 × C.I. 187-2
Rojo Vinoso de Aragónc
Doré de Gomerc
Wisc. Exp. Single cross
Corn Belt (USA)
A78 × A109
Corn Belt (USA)
Divergent Selection Procedure for LIBR in Both Synthetic Varieties
Divergent masal selection on both sexes was carried out in each synthetic variety (additional file 1). In 2003, approximately 600 plants were shoot-bagged for selection. When approximately 90% of the plants had been shoot-bagged, the length of the internode basal ring (LIBR) was measured in the third internode above ground level. The LIBR refers to the area located between the node and the pulvinus line in the internode, as shown in Figure 1b. Following the methodology of Santiago et al. , the sheath over the tissue was partially removed to measure this area. The LIBR (in mm) was measured in all normal plants, and each individual plant was labeled. According to cut-off points in either direction of selection, plants with lower values for LIBR were randomly mated to obtain the first cycle for short-length of the internode basal ring (Short_LIBR) and plants with higher values for LIBR were randomly mated to obtain the first cycle for large-length of the internode basal ring (Large_LIBR). Selection was set to apply 10% selection intensity. In 2004, second selection cycles were obtained from Short_LIBRC1 and Large_LIBRC1. In the Short_LIBRC1, plants with short LIBR were selected and mated to obtain Short_LIBRC2; in the Large_LIBRC1, plants with large LIBR were selected and mated to obtain Large_LIBRC2. In 2005, third selection cycles from Short_LIBRC2 and Large_LIBRC2 were conducted in the same way as that described above.
Evaluation of the LIBR Response in the Selection Program
Seeds for this study were renewed by intermating at least 100 plants from each of the six cycles of selection (Large_LIBRC1, Large_LIBRC2, Large_LIBRC3 and Short_LIBRC1, Short_LIBRC2, Short_LIBRC3) and the original cycles of EPS20 and EPS21 in 2006. Field experiments for evaluations were conducted at Pontevedra (42°24' N, 8°38' W, 20 m above sea level) in 2007 and 2008. For field experiments, plants were grown in a randomized complete block design with three replications. Each plot had two rows spaced 0.80 m apart and each row consisted of 25 two-kernel hills spaced 0.21 m apart. After thinning to one plant per hill, plant density was approximately 60,000 plants ha -1. The soil type is acid sandy loam. Trials were irrigated as necessary, and cultivation operations, fertilization, and weed control were carried out according to local practices. To accurately define the silking time of each genotype, plots were checked until 50% of plants showed silks. At silking, 10 plants were infested with a mass of approximately 40 MCB eggs, reared as described by Eizaguirre and Albajes . At 30 days after silking, another 10 plants where evaluated to determine the characteristics of the LIBR, and plant and ear heights. The LIBR was measured as described above. Ear and plant heights were measured as the distance from the soil to the ear attachment node and to the collar of the flag leaf, respectively. At harvest, ears of infested plants were collected and kernel damage was scored on a nine-point subjective scale, as follows: 1 = 91 to 100% damage; 2 = 71 to 90%; 3 = 61 to 70%; 4 = 51 to 60%; 5 = 41 to 50%; 6 = 25 to 40%; 7 = 11 to 24%; 8 = 1 to 10%, and 9 = without damage. The stems of these plants were split into two longitudinal parts and the length of tunnels produced by larval feeding was measured (cm). The yield of uninfested plants (second row of each plot) was recorded, adjusted to kernel moisture of 140 g H2O kg-1 and expressed as Mg ha-1.
Biochemical Analysis of LIBR and Upper Sections
Original C0, Large_LIBRC3, and Short_LIBRC3 of each synthetic variety were grown at Pontevedra (42°24' N, 8°38' W, 20 m above sea level) in 2009. The field experimental design was a randomized complete block design with three replicates. Each plot had two rows spaced 0.8 m apart and each row consisted of 15 two-kernel hills spaced 0.21 m apart. After thinning to one plant per hill, plant density was approximately 60,000 plants ha -1. Cultivation operations, fertilization, and weed control were carried out according to local practices and crop requirements.
The fourth internode above ground level was collected from 12 plants for biochemical analyses. Based on previous studies, samples for analysis were collected 30 days after silking when internode elongation had ceased . For each internode, the basal parts of the internode corresponding to the LIBR area and a region 2 cm up from the LIBR area were separated into cylindrical stalk sections with a variable width (0.3-0.8 mm depending on the LIBR area). For simplicity, the LIBR area and the region above it are hereafter referred to as I1 and I2, respectively (Figure 1b). The outer rind (including the cuticle, epidermis, xylem elements, and phloem) was separated from the central pith tissue of each section. The pith tissue consisted of mostly parenchyma cells and randomly distributed vascular strands. Internode sections were frozen (-20 °C), lyophilized, and ground through a 0.75 mm screen in a Pulverisette 14 rotor mill (Fritsch GmbH, Oberstein, Germany).
For DIMBOA analysis, ground material samples (each 100 mg) were weighed into screw-capped 15 mL polypropylene Falcon tubes and 5 mL HPLC grade methanol and 50 μL acetic acid were added. The tubes were vortexed and placed in a sonicator waterbath for 60 minutes at 60°C. The supernatant (0.5 mL) was combined with 0.5 mL distilled water in a microcentrifuge tube, vortexed, and centrifuged for 5 min at 1000 g. The supernatants were transferred into vials for analysis by HPLC. Analyses were performed using a 2690 Waters Separations Module (Waters, Milford, MA, USA) equipped with a 996 Photodiode Array Detector (Waters) with a Waters YMC ODS-AM (Waters, Milford, MA, USA) narrow bore column (100 × 2 mm i.d.; 3 μM particle size). For elution, the mobile phase system consisted of acetotrinile (Solvent A) and trifluoroacetic acid (0.05%) in water (solvent B) delivered in the following gradient conditions: initial A: B ratio of 10:90, changing to 30:70 in 3.5 min, then to 32:68 in 6.5 min, then to 100:0 in 4 min, then isocratic elution with 100:0 for 4.5 min, finally returning to the initial conditions after 3 min. The mobile phase flow rate was 0.3 mL/min and the total analysis time was 21.5 min. The sample injection volume was 4 μL, and the elution profiles were monitored on-line by UV absorbance at 325 and 254 nm. Retention times were compared with those of freshly prepared standard solutions. The DIMBOA standard was kindly provided by Dr. Carlos Souto from Vigo University.
Analysis of Hydroxycinnamic Acids
Ground material (500 mg) was extracted in 30 mL 80% methanol and mixed with a Polytron mixer (Brinkman Instruments, Westbury, NY). Samples were extracted for 1 h and then centrifuged for 10 min at 1000 g. The remaining pellet was then shaken in 20 mL 2 N NaOH under nitrogen flow for 4 h. Digested samples were neutralized with 6 N HCl, and the pH was adjusted to 2.0. After centrifugation, the supernatant was collected and the pellet washed twice with distilled water (10 mL each). Supernatants were pooled and then extracted twice with ethyl acetate (40 mL each). Collected organic fractions were combined and reduced to dryness using a Speed Vac (Savant Instruments, Holbrook, NY). The final extract was dissolved in 1.5 mL methanol and stored at -20°C prior to HPLC analysis according to the method described by Santiago et al. .
Retention times and UV spectra were compared with those of freshly prepared standard solutions of PCA and FA (Sigma, St. Louis, MO), and 5-5-DFA, the latter kindly provided by the laboratory of Dr. J.T. Arnason (University of Ottawa, Ontario, Canada). The UV spectra of other DFAs were compared with previously published spectra . We identified and quantified four isomers of DFA: 5-5' DFA, 8-5' DFA (sum of 8-5'-non cyclic and 8-5'-benzofuran forms), and 8-o-4' DFA. The role of DFAs in resistance was based on the DFA total content (DFAT), which is commonly related to cell wall strength .
Acid Detergent Fiber (ADF) and Acid Detergent Lignin (ADL) Analyses
Fiber is composed largely of cellulose, hemicellulose, and lignin, which are the primary components of plant cell walls. ADF is composed of mostly cellulose and lignin, while ADL is primarily lignin . Determinations of ADF and ADL were carried out using the AOAC Official Method 973.18: "Fibre (Acid detergent) and lignin (H2SO4) in animal feed" .
Combined analyses of variance (over years and synthetic varieties) (ANOVA) for LIBR, MCB damage, and other agronomic traits were conducted using the PROC GLM routine of SAS . The sources of variation were years, replications within years, cycles of selection of synthetic varieties, and their interactions. All sources of variation, except for synthetics and cycles of selection, were considered random. The genetic progress of selection in each synthetic line was estimated by the linear regression coefficients of the LIBR plotted against cycles of selection. Progress up and down from the original cycles was estimated using the model proposed by Eberhart . For each synthetic variety, sums of squares of cycles were partitioned into sums of squares due to linear and quadratic regressions and deviations from the model. Furthermore, sums of squares for linear and quadratic regressions were partitioned into average regression, and between regressions. This analysis is appropriate when two or more populations are developed from the same base population by different methods of selection, as in our study, where we compared short and large LIBRs. Estimates of average linear and quadratic coefficients for both selection directions were also calculated using the Eberhart model . Simple linear regression coefficients of LIBR plotted against tunnel length and several other traits of economic importance were determined using the PROC REG routine of SAS .
For biochemical analyses, we combined cycles of selection of synthetic varieties and sections to compare data on the contents of diverse compounds by least significant differences (LSD) tests. All analyses were performed using the SAS program .
Results and Discussion
Responses to LIBR Selection and Relationship with Borer Resistance
As estimated by the Eberhart model, the progress of selection for larger LIBR (b11) in the maize synthetic EPS20 was 0.074 mm per cycle (P = 0.27), whereas that for shorter LIBR (b12) in this synthetic was -0.10 mm (P = 0.12). Similarly, the linear progress of selection for larger LIBR (b11) in the maize synthetic EPS21 was 0.064 mm (P = 0.34) per cycle, whereas that for shorter LIBR (b12) was -0.27 mm (P = 0.001). The quadratic coefficients were non-significant. Previous studies have emphasized that the synthetic variety EPS21 displays higher genetic variability; therefore, a better linear response of this synthetic to selection was predictable [24, 25]. Non-significant linear changes with three cycles of selection, except for shortening the LIBR in EPS21, suggest that multiple genes with small effects influence the phenotype of the LIBR.
Means of different traits evaluated in three cycles of divergent selection to lengthen or shorten the length of the internode basal ring (LIBR) in the synthetic varieties EPS20 and EPS21
Simple linear regressions of agronomic and resistance traits on LIBR in synthetic varieties EPS20 and EPS21
Pr > F
Tunnel length (cm) **
Kernel damage (1-9) *
Plant height (cm)
Ear height (cm)
Yield (Mg ha-1)
Tunnel length (cm)
Kernel damage (1-9)
Plant height (cm)
Ear height (cm)
Yield (Mg ha-1)
In terms of MCB resistance, we assumed that the LIBR region was related to resistance because this is the area of borer establishment and entry. Any progress in selection that results in changes to this area could affect resistance. The mean tunnel length in EPS20_Large_LIBRC3 (21.57 cm) was significantly greater than that in EPS20_Short_LIBRC3 (10.36 cm) (Table 2). Moreover, the simple regression coefficient of tunnel length (dependent variable) on LIBR (independent variable) was 15.15 mm in EPS20 (R2 = 0.91, P = 0.001) (Table 3). These results indicated that our hypothesis was correct for EPS20, as shorter LIBR was associated with greater resistance. In addition, in the present study, the selection to shorten the LIBR in EPS20 showed a comparable improvement to that achieved via recurrent selection for resistance to MCB in EPS12 . Sandoya and co-workers  reported a linear decrease for tunnel length of -1.80 cm cycle-1; similar to the tunnel length reduction between EPS20 and EPS20_Short_LIBRC3 of -1.84 cm cycle-1. Moreover, we were able to obtain one cycle per year in the masal selection procedure used in the present study to reduce the LIBR, whereas the recurrent selection program used by Sandoya and co-workers  required 3 years to complete one selection cycle.
There were non-significant differences in tunnel length between C0 (12.44 cm), Large_LIBRC3 (14.62 cm), and Short_LIBRC3 (12.28 cm) in EPS21 (Table 2). Moreover, the simple regression coefficient of tunnel length on LIBR in EPS21 was non-significant (R2 = 0.12, P = 0.437) (Table 3). It may be that one or more additional resistance mechanisms in the base material of EPS21 masks the relationship between LIBR and resistance in this synthetic variety. For example, the inbred line CO125 contained high concentrations of diferulic acids--cell wall compounds related to MCB resistance [35, 36, 51], and the variety PB130 had thick cell walls that were positively related to MCB resistance . In addition, the differences between the two synthetic varieties in terms of the biochemical composition of the LIBR could be important, as discussed below.
The Reid-line synthetic EPS20, which showed smaller responses to LIBR selection, partially because of its lower variability, was the synthetic variety that showed the greatest indirect response for tunnel length. This trend suggested a single resistance mechanism related to the LIBR in most of the inbred lines that make up EPS20. Butrón et al.  compared different germplasm groups, and proposed that the Reid germplasm has genetic mechanisms for stem-damage resistance to the MCB. Those mechanisms could be related to stalk-breakage resistance derived from the Iowa Stiff Stalk Synthetic .
Previous studies on maize found that there was no relationship between ear and stem resistance to the MCB [53, 54]; therefore, the kernel damage response to MCB was not predictable at the start of these experiments. The healthiest ears were found in EPS20_Short_LIBRC3 (8.68) and EPS21_Short_LIBRC1 (8.70), while the more damaged ears were found in EPS20_Large_LIBRC3 (7.88) and EPS21_Large_LIBRC1 (8.28). Significant differences between opposite third cycles of selection were observed in the synthetic EPS20 (Table 2). In addition, the regression coefficient for kernel damage was negative (-0.84) and significant in EPS20 (R2 = 0.62, P = 0.034) (Table 3). The negative value indicates that larger LIBR was associated with greater ear damage; however, according to the nine-point rating scale, the ears were barely damaged in both cycles and synthetics (8 = 1 to 10% damaged).
Biochemical Resistance Mechanisms of the LIBR against Borer
We screened the diverse biochemical traits related to MCB attack in the basal internode area. For these analyses, we evaluated the composition of rind, which is the initial entry point for larvae, and the pith, which is the tissue upon which the larvae feed. In addition to the LIBR (I1), we also analyzed the area higher up the stem (I2) (Figure 1b).
Larvae Entry Point
Biochemical compounds in rind and pith of two internode sections in two synthetic varieties and their derivatives with lengthened or shortened length of the basal internode ring (LIBR)
We detected DIMBOA in the I1 section (LIBR area) of the original EPS21 and Short and Large C3 cycles of EPS21. However, in the EPS20 synthetic variety, we detected DIMBOA in the I1 section of only the original EPS20. The highest concentration of DIMBOA was in EPS21_Large_LIBRC3 (217 μg/g dry weight) (Table 4). It is important to note that DIMBOA was not detected in any I2 sections (2-cm up from the I1) (Table 4). Consistent with these results, previous studies on individual leaves noted high initial concentrations of hydroxamic acids, which declined rapidly as the leaf aged and expanded . Attending to our previous hypothesis, the less developed cells in the LIBR section contained residual DIMBOA, while the DIMBOA concentrations decreased to zero further up the internode.
In maize, the hydroxamic acid concentration increases rapidly and reaches a maximum a few days after germination, and then decreases as the plant ages [27, 55–58]. Bergvinson et al.  reported DIMBOA concentrations of approx. 300 μg/g dry weight in the pith, rind, and sheath tissues at early silking. In the current study, we determined DIMBOA concentrations in localized sections of the internode (I1) in mature plants at 30 days after silking, when internode elongation had ceased.
Regarding the inhibitory effect of DIMBOA on larvae, Barry et al.  concluded that less than 100 μg/g is insufficient for resistance to ECB and that a concentration of at least 400 μg/g would be a desirable target for ECB-resistance in a breeding program. In the current study, only the EPS21_Large_LIBRC3 contained significant quantities of DIMBOA (217 μg/g); this level may inhibit larval development (Table 4). There may be higher concentrations of DIMBOA at early silking, just after larvae hatching. The presence and amount of DIMBOA may be at least partly responsible for the lack of relationship between the LIBR and borer resistance in EPS21.
We analyzed the hydroxycinnamic acids bound in the cell walls of EPS20 and EPS21 and their cycles of selection. The major hydroxycinnamic compound was PCA, followed by FA, and DFAT (Table 4). In cells, PCA is mainly esterified to the γ -position of phenylpropanoid sidechains of S units in lignin [33, 59, 60]. Although very small quantities of PCA are esterified to arabinoxylans in immature tissues, most PCA accretion occurs in tandem with lignification [61, 62]. FA is intracellularly esterified to the C5-hydroxyl of α-L-arabinose sidechains of xylans and deposited into primary and secondary walls [43, 63, 64]. During cell wall deposition and lignification, xylans are cross-linked by peroxidase-mediated coupling of ferulate monomers into a complex array of dimers and trimers, and by extensive copolymerization of these FA, into lignin . Oxidative coupling of FA probably contributes to wall stiffening, lignin formation, cessation of growth, limited cell wall degradability by ruminants, and resistance to pests and diseases [16, 35, 36, 64, 66–70].
The levels of hydroxycinnamic acids detected in rind tissues were consistent with those determined in previous studies on various maize inbred lines . There were greater concentrations of PCA and FA in the rind than in the pith, while DFAT concentrations showed the opposite trend  (Table 4). Rind tissues generally had greater concentrations of PCA and FA esters than pith tissues. This was expected, because rind vascular tissues lignify to a greater extent to support the conductive and supportive tissues of the internode . PCA was the only hydroxycinnamic acid that showed significant differences between cycles of selection in the rind. In the I1 section, there were significant differences in PCA concentrations between some of the EPS20 cycles; that is, C0 contained higher levels of PCA than Short_LIBRC3 (19524.3 and 17789.0 μg/g dry weight, respectively), although the difference between the PCA contents in Large or Short cycles was insignificant (18976.7 and 17789.0 μg/g dry weight, respectively) (Table 4). There were no significant differences in PCA concentrations among the I1 sections of EPS21 cycles (Table 4). From those results, we could not conclude that PCA has a functional role in resistance of the rind internode basal ring area.
Among the literature on the evolution of cell wall hydroxycinnamic acids in maize internodes [43, 61, 72–74], the study by Scobbie et al.  is the most consistent with our results. Scobbie et al.  sectioned individual maize internodes into ten sections of equal length, and found that the lower three sections of the internode were significantly less developed than the remaining upper seven segments. They detected similar concentrations of esterified FA in all of the subsections of the internodes, but found progressively greater concentrations of esterified PCA in the upper internode sections of successively older internodes (progressing from top internodes down the stalk). Furthermore, Hatfield et al.  noted that the tissues at the top of a given internode contained more PCA than tissues in the lower part of the internode. In the current study, there were no differences in PCA and FA contents among the various rind sections. There are three points of difference between the previous studies and this study: Scobbie et al.  analyzed pith and rind jointly in each section, Hatfield et al.  mainly analyzed half-internode sections, and both evaluated single inbred lines. In the present study, we analyzed pith and rind separately for each section, the analyzed sections were from the lower half of the internode, and the genotypes used were synthetic varieties, each composed of eight inbred lines.
In the leaf sheaths, increased levels of NDF, ADF, cellulose, and lignin were reported to correspond to increased resistance to ECB feeding on that tissue [75–77]. In the current study, there were significant differences among cycles of selection for ADF and ADL (Table 4). In the I1 section of EPS20, there were significant differences in ADF; C0 contained 37.0% ADF and Large _LIBRC3 contained 40.7%. However, the difference in ADF between Large and Short cycles was not significant (40.7 and 39.5% ADF, respectively). No significant differences in ADF in the I1 section were found in EPS21 synthetic variety (Table 4). Furthermore, there were no significant differences in ADL in the I1 section in any of the maize synthetics or selection cycles (Table 4).
However, there were differences in ADF and ADL between the two rind sections (Table 4). The I2 sections contained higher concentrations of ADF and ADL than I1 sections. This result was consistent with previous studies showing progressively greater lignin concentrations from the base to the top of internode sections [73, 74]. This reflects the greater lignin content and higher degree of lignification in the more mature tissues/cells. In this sense, and according to our original hypothesis, the lower ADF and lignin contents in the rind of the I1 section could make this site more readily penetrable by the larvae. There were no differences in ADF or ADL between Short and Large cycles of selection. However, in Large_LIBRC3, the larger area with lower ADF and ADL content could increase its susceptibility to borer entry. Conversely, the shorter LIBR in EPS20_Short_LIBRC3 could result in higher resistance by decreasing the size of the larval entry area. Nevertheless, the role of this mechanism in other genetic backgrounds, such as in the synthetic EPS21, could be obscured by other traits, such as the presence of DIMBOA as described above, or other factors.
Tissues Consumed by Larvae
In the pith, we observed differences in DIMBOA, PCA, and DFAT concentrations between cycles of selection (Table 4). The DIMBOA concentrations in the pith were lower than those in rind tissues, and the differences were similar to those observed in the rind. That is, we detected DIMBOA in the I1 section of the original EPS21 and EPS20, and in the Short and Large C3 cycles of EPS21. EPS21_Large_LIBRC3 contained a high concentration of DIMBOA (217 μg/g dry weight) (Table 4). In the same way, we did not detect DIMBOA in I2 sections (Table 4). As mentioned previously, the presence and level of DIMBOA in rind and pith tissues at 30 days after silking may partly explain the lack of correlation between the LIBR and borer resistance in EPS21.
The concentrations of PCA and FA were lower in the pith than in the rind, while DFAT concentrations showed the opposite trend (Table 4). These findings are consistent with previous reports, which showed that pith tissues have a lower degree of lignification, and that DFAT has a major role as a cross-linking agent to stiffen and strengthen these tissues [34, 36, 71]. The lower degree of lignification is reflected by the lower levels of ADF and ADL in the pith (Table 4). In addition, no significant variations of ADF and ADL were observed among the pith sections evaluated (Table 4).
Regarding the I1 section, there were no significant differences in PCA and DFAT concentrations between cycles of selection in EPS21 and EPS20 (Table 4), although it is interesting to note that I2 sections of EPS20 contained higher concentrations of DFAT. In agreement with these results, in a study on floating rice, Azuma et al. [78, 79] showed that 5-5 diferulic acid was present at the lowest level around the intercalary meristem and increased as the distance from the meristematic zone increased toward the upper part of the internode. Those results suggested that the cell wall deposition of diferulic acids is not a consequence but a cause of the cessation of cell elongation in floating rice internodes. The current study is the first to describe variations in diferulates (DFAT) between two sections of maize internodes. Diferulates were not quantified in previous studies because of a lack of reliable diferulate standards, and because of the poor recovery of these compounds using traditional analytical techniques [43, 72]. The role of DFAT in borer resistance, especially that of pith tissues, is well characterized [35, 36, 51, 71]. It is possible that DFAT has a role in cessation of growth of the maize internode in some specific backgrounds, but this should be examined more closely in future studies. On the other hand, the ubiquitous presence of DFAT in EPS21, as well as the presence of DIMBOA, suggests that these and other substances may mask the effects of the LIBR on borer resistance.
In summary, the LBIR showed positive responses to selection in both of the synthetic maize varieties, EPS20 and EPS21. There was a relationship between large LIBR and decreased MCB resistance in EPS20, a more uniform germplasm derived from the US Corn Belt population "Reid". A large LIBR could increase the area in which larvae can enter the stem, while a short LIBR could decrease this area, making the plant more resistant to this pest.
Structural reinforcement of the cell walls appears to be the most significant trait involved in the relationship between the LIBR and borer resistance. Lower contents of ADF and ADL in the rind of the LIBR section facilitated the entry of larvae through this area in both synthetic varieties, while lower concentrations of DFAT in the pith LIBR sections facilitated larval feeding in EPS20. We detected the antibiotic compound DIMBOA in the LIBR section at 30 days after silking in both synthetic varieties. The higher concentrations of DIMBOA in EPS21 could be partly responsible for the lack of relationship between the LIBR and borer resistance in this variety.
These experiments using selection in two genetic backgrounds enabled us to study the relationship between the basal area of maize internodes and borer resistance. Our results suggest that synthetic varieties combining diverse germplasms could contain diverse resistance mechanisms, which can mask the role of the LIBR in borer resistance. This was demonstrated in the synthetic variety EPS21, which has the most variable background. The LIBR as a resistance trait could be useful for breeding borer-resistant genotypes in maize breeding programs, especially working with "Reid" materials.
This research was supported by the National Plan for Research and Development of Spain (Projects Cod. AGL2006-13140, AGL 2009-09611). R. Santiago acknowledges postdoctoral contracts "Juan de la Cierva" partially financed by the European Social Fund and "Isidro Parga Pondal" financed by the Autonomous Government of Galicia and the European Social Fund.
- Anglade P: Les Sesamia. Entomologie appliqué á l'agriculture. Tomo II, Lépidoptéres, II. Edited by: Balachowsky AS. 1972, Masson et Cie, Paris, France, 1389-1400.
- Cordero A, Malvar RA, Butrón A, Revilla P, Velasco P, Ordás A: Population dynamics and life-cycle of corn borers in South Atlantic European coast. Maydica. 1998, 43: 5-12.
- Velasco P, Revilla P, Monetti L, Butrón A, Ordás A, Malvar RA: Corn borers in northwestern Spain. Population dynamics and distribution. Maydica. 2007, 52: 195-204.
- Kumar H, Mihm JA: Assessing damage by second-generation southwestern corn borer, Diatraea grandiosella (Dyar) and sugarcane borer, Diatraea saccharalis (Fabricious) and development of sources of resistance in maize. Maydica. 1997, 42: 59-71.
- Butrón A, Malvar RA, Revilla P, Soengas P, Ordás A: Rind puncture resistance in maize: inheritance and relationship with resistance to pink stem borer attack. Plant Breeding. 2002, 121: 378-382. 10.1046/j.1439-0523.2002.716313.x.View Article
- Smith CM: An overview of the mechanism and bases of insect resistancein maize. In Proceedings of an International Symposium held at theInternational Maize and Wheat Improvement Center (CIMMYT): 23 November-3December 1994. Edited by: Mihm JA. CIMMYT, Mexico; 1997:1-12.
- Malvar RA, Butrón A, Ordás B, Santiago R: Causes of natural resistance tostem borers in maize. Crop protection research advances Nova SciencePublishers; 2008, 51-96.
- Malvar RA, Cartea ME, Revilla P, Ordás A, Álvarez A, Mansilla JP: Sources of resistance to pink stem borer and European corn borer in maize. Maydica. 1993, 38: 313-319.
- Schön CC, Lee M, Melchinger AE, Guthrie WD, Woodman WL: Mapping and characterization of quantitative trait loci affecting resistance against second-generation European corn borer in maize with the aid of RFLPs. Heredity. 1993, 70: 648-659. 10.1038/hdy.1993.93.View Article
- Melchinger AE, Kreps R, Spath R, Klein D, Schulz B: Evaluation of early-maturing European maize inbreds for resistance to the European corn borer. Euphytica. 1998, 99: 115-125. 10.1023/A:1018305316853.View Article
- Krakowsky MD, Lee M, Woodman-Clikeman WL, Long MJ, Sharpova N: QTL mapping of resistance to stalk tunneling by the European corn borer in RILs of maize population B73 × DE811. Crop Sci. 2004, 44: 274-282. 10.2135/cropsci2004.0274.View Article
- Abedon BG, Tracy WF: Corngrass1 of maize (Zea mays L) delays development of adult plant resistance to common rust (Puccinia sorghi Schw) and European corn borer (Ostrinia nubilalis Hübner). J Heredity. 1996, 87: 219-223.View Article
- Williams WP, Buckley PM, Davis FM: Vegetative phase change in maize and its association with resistance to fall armyworm. Maydica. 2000, 45: 215-219.
- Kumar H, Saxena KN: Oviposition by Chilo partelus (Swinhoe) in relation to its mating, diurnal cycle and certain non plant surfaces. Appl Entomol Zool. 1985, 20: 218-221.
- Davis FM, Baker HT, Williams WP: Anatomical characteristics of maize resistant to leaf feeding by southwestern corn borer and fall armyworm. J Agric Entomol. 1995, 12: 55-65.
- Bergvinson DJ, Arnason JT, Hamilton RI: Phytochemical changes during recurrent selection for resistance to the European corn borer. Crop Sci. 1997, 37: 1567-1572. 10.2135/cropsci1997.0011183X003700050026x.View Article
- Groh S, González-de-León D, Khairallah MM, Jiang C, Bergvinson D, Bohn M, Hoisington DA, Melchinger AE: QTL mapping in tropical maize: Genomic regions for resistance to Diatraea spp. and associated traits in two RIL populations. Crop Sci. 1998, 38: 1062-1072. 10.2135/cropsci1998.0011183X003800040030x.View Article
- Santiago R, Souto XC, Sotelo J, Butrón A, Malvar RA: Relationship between maize stem structural characteristics and resistance to pink stem borer (Lepidoptera: Noctuidae) attack. J Econ Entomol. 2003, 96: 1563-1570. 10.1603/0022-0493-96.5.1563.PubMedView Article
- Grier SL, Davis DW: Infestation procedures and heritability of characters used to estimate ear damage caused by second-brood European corn borer (Ostrinia nubilalis, Hübner) on corn. J Am Soc Hort Sci. 1980, 105: 3-8.
- Davis FM, Baker HT, Williams WP: Anatomical characteristics of maize resistant to leaf feeding by southwestern corn borer and fall armyworm. J Agric Entomol. 1995, 12: 55-65.
- Jung HG, Morrison TA, Buxton DR: Degradability of cell-wall polysaccharides in maize internodes during stalk development. Crop Sci. 1998, 38: 1047-1051. 10.2135/cropsci1998.0011183X003800040027x.View Article
- Collings DA, Winter H, Wyatt SE, Allen NS: Growth dynamics and cytoskeleton organization during stem maturation and gravity-induced stem bending in Zea mays L. Planta. 1998, 207: 246-258. 10.1007/s004250050480.PubMedView Article
- Kiesselbach TA: The stem. The structure and reproduction of corn (50th Anniversary Edition). New York; 1999, 27-30.
- Butrón A, Tarrío R, Revilla P, Malvar RA, Ordás A: Molecular evaluation of two methods for developing maize synthetic varieties. Plant Breeding. 2003, 12: 329-333.
- Butrón A, Revilla P, Romay MC, Ordás A, Malvar RA: Causes of agronomic differences between synthetics developed by the random and convergent cross methods. Field Crops Res. 2009, 110: 229-234. 10.1016/j.fcr.2008.09.003.View Article
- Klun JA, Brindley TA: Role of 6-methoxybenzoxazolinone in inbred resistance of host plant (maize) to first brood larvae of European corn borer. J Econ Entomol. 1966, 59: 711-718.View Article
- Klun JA, Robinson JF: Concentration of 2 1,4-benzoxazinones in dent corn at various stages of development of plant and its relation to resistance of host plant to European corn borer. J Econ Entomol. 1969, 62: 214-220.View Article
- Gutiérrez C, Castañera P: Efecto de los tejidos de maíz con alto y bajo contenido en DIMBOA sobre la biología del taladro Sesamia nonagrioides Lef. (Lepidoptera: Noctuidae). Investigaciones Agrarias: Producción y Protección vegetal. 1986, 1: 109-119.
- Ortego F, Ruiz M, Castañera P: Effect of DIMBOA on growth and digestive physiology of Sesamia nonagrioides (Lepidoptera: Noctuidae) larvae. J Insect Physiol. 1998, 44: 99-101.View Article
- Mihm JA: Breeding for host plant resistance to maize stem borers. Insect Sci Appl. 1985, 6: 369-377.
- Scriber JM, Slansky F: The nutritional ecology of immature arthropods. Ann Rev Entomol. 1981, 26: 183-211. 10.1146/annurev.en.26.010181.001151.View Article
- Ralph J, Helm RF, Quideau S, Hatfield RD: Lignin-feruloyl ester cross-links in grasses. Part 1. Incorporation of feruloyl esters into coniferyl alcohol dehydrogenation polymers. J Chem Soc Perkin Trans. 1992, 1: 2961-2969.View Article
- Ralph J, Hatfield RD, Quideau S, Helm RF, Grabber JH, Jung HJG: Pathway of p-coumaric acid incorporation into maize lignin as revealed by NMR. J Am Chem Soc. 1994, 116: 9448-9456. 10.1021/ja00100a006.View Article
- Bunzel M: Chemistry and occurrence of hydroxycinnamate oligomers. Phytochem Rev. 2010, 9: 47-64. 10.1007/s11101-009-9139-3.View Article
- Santiago R, Butrón A, Arnason JT, Reid LM, Souto XC, Malvar RA: Putative role of pith cell wall phenylpropanoids in Sesamia nonagrioides (Lepidoptera: Noctuidae) resistance. J Agric Food Chem. 2006, 54: 2274-2279. 10.1021/jf0524271.PubMedView Article
- Santiago R, Sandoya G, Butrón A, Barros J, Malvar RA: Changes in phenolic concentrations during recurrent selection for resistance to the Mediterranean corn borer (Sesamia nonagrioides Lef.). J Agric Food Chem. 2008, 56: 8017-8022. 10.1021/jf800922j.PubMedView Article
- Ramputh AI: Soluble and cell wall bound phenolic-mediated insectresistance in corn and sorghum. PhD thesis Ottawa-Carleton Institute ofBiology, Ontario, Canada; 2002.
- Coors JG: Resistance to the European corn borer, Ostrinia nubilalis (Hübner), in maize, Zea mays L., as affected by soil silica, plant silica, structural carbohydrates, and lignin. Genetic aspects of plant mineral nutrition.Edited by: Gabelman WH, Loughman BC. Martinus Nijhoff publishers, Dordrecht, The Netherlands; 1987:445-456.View Article
- Beeghly HH, Coors JG, Lee M: Plant fiber composition and resistance to European corn borer in four maize populations. Maydica. 1997, 42: 297-303.
- Messmer MM, Melchinger AE, Lee M, Woodman WL, Lee EA, Lamkey KR: Genetic diversity among progenitors and elite lines from the Iowa staff stalk synthetic (BSSS) maize population: comparison of allozyme and RFLP data. Theor Appl Genet. 1991, 83: 97-107.PubMedView Article
- Gerdes JT, Behr CF, Coors JG, Tracy WF: Compilation of North AmericanMaize Breeding Germplasm. Crop Science Society of America Inc.,Madison, USA; 1993.
- Eizaguirre M, Albajes R: Diapause induction in the stem corn borer, Sesamia nonagrioides (Lepidoptera: Noctuidae). Entomol Gener. 1992, 17: 277-283.View Article
- Jung HJG: Maize stem tissues: Ferulate deposition in developing internode cell walls. Phytochem. 2003, 63: 543-549. 10.1016/S0031-9422(03)00221-8.View Article
- Waldron KW, Parr AJ, Ng A, Ralph J, Williamson G: Cell wall esterified phenolic dimers: identification and quantification by reversed phase high performance liquid chromatography and diode array detection. Phytochem Anal. 1996, 7: 305-312. 10.1002/(SICI)1099-1565(199611)7:6<305::AID-PCA320>3.0.CO;2-A.View Article
- Van Soest PJ: Nutritional Ecology of the Ruminant. 2 edition. CornellUniversity Press, Ithaca, NY; 1994.
- AOAC Official Method 973.18, Fiber (Acid Detergent) and Lignin inAnimal Feed. Official Methods of Analysis of AOAC International. 16 edition.AOAC International, Arlington, VA; 1997, 28-29, Chapter 4,.
- Institute SAS: The SAS System. SAS Online Doc. HTML Format Version eightSAS Institute Inc., Cary, North Carolina; 2007.
- Eberhart SA: Least squares method for comparing progress among recurrent selection methods. Crop Sci. 1964, 4: 230-231. 10.2135/cropsci1964.0011183X000400020036x.View Article
- Barros J, Malvar RA, Butrón A, Santiago R: Combining abilities in maize for the length of the internode basal ring, the entry point of the Mediterranean corn borer larvae. Plant Breeding. 2011, 130: 268-270. 10.1111/j.1439-0523.2010.01789.x.View Article
- Sandoya G, Butrón A, Alvarez A, Ordás A, Malvar RA: Direct response of a maize synthetic to recurrent selection for resistance to stem borers. Crop Sci. 2008, 48: 113-118. 10.2135/cropsci2007.02.0084.View Article
- Santiago R, Butrón A, Reid LM, Arnason JT, Sandoya G, Souto XC, Malvar RA: Diferulate content of maize sheaths is associated with resistance to the Mediterrranean corn borer Sesamia nonagrioides (Lepidoptera: Noctuidae). J Agric Food Chem. 2006, 54: 9140-9144. 10.1021/jf061830k.PubMedView Article
- Butrón A, Malvar RA, Velasco P, Vales MI, Ordás A: Combining abilities for maize stem antibiosis, yield loss, and yield under infestation and no infestation with pink stem borer attack. Crop Sci. 1999, 39: 691-696. 10.2135/cropsci1999.0011183X003900020015x.View Article
- Butrón A, Malvar RA, Velasco P, Cartea ME, Ordás A: Combining abilities and reciprocal effects for maize ear resistance to pink stem borer. Maydica. 1998, 43: 117-122.
- Velasco P, Soengas P, Revilla P, Ordás A, Malvar RA: Mean generation analysis of damage caused by Sesamia nonagrioides (Lepidoptera: Noctuidae) and Ostrinia nubilalis (Lepidoptera: Crambidae) in sweet corn ears. J Econ Entomol. 2004, 97: 120-126. 10.1603/0022-0493-97.1.120.PubMedView Article
- Morse S, Wratten SD, Edwards PJ, Niemeyer HM: Changes in the hydroxamic acid content of maize leaves with time and after artificial damage; implications for insect attack. Ann Appl Biol. 1991, 119: 239-249. 10.1111/j.1744-7348.1991.tb04862.x.View Article
- Guthrie WD, Wilson RL, Coats JR, Robbins JC, Tseng CT, Jarvis JL, Russell WA: European corn borer (Lepidoptera: Pyralidae) leaf-feeding resistance and DIMBOA content in inbred lines of dent maize grown under field versus greenhouse conditions. J Econ Entomol. 1986, 79: 1492-1496.View Article
- Barry D, Alfaro D, Darrah LL: Relation of European corn borer (Lepidoptera: Pyralidae) leaf feeding resistance and DIMBOA content in maize. Environ Entomol. 1994, 23: 177-182.View Article
- Cambier V, Hance T, Hoffmann E: Variation of DIMBOA and related compounds content in relation to the age and plant organ in maize. Phytochemistry. 2000, 53: 223-229. 10.1016/S0031-9422(99)00498-7.PubMedView Article
- Grabber JH, Quideau S, Ralph J: p-Coumaroylated syringyl units in maize lignin; implications for β-ether cleavage by thioacidolysis. Phytochemistry. 1996, 43: 1189-1194. 10.1016/S0031-9422(96)00431-1.View Article
- Lu F, Ralph J: Detection and determination of p-coumaroylated units in lignins. J Agric Food Chem. 1999, 47: 1988-1992. 10.1021/jf981140j.PubMedView Article
- Morrison TA, Jung HJG, Buxton DR, Hatfield RD: Cell-wall composition of maize internodes of varying maturity. Crop Sci. 1998, 38: 455-460. 10.2135/cropsci1998.0011183X003800020031x.View Article
- Vailhe MAB, Provan GJ, Scobbie L, Chesson A, Maillot MP, Cornu A, Besle JM: Effect of phenolic structures on the degradability of cell walls isolated from newly extended apical internode of tall fescue (Festuca arundinacea Schreb.). J Agric Food Chem. 2000, 48: 618-623. 10.1021/jf9906329.PubMedView Article
- Migne C, Prensier G, Utille JP, Angibeaud P, Cornu A, Grenet E: Immunocytochemical localisation of p-coumaric acid and feruloyl-arabinose in the cell walls of maize stem. J Sci Food Agric. 1998, 78: 373-381. 10.1002/(SICI)1097-0010(199811)78:3<373::AID-JSFA129>3.0.CO;2-I.View Article
- MacAdam JW, Grabber JH: Relationship of growth cessation with the formation of diferulate cross-links and p-coumaroylated lignins in tall fescue. Planta. 2002, 215: 785-793. 10.1007/s00425-002-0812-7.PubMedView Article
- Grabber JH, Ralph J, Lapierre C, Barrière Y: Genetic and molecular basis of grass cell wall degradability. I. Lignin-cell wall matrix interactions. Comptes Rendus Biol. 2004, 327: 455-465. 10.1016/j.crvi.2004.02.009.View Article
- Kamisaka S, Takeda S, Takahashi K, Shibata K: Diferulic and ferulic acids in the cell wall of oat coleoptiles--their relationships to mechanical properties of the cell wall. Physiol Plant. 1990, 78: 1-7. 10.1111/j.1399-3054.1990.tb08706.x.View Article
- Schopfer P: Hydrogen peroxide-mediated cell-wall stiffening in vitro in maize coleoptiles. Planta. 1996, 199: 43-49.View Article
- Hatfield RD, Wilson JR, Mertens DR: Composition of cell walls isolated from cell types of grain sorghum stems. J Sci Food Agric. 1999, 79: 891-899. 10.1002/(SICI)1097-0010(19990501)79:6<891::AID-JSFA304>3.0.CO;2-#.View Article
- Grabber JH, Ralph J, Hatfield RD: Model studies of ferulate-coniferyl alcohol cross-product formation in primary maize walls: Implications for lignification in grasses. J Agric Food Chem. 2002, 50: 6008-6016. 10.1021/jf0205312.PubMedView Article
- Bily AC, Reid LM, Taylor JH, Johnston D, Malouin C, Burt AJ, Bakan B, Regnault-Roger C, Pauls KP, Arnason JT, Philogene BJR: Dehydrodimers of ferulic acid in maize grain pericarp and aleurone: Resistance factors to Fusarium graminearum. Phytopathology. 2003, 93: 712-719. 10.1094/PHYTO.2003.93.6.712.PubMedView Article
- Barros J, Malvar RA, Jung HG, Santiago R: Cell wall composition as a maize defense mechanism against corn borers. Phytochemistry. 2011, 72: 365-371. 10.1016/j.phytochem.2011.01.004.View Article
- Jung HG, Casler MD: Maize stem tissues: Cell wall concentration and composition during development. Crop Sci. 2006, 46: 1793-1800. 10.2135/cropsci2005.02-0085.View Article
- Hatfield RD, Marita JM, Frost K: Characterization of p-coumarate accumulation, p-coumaroyl transferase, and cell wall changes during the development of corn stems. J Sci Food Agric. 2008, 88: 2529-2537. 10.1002/jsfa.3376.View Article
- Scobbie L, Russell W, Provan GJ, Chesson A: The newly extended maize internodes: a model for the study of secondary cell wall formation and consequences for digestibility. J Sci Food Agric. 1993, 61: 217-225. 10.1002/jsfa.2740610213.View Article
- Klenke JR, Russell WA, Guthrie WD: Recurrent selection for resistance to European corn borer in a corn synthetic and correlated effects on agronomic traits. Crop Sci. 1986, 26: 864-868. 10.2135/cropsci1986.0011183X002600050005x.View Article
- Coors JG: Nutritional factors related to European corn borer resistance inmaize. In Proceedings of the 42nd Annual Corn and Sorghum ResearchConference. Edited by: Wilkinson D. American Seed Trade Association,Washington DC; 1988:79-88.
- Buendgen MR, Coors JG, Grombacher AW, Russell WA: European corn borer resistance and cell wall composition of three maize populations. Crop Sci. 1990, 30: 505-510. 10.2135/cropsci1990.0011183X003000030005x.View Article
- Azuma T, Okita N, Nanmori T, Yasuda T: Changes in cell wall-bound phenolic acids in the internodes of submerged floating rice. Plant Prod Sci. 2005, 8: 441-446. 10.1626/pps.8.441.View Article
- Azuma T, Okita N, Nanmori T, Yasuda T: Relationship between the deposition of phenolic acids in the cell walls and cessation of rapid growth in internodes of floating rice. Plant Prod Sci. 2005, 8: 447-453. 10.1626/pps.8.447.View Article
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