Effect of Phosphorus and Arbuscular Mycorrhizal Fungi (AMF) Inoculation on Growth and Productivity of Maize (Zea mays L.) in a Tropical Ferralsol

The experimental soil was collected on an old maize farm located in the Luano area, Lubumbashi, DR Congo (−11,60233°S; 27,50897°E to −11,60234°S; 27,50908°E, altitude 1200 m asl). It is a red and deep sandy clay loam soil whose available laboratory data are summarized in Table 1.

Spores were extracted from a 100 g sample of soil by using the standard wet sieving and decantation method (45 µm and 1 mm mesh) followed by counting using an Olympus SZ61 stereo microscope according to Walker et al. (2006). AMF morpho-species identification was done under microscope of 40 and 100 X on three to five spores of similar morphology, assembled on a strip in the polyvinyl lacto-glycerol. Spore shapes, their colors and sizes, occurrence or not of pedicels, number of spore wall layers and wall surface ornamentation were main criteria used for identification (Oehl et al. 2011a; Trappe 1992). The mean density was of 150 spores 100 g⁻¹ soil with predominance of genus belonging to Gigaspora, Acaulospora and Archaeospora. The maize variety “Katanga” was used as test crop in the experiment. This local variety blooms from 60 to 65 days after sowing and presents a maximal height of 191 cm depending on growing conditions. Grains are white and have a weight nearing 168 ± 25 g cob⁻¹, i.e. 380 g per 1000 grains. Before sowing, the grains were disinfected with sodium hypochlorite (1%) during 5 min, then with the alcohol (75%) and rinsed with tap water afterwards.

The inoculum was obtained from red Sorghum (Sorghum vulgare L.) cultivated in pots, to have high AMF spore density and root colonization; as described by Mukerji et al. (2002), and Selvaraj and Chellappan (2006). The pots had 28 cm diameter (0.4396 m²) and depth 28 cm. Sorghum was sown in a litter substrate at 25 to 30 plants per pot. At 3.5 months later, root and AMF spores from Sorghum crop were extracted and used as inoculum. The litter substrate was collected from Miombo woodland dominated by Brachystegia and Julbernardia. The choice of this substrate is justified by its high porosity. This is a reasonable method of AMF inoculum production contrary to the high cost of commercial inoculum and their scarcity in the Lubumbashi region. The inoculum produced had a spore mean density of 250. 100 g⁻¹ of substrate and 10 g of colonized roots at the frequency of 70 to 80%. Acaulospora and Ambispora were the most dominant genera.

Di-ammonium phosphate (DAP—18-46-0) and potassium chloride (KCl—60% K₂O) were used as basal fertilizers and urea (46% N) was added as top fertilizer to cover the N crop demand. The K and N were maintained constant while P was added as DAP in 3 doses: 60 kg P₂O₅ ha⁻¹, which is the normal dose, recommended for maize in tropical conditions (Raemaekers 2001), 30 kg P₂O₅ ha⁻¹ as the half of recommended dose and 0 kg P₂O₅ ha⁻¹ as the control.

The experiment was conducted in pots of 28 cm diameter and 28 cm depth in a factorial design 2 × 3 with 5 replications. Two levels of AMF inoculation and 3 levels of phosphorus application were used as treatments:

The maize plants were watered during the 3 first months (September to November 2017), every 2 days with 1 liter of tap water per pot having 1 plant each. The experiment took place in a shade house from September 2017 to January 2018. The last two months (December 2017 and January 2018) of experiment were rainy. During the experimental period, the prevailing temperature varied between 15 to 32 °C and a mean relative humidity of 79% and 12 h sunshine.

The effect of inoculation and P application on maize was significant for the number of days before flowering. Plants that were inoculated with AMF flowered earlier than non-inoculated plants (Table 2). The combination of inoculation with P application increased maize flowering precocity while control plants were the latest to flowering. The effect of inoculation was not significant for plant height, number of leaves and chlorophyll content while, P application significantly increased the number of leaves per plant and leaves chlorophyll content. The effect of AMF inoculation and P application was significant on maize root colonization. Root colonization was more important on inoculated plants than on plants that were not inoculated. For non-inoculated plants, increasing P application proportionally increased their ability to be colonized by soil indigenous mycorrhiza. However, for inoculated plants, the maize which did not receive any P showed the highest rate of root colonization, followed by those that received 60 kg P₂O₅ ha⁻¹ and the one that received 30 kg P₂O₅ ha⁻¹ had the lower rate of colonization.

At 60 days after sowing, the most common mycorrhizae structures on all treatments were intra or extra-radical hyphae. Vesicles were found only on inoculated plants on which there was no P application and those that received 30 kg P₂O₅ ha⁻¹. In the same way, arbuscles were found only on plants that were inoculated and did not receive any P application (Table 3).

Yield results (Table 4) shows that the AMF treatments had a significant effect on yield parameters, except cob height insertion and cob length, which varied more with P treatments than with AMF inoculum. The height at the cob insertion, cob weight, cob length, cob diameter and the number of seed rows varied more with P than with AMF inoculum applied. Obtained averages under P influence were double or threefold higher than the control and AMF treatment alone. Cobs were then inserted between 73 and 103 cm height for 30 or 60 kg P₂O₅ ha⁻¹, whereas without P cob insertion was observed between 30 cm (for the control) and 40 cm (for inocula alone). The highest cob weight was obtained on treatments with 60 kg P₂O₅ ha⁻¹ with or without inocula, i.e. 145 to 146 g. The length of these cobs measured on average 15 cm. A fertilization with 30 kg P₂O₅ ha⁻¹ gave cobs weighing 79 to 107 g with a length of 12 to 13 cm. The lowest cob weight was obtained on inocula alone and the control, respectively 4 to 13 g, and a cob length of 6 to 7 cm. The cob diameter was the same for 30 kg and 60 kg P₂O₅ ha⁻¹, being 42 to 45 mm. The AMF only treatment had 24 mm of cob diameter, double compared to the control. Cobs from the 30 and 60 kg P₂O₅ ha⁻¹ treatments without inoculum contained 13 seed rows, whereas they were empty for the control treatment. AMF combined to 60 kg P ha⁻¹ had 13 seed rows followed by AMF combined with 30 kg P₂O₅ ha⁻¹ with 11 seed rows, cobs from the AMF only treatment had 7 rows. The comparison of the treatments 30 kg P₂O₅ ha⁻¹ with AMF and 30 kg P₂O₅ ha⁻¹ without AMF considering grain weight, grain yield and grain phosphorus content parameters shows better the influence of AMF on P uptake. The addition of 30 kg P₂O₅ ha⁻¹ produced 59 g of grains per cob, the AMF inoculation offer 12 g of grains per cob, whereas the control treatment had cobs without grains. The results found indicate that the AMF treatments had a highly significant effect on P uptake. The P treatments and their interaction with AMF also had a strong effect. Grains from inoculated plants had a double content of phosphorus in comparison with un-inoculated plants. The highest phosphorus content in maize grains was 1.41 mg phosphorus g⁻¹ obtained on AMF inoculation alone followed by inoculum +60 kg of P₂O₅ ha⁻¹ and inoculum +30 kg of P₂O₅ ha⁻¹.

Plaxton and Tran (2011) and Stigter and Plaxton (2015) have shown the phosphorus implication in plant physiology already which lead to the amine acid and protein constitution; and its deficiency in the soil can reduce severely the grain’s production. AMF contribution to maize growth was strongly observed on male precocity on the plants inoculated and fertilized (59 and 62 days after sowing) in comparison to the control (93 days after sowing). Inoculating crops conferred an advance of 30 days duration at flowering, which is explained by P acquiring which is the first benefit of the symbiosis. Oehl et al. (2011b) demonstrated that for plants inoculated with AMF and fertilized, flowering occurred earlier compared to those that were not inoculated. The same average was obtained for plant height, leaves number and chlorophyll rate in leaves especially on treatments inoculated and fertilized with 30 or 60 kg P₂O₅ ha⁻¹. This joins the allegations of Davies and Linderman (1990) and Aguegue et al. (2017) showing that the only micro-doses of chemical fertilizers (half of the crop demand) are sufficient to promote plant growth when AMF have been applied. Munir et al. (2003) also showed that the addition of phosphorus decreases the mycorrhizal symbiosis because the plant’s growth depends on the chemical fertilizer.

Root colonization was very intense (73%) on inoculated plants without P addition and less intense (25%) on control plants, the difference being 48%. The inoculated plants were more colonized (57%) than un-inoculated plants, which had a mean of 40% root colonization rate. This root colonization rate can be explained by AMF previously existing in the experimental soil. As shown in the methodology, the experimental soil harboured 150 mycorrhizae spores per 100 g soil, a spore density sufficient to colonize the roots of a given crop. This is sufficiently proving the ubiquist character of AMF in soils as underlined by Liu et al. (2016), Cozzolino et al. (2013) and Ambrosini et al. (2015). Although most soils contain AMF, inoculation is still very important because it provides new AMF propagules capable of colonizing the newly established crop as quickly as possible. While assessing the root colonization, fungal hyphae as primary structure of symbiosis were present in all treatments. However, vesicles were only found in treatments with inoculum alone or combined to the small dose of 30 kg P₂O₅ ha⁻¹. The dose of 60 kg P₂O₅ ha⁻¹ seemed to compromise the vesicle formation on roots. The highest dose of P₂O₅ (60 kg ha⁻¹) reduces fungi activity in the root and compromises arbuscles or vesicles formation, as was also observed by Braunberger et al. (1991).

The height at the cob insertion, the weight of cobs, their length and diameter were not directly influenced by AMF inoculum but rather by phosphorus applications. Fertilization with 30 kg P₂O₅ ha⁻¹ seemed to be sufficient to improve the nutritional status of the Ferralsol used as substrate for this experiment, compared to the dose of 60 kg P₂O₅ ha⁻¹ which is low cost effectiveness. These results are nearing those found by Aguegue et al. (2017) in Ferralsol in southern Benin, indicating that Glomus cubens species combined to a half dose of chemical fertilizers of NPK (7.5 P₂O₅ kg ha⁻¹) allow to get an equivalent production of maize to that obtained using the recommended dose of NPK (15 P₂O₅ kg ha⁻¹) alone. The AMF inoculum alone given cobs well filled with grains, thus much better than plants of the control (without phosphorus neither AMF inoculum) given cobs without grains. The AMF showed P efficiency in the experimental soil; this induced the fruition. Several researchers such as Pandey et al. (2005) and Huang et al. (2017) have demonstrated the mycorrhiza efficiency in plant production. Grain P concentration increased with both inoculation and P fertilization. The highest P concentration was obtained with the treatment of inocula alone. This proves that mycorrhizae can be used as biofertilizers as confirmed by Miransari (2011) and Zhang et al. (2017), and that these fungi enhance chemical P uptake through fungal hyphae. Results of this study showed that the grain P concentration was 2 to 3 times lower than the standard P concentration (210 mg 100 g⁻¹) contained in maize grains (Messiaen and Fakorede 2006). This gap could be explained by root concentration in the pot experiment culture that uptakes only mineral fertilizers than field experiments which benefit also the soil minerals.