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  • Author or Editor: Tao Xie x
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Plants growing in salt-affected soils may have retarded growth and inhibited or altered metabolic processes. This study aims at investigating the impact of subsurface soil salinity on root growth and metabolic processes in perennial ryegrass (Lolium perenne). The seeds of perennial ryegrass (cv. Quick Start II) were planted in polyvinyl chloride (PVC) tubes (10 cm diameter × 42 cm long) for 2 months. The experiment consisted of three treatments: 1) control, 40 cm filled with sand–peat mixture (7 sand : 3 peat wt/wt); 2) T20, a 20-cm-deep layer of saline soil covered with a 20-cm-deep layer of sand–peat mixture; and 3) T30, a 30-cm-deep layer of saline soil covered with a 10-cm-deep layer of sand–peat mixture. Our study showed that soil salinity at the subsurface inhibited the growth of perennial ryegrass roots. Compared with the control, the root activity in saline soil layer decreased, whereas it remained high in the mixture-soil zone. The content of amino acids in the roots obtained from the surface soil (0–10 cm) in T30 was greater than that in both the T20 and the control regimes. The content of soluble sugars in the roots went up with the decrease of the depth of sand–peat mixture. The increased root activity and free amino acids content in the roots sampled from the upper soil layers coupled with the increased soluble sugars in the roots subjected to soil salinity stress in the bottom soil layer represents some adaptive responses and regulative mechanisms in perennial ryegrass.

Free access

In the actual cultivation process, blind fertilizer application was widespread, resulting in a serious decline in the yield of Pseudostellaria heterophylla. We used the 3414 fertilizer experiment design to study the effects of combined Boron (B), Molybdenum (Mo), and Copper (Cu) on the growth indexes, diurnal changes of photosynthesis, and rapid fluorescence induction dynamics in P. heterophylla. Our results show that the optimal combination of B, Mo, and Cu simultaneously promoted the growth of underground and aboveground parts, and significantly improved the quality of single root tuber and yield per unit area. The best combination was treatment 9 (T9 = B, 1 g/L; Mo, 0.08 g/L; Cu, 0.05 g/L), and resulted in a 35.1% increase in yield per unit area compared with the control group (T1). Although the optimal combined application of microfertilizers did not change the bimodal trend of diurnal variation of photosynthesis, it effectively increased the daily average, peak, and valley values of the photosynthetic rate by alleviating the nonstomatal limitation and the photosynthetic midday depression. Pseudostellaria heterophylla leaves showed greater photochemical activity and less photoinhibition of photosystem II in T9. Major effects were that it helped protect the activity of the oxygen-evolving complex to reduce the oxidative damage of chloroplasts and prevent the dissociation of thylakoid. The microfertilizer application also enhanced the electron receiving ability of the QB and plastoquinone (PQ) electronic pools, thereby increasing the ability of electron transfer from QA to QB. The number of reaction centers per unit area was promoted notably by the fertilization treatment.

Open Access

In natural conditions, it takes more than 3 years to complete the Ananas juvenile phase, and another 2 years for adult vegetative growth of the plantlet from in vitro buds. Ethylene has often been used to shorten the juvenile and vegetative phases to produce earlier flowering. It is important to induce in vitro flowering of Ananas plants to understand the flowering mechanism more completely, which is also related to flower organ differentiation and development as well as the pineapple fruit eye development. In this study, Murashige and Skoog (MS) basal medium was used to select the best combination for adventitious bud induction from the callus of Ananas bracteatus var. tricolor (A. tricolor). Flower induction from the callus was studied using 6-benzyladenine (6-BA) and 1-naphthylacetic acid (NAA) at four different concentrations (0, 1.0, 2.0, and 3.0 mg⋅L–1). Our results showed that when MS was added with 3 mg⋅L–1 6-BA and 2 mg⋅L–1 NAA under 2000 μmol⋅m–2⋅s–1 of light for 16 hours per day at a temperature of 20 °C, the callus of A. tricolor grew quickly, and adventitious buds were induced. After more than four successive subcultures (at day 80), differentiation of flower buds was observed on the aging callus tissue before a complete floral organ developed. This research could be used for the flowering regulation of Ananas plants in the future. Inducing flowers directly from the callus has important scientific significance for the differentiation and morphogenesis of Ananas plants.

Open Access