Root anatomy and spatial pattern of radial oxygen loss of eight true mangrove species

The root anatomical features of eight mangrove species in Hong Kong were similar, with large aerenchymal lacunae in the cortex for efficient internal oxygen transfer and an outer barrier consisting of an epidermis and hypodermis to prevent oxygen loss. The spatial pattern of radial oxygen loss (ROL) was also comparable, with more oxygen lost from the tip than that from the basal and mature zones. However, the aerenchyma in the cortex, the barrier and the extent of ROL varied along the root and these variations were species-specific. The whole root of Avicennia marina (Forsk.) Vierh., Acanthus ilicifolius L., Aegiceras corniculatum (Linn.) Blanco, Kandelia obovata Sheue, Liu & Yong (previously known as Kandelia candel (L.) Druce) and Heriteria littoralis Dryand. ex W. Ait. had schizogenous aerenchyma, while the aerenchyma of Lumnitzera racemosa Willd. and Bruguiera gymnorrhiza (L.) Poir changed from schizogenous in the root tip to lysigenous in the other parts of the root. Excoecaria agallocha L. displayed the opposite pattern, from lysigenous in the root tip to schizogenous further up. Among the eight species, the roots of A. marina and A. ilicifolius had the largest areas of aerenchyma air spaces, but they also had the weakest barrier. On the other hand, H. littoralis had the least longitudinal oxygen transfer because of its smaller area of aerenchyma air spaces in its root. The tolerance of mangrove species to waterlogged soil followed the order of A. marina (most foreshore species) > A. ilicifolius > K. obovata > A. corniculatum > B. gymnorrhiza > E. agallocha > L. racemosa > H. littoralis (most landward species), which is related to their anatomical features of root cortex, epidermis and hypodermis.     

The influence of oxygen deficiency on ethylene synthesis, 1-aminocyclopropane-1-carboxylic acid levels and aerenchyma formation in roots of Zea mays

The relationship between ethylene production, 1-aminocyclopropane-l-carboxylic acid (ACC) concentration and aerenchyma formation (ethylene-promoted cavitation of the cortex) was studied using nodal roots of maize (Zea mays L. cv. LG11) subjected to various O₂ treatments. Ethylene evolution was 7–8 fold faster in roots grown at 3 kPa O₂ than in those from aerated solution (21 kPa O₂), and transferring roots from aerated solution to 3 kPa O₂ enhanced ethylene synthesis within less than 2 h. Ethylene production and ACC accumulation were closely correlated in different zones of hypoxic roots, regardless of whether O₂ was furnished to the roots through aerenchyma or external solution. Both ethylene production and ACC concentrations (fresh weight basis) were more than 10-fold greater in the distal 0–10 mm than in the fully expanded zone of roots at 3 kPa O₂. Aerenchyma formation occurred in the apical 20 mm of these roots. Roots transferred from air to anoxia accumulated less than 0. 1 nmol ACC (mg protein)^-1 for the first 1.75 h; no ethylene was produced in this time. The subsequent rise in ACC levels shows that ACC can reach high concentrations even in the absence of O₂, presumably due to a de-repression of ACC synthase. The hypothesis was therefore tested that anoxia in the apical region of the root caused enhanced synthesis of ACC, which was transported to more mature regions (10–20 mm behind the apex), where ethylene could be produced and aerenchyma formation stimulated. Surprisingly, exposure of intact root tips to anoxia inhibited aerenchyma formation in the mature root axis. High osmotic pressures around the growing region or excision of apices had the same effect, demonstrating that a growing apex is required for high rates of aerenchyma formation in the adjacent tissue.     

An overview of oxygen transport in plants: diffusion and convection

The movement of gases within plants is crucial for species that live in flood-prone areas with limited soil oxygen. These plants adapt to hypoxia/anoxia not by using oxygen more efficiently, but by ensuring a steady oxygen supply to their cells. Wetland plants typically form gas-filled spaces (aerenchyma) in their tissues, providing a low-resistance pathway for gas movement between shoots and roots, especially when the shoots are above water, and the roots are submerged. Oxygen movement in plant roots is mainly through diffusion. However, in certain species, such as emergent and floating-leaved plants, pressurized flows can also facilitate the movement of gases within their stems and rhizomes. Three types of pressurized (convective) flows have been identified: humidity-induced pressurization (positive pressure), thermal osmosis (positive pressure with air flow against the heat gradient), and venturi-induced suction (negative pressure) caused by wind passing over broken culms. A clear diel variation in pressurized flows exists, with higher pressures and flows during the day and negligible pressures and flows during the night. This article discusses some key aspects of these mechanisms for oxygen movement.     

Maintenance of 32P uptake and transport in Pinus serotina seedlings under hypoxic growth conditions

In the present study, we examined the effects of long- and short-term hypoxia on net uptake and transport of phosphorus to shoots of pond pine (Pinus serotina Michx.), a moderately flood-tolerant southern pine, and the influence aerenchyma formation might have in maintenance of P uptake and transport. Seedlings were grown under aerobic (250 μM O₂) or hypoxic (≤50 μM O₂) solution conditions for 5.3 weeks in continuously flowing solution culture containing 100 μM P. Intact seedlings were then labeled with ³²P for up to 24 h to determine how short- and long-term hypoxic solution conditions affected rates of unidirectional influx and the accumulation of ³²P in roots and shoots. Seedlings in the long-term hypoxic treatment were grown for 5.3 weeks in hypoxic solution and also labeled in hypoxic uptake solution. The short-term hypoxic treatments included a 24-h hypoxic pretreatment followed by time in labeled hypoxic uptake solution for seedlings grown under aerobic or hypoxic conditions; in the latter case, diffusion of atmospheric O₂ entry into stem and root collar lenticels was blocked, thus removing any influence that aerenchyma formation might have had on enhancing O₂ concentrations of root tissue. Although unidirectional influx rates of ³²P in roots of seedlings grown under long-term hypoxic conditions were 1.4 times those of aerobically grown seedlings, accumulation of ³²P in roots was similar after 24 h in labeled uptake solution. These results suggest that ³²P efflux was also higher under hypoxic conditions. Higher shoot/root fresh weight ratios and lower shoot P concentrations in seedlings grown under hypoxic solution conditions suggest that the “shoot P demand” per unit root should be high. Yet accumulation of ³²P in shoots was reduced by 50% after 24 h in hypoxic uptake solution. Both short-term hypoxic treatments decreased accumulation of ³²P in roots by more than 50%. Short-term hypoxia decreased shoot accumulation in seedlings grown under aerobic and hypoxic conditions by 84 and 50%. respectively. Short- and long-term hypoxic conditions increased the percentage of root ³²P in the nucleic acid and chelated-P pools, resulting in a significantly smaller percentage of ³²P in the soluble inorganic phosphate (p_i) pool, the pool available for transport to the shoot. However, a reduction in pool size or in labeling of the pool available for transport cannot fully account for the large reduction in accumulation of ³²P in shoots, particularly in the short-term hypoxic treatment of aerobically grown seedlings. Our results suggest that both influx and transport of ³²P to shoots of pond pine seedlings are O₂-dependent processes, and that the transport of ³²P to shoots may be more sensitive to hypoxic solution conditions than influx at the cortical and epidermal plasmalemma, with aerenchyma formation supporting a substantial amount of both ³²P uptake and transport.     

Lacunal allocation and gas transport capacity in the salt marsh grass Spartina alterniflora

Summary Lacunal allocation as the fraction of the total cross sectional area of leaves, stem bases, rhizomes, and roots was determined in both tall and short growth forms of Spartina alterniflora collected from natural monospecific stands. The results indicate that in both growth forms lacunal allocation is greater in stem bases and rhizomes than in leaves and roots and that tall form plants allocate more of their stem and rhizome to lacunae than short form plants.Measurements made in natural stands of Spartina alterniflora suggest that total lacunal area of the stem base increases with increasing stem diameter and that stem diameter increases with increasing plant height and above-ground biomass. However, the fraction of cross section allocated to lacunae was relatively constant and increased only with the formation of a central lacuna.Experimental manipulations of surface and subsurface water exchange were carried out to test the influence of flooding regime on aerenchyma formation. No significant differences in lacunal allocation were detected between plants grown in flooded (reduced) and drained (oxidized) sediments in either laboratory or field experiments. While aerenchyma formation in Spartina alterniflora may be an adaptation to soil waterlogging/anoxia, our results suggest that lacunal formation is maximized as a normal part of development with allocation constrained structurally by the size of plants in highly organic New England and Mid-Atlantic marshes.The cross sectional area of aerenchyma for gas transport was found to be related to the growth of Spartina alterniflora with stands of short form Spartina alterniflora exhibiting a lower specific gas transport capacity (lacunal area per unit below ground biomass) than tall form plants despite having a similar below-ground biomass supported by a 10 fold higher culm density. The increased specific gas transport capacity in tall vs. short plants may provide a new mechanism to explain the better aeration, higher nutrient uptake rates and lower frequency of anaerobic respiration in roots of tall vs. short Spartina alterniflora.     

A linkage map of maize × teosinte <Emphasis Type="Italic">Zea luxurians</Emphasis> and identification of QTLs controlling root aerenchyma formation

The objectives of this study were to construct a linkage map and identify quantitative trait loci (QTLs) controlling root aerenchyma formation in drained soil conditions using 195 F₂ individuals derived from a cross between maize inbred line B73 × teosinte Zea luxurians. A 107 SSR marker based map covering 1,331 cM across all ten chromosomes was developed. One significant difference between the parents utilized in the study was that under non-flooding conditions, B73 exhibits a minor capacity to develop root aerenchyma, whereas Z. luxurians exhibits a high tendency to form aerenchyma. Linkage analysis indicated segregation distortion regions on chromosomes 2, 4 and 8, and severe recombination suppression on the long arm of chromosome 4. Multiple interval mapping analysis suggests that five QTLs for aerenchyma formation in non-flooding conditions are located on chromosomes 2, 3, 5, 9 and 10, and these explained 36.3% of the total phenotyphic variance. The Z. luxurians alleles in all five QTLs increased the capacity to form aerenchyma and the locations of these QTLs did not overlap those previously identified in the teosinte Z. nicaraguensis. By transferring aerenchyma-forming QTLs from both Z. luxurians and Z. nicaraguensis, it may be possible to pyramid these genes and develop a maize line with exceptional aerenchyma formation and a high level of tolerance to flooding conditions.     

Adaptations of Central Amazon Tree Species to Prolonged Flooding: Root Morphology and Leaf Longevity

Abstract: Várzeas are species-rich forest communities of the Central Amazon floodplains, inhabited by highly adapted tree species that can withstand long flooding periods. The leaf shedding behaviour and morphological traits that may contribute to adaptation to low oxygen levels were studied at the Ilha de Marchantaria on the lower Solimoes-Amazonas river, Brazil, and in greenhouse experiments with cuttings of six tree species typical of the Amazon floodplain. Comparison of deciduousness in situ revealed that four of the species under investigation, Salix martiana , Tabernaemontana juruana , Laetia corymbulosa and Pouteria glomerata , are able to maintain their leaf system during the aquatic period. Adventitious roots were formed by S. martiana and T. juruana , but anatomical characteristics differed between the species. Whereas S. martiana developed lysigenous aerenchyma in its roots during aerobic and anaerobic growth, only small intercellular spaces of schizogenous origin were formed in the root cortex of T. juruana . Similar to the latter species, such spaces were constitutively formed in the deciduous species Crateva benthami and Vitex cymosa . Suberin deposits were observed in tangential and radial cell walls of the hypodermis of roots from T. juruana , L. corymbulosa and P. glomerata . Suberin deposits were less pronounced in roots of S. martiana and absent in V. cymosa and C. benthami . The data show that different, almost contrasting, survival mechanisms have evolved in roots of plants with similar life forms in the same habitat. The results further suggest that the morphological traits of the investigated trees are causally linked with the in situ leaf shedding behaviour.     

Cellular Dimorphism in the Maize Root Cortex: Involvement of Microtubules,Ethylene and Gibberellin in the Differentiation of Cellular Behaviour in Postmitotic Growth Zones

Detailed morphometric analysis of cell shapes and an immunofluorescent study of microtubules were carried out on primary roots of Zea mays L. Two types of cells were found to be formed within the postmitotic isodiametric growth (PIG) region of the root cortex that were differentially responsive to low level of exogenous ethylene. The innermost and central cell rows of the cortex were sensitive to ethylene treatment and showed a disturbed distribution of cortical microtubules (CMTs) as well as changed polarity of cell growth, whereas the 2–3 outermost cell rows were less sensitive in this respect. This suggests that post-mitotic cells of the inner cortex are specific targets for ethylene action. These properties of the inner cortex are compatible with its cells being involved in the formation of aerenchyma; they may also favour root growth in compacted soil. By contrast, the specific properties of the outer cortex indicate that this tissue domain is necessary for the gaseous impermeability and the mechanical strengthening of subjacent aerenchymatous cortex, especially in the mature region of the root. Ethylene affected neither the pattern of cortical cell expansion in the meristem nor the position of the PIG region with respect to the root tip. This contrasts with gibberellin-deficiency which affected these parameters in both parts of the cortex. These observations indicate a fundamental difference between the role of these two phytohormones in the morphogenesis and development of maize roots.     

Mycorrhizal colonisation in plants from intermittent aquatic habitats

Several plant species with amphibious characteristics from intermittent aquatic habitats were examined for colonisation with arbuscular mycorrhizal fungi (AM), dark septate endophytes (DSE) and the ratio of aerenchyma in root tissue. We studied submerged specimens of Alisma plantago-aquatica, Mentha aquatica, Myosotis scorpioides, Oenanthe fistulosa, Gratiola officinalis, Glyceria fluitans, Sium latifolium and Teucrium scordium. In the first four, we also examined the emerged growth forms, which were grown under experimental conditions. Roots of all species were mycorrhizal and showed AM and DSE colonisation. The results suggest that AM colonisation may also be abundant in plants of aquatic environment. Arbuscules were not found in submerged specimens of M. aquatica, O. fistulosa and S. latifolium. The AM colonisation was generally higher in emerged specimens as compared to submerged ones. The aerenchyma ratio in root cross-sections ranged from 10 to 50% and in most cases did not differ between submerged and emerged specimens. No clear relationship between AM colonisation and aerenchyma ratio was recognized, while a positive correlation between AM and plant available phosphorous was established.