P-deficient Plants Research Articles

Leaf Phosphate Status, Photosynthesis, and Carbon Partitioning in Sugar Beet (IV. Changes with Time Following Increased Supply of Phosphate to Low-Phosphate Plants).

Changes in photosynthesis, carbon partitioning, and growth following resupply of orthophosphate (Pi) to moderately P-deficient plants (low-P) were determined for sugar beets (Beta vulgaris L. cv F58-554H1) cultured hydroponically in growth chambers. One set of plants was supplied with 1.0 mM Pi in half-strength Hoagland solution (control plants), and a second set (low-P plants) was supplied with 0.05 mM Pi. At the end of 2 weeks, the low-P plants were resupplied with 1.0 mM Pi. Low-P plants rapidly accumulated large amounts of Pi, and the photosynthesis rate increased to control values within 4 to 6 h. The rate of photosynthesis appeared to be controlled by ribulose-1,5-bisphosphate (RuBP); low P reduced photosynthesis and RuBP levels, and P resupply increased photosynthesis and RuBP in a manner parallel with time. Low-P treatment reduced adenylate levels substantially but not nicotinamide nucleotides; adenylate levels recovered to control values over 3 to 6 h. With low P, more photosynthate is allocated to non-P carbon compounds (e.g. starch, sucrose) than to sugar phosphates. When P is resupplied, sugar phosphates increase as starch and sucrose pools decrease; this increase in leaf (chloroplast) sugar phosphates was most likely responsible for the increases in RuBP and photosynthesis and may have increased adenylate levels (through enhanced levels of ribose-5-phosphate).

Influence of Species of Vesicular-Arbuscular Mycorrhizal Fungi and Phosphorus Nutrition on Growth, Development, and Mineral Nutrition of Potato (Solanum tuberosum L.).

Growth, development, and mineral physiology of potato (Solanum tuberosum L.) plants in response to infection by three species of vesicular-arbuscular mycorrhizal (VAM) fungi and different levels of P nutrition were characterized. P deficiency in no-P and low-P (0.5 mM) nonmycorrhizal plants developed between 28 and 84 d after planting. By 84 d after planting, P deficiency decreased plant relative growth rate such that no-P and low-P plants had, respectively, 65 and 45% less dry mass and 76 and 55% less total P than plants grown with high P (2.5 mM). A severe reduction in leaf area was also evident, because P deficiency induced a restriction of lateral bud growth and leaf expansion and, also, decreased the relative plant allocation of dry matter to leaf growth. Root growth was less influenced by P deficiency than either leaf or stem growth. Moreover, P-deficient plants accumulated a higher proportion of total available P than high-P plants, indicating that P stress had enhanced root efficiency of P acquisition. Plant P deficiency did not alter the shoot concentration of N, K, Mg, or Fe; however, the total accumulation of these mineral nutrients in shoots of P-stressed plants was substantially less than that of high-P plants. P uptake by roots was enhanced by each of the VAM symbionts by 56 d after planting and at all levels of abiotic P supply. Species differed in their ability to colonize roots and similarly to produce a plant growth response. In this regard, Glomus intraradices (Schenck and Smith) enhanced plant growth the most, whereas Glomus dimorphicum (Boyetchko and Tewari) was least effective, and Glomus mosseae ([Nicol. and Gerd.] Gerd. and Trappe) produced an intermediate growth response. The partial alleviation of P deficiency in no-P and low-P plants by VAM fungi stimulated uptake of N, K, Mg, Fe, and Zn. VAM fungi enhanced shoot concentrations of P, N, and Mg by 28 d after planting and, through a general improvement of overall plant mineral nutrition, promoted plant growth and development.

Effect of withdrawal of phosphorus on nitrate assimilation and PEP carboxylase activity in tomato

Tomato plants (Lycopersicon esculentum) grown in a complete nutrient solution for 8 days were transferred to a P-free solution of pH 6.0. Within 2 days of transfer the rate of alkalinization of the nutrient solution declined and by 4 days the solution had become acid. Nitrate transferred from roots to leaves was depressed over this period, and the rate of nitrate reductase activity in the leaves (the main site of assimilation of nitrate in tomato) had declined by 60% within 5 days of transfer. The activity of PEP carboxylase in the leaves of the P-deficient plants increased after 3 days, eventually becoming 3 times greater than in the leaves of plants adequately supplied with P. The PEP carboxylase activity in the roots of the P-deficient plants increased within 2 days, becoming 4 times greater after 8 days' growth. These results are discussed in relation to mechanisms for enhancement of P acquisition and maintenance of cation and anion uptake during P-deficiency.

Polyamine Concentration and Ethylene Evolution in Tomato Plants under Nutritional Stress

Polyamine accumulation in foliage was assessed in relation to ammonium accumulation and ethylene evolution in tomato (Lycopersicon esculentum Mill.) under nutritional stress. Nutritional stresses were induced in greenhouse-grown plants in quartz sand with an NH4-based solution or with NO3-based solutions without P, K, Ca, or Mg. Plants receiving NH4-based nutrition had higher putrescine and lower spermidine concentrations than plants receiving NO3-based nutrition. Adding AOA (10-5m) to the nutrient solution of plants receiving NH4-based nutrition suppressed putrescine accumulation but had no effect on spermidine; silver thiosulfate (10-5 m) had no effect on polyamine accumulation. Deficiencies had no consistent effect on polyamine accumulation relative to its accumulation under full-nutrition conditions, but adding AOA restricted putrescine and spermidine accumulation in all nutrient-deficient regimes. Foliar spermine accumulation was not affected by nutritional regime. Ammonium-based nutrition resulted in enhanced putrescine and ammonium accumulation and accelerated ethylene evolution rates relative to plants receiving NO3-based nutrition. All nutrient-deficient plants had higher ammonium accumulation, and all but P-deficient plants had higher ethylene evolution than those receiving full NO3-based nutrition. Although some variability occurred among treatments, an association among putrescine accumulation, ammonium accumulation, ethylene evolution. and stress-induced symptoms was apparent. Chemical name used: (aminooxy) acetic acid (AOA).

Influence of Vesicular-Arbuscular Mycorrhizal Fungi on the Response of Potato to Phosphorus Deficiency.

Morphological and biochemical interactions between a vesicular-arbuscular mycorrhizal (VAM) fungus (Glomus fasciculatum [Thaxt. sensu Gerdemann] Gerdemann and Trappe) and potato (Solanum tuberosum L.) plants during the development of P deficiency were characterized. Nonmycorrhizal (NM) plants grown for 63 d with low abiotic P supply (0.5 mM) produced 34, 52, and 73% less root, shoot, and tuber dry matter, respectively, than plants grown with high P (2.5 mM). The total leaf area and the leaf area:plant dry weight ratio of low-P plants were substantially lower than those of high-P plants. Moreover, a lower shoot:root dry weight ratio and tuber:plant dry weight ratio in low-P plants than in high-P plants characterized a major effect of P deficiency stress on dry matter partitioning. In addition to a slower rate of growth, low-P plants accumulated nonreducing sugars and nitrate. Furthermore, root respiration and leaf nitrate reductase activity were lower in low-P plants than in high-P plants. Low abiotic P supply also induced physiological changes that contributed to the greater efficiency of P acquisition by low-P plants than by high-P plants. For example, allocation of dry matter and P to root growth was less restricted by P deficiency stress than to shoot and tuber growth. Also, the specific activities of root acid phosphatases and vanadate-sensitive microsomal ATPases were enhanced in P-deficient plants. The establishment of a VAM symbiosis by low-P plants was essential for efficient P acquisition, and a greater root infection level for P-stressed plants indicated increased compatibility to the VAM fungus. By 63 d after planting, low-P VAM plants had recovered 42% more of the available soil P than low-P NM plants. However, the VAM fungus only partially alleviated P deficiency stress and did not completely compensate for inadequate abiotic P supply. Although the specific activities of acid phosphatases and microsomal ATPases were only marginally influenced by VAM infection, VAM roots characteristically had a higher protein concentration and, consequently, enhanced microsomal ATPase and acid phosphatase activities on a fresh weight basis compared with NM roots. Morphological and ultrastructural details of VAM plants are discussed in relation to the influence of the VAM symbiosis on P nutrition of potato.

Resistance Responses of Potato to Vesicular-Arbuscular Mycorrhizal Fungi under Varying Abiotic Phosphorus Levels

In mycorrhizal symbioses, susceptibility of a host plant to infection by fungi is influenced by environmental factors, especially the availability of soil phosphorus. This study describes morphological and biochemical details of interactions between a vesicular-arbuscular mycorrhizal (VAM) fungus and potato (Solanum tuberosum L. cv Russet Burbank) plants, with a particular focus on the physiological basis for P-induced resistance of roots to infection. Root infection by the VAM fungus Glomus fasciculatum ([Thaxt. sensu Gerdemann] Gerdemann and Trappe) was extensive for plants grown with low abiotic P supply, and plant biomass accumulation was enhanced by the symbiosis. The capacity of excised roots from P-deficient plants to produce ethylene in the presence or absence of exogenous 1-amino cyclopropane-1-carboxylic acid (ACC) was markedly reduced by VAM infection. This apparent inhibition of ACC oxidase (ACC(ox)) activity was localized to areas containing infected roots, as demonstrated in split-root studies. Furthermore, leachate from VAM roots contained a potent water-soluble inhibitor of ethylene generation from exogenous ACC by nonmycorrhizal (NM) roots. The leachate from VAM-infected roots had a higher concentration of phenolics, relative to that from NM roots. Moreover, the rates of ethylene formation and phenolic concentration in leachates from VAM roots were inversely correlated, suggesting that this inhibitor may be of a phenolic nature. The specific activity of extracellular peroxidase recovered in root leachates was not stimulated by VAM infection, although activity on a fresh weight basis was significantly enhanced, reflecting the fact that VAM roots had higher protein content than NM roots. Polyphenol oxidase activity of roots did not differ between NM and VAM roots. These results characterize the low resistance response of P-deficient plants to VAM infection. When plants were grown with higher abiotic P supply, the relative benefit of the VAM symbiosis to plant growth decreased and root infection was lower. The in vivo ACC(ox) activity was also greater in roots of plants grown on high levels of P compared with those grown on low levels, although the influence of VAM infection was partially to counteract the nutritional effect of P on ACC(ox) activity. Similar to ACC(ox) activity, extracellular peroxidase activity of roots increased linearly with increasing abiotic P supply, thus indicating a greater potential for resistance to VAM infection. These findings suggest that VAM fungi may alter phenolic metabolism of roots so as to hinder ethylene production and the root's ability to invoke a defense response. Raising the abiotic P supply to plants at least partially restores the capacity of roots to produce ethylene and may, in this way, increase the root's resistance to VAM infection.

Responses of Transpiration and Hydraulic Conductance to Root Temperature in Nitrogen- and Phosphorus-Deficient Cotton Seedlings

Suboptimal N or P availability and cool temperatures all decrease apparent hydraulic conductance (L) of cotton (Gossypium hirsutum L.) roots. The interaction between nutrient status and root temperature was tested in seedlings grown in nutrient solutions. The depression of L (calculated as the ratio of transpiration rate to absolute value of leaf water potential [Psi(w)]) by nutrient stress depended strongly on root temperature, and was minimized at high temperatures. In fully nourished plants, L was high at all temperatures >/=20 degrees C, but it decreased greatly as root temperature approached the chilling threshold of 15 degrees C. Decreasing temperature lowered Psi(w) first, followed by transpiration rate. In N- or P-deficient plants, L approached the value for fully nourished plants at root temperatures >/=30 degrees C, but it decreased almost linearly with temperature as roots were cooled. Nutrient effects on L were mediated only by differences in transpiration, and Psi(w) was unaffected. The responses of Psi(w) and transpiration to root cooling and nutrient stress imply that if a messenger is transmitted from cooled roots to stomata, the messenger is effective only in nutrient-stressed plants.

Environmental pollution and impacts on soils and forests nutrition in North America

The effects of acid deposition, excess N deposition, and elevated CO2 on forest soils and nutrition in North America are reviewed. While there remains the possibility that acid deposition and excess N deposition are contributing to declines in red spruce, sugar maple, and southern pines, clearcut cause and effects are still not evident. Climate is clearly a major factor in red spruce decline in the northeastern U.S., but air pollution may contribute. There is some evidence that soil solution Al may be approaching deleterious levels in southeastern red spruce forests. Lack of proper management may be a major factor in the sugar maple and southern pine declines, but once again, air pollution as a potential contributor cannot be ignored. Nutrient budget analyses and discoveries of soils base cation depletion in certain sites suggest that base cation status is declining in forests of the southeastern U.S., but thus far, base cation deficiencies are uncommon. Recent research has revealed that there are more cases of N-saturated forests in North America than was previously suspected. These systems are characterized by high rates of soil N mineralization, high atmospheric N inputs, low uptakes, or some combination of these factors. Soil leaching and Al mobilization in such systems is often dominated by nitrate. However, the geographical extent of these types of systems is limited, and the traditional view that most forest ecosystems are N limited remains valid, especially where forest management is intensive. The limited information available on tree response to CO2. suggests N-deficient plants often grow faster with elevated CO2, whereas P-deficient plants often do not. Research is needed to 1) determine if the differences in response between N- and P-deficient plants is common, 2) the responses of plants deficient in other nutrients to elevated CO2, and 3) the interactions of CO2 increase, nutrient deficiencies, climate change.

Phosphate Uptake by Spirodela and Lemna during Early Phosphorus Deficiency

Growth, internal P concentration and Pi uptake was investigated in sterile cultures of Spirodela oligorrhiza (Kurz) Hegelm. and Lemna major L. plants during early P-deficiency. Within 12 h of transfer to a P-deficient medium, Pi uptake rates by P-deficient (- P) plants were enhanced 30-120% compared with P adequate (+ P) controls at 1-1000 �M external [Pi]. The enhancement in Pi uptake rates with P-deficiency normally preceded, and was more pronounced than, other effects of P-deficiency such as reduced growth, reduced internal [P] and appearance of visual symptoms. Enhanced Pi uptake rates in - P compared with +P plants resupplied with Pi was more closely correlated with a fall in the internal [Pi] (r = -0.93 to -0.98) than with a fall in the concentration of three other P fractions (i.e. ester P, lipid P, and residual P). The role of tissue [Pi] in Spirodela and Lemna plants as a possible determinant of Pi uptake rates is discussed. Kinetic analysis showed that enhanced Pi uptake in -P compared with + P plants resupplied with Pi was the result of a 2-4-fold increase in V*max of two first- order systems and not by an increased affinity (i.e. reduced K*m) of the carrier for the phosphate ion.

Increased Arginine Biosynthesis during Phosphorus Deficiency

The accumulation of arginine in leaves of four citrus rootstock cultivars during P deficiency has been demonstrated to be due to increased de novo synthesis rather than decreased catabolism or increased protein degradation (E Rabe, CJ Lovatt, 1984, Plant Physiol 76: 747-752). In this report, we provide evidence (a) that the increased activity of the arginine biosynthetic pathway observed for citrus rootstocks grown under P-deficient conditions for 7 months is due to an increase in the concentration of ammonia in leaves of P-deficient plants and (b) that ammonia accumulation and removal through arginine systhesis are early responses to phosphorus deficiency for both a woody perennial, rough lemon (Citrus limon), and an herbaceous annual, summer squash (Cucurbita pepo). Transferring 5-day-old squash plants to a phosphorus-deficient nutrient solution for only 10 days resulted in a 2-fold increase in the concentration of nitrate in the youngest fully expanded leaves (YFE). Concomitantly, the specific activity of nitrate reductase doubled and the ammonia content of P-deficient YFE leaves increased to a concentration significantly greater that of leaves from healthy control plants (P < 0.05). Consistent with increased availability of ammonia, the incorporation of NaH(14)CO(3) into arginine plus urea doubled during phosphorus deficiency and arginine accumulated. Despite the accumulation of nitrate and ammonia in YFE leaves during phosphorus deficiency, the total nitrogen content of these leaves was less than that of the healthy control plants. Similar results were obtained for rough lemon. Nitrate content of the YFE leaves increased 1.5- and 3.0-fold in plants deprived of phosphorus for 6 and 12 weeks, respectively. Ammonia content of the leaves increased as P deficiency progressed to 1.4 +/- 0.08 mg (+/- se, n = 4) per gram dry weight, a level 1.8-fold greater than that of the P-sufficient control plants. During P deficiency de novo arginine biosynthesis in rough lemon increased 10-fold. Immersing the petiole of YFE leaves from P-sufficient squash and rough lemon plants in 50 millimolar NH(4) (+) for 3 hours resulted in the accumulation of ammonia in the leaves, and a 4-fold increase in the incorporation of NaH(14)CO(3) into arginine plus urea. Taken together, these results provide strong evidence that the accumulation of nitrate and ammonia in leaves is an early response of both woody and herbaceous plants to P deprivation. The data are consistent with the hypothesis that increased de novo arginine biosynthesis in leaves during P deficiency is in response to ammonia content of the leaves.

Growth and the distribution of phosphorus in wheat developed under various phosphorus and temperature regimes

Experiments were designed to examine the effect of the level and duration of application of phosphorus (P) on yield in wheat and the effect of growth conditions prior to anthesis on the utilisation of P taken up during the early stages of development. In the first experiment, wheat (Triticum aestivum cv. Kite) was grown in sand and supplied with a complete nutrient solution containing either 1 mM phosphate or 0.25 mM phosphate. The supply of P was maintained until grain maturity, or stopped at different stages of development (floral initiation, flag leaf emergence, anthesis). The increase in total plant dry matter over this period ranged from 8.8 to 17.6 g/plant, with the 1.0 mM P supply and from 4.1 to 9.5 g/plant with the 0.25 mM P supply. Supply of P beyond anthesis resulted in more tiller dry matter and increased the P content of the grain, but did not increase grain yield at either level. With 1 mM P to maturity, up to 21% P of the grain P could be attributed to retranslocation of P within the plant after anthesis. With 0.25 mM P to floral initiation, 58% of the grain P could be attributed to such retranslocation. In a second experiment plants (cv. Kite) were grown initially at 18/13�C with 0.25 mM P until floral initiation and thereafter with a P-free solution until maturity. Between floral initiation and anthesis plants were placed in six dayhight temperatures, extending (in 3�C steps) from 15/10�C to 30/25OC, and then returned to the standard condition of 18/13�C. Higher pre-anthesis temperatures reduced the pre-anthesis growth period and the plant height, but increased the leaf phosphorus concentration and uptake of phosphorus per plant in both the pre- and post-anthesis periods. Net CO2 exchange indicated that leaf senescence in P-deficient plants was closely associated with the export of nitrogen as well as the export of P. Grain P increased from 0.15% to 0.3% when the preanthesis temperature was increased from 15/10 to 30/25�C, although grain yield per main culm did not vary greatly. These findings highlight the importance of environmental conditions in determining the level of P deficiency in wheat, and show that grain yield is not limited by the amount of P in the grain.

De Novo Arginine Biosynthesis in Leaves of Phosphorus-Deficient Citrus and Poncirus Species

Young, fully expanded leaves from 7-month-old P-deficient citrus rootstock seedlings had levels of nonprotein arginine that were 10- to 50-fold greater than those from P-sufficient control plants. Arginine content of the protein fraction increased 2- to 4-fold in P-deficient leaves. Total arginine content, which averaged 72 +/- 6 micromoles per gram dry weight of P-sufficient leaf tissue (mean +/- se, n = the four rootstocks) was 207, 308, 241, and 178 micromoles in P-deficient leaves from Citrus limon cv rough lemon, Poncirus trifoliata x C. sinensis cv Carrizo citrange and cv Troyer citrange, and P. trifoliata cv Australian trifoliate orange, respectively. For each rootstock, the accumulation of arginine paralleled an increase in the activity of the pathway for the de novo biosynthesis of arginine. The ratio of the nanomoles NaH(14)CO(3) incorporated into the combined pool of arginine plus urea per gram fresh weight intact leaf tissue during a 3-hour labeling period for P-deficient to P-sufficient plants was 91:34, 49:11, 35:11, and 52:41, respectively. When P-deficient plants were supplied with P, incorporation of NaH(14)CO(3) into arginine plus urea was reduced to the level observed for the P-sufficient control plants of the same age and arginine ceased to accumulate. Arginase and arginine decarboxylase activity were either unaffected or slightly increased during phosphorus deficiency. Taken together, these results provide strong evidence that arginine accumulation during phosphorus deficiency is due to increased activity of the de novo arginine biosynthetic pathway.

Stomatal Responses to Water Stress and to Abscisic Acid in Phosphorus-Deficient Cotton Plants

Cotton (Gossypium hirsutum L.) plants were grown in sand culture on nutrient solution containing adequate or growth-limiting levels of P. When water was withheld from the pots, stomata of the most recently expanded leaf closed at leaf water potentials of approximately -16 and -12 bars in the normal and P-deficient plants, respectively. Pressure-volume curves showed that the stomata of P-deficient plants closed when there was still significant turgor in the leaf mesophyll. Leaves of P-deficient plants accumulated more abscisic acid (ABA) in response to water stress, but the difference was evident only at low water potentials, after initiation of stomatal closure. In leaves excised from unstressed plants, P deficiency greatly increased stomatal response to ABA applied through the transpiration stream. Kinetin blocked most of this increase in apparent sensitivity to ABA. The effect of P nutrition on stomatal behavior may be related to alterations of the balance between ABA and cytokinins.

Accumulation of ammonium-N and amino-N in theAzolla-Anabaena association

Expanded pools of ammonium and amino-N were found in fronds of Azolla plants experiencing P deficiency and crowding. A larger and more rapid increase in pool size of these compounds was found in P-deficient plants than in crowded populations. High temperature did not limit their accumulation in P-deficient fronds of all the strains examined exceptA. caroliniana.

Studies of phosphorus and potassium deficiencies in Trifolium subterraneum based on electrical measurements

Electrical measurements were used to indicate changes in plant tissue due to alterations in nutrient status. An experiment with Trifolium subterraneum L., grown in soil at five rates of applied P, showed that inadequate P produced high values for (1) resistance to low frequency current (RLM) and (2) radius of the impedance locus (r). With increasing P the values of these two parameters fell, reaching a minimum at the P level giving maximum growth. Increasing the P supply above the optimum had no further effect.A study of K-deficient and of P-deficient plants showed the feasibility of diagnosing either deficiency or of discriminating between the two deficiencies, from changes in certain impedance parameters of the petiole tissue following correction of the deficiencies. Changes in membrane phase angle were consistent with K deficiency delaying and P deficiency hastening aging of the plasma membrane. RLF of both petioles and leaflets was increased by P deficiency, and the value for attached but not detached petioles from P-deficient plants was reduced by treatment with phosphate. RLF values for attached P-deficient leaflets decreased in response to phosphate treatment during leaf development but no longer responded (within 6 days of treatment) after a certain stage of maturity.Changes in RLF and r resulting from the correction of P deficiency show that some factor in addition to increase in tissue K is involved, most likely the plasmodesmata. The differences between RLF changes due to correction of nutrient deficiencies and those due to injury are noted.

Untersuchungen zur Steigerung der Flavonol-Akkumulation durch P- and N-Mangel in Fagopyrum esculentumMoench

Summary Plants grown under P- and N-deficiency accumulate flavonols to a higher extent than those receiving a complete set of nutrients ( Krause and Reznik , 1972). This may be due to an increased PAL-activity or a decreased turnover of the flavonol. In fact PAL-activity related to fresh weight is higher in plants under P- and N-deficiency than in those growing in the presence of all nutrients. This seems to support the dominating role of PAL in controlling phenylpropane levels in plants. On the other hand P-deficient plants show a dramatic increase in phenylpropane content (rutin and chlorogenic acid) during continuation of the experiment, although PAL-activity decreases. Calculations based on in vitro measure ments under V max -conditions show that even decreasing levels of PAL are sufficient to cause the observed increase in flavonol level. In contrast to this situation N-deficient plants and those with complete nutrition do not increase their flavonol content although their PAL-activity based on fresh weight remains at comparable levels as in P-deficient plants. Therefore flavonol levels cannot simply be related to levels of PAL-activity, but other factors have to be taken into account. The fact that completion of the nutrient solution is able to accelerate the retarded growth of P-deficient plants suggested that a possibly retarded turnover of flavonol may also be increased by P-supplement. Fig. 3 a shows that phosphate addition does not reduce the absolute amount of rutin per leaf, although its content based on fresh weight decreases due to an increase of fresh weight per leaf. On the other hand phosphate addition during the time of flavonol increase in P-deficient plants results in a complete stop of this increase keeping the flavonol content at the level reached at the time of phosphate addition. These results indicate that in vivo turnover of flavonoids is not of such importance as suggested from experiments in vitro or with tissue cultures.

Response of Weeds to Soil Phosphorus and Potassium

Ten warm-season and seven cool-season weed species were grown in the glasshouse on Hartsells fine sandy loam taken from field plots that had been in long-term fertility studies. The soil pH was 5.9 and phosphorus (P) levels ranged from 8 to 95 kg/ha and the potassium (K) levels from 40 to 213 kg/ha. Growth response to P and K levels was measured by dry herbage yield. Redroot pigweed (Amaranthus retroflexus L.), jimsonweed (Datura stramonium L.), and Florida beggarweed [Desmodium tortuosum (Sw.) DC] were the most responsive warm-season weed species to P, whereas chickweed [Stellaria media (L.) Cyrillo] was the most responsive cool-season weed to P. Extreme P deficiency symptoms were evident on species giving a high response to P. P-deficient plants were severely stunted and exhibited a characteristic reddish-purple color. Showy crotalaria (Crotalaria spectabilis Roth), tall morningglory [Ipomoea purpurea (L.) Roth], sicklepod (Cassia obtusifolia L.), Carolina geranium (Geranium carolinianum L.), and coffee senna (Cassia occidentalis L.) were the most tolerant to low soil P. Redroot pigweed, jimsonweed, and Florida beggarweed were the most responsive warm-season weeds to K. Wild mustard [Brassica kaber (DC.) L.C. Wheeler var. Pinnatifida (Stokes) L.C. Wheeler] and annual bluegrass (Poa annua L.) were the most responsive cool-season weeds to K. Potassium deficiency symptoms were characterized primarily by severe stunting. Buckhorn plantain (Plantago lanceolata L.), Carolina geranium, and curly dock (Rumex crispus L.) were the most tolerant cool-season weeds to low soil K. Generally, weeds were more sensitive to low soil-test P than K.

EMERSON ENHANCEMENT EFFECT AND THE REACTIVATION OF PHOTOSYNTHESIS IN PHOSPHATE DEFICIENT LEMNA MINOR*

SUMMARY Photosynthetic enhancement, studied in the wavelength pair 650/717 nm, is expressed as and as . The maximum values of enhancement are considered to represent the ratio between the “potential cooperative activities” (PCA) of the two photosystems: Under conditions of P-deficiency E650(717)max tends to increase. However, when deficient plants have reactivated their photosynthesis (PS) by P-uptake, it decreases. This result demonstrates that far red light to a certain degree overcomes the inhibiting effect of P-deficiency. A tentative explanation is based on the hypothesis that in P-deficient plants PS operates with the less efficient pseudocyclic photophosphorylation at 650 nm as a 12-quanta process, whereas with background light of 717 nm a switch takes place to a more efficient PS, operating with cyclic photophosphorylation. PS, making use of the cyclic pathway, is thought to operate in plants with normal P-content, thus showing the normal high efficiency.

Accumulation of damaging concentrations of phosphorus by leaves of selkirk wheat

Leaves of P-deficient wheat plants were damaged after 1 mM P was included in the previously zero P nutrient solution. Wheat plants continuously grown in 1 mM P in modified Hoagland's solution were not damaged. Maximum damage and P accumulation occurred in the apical regions of the youngest leaves. We attributed this leaf damage to the accumulation of abnormally high (in excess of 3 per cent dry weight) amounts of P in the leaves of P-deficient plants from nutrient solution that was nontoxic to plants containing adequate P. re]19720721

ACCUMULATION OF TOXIC LEVELS OF PHOSPHORUS IN THE LEAVES OF PHOSPHORUS-DEFICIENT BARLEY

Leaves of P-deficient barley (Hordeum vulgare L.) plants were damaged after the addition of P to the hydroponic solution. These damaged leaves accumulated abnormally high percentages of P. Damage was severest in the apical regions of the youngest leaves. The facts that P accumulated in the leaf tips of P-deficient plants after P exposure whereas N did not, and that continuous exposure to high-solution P did not result in high tissue percent P, suggested that a source-sink control mechanism, and not just transpirational uptake and accumulation was involved.