Propagation of lettuce (Lactuca sativa) breeding material by tissue culture

A tissue culture method using Murashige and Skoog's (MS) medium was devised to propagate healthy plants from field grown lettuce plants selected for seed production. Explants (2–3 mm long) from axillary buds were successfully grown on MS + 1.0 or 2.0 mg litre^-1 kinetin and 6.4 mg litre^-1 IAA to promote shoot growth. Concentrations of 0.5 and 4.0 mg litre^-1 kinetin gave poor shoot growth. The cultures were successfully rooted after 3–4 wk on MS + 6.4 mg litres^-1 IAA after transfer from MS + 1.0 mg litre^-1 kinetin and on MS + 4.8 mg litre^-1 IAA after transfer from MS + 2.0 mg litre^-1 kinetin. Concentrations of 3.2 and 8.0 mg litre^-1 IAA gave poor root initiation. Root initiation was more successful when cultures were grown at 40 Wm^-2 than in cultures grown at 5 Wm^-2. Rooted cultures were established in compost with a 90–95% success rate and the regenerated plants flowered c. 18 wk after the cultures were initiated.     

EFFECT OF TEMPERATURE ON LIGHT-LIMITED GROWTH AND CHEMICAL COMPOSITION OF SKELETONEMA COSTATUM (BACILLARIOPHYCEAE)1

Phytoplankton growth rate in response to irradiance can be approximated by a hyperbola defined by three coefficients: i) initial slope (α); ii) asymptote (μ_m); and, iii) X-axis intercept or compensation irradiance (I_c). To mathematically represent the interaction of temperature and irradiance on growth rate, one must describe the relationship between these constants and temperature. The marine diatom, Skeletonema costatum (Greville) Cleve, was grown in unialgal culture at different levels of irradiance and 2-3 photoperiods at 0, 5, 10, 16 and 22 C. The value of I_c is ca. 1.0 ly·day^?1 or less at all temperatures. The initial slope (div·ly^?1) is a “u-shaped” function of temperature described by the second degree polynomial, α= 0.25–0.02T+0.001T². Within the range 0–10 C, μ_m (div·day^?1) is an exponential function of temperature described by the equation, μ_m= 0.48 exp (0.126T). At each temperature and selected levels of irradiance, cell size and cellular content of C, N and chl a were determined. The C:chl a and N:chl a ratios increased with irradiance because of increases in C and decreases in chl a. At lower temperatures (0, 5, 10 C), the rate of increase of both ratios with irradiance was greater than at the higher temperatures (16, 22 C). Cellular content of N was independent of irradiance and temperature, and the C:N ratio ranged from 5 to 8 with a slight tendency to lower values at low irradiance. Cell volume was not influenced by either temperature or irradiance.     

Post-harvest age-induced seed dormancy of Acer ginnala and its alleviation by growth regulator and low temperature treatments

One-month-old fruits of Acer ginnala with winged pericarp attached gave 44% germination and this was not increased by cold treatment at 4°C for 0, 10, 20, or 30 days, gibberellic acid treatment at 0, 1, 10, 100 or 1000 mg litre^-1, or ethephon treatment at 0, 2, 20, 200 or 2000 mg litre^-1. After 6 months of storage at 20–25 °C, germination of untreated fruits fell to 5% but could be restored to that of 1-month-old fruits by incubation at 4 °C for 30 days. After 9 months storage, no germination occurred in untreated fruits. Cold treatment (30 days at 4 °C partially restored germination (26%). Treatment with either gibberellic acid (1000 mg litre^-1) and 30 days at 4 °C (40%) or ethephon (100 mg litre^-] and 30 days at 4 °C improved germination (69%). The combination of all three treatments, i.e. 100 mg litre^-1 gibberellic acid, 100 mg litre^-1 ethephon and 30 days at 4 °C, optimised germination (86%). Thus, dormancy of A. ginnala developed during storage but could be reversed by a combination of treatment with low temperature and growth regulators. The highest germination (86%) was achieved after low temperature and growth regulator treatment of stored fruit.     

Nitrogen nutrition,photosynthesis and carbon allocation in ectomycorrhizal pine

Summary Studies examined net photosynthesis (Pn) and dry matter production of mycorrhizal and nonmycorrhizalPinus taeda at 6 intervals over a 10-month period. Pn rates of mycorrhizal plants were consistently greater than nonmycorrhizal plants, and at 10 months were 2.1-fold greater. Partitioning of current photosynthate was examined by pulse-labelling with¹⁴CO₂ at each of the six time intervals. Mycorrhizal plants assimilated more¹⁴CO₂, allocated a greater percentage of assimilated¹⁴C to the root systems, and lost a greater percentage of¹⁴C by root respiration than did nonmycorrhizal plants. At 10 months, the quantity of¹⁴CO₂ respired by roots per unit root weight was 3.6-fold greater by mycorrhizal than nonmycorrhizal plants. Although the stimulation of photosynthesis and translocation of current photosynthate to the root system by mycorrhiza formation was consistent with the source-sink concept of sink demand, foliar N and P concentrations were also greater in mycorrhizal plants.Further studies examined Pn and dry matter production ofPinus contorta in response to various combinations of N fertilization (3, 62, 248 ppm), irradiance and mycorrhizal fungi inoculation. At 16 weeks of age, 6 weeks following inoculation with eitherPisolithus tinctorius orSuillus granulatus, Pn rates and biomass were significantly greater in mycorrhizal than nonmycorrhizal plants. Mycorrhizal plants had significantly greater foliar %P, but not %N, than did nonmycorrhizal plants. Fertilization with 62 ppm N resulted in greater mycorrhiza formation than either 3 or 248 ppm. Increased irradiance resulted in increased mycorrhiza formation.     

Direct plant regeneration from leaf explants of Plumbago species and its genetic fidelity through RAPD markers

In vitro plant regeneration was achieved from leaf explants of Plumbago rosea and Plumbago zeylanica on Murashige & Skoog (1962) medium supplemented with 1.5 mg litre^?1 6‐benzylaminopurine, 0.25 mg litre^?1 indole‐3‐acetic acid, 50 mg litre^?1 adenine sulfate and 3% (w/v) sucrose. The shoot initials developed within 2–3 wk on the leaf margin as well as from the wounds of the leaf. High frequency shoot‐bud regeneration was achieved on similar medium in subsequent subcultures. The semi‐mature leaves produced more shoot‐buds as compared to the younger leaves. Mature leaves did not show any response for shoot bud initiation. More than 85% of the semi‐mature explants produced shoot‐buds per leaf explant within 4 wk of culture. Shoots rooted easily on medium having half‐strength basal Murashige & Skoog (1962) medium supplemented with 0.25 mg litre^?1 indole‐3‐butyric acid and 2% (w/v) sucrose; 84–92% of the in vitro rooted plantlets survived in the greenhouse. The regenerated plantlets appeared morphologically similar to the mother plants. No variation was detected among the regenerated plants by the use of Randomly Amplified Polymorphic DNA (RAPD) markers. This method might be useful for assessing plant improvement programmes.     

The effect of imazalil in the control of decay in yellow yam caused by Penicillium sclerotigenum

A strain of Penicillium sclerotigenum isolated from decaying yellow yams (Dioscorea cayenensis) was found to have developed resistance to benzimidazole fungicides and the use of imazalil was investigated as an alternative agent for controlling it. Two formulations were tested and proved to be equally effective in controlling decay at a concentration of 50 mg imazalil litre^-1 if the yams were dipped in it for 5 s; concentrations down to 10 mg litre^-1 were effective if the immersion time was increased to 5 min or more. These treatments gave good control of decay when applied up to 24 h after inoculation but were less effective when application was 48 h after inoculation, although at 500 mg litre^-1 there was some indication that levels of decay were decreased when compared with untreated tubers. Fungal penetration was unaffected or increased by increasing delays in the time of the fungicide application depending on the concentration applied. In trial shipments of yams from Jamaica to Britain imazalil alone was less effective in controlling overall decay because of the presence of a Rhizopus species. This could be controlled by the addition of dichloran to the dip. Imazalil residues were highest in the peel; levels in the peeled tuber varied and tended to decrease during storage but were generally in the range of 0·5 - 0·8 mg kg^-1 which is higher than the maximum levels accepted for other produce. A simple cooking test showed that residues in treated yam slices declined by about one third after boiling the slices in water for 45 min.     

Effects of carbonyl sulfide, methyl iodide, and sulfuryl fluoride on fruit phytotoxicity and insect mortality

Three potential chemical fumigants: carbonyl sulfide (COS), methyl iodide (MI) and sulfuryl fluoride (SF) were tested at selected dosages on lemons against California red scale (Aonidiella aurantii) and MI and COS were tested on nectarines against codling moth (Cydia pomonella). In nectarines, COS was tested at 0, 20, 40, 60 and 80 mg litre^?1, MI at 0, 10, 15, 20 and 25 mg litre^?1. Both fumigants intensified nectarine peel color, delayed fruit softening, but did not alter overall fruit quality. COS at 80 mg litre^?1 resulted in 87% codling moth mortality, but the fumigant dosage was insufficient to reach the desired probits 9 level (99.9968%). MI gave 100% codling moth mortality at 25 mg litre^?1. Lemons were treated with MI at 0,10,20,40,60 mg litre^?1, SF at 0,10,20,40, 80 mg litre^?1 and COS at 0,20,40, 60 and 80 mg litre^?1. MI gave 100% red scale mortality at ≥40 mg litre^?1 but caused significant fruit injury. Conditioning lemons at 15°C for 3 days before MI fumigation lessened lemon phytotoxicity. Forced aeration at 3.5 standard litres per minute of lemons for 24 h following MI fumigation at 20 mg litre^?1 significantly reduced phytotoxicity compared to 2 h postfumigation aeration after MI treatment. SF at ≥40 mg litre^?1 gave 100% red scale mortality but resulted in commodity phytotoxicity. Lemons treated with the highest selected dose of 80 mg litre^?1 COS gave only 87% kill of red scale, but failed to reach the desired probit 9 level.     

Morphactin and Adventitious Root Formation in Pea Cuttings

Stock plants of pea (Pisum sativum L. cv. Alaska) were grown at different controlled levels of irradiance (4, 16 or 38 W m^?2) for 11 days from sowing. Morphactin (CFM, methyl-2-chloro-9-hydroxy-fluorene-9-carboxylate) was applied to the apex of the stock plants 3 days before cuttings were excised. The cuttings were rooted at 16 W m^?2. High levels of morphactin (>5 × 10^?3 mg l^?1) inhibited root formation in the cuttings. Low concentrations of CFM (5 × 10^?5 mg l^?1) promoted the formation of adventitious roots in cuttings from plants grown at all three levels of irradiance, with the most pronounced effect in cuttings from 4 W m^?2. Measurements of ethylene evolution by CFM-treated plants 3 days after application, revealed a stimulatory effect on ethylene production by high CFM concentrations.     

Effect of imidacloprid on the sivlerleaf whitefly, Bemisia argentifolii Bellows and Perrring (Homoptera: Aleyrodidae), and whitefly parasitism

Bioassays were conducted under greenhouse conditions to determine the effect of imidacloprid on adult and nymphal stages of the silverleaf whitefly, Bemisia argentifolii Bellows and Perring, and parasitism by Encarsia formosa (Gahan). A flowable formulation (24Oglitre^-1) of imidacloprid at six rates (0.09, 0.04 and 0.02 g a.i. litre^-1 pot volume for experiments 1 and 2; 0.009, 0.004, and 0.002 g a.i. litre^-1 pot volume for experiment 3) was evaluated. After a 48 h exposure to treated plants, high mortality of adult whitefly (>94%) was observed. Adults exposed to poinsettias treated 150 days earlier also had significantly greater mortality (>79%) than the adults on control plants. When exposed to treated plants for only 6 h, >65% of adults were killed. All three rates of imidacloprid caused >97% mortality of immature whiteflies by day 19. When treated plants were continually exposed to adult whiteflies, immature mortality was 100% for the three higher rates of imidacloprid up to and including 88 days after treatment. During the same time, emerging adults were reduced significantly. Immatures reinfested on plants treated 161 days earlier, incurred 80% mortality at the higher rate 0.09 g a.i. litre^-1 pot volume and 38% mortality at 0.02 g a.i. litre^-1 pot volume. At lower treatment rates, results varied. At 0.009 g a.i. litre^-1 of pot volume, mean percentage whitefly mortality (65%) 25 days after treatment was significantly higher than the controls; however, whitefly mortality at 0.004 and 0.002 g a.i. litre^-1 pot volume was not significantly different from controls or plants treated with the higher rate. Parasitoids could develop to the adult stage on whiteflies infesting imidacloprid treated plants. Parasitism occurred at low levels (< 10%), doe to high levels of whitefly mortality on treated plants. No phytotoxicity was observed for any treatment throughout the length of the trials that lasted through flowering.     

Photoheterotrophy and light-dependent uptake of organic and organic nitrogenous compounds by Planktothrix rubescens under low irradiance

1. Planktothrix rubescens is the dominant photoautotrophic organism in Lake Zürich, a prealpine, deep, mesotrophic freshwater lake with an oxic hypolimnion. Over long periods of the year, P. rubescens accumulates at the metalimnion and growth occurs in situ at irradiance near the photosynthesis compensation point. Experiments were conducted to evaluate the contribution of photoheterotrophy, heterotrophy and light‐dependent uptake of nitrogenous organic compounds to the carbon and nitrogen budget of this cyanobacterium under conditions of restricted availability of light quanta. 2. We used both purified natural populations of P. rubescens from the depth of 9 m and an axenic culture grown under low irradiance at 11 μmol m^?2 s^?1 on a light : dark cycle (10 : 14 h) to determine the uptake rates of various amino acids, urea, glucose, fructose, acetate and inorganic carbon. The components were added to artificial lake water in low amounts that simulated the naturally occurring potential concentrations. 3. The uptake rates of acetate and amino acids (glycine, serine, glutamate and aspartate) were strongly enhanced at low irradiance as compared with the dark. However, no difference was observed in the uptake of arginine, which was taken up at high rates under both treatments. The uptake rates of glucose, fructose and urea were very low under all conditions. Similar results were obtained for both axenic P. rubescens and for purified natural populations of P. rubescens that were separated from bacterioplankton and other phytoplankton. 4. Metalimnetic P. rubescens that was stratified at low irradiance for weeks exhibited much higher uptake rates than filaments that were entrained in the deepening surface mixed layer and experienced higher irradiance. The added organic compounds contributed up to 62% to the total carbon uptake of metalimnetic P. rubescens. On the basis of a molar C : N ratio of 4.9, the nitrogen uptake as organic compounds satisfied up to 84% of the nitrogen demand. 5. The experiments indicate that photoheterotrophy and light‐dependent uptake of nitrogenous organic compounds may contribute significantly to the carbon and nitrogen budget of filaments at low irradiance typical for growth of P. rubescens in the metalimnion and at the bottom of the surface mixed layer.     

模拟N沉降对太岳山油松人工林和天然林草本群落的影响

由于人类活动氮沉降呈逐年增加的趋势,进而增加了陆地生态系统氮的输入,从而影响陆地生态系统多样性、物种组成和功能。为揭示氮沉降增加对油松林草本群落的影响,于2009年7月在太岳山油松人工林和天然林,设计4个施氮水平:对照(CK,0 kg N hm-2a-1),低氮(LN,50 kg N hm-2a-1),中氮(MN,100 kg N hm-2a-1)和高氮(HN,150 kg N hm-2a-1),研究草本群落的生物多样性、生物量以及草本元素含量对模拟N沉降的响应。研究结果表明:模拟N沉降未能显著影响人工林草本群落的生物多样性(P0.05),而中氮、高氮显著降低了天然林草本群落的生物多样性(P0.05);从Jaccard指数和Sorensen指数分析得出人工林不同氮水平之间草本群落差异性较小,而天然林不同氮水平之间草本群落差异性较大。模拟N沉降没有显著改变人工林草本群落生物量(P0.05),而高氮明显促进天然林草本群落生物量的增加(P0.05)。与对照相比,模拟N沉降提高了人工林和天然林羊胡子苔草叶根中的全N含量(P0.05),而降低了全Mg的含量(P0.05),并且根部元素含量变化与土壤养分含量变化较为一致。施氮提高了N/K、N/Ca、N/Mg(P0.05)的比值。说明油松林下草本群落对氮沉降的响应因林分土壤N饱和程度以及林地利用历史的不同而产生差异,其中天然林响应最为敏感。     

Effects of N addition rates on the productivity ofPicea Sitchensis,Thuja plicata,andTsuga heterophylla seedlings

Seedlings ofPicea sitchensis, Thuja plicata andTsuga heterophylla were supplied N hydroponically at one of four exponentially increasing rates of addition (0.09, 0.07, 0.05, or 0.025 gN^-1 day^-1) for up to 3 months in a naturally illuminated glasshouse. Relative growth rates (RGR) were analyzed as a function of N uptake, the allocation of assimilated N to foliage (LNFR), foliar N concentrations (N_la) and met assimilation rates (NAR), which were combined to estimate N productivity (RGR per unit whole-plant N concentration). Nitrogen accumulation, biomass and N partitioning and RGR and its components varied with species in response to the different N regimes.T. heterophylla had the lowest maximum wholeplant N concentrations (wpN) and specific absorption rates for N and exhibited the least plasticity in root: shoot ratios as wpN increased from 11–21 mg g^-1. In all species, RGR increased linearly with wpN, while LNFR increased curvilinearly. Foliar N (N_la) increased linearly with wpN and NAR increased linearly with N_la. The RGRs ofT. heterophylla were highest at wpNs up to 18 mg g^-1, a result of higher foliar N use efficiencies (NAR/N_la). However, RGR increased more with wpN inT. plicata andP. sitchensis. Although LNFR increased with wpN in all species, foliar N use efficiency declined, possibly due to an increased partitioning of foliar soluble N to non-photosynthetic compounds. Thus, in each species, N productivity did not increase above intermediate levels of wpN: 14 mg g^-1 inT. heterophylla, 16 mg g^-1 inP. sitchensis and 17 mg g^-1 inT. plicata.     

降水和氮沉降增加对草地土壤酶活性的影响

为探究降水和氮沉降增加对草地生态系统土壤酶活性的影响,于2014年生长季在内蒙古温带典型羊草草原开展了野外原位控制实验。试验共设置降水(对照,W0,自然降水;W15,增加15%的年均降水量)、施氮(对照,CK,0 kg N hm~(-2)a~(-1);低氮,LN,25 kg N hm~(-2)a~(-1);中氮,MN,50 kg N hm~(-2)a~(-1);高氮,HN,100 kg N hm~(-2)a~(-1))及其交互作用等8个不同的处理水平来模拟降水和氮沉降增加的全球变化情景,分别定量探讨了不同水、氮添加条件下草地表层土壤中与氮循环相关的蛋白酶,脲酶,硝酸还原酶,亚硝酸还原酶活性的月动态变化及其与土壤理化性质之间的相关性。研究结果表明:在自然降水条件下,不同施氮水平蛋白酶、脲酶和硝酸还原酶活性无显著差异,亚硝酸还原酶活性相比于对照显著降低;在增加降水条件下,不同施氮水平对蛋白酶和硝酸还原酶活性未产生显著性影响,高氮水平显著降低脲酶和亚硝酸还原酶活性。不同施氮水平是否添加降水对亚硝酸还原酶活性无影响,而增添降水使低氮处理的蛋白酶活性和中、高氮处理水平的硝酸还原酶活性增加、高氮处理的脲酶活性降低。降水在影响蛋白酶和硝酸还原酶活性方面具有主效应,氮沉降在影响亚硝酸还原酶活性方面具有主效应,而降水和施氮处理未表现出明显地交互作用。土壤亚硝酸还原酶活性与土壤碳氮比和NH~+_4-N含量极显著正相关,与NO-3-N含量显著正相关。     

Effects of nitrogen supply and irradiance on growth and nitrogen status in the moss Dicranum majus from differently polluted areas

Abstract

A growth experiment was undertaken to study the effects of nitrogen supply and irradiance on growth and nitrogen status in the moss Dicranum majus Sm. from two areas receiving different amounts of atmospheric nitrogen deposition. Intact samples of D. majus carpets were taken from two Picea abies forests, one located in southern Norway (high-N site) and the other in central Norway (low-N site). The moss carpets were grown for 120 days at three irradiance levels (PPFD: 20,40 or 80 μmol m^?2 s^?l) and sprayed daily with equal amounts of a nutrient solution containing 30, 180 or 330 μM nitrogen as NO₃ - and NH₄ +. Concentrations and total amounts of nitrogen, soluble proteins and chlorophyll were highest in moss plants from the high-N site, both at the start and the end of the experiment. The elongation growth was highest at the lowest irradiance level. As total biomass production did not differ between nitrogen and light treatments, moss growth was presumably limited by other factors, even at the lowest supply rates. Concentrations and total amounts of nitrogen increased with increasing nitrogen supply in moss plants from both sites. Accumulated nitrogen was partly stored as protein and chlorophyll. Recycling of nitrogen from old to young tissues is discussed as a possible explanation for the rather low nitrogen demand in D. majus and the persistently higher nitrogen contents in moss plants from the high-N site.     

Complementary limiting factors of astaxanthin synthesis during photoautotrophic induction of <Emphasis Type="Italic">Haematococcus pluvialis</Emphasis>: C/N ratio and light intensity

We investigated the effect of carbon/nitrogen (C/N) ratio on astaxanthin synthesis in Haematococcus pluvialis during photoautotrophic induction by continuous input of both CO₂–air mixture and intense light. When H. pluvialis was induced by constant irradiance induction at 200 μmol photon m⁻² s⁻¹, there was a positive correlation with astaxanthin content and C/N ratio, which was similar to the case for heterotrophic induction. Lower C/N ratios did not retard Haematococcus encystment, but did increase culture biomass, resulting in a decrease in astaxanthin production because of light limitation. However, induction using variable irradiance showed that reduction of astaxanthin production at low C/N ratios was successfully overcome by simply increasing the light intensity from 200 to 300 μmol photon m⁻² s⁻¹ to overcome the light limitation. This resulted in a greatly enhanced astaxanthin synthesis in proportion to cell density in cultures with low C/N ratios. Our results indicate that light intensity is more critical than C/N ratio in astaxanthin production by H. pluvialis during photoautotrophic induction.     

Influence of Nitrogen and Sucrose in the Medium and of Irradiance of the Stock Plants on Root Formation in Pelargonium Petioles Grown in vitro

In vitro root formation was studied in petiole explants from Pelargonium×hortorom Bailey cv. Radio exposed to different irradiance (2.5. 11.6 or 23.0 W/m²). Optimal root formation was found when stock plants were subjected to 2.5 W/m² and explants were grown on a medium with 20 g/I of sucrose and 5.0 mM of nitrogen. The number of roots per explant decreased with increasing nitrogen or sucrose concentrations in the growth medium and with increasing irradiance applied to the stock plants. Variation in temperature (17, 21 or 25°C) did not affect root formation. The number of roots per explant was higher in explants from young petioles than in explants from older petioles. The initial nitrogen content of the explants was highest at the lowest irradiance. The content of reducing sugars and sucrose increased with increasing irradiance. The endogenous levels of lysine, arginine and ornithine were highest at 2.5 W/m² and the levels of proline. alanine, γ-aminobutyric acid, glutamic acid, glutaminc, aspartic acid and asparagine were highest at 23.0 W/m². With rising nitrogen concentration in the medium, the final endogenous content of nitrogen in the explants increased, whereas the content of reducing sugars decreased. When the sucrose concentration in the medium increased, the endogenous content of reducing sugars rose, and the nitrogen level was lowered. Variations in the nitrogen concentration in the growth medium influenced the final level of free amino acids in the explants.     

The use of hydrogen peroxide to control postharvest decay on 'Galia' melons

Sanosil-25, a disinfectant containing 48% hydrogen peroxide and silver salts as stabilising agents, inhibited the mycelial growth of the two main decays causing fungi of melons, Alternaria alternata and Fusarium solani in vitro at concentrations between 5000 and 10 000 μl litre^-1. However, in in vivo experiments, Sanosil-25 markedly decreased decay at a concentration of 5000 μl litre^-1 when incorporated into a wax treatment and produced no phytotoxic effect. This treatment may provide an alternative to imazalil which, although more effective, gives problems with residue levels. A concentration of 10 000 μl litre^-1 proved phytotoxic.     

Fate of nitrogen applied as Azolla and blue-green algae (Cyanobacteria) in waterlogged rice soils—a15N tracer study

Summary ¹⁵N tracer was used to detect the extent to which nitrogen of appliedAzolla caroliniana, Anabaena variabilis andNostoc muscorum was available for assimilation by the growing rice plants in pots under 4 cm flood water for 60 days. The rate of release of nitrogen from the above biofertilizers, the amount of nitrogen remaining in the soils and the amount that was lost from the soils during this period were also examined. Previously¹⁵N-labelled biomass of Azolla, Anabaena and Nostoc to provide 40 mg N was mixed thoroughly with 0.5 kg silt loam Bangladesh soil (Sonatola series) in each of three pots used for a single treatment. Each pot received four 16 days old IR8 rice seedlings. A parallet set of experiments was conducted without rice plants.It was found that nitrogen uptake in the rice plants was increased by 91, 176 and 215% on using Azolla, Anabaena and Nostoc which resulted in increased total dry matter yields (shoot plus root) of 74, 105 and 125%, respectively. Of the total¹⁵N applied at the start, 26, 49 and 53% was released from Azolla, Anabaena and Nostoc; about 7, 14 and 13% was lost by denitrification and 74, 51 and 47% remained in the soils as the undecomposed part of the biofertilizers, respeciively, after 60 days. Of 15.76, 22.72 and 25.92 mg N assimilated by the rice plants, 48, 61 and 62% was supplied by Azolla, Anabaena and Nostoc, respectively. The rest was obtained from the soil used.In the absence of the rice plants 30, 43 and 45% of applied¹⁵N of Azolla, Anabaena and Nostoc was released, respectively, in 60 days of which 93–96% was lost as N₂ through denitrification.     

连续氮添加14年对温带典型草原土壤碳氮组分及物理结构的影响

全球氮沉降对生态系统造成了深远的影响,研究长时间氮沉降对草地生态系统土壤理化特征的影响有助于加强生态系统对氮沉降响应的长效机制的理解。通过连续14年长期施加N0（0 g N m^-2 a^-1）、N2（2 g N m^-2 a^-1）、N4（4 g N m^-2 a^-1）、N8（8 g N m^-2 a^-1）、N16（16 g N m^-2 a^-1）、N32（32 g N m^-2 a^-1）六种浓度尿素模拟氮沉降,并将土壤分成0-10、10-20和20-40 cm三个深度土层,研究温带草原生态系统土壤碳氮组分及物理结构对氮添加的响应及其相互关系,结果表明：（1）氮添加显著降低0-10 cm土壤酸碱度及土壤微生物量碳含量,N32相比N0分别下降了27.63%和58.40%（P<0.05）;各土层总有机碳和全氮含量对氮添加处理无显著响应,0-10 cm土层显著高于20-40 cm土层。（2）同一土层深度不同梯度氮添加处理显著增加土壤无机氮离子含量（P<0.05）,0-10 cm土层铵态氮含量N32相比N0增加了88.72%,20-40 cm土层硝态氮含量N32相比N0增加了19.55倍,土壤深度与氮添加对无机氮离子含量影响具有显著的交互效应。（3）同一土壤深度不同梯度氮添加处理土壤粒度分形维数及土壤团聚体差异不显著,相关分析表明土壤碳氮元素含量与土壤结构显著相关。土壤碳氮组分在适宜浓度氮添加的增加趋势说明氮添加在一定程度上可能促进土壤理化性质的改良,氮添加对土壤物理结构的影响还需要进一步的深入研究。     

Nitrogen concentration of cauliflower organs as determined by organ size,N supply,and radiation environment

Data from field experiments carried out in three consecutive years under contrasting N supply and radiation environment altered by artificial shading were used to identify (a) the relationship between N concentration and organ size under conditions of unrestricted N supply and (b) critical levels of soil nitrate (Nmin_crit), where nitrogen concentration of cauliflower organs begin to decline because of N limitations. The decline of N concentrations in cauliflower was analysed at different levels of morphological aggregation, i.e., the whole shoot level, the organ level (leaves, stem, and curd), and within different leaf groups within the canopy. Nmin_crit values (0–60 cm soil depth) for total nitrogen concentration of cauliflower organs leaves, stem and curd were estimated at 85, 93 and 28 kg N ha^–1, respectively. Within the canopy, Nmin_crit values for total N of leaves increased from the top to the bottom from 44 to 188 kg N ha^–1. Nmin_crit values for protein N in leaves from different layers of the canopy were much lower at around 30 kg N ha^–1, without a gradient within the canopy. It is discussed that these differences in Nmin_crit values are most likely a consequence of N redistribution associated with nitrogen deficiency. The decline of average shoot nitrogen concentrations, [Nm] (%N DM), with shoot dry matter, W _sh, (t ha^–1) under conditions of optimal N supply was [Nm]= 4.84 (±0.071) W _sh ^{–0.089(± 0.011)}, r ²=0.67 (±S.E.). The reduction of radiation intensity by artificial shading (60% of control) had no significant influence on total nitrogen concentrations of leaves and only a small influence on protein nitrogen concentrations in lower layers of the canopy. The leaf nitrate nitrogen fraction of nitrogen, f _nitr (–), within the canopy decreased linearly with increased average incident irradiance in different canopy layers (I _av, W PAR m^–2) (f _Nitr. = 0.2456(±0.0188) – 0.0023(±0.0004)I _av, r ² = 0.67.