International Rice Research Newsletter Vol.13 No.2

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    IRRN GUIDELINES

    The International Rice Research

    Newsletter objective is:

    To expedite communication among

    scientists concerned with the

    development of improved technology

    for rice and for rice-based cropping

    system. This publication will reportwhat scientists are doing to increase

    the production of rice. inasmuch as

    this crop feeds the most densely

    populated and land-scarce nations in

    the world . . . IRRN is a mechanism

    to help rice scientists keep each other

    informed of current research

    findings.

    The concise reports contained in

    IRRN are meant to encourage rice

    scientists and workers to communicate

    with one another. In this way, readerscan obtain more detailed information on

    the research reported.

    guidelines, and research categories that

    follow.If you have comments or suggestions,

    please write the editor, IRRN, IRRI,

    P.O. Box 933, Manila. Philippines. We

    look forward to your continuing interest

    in IRRN.

    Criteria for IRRNresearch reports

    Please examine the criteria,

    has International, or pan-national,

    has rice environment relevance advances rice knowledge uses appropriate research design

    and data collection methodology

    reports appropriate, adequate data applies appropriate analysis, using

    appropriate statistical techniques reaches supportable conclusions

    relevance

    Guidelines forcontributorsThe International Rice ResearchNewsletteris a compilation of research

    briefs on topics of interest to rice

    scientists all over the world.

    Contributions to IRRN should bereports of recent work and work-in-

    progress that have broad interest and

    application. Please observe these

    guideline in preparing submissions:

    The report should not exceed twopages of double-spaced typewritten

    text. No more than two figures

    (graphs, tables, or photos) may

    accompany the text. Do not cite

    references or include a

    bibliography. Items that exceed the

    specified length will be returned.

    research objectives and project

    design. The discussion should be

    brief, and should relate the results

    of the work to its objectives. Report appropriate statistical

    analysis.

    Provide genetic background fornew varieties or breeding lines.

    Specify the environment (irrigated,rainfed lowland, upland, deep

    water, tidal wetlands). If you must

    use local terms to specify landforms

    or cropping systems, explain or

    define them in parentheses.

    Specify the type of rice culture(e.g., transplanted, wet seeded, dry

    seeded).

    Specify seasons by characteristicweather (wet, dry, monsoon) and

    by months. Do not use national or

    local terms for seasons or, if used,define them.

    When describing the rice plant andits cultivation, use standard,

    internationally recognized

    designators for plant parts and

    growth stages, environments,

    management practices, etc. Do notuse local terms.

    Include a brief statement of

    When reporting soil nutrientstudies, be sure to include standard

    soil profile description,

    classification, and relevant soil

    properties.

    diseases, insects, weeds, and cropplants; do not use common names

    or local names alone.

    Provide scientific names for

    Survey data should be quantified(infection percentage, degree of

    severity, sampling base, etc.).

    When evaluating susceptibilityresistance, tolerance, etc., report the

    to stress used to assess level or

    incidence. Specify the

    measurementsused.

    actual quantification of damage due

    Use international measurements.Do not use local units of measure.

    Express yield data in metric tons

    per hectare (t/ha) for field studies

    and in grams per pot (g pot) or per

    row (g row) for small-scale studies. Express all economic data in terms

    of the US$. Do not use national

    monetary units. Economic

    Information should be presented at

    the exchange rate $:local currency

    at the time data were collected.

    Use generic name, not tradename, for all chemicals.

    When using acronyms orabbreviations, write the name in full

    on first mention, following it with

    the acronym or abbreviation in

    parentheses. Thereafter, use the

    abbreviation.

    Define in a footnote or legend anynonstandard abbreviation or

    symbols used in a table or figure.

    Categories of researchreportedGERMPLASM IMPROVEMENT

    genetic resources

    genetics

    breeding method

    yield potentialgrain quality and nutritional value

    disease resistance

    insect resistance

    drought tolerance

    excess water tolerance

    adverse temperature tolerance

    adverse soils tolerance

    integrated germplasm improvement

    seed technology

    research techniques

    data management and computer

    modeling

    CROP AND RESOURCE

    MANAGEMENT

    soils and soil characterization

    soil microbiology and biological Nfertilizer

    physiology and plant nutrition

    crop management

    soil fertility and fertilizer managemendisease management

    insect management

    weed management

    managing other pests

    integrated pest management

    water management

    farm machineryenvironmental analysis

    postharvest technology

    farming systems

    research methodology

    data management and computer

    modeling

    SOCIOECONOMIC AND

    ENVIRONMENTAL IMPACT

    environment

    production

    livelihood

    EDUCATION ANDCOMMUNICATION

    training and technology transfer

    communication research

    Information storage and retrieval

    research

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    CONTENTS

    GERMPLASM IMPROVEMENT

    Genetics

    4 Genetics of seedling elongation in rice

    Breeding methods

    production

    4 Use of Purple Puttu rice variety as a pollen barrier in CMS line seed

    4 Inbreeding depression of yield in rice hybrids

    5 Micropropagation of cytosterile rice stocks

    6 Tissue culture for Argentine rice (O. sativa L.) improvement

    6 Morphoanatomy of rice embryoid development

    Yield potential

    7 Models for predicting rice flowering

    Grain quality and nutritional value

    8 Optical determination of rice grain chalkiness (Clk)

    9 Protein content variation among rice varieties

    Disease resistance

    9 Multiple resistance to bacterial blight (BB) and four fungal diseases

    10 Isolation of a plasmid from strains of Xanthomonas campestrispv. oryzae

    11 Screening for blast (Bl) resistance in Hangzhou, China

    11 Background resistance to bacterial blight (BB) hill and leaf infection

    12 Neck blast (Bl) in newly released upland rice varieties in Brazil

    13 Maintenance of virulence in Xanthomonas campestrispv. oryzae cultures

    13 Leaf blast (Bl) outbreak at Faizabad, India

    that cause bacterial blight (BB) in rice

    Adverse temperature tolerance

    14 Screening rice varieties for cold tolerance at seedling and reproductive

    stages

    Adverse soils tolerance

    15 Effect of acidity on germination and growth of rice seeds

    CROP AND RESOURCE MANAGEMENT

    Soils and soil characterization

    15 Influence of soil texture on rice crop performance

    Soil microbiology and biological N fertilizer

    16 Early, uniform stem nodulation in Sesbania rostrata after spray of

    Rhizobium culture

    Physiology and plant nutrition

    different seasons

    16 Influence of nitrogen and zinc application on nutrient uptake by rice in

    Crop management

    17 Environmental limitations to rice cultivation in the Punjab

    Soil fertility and fertilizer management17 Effect of farmyard manure (FYM) supplemented with N, P, K on gra

    18 Phosphorus requirements in a rice - wheat cropping system

    18 Effect of two phosphorus sources with or without azolla incorporation

    yield

    rice yield in the Senegal River valley

    Disease management

    oryzae

    Bangladesh

    19 Four fungicides for control of grain infection caused by Helminthosporiu

    20 Distribution and severity of rice seedling diseases in boro seedbeds

    20 Managing rice sheath rot (ShR) disease in Kerala, India

    21 Greenhouse trials of seed dress method for controlling sheath blight (Sh

    22 Rice ragged stunt virus (RSV) in aquatic weed Monochoria vaginalis

    Insect management

    22 Influence of time of day and sweeping pattern on catches of gre

    22 Effect of flooding on black bug Scotinophara coarctata (F.) e

    23 Host range and overwintering of rice pink stem borer (PSB) in a hilly regi

    24 Chemical control of rice stem borers (SB) in the Punjab

    24 Monitoring susceptibility of rice pests to insecticides

    leafhoppers (GLH)

    parasitization

    of India

    Water management

    requirement

    25 Influence of planting method and irrigation practices on rice wa

    Farm machinery

    26 Manual rice transplanter use in Burma

    Farming systems

    26 Pigeonpea genotypes and rice yield in an intercropping system

    27Rice

    -

    based cropping systems for optimum production under resouconstraints

    ERRATA

    ANNOUNCEMENTS

    28 INSURF Planning Workshop

    28 New IRRI publications

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    were no anther sacs, and pollen grains

    averaged 0.33 (see table).

    At least 3 lines of Purple Puttu at 15

    10-cm or closer spacing around CM

    line seed production plots can effective

    intercept pollen and anther sac dispers

    between different cytosterile lines. An

    added advantage is that Purple Puttus purple foliage distinguishes it from oth

    varieties.

    sunlight to 1000 h. The petri dishes were

    placed 15 cm from the first stake at the

    level of the glass slides and the muslin

    cloth removed to allow anther sacs and

    pollen grains to disperse by natural wind

    velocity (7.2 km/ h to a height of 3 m).

    Three such dispersals were made.

    The slides were collected and thenumber of anther sacs and pollen grains

    per square inch counted. Where there

    were no plants of Purple Puttu in front

    of the slide, anther sacs averaged 2.33

    and pollen grains 12.66. After the first

    row of Purple Puttu, anther sacs

    averaged 1.66 and pollen grains 6.33 per

    square inch; after the second row, there

    Use of Purple Puttu rice

    variety as a pollen barrier in

    CMS line seed production

    GERMPLASM IMPROVEMENT

    Genetics

    Genetics of seedling

    elongation in rice

    R. S. Tripathi, Agriculture Research Station,

    Banswara, India

    We studied the inheritance of seedling

    elongation ability in an F2 population of

    Pankaj/Nageribao under deepwater

    conditions during the 1977 wet season at

    the Central Rice Research Institute,

    Cuttack. F2 30-day-old seedlings and

    parental lines raised in shallow pans

    were submerged in 80 cm water.

    Seedling height was recorded after 10 d.

    The frequency distributions of F2s and

    parents are presented in the table.

    Frequency distribution of parents and F2 for

    seedling elongation in Pankaj/Nageribao.

    Cuttack, India, 1977.

    Frequency distribution

    Plantheight

    (cm)

    Parents F2

    Pankaj Nageribao

    0-10 10-20 220-30 30-40

    64

    40-50 550-60 3 17

    60-70 19 26

    70-80 8 4680-90 2 70

    90-100 8 99100-110 16 97110-120 3 61120-130 1 11130-140 2

    Range (cm) 54.0-78.2 89.4-120.7

    Average 67.2 110.4

    In 446 F2 plants, 270 were 90-140 cm

    tall, with elongation rates equal to tha

    of the Nageribao parent; 60 plants

    showed poor elongation (10-70 cm),

    comparable to Pankaj; and 116 were

    intermediate (70-90 cm), elongation

    ability better than that of Pankaj but

    not equal to that of Nageribao.

    The data are consistent with two

    dominant complementary genes for

    elongation ability. Presence of both

    genes (Sel 1 and Sel 2) gave elongation

    ability like that of the Nageribao paren

    Absence of either of the genes resulted

    in segregants with intermediate

    elongation ability; absence of both

    resulted in plants like the Pankaj

    parent.

    Breeding methods

    M. Rangaswamy, K. Natarajamoorthy, andS. R. Sree Rangasamy, School of Genetics,

    Tamil Nadu Agricultural University,

    Coimbatore 641003, Tamil Nadu, India

    We assessed the distance of pollen

    dispersal across lines of Purple Puttu

    90 d after sowing, which coincides with

    anthesis in the CMS lines now available

    at the Coimbatore Paddy Breeding

    Station. Purple Puttu has long duration

    (150 d) and is highly photoperiod

    sensitive (120 d to flowering in the wet

    season, does not flower in the dry).

    acetocarmine-glycerine were tied at

    60 cm high to bamboo stakes between

    six rows (15- 10-cm spacing) of

    Purple Puttu. One gram fresh anthers

    collected at 0800 h from a number of

    varieties were bulked and kept in closed

    muslin cloth bags in a petri dish under

    Glass slides smeared with vaseline and

    Rice pollen dispersal a with Purple Puttu as a

    pollen barrier.

    Purple Puttu Av for 3 applicationsrow number

    Anthers/inch2 Pollen/inch2

    0 row 2.33 12.66Row 1 1.66 6.33

    Row 2 0.33Row 3 0.33Row 4

    Row 5

    a Wind velocity at 3 m = 7.2 km/h.

    Inbreeding depression of yiel

    in rice hybrids

    M. Rangaswamy, H. Natarajamoorthy, an

    S. R. Sree Rangasamy, School of Genetics

    Tamil Nadu Agricultural University,

    Coimbatore 641003, Tamil Nadu, India

    Seven IRRI medium-duration hybrids

    (130-140 d) were tested in 1986 wet

    season as F1 (3 replications) and in 198

    dry season as F2 (4 replications) for

    inbreeding depression of grain yield.

    Grain yields in the F2 ranged from

    -28.59 to 3.62% compared to the F1(see table). The same F1 and F2 were

    4 IRRN 13:2 (April 1988)

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    compared with standard variety CO 43.

    Inbreeding depression ranged from

    -30.69 to -0.43%. Hybrids

    IR54752A/ IR19392-2 11-1 and

    IR54752A/ IR4422-480-2-3-3 had yield

    stability in the F2, with low inbreeding

    depression (-0.43 and -0.58%,

    respectively). Their standard heteroses

    were not significant.

    Inbreeding depression (ID) of grain yield in hybrid rice.a Tamil Nadu, India, 1986-87.

    F1 yield F2 yield

    Hybrid, variety (t/ha) heterosis (t/ha) heterosis ID standard standard

    1986 WS 1987 DS

    F1 yield Standard F2 yield Standard over over ID overstandard

    1986 WS (%) 1987 DS (%) (% ) (%) (%) (%)

    IR46828A/IR13524-21-2-3-3-2-2 4.5 29.0 3.9 40.8 14.0 71.0 59.216.6

    IR46830A/IR13292-5-3 4.5 29.0 4.5 32.1 1.4 71.0 67.9 4.3

    IR54752A/IRl4753-120-3 7.0 +10.6 5.6 14.8 20.6110.6 85.2 23.0

    IR54752A/IR19392-211-1 6.4 + 0.4 6.2 0.1 2.5 100.4 100.0 0.4

    IR54752A/IR4422-480-2-3-3 4.2 34.2 4.4 33.8 + 3.6 65.8 66.2 0.6

    IR54752A/IR20933-68-28-1-2 5.5 14.1 3.9 40.5 28.6 85.9 59.5 30.7

    IR54752A/IR54 6.0 6.4 4.8 26.2 18.8 93.6 73.8 21.1

    CO 43 (standard) 6.4 6.6 + 3.0 100.0 100.0

    LSD 1.1 1.0

    Micropropagation of

    cytosterile rice stocks

    D. S. Kumari, N. P. Sarma, and G. J. N.

    Rao, Central Rice Research Institute

    (CRRI), Cuttack 753006, India

    We have propagated cytosterile rice

    stocks by regenerating plants in callus

    culture. The important consideration in

    applying in vitro methods for

    propagation is to retain the geneticintegrity of the original stock. There is a

    risk of genetic variation in plants

    regenerated after an intermediate callus

    growth phase.

    In vitro propagation of rice by

    inducing axillary shoots or regeneration

    from nodal buds ensures against the

    possibility of genetic variation among

    the regenerants.

    of cytosterile stock V20A were

    germinated on Murashige and Skoogs

    (MS) medium with 50 g sucrose/liter but without auxins. Six-day-old excised

    seedling shoots, without radicle and

    endosperm, were implanted on fresh MS

    medium supplemented with

    benzyladenine (BA) at 0.5, 1, 1.5, and

    2 mg/liter. The cultures were

    maintained at 25 + 1 C with 16 h

    photoperiod/d.

    Dehusked and surface sterilized seeds

    After 3 wk, multiple axillary shoots

    formed from the basal region of the

    implanted shoots. Axillary shoot

    formation was highest with 2 mg

    BA/liter (Table 1).

    about 1 cm long, they were separated

    When clumps of multiple shoots were

    Table 1. Multiple shoot formation of the cyto -sterile stock V20A after 3 wk in culture. CRRI,

    Cuttack, India.

    Shoots Axillary shoots

    (no.) after 3 wk

    Mediuma implanted (no.) induced

    MS + 0.5 mg BA 17 40MS + 1.0 mg BA 18 58MS + 1.5 mg BA 17 80MS + 2.0 mg BA 16 82

    aMS basic medium with 50 g sucrose/liter.

    and used as fresh implants on MS

    medium containing different levels of

    BA, kinetin (K), naphthalene acetic aci

    (NAA), and indolebutyric acid (IBA)

    (Table 2).

    The number of shoots increased

    slightly with the addition of K to the

    medium. The best results were with BA

    Adding NAA with BA did not promot

    root growth; adding IBA with BA

    induced weak roots. Root growth was

    vigorous in MS medium supplementedwith NAA alone, but axillary shoots

    were suppressed.

    multiple axillary shoots in vitro is

    feasible for the micropropagation of

    valuable cytosterile stocks. Continuous

    axillary shoot production is possible,

    These results suggest that induction

    Table 2. Effect of different growth regulators in multiple shoot and root formation. CRRI, CuttackIndia.

    Growth regulators (mg/liter) Shoots Axillary shoots RootMediuma implanted

    BA K NAA IBA

    produced

    (no.) (no.)

    MS-1 2 26 100

    MS-2 0.5 24 372 0.5

    MS-4

    14 432 1

    MS-520 68

    2 0.5 1 20MS-6

    54 0.5 1 18 31 ++

    1 12 211.5 12 12 +++

    MS-3++

    MS-7 2MS-8

    +

    aMS basic medium with 50 g sucrose/liter. b+ = weak, ++ = good, +++ = very good.

    IRRN 13:2 (April 1988)

    a ID =F2 - F1

    F 100

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    eliminating the risk of somaclonal

    variation in successive subcultures. A

    logical extension of the rate of

    multiplication through successive

    cultures should yield 1 5n axillary

    shoots, where n is the number of

    subcultures, with each cycle requiring

    3-4 wk. Since rooting is essential to

    establish the shoots in soil, an additional

    cycle on MS medium supplementedwith root-inducing auxin NAA at

    1.5 mg/liter may be necessary.

    Table 1. Variation among the first progeny of Gualeyan P. A. regenerated plants (R2) and progen

    of the original variety. Buenos Aires, Argentina, 1987.

    Trait Gualeyan

    Mean Range

    Panicle length (cm) 17.66 22.08 12.09-25.6 **Grain with husk

    Length (mm) 9.35 9.13 8.5 - 9.85 **

    Grain without husk3.82 3.52 4.0 - 3.0 **

    Length (mm) 7.11 7.78 6.3 - 1.85 **Width (mm) 3.11 2.89 2.5 - 3.15 **

    R2 progenyF tes

    Width (mm)

    a ** = significant at 1% level.

    Table 2. Variation among the first progeny of Yerua F. A. regenerated plants (R2) and progeny othe original variety. Buenos Aires, Argentina, 1987.

    Tissue culture for Argentine-

    rice (O. sativa L.)

    improvementTrait

    R2 progenyYerua F tes

    Mean Range

    M. A. Rapela and M. A. Marassi, Instituto

    Fitotcnico de Santa Catalina, Facultad de

    Agronomia, Universidad Nacional de la

    Plata, C. C. 4, 1836 Llavallol, Buenos Aires,Argentina

    Seeds of Argentine rice varieties Yerua

    F.A. and Gualeyan P.A. were cultured

    on Murashige and Skoogs (MS) basic

    salts supplemented with 2 mg 2,4-D/liter

    of medium in darkness at 28 C. Callus

    formed 15 d after inoculation. Callus

    induction was 100% in both varieties.

    regeneration medium with the same

    basic salts supplemented with 1 mg

    BAP/liter. Plant regeneration was 30%

    in Yerua, 50% in Gualeyan.

    The plantlets were transferred to pots

    containing sterile vermiculite and

    watered with 1/4 MS salts. After 1 wk,

    they were transplanted to the

    greenhouse and grown to maturity.

    Seeds were obtained from all the plants,

    although fertility was not 100%.

    Seeds from the regenerated plants and

    seeds from the original varieties were

    planted at 20- 20-cm spacing and

    conventional cultivation procedures

    followed. At maturity, sample plants

    were collected to evaluate agronomic

    traits; the rest were used for testing yield

    characteristics and blast resistance.

    regenerated from Gualeyan (R2 ) showed

    higher tillering ability than the original

    variety; 20% had a different husk color.

    Calli were subcultured on a

    The first progeny of plants

    Panicle length (cm) 21.14Grain with husk

    Length (mm) 10.34Width (mm) 3.54

    Length (mm) 7.94Width (mm) 3.1

    aSignificant at 1% (**) and 5% (*) levels.

    Grain without husk

    Panicle length and two grain

    dimensionswith and without husk

    also significantly differed (Table 1). The

    first progeny of plants regenerated from

    Yerua (R2 ) showed low plant height and

    significant differences for panicle length,

    grain width with husk, and grain length

    Morphoanatomy of rice

    embryoid development

    F. J. Zapata and D. C. de Castro, Tissue

    Culture Laboratory, Plant Breeding

    Department, IRRI

    Histological studies of cultured embryos

    during the early stages of cell

    proliferation provide information about

    the initial sites and patterns of cell

    division activity and subsequent

    differentiation. Morphological

    observations through the scanning

    electron microscope (SEM) provide a

    clear picture of the natural concave-

    convex appearance of the various stages

    of embryoid development.

    22.30 12.3 - 3.0 **

    9.67 11.0 - 6.53.74 3.25- 4.3 *

    7.51 *3.04

    ns

    6.5 - 8.7

    26.5 - 4.1 **

    without husk (Table 2).

    This study showed a definite trend

    toward more somaclonal variation in

    Gualeyan than in Yerua. The tissue

    culture-derived plants may be useful as

    sources of new germplasm.

    Dehulled mature seeds of rice variety

    Tetep were sterilized and inoculated in

    Linsmaier and Skoogs (LS) medium,

    each liter containing 1 mg 2,4-

    dichlorophenoxyacetic acid (2,4-D)

    gelled with 1% agar. Cultures were

    maintained in darkness at 26-27 C.

    The scutella were isolated from

    embryos still embedded in the seed afte

    1 wk in culture. Samples for histologica

    and SEM analysis were taken 2, 4, 6, 8

    10, and 12 d after seed inoculation;

    subsequent samples from subcultures

    were taken every 4 wk.

    were transferred to Murashige and

    Skoogs (MS) medium, each liter

    containing 4 mg benzylaminopurine

    For plant regeneration, 3-mo-old cal

    6 IRRN 13:2 (April 1988)

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    (BAP), 0.5 mg indole-3-acetic acid

    (IAA), 0.5 mg naphthalene acetic acid

    (NAA), 500 mg casein hydrolysate, and

    3% sucrose gelled with 0.8% agar. The

    calli were incubated at 26-27 C in

    continuous 3000 lux light intensity.

    Active cell division took place in the

    scutellum, especially on the

    subepidermal (sep) portion (see figure,

    1-2). Calli formed on day 6 of culture.

    Elongated structures were visible at the

    periphery of the scutellum on day 10 (3).

    Cells pushed out the epithelial layer,

    giving the scutellum a wavy appearance.

    Active cell division was visible on day

    12. Smooth, compact, round and

    whitish embryoids were obtained after 3

    wk in culture (4).

    Anatomical observations showed

    embryogenic calli with densely packed

    cells, prominent nucleus, and thin cell

    walls (5). Nonembryogenic calli had

    loosely packed cells, hardly visible

    nuclei, and thick cell walls (5).

    A SEM study (7) showed globular

    and organized structures (e) proliferating

    at the surface of the nonembryogenic

    calli (ne). Embryoids containing the

    scutellar portion, coleorhiza, and a

    developing coleoptile (8) were exactly

    Yield potential

    Models for predicting rice

    flowering

    A. B. Dua and D. P. Garrity, Multiple

    Cropping Department, IRRI

    Models for predicting flowering in

    cereals are often location specific. We

    developed simple temperature-

    dependent regression models that can

    estimate flowering in lowland irrigatedrice. Data from 43 rice experiments

    conducted at 23 irrigated sites in Asia,

    Africa, and Latin America that ranged

    from 09'S latitude (Ahero, Kenya) to

    3716'N latitude (Suweon, Korea) were

    evaluated for relationships between

    mean temperature, photoperiod, and

    flowering date.

    cultivars IR9729-67-3 (very early), IR36

    Three maturity groups, represented by

    like the zygotic embryo, but sometimes

    did not have synchronized developmen

    Embryogenic calli transferred to

    regeneration medium produced prolific

    shoots and plantlets from embryoids

    after 3 wk in culture.

    and BG35-2 (early), and Taichung SenYu 285 (medium), were tested for best

    fit to generalized thermal or

    photoperiod models. Thermal units (Tu

    for each 24-h interval had been recorded

    in agrometeorological stations in the

    vicinity of the experiments. Daily

    thermal units were calculated as the

    mean of the daily maximum (T max) and

    minimum (Tmin) temperatures and

    summed for the period from seeding to

    flowering (SF).

    Accumulated thermal units for the

    period transplanting to flowering (TF)also were computed. Photoperiod (p) at

    panicle initiation was estimated, using

    meteorological algorithms. Reciprocals

    of the durations of SF and TF were

    calculated as the average rate of

    progress toward flowering. Average rat

    of progress toward flowering showed a

    curvilinear trend with mean temperature

    (see figure). This relationship was

    derived from data across the four

    Rice embryoid development: 1 = longitudinalsection of a seed embryo showing the coleorhiza (cr),

    coleoptile (cl), scutellum (sc), and subepidermallayer (sep); 2 = callus formation at the subepidermallayer of the sc; 3 = thallus structure proliferatingfrom the surface of the sc; 4 = 3-mo-old smooth,compact, round, and whitish embryoids; 5 = anembryogenic callus; 6 = a nonembryogenic callus; 7= scanning electron micrograph of embryogeniccalli (e) proliferating at the surface of nonembryo-genic (ne) calli; 8 = scanning electron micrograph ofan embryoid with sc, cr, and a developing cl. IRRI,1987. Rate of development from seeding to flowering of IR36 (1/f) vs mean temperature.

    IRRN 13:2 (April 1988) 7

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    Optical determination of rice

    grain chalkiness (Clk)

    Jin Qingsheng and Qiu Baiqin, Crop

    Institute, Zhejiang Academy of Agricultural

    Sciences (ZAAS), Hangzhou, China

    We used a digital grain translucency

    meter (DWY-1A model, manufactured

    by ZAAS) to measure grain

    translucency of 17 IR varieties grown in

    early season 1986. Samples of whole

    milled rice were tested, with three

    replications.

    Mean translucency and corresponding

    Clk scale are shown in the table. Asignificant negative correlation was

    found between grain translucency and

    Clk (see figure). For rice breeding work

    or in grading for market value, this

    meter can be used instead of visual

    rating to measure the degree of Clk.

    Optical determination of Clk is not

    possible with waxy rice because the

    opaque endosperm also reduces grain

    translucency.

    Photo-thermal models for predicting flowering in IR36 across locations. Screened data set of 43trials from a global rice-weather study. 1987.

    ModelRegression coefficientsa

    a b cR2 CV

    d

    Seeding to flowering1. 1/f = a + b*Tmean 0.00165ns 0.00471** 0.39 13.0

    2. 1/f = a + b*TU 0.02171** 0.0000425** 0.75 8.2

    3. 1/f = a + b *TU+c*p+d*p2 0.0733** 0.00000385** 0.0148** 0.000579** 0.79 6.8

    (0.00233) (0.00009)

    (0.000994) (3.93 E-07)

    (0.0236) (4.57 10 E-10) (0.00366) (0.000141)Transplanting to flowering

    1. 1/f = a + b*Tmean 0.00334ns +0.000695** 0.37 12.7(0.00359) (0.00138)

    2. 1/f = a + b*TU 0.0302** 8.64 E-06** 0.81 7.0

    3. 1/f = a + b*TU+c*p+d*p2 0.0707* 8.15 E-06** +0.0156** 0.000607** 0.78 6.3

    (0.00117) (6.44 E-07)

    (0.0307) (8.28 E-07) (0.00476) (0.00184)

    level. 1/f = progress toward flowering, i.e., the reciprocal of the time from seeding to flowering (SF)

    a*, ** = 0.05 and 0.01 significance levels, respectively, ns = estimated values not significant at the 5%

    or transplanting to flowering (TF). p = photoperiod. TU = accumulated thermal units. Tmean =mean temperature (C) from seeding to flowering.

    latitude groups. The optimum

    temperature for maximum developmen

    rate in IR36 was 26.8 C.

    A simple model using accumulated

    thermal units accurately estimated the

    rate of progress toward flowering (see

    table). Best fit models included a

    quadratic photoperiod term (p) that

    accounted for daylength effects. Model

    for genotypes maturing earlier (IR9729

    67-3 and BG35-2) and later (Taichung

    Sen Yu 285) than IR36 were very simil

    in performance.

    developing simulation models of rice

    growth and development that rely on a

    accurate prediction of phenological

    events under a wide range of

    temperatures and daylengths.

    These data may be useful in

    Grain quality and nutritional value

    Grain translucency and Clk rating in milled rice

    of 17 IR varieties, evaluated by digital trans-lucency meter. Hangzhou, China, 1986.

    Variety

    IR22 90.7 1.4

    IR24 81.0 2.8IR28 84.0 2.6IR30 70.0 6.5IR34 88.0 3.3

    IR36 86.3 3.2

    IR38 80.7 5.2IR43 79.7 3.9IR44 84.3 3.6IR45 86.7 5.0IR46 82.3 1.0IR52 78.7 1.4IR54 89.0 1.5

    IR56 85.0 1.0IR60 85.7 1.0IR62 90.7 1.0

    IR64 77.3

    Translucency

    (%)Clk

    4.1Relationship between Clk scale and translucency measured in milled rice of 17 IR varieties, 1986.

    8 IRRN 13:2 (April 1988)

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    Protein content variation

    among rice varieties

    M. Jayapragasam, A. Manickam, N. M.

    Ahamad, and B. Thayumanavan,

    Biochemistry Department, Tamil Nadu

    Agricultural University, Coimbatore 641003,

    India

    We analyzed the grain of 294 ricegenotypes raised in the same field under

    similar cultural operations for protein

    content, using conventional micro-

    Kjeldahl method. Grain samples were

    dehusked by hand- pounding. Brown rice

    protein content was expressed as dry

    weight % after multiplying by 5.95.

    Total protein varied from 4.94% in

    Ratna and Sona to 12.86% in ADT21.

    ASD10, T3 (Tainan), and T8 had

    protein contents higher than 12%. Thirty

    samples contained more than 10%

    protein; 112 samples, 8-10%; 137

    samples, 6-8%; and 15 samples, less than

    6%. Ten of 40 ADT varieties had more

    than 10% protein. TKM and ADT

    Disease resistance

    Multiple resistance to

    bacterial blight (BB) and four

    fungal diseases

    R. N. Singh and A. T. Khan, N. D.

    University of Agriculture and Technology,

    P. O. Dabha Semar, District Faizabad

    224133, U. P. India

    We tested 233 rice varieties and lines in

    the 1986 National Screening Nursery

    and Multiple Resistance Screening Trial

    for resistance to BB, sheath rot (ShR),

    brown spot (BS), false smut (FS), and

    narrow brown leaf spot (NBLS) diseases

    during 1986-87 wet season. Each test

    entry was planted in 2-m-long rows at20- 15-cm spacing.

    Plants in half of the rows were clip-

    inoculated with a suspension of a local

    isolate of Xanthomonas campestrispv.

    oryzae (Ishiyama) Dye at maximum

    tillering. BB was rated at 15 and 30 d

    after inoculation. Reactions to high

    natural BS, NBLS, ShR, and FS disease

    Mean and dispersal coefficient of variation of protein content of grain of some rice varieties. Tam

    Nadu, India.

    Soluble protein Total protein

    Samples Mean CV (%) Samples Mean CV (%Varieties

    (no.) (%) (no.) (%)

    ADT varieties 39 0.5 1 63.3 40 9.08 17.9

    ASD varieties 18 0.97 38.7 18 8.87 18.7

    CO varieties 18 0.68 36.8 28 8.1 1 12.8

    CO32 mutants 4 0.5 6 24.3 4 7.32 14.6

    CO33 mutants 10 0.81 32.3 10 8.50 18.8

    IR varieties 6 0.48 37.3 8 7.18 12.1

    Ponni/IR8 (F4) 39 8.45 5.5

    Tainan varieties 50 1.05 30.0 50 8.74 16.1

    TKM varieties 8 0.89 39.7 8 9.10 17.4

    TKM6 mutants 11 1.00 24.0 11 7.64 20.8

    Other varieties 77 0.57 40.4 78 7.62 17.3

    All genotypes 24 1 0.74 48.2 294 8.26 17.2

    varieties had the highest average protein

    content, 9.1%.

    Hot-water soluble protein estimated

    colorimetrically by Lowry's method

    showed greater variation than total

    protein (see table). The Tainan types

    had the highest average soluble protein

    content (1.05%). Total protein and

    soluble protein contents of the grain

    were not significantly correlated. Prot

    of 62 varieties soluble in 0.1 M NaOH

    and determined by Lowrys method w

    very highly significantly correlated wit

    micro-Kjeldahl protein (r = 0.93**). T

    coefficient of variation for data from

    Lowry's method (18.11%) was slightly

    lower than that for the micro-Kjeldah

    method (19.41%).

    Resistance of varieties and lines to BB, ShR, BS, FS, and NBLS.a

    Uttar Pradesh, India, 1986-87 w

    season.

    Varieties (%)

    Disease-free Resistant Moderately susceptible SusceptiDisease

    BB 0 42.0 47.2 10.7ShR 0.4 45.4 48.5 5.BS 0 23.2 73.0 3.FS 26.2 43.0 24.0 6.

    NBLS 65.7 3.4 13.7 17.

    aData based on 233 varieties except for FS and NBLS, where observations were recorded on 221 231 lines. respectively.

    pressure were taken on plants in the

    other half of the rows.

    No variety or line escaped BB and BS

    (see table). Only one remained free of

    ShR; 26.2% escaped FS. Because NBLS

    appeared late in the season, a majority

    of the varieties (65.67%) escaped thedisease; however, the highest number of

    entries showed susceptibility. More

    varieties showed resistance to ShR

    (45.45%) and moderate susceptibility to

    BS (72.96%); fewer were resistant

    (3.43%) and moderately susceptible

    (13.74%) to NBLS.

    IET8958, IET9313, IET9843, and

    IR50 showed multiple resistance to BB

    ShR, BS, and FS; IET8340 showed

    resistance to BB, ShR, FS, and NBLS

    Entries with multiple resistance to thre

    diseases included IET7511, IET7720,

    IET7978, RP16691-2897-5526, and

    IR29652-65-2-3 to ShR, BS, and FS;IET8022, IET8023, IET9965, and

    IR32429-45-3-2-6 to BB, ShR, and BS

    IET8364, IET8653, IET8611, and

    IET9799 to BB, BS, and FS; and

    IET8588 to ShR, FS, and NBLS. A

    large number of entries possess

    resistance to two diseases, many others

    are resistant to one disease.

    IRRN 13:2 (April 1988)

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    Isolation of a plasmid from

    strains ofXanthomonas

    campestris pv. oryzae that

    cause bacterial blight (BB) in

    rice

    Vijai Pal, Plant Pathology Department,

    Haryana Agricultural University, Hisar

    125004, India; and L. Gardan and M.Charles, Institut National de la Recherche

    Agronomique (INRA), Station de

    Pathologie Vegetale et Phytobacteriologie,

    Beacouze 49000 Angers, France

    One or more indigenous plasmids in

    several phytopathogenic spp. of

    Agrobacterium, Corynebacterium,

    Erwinia, Pseudomonas, and

    Xanthomonas have been demonstrated

    to carry the determinants of bacterial

    pathogenicity. We investigated the

    presence of plasmids in various strainsof Xanthomonas campestrispv. oryzae

    and evaluated their physical and

    pathological properties.

    national collection of phytopathogenic

    bacteria, INRA, Angers, and strains

    XCOH-9 and XCOH-40 from Haryana

    Agricultural University, Hisar, India.

    Strain L5-30 of Rhizobium meliloti with

    plasmid pRMe, molecular weight (MW)

    89 106 dalton; strain M 175.4 of

    Enterobacter cloacae with 2 plasmids,

    MW 155 106 and 71 106 dalton;strain V-517 ofEscherichia coli with

    Strains 1948 and 1981 came from the

    1. Agarose gel electrophoresis of plasmid DNA of

    known MW along with the 4 strains of X. campestris

    pv. oryzae. Track 1, lysate from strain 1948; 2, lysate

    from strain XCOH-9; 3, lysate from Rhizobium

    meliloti strain L5-30 carrying plasmid pRMe (MW

    89 106 dalton); 4, strain 1981; 5, lysate from E. coli

    strain V-517 carrying plasmid pVA517A(MW 35.8

    106 dalton); 6, lysate from E. cloacae strain M

    175.4 carrying plasmids pRE-175 upper band (MW

    155.3 106 dalton) and lower band (MW 71.5

    106 ); 7, lysate from XCOH-40.

    10 IRRN 13:2 (April 1988)

    2. Electron microphotograph of plasmid DNA isolated from Xanthomonas campestrispv. oryzae.

    plasmid pVA517A, MW 35.8 106 physical measurement. The MW of the

    dalton; and several other plasmids plasmid of X. c.pv. oryzae was about

    ranging in size from 1.36 106 dalton to 20.3 106 to 21 106 dalton as

    4.8 106 dalton were used as reference determined by electron microscopy and

    strains for measuring the MW of the agarose gel electrophoresis (Fig. 2).

    plasmid species of X. c.pv. oryzae. Taichung Native 1 rice seedlings

    All the strains were grown overnight grown in plastic pots (12 cm diam) wer

    in 5 ml broth in a shaker at 28 C. The individually inoculated by tip clipping a

    cells were harvested by centrifuging at 90 d after sowing with all the test strain

    8000 g 10 min and thoroughly of X. c.pv. oryzae. Each strain was

    resuspended in 2 ml of E- buffer (40 mM reisolated from diseased seedlings (afte

    Tris-acetate, pH 9, 2 mM sodium five pathological tests in serial) and the

    EDTA). The suspension was lysed by plasmids again analyzed by geladding 4 ml of lysis solution (3% sodium electrophoresis.

    dodecyl sulfate in 50 mM Tris-OH All four reisolated strains showed the

    buffer, pH 12.6) at 90 C for 20 min. presence of a plasmid with the same

    The lysate was emulsified with 6 ml of MW, indicating the stability of this

    phenol-chloroform mixture (1:1 by plasmid in the different strains. The

    volume) and centrifuged for 10 min at presence of a plasmid in X. c.pv. oryza

    8000 g. strains may provide an opportunity for

    recovered and used for agarose gel indigenous plasmids in BB

    electrophoresis (0.7% agarose in a development.

    vertical Lucite slab gel apparatus). The

    gels were stained in ethidium bromide

    solution (0.4 g/ml) and visualized overan UV-transilluminator (Fig. 1). The International Rice Research

    estimated by electron microscopy and

    by plotting the relative mobility of

    against the logarithm of plasmid MW of 933, Manila, Philippines.reference standards determined

    previously by electron microscopic and

    The upper aqueous phase was understanding the involvement of

    The MW of the plasmid was Newsletter is mailed free to individualsand institutions engaged in rice researchand training. For further information,write IRRI, Communication and

    plasmid DNA bands in the agarose gel Publications Dept., Division R, P.O. Box

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    Varieties or lines resistant to B1 at CNRRI,

    Fuyang Experiment Station, Hangzhou, China,

    1987.

    Variety or line

    BG380-2C712035C721313C731110HPU5010-PLP21-2-1BIR13524-21-2-3-3-2-2IR19349-135-2-3-2-1IR19670-57-1-1-3IR31868-64-2-3-3-3IR32429-122-3-1-2IR35353-94-2-1-3IR35410-16-3-2-2-2-2IR37865-29-3-1-3IR39379-20-1-2-1-1

    IR7732-RGA-B-A96-1SR9713-31-2-3

    Suakoko 8 (2526)

    Tetep32-Xuan-5-BEr Jiu Feng (resistant

    check)Guang Lu Ai No. 4 9 5 9

    (susceptible check)

    Score a

    Seedling Leaf Neck

    5 0 14 1 03 1 03 1 04 0 04 0 03 0 03 1 34 0 04 0 03 0 03 3 04 0 02 0 0

    4 2 00 0 03 1 33 3 0

    4 0 35 2 5

    a By the Standard evaluation system for rice 0-9scale.

    Screening for blast (Bl)

    resistance in Hangzou,

    China

    Shen Ying, Yuan Xiao-ping, and Huang Shi-

    wen, China National Rice Research Institute

    (CNRRI); and Lu Fu-ying, Zhejiang

    Agricultural University, Hangzhou,

    Zhejiang, China

    Rice Bl is one of the most widely

    distributed diseases in China. Heavy

    infections on panicles are often

    detrimental to rice yields. We screened

    113 entries under natural disease

    pressure at the CNRRI Fuyang

    Experiment Station during 1987.

    One-month-old seedlings were

    transplanted in 2 rows at 20- 20-cm

    spacing. One row each of susceptible

    checks Yuan Feng Zao and Guang Lu

    Ai No. 4 and resistant check Er JiuFeng were transplanted between each

    entry and on all sides. Soil was sandy

    loam with medium fertility. Fertilizer

    was applied at 75-37.5-25 kg NPK/ ha.

    A local predominant strain of the Bl

    pathogen was collected and isolated

    from naturally infected leaves and a

    spore suspension sprayed at 2 wk after resistant to Bl (see table). C721313,

    transplanting to help initiate infection. C731110, HPU5010-PLP21-2-1B,

    The spore suspension concentration was IR13524-21-2-3-3-2-2, IR31868-64-2-3-3

    adjusted to 5 10 5/ml. Seedling, leaf, 3, IR32429-122-3-1-2, IR39379-20-1-2-1

    and neck Bl were scored at four leaf 1, IR7732-RGA-B-A96-1 have good

    ages, maximum tillering, and maturity. grain quality and high yield potential.Of 113 entries screened, 19 were

    Background resistance to

    bacterial blight (BB) hill and

    leaf infection

    T. W. Mew and C. M. Vera Cruz, IRRI

    In the Philippines, rices with the Xa-4

    gene for resistance to race 1 of

    Xanthomonas campestrispv. oryzae are

    affected by the virulence of race 2, the

    dominant bacterial pathogen

    population. Although more than 80% ofthe rice area is planted to varieties with

    such resistance, BB occurs endemically

    in specific localities. The level of

    infection varies, even though the same

    resistance gene Xa-4 confers resistance.

    We assessed reactions of commonly

    planted varieties to both virulent and

    avirulent races to determine if other

    components influence their resistance.

    Races 1 and 2 and IR20, IR22, IR26,

    IR36, IR42, IR48, IR50, IR54, IR56,

    IR58, IR60, and IR62 (all known to

    carry Xa-4) were used.

    Plants raised in the screenhouse wer

    inoculated at 21 d after sowing with

    isolate PXO 61 of race 1 (avirulent) an

    PXO 86 of race 2 (virulent). IR24,

    which carries no gene for BB resistanc

    was the susceptible check. Hill and

    leaf/ hill infection was measured at thr

    growth stages.

    The relative resistance index (RI) us

    Resistance or susceptibility of IR cultivars carrying Xa-4 gene for BB resistance to 2 races ofXathomonas campestris pv. oryzae at 3 growth stages. a IRRI, 1986 dry season.

    Early tillering Maximum tillering

    Variety Hill Leaf Hill Leaf Hill

    Booting stage

    Leaf

    infection infection infection infection infection infecti

    (%) (%) (%) (%) (%) (%)

    PXO 61IR24 b 91.6 29.6 91.6 23.8 52.0 14.8IR56 91.6 28.4 87.4 17.0 52.0IR50

    9.645.8 11.4 50.0 5.4 8.2 0.8

    IR60 43.8 11.8 33.4 3.2 4.2IR42 37.6

    0.211.2 6.2 0.2

    IR22 33.4 7.2 12.4IR58 33.4

    1.8 6.8 18.8 1.8 4.2 0.6

    IR62 27.0IR36

    7.4 29.2 3.8 10.427.0

    2.29.6 20.8 1.6

    IR200

    25.0 7.6 12.4 1.6 14.6IR54

    1.820.8

    IR265.6 35.4 2.2 2.2 0

    18.8 3.8 6.2 0.6 2.0 0.4

    IR24 b 73.0 23.8 87.6 25.6 75.0 24.0IR56 95.8 30.8 91.6 20.0

    IR50 98.0

    73.0 13.4

    31.8 100IR60

    21.491.6

    70.829.2

    16.8

    IR4277.0 14.4 58.4

    70.810.0

    23.0 60.4 12.0 IR22 75.0 25.0 62.4 12.4IR58 58.4 16.8 81.2 20.8IR62

    70.8 20.868.8 17.8 79.0

    IR3619.4

    66.6 15.6 60.4 9.270.8

    85.418.2

    IR2016.4

    43.8IR54

    22.4 58.4 56.2 12.039.6

    13.211.8 67.6

    IR2624.0

    75.060.8

    26.2 64.6 19.8 60.4 18.621.8

    a Mean of 2 replications. b Susceptible check.

    PXO 86

    IRRN 13:2 (April 1988) 1

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    to measure resistance is based on a

    comparison of the amount of disease on

    IR24. The effect ofXa-4 on the

    individual race was estimated by the

    formula

    DL of IR24 - DL of IR cultivar

    100RI =

    DL = disease level (% hill infection, %

    leaf infection, % lesion area)A zero RI means that resistance equals

    that of IR24.

    A wide range of hill and leaf infection

    with the two races was observed (see

    table). Infection with the virulent race

    was higher than with the avirulent race

    at both maximum tillering and booting.

    Based on hill infection, the RI of

    varieties infected with the avirulent race

    increased as the plants matured (see

    figure). The RI of varieties infected with

    the virulent race also increased.The data seem to suggest that these

    varieties possess a distinct background

    Relative resistance index, based on hill infection, of selected IR varieties to races 1 (PXO61) and 2 (PXO86) of Xanthomonas campestrispv. oryzae as compared to that of IR24, the susceptible variety, at 3 growth stages,

    IRRI, 1986 dry season, + = more resistant than IR24, - = more susceptible than IR24.

    12 IRRN 13:2 (April 1988)

    resistance that increased as the plant

    matured. Using hill and leaf infection as

    parameters, such background resistanc

    may not be shown at early tillering.

    Because difference in disease level

    induced by PXO 61 and PXO 86 is

    related to the effect ofXa-4, the DL of

    test variety not matched by PXO 86 is a

    measure of background resistance.

    Although the measurement is indirect,differences at different growth stages

    were clear. Perhaps this background

    resistance slows down epidemics in

    farmers fields in the Philippines, even

    though the race 2 population is

    increasing with an increase in hectarage

    planted to varieties with similar genetic

    backgrounds. Background resistance

    could be an attribute of the durability o

    resistance of IR cultivars carrying the

    Xa-4 gene.

    For instructions on preparation of brief

    reports of rice research to submit for

    publication in IRRN, see the inside fron

    cover of this issue.

    Neck blast (BI) in newly

    released upland rice varieties

    in Brazil

    E. P. Guimaraes, O. P. de Morais, and M.

    H. G. L. Chatel, National Research Center for Rice and Beans (EMBRAPA/CNPAF)

    Caixa Postal 179, 74000 Goiania, GO, Braz

    Upland rice varieties Rio Paranaiba

    (IAC47/63-83), Araguaia

    (IAC47/TOS2578/74-2-3-B2), and

    Cabau (mutant of IRAT79) were

    released to the Cerrado Region in

    Brazil. They were evaluated in

    consecutive years 1984-85, 1985-86, and

    1986-87 in Goiania with local check

    IAC47.

    Neck Bl increased and grain yielddecreased for all varieties tested (see

    table). The increase in all cultivars was

    independent of the degree of resistance.

    Disease and yield were significantly

    different between IAC47 and the

    improved varieties. The newly released

    upland varieties had higher neck Bl

    resistance, and yielded more.

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    Neck Bl incidencea and grain yield of newly released upland rice cultivars and local check IAC47.b Goiania, GO, Brazil, 1986-87.

    IAC47 Rio Paranaiba Araguaia Cabacu Year mean

    Growingseasonc Neck B1 Grain Neck B1 Grain Neck B1 Grain Neck B1 Grain Neck B1

    yield yield yield yield y

    (t/ha) (t/ha) (t/ha) (t/ha) (

    1984-85 (6) 3.2 2.6 1.3 3.4 1.l 2.8 1.2 2.9 1.7 c 2

    1985-86 (4) 3.9 1.3 3.0 2.0 2.7 2.1 2.9 1.9 3.9 b

    1986-87 (4) 8.7 0.8 5.6 1.6 5.1 1.6 5.4 1.3 6.2 a 1

    1

    Cultivar mean 6.2 a 1.6 b 3.2 b 2.4 a 2.9 b 2.2 a 3.1 b 2.1 a

    aDisease evaluation scale 1 to 9, Standard evaluation system for rice. bMeans were compared using Tukey's test at 5% level of significance. abc show ferences among year means; ABC show differences among cultivar means. c Figures in parentheses = number of trials.

    Maintenance of virulence in

    Xanthomonas campestris pv.

    oryzae cultures

    J. C. Durgapal, Division of Mycology and

    Plant Pathology, Indian Agricultural

    Research Institute, New Delhi 110012, India

    The loss of virulence in phytopathogenic

    bacterial cultures maintained on culture

    medium is a common phenomenon. In

    the absence of lyophilization facilities,

    cultures of Xanthomonas campestrispv.

    oryzae, the pathogen of bacterial blight,

    not only decline in virulence but

    occasionally even lose viability within a

    year of maintenance on a culture

    medium under refrigeration. We

    evaluated the suitability of sterile

    distilled water columns, top layeredwith liquid paraffin, for long-term

    maintenance of the bacterium.

    in round- bottomed, screw-capped test

    tube (about 7.5 cm high, 1.5 cm outer

    diameter) was provided with a 0.5-cm-

    thick top layer of medical grade liquid

    paraffin and autoclaved at 15 lb pressure

    for 30 min. Bacterial growth from

    nutrient agar slant 48 h old was

    transferred aseptically to the column

    and stored at 10 C.

    In Oct 1980, cultures of three virulentgradeshighly, moderately, and weakly

    virulentwere preserved by this

    technique. An identical set was

    maintained under refrigeration on

    culture medium (modified Wakimotos

    medium: 5 g peptone, 20 g sucrose, 0.5 g

    Ca(NO3)2. 4 H2O, 0.5 g FeSO4

    .7H2O,

    2 g Na2HPO4 2H2 O; 20 g agar, 1000 ml

    A distilled water column 2.5 cm high

    distilled water, pH adjusted to 6.8), with

    subculturing at 6-mo intervals.

    The viability of the preserved cultures

    was tested. With a wire-loop, a minute

    amount of the bacterial mass available

    as sediment at the bottom of the water

    columns was transferred to medium

    slants and incubated at 27 C. An

    aqueous suspension of 48-h-old fresh

    culture at about 109 cells/ml served as

    inoculum.

    About 20 fully developed young

    leaves of TN1 rice plants at the

    maximum tillering stage were inoculated

    by leaf tip cutting. Virulence was

    determined by average lesion length

    measured 15 d after inoculation. The

    cultures were graded weakly (0.1-

    5.0 cm), moderately (5.1-12.0 cm), or

    highly (>12.0 cm) virulent.Cultures preserved in the water

    column and those maintained on culture

    medium were tested for viability and

    virulence at 1, 3, and 6 yr.

    Each culture in a water column was

    still viable in the last test in 1986, with

    no appreciable decline in initial

    virulence. In the cultures maintained on

    culture medium, the moderately and

    weakly virulent types survived to the last

    test, but 2 of the 3 highly virulent

    cultures lost viability within 1 yr.

    The pathogenicity test furtherrevealed a gradual loss of virulence in

    highly and moderately virulent cultures.

    In the last test, three cultures (one highly

    virulent and two moderately virulent)

    became avirulent; the rest reacted as

    weakly virulent.

    Sterile distilled water columns top

    layered with liquid paraffin served as a

    remarkably suitable and effective

    medium for long-term maintenance of

    X. c.pv. oryzae cultures. The preserve

    cultures not only remained viable, but

    retained their original pathological

    characteristics for several years. This

    inexpensive and easily manageable

    device could be a reliable base for

    maintaining the bacterium in its virule

    form in laboratories lacking

    lyophilization facilities.

    Leaf blast (BI) outbreak at

    Faizabad, India

    P. Mukerjee, S. P. S. Rathi, and D. M.

    Maurya, Crop Research Station, Narendra

    Deva University of Agriculture andTechnology, Masodha, P.O. Dabha Semar

    Faizabad, India

    Severe leaf Bl caused by Pyricularia

    oryzae had not been observed around

    Faizabad, specifically Masodha and

    Sohawal block, for 10 yr. During the

    1986 wet season (Jun-Dec) at C. R. S.

    Masodha, it appeared only on N22 at

    the milk stage, and only on the upper

    and flag leaves; the neck was not

    affected. During the 1987 wet season,

    N22 and Bagri showed severe infectioin early Aug at tillering; plants were

    completely killed by the second week

    Aug.

    Under upland rainfed conditions in

    trials at C. R. S. Masodha, where

    disease pressure was highest, some new

    developed lines showed high resistance

    to leaf Bl; indigenous varieties were

    IRRN 13:2 (April 1988)

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    highly susceptible. Satha D, Akashi, Lalmati-A, Lurkan, Miriti, Kachni,

    Bagri, and N22 were most susceptible. Rani Kajal, Satha-F, and Sarya had

    Bagri Black, Bagri White, Bhadaila kala, moderate infection.

    Budhi, Gorakhpur local, Kudia, In farmers' fields, severe leaf B1

    Adverse temperature tolerance

    Screening rice varieties for

    reproductive stages showed low tolerance for cold at the

    yellowing and plant height were scored

    at 25, 45, and 55 d after sowing (DAS).cold tolerance at seedling and Two new lines ES1-2-3 and ES1-1-1

    S. K. Sinha, S. Biswas, and S. K. B. Roy,

    Rice Research Station, Chinsurah 712102,

    India

    seedling stage and flowered earlier than

    the check variety IR50. Both lines had

    similar seedling height and leaf number

    at 55 DAS; number of tillers/plant at

    Cold tolerance at the seedling stage as

    well as at the reproductive stage is

    essential for early dry season rice in

    West Bengal. We screened a number of

    newly developed lines and three hillvarieties in 1984-85 to identify genotypes

    possessing both characters.

    Seeds were sown 21 Nov 1984. Leaf

    harvest was lower than that of IR50 (see

    table).

    Two hill rice varieties introduced

    from Bhutan, MAAP and KAAP,

    showed high seedling tolerance for cold,and flowered earliest. But number of

    tillers/ plant was very low. Khonorullo,

    another hill rice, showed cold

    Characters related to cold tolerance at different growth stages. a West Bengal, India, 1984-85.

    was observed on popular indigenous

    varieties Lalmati, Mutmuri, N22,

    Mutmuriya, and Bagri.

    susceptibility at all growth stages, with

    delayed heading. CB-1 (Chinsurah

    Boro-1) exhibited high seedlingtolerance for cold but flowered late.

    Awned and red grains also restrict CB-1

    use.

    Varieties that flowered around mid-

    Mar in West Bengal usually experience

    temperatures of 22-25 C during panicl

    development and produce a higher

    percentage of filled spikelets/ panicle.

    Using the Bhutanese varieties that

    flower between 17-19 Mar in the

    hybridization program may provide

    plants that flower early, with cold

    tolerance at both seedling andreproductive stages, suitable for dry

    season (boro) rice in West Bengal.

    Leaf yellowinga Seedling ht (cm)Genotype

    Leaf no. a

    SourceTillers

    Days

    25 DAS 45 DAS 55 DAS 25 DAS 45 DAS 55 DAS 25 DAS 45 DAS 55 DAS(no./plant)

    heading

    New lines

    IR9262-5-2-2-2 IRRI 5 7 7 6 8 10 3 3 4 10 125

    IR15579-135-3 3 5 5 7 9 12 3 4 5 9

    IR7167-33

    -2-4-2

    -3 IRRI

    125

    5 7 7 6 8 9 35 7 7 6 9 12

    3 5 9 131IR13155-60-3-1 IRRI 3 3 5 10 127

    IR5716-18-1 IRRI 5 5 5 7 8 10 3 4 5 9 127

    IR8866-30-3-1-4-2 IRRI 5 7 7 6 8 10 3 4 4 9 131ES1-2-3 India 3 5 5 5 9 10 3 4 4 6 117ESl-1-1 India 5 5 5 5 9 10 3 4

    IR50

    4

    IRRI 5 7 9 6 8 9 3 4 5 10 129

    7 118

    Hill rice

    MAAP Bhutan 1 1 1 10 12 15 3 4KAAP Bhutan 1 5 7 8 12 3 4

    516 5

    IRRI

    3 1154 113

    Khonorullo Bhutan 5 7 7 6 9 11 3 4 5 7 131

    Local checkCB-1 India 1 1 1 12 15 20 3 4 5 13 139

    Average diurnal temp (C) 20 19 18

    a By the Standard evaluation system for rice scale.

    The International Rice Research Newsletter invites contributions of concise summaries of significant current rice research for

    publication. Contributions should be limited to no more than 2 pages typed double-spaced, accompanied by no more than 2 figures,

    tables, or photographs. Contributions are reviewed by appropriate IRRI scientists and those accepted are subject to editing and

    abridgment to meet space limitations. Authors are identified by name and research organization. See inside front cover for more

    information about submissions.

    14 IRRN 13:2 (April 1988)

    to

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    measured (see table).

    2.0. All seeds germinated at pH 3.0 an

    above except for CSR4 and IR28222-

    Adverse soils tolerance No seeds germinated at pH 1.0 and

    Effect of acidity on 3.0, 4.0, 5.0, 6.0, and 7.0 by adding 2-2-2-2. No variety produced root that

    germination and growth of

    rice seeds

    A. K. Bandyopadhyay, Central Soil Salinity

    Research Institute, Regional Research

    Station Canning, PO:Canning Town, Dist:

    24-Pgs, West Bengal, India

    Germination is an acute problem in

    coastal acid saline soils that remain

    highly acidic during the premonsoon dry

    hydrochloric acid. Ten seeds were kept could be measured at pH 3.0. BG35-2

    in each solution in petri dishes, with BW100, B2149B-PN-26-1-1, and RD

    three replications. Water volume was appear highly promising for coastal ac

    maintained by adding solution. After 4 saline soils where germination is a

    d, the germinated seeds were counted problem.

    and seedling height and root length

    Effect of acidity (pH 3, 4, 5, 6, 7) on growth of rice seeds. West Bengal, India.

    Seedling ht (cm) Root length (cm)

    3 4 5 6 7 3 4 5 6 7Variety

    period. We screened 118 IRRI

    germplasms in acid saline soils havingBWl00 4.5 6.3 6.7 6.0 5.4

    pH 3.5. Nine varieties were selected.5.5 7.0 8.0 8.

    A laboratory experiment was IR28222-9-2-2-2-2 1.2 7.3 1.7 6.2 6.3 r 2.5 3.5 5.0 5.

    conducted to evaluate comparative3.0 5.5 5.6 5.2 4.3 a 2.0 5.0 3.5 4.1.2 6.0 5.3 4.5 4.5 c 5.5 8.0 6.0 7.

    tolerance of the selected varieties for Mahsuri 1.2 5.5 5.2 4.7 5.2 e 5.0 6.5 3.0 3.

    BG35-2 3.5 6.3 6.0 6.0 5.7 5.5 5.5 3.5 3.

    B2149B-PN-26-1-1 3.4 6.7 7.7 7.0 5.4 T 3.0 4.0 4.5 3.

    IR44ITA230

    graded acidity levels. Tap water (EC 1.0, IR8067-41-1E-P1 2.7 6.3 7.0 6.5 6.0 s 2.5 2.5 2.0 2.

    pH 7.2) was used as the medium. RD15 3.3 6.2 6.3 6.7 5.3 4.5 4.5 2.0 2.

    Solution pH was adjusted to 1.0, 2.0,CSR4 0.5 6.0 6.3 5.5 5.8 9.0 9.0 11.0 6.

    CROP AND RESOURCE MANAGEMENT

    Soils and soil characterization

    Influence of soil texture on Influence of soil type on root production andrice crop performance

    grain yield. Tamil Nadu, 1983.

    Root dry weight

    M. A. Salam, Cropping Systems Research (g/pot) Grain

    Centre, Karamana 695002, Trivandrum; and yield

    S. Subramanian, Tamil Nadu AgriculturalTillering Panicle (g/pot)

    University, Coimbatore 641003, Indiainitiation

    Sandy clay loam 3.43 6.44 15.7

    We studied the performance of IR20 Clay loam 3.98 7.39 21.1

    rice in two soils of different textures inLSD (0.05) 0.14 0.17 0.4

    CV (%) 7.3 5.3 2.4

    pot culture under natural light during Difference 0.6 1.0 5.4

    summer 1983 (Feb-Jun). % increase 16 15 34

    ~

    The soils were clay loam (42.4% clay,

    The crops received standard

    management practices and

    recommended nutrients. Root dry

    weight was recorded at tillering and

    panicle initiation. Grain yield wasmeasured at 14% moisture. The

    differences in root production and grain

    yield are given in the table.

    Root production and grain yield were

    higher in fine textured clay loam than in

    coarse textured sandy clay loam. Grain

    yield and root dry weight had significan

    positive correlation.

    The better performance of rice in clay

    loam soil was due to enhanced root

    production.

    30.2% silt, 23.4% coarse sand, 4% finesand, 99-8-254 ppm available NPK, 0.7

    ppm DTPA extractable Zn, 1.0% The International IPM Newsletter is published for researchers in the development and

    organic C, pH 8.2, and EC 0.3 dS/m) transfer of integrated pest management (IPM) technology in rice production. Its content

    and sandy clay (23.6% clay, 6.8% silt, focuses on discussions of current issues; it does not publish research reports. For more

    26.5% coarse sand, 37.2% fine sand, information, write Dr. B. M. Shepard, IPM Newsletter, IRRI, P.O. Box 933, Manila,

    100-4-140 ppm available NPK, 0.4 ppm Philippines.

    DTPA extractable Zn, 0.42% organic C,

    pH 7.8, and EC 0.17 dS/m).

    IRRN 13:2 (April 1988) 1

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    Soil microbiology and biological N fertilizer was tested in the field.isolated and tested. One culture (TCSR

    Early, uniform stem

    nodulation in Sesbania

    rostrata after spray of

    Rhizobium culture

    A. S. Bhagwat, D. C. Joshua, and C. R.

    Bhatia, Nuclear Agriculture Division,

    Bhabha Atomic Research Centre, Trombay,

    Bombay 400085, India

    Sesbania rostrata plants grown in pots

    filled with local Trombay soil did not

    produce any stem nodules. Plants raised

    in pots filled with a mixture of local soil

    and soil from Paddy Breeding Station,

    Tamil Nadu Agricultural University,

    Coimbatore, or inoculated with

    homogenized stem nodules nodulated

    profusely.

    Those fully grown stem nodules were

    removed, cleaned in tap water, surface-

    sterilized with 0.1% HgCl2 for about

    4 min, and washed in sterile distilled

    water. The nodules were crushed,

    inoculated in Luria broth (tryptone 1%,

    yeast extract 0.5%, and NaCl 0.5%), and

    incubated at 28 C. After 48 h, the

    culture was plated on Congo red yeast

    extract mannitol agar. Colorless

    mucoid, slow growing colonies were

    For field inoculation, culture grown

    in Luria broth (about 10 8 cells/ml) wa

    sprayed on 35-d-old S. rostrata (25

    plants with 4 replications). At this stag

    plants were 75-80 cm tall and had no

    stem nodules.

    Nodules developed on inoculated plants within 10 d. Stem nodules on 5

    plants from each replication were

    counted 20 d after inoculation.

    repeatable nodulation. At 55 d after

    sowing, the mean number of stem

    nodules on inoculated plants was

    180+16, compared to 22+4 in control

    plants. This culture is available on

    request.

    The rhizobia1 culture induced early,

    Physiology and plant nutrition N benefited uptake of N, P, K, Zn,

    Influence of nitrogen and zinc

    application on nutrient uptake

    by rice in different seasons

    M. A. Salam, Kerala Agricultural

    University, Cropping Systems Research

    Centre, Karamana 695002; and S.

    Subramanian, Tamil Nadu Agricultural

    University (TNAU), Coimbatore 641003,

    India

    We studied the uptake of major and

    micro nutrients by rice in three seasons:

    1982 southwest monsoon Jun-Oct, 1982

    northeast monsoon Oct-Jan, and 1983

    summer Feb-Jun. The experiment was

    laid out in a factorial combination of 4

    levels of N (0, 60, 90, and 120 kg N/ha)

    and 2 levels of Zn (no ZnSO4 and 25 kg

    ZnSO4/ha) in a randomized block

    design with 6 replications, in a different

    field each season.

    The soil at TNAU (11 N, 77 E and

    427 m above mean sea level) was a

    Vertisol (clay loam) containing 1.1%

    organic C, 196-9.5-200 ppm available NPK, 598 ppm total soil N, and

    0.4 ppm DTPA extractable Zn. The test

    variety was IR20. Standard

    management practices were used.

    Nutrient uptake was estimated using

    standard procedures.

    Fe, Mn, and Cu in all seasons; in

    general, the effect persisted up to 90 kg

    N/ ha (see table). Zn also increased N,

    Zn, and Fe uptake in all seasons. This

    can be ascribed to the positive effect of

    Zn on root dry weight and root volume

    (data not given).

    N up to 90 kg/ ha and ZnSO4 at

    25 kg/ ha increased grain yield in all

    seasons. Simple regressions and

    coefficients of determination revealedsignificant positive correlations in all

    seasons.

    A comparison between seasons

    showed that uptake of N, P, K, Zn, Fe

    Mn, and Cu was low during northeast

    monsoon season.

    N-Zn interactions were not consisten

    Nutrient and micronutrient uptake by season.a TNAU, Coimbatore, India, 1982-83.

    N uptake (kg/ha) P uptake (kg/ha) K uptake (kg/ha) Zn uptake (g/ha) Fe uptake (kg/ha)

    SWM NEM SUM SWM NEM SUM SWM NEM SUM SWM NEM SUM SWM NEM SU

    N and Zn levels

    N0 67 46 57 18 13 19 74 74 132 137 N60 87 55 79 2116 19 96

    97 146 1.18 0.53 1.95 117 208 159 217 1.68 0.97 1.

    N90 96 60 89 22 18 22 101 136 143 209 168198 1.62 1.10 1. N120 104 70 91 21 17 23 162 142 164 239 181211 2.00 0.97 1.

    LSD (0.05) 7 7 8 2 1 4 25 20 22 21 16 22 0.17 0.12 0.

    Zn0 84 53 76 18 15 19 101 106 131 185 126 180 1.45 0.84 1.

    Zn 1 93 63 81 23 17 22 115 117 146 212 162 206 1.77 0.95 1.

    LSD (0.05) 5 5 ns 1 1 3 ns ns ns 15 12 16 0.12 0.08 0.

    aSWM = southwest monsoon, NEM = northeast monsoon, SUM = summer.

    16 IRRN 13:2 (April 1988)

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    Effect of farmyard manure

    (FYM) supplemented with N,

    P, K on grain yieldG. B. Chettri and R. B. Rai, Centre for

    Agicultural Research and Development

    (CARD), Wangdiphodrang, Bhutan; and

    A. R. Samiano, Training and Technology

    Transfer Department, IRRI

    FYM is an important source of plant

    nutrients for irrigated rice in Bhutan. Inthe Wangdiphodrang-Punakha valley,

    FYM is predominantly composed of

    animal manures mixed with rice straw invarious stages of decomposition. An

    estimated average of 7 t FYM (fresh

    weight)/ha is applied before

    transplanting. The actual rate varies

    widely, from zero to 20 t/ha.

    As fertilizer-responsive rice varieties

    become more widespread, FYM

    probably will continue to contribute

    significantly to crop nutrition and soil

    condition.

    We supplemented FYM with N, P, K

    to evaluate its effect on grain yield of

    IR36. IR36 seedlings raised in dry bed

    nurseries were transplanted in mid-Junat 49 d after seeding with 20- 20-cm

    spacing in 4- 6-m bunded plots, in a

    completely randomized block design

    with 7 treatments and 3 replications.

    The soil was a loam with pH 6.6,

    1.2% organic C, 9.3 meq CEC/100 g,

    4.6 ppm available P (Olsens), 0.332 meq

    Crop management

    Environmental limitations to

    rice cultivation in the Punjab

    J. S. Sawhney and K. R. Sharma, Soils

    Department, Punjab Agricultural University,

    Ludhiana 141004, India

    Five sites representing typical rice-

    growing areas of the Punjab were

    selected to evaluate suitability for rice

    production. On the basis of soil-site

    characteristics (see table), four suitability

    classes have been defined, from highly

    suitable to currently not suitable.

    Average rice yields under controlled

    conditions with fertilizer (50-12-12 kg

    NPK/ ha) based on soil test suggest that

    the yield data correlate well with soil-

    site suitability class.

    Punjab is controlled by rainfall during

    growing season, soil texture, drainage,

    infiltration, soil reaction, and soluble

    salts. It is possible to make yield

    predictions at different levels of the

    suitability class on the basis of soil-site

    The yield potential of rice soils in the

    characteristics and their degree of

    limitation. The study predicts the

    following environmental limitations for

    sustained rice cultivation:

    Rainfallless than 300 mm during

    Soil typefine loamy surface and

    growing season Jul-Sep is limiting.

    subsurface texture with more than

    16% clay.

    Drainageoptimum from moderately

    well to imperfectly drained.

    Soil reactionoptimum pH 7-8.3.

    Soluble saltssalinity and alkalinity

    are the primary obstacles.

    Soil and site suitability characteristics and their limitations.a Ludhiana, India.

    Soil

    Rainfall Water

    (annual) cumulativeJul-Sep (mm)

    (mm) intakeDrainage pH

    6h

    Rawalpindi clay loam 202 29 Imperfect 8.6

    (Aquic Ustochrepts) (315) (8.4)

    Degree of limitation 2 0 0 1

    Samana sandy loam 474 58 Well 7.4

    (Udic Ustochrepts) (680) (7.6)

    Degree of limitation 0 3 3 0

    Bhoewal loam 532 42 Moder- 7.4

    (Typic Haplustalfs) (7 13) ately well (8.2)

    Degree of limitation 0 1 1 0

    Narike sandy loam 290 40 Moder- 9.4

    (Natraquic Calciorthid) (425) ately well (9.3)

    Degree of limitation 2 1 1 4

    Gurdaspur loam 603 48 Moder- 7.2

    (Udic Haplustalfs) (88.6) ately well (7.3)

    Degree of limitation 0 1 1 0

    10-3 sodium Silt Clay

    ECe Exchangeable

    dS/m percentage

    1.6 15.6

    (1.7) (9.3)

    1 2

    1.0 6.9

    (0.7) (6.6)

    0 0

    1 .0 7.4

    (0.8) (8.2)

    0 0

    2.4 40

    (3.6) (43)

    3 4

    0.4 2.5

    (0.4) (1.1)

    0 0

    41.5 30.0(33.0) (34.1)

    0 0

    18.8 12.7(29.9) (15.7)

    2 2

    50.3 25.9(48.8) (29.2)

    0 0

    20.6 18.2(29.7) (22.8)

    0 1

    30.6 10.4

    (40.7) (15.7)

    0 0

    Yield (t/ha)OrganicOverall

    Land

    Climitation

    suitability Control Recommende

    (%) classb fertilizer base

    on soil-teste

    0.45 1-2 S2 3.7(0.22)

    6.1

    0

    0.35 2-3 S3 2.8 5.1(0.17)

    1

    0.72 0-1 S1 4.6(0.26)

    0

    0.17 3-4 S4 1.2 1.7

    7.8

    (0.12)

    2

    0.59 1-2 S1-2 4.1 7.4

    (0.29)

    0

    aValues in brackets indicate weighted mean of the column. bS1 = highly suitable, S4 = currently not suitable. cAverage of 5 yr.

    Soil fertility and fertilizer management

    IRRN 13:2 (April 1988) 17

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    K/100 g, and 1.2 ppm available Zn. The

    FYM contained 1.8% N and 0.45 pprn

    total P. FYM, all P and K, and 35 kg

    N/ ha were applied basally; the

    remaining N was topdressed at panicle

    initiation. Grain yield was computed at

    14% moisture.

    No significant pest or disease damage

    or water stress occurred during crop

    development. All fertilizer treatmentsincreased yield significantly (see table).

    Mean yield from plots given FYM alone

    was 20% higher than check plots.

    Supplementing FYM with extra N had

    no effect. FYM plus P significantly

    increased yield 18% over FYM alone.

    Yields with FYM supplemented with

    Phosphorus requirements in a

    rice - wheat cropping system

    J. S. Kolar and H. S. Grewal, Agronomy

    Department, Punjab Agricultural University,

    Ludhiana 141004, Punjab, India

    We studied P requirements of rice

    grown in sequence with wheat in the

    field 1983 to 1987. Different

    combinations of P level (0, 13, and

    26 kg P/ ha) and P application (applying

    P to rice alone, wheat alone, or both

    rice and wheat) were laid out in a

    randomized block design with 4

    replications.At the beginning of the experiment in

    1983, the soil (sandy loam, Typic

    Ustochrept) had pH 8.1, 0.29% organic

    C, and 14.5 kg Olsen's P/ha. All plots

    received 120 kg N and 23 kg K/ha. All

    Effect of two phosphorussources with or without azolla

    incorporation on rice yield in

    the Senegal River valley

    H. F. Diara and I. Camara, West Africa

    Rice Development Association (WARDA)

    Regional Research Station on Irrigated Rice,

    Saint-Louis, Senegal

    We compared a soluble-type P (triple

    superphosphate with 45% P2O5 ) and a

    natural type P (aluminum phosphate

    18 IRRN 13:2 (April 1988)

    N+P and from plots fertilized with

    N+P or N+P+K only did not differ

    significantly from yields with FYM+P.

    nitrogen in FYM may be seriously

    limited by inadequate soil P. In

    Wangdiphodrang-Punakha, soil

    analyses now show that available P

    levels are generally low (less than 10

    ppm). Available K and other plantnutrients appear to be adequate. These

    preliminary results suggest that in a

    region where use of inorganic fertilizer is

    very low but use of FYM is routine,

    more benefit could be obtained from

    supplementing FYM with P.

    The results indicate that utilization of

    Effect of FYM supplemented with N and P o

    yield of IR36. CARD, Wangdiphodrang, Bhuta

    1986.

    Fertilizer treatment a Grain

    FYM b Nyield

    P K (t/ha)(t/ha) (kg/ha) (kg/ha) (kg/ha)

    0 0 0 0 4.8 7.5 0 0 0 5.8 b7.5 35 0 0 5.3 bc

    7.5 0 50 0 6.9 a7.5 35 50 0 7.0 a00

    75 50 0 6.6 a75 50 40 6.9 a

    CV (%) 4.5

    a N as urea, P as single superphosphate, K muriate of potash. b Fresh weight. c Meseparation in a column by DMRT at the 5level.

    Influence of P on rice yield in a rice - wheat cropping system. Punjab, India, 1983-87.

    P (kg/ha) Grain yield (t/ha)

    Rice Wheat 1983 1984 1985 1986 1987 Mean

    1984-8

    0 013 026 0

    0 130 26

    13 1313 2626 1326 26

    LSD (0.05)

    7.4

    7.37.57.56.87.1

    7.57 .07.5

    ns

    5.7

    6.86.96 .06.06.7

    6.86.86.6

    0.7

    6.2 6.47.2 8.47.2 8.4

    6.5 7.26.5 7.37.4 8.37.2 8.47.1 8.37.1 7.9

    0.4 0.9

    5.68.48.6

    6.87.68.58.68.57.4

    0.7

    6.07.77.8

    6.66.87.77.87.77.2

    0.7

    P and K and 1/3 N were applied before table). Rice grown on the residue oftransplanting. The remaining N was 25 kg P/ha applied to the preceding

    applied at 21 d and 42 d after wheat showed no response. Increasing

    transplanting. to 26 kg/ha for both rice and wheat

    application of up to 13 kg P/ ha (see

    Rice responded significantly to direct slightly depressed rice yield.

    Soil analysis. Fanaye P4 (Paleustollic Torrerts), Fanaye Station, Senegal.

    pH Organic CEC c Available P TotalAdsorbed P e a

    Texture a Clay Sand SiltSoil:water KC1 (%) (%) (%) (%)

    matterb (meq/ BRAY II Pd

    the soil solutio

    (1:1) 1 N100 g) (ppm) (ppm)

    (g P/g of soil

    6.2 4.4 Clay 46.5 29.9 23.6 0.35 31.26 1.50 240 330

    a Bouyoucos method. bWalkley - Black method. c Cobaltihexamine method (Orsini et Remy 1976d Perchloric acid digestion. e Fox and Kamprath method (1970).

    with 34% P2O5 ). We also evaluated the The trial for four consecutive

    influence of azolla incorporation on cropping seasons was conducted on a

    assimilation of P by rice. fine clayey soil Paleustollic Torrerts (se

    0.2 ppm P in

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    Effects of 2 P sources, applied with and without azolla incorporation, on grain yield of rice variety Sri Malaysia.

    Fanaye Research Station, Senegal River valley, 1985 rainy season. Basal appl ication of P, except in treatmen

    6, where P was split-applied.

    table). The design was a randomized

    complete block with three replications.

    Treatments were no N or P, no N plus

    either of the 2 sources of P at the rate of

    52 kg P/ha, 120 kg N (urea) plus either

    of the 2 sources of P at 52 kg P/ha, and

    60 kg N (urea) + 60 kg N (azolla)/ha

    and O or 52 kg P, applied either split or

    all at once. Two crops ofAzolla pinnata

    var. imbricata, of Indian origin (20 t/haeach, equivalent to 30 kg N/ha) were

    grown successively and incorporated

    before rice transplanting. The rice

    variety was Sri Malaysia.

    After the third cropping season, rice

    yield showed no influence from P. After

    the fourth cropping season, during the

    1985 rainy season, no significant

    difference in yield between the two P

    so urces had occurred (see figure).

    equivalent with triple superphosphate,

    yields were higher when azolla wasincorporated. Uptake of P from a split more pronounced with aluminum the fourth cropping season, the lack of

    application and assimilated by azolla phosphate; the split application P had caused an important yield

    seems better. The response of rice was produced 0.9 t/ha more. By the end of reduction (2.0 and 3.0 t/ha).

    However, although N and P levels were

    Disease management

    Four fungicides for control of

    grain infection caused by

    Helminthosporium oryzae

    A. S. Prabhu and A. B. Santos, National

    Research Center for Rice and Beans

    (EMBRAPA/CNPAF) - Caixa Postal 179,

    74000 Goiania, Goias, Brazil

    Grain discoloration caused by

    Helminthosporium oryzae Breda de

    Haan, the causal agent of brown spot

    (BS), is a major problem in the 35,000

    ha irrigated Rio Formoso rice project. A

    disease outbreak in Feb 1983, during the

    vegetative phase of the fourth successive

    planting of lowland rice variety IAC899

    in CNPAF experimental fields

    indicated the possible role of infected

    plant debris. Despite 3 sprayings with

    maneb fungicide at 10-d intervals to

    control leaf infection, the disease

    retarded plant growth.

    We evaluated four marketed spray

    fungicides for grain infection control in

    the same fields. The experiment used 8

    m2 direct seeded plots in a randomized

    block design with 8 replications.

    Fungicides were sprayed at

    recommended doses 3 times at 7-d

    intervals, beginning at 50% heading

    (92 d after seeding). Untreated controls

    were not maintained because in similar

    experiments, sprayed plots adjacent to

    untreated plots exhibited abnormally

    high disease intensities.

    Effect of fungicide spray on BS control.a Goiania, Goias, Brazil, 1983.

    FungicideFlag leaf lesions (no./leaf) Diseased grains/panicle (%) Unfilled grains/ Grain

    112 DAS 119 DAS 108 DAS 115 DASpanicleb yield

    (%) (t/ha)

    Rate(kg ai/ha)

    Ziram 50% EC 1.5 8.91 a 27.47 a 27.76 a 44.58 ab 41.75 a 2.05 a

    Thiophanate-methyl (20%) + 1.4 7.43 b 22.19 b 26.56 ab 45.64 a 41.16 achlorothalonil 50% WP

    2.03 a

    Maneb 80% WP 1.6 8.59 ab 23.26 ab 25.71 ab 39.52 b 38.70 a 2.22 a

    Captafol 48% EC 0.96 9.14 a 25.91 ab 23.30 b 39.34 b 34.83 a 2.41 a

    CV (%) 12.0 13.5 11.8 10.2 17.2 15.2

    a Means of 8 replications. In a column, means followed by a common letter are not significantly different by Tukey test at the 5% level. DAS = days afte

    seeding. bUnfilled grain percentage was based on 10 panicles/plot.

    IRRN 13:2 (April 1988) 19

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    Disease intensity on flag leaves and

    panicles, unfilled grain percentage, and

    grain yield were measured. Flag leaf

    lesion counts and percentage of diseased

    grains/panicle were based on 50

    randomly collected tillers/ plot.

    Distribution and severity ofrice seedling diseases in boro

    seedbeds in Bangladesh

    A. H. Mondal, M. M. Rahman, and S. A.

    Miah, Plant Pathology Division, Bangladesh

    Rice Research Institute, Joydebpur, Gazipur,

    Bangladesh

    We surveyed rice seedbed diseases in

    some northwestern districts during the

    Nov-Mar boro season. Six diseases

    bakanae (Bak), blast (Bl), brown spot

    (BS), damping-off (DO), root knot(RK), and seedling blight (Sb)were

    found in 48 locations. Commonly grown

    rice were BR1, BR3, BR8, BR9, IR8,

    Pajam, Purbachi, and some local

    varieties.

    DO was found everywhere,

    irrespective of variety (see table). RK

    was the second most common disease; it

    was not found in alkaline belts of

    Rajshahi district. Its intensity and

    severity were highest in sandy soil,

    especially near riverbanks, even in

    seedbeds with little standing water,irrespective of varieties sown.

    BS was found in seedbeds that

    suffered from water stress. Bak affected

    seedlings of Purbachi, Khaily boro

    (local cultivar), and BR16. Bl was found

    mainly on Pajam and Iratom seedlings.

    Treatments differed significantly, but but differences among the test fungicid

    did not reduce flag leaf and grain were not significant. Blotter test

    infection much (see table). Grain determined that 75% of seeds collectedinfection was negatively correlated with from sprayed fields were associated w

    percentage of unfilled grain (r = H. oryzae. That seed lot showed only

    -0.84**) and grain yield (r= -0.84**), 39% germination.

    Distribution of seedling diseases as observed in boro seedbeds during January 1987 in northwest

    districts of Bangladesh.

    Disease frequency in survey areaa

    Bak Bl BS DO RK Sb T

    District

    Bogra

    Dinajpur

    Gaibandha

    Gazipur

    Jamalpur

    Lalmonirhat

    Mymensingh

    Natore

    Pabna

    Rajshahi

    Rangpur

    Tangail

    Total

    DI

    6(18.2)

    0

    2(25.0)

    0

    1

    (12.5)1

    (33.3)2

    (11.8)1

    (11.1)0

    0

    2(14.3)

    0

    15(11.0)

    4 [3-5]

    0

    0

    0

    2

    (12.5)0

    0

    3

    (17.6)0

    0

    0

    1

    (7.1)3

    (16.7)

    9

    (6.6)

    8 [7-9]

    6(18.2)

    0

    2

    (25.0)1

    (25.0)1

    (12.5)0

    3

    (17.6)3

    (33.3)3

    (37.5)2

    (33.3)1

    (7.1)2

    (11.1)

    24

    (17.6)

    5 [3-7]

    12(36.4)

    2(50.0)

    2

    (25.0)2

    (25.0)3

    (37.5)1

    (33.3)6

    (35.3)3

    (33.3)4

    (50.0)2

    (33.3)5

    (35.7)6

    (33.3)

    48(35.3)

    6 [ 3-9]

    9(27.2)

    2(50.0)

    2(25.0)

    2

    (25.0)

    3(37.5)

    1(33.3)

    3(17.6)

    2

    (22.2)1

    (12.5)1

    (16.7)5

    (35.7)7

    (38.9)

    38(27.9)

    5 [3-7]

    0

    0

    0

    1(12.5)

    0

    0

    0

    0

    0

    1

    (16.7)0

    0

    2

    (1.5)

    3 [ 1-5]

    3

    l

    13

    a Figures in parentheses show percentage of the disease in the district; those within brackets showdisease index. DI 1 = lowest disease intensity, 9 = highest disease intensity.

    Severity as high as disease index 8 was found in only two locations. More tha

    concentrated in Mymensingh, Tangail, one disease was observed in the same

    Gazipur, and Rangpur districts. Sb was seedbed in some locations.

    Managing rice sheath rot

    (ShR) disease in Kerala, India

    B. K. Nair, Agriculture Department, Kerala;B. Balakrishnan, Regional Agricultural

    Research Station, Kumarakom, Kottayam,

    Kerala; and M. C. Nair, Plant Pathology

    Department, College of Agriculture,

    Vella-vani, Kerala, India

    Field trials to evaluate crop nutrition

    schedules for managing rice ShR disease

    20 IRRN 13:2 (April 1988)

    have shown that sources of N and

    method of application can influence

    disease incidence and grain damage.

    A field experiment during the firstcrop season (May-Sep 1985) at the

    Cropping Systems Research Centre,

    Karamana, used susceptible variety

    Jyothi to evaluate crop nutrition

    schedules for managing ShR.

    The fertilizer level used was 70-35-

    52.5 kg NPK/ ha, the recommended rate

    in disease endemic areas. Sources were

    farmyard manure (FYM), urea, and

    ammonium sulfate for N; super-

    phosphate for P; and muriate of pota

    for K. Except for FYM, all forms of Nwere applied in three splits, half as bas

    and half in two equal topdressings. K

    was applied in two equal splits, basal

    and as topdressing. All P was applied

    basal.

    Carboxin (0.1% spray), widely

    recommended for ShR control, was

    sprayed with two fertilizer treatments

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    Effect of fertilizer and organic manure on ShR intensity and rice grain yield. Kerala, India, 1985.

    Disease intensitya Grain yield (t/ha)

    Treatment Without With Without With

    fungicide fungicide fungicide fungicide

    (F0) (F1) (F0) (F1)

    Organic manure (OM) 4.9 3.5 3.0 2.8alone @ 5 t/ha in soil

    at planting

    OM + N1

    (urea) and K 6.7 5.0 4.6 4.6

    soil application

    OM + N2 (ammonium 7.5 4.5 4.4 4.5sulfate) and K soil application

    OM + N1 and K, last split 5.9 5.9 4.6 5.0of both N and K as foliar sprays

    OM + N2 and K, last split 4.1 8.1 4.4 4.6of both N and K as foliar sprays

    OM + N1 + K + Zn and Mn 8.2 6.1 4.6 4.7

    foliar sprays

    OM + N2 + K + Zn and Mn 9.2 6.7 4.4 4.5

    foliar sprays

    LSD for treatment (T) 2.1 197.1

    LSD for T fungicide 3.0

    a

    By the Standard evaluation system for rice 1 to 9 scale.

    45 and 60 d after transplanting.

    Five random 1-m2 samples were

    observed in each 24-m2 plot. Each hill

    was scored on type and