土壤药剂处理结合阳光消毒防治番茄根结线虫技术评价

为了筛选安全、高效、实用的化学防治技术,对国内外生产的5种杀线虫剂(棉隆、1,3 二氯丙烯·氯化苦、威百亩、噻唑磷、溴甲烷)土壤处理结合阳光消毒防治番茄根结线虫的效果进行了评价。结果表明,使用98%棉隆微粒剂450 kg/hm2或10%噻唑磷颗粒剂30 kg/hm2防治番茄根结线虫(Meloidogyne incognita),结合夏季高温进行阳光消毒,能有效地降低番茄根结线虫的数量,减轻根结线虫的危害程度,节省农户的生产成本,提高番茄的产量和农户的经济效益,是夏季防治番茄根结线虫的有效措施。     

Inactivation of Escherichia coli in soil by solarization

Abstract

Contamination of agricultural soil by fecal pathogenic bacteria poses a potential risk of infection to humans. For the biosafety control of field soil, soil solarization in an upland field was examined to determine the efficiency of solarization on the inactivation of Escherichia coli inoculated into soil as a model microorganism for human pathogenic bacteria. Soil solarization, carried out by sprinkling water and covering the soil surface with thin plastic sheets, greatly increased the soil temperature. The daily average temperature of the solarized soil was 4–10°C higher than that of the non-solarized soil and fluctuated between 31 and 38°C. The daily highest temperature reached more than 40°C for 8 days in total in the solarized soil during the second and third weeks of the experiment. Escherichia coli in the solarized soil became undetectable (< 0.08 c.f.u. g^?1 dry soil) within 4 weeks as a result, whereas E. coli survived for more than 6 weeks in the non-solarized soil. Soil solarization, however, had little influence on the total direct count and total viable count of bacteria in the soil. These results indicate that soil solarization would be useful for the biosafety control of soil contaminated by human pathogens via immature compost or animal feces.     

Soil Solarization: An Organic Weed-Management Approach in Cauliflower

Studies were conducted at KPK Agricultural University, Peshawar, Pakistan, in June 2008 and 2009 using a randomized complete block design. Plots were covered with transparent polyethylene films for different periods (0, 2, 4, 6, 8, and 10 weeks). The temperature inside the film was about 10 °C greater than the atmospheric temperature. Solarization increased nitrogen (N) and organic-matter levels in both years, probably because of decomposition of plant residues. Increasing the period of solarization decreased weed density and both fresh and dry biomass. The effectiveness of solarization was species specific. In 2008, Cirsium arvense L. was controlled in the solarized soil, whereas Vicia sativa germination was stimulated by solarization. In 2009, suppressed weeds included Sorghum halepense whereas Chenopodium album L., Cyperus rotundus, and Rumex crispus L. were unaffected. Solarization increased yield of cauliflower (Brassica oleracea L.) in both years. These results suggest that solarization should be practiced before planting horticultural crops in areas with a hot climate.     

Loss of Viability of Dematophora necatrix in Solarized Soils

To study the relationship between temperature regimes and loss of viability of Dematophora necatrix in soil, two field experiments were conducted to determine the effectiveness of soil solarization on reducing the population of D. necatrix colonizing avocado root segments buried at a depth of 15–60cm. Increase of maximum hourly temperatures attributable to soil solarization reached, depending on depth, 6.7–4.6°C in unshaded areas and 3.9–1.5°C for shaded areas in the first experiment (starting in early June, 1995). The better environmental conditions in the second experiment (starting by mid-July, 1995) led to higher temperature increases (8.6–5.6°C, depending on depth) when solarization was conducted in unshaded areas. One, 4, 5 and 6 weeks of solarization were required to eliminate the viability of D. necatrix at 15, 30, 45 and 60cm depths in the first experiment, whereas only 8, 10, 15 and 22 days of solarization were needed for the loss of viability of D. necatrix at the same depths in the second experiment. In shaded areas, however, soil solarization attained significant effectiveness at 15cm depth.Regression analyses of fungal viability (ln-transformed data) over accumulated temperature–time showed best fits when the minimum threshold temperature was 30°C. Although eradication of D. necatrix in soil can be achieved down to 60cm depth in solarized plots, and at 15cm depth in unsolarized unshaded plots, the accumulation of temperature–time appeared less effective in reducing inoculum viability in the latter.     

A solar collector for soil disinfestation

A solar collector to be used for disinfestation of substrates for plant propagation is described. At a high solar radiation intensity (more than 1 cal cm^–2 min^–1), one day of treatment was sufficient for disinfestation of soil infested withSclerotium rolfsii, Sclerotinia sclerotiorum, Fusarium solani f.sp.phaseoli orPythium aphanidermatum.Treatment of soil in the solar collector strongly reduced the total numbers of fungi, bacteria and actinomycetes. The nutrient status of the soil was only slightly changed and did not result in an effect on plant growth.     

Implementation of soil solarization in Greece: conclusions and suggestions

The use of soil solarization in Greece is described, indicating methods of reducing the period of solarization by using impermeable plastic sheets and combining it with the addition of antagonistic bacteria.     

Compositional shifts of bacterial groups in a solarized and amended soil as determined by denaturing gradient gel electrophoresis

Soil solarization is a widespread, nonchemical agricultural practice for disinfesting soils, which is often used in combination with organic amendment, and whose action represents an important factor impacting on soil bacterial communities structure and population dynamics. The present study was conducted to investigate whether and to which extent a 72-day plot-scale soil solarization treatment, either combined or not with organic amendment, could stimulate compositional changes in the genetic structure of indigenous soil bacterial communities. Soil solarization with transparent polyethylene film, in combination or not with farmyard manure addition, was carried out during a summer period on a clay loam agricultural soil located in Southern Italy. Soils from a four-treatment (NS, nonsolarized control soil; S, solarized soil; MA, manure-amended nonsolarized soil; MS, manure-amended and solarized soil) plot block were sampled after 0, 8, 16, 36 and 72 days. Compositional shifts in the genetic structure of indigenous soil bacterial communities were monitored by denaturing gradient gel electrophoresis (DGGE) fingerprinting of 16S rRNA gene fragments amplified from soil-extracted community DNA using primers specific for Bacteria, Actinomycetales, α- and β-Proteobacteria. Changes in soil temperature, pH, and electrical conductivity (EC_1:1) were also monitored from 0 to 72 days. Beneath the polyethylene film the average soil temperature at 8-cm depth reached 55 °C compared to 35 °C in nonsolarized soil. In general, without amendment both soil pH and EC_1:1 were not significantly affected by solarization, whereas in manured plots either variables were greatly increased (from 7.0 to 8.0 pH and from 271 to 3021 μS cm⁻¹ EC_1:1), and both showed long-lasting effects due to soil solar heating. The eubacterial DGGE profiles revealed that soil solarization was the main factor inducing strong time-dependent population shifts in the community structure either in unamended or amended soils. Conversely, the addition of organic amendment resulted in an altered bacterial community, which remained rather stable over time. A similar behaviour was also observed in the DGGE patterns of β-proteobacterial and actinomycete populations, and also, albeit to a lesser extent, in the DGGE profiles of α-Proteobacteria. An increased bacterial richness was evidenced by DGGE fingerprints in 16- and 36-day samplings, followed by a decrease appearing in 72-day samplings. This could be explained, other than by a direct thermal effect on soil microflora, by solarization-induced changes in the physico-chemical properties of soil microbial habitats or by other ecological factors (e.g. decreased competitiveness of dominating bacterial species, reduced grazing pressure of microfaunal predators, increased nutrient availability).     

Effects of solar treatment on germination of sclerotia (Sclerotium rolfsii Sacc.) and on other soil mycoflora

Summary Only 10% of sclerotia germinated in a tarpcovered plot after 45 days of treatment while 50% of sclerotia germinated in the control plot. However, complete inhibition of sclerotia germination was not achieved. The maximum temperature recorded was 53°C, after 45 days of treatment in a tarped plot at 1 cm depth. The incidence of Acrophialophora fusispora, Aspergillus spp., Spicaria sp., and Trichoderma viride increased in soil after 45 days of the solar treatment.     

Displacement of native rhizobia nodulating chickpea (Cicer arietinum L.) by an inoculant strain through soil solarization

Summary Soil solarization greatly reduced the native chickpea Rhizobium population. With inoculation, it was possible to increase the population of the Rhizobium in solarized plots. In the 1st year, 47% nodulation was obtained with chickpea inoculant strain IC 59 when introduced with a cereal crop 2 weeks after the soil solarization and having a native Rhizobium count of <10 g^-1 soil, and only 13% when introduced 16 weeks after solarization at the time the chickpeas were sown, with 2.0×10² native rhizobia g^-1 soil. In the non-solarized plots inoculated with 5.6×10³ native rhizobia g^-1 soil, only 6% nodulation was obtained with the inoculant. In the succeeding year, non-inoculated chickpea was grown on the same plots without any solarization or Rhizobium inoculation. The treatment that showed good establishment of the inoculant strain in year 1 formed 68% inoculant nodules. Other treatments indicated a further reduction in inoculant success, from 1%–13% to 1%–9%. Soil solarization thus allowed an inoculant strain to successfully displace the high native population in the field and can serve as a research tool to compare strains in the field, irrespective of competitive ability. In year 1, Rhizobium inoculation of chickpea gave increased nodulation and increased plant growth 20 and 51 days after sowing, and increased dry matter, grain yield, and grain protein yield at maturity. These beneficial effects of inoculation on plant growth and yield were not measured in the 2nd year.Submitted as Journal Article No. JA 945 by the International Crops Research Institute for the Semi-Arid Tropics (ICRISAT), Patancheru, Andhra Pradesh 502 324, India     

Integrated management of Meloidogyne incognita‐Fusarium oxysporum f. sp. ciceri wilt disease complex in chickpea

A field experiment was conducted to study the management of a root‐knot nematode, Meloidogyne incognita (Kofoid and White) Chitw. (Tylenchida: Heteroderidae)‐wilt inducing fungi, Fusarium oxysporum Schlecht. emend. Snyd & Hans. f. sp. ciceri (Padwick) Snyd. & Hans. (Moniliales: Tuberculariaceae) wilt disease complex in chickpea (Cicer arietinum L.). cv. Annegiri. The results indicated that integration of soil solarization (for 6 weeks), VA mycorrhizal fungus (VAM), Glomus fasciculatum inoculation (12g/hill) and seed treatment with carbosulfan (3% w/w) was highly effective in reducing population levels of both pathogens, root‐knotdisease and wilt incidence and in increasing chickpea grain yield significantly. However, seed treatment with carbendazim (0.25% w/w) together with carbosulfan (3% w/w) was not only effective in reducing the wilt disease complex but also economic with an incremental cost: benefit ratio of 1: 2.4.