Survival of Phytophthora cinnamomi in Buried Eucalyptus Roots

Colonization and survival of Phytophthora cinnamomi in roots was tested in 3 months old, axenically grown seedlings of Eucalyptus maculata (field resistant) and E. sieberi (susceptible). The roots were inoculated, then one week later were excised and buried in three non-sterile, conducive soils; a lateritic gravel, an infertile duplex soil, a loamy sand as well as in a fertile, suppressive krasnozem. Pathogen viability, percentage root colonization and chlamydospore numbers were examined at matric potentials of ?1/3, ?5 and ?10 bar after periods of 10, 100 and 200 days at 21°C. At 10 days, survival was 100% in the form of mycelium and the only significant difference was between the two Eucalyptus species. At 100 days survival was solely due to chlamydospores, but the pathogen was viable in all inoculated roots and at each matric potential. At 200 days soils had dried to less than ?10 bars and the pathogen failed to survive. No significant differences were found between the two pathogen isolates but significant differences were obtained between the susceptible and field resistant Eucalyptus species. Pathogen viability, percentage root colonization and chlamydospore number were highly correlated with soil types and matric potential. These components declined with decreasing soil matric potential. The Krasnozem was only suppressive at relatively high soil matric potentials (?1/3 bar). At lower values (?5, ?10 bar) survival of the pathogen, chlamydospore numbers and percentage colonization of the roots in the Krasnozem were comparable with that of the 3 conducive soils tested. Chlamydospores were present, but in low numbers in roots buried in the suppressive soil at ?1/3 bar.     

Behaviour of Phytophthora citrophthora and P. nicotianae var. in soil, and Differences in Their Tolerance to Antimicrobial Components of Selective Media Used for Isolation of Phytophthora spp.

Phytophthora citrophthora was inhibited to a greater extent than P. nicotianac var. parasitica by chloramphenicol, hymexazol, PCNB and pimaricin at concentrations used in selective media for the isolation of Phytophthora spp. Reduced concentrations of the antimicrobial components of the selective media to tolerant levels for P. citrophthora markedly increased the recovery of the two brown rot pathogens from soil. Mycelium of both Phytophthora spp. survived in air-dried soil for at least 5 months while mycelium of most Phytophthora spp. do not survive in dry soil. In moist soil, P. nicotianae var. parasitica produced hyphal swellings, sporangia and chlamydospores. P. citrophthora produced hyphal swellings and sporangia, but no chlamydospores. No oospores were produced, even in pairing cultures on agar plates with isolates obtained from several locations of citrus groves andfruits by both species. Sporania were obtained in both species in citrus groves on mycelium mats, in the rhizosphere, in infected leaves and fruits buried at soil depths of 5–35 cm. Numbers of propagules declined during the incubation period, but conside, rable numbers survived throughout the experimental period (6 months). Although P. nicotianae var. parasitica produced chlamydospores while P. citrophthora did not, numbers of surviving propagules recovered from soil after 6 months were comparable with both species. The brown rot pathogens survived in soil both as colonizers of detached leaves and fruits and as parasites in living root tissues.     

Growth and survival of Verticillium chlamydosporium goddard,a parasite of nematodes,in soil

Selective media for the isolation of the nematophagous fungus Verticillium chlamydosporium, are described. These enabled densities > 500 colony forming units (CFU) g^‐1 soil to be reliably estimated. However, there was little relationship between estimates of the Verticillium biomass in a sterilized soil and the numbers of CFU which developed on the selective media. The growth and survival of the fungus infield soils were studied and estimates of the numbers of CFU in soils in which cyst‐nematode multiplication was suppressed were greater than in those in which the nematode multiplied. Isolates of the fungus differed in their ability to proliferate in soil, but some increased rapidly from applications of chlamydospores or a mixture of hyphae and conidia in alginate granules containing wheat bran. The energy source (wheat bran) was essential for the establishment of the fungus from granular applications. Numbers of CFU greatly exceeded those of chlamydospores, but there was considerable variation in the relationship in different soils. Some isolates of V. chlamydosporium proliferated in soil and survived in considerable numbers for at least 3 months. Hence, pre‐cropping applications of the fungus should survive long enough to kill nematode eggs and females that develop on roots of spring‐sown crops.     

Extraction of extraradical arbuscular mycorrhizal mycelium from compartments filled with soil and glass beads

This study presents a novel method for the extraction and quantification of extraradical mycelium (ERM) of arbuscular mycorrhizal fungi (AMF) from a substrate that simulates soil better than previously used artificial growth media. Fungal compartments were constructed from small net pots with a latticed wall and filled with a mixture of glass beads and 40 m wet sieved soil. The net pots were surrounded by a 30-m mesh membrane through which hyphae but not roots could grow. They were inserted into soil where a Glomus intraradices (BEG 110) colonized potato plant was growing. The ERM that had grown out from roots through the membrane was successfully collected and quantified after harvest by washing out the soil/glass bead mixture through a sieve with a mesh width of 40 m. Concentrations of P, Zn, Cu and Mn in the AMF ERM were analysed.     

EFFECT OF THE NON-MYCORRHIZAL PIONEER PLANT SALSOLA KALI L. (CHENOPODIACEAE) ON VESICULAR-ARBUSCULAR MYCORRHIZAL (VAM) FUNGI

The effects of Salsola kali (Russian thistle) on chlamydospore numbers and viable propagules of the vesicular-arbuscular mycorrhizal fungus Glomus fasciculatum were monitored for 18 wk under laboratory conditions. When S. kali or Agropyron smithii (a mycorrhizal species) were grown for 6 wk, the number of chlamydospores in soil declined to the same number as in the control (non-planted) soil; the number of chlamydospores in the S. kali and control soils continued to decline over the 18 wk period. However, using a Zea mays bioassay, the per cent colonization of corn roots obtained from soil in which S. kali grew for 6, 12, or 18 wk was significantly greater than in the control soil. These results suggest that S. kali may stabilize mycorrhizal infectivity of disturbed soils for at least short periods of time.     

Survival ofalginate-ecapsulated Pseudomonas fluorescens cells in soil

Alginate-encapsulated and unencapsulated cells of Pseudomonas fluorescens Rsf were introduced into soil microcosms with and without wheat plants to evaluate bacterial survival and colonization of the rhizoplane and rhizosphere. Encapsualtion of cells in alginate amended with skim milk or with skim milk plus bentonite clay significantly enchanced long-term survival of the cells. There was a negligible effect on long-term bacterial survival when cells were encapsulated in alginate amended with TY medium or soil extract, as compared to water. Drying of beads resulted in a significant reduction in bacterial viability. After addition to soil, cells in dried beads increased in numbers and exhibited stable population densities, whereas cells added in moist beads showed stable dynamics at a higher level. Cells encapsulated in dried beads or fresh beads survived better than unencapsulated cells added to soil. Both cells in moist and dried alginate beads also survide a dry/wet cycle in soil, whereas unencapsulated cells were sensitive to these moisture fluctuations. Shortly after inoculation and 63 days after this, cells from moist beads colonized wheat roots at significantly higher levels than unencapsulated cells, whereas cells in dried beads did so at levels similat to unencapsulated cells. Cells in beads initially placed at different distance from developing root mat were able to move towards and colonize the rhizosphere, at levels of roughly 10⁴ to 10⁶ colony-forming units fo P. fluorescens R2f per gram of dry soil. Correspondence to: J. T. Trevors or J. D. van Elsas     

Evaluation of Pochonia chlamydosporia var. chlamydosporia as a control agent of Meloidogyne javanica on pistachio

The potential of isolates of Pochonia chlamydosporia var. chlamydosporia as biocontrol agents for root-knot nematodes was investigated in vitro and on pistachio plants. On potato dextrose agar, growth of all isolates started at temperatures above 10°C, reached maximum between 25 and 28°C and slowed down at 33°C. On water agar, all isolates parasitized more than 85% of the eggs of Meloidogyne javanica at 18°C after 3 weeks. Filtrates of isolates grown on malt extract broth did not cause more than 5% mortality on second-stage juveniles of M. javanica after 48 h of incubation. A single application of 10×10³ chlamydospores (produced on sand–barley medium) g^–1 soil, was applied to unsterilised soil planted with pistachio cv. Kalehghochi, and plants were inoculated with 3000 nematode eggs. After 120 days in the glasshouse, nematode multiplication and damage were measured. Ability of fungus isolates to survive in the soil and to grow on roots were estimated by counting colony forming units (cfu) on semi-selective medium. Fungal abundance in soil increased nearly 3-fold and 10×10³ and 20×10³ cfu g^–1 root of pistachio were estimated in pots treated with isolates 40 and 50, respectively. Strain 50 was more abundant in soil and on the roots, infected more eggs (40%) on the roots and controlled 56% of total population of M. javanica on pistachio roots, whereas isolate 40 parasitized 15% of the eggs on the roots and controlled ca. 36% of the final nematode population.     

Suppression of nematophagous fungi by enchytraeid worms: a field exclosure experiment

The feeding biology of Enchytraeus crypticus and other enchytraeids is poorly understood as is their effect on nematophagous fungi. Because enchytraeids had been associated with nematophagous fungi in the field and had suppressed these fungi in soil microcosms, we tested the hypothesis that exclusion of enchytraeids, largely E. crypticus, would improve establishment of certain nematophagous fungi in field plots. The fungi, Hirsutella rhossiliensis and Monacrosporium gephyropagum, are being studied as potential control agents of plant-parasitic nematodes and were formulated as hyphae in alginate pellets. The pellets were mixed into soil without enchytraeids and placed in cages (PVC pipe, 80 cm³ volume) with fine (20 μm) or coarse (480 μm) mesh; cages were buried 15 cm deep in field plots and then recovered after 6–52 days. When fine mesh was used, enchytraeids were excluded and the fungi increased to large numbers. When coarse mesh was used, enchytraeid numbers in cages increased rapidly and the fungi did poorly. Although mesh also affected other potential fungivores, including collembolans and large dorylaimid nematodes, we suspect that enchytraeids were more important because large numbers were consistently found in cages with coarse mesh soon after the cages were placed in soil. Organisms smaller than enchytraeids (bacteria, fungi, and protozoa) also appeared to be important because the fungi did better in heat-treated soil than in non-heat-treated soil, regardless of mesh size. The rapid increase in enchytraeid numbers in cages with hyphal pellets and coarse mesh was probably caused by movement of enchytraeids toward the pellets with hyphae: increase in enchytraeid numbers was minimal when movement into cages was blocked (or when cages contained pellets without hyphae). Overall, the data were consistent with the hypothesis that enchytraeids, or other meso- or macrofauna, contributed to suppression of nematophagous fungi in our field plots. Received: 22 April 1997 / Accepted: 16 June 1997     

Persistence of a streptomycin-resistant variant of Corynebacterium insidiosum in soil and alfalfa roots in soil

Summary A pathogenic, streptomycin-resistant variant of Corynebacterium insidiosum, the alfalfa wilt bacterium, was used to determine the persistence of the bacterium in soil and in infected alfalfa roots buried in soil subjected to fluctuating temperatures and different moisture regimes. Use of streptomycin in the agar medium reduced the numbers of soil micro-organisms significantly and enabled colonies of C. insidiosum to be detected at low soil dilutions. In soils incubated at 20°C and moistened to field capacity, the pathogen was not recovered after 7 days from a Malmo silt loam but remained viable for 20 days in the A and C horizons and for 31 days in the B horizon of a Lethbridge silt loam. In excised alfalfa roots held in a Lethbridge silt loam, the pathogen persisted for 50 weeks in soil at the wilting point, regardless of temperature, and in soil subjected to temperatures fluctuating between -5 and +5°C, regardless of moisture. However, in excised alfalfa roots held at a mean temperature of 20°C and under saturated moisture conditions, C. insidiosum did not persist beyond 16 weeks. re]19730925     

土壤石砾含量对掌叶木幼苗生长和根系特征的影响

为探讨土壤石砾含量对珍稀濒危植物掌叶木幼苗生长和根系的影响,该研究以1个月生掌叶木幼苗为试验材料,进行5种不同土壤石砾含量[0(CK),20%,40%,60%和80%]盆栽试验,筛选最适宜掌叶木幼苗生长的土壤石砾含量。结果表明:(1)土壤石砾含量对掌叶木幼苗生长有极显著影响,其中幼苗苗高和地径相对增长率、叶面积、苗木质量指数、生物量(根、叶和全株)和根冠比均在土壤石砾含量为40%时最大。(2)土壤石砾含量对掌叶木幼苗根系形态具有极显著影响,总根长和根表面积在土壤石砾含量为40%时最大; 而根系平均直径随石砾含量增加逐渐减小,当土壤石砾含量高达80%时,根系平均直径最小。(3)土壤石砾含量对掌叶木幼苗根系拓扑结构和分形特征无显著影响,而对根系平均连接长度和分叉数有极显著影响,其中各处理根系拓扑指数(TI)、修正拓扑指数(q_a和q_b)均趋近于1,即掌叶木幼苗根系在不同土壤石砾含量中分支模式更趋近于鱼尾形分支; 根系平均连接长度随石砾含量增加先增大后减小,在土壤石砾含量40%时最大; 根系分叉数随石砾含量增加逐渐减小。(4)综合评价幼苗生长和根系形态与构型指标表明,掌叶木幼苗在40%土壤石砾含量中地下根系和地上茎叶生长状况最好。因此,土壤添加适量石砾能促进掌叶木幼苗生长,当石砾含量为40%时幼苗生长效果最好,苗木质量指数最高,最适宜掌叶木幼苗生长。     

Studies on the relation between density of Longidorus elongatus and growth of sugar beet, with supplementary observations on Trichodorus spp

Longidorus elongatus attacks sugar beet on light sandy soils in the West Midlands. Severely damaged plants may die or recover, producing fanged roots. Up to 335 L. elongatus/200 g of soil were found around attacked seedling plants and were often visible to the unaided eye on the roots of freshly lifted plants. Five experiments were made and regressions computed of yield of beet, total numbers of plants and numbers of normal and fanged beet on L. elongatus numbers. Between 24% and 50% of roots per 100 L. elongatus/ 200 g were killed or became fanged. Corresponding figures for loss of plant were between 7.5% and 33%. Estimated loss of yield varied between 0.8 and 7.3 tons (2.0–18.3 t/ha)/acre/100 L. elongatus/200 g, the former where the potential yield was high and the latter where poor growing conditions hindered recovery. Large numbers of Trichodorus occurred in two trial sites and there is some evidence of competition between the two genera. Significant negative regressions for Trichodorus spp. were obtained in one trial suggesting a loss of 12% total and 17% normal roots per 100 Trichodorus spp./200 g.     

Assessment of artificial substrates for evaluating groundwater microbial quality

Protection of groundwater resources requires the development of reliable ecological indicators. Microorganisms involved in ecological services or being associated with particular hosts or habitats could be used for this purpose. Nevertheless, their tracking remains limited because of sampling issues, and a lack of devices for their long term monitoring. In the present study, three artificial substrates (glass and clay beads, and gravel particles) were tested in terms of efficacy at favoring bacterial growth, and at capturing bacterial diversity of waters (i.e., groundwater, surface water and wastewater). Total proteins, total carbohydrates, dehydrogenase and hydrolytic activities were used to monitor biofilm development on these artificial substrates. Fingerprinting analyses based on rrs (16S rRNA) − rrl (23S rRNA) spacer analyses (ARISA) and next generation sequencing (NGS) of partial rrs DNA segments (V5-V6) were used to compare operating taxonomic units (OTUs), and infer bacterial genera trapped on these substrates. Glass beads were found less efficient than the other two artificial substrates at increasing protein contents and microbial activities (hydrolytic and dehydrogenase activities). ARISA showed a discrimination of bacterial communities developing on artificial substrates that was matching water types. An incubation period of 7 days allowed a reliable assessment of bacterial diversity. From this incubation period, around 75% of water genera with more than four V5-V6 rrs DNA sequences detected in a water type were recovered from biofilms growing on artificial substrates. Based on relative abundances of genera, clay beads and gravel particles were more efficient than glass beads to capture and obtain bacterial communities matching those of the initial waters. Between 45–67% of similarities were found for these artificial substrates while it was between 36 and 43% for glass beads. This study demonstrated clay beads and gravel particles as being efficient tools for capturing bacterial diversity and monitoring bacterial growth. Overall, clay beads appeared the best choice for field monitoring because of the ease of their size standardization in comparison with gravel particles.     

Field and laboratory studies for evaluating the toxicity of the insecticide Reldan on soil fungi

The response of soil fungi to the insecticide Reldan (chlorpyrifos-methyl) was studied under field and laboratory conditions. The colony forming units (CFU) of fungi were determined by means of serial dilution technique after 1 day, 7, 14, and 28 days of the insecticide application in soil. The plate count data indicated that the insecticide affected the number of fungi in treated soil compared with the untreated soil; the developed colonies decreased after 1–7 days of insecticide application and then increased with increasing application time. The effect of different concentrations of insecticide on the morphological features and sporogenesis of Aspergillus flavus, Fusarium culumorum, and Drechslera biseptata was studied. Relative conidiospore formation was sharply decreased and the conidiophores were deformed in A. flavus, while F. culumorum and D. biseptata failed to produce conidiospores, although chlamydospores were formed in large numbers when cultivated on the growth medium containing insecticide.     

Patterns of rhizosphere carbon flux in sugar maple (Acer saccharum) and yellow birch (Betula allegheniensis) saplings

Despite its importance in the terrestrial C cycle rhizosphere carbon flux (RCF) has rarely been measured for intact root–soil systems. We measured RCF for 8‐year‐old saplings of sugar maple (Acer saccharum) and yellow birch (Betula allegheniensis) collected from the Hubbard Brook Experimental Forest (HBEF), NH and transplanted into pots with native soil horizons intact. Five saplings of each species were pulse labeled with ¹³CO₂ at ambient CO₂ concentrations for 4–6 h, and the ¹³C label was chased through rhizosphere and bulk soil pools in organic and mineral horizons for 7 days. We hypothesized yellow birch roots would supply more labile C to the rhizosphere than sugar maple roots based on the presumed greater C requirements of ectomycorrhizal roots. We observed appearance of the label in rhizosphere soil of both species within the first 24 h, and a striking difference between species in the timing of ¹³C release to soil. In sugar maple, peak concentration of the label appeared 1 day after labeling and declined over time whereas in birch the label increased in concentration over the 7‐day chase period. The sum of root and rhizomicrobial respiration in the pots was 19% and 26% of total soil respiration in sugar maple and yellow birch, respectively. Our estimate of the total amount of RCF released by roots was 6.9–7.1% of assimilated C in sugar maple and 11.2–13.0% of assimilated C in yellow birch. These fluxes extrapolate to 55–57 and 90–104 g C m^?2 yr^?1 from sugar maple and yellow birch roots, respectively. These results suggest RCF from both arbuscular mycorrhizal and ectomycorrhizal roots represents a substantial flux of C to soil in northern hardwood forests with important implications for soil microbial activity, nutrient availability and C storage.     

In vitro Organogenesis in Explants from Different Cultivars of Begonia X hiemalis

Petiole explants from 17 cultivars of Begonia X hiemalis were grown on a basal agar medium with different combinations of NAA and BA as well as on media lacking microelements or vitamins. The stock plants were kept either under short days (7–8 h of light perday) at 15°C or under long days (15–16 h of light) at 18–21°C. The day length during the in vitro culture was 20 h of light and the temperature 21°C. Explants from short-day treated stock plants did not show any differentiation. In explants from long-day treated stock plants, the percentage of explants with shoot, root and with both shoot and root initiation were recorded after 55 days. Explants forming both shoots and roots were transferred to soil, and plantlet formation was observed after another 55 days. The percentage of explants with organ and plantlet formation differed between cultivars. With increasing NAA and decreasing BA concentrations, the percentage of explants forming only roots increased, whereas the percentage of explants with only shoots decreased. Plantlet formation was most frequent in explants from NAA: BA ratios of 2: 1 and 10: 1, and a variation was found between different cultivars. When the vitamin fraction was not added to the medium, this did not influence formation of shoots, roots and plantlets. When the microelements were omitted. shoots, roots and callus were formed, but no plantlets.     

Cadmium phytoextraction from loam soil in tropical southern China by Sorghum bicolor

The cadmium (Cd) uptake characteristics by Sorghum bicolor cv. Nengsi 2# and Cowley from the acidic sandy loam soil (pH = 6.1) during the entire growth period (100 days) were investigated in pot outdoors in a tropical district of southern China, Hainan Island. The Cd-spiked levels in soil were set as 3 and 15 mg/kg. Correspondingly, the available Cd levels in soil extracted by Mehlich III solution were 2.71 and 9.41 mg/kg, respectively. Basically, two varieties in a full growth period (100 days) did not show a significant difference in their growth and Cd uptake. Under high Cd stress, the plant growth was inhibited and its biomass weight and height decreased by 38.7–51.5% and 27.6–28.5%, respectively. However, S. bicolor showed higher bioaccumulation capability of Cd from soil to plant [bioconcentration factor (BCF)>4], and higher transfer capability of Cd from roots to shoots [translocation factor (TF)>1] under high Cd stress; Cd contents in the roots, stems, and leaves of S. bicolor reached 43.79–46.07, 63.28–70.60, and 63.10–66.06 mg/kg, respectively. S. bicolor exhibited the potential phytoextraction capability for low or moderate Cd-contamination in acidic sandy loam soil.     

The growth of external AM fungal mycelium in sand dunes and in experimental systems

We estimated the biomass and growth of arbuscular mycorrhizal (AM) mycelium in sand dunes using signature fatty acids. Mesh bags and tubes, containing initially mycelium-free sand, were buried in the field near the roots of the dune grass Ammophila arenaria L. AM fungal mycelia were detected at a distance of about 8.5 cm from the roots after 68 days of growth by use of neutral lipid fatty acid (NLFA) 16:1ω5. The average rate of mycelium extension during September and October was estimated as 1.2 mm day⁻¹. The lipid and fatty acid compositions of AM fungal mycelia of isolates and from sand dunes were analysed and showed all to be of a similar composition. Phospholipid fatty acids (PLFAs) can be used as indicators of microbial biomass. The mycelium of G. intraradices growing in glass beads contained 8.3 nmol PLFAs per mg dry biomass, and about 15% of the PLFAs in G. intraradices, G. claroideum and AM fungal mycelium extracted from sand dunes, consisted of the signature PLFA 16:1ω5. We thus suggest a conversion factor of 1.2 nmol PLFA 16:1ω5 per mg dry biomass. Calculations using this conversion factor indicated up to 34 μg dry AM fungal biomass per g sand in the sand dunes, which was less than one tenth of that found in an experimental system with Glomus spp. growing with cucumber as plant associate in agricultural soil. The PLFA results from different systems indicated that the biomass of the AM fungi constitutes a considerable part of the total soil microbial biomass. Calculations based on ATP of AM fungi in an experimental growth system indicated that the biomass of the AM fungi constituted approximately 30% of the total microbial biomass. This revised version was published online in June 2006 with corrections to the Cover Date.     

SEEDLING GROWTH AND ROOT CONTRACTION IN THE SOAP PLANT,CHLOROGALUM POMERIDIANUM (LILIACEAE)

Radicles and adventitious roots of the soap plant are contractile and through their activity, mature bulbs of this species are buried to depths of 20–30 cm. Experiments were performed to determine rates of contraction and displacement of the shoot apex resulting from activity of the contractile radicle and the first several adventitious roots. The average displacement was 23.2 mm over a 10-wk period and 63.8 mm over 29 weeks. Small glass beads and abortive seeds served as controls and showed no displacement through the soil column. Measurements from longitudinal and transverse sections of contracted and uncontracted portions of radicles revealed average increases of 26–64% in radial dimensions and 40–56% decreases in longitudinal dimensions of inner and middle cortical cells (excluding the endodermis) following contraction. Cells of the outermost cortex (excluding the exodermis) decreased in average longitudinal dimensions by 18–26% before becoming distorted and collapsed as contraction was completed. Average volumes of innermost cortical cells decreased by 15–54%, while two or three cell layers of the middle cortex, adjacent to collapsed outer cortical cells, increased in volume up to 75%. These middle cortical cells are identified as the “active” cells which, by their growth, are responsible for the shortening of the root. Throughout the process of contraction, the stele remains straight and undistorted, although the closer spacing of tracheary element secondary wall thickenings following contraction suggests longitudinal compression of the stele. The average number of cortical cells per transverse section does not differ in contracted and uncontracted roots and no evidence is found to support the “interdigitation” hypothesis of root contraction. However, reorientation of middle cortical cell expansion may be the mechanism of root contraction in Chlorogalum pomeridianum.     

Detection of Cryptomeria japonica roots with ground penetrating radar

Abstract

Coarse tree roots, which are responsible for most root carbon storage, are usually measured by destructive methods such as excavation and coring. Ground penetrating radar (GPR) is a non-destructive tool that could be used to detect coarse roots in forest soils. In this study, we examined whether the roots of Cryptomeria japonica, a major plantation species in Japan, can be detected with GPR. We also looked for factors that impact the analysis and detection of roots. Roots and wooden dowels of C. japonica were buried 30 cm deep in sandy granite soil. From GPR measurements with a 900 MHz antenna, the distribution and diameter of samples in several transects were recorded. The buried roots were detected clearly and could be distinguished at diameters of 1.1–5.2 cm. There were significant positive relationships between root diameter and parameters extracted from the resultant GPR waveform. The difference in water content between roots and soil is a crucial factor impacting the ability to detect roots with GPR. We conclude that GPR can be used as a non-destructive tool, but further investigation is needed to determine optimal conditions (e.g. water content) and analytical methods for using GPR to examine roots in forest sites.     

The inter-relationship between the age of carrot roots at harvest and infection by Mycocentrospora acerina in storage

Infection of carrot roots by Mycocenlrospora acerina in chill storage (3.5 °C) following inoculation with chlamydospores was studied in 1973–74 and 1974–75. AREAS of intact periderm were only rarely infected, and the high level of periderm resistance predominated over other variables. However, wound infection tended to increase with depth of wound and with increasing age of the plants at harvest. Irrespective of age of root or depth of wound, roots were comparatively resistant to infection at harvest and early in storage, resistance being expressed as a restriction of mycelial growth on the wound surface or localisation of the lesion. Increasing susceptibility with time in storage, depth of wounds, or age at harvest, resulted in larger numbers of inoculated sites becoming infected and a more rapid development from localised to progressive lesions.