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RESEARCH ARTICLE

First record of stubby-root nematode (Paratrichodorus porosus) associated with barley in Australia

J. G. Sheedy A C , T. G. Clewett A , M. Hodda B and J. P. Thompson A
+ Author Affiliations
- Author Affiliations

A Leslie Research Centre, Agri-Science Queensland, Department of Employment, Economic Development and Innovation, PO Box 2282, Toowoomba, Qld 4350, Australia.

B CSIRO Entomology, GPO Box 1700, Canberra, ACT 2601, Australia.

C Corresponding author. Email: jason.sheedy@deedi.qld.gov.au

Australasian Plant Disease Notes 5(1) 66-69 https://doi.org/10.1071/DN10024
Submitted: 26 November 2009  Accepted: 3 June 2010   Published: 17 June 2010

Abstract

High populations (5000 to 20 000/kg soil) of the stubby-root nematode Paratrichodorus porosus were identified morphologically from soil samples taken under patches of poorly growing barley in a field between Yuleba and Surat in western Queensland, Australia. Lower populations (<4000/kg soil) were recovered from soil samples taken from asymptomatic barley. This is the first record of this nematode species on barley in Australia.

In 2008, a 130-ha irrigated crop of barley (Hordeum vulgare cv. Dictator) being grown for hay on a brown Kandosol (Isbell 2002) (pH 6.0; 88% sand; 5% silt; 7% clay) between Yuleba and Surat, Queensland (26.98547°S 149.27344°E, 244 m elevation) had large patches of poor growth over a 20-ha portion of the field. The crop had been planted on June 14 with 40 kg/ha monoammonium phosphate (MAP: 10% N, 22% P, 1.5% S) and fertilised with 200 kg/ha urea (46% N) on July 15 and then irrigated. At the beginning of anthesis, asymptomatic plants had normal growth, biomass and a height over 1 m, whereas symptomatic plants were visibly stunted (<30 cm high) with severely reduced biomass. Three samples each of symptomatic and asymptomatic groups of whole plants from 20 cm of row and soil to 15-cm depth were collected from different areas within the 20-ha portion.

Each soil and root sample was thoroughly mixed with roots cut into ~1-cm lengths. Gravimetric moisture content was determined by drying a 100-g subsample at 105°C for 48 h. Nematodes were extracted from a 200-g subsample from each soil sample using the Whitehead tray method (Whitehead and Hemming 1965) for 48 h at 22°C and collected on a 20-μm-aperture sieve. Samples were stored in ~15 mL of water at 3°C. Nematode populations were counted under a compound microscope (100×) using a Hawksley slide counting chamber of 1-mL capacity. After assessment, nematodes were submitted to the Australian National Insect Collection (Canberra, Australia) for species identification.

Morphological identifications were conducted initially on immobilised specimens in water. Identifications were confirmed on specimens fixed in formaldehyde for 2 weeks, then processed to glycerol by the slow method and mounted on permanent slides (Hooper 1986).

The nematodes were on average 353 μm long (307–378 μm), average vulval position of 54% (52–56%), had onchiostyles between 42 and 50 µm long, excretory pore anterior to pharynx base, medioventral body pores, anterodorsal overlap of intestine, oesophageal bulb, no males, pore-shaped vulva in ventral view, oval, oblique and separated vaginal cuticular pieces and a convex-conoid tail. The most distinctive diagnostic characters were the excretory pore much anterior to the oesophago-intestinal junction, the anterodorsal overlap of the oesophagus of the intestine and the absence of males. Female body length was shorter than, but vulval position was consistent with published ranges; however, neither trait is generally considered diagnostic (Decraemer 1995). Of the seven species of Paratrichodorus identified in Australia (P. minor, P. lobatus, P. porosus, P. renifer, P. queenslandensis, P. orrae and P. mirzai) (Decraemer and Reay 1991; McLeod et al. 1994), this combination of characters is present in P. porosus only (Table 1).


Table 1.  Distinguishing features of Australian species of Paratrichodorus (after Decraemer and Reay 1991; Decraemer 1995)
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P. porosus populations were 5053, 10139 and 20216/kg soil (oven-dry equivalent) in samples from areas with symptomatic plants and 320, 507 and 4101/kg soil in samples from areas with asymptomatic plants. Examination of the root systems showed that asymptomatic plants had normal root development while symptomatic plants had severe root damage including black lesions, stunting of lateral roots and absence of root-hairs.

Further investigation was done in a glasshouse pot study using pregerminated barley cv. NRB04182 plants in 7-cm-square by 15-cm-high plastic pots containing 330 g of remnant soil from the poor growth area with a P. porosus concentration of 5053/kg. Each pot was fertilised with 1 g of Osmocote® Native Gardens plus micronutrients (17–1.6–8.7 NPK) slow-release fertiliser mixed through the soil and grown on glasshouse benches fitted with a bottom watering system regulated by a float valve set to a water tension of 2 cm. After 10 weeks growth, root systems were visually examined and a 1-g subsample stained for root-infecting fungi (Phillips and Hayman 1970). No evidence of phytoparasitic fungi was observed on the root systems of the glasshouse-grown barley cv. NRB04182, which displayed similar symptoms to the barley cv. Dictator root systems observed from symptomatic field plants (Fig. 1).


Fig. 1.  Root system of barley cv. NRB04182 showing blackening, stunting of lateral roots and no root-hair production after 10 weeks glasshouse growth in field soil infested with 5053 Paratrichodorus porosus/kg.
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P. porosus has previously been recorded in Queensland, New South Wales and Western Australia (McLeod et al. 1994) with the most recent report specifically indentifying P. porosus in a survey of Queensland sugarcane fields where it occurred in <1% of samples (Blair et al. 1999). However, Paratrichodorus spp. have previously been associated with sugarcane (Saccharum sp.) (Blair et al. 1999; Blair and Stirling 2007), citrus (Citrus spp.) (Brown 1978; Walker and Morey 1999) and other fruit trees (Sauer 1981), leeks (Allium ampeloparsum) (Hall et al. 2007), grapes (Vitis sp.) (Stirling 1976; Harris 1983), carrot (Daucus carota) (Walker 2004) and wheat (Triticum aestivum) (Suatmadji 1984). These reports have identified Paratrichodorus spp. in a range of soil types; however, high sand-content soils were most common with Blair et al. (1999) finding that the mean densities of Paratrichodorus spp. were significantly higher in sandy loams with greater than 75% sand (coarse and fine) than all other soil types. A recent review by Hodda and Nobbs (2008) found that of the seven species of Paratrichodorus present in Australia, only P. minor and P. porosus have been associated with damage of major agricultural species outside the Australasian region.

This is the first report of P. porosus associated with poor growth of barley in Australia. Observations by the property owners suggested that barley cv. Fitzroy and a mixed planting of barley cvv. Mackay and Grout also suffered from patchy poor growth during 2007 and 2009, respectively. Little is known of the distribution of P. porosus in broadacre cropping systems or the host status of many of the economically important crops in Queensland. Initially, glasshouse studies would be valuable to assess the host status of economically important crop species and cultivars. Additionally, targeted sampling of lighter-textured soils would be useful to ascertain the extent of P. porosus distribution.



Acknowledgements

The authors thank Lindsay Ward (Ward Agriculture) and Greg Platz (Agri-Science Queensland) for initial collection of soil and plant samples and David and Matthew McInnerney for allowing sampling to be done on their property.


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