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1.10Yam scale

Aspidiella hartii

Members of the Diaspididae family are called armoured scales because they produce a hard, fibrous, wax-like covering (Carver et al. 1991) that attaches them to the host plant. Unlike the soft scales, armoured scales do not produce the honeydew-like secretions that commonly cause sooty mould to develop (Beardsley and Gonzalez 1975).

Feeding by armoured scales affects their hosts by removing sap, and injected saliva contains toxic enzymes that can damage the host plant (Beardsley and Gonzalez 1975). Leaf chlorosis and other localised effects are often associated with armoured scale infestations (Beardsley and Gonzalez 1975). High populations of scales can cause the death of branches or even entire trees (Beardsley and Gonzalez 1975; Watson 2011).

Scale nymphs typically settle and feed on the host plant, becoming immobile as they develop into late instar nymphs (Beardsley and Gonzalez 1975). The female reaches sexual maturity without undergoing true metamorphosis, remaining legless and immobile on the host plant. There is no pupal stage in the female lifecycle. The male scale has a pupal stage, subsequently emerging as a winged adult form. The female life stages are egg, nymph and adult, while the male has egg, nymph, pre-pupal, pupal and adult stages (Beardsley and Gonzalez 1975).

The scale covering the mature adult female Aspidiella hartii is circular, brown to brownish grey, and around 1–2.5 mm in diameter (Mau and Martin Kessing 1992b; Watson 2011). The scale cover of the mature male is smaller and more elongate than that of the female (Watson 2011). The adult males of most armoured scales are winged and capable of flight. They are tiny, fragile and lack functional mouthparts, so cannot feed. They are short-lived, generally living for only a few hours (Beardsley and Gonzalez 1975).

Reproduction in most armoured scales is sexual, although some reproduce by parthenogenesis, and some species have both sexual and parthenogenetic races (Beardsley and Gonzalez 1975; Watson 2011). Aspidiella hartii reproduces sexually (Mau and Martin Kessing 1992b; Watson 2011). After fertilization, the female starts to lay eggs under her scale.

1.10.1Probability of entry

Probability of importation

• 
  Aspidiella hartii may be found on ginger rhizomes (Stout 1982; Mau and Martin Kessing 1992b) and is likely to survive transport on ginger.
  
• 
  Aspidiella hartii is a major pest during storage of ginger rhizomes (Devasahayam and Abdulla Koya 2005).
  
• 
  Aspidiella hartii was the most commonly detected ginger pest intercepted in New Zealand on fresh ginger imported from Fiji between 2000 and 2010 (NZ pest interception data).
  
• 
  Only first instar crawlers and male adults are active, which are likely to be dislodged during harvest and processing.
  
• 
  Other stages are sessile under a protective scale and unable to move.
  
• 
  Adult males do not live for more than a day, so are not likely to be present on imported ginger rhizomes, unless they emerge from pupation during transit.
  
• 
  Eggs are laid within the puparium (scale) (Mau and Martin Kessing 1992b) and may remain intact during processing and transit if not detected.
  
• 
  The harvested ginger is individually washed with high pressure water to remove soil, and this may remove some scales present on the ginger. However, live Diaspididae scales are difficult to remove with high pressure water spray, and a small percentage are likely to remain attached (Walker et al.1999).
  
• 
  Armoured scales are small and may not be noticed at harvest or during pre-export processing, particularly when present in low numbers. Adult females of Aspidiella hartii are light brown to grey and are around 1 mm in diameter (Mau and Martin Kessing 1992b).
  

Probability of distribution

• 
  The first-stage larvae of armoured scales are the active crawlers, while the second-stage larvae, pupae and adult females are immobile (Mau and Martin Kessing 1992b). Aspidiella hartii eggs, larvae, pupae and adult females would remain fixed to rhizomes under their protective scales.
  
• 
  If viable eggs hatch whilst the ginger is in storage, the first instar crawlers may be able to spread to other products in the storage facility.
  
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  Although the ginger is intended for human consumption, some material will be discarded as waste. Disposal of waste is likely to be via municipal or commercial waste systems, where pests would have limited opportunity to be in the proximity of host plants.
  
• 
  Some ginger may be discarded in a domestic garden or other exposed outdoor environment where potential hosts may be present.
  

• 
  Hosts of Aspidiella hartii include sweet potato, taro, turmeric and yams (Watson 2011).
  
• 
  Crawler wandering generally serves to disperse young scales away from the mother onto new growth of the same host, and movement between plants seldom occurs unless such plants are in contact (Beardsley and Gonzalez 1975). Diaspid crawlers can only move for short distances, and with great difficulty, across sand or bare soil (Beardsley and Gonzalez 1975).
  
• 
  The period of crawler mobility is limited by their small energy reserves and need to feed (Beardsley and Gonzalez 1975).
  

However, if rhizomes infested with yam scales were planted and established, then the scales would have a high likelihood of having available host plants on which to establish.

Probability of entry (importation × distribution)

1.10.2Probability of establishment

• 
  The main risk for establishment is posed by the first instar larvae, as they are capable of seeking out suitable hosts over short distances if introduced into the environment.
  
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  First instar larvae may be blown off the ginger during transport. However, the likelihood of these larvae landing on or near suitable hosts via wind dispersal would be very low.
  
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  Aspidiella hartii is thought to reproduce sexually (Watson 2011), like most other armoured scales (Beardsley and Gonzalez 1975).
  
• 
  Adult males of sexually reproducing Diaspididae may have flight capability, but are unable to establish populations (Moran and Goolsby 2010).
  
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  Adult males only live for a few hours, so have a limited period in which to find a mate.
  
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  An imported single gravid female may be all that is necessary to initiate an infestation (Beardsley and Gonzalez 1975). However, establishment of a population would require both male and female crawlers to find hosts in close proximity and complete their development, and then for the flying adult male to locate an adult female for mating.
  
• 
  Receptive adult female scales release pheromones to attract males. Information on flight ability of male Aspidiella hartii is not available, but the males of California red scale (Aonidiella aurantii) have been recovered up to 189 m downwind and 92 m upwind from release points. However, they were unable to fly upwind when the wind velocity exceeded 1.6 km per hour (Beardsley and Gonzalez 1975).
  
• 
  Cold winter temperatures are likely to be a limiting factor in the potential establishment of Aspidiella hartii (Soltic and Peacock 2006). Climatic conditions, particularly temperature, humidity and rainfall, influence the rate of development and survival of armoured scale species (Beardsley and Gonzalez 1975).
  

1.10.3Probability of spread

• 
  Once established, Aspidiella hartii is likely to spread wherever suitable host plants and favourable climate occur.
  
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  Natural spread would occur slowly through the movement of crawlers blown by the wind or carried by flying insects or birds (Watson 2011), although specific information on movement of Aspidiella hartii is lacking.
  
• 
  Dispersal of crawlers via wind or animals is not directional, reducing the likelihood of the crawlers locating a suitable host.
  
• 
  First instar crawlers of Diaspididae have limited ability to move unassisted. In the absence of wind or other assisted dispersal, crawlers normally settle on the same host plants as the parents (Magsig-Castillo et al. 2010).
  
• 
  The movement of infested tubers or rhizomes of tropical root crops, especially if they are used for planting purposes or stored with other root crops to be used for planting, is the most likely means of long distance dispersal for Aspidiella hartii (Watson 2011).
  
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  The small size and sessile habits of this species mean that an infestation may not be discovered until it is too late to eradicate it (Beardsley and Gonzalez 1975).
  

1.10.4Probability of entry, establishment and spread

1.10.5Consequences

1.10.6Unrestricted risk estimate

Unrestricted risk is the result of combining the probability of entry, establishment and spread with the outcome of overall consequences. Probabilities and consequences are combined using the risk estimation matrix shown in Table 2.5.

The unrestricted risk estimate for Aspidiella hartii of ‘low’ exceeds Australia’s ALOP. Therefore, specific risk management measures are required for this pest.