Nephotettix cincticeps (rice green leafhopper)
Identity
- Preferred Scientific Name
- Nephotettix cincticeps (Uhler) 1956
- Preferred Common Name
- rice green leafhopper
- Other Scientific Names
- Nephotettix apicalis Melichar
- Nephotettix apicalis cincticeps Esaki & Hashimoto
- Nephotettix apicalis var. cincticeps
- Nephotettix bipunctatus cincticeps Esaki & Hashimoto
- Nephotettix bipunctatus fabricius forma cincticeps Esaki & Ito
- Nephotettix cincticeps Linnavuori
- Nephotettix cincticeps Matsumura
- Selenocephalus cincticeps Uhler, 1896
- International Common Names
- Englishgreen leafhoppergreen rice leafhopperspotted jassid
- Spanishcigarrita verde del arroz
- Frenchcicadelle verte du riz
- Local Common Names
- Chinahei wei ye chan
- GermanyZikade, Gruene Japanische Reis-Zikade, Gruene Reis-
- Japantsumaguro yokobae
- Korea, DPRgoodong manicheung
- EPPO code
- NEPHCI (Nephotettix cincticeps)
Pictures
Distribution
Host Plants and Other Plants Affected
Host | Host status | References |
---|---|---|
Alopecurus aequalis (Dent foxtail) | Wild host | |
Avena fatua (wild oat) | Wild host | |
Echinochloa frumentacea (Japanese millet) | Wild host | |
Leersia japonica (japanese cutgrass) | Wild host | |
Oryza sativa (rice) | Main | |
Phalaris arundinacea (reed canary grass) | Wild host | |
Phragmites australis (common reed) | Wild host | |
Poa annua (annual meadowgrass) | Wild host |
Symptoms
Both nymphs and adults of N. cincticeps suck sap primarily from leaves and leaf sheaths of rice plants. Populations are rarely high enough to cause direct feeding damage. N. cincticeps is the vector of rice dwarf disease, rice yellow dwarf disease and transitory yellowing (Ou, 1985).
List of Symptoms/Signs
Symptom or sign | Life stages | Sign or diagnosis |
---|---|---|
Plants/Leaves/honeydew or sooty mould | ||
Plants/Leaves/yellowed or dead | ||
Plants/Stems/honeydew or sooty mould |
Prevention and Control
Cultural Control
In Japan, the cultivation of early-planted rice crops contributed to an increase in the importance of Rice dwarf virus disease (Kiritani, 1983). Hokyo (1976) advocated later planting of rice crops so that fewer immigrants would be able to colonize rice fields. This could be achieved by developing mechanical transplanting techniques for older seedlings. However, these measures were often not considered practical. Ploughing fallow rice fields in the winter is recommended with the objective of reducing numbers of overwintering adults and nymphs of N. cincticeps and thus reducing the incidence of Rice dwarf virus disease (Nakasuji and Kiritani, 1977). Widiarta et al. (1992) showed that ploughing during the peak oviposition period of N. cincticeps females was the most effective strategy to reduce the density of leafhoppers invading rice crops. In Korea, lower population densities of N. cincticeps were recorded in direct-seeded rice fields than in fields where machine transplanting was practised (Lee and Ma, 1997). Population development of rice leafhoppers and planthoppers is enhanced by the application of high levels of inorganic nitrogen fertilizer (Cook and Denno, 1994). Researchers in Japan reported that the density of N. cincticeps in an organically-farmed rice field was lower than that in a field where chemical inputs were used (Kajimura et al., 1993). Based on this and related studies it was suggested that fertilizer practices could be modified to manage populations of both leafhoppers and planthoppers in Japan (Kajimura et al., 1995).
In Japan, the cultivation of early-planted rice crops contributed to an increase in the importance of Rice dwarf virus disease (Kiritani, 1983). Hokyo (1976) advocated later planting of rice crops so that fewer immigrants would be able to colonize rice fields. This could be achieved by developing mechanical transplanting techniques for older seedlings. However, these measures were often not considered practical. Ploughing fallow rice fields in the winter is recommended with the objective of reducing numbers of overwintering adults and nymphs of N. cincticeps and thus reducing the incidence of Rice dwarf virus disease (Nakasuji and Kiritani, 1977). Widiarta et al. (1992) showed that ploughing during the peak oviposition period of N. cincticeps females was the most effective strategy to reduce the density of leafhoppers invading rice crops. In Korea, lower population densities of N. cincticeps were recorded in direct-seeded rice fields than in fields where machine transplanting was practised (Lee and Ma, 1997). Population development of rice leafhoppers and planthoppers is enhanced by the application of high levels of inorganic nitrogen fertilizer (Cook and Denno, 1994). Researchers in Japan reported that the density of N. cincticeps in an organically-farmed rice field was lower than that in a field where chemical inputs were used (Kajimura et al., 1993). Based on this and related studies it was suggested that fertilizer practices could be modified to manage populations of both leafhoppers and planthoppers in Japan (Kajimura et al., 1995).
Biological Control
The major focus of biological control strategies for N. cincticeps has been to enhance the regulation of leafhopper populations through the conservation of natural enemies, particularly spiders (Kiritani et al., 1970). Spiders, including Pardosa pseudoannulata, Pirata subpiraticus and Ummeliata insecticeps, are important predators of N. cincticeps in rice fields (Li and Zhao, 2002; Ishijima et al., 2006; Lou et al., 2013). Field studies in Japan showed that populations of predatory wolf spiders (P. pseudoannulata and P. subpiraticus) were higher in paddy fields with no tillage than in conventionally tilled paddy fields (Ishijima et al., 2004).
The hydrometrid Hydrometra procera has also shown potential as a biological control agent of N. cincticeps in paddy fields in Japan (Murata, 2009). The mirid Cyrtorrhinus livdipennis is a predator of eggs of N. cincticeps, and the veliid Microvelia horvathi and the staphylinid Paederus fuscipes are predators of adults and nymphs of N. cincticeps on rice in China (Lou et al., 2013). A comprehensive list of the parasitoids of hemipteran pests of rice in Asia, including N. cincticeps, is provided in Gurr et al. (2011), and the prospects for enhancing the biological control of rice planthoppers by ecological engineering is discussed. Nitta and Grey (1996) reported that good control of N. cincticeps in the field was achieved with Beauveria bassiana (strain TB.274) when applied as a conidial dust to first-generation adults. The application of B. bassiana gave effective control of the overwintering generation (77-81%) and second generation (73-83%) of N. cincticeps in rice fields in Hunan province, China (Bao and Gu, 1998, in Lou et al., 2013).
Host-Plant Resistance
In laboratory feeding studies, Kawabe (1985) found that N. cincticeps fed for a much longer time from the xylem in resistant than in susceptible rice varieties. Similarly, very low levels of amino acids and sugar were recorded in adults fed on a new resistant variety, Norin-PL6, suggesting that feeding from the phloem was severely restricted (Jung et al., 1995). Sato and Sogawa (1981) showed that there were variations among populations of N. cincticeps in their ability to survive and reproduce on resistant varieties.
There are few sources of resistance to N. cincticeps in the japonica germplasm but resistant donors from indica varieties are also utilized in breeding programmes (see e.g. Wang et al., 2003, 2004). An African rice cultivar, Oryza glaberrima (IRGC104038), has been shown to be highly resistant to N. cincticeps at the booting stage and the genetic basis for this resistance was investigated (Fujita et al., 2010). A simple and rapid method has been developed for evaluating resistance in rice to N. cincticeps based on nymphal growth (Hirae, 2011). Genetic studies are concentrating on molecular mapping of host plant resistant gene(s) to N. cincticeps in order to facilitate marker-assisted selection of resistance in rice breeding programmes (Yasui, 2007; Jena and Mackill, 2008; Fujita et al., 2010; Park et al., 2013).
In laboratory feeding studies, Kawabe (1985) found that N. cincticeps fed for a much longer time from the xylem in resistant than in susceptible rice varieties. Similarly, very low levels of amino acids and sugar were recorded in adults fed on a new resistant variety, Norin-PL6, suggesting that feeding from the phloem was severely restricted (Jung et al., 1995). Sato and Sogawa (1981) showed that there were variations among populations of N. cincticeps in their ability to survive and reproduce on resistant varieties.
There are few sources of resistance to N. cincticeps in the japonica germplasm but resistant donors from indica varieties are also utilized in breeding programmes (see e.g. Wang et al., 2003, 2004). An African rice cultivar, Oryza glaberrima (IRGC104038), has been shown to be highly resistant to N. cincticeps at the booting stage and the genetic basis for this resistance was investigated (Fujita et al., 2010). A simple and rapid method has been developed for evaluating resistance in rice to N. cincticeps based on nymphal growth (Hirae, 2011). Genetic studies are concentrating on molecular mapping of host plant resistant gene(s) to N. cincticeps in order to facilitate marker-assisted selection of resistance in rice breeding programmes (Yasui, 2007; Jena and Mackill, 2008; Fujita et al., 2010; Park et al., 2013).
Field and laboratory studies are being carried out to assess the effects of transgenic rice expressing Bacillus thuringiensis (Bt) toxins against other insect pests on N. cincticeps as a non-target organism. One study showed that female longevity, oviposition duration and fecundity of N. cincticeps were higher/longer on two Bt rice lines than on a wild type cultivar (Zhou et al., 2005), while other studies have shown no adverse effects of tested Bt rice lines on the population density of N. cincticeps and/or on the population dynamics of their spider predators (e.g. Liu et al., 2002; Chen et al., 2006; Lu et al., 2014).
Chemical Control
Due to the variable regulations around (de-)registration of pesticides, we are for the moment not including any specific chemical control recommendations. For further information, we recommend you visit the following resources:
•
EU pesticides database (http://ec.europa.eu/food/plant/pesticides/eu-pesticides-database/)
•
PAN pesticide database (www.pesticideinfo.org)
•
Your national pesticide guide
Impact
Rice dwarf virus (RDV) and Rice gall dwarf virus (RGDV) are transmitted by N. cincticeps in a persistent manner (Sasaya et al., 2014). N. cincticeps is regarded as a major pest of rice in Japan, particularly in the south of the country where Rice dwarf virus disease is present (Kiritani, 1980). Direct feeding damage to the rice plant may occur as the insertion of the insect's stylets disrupts the translocation of water and photosynthetic products to the panicles (Naba, 1988). Potential yield loss is greater in early-maturing varieties, but field populations of N. cincticeps are rarely high enough to cause serious damage.
Few data are available for economic losses caused by Rice dwarf virus disease. Kiritani (1983) argued that changes in cultivation practices, such as the winter and spring ploughing of fallow rice fields, has contributed to a decline in the duration and frequency of Rice dwarf virus disease.
Information & Authors
Information
Published In
Copyright
Copyright © CABI. CABI is a registered EU trademark. This article is published under a Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
History
Published online: 21 November 2019
Language
English
Authors
Metrics & Citations
Metrics
SCITE_
Citations
Export citation
Select the format you want to export the citations of this publication.
EXPORT CITATIONSExport Citation
View Options
View options
Get Access
Login Options
Check if you access through your login credentials or your institution to get full access on this article.