The Auchenorrhyncha of Central Europe. Die Zikaden Mitteleuropas, Volume 1: Fulgoromorpha, Cicadomorpha excl. Cicadellidae

Holzinger, Werner E.; Kammerlander, Ingrid; Nickel, Herbert

doi:10.1163/9789004231108

Cited by 106 publications

(45 citation statements)

References 0 publications

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…China: Ningxia; Algeria ( Nast 1972 , Holzinger et al 2003 ) Austria ( Nast 1972 , Holzinger et al 2003 ) Belgium ( Nast 1972 , Holzinger et al 2003 ); Canada: Alberta, British Columbia, Manitoba, New Brunswick, Newfoundland, Nova Scotia, Ontario, Quebec, Saskatchewan ( Bartlett et al 2014 ) Czechoslovakia ( Nast 1972 , Holzinger et al 2003 ); Denmark ( Nast 1972 , Holzinger et al 2003 ); Finland ( Nast 1972 , Holzinger et al 2003 ); France ( Nast 1972 , Holzinger et al 2003 ); Germany ( Nast 1972 , Holzinger et al 2003 ); Great Britain ( Nast 1972 , Holzinger et al 2003 ); Hungary ( Nast 1972 , Holzinger et al 2003 ); Italy ( Nast 1972 , Holzinger et al 2003 ); Japan: Hokkaido, Honshu; Macedonia; Morocco; Netherlands; Norway; Poland; Romania; Russia; Serbia; Spain; Sweden; Switzerland; Tunisia; USA: Alaska, Arizona, California, Colorado, Connecticut, Delaware, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Maine, Maryland, Massachusetts, Michigan, Minnesota, New Hampshire, New Jersey, New Mexico, New York, North Carolina, Ohio, Oregon, Pennsylvania, Rhode Island, South Dakota, Tennessee, Utah, Vermont, Virginia, Washington, Wisconsin ( Bartlett et al 2014 ).…”

Section: Checklistsmentioning

confidence: 99%

“…China: Guangxi, Guizhou, Zhejiang; France ( Ribaut and Lacroix 1958 ); Germany ( Holzinger et al 2003 ); UK ( Holzinger et al 2003 ); Iran: Kandovān ( Mozaffarian and Wilson 2011 ); Netherlands ( De Haas and Den Bieman 2018 ); Poland ( Gebicki et al 2013 ).…”

Section: Checklistsmentioning

confidence: 99%

“…China: Nei-Mongol, Heilongjiang; Iran: bādeh, Albāji, Bampur, Bazmān, Birjand, Chābahār, Dālaki, Evin, Gambuyeh, Gāvbandi, Gharechaman, Hafttappeh, Hamidieh, Hāresābād, Hashtpar, Irānshahr, Kandovān (Māzandarān), Marand, Miāneh-ZanjānRd, Minushahr, Mollāsāni, Shādegān, Shieh, Susangerd, Suza, Tabriz, Varāmin, Zābol ( Kalkandelen 1990 ); Afghanistan ( Nast 1972 , Holzinger et al 2003 ); Albania; Algeria: ( Nast 1972 , Holzinger et al 2003 ) Armenia; Austria; Azerbaijan ( Nast 1972 , Holzinger et al 2003 ); Belgium: ( Nast 1972 , Holzinger et al 2003 ); Cyprus; Czech Republic; Denmark: ( Nast 1972 , Holzinger et al 2003 ); Estonia: ( Nast 1972 , Holzinger et al 2003 ); Finland: ( Nast 1972 , Holzinger et al 2003 ); France: ( Nast 1972 , Holzinger et al 2003 ); Georgia: ( Nast 1972 , Holzinger et al 2003 ); Germany: ( Nast 1972 , Holzinger et al 2003 ); UK: ( Nast 1972 , Holzinger et al 2003 ); Greece: ( Nast 1972 , Holzinger et al 2003 ); Hungary: ( Nast 1972 , Holzinger et al 2003 ); Ireland: ( Nast 1972 , Holzinger et al 2003 ); Israel: ( Nast 1972 , Holzinger et al 2003 ); Italy: ( Nast 1972 , Holzinger et al 2003 ); Jordan: ( Nast 1972 ); Kazakhstan: ( Holzinger et al 2003 ); Kyrgyzstan: ( Nast 1972 , Holzinger et al 2003 ); Libya: ( Nast 1972 ); Lithuania; Moldova: ( Holzinger et al 2003 ); Mongolia; Netherlands: ( Nast 1972 , Holzinger et al 2003 ); Poland: ( Nast 1972 , Holzinger et al 2003 ); Portugal: ( Nast 1972 , ...…”

Section: Checklistsmentioning

confidence: 99%

See 2 more Smart Citations

Distribution patterns of Chinese Cixiidae (Hemiptera, Fulgoroidea), highlight their high endemic diversity

Yang¹,

Bourgoin²,

Zhang³

et al. 2022

BDJ

View full text Add to dashboard Cite

Cixiidae are small strictly phytophagous hemipteran insects worldwide distributed. Ecology and systematics of Chinese fauna remains poorly investigated. For instance, does their distribution follows the patterns of biogeogaphical distribution established for their host plants or other related-taxa because they are all obligatory phytophagous taxa? Do they follow the usual distributional Chinese realms and boundaries already recognized? Which zoogeographical Chinese regions and connections between them do they depict. To investigate these issues, we provide here a referenced and comprehensive checklist of the 250 cixiid species currently reported from China (77 new records), with their precise distribution at the regional level. In the 8 Chinese main zoogeographical regions usually recognized and 2 adjacent areas, we analyzed further their diversity at the tribal, generic, and specific levels using a non-metric multidimensional scaling and an unweighted pairwise group analysis using an arithmetic mean cluster analyses. The observed distribution patterns shown that an intercalary Sino-Japanese realm is recognisable between the Palaearctic and Oriental realms. At the regional level, the South China region clusters more closely with the Southwest, Central and North China regions. Taiwan, clearly separated from the South China region and mainland China, is more closely related to the Qinghai-Tibet region and Indochina countries. Although Central and South China regions remain close to each other, the Qinghai-Tibet region appears singularly different. An updated checklist of the 250 Cixiidae species, known to occur in China and counting for 10% of the Chinese planthopper fauna, is presented based on literature, recent collections, and museum records. More than 400 records distributed among the 28 provinces and 8 regions in China are extensively provided, including 77 new records. Of these, more than 80% of the species (205 species, 82%) have been only reported from China, and most of them are endemic species, which could reflects the great diversity degree of the Chinese regions and local biotypes highlights the uniqueness of this fauna. These species are found in 8 Chinese zoogeographical regions: The Taiwan region is the most diversified with 161 species and the highest rate of endemic species (69.57%), followed by South China (78 species, 17.95%), Central China (60 species, 33.33%), Southwest China (43 species, 39.53%), North China (29 species, 34.48%), Qinghai-Tibet region (10 species, 20%), Northeast China (8 species, 12.5%), and 5 species found in the Inner Mongolia-Xinjiang region that are not endemic ones. Endemism was analyzed for each region and repeated for species distribution patterns across them, 9 being bi-regionally and tri-regionally distributed. The South China-Taiwan pattern is the most richest one, followed by the Central-South China-Taiwan pattern. Semonini and Pentastirini tribes are widespread among all the zoological regions, representing respectively 21.20% and 17.20% of all the species, while Cixiini being is the most common tribe with 45.20%, remains absent from the North-Eastern China region. Andini with only 5.20% of the species is distributed in the Sino-Japanese - Oriental Region; Eucarpini (6.40%) and Borysthenini (2.00%) are mainly concentrated in the south of the Qingling Mountain-Huai River. The remaining four tribes, Bennini (0.40%), Briixini (0.80%), Oecleini (1.20%) and Stenophlepsiini (0.40%) are relatively rare and restricted to Taiwan. At the generic level, Kuvera (7.2%) is the most widely distributed genus in China while Cixius, Betacixius, Kuvera, Oecleopsis and Andes are the more diversified. One genus (Oliparisca) is distributed only in the Tibet region, while 10 genera are distributed only in the Taiwan region. In addition, nearly half of the genera (16 genera, 48.48%) are distributed south of the Palearctic/Oriental boundary. A non-metric multidimensional scaling and an unweighted pairwise group method analysis using arithmetic mean clustering based on the Jaccard similarity coefficient matrix support a Palaearctic/Sino-Japanese boundary and a South China region closer to the Southwest, Central and North China regions. The Taiwan region appears clearly separated from the South China region and to mainland China, and more closely related to the Qinghai-Tibet region and Indochina countries. The Central and South China regions appear close to each other, but the Qinghai-Tibet region is singularly isolated.

show abstract

Section: Checklistsmentioning

confidence: 99%

Section: Checklistsmentioning

confidence: 99%

Section: Checklistsmentioning

confidence: 99%

See 1 more Smart Citation

Distribution patterns of Chinese Cixiidae (Hemiptera, Fulgoroidea), highlight their high endemic diversity

Yang¹,

Bourgoin²,

Zhang³

et al. 2022

BDJ

View full text Add to dashboard Cite

show abstract

“…The planthopper Pentastiridius leporinus (Linnaeus 1761) is a member of the Cixiidae (Hemiptera, Fulgoromorpha) family, which comprises almost 2000 species worldwide 1 . The insect has a palearctic distribution but does not occur in northern regions 2 . In natural ecosystems, adult P. leporinus are known to feed on the above‐ground parts of reed grass ( Phragmites australis ) but no information is available on host plants used by the immature stages that ingest phloem sap from roots 1–3 .…”

Section: Introductionmentioning

confidence: 99%

“…The insect has a palearctic distribution but does not occur in northern regions 2 . In natural ecosystems, adult P. leporinus are known to feed on the above‐ground parts of reed grass ( Phragmites australis ) but no information is available on host plants used by the immature stages that ingest phloem sap from roots 1–3 . In agricultural systems, P. leporinus feeds on sugar beet ( Beta vulgaris ) leaves, thereby transmitting the phloem‐restricted γ‐3 proteobacterium ‘ Candidatus Arsenophonus phytopathogenicus’ that causes a disease known as syndrome ‘basses richesses’ (SBR) 4–6 .…”

Section: Introductionmentioning

confidence: 99%

Life history traits and a method for continuous mass rearing of the planthopper Pentastiridius leporinus, a vector of the causal agent of syndrome ‘basses richesses’ in sugar beet

Pfitzer¹,

Varrelmann²,

Schrameyer

et al. 2022

Pest Management Science

View full text Add to dashboard Cite

BACKGROUND The planthopper Pentastiridius leporinus (Hemiptera: Cixiidae) is the main vector of the γ‐3 proteobacterium ‘Candidatus Arsenophonus phytopathogenicus’ which causes the syndrome ‘basses richesses’ (SBR) in sugar beet. SBR is a new and fast‐spreading disease in Central Europe that leads to high yield losses. To date, the development of management strategies has been hampered by insufficient knowledge about general life history traits of the planthopper and, most importantly, the year‐round availability of insects reared under controlled conditions. Rearing of P. leporinus has been considered challenging and to date no protocol exists. RESULTS Here we describe a method for mass rearing P. leporinus on sugar beet from egg to adult that has produced five generations and over 20 000 individuals between June 2020 and March 2022. An alternative host such as wheat is not necessary for completing the life cycle. No‐choice experiments showed that P. leporinus lays 139.1 ± 132.9 eggs on sugar beet, whereas no oviposition was observed on its nymphal host wheat. Head capsule width was identified as a trait that unequivocally distinguished the five nymphal instars. Developmental time from first instar to adult was 193.6 ± 35.8 days for males and 193.5 ± 59.2 days for females. Infection rates of adults were tested with a nested polymerase chain reaction. The results demonstrated that 70%–80% of reared planthoppers across all generations carried the SBR proteobacterium. CONCLUSION The mass‐rearing protocol and life history data will help overcome an important bottleneck in SBR research and enhance efforts in developing integrated pest management tools. © 2022 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

show abstract

Habitat area and local habitat conditions outweigh fragmentation effects on insect communities in vineyards

Bosco

Moser

Jones

et al. 2023

Ecol Sol and Evidence

View full text Add to dashboard Cite

1. Fragmentation of habitat, for example by intensive agricultural practices, can be detrimental to local biodiversity. However, it often remains unclear whether such biodiversity declines are caused by loss of habitat area or increased fragmentation, and how habitat quality factors into it. In our study system, vegetated vineyards are typically small, and isolated from one another, potentially limiting the distribution and dispersal of organisms.2. In a full-factorial experiment of a priori selected vegetated vineyard patches of differing size and fragmentation, we aimed to disentangle the effects of habitat area (area of vegetated vineyards), habitat fragmentation (number of vegetated vineyards per 100 ha) and field-scale ground vegetation density on ground beetle, leafhopper and wild bee communities using a combined framework of multiscale and multispecies modelling (Hierarchical Model of Species Communities).

show abstract

The Auchenorrhyncha of Central Europe. Die Zikaden Mitteleuropas, Volume 1: Fulgoromorpha, Cicadomorpha excl. Cicadellidae

Cited by 106 publications

References 0 publications

Distribution patterns of Chinese Cixiidae (Hemiptera, Fulgoroidea), highlight their high endemic diversity

Distribution patterns of Chinese Cixiidae (Hemiptera, Fulgoroidea), highlight their high endemic diversity

Life history traits and a method for continuous mass rearing of the planthopper Pentastiridius leporinus, a vector of the causal agent of syndrome ‘basses richesses’ in sugar beet

Habitat area and local habitat conditions outweigh fragmentation effects on insect communities in vineyards

Contact Info

Product

Resources

About