2022
DOI: 10.1111/eva.13381
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Genome‐scale phylogeography resolves the native population structure of the Asian longhorned beetle, Anoplophora glabripennis (Motschulsky)

Abstract: Human‐assisted movement has allowed the Asian longhorned beetle (ALB, Anoplophora glabripennis (Motschulsky)) to spread beyond its native range and become a globally regulated invasive pest. Within its native range of China and the Korean peninsula, human‐mediated dispersal has also caused cryptic translocation of insects, resulting in population structure complexity. Previous studies used genetic methods to detangle this complexity but were unable to clearly delimit native populations which is needed to devel… Show more

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Cited by 10 publications
(13 citation statements)
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“…Hence, the inclusion of a wider collection of native populations is recommended. For example, in the SNP discovery to study the population structure of the Asian longhorned beetle, the longhorned beetle samples from a wide coverage area in China and Korea were used [ 54 ].…”
Section: Discussionmentioning
confidence: 99%
“…Hence, the inclusion of a wider collection of native populations is recommended. For example, in the SNP discovery to study the population structure of the Asian longhorned beetle, the longhorned beetle samples from a wide coverage area in China and Korea were used [ 54 ].…”
Section: Discussionmentioning
confidence: 99%
“…Most ALB beetles fly up to ∼30 m at a time, and the dispersal distance of the first generation is generally less than 200 m if hosts are continuously distributed (He & Huang, 1993). In China, ALB is recorded throughout most of the country, except Taiwan, Hong Kong, and Macao (Li et al, 2020a;Cui et al, 2022). ALB has caused extensive damage since the 1980s, especially north of the Yangtze River.…”
Section: Distribution and Damage Caused By Albmentioning
confidence: 99%
“…, 2020a; Cui et al. , 2022). ALB has caused extensive damage since the 1980s, especially north of the Yangtze River.…”
Section: Distribution and Damage Caused By Albmentioning
confidence: 99%
“…In the amplification step, we used 5 µL of eluted DNA in each PCR, 10 µL of 5 × Q5 buffer, 10 µL of Q5 enhancer solution, 1 µL of 10 mmol/L dNTP, 0.3 µL of 10 µmol/L Iron Forward PCR Primer, 0.3 µL of 10 µmol/L Iron Reverse PCR Primer, 0.5 µL of Q5 High-fidelity polymerase, and 22.9 µL of H 2 O. Our PCR amplification was performed using an initial denaturation step at 75 °C for 5 min, followed by 5 cycles at 98 °C for 10 s, 55 °C for 30 s, and 72 °C for 30 s; 7 cycles at 98 °C for 10 s, 65 °C for 30 s, and 72 °C for 30 s; and a final elongation step at 72 °C for 5 min, and subsequently held at 4 °C (Abed et al, 2019;Cui et al, 2022).…”
Section: Gbs Proceduresmentioning
confidence: 99%