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1

Ilyasov, Rustem A., Junhyung Park, Junichi Takahashi, and Hyung Wook Kwon. "Phylogenetic Uniqueness of Honeybee Apis Cerana from the Korean Peninsula Inferred from The Mitochondrial, Nuclear, and Morphological Data." Journal of Apicultural Science 62, no. 2 (2018): 189–214. http://dx.doi.org/10.2478/jas-2018-0018.

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Abstract Apis cerana is an Eastern honeybee species distributed throughout Asia and closely related to the Western honeybee species Apis mellifera distributed across all of Africa, Europe and Western Asia, and subdivided into thirty confirmed subspecies. Currently, A. cerana is an endangered bee species in contrast to A. mellifera. We sequenced and annotated the complete mitochondrial genome of A. cerana from the Jeollanam-do province of South Korea and uploaded to the DDBJ/Genbank database(AP018431). MtDNA sequence is 15.925 bp long, has 84% AT-content and 16% GC-content and contains 22 tRNA
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2

Donkersley, Philip, Lucy Covell, and Takahiro Ota. "Japanese Honeybees (Apis cerana japonica Radoszkowski, 1877) May Be Resilient to Land Use Change." Insects 12, no. 8 (2021): 685. http://dx.doi.org/10.3390/insects12080685.

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Pollinators are being threatened globally by urbanisation and agricultural intensification, driven by a growing human population. Understanding these impacts on landscapes and pollinators is critical to ensuring a robust pollination system. Remote sensing data on land use attributes have previously linked honeybee nutrition to land use in the Western Honeybee (Apis mellifera L.). Here, we instead focus on the less commonly studied Apis cerana japonica—the Japanese Honeybee. Our study presents preliminary data comparing forage (honey and pollen) with land use across a rural-urban gradient from
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3

SUGAHARA, Michio. "Defensive behaviour of Apis cerana japonica against predatory hornets." Hikaku seiri seikagaku(Comparative Physiology and Biochemistry) 30, no. 2 (2013): 68–75. http://dx.doi.org/10.3330/hikakuseiriseika.30.68.

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4

Sakamoto, Y., T. Maeda, M. Yoshiyama, F. Konno, and J. S. Pettis. "Differential autogrooming response to the tracheal mite Acarapis woodi by the honey bees Apis cerana and Apis mellifera." Insectes Sociaux 67, no. 1 (2019): 95–102. http://dx.doi.org/10.1007/s00040-019-00732-w.

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AbstractThe infestation of honey bees by the endoparasitic tracheal mite Acarapis woodi was first discovered in Apis mellifera on the Isle of Wight, England, and the mite has since spread to all continents except Australia. Since 2010, this tracheal mite has spread rapidly in the Japanese honey bee, Apis cerana japonica, of mainland Japan, causing considerable colony mortality. In contrast, infestations by the mites in the imported and managed European honey bee, A. mellifera, have rarely been observed in Japan. A previous laboratory experiment revealed a difference in susceptibility by demons
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5

Fujiwara, S., H. Miura, T. Kumagai, et al. "Drone congregation of Apis cerana japonica (Radoszkowski, 1877) above large trees." Apidologie 25, no. 3 (1994): 331–37. http://dx.doi.org/10.1051/apido:19940309.

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6

FUCHIKAWA, TARO, and ISAMU SHIMIZU. "Circadian rhythm of locomotor activity in the Japanese honeybee, Apis cerana japonica." Physiological Entomology 32, no. 1 (2007): 73–80. http://dx.doi.org/10.1111/j.1365-3032.2006.00543.x.

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7

ROZALSKI, J. Robert, Koji TSUCHIDA, and Hironori SAKURAI. "A Preliminary Report of PCR Amplifications of Apis cerana japonica Genomic DNA." Applied Entomology and Zoology 32, no. 1 (1997): 259–61. http://dx.doi.org/10.1303/aez.32.259.

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8

Yokoi, Tomoyuki. "Visitation and gnawing behaviour of Japanese honeybee Apis cerana japonica to lettuce." Apidologie 46, no. 4 (2014): 489–94. http://dx.doi.org/10.1007/s13592-014-0340-z.

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9

Yoshiyama, Mikio, and Kiyoshi Kimura. "Characterization of antimicrobial peptide genes from Japanese honeybee Apis cerana japonica (Hymenoptera: Apidae)." Applied Entomology and Zoology 45, no. 4 (2010): 609–14. http://dx.doi.org/10.1303/aez.2010.609.

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10

Yoshiyama, Mikio, Masanori Kubo, and Kiyoshi Kimura. "Intestinal bacteria across life stages of the Japanese honey bee Apis cerana japonica." Journal of Apicultural Research 49, no. 2 (2010): 218–20. http://dx.doi.org/10.3896/ibra.1.49.2.14.

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11

Morii, Kiyohito, and Yoshiko Sakamoto. "Off-Season Swarming in the Japanese Honey Bee (Apis Cerana Japonica)." Journal of Apicultural Science 68, no. 1 (2024): 51–55. http://dx.doi.org/10.2478/jas-2024-0005.

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Abstract Several studies have reported fragmentary evidence that climate change is altering the phenology and behavior of honey bees. We compiled records of off-season swarming of the Japanese honey bee (Apis cerana japonica) between autumn and winter to improve our understanding of the impact of climate change on the subspecies’ swarming phenology. Based on a survey of 311 beekeepers, eleven off-season swarming records were collected, with ten of them are from 2020 onward. The beekeepers who reported off-season swarming records had eight to twenty years of beekeeping experience, and they decl
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12

Fuchikawa, Taro, and Isamu Shimizu. "Effects of temperature on circadian rhythm in the Japanese honeybee, Apis cerana japonica." Journal of Insect Physiology 53, no. 11 (2007): 1179–87. http://dx.doi.org/10.1016/j.jinsphys.2007.06.013.

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13

Yoshida, T., J. Saito, and N. Kajigaya. "The mating flight times of native Apis cerana japonica Radoszkowski and introduced Apis mellifera L in sympatric conditions." Apidologie 25, no. 4 (1994): 353–60. http://dx.doi.org/10.1051/apido:19940401.

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14

Shimizu, Isamu, Yutaka Kawai, Masanori Taniguchi, and Setsuyuki Aoki. "Circadian Rhythm and cDNA Cloning of the Clock Geneperiodin the Honeybee Apis cerana japonica." Zoological Science 18, no. 6 (2001): 779–89. http://dx.doi.org/10.2108/zsj.18.779.

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15

MAEDA, Taro. "Effects of tracheal mite infestation on Japanese honey bee, Apis cerana japonica." Journal of the Acarological Society of Japan 25, Supplement1 (2016): S109—S117. http://dx.doi.org/10.2300/acari.25.suppl_109.

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16

Takahashi, Jun-ichi, Takeshi Wakamiya, Takuya Kiyoshi, et al. "The complete mitochondrial genome of the Japanese honeybee, Apis cerana japonica (Insecta: Hymenoptera: Apidae)." Mitochondrial DNA Part B 1, no. 1 (2016): 156–57. http://dx.doi.org/10.1080/23802359.2016.1144108.

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17

YOKOI, Kakeru, Hironobu UCHIYAMA, Takeshi WAKAMIYA, et al. "The draft genome sequence of the Japanese honey bee, Apis cerana japonica (Hymenoptera: Apidae)." European Journal of Entomology 115 (November 14, 2018): 650–57. http://dx.doi.org/10.14411/eje.2018.064.

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18

Wu, Meihua, Yuya Sugimura, Noriko Takaya, et al. "Characterization of bifidobacteria in the digestive tract of the Japanese honeybee, Apis cerana japonica." Journal of Invertebrate Pathology 112, no. 1 (2013): 88–93. http://dx.doi.org/10.1016/j.jip.2012.09.005.

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19

Takashima, Shunsuke, Yuma Ohari, and Tadashi Itagaki. "Prevalence of Nosema species infections in Apis cerana japonica and Apis mellifera honeybees in the Tohoku region of Japan." Parasitology International 83 (August 2021): 102361. http://dx.doi.org/10.1016/j.parint.2021.102361.

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20

Kawakita, Satoshi, Kotaro Ichikawa, Fumio Sakamoto, and Kazuyuki Moriya. "Sound recordings of Apis cerana japonica colonies over 24 h reveal unique daily hissing patterns." Apidologie 50, no. 2 (2019): 204–14. http://dx.doi.org/10.1007/s13592-018-0631-x.

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21

Sasaki, M., M. Ono, S. Asada, and T. Yoshida. "Oriential orchid (Cymbidium pumilum) attracts drones of the Japanese honeybee (Apis cerana japonica) as pollinators." Experientia 47, no. 11-12 (1991): 1229–31. http://dx.doi.org/10.1007/bf01918392.

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22

Tsuruta, T., M. Matsuka, and M. Sasaki. "Temperature as a causative factor in the seasonal colour dimorphism of Apis cerana japonica workers." Apidologie 20, no. 2 (1989): 149–55. http://dx.doi.org/10.1051/apido:19890205.

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23

OKABE, Kimiko, Tatsuya NAKAMURA, and Tetsuo GOTOH. "Preliminary Study of Mites Associated with the Japanese Honey Bee, Apis cerana japonica Radoszkowski (Hymenoptera: Apidae)." Journal of the Acarological Society of Japan 9, no. 1 (2000): 23–30. http://dx.doi.org/10.2300/acari.9.23.

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24

YOSHIDA, Tadaharu. "Difference in Drone Congregation Areas of Native Apis cerana japonica RAD. and Introduced A. mellifera L." Japanese journal of applied entomology and zoology 38, no. 2 (1994): 85–90. http://dx.doi.org/10.1303/jjaez.38.85.

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25

Nagamitsu, Teruyoshi, Mika Yasuda, Fuki Saito-Morooka, et al. "Genetic Structure and Potential Environmental Determinants of Local Genetic Diversity in Japanese Honeybees (Apis cerana japonica)." PLOS ONE 11, no. 11 (2016): e0167233. http://dx.doi.org/10.1371/journal.pone.0167233.

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26

Maeda, Taro, and Yoshiko Sakamoto. "Tracheal mites, Acarapis woodi, greatly increase overwinter mortality in colonies of the Japanese honeybee, Apis cerana japonica." Apidologie 47, no. 6 (2016): 762–70. http://dx.doi.org/10.1007/s13592-016-0434-x.

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27

Sumitani, Megumi, Jae Min Lee, Masatsugu Hatakeyama, and Kugao Oishi. "Cloning and characterization ofAcmar1, amariner-like element in the asiatic honey bee,Apis cerana japonica (Hymenoptera, Apocrita)." Archives of Insect Biochemistry and Physiology 50, no. 4 (2002): 183–90. http://dx.doi.org/10.1002/arch.10043.

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28

Fujiwara, Ayumi, Masami Sasaki, and Izumi Washitani. "First report on the emergency dance of Apis cerana japonica , which induces odorous plant material collection in response to Vespa mandarinia japonica scouting." Entomological Science 21, no. 1 (2017): 93–96. http://dx.doi.org/10.1111/ens.12285.

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29

Chen, Yi, Michael Meissle, Jiabao Xue, et al. "Expression of Cry1Ab/2Aj Protein in Genetically Engineered Maize Plants and Its Transfer in the Arthropod Food Web." Plants 12, no. 23 (2023): 4057. http://dx.doi.org/10.3390/plants12234057.

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While transgenic Bacillus thuringiensis (Bt) maize provides pest resistance and a reduced application of chemical pesticides, a comprehensive environmental risk assessment is mandatory before its field release. This research determined the concentrations of Bt protein in plant tissue and in arthropods under field conditions in Gongzhuling City, northeastern China, to provide guidance for the selection of indicator species for non-target risk assessment studies. Bt maize expressing Cry1Ab/2Aj and non-transformed near-isoline were grown under identical environmental and agricultural conditions.
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30

WONGCHAWALIT, Jintanart, Takeshi YAMAMOTO, Hiroyuki NAKAI та ін. "Purification and Characterization of α-Glucosidase I from Japanese Honeybee (Apis cerana japonica) and Molecular Cloning of Its cDNA". Bioscience, Biotechnology, and Biochemistry 70, № 12 (2006): 2889–98. http://dx.doi.org/10.1271/bbb.60302.

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31

Maeda, Taro, and Yoshiko Sakamoto. "Range expansion of the tracheal mite Acarapis woodi (Acari: Tarsonemidae) among Japanese honey bee, Apis cerana japonica, in Japan." Experimental and Applied Acarology 80, no. 4 (2020): 477–90. http://dx.doi.org/10.1007/s10493-020-00482-6.

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32

Maeda, Taro, and Yoshiko Sakamoto. "Field application of menthol for Japanese honey bees, Apis cerana japonica (Hymenoptera: Apidae), to control tracheal mites, Acarapis woodi (Acari: Tarsonemidae)." Experimental and Applied Acarology 70, no. 3 (2016): 299–308. http://dx.doi.org/10.1007/s10493-016-0072-z.

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33

Chikano, Mao, and Jun-ichi Takahashi. "Complete mitochondrial DNA sequence of the yeast Zygosaccharomyces siamensis (Saccharomycetes: Saccharomycetales) from fermented honey of the Apis cerana japonica in Japan." Mitochondrial DNA Part B 5, no. 3 (2020): 2645–47. http://dx.doi.org/10.1080/23802359.2020.1785961.

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34

Wu, Meihua, Yuya Sugimura, Kyoko Iwata, et al. "Inhibitory Effect of Gut Bacteria from the Japanese Honey Bee,Apis cerana japonica, AgainstMelissococcus plutonius, the Causal Agent of European Foulbrood Disease." Journal of Insect Science 14, no. 129 (2014): 1–13. http://dx.doi.org/10.1673/031.014.129.

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35

Ono, M., I. Okada, and M. Sasaki. "Heat production by balling in the Japanese honeybee,Apis cerana japonica as a defensive behavior against the hornet,Vespa simillima xanthoptera (Hymenoptera: Vespidae)." Experientia 43, no. 9 (1987): 1031–34. http://dx.doi.org/10.1007/bf01952231.

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36

Yoshiyama, Mikio, and Kiyoshi Kimura. "Bacteria in the gut of Japanese honeybee, Apis cerana japonica, and their antagonistic effect against Paenibacillus larvae, the causal agent of American foulbrood." Journal of Invertebrate Pathology 102, no. 2 (2009): 91–96. http://dx.doi.org/10.1016/j.jip.2009.07.005.

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37

Kobayashi, Shun, Tetsuo Denda, Shigehiko Mashiba, Toshitaka Iwamoto, Teruo Doi, and Masako Izawa. "Pollination partners of Mucuna macrocarpa (Fabaceae) at the northern limit of its range." Plant Species Biology 30, no. 4 (2015): 272–78. https://doi.org/10.5281/zenodo.13448194.

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(Uploaded by Plazi for the Bat Literature Project) Mucuna macrocarpa is a plant found in tropical and subtropical regions that requires an "explosive opening." Explosive opening is the process that exposes the stamen and pistil from the opening of the carina. This process is needed for cross pollination; however, the plant cannot open itself and opening by an animal is needed. The most common opener of Mucuna flowers is several nectar-eating bats (e.g., Syconycteris), but the flying fox, Pteropus dasymallus, is the only opener of M. macrocarpa on the subtropical island of Okinawajima. Here, we
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38

Kobayashi, Shun, Tetsuo Denda, Shigehiko Mashiba, Toshitaka Iwamoto, Teruo Doi, and Masako Izawa. "Pollination partners of Mucuna macrocarpa (Fabaceae) at the northern limit of its range." Plant Species Biology 30, no. 4 (2015): 272–78. https://doi.org/10.5281/zenodo.13448194.

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(Uploaded by Plazi for the Bat Literature Project) Mucuna macrocarpa is a plant found in tropical and subtropical regions that requires an "explosive opening." Explosive opening is the process that exposes the stamen and pistil from the opening of the carina. This process is needed for cross pollination; however, the plant cannot open itself and opening by an animal is needed. The most common opener of Mucuna flowers is several nectar-eating bats (e.g., Syconycteris), but the flying fox, Pteropus dasymallus, is the only opener of M. macrocarpa on the subtropical island of Okinawajima. Here, we
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39

Kobayashi, Shun, Tetsuo Denda, Shigehiko Mashiba, Toshitaka Iwamoto, Teruo Doi, and Masako Izawa. "Pollination partners of Mucuna macrocarpa (Fabaceae) at the northern limit of its range." Plant Species Biology 30, no. 4 (2015): 272–78. https://doi.org/10.5281/zenodo.13448194.

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(Uploaded by Plazi for the Bat Literature Project) Mucuna macrocarpa is a plant found in tropical and subtropical regions that requires an "explosive opening." Explosive opening is the process that exposes the stamen and pistil from the opening of the carina. This process is needed for cross pollination; however, the plant cannot open itself and opening by an animal is needed. The most common opener of Mucuna flowers is several nectar-eating bats (e.g., Syconycteris), but the flying fox, Pteropus dasymallus, is the only opener of M. macrocarpa on the subtropical island of Okinawajima. Here, we
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40

Kobayashi, Shun, Tetsuo Denda, Shigehiko Mashiba, Toshitaka Iwamoto, Teruo Doi, and Masako Izawa. "Pollination partners of Mucuna macrocarpa (Fabaceae) at the northern limit of its range." Plant Species Biology 30, no. 4 (2015): 272–78. https://doi.org/10.5281/zenodo.13448194.

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(Uploaded by Plazi for the Bat Literature Project) Mucuna macrocarpa is a plant found in tropical and subtropical regions that requires an "explosive opening." Explosive opening is the process that exposes the stamen and pistil from the opening of the carina. This process is needed for cross pollination; however, the plant cannot open itself and opening by an animal is needed. The most common opener of Mucuna flowers is several nectar-eating bats (e.g., Syconycteris), but the flying fox, Pteropus dasymallus, is the only opener of M. macrocarpa on the subtropical island of Okinawajima. Here, we
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41

Kobayashi, Shun, Tetsuo Denda, Shigehiko Mashiba, Toshitaka Iwamoto, Teruo Doi, and Masako Izawa. "Pollination partners of Mucuna macrocarpa (Fabaceae) at the northern limit of its range." Plant Species Biology 30, no. 4 (2015): 272–78. https://doi.org/10.5281/zenodo.13448194.

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(Uploaded by Plazi for the Bat Literature Project) Mucuna macrocarpa is a plant found in tropical and subtropical regions that requires an "explosive opening." Explosive opening is the process that exposes the stamen and pistil from the opening of the carina. This process is needed for cross pollination; however, the plant cannot open itself and opening by an animal is needed. The most common opener of Mucuna flowers is several nectar-eating bats (e.g., Syconycteris), but the flying fox, Pteropus dasymallus, is the only opener of M. macrocarpa on the subtropical island of Okinawajima. Here, we
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42

SUGAHARA, Michio. "Oriental orchid (Cymbidium floribundum) attracts the Japanese honeybee (Apis cerana japonica) with a mixture of 3-hydroxyoctanoic acid and 10-hydroxy-(E)-2-decenoic acid." Hikaku seiri seikagaku(Comparative Physiology and Biochemistry) 30, no. 1 (2013): 11–17. http://dx.doi.org/10.3330/hikakuseiriseika.30.11.

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43

Sugahara, Michio, Kazunari Izutsu, Yasuichiro Nishimura, and Fumio Sakamoto. "Oriental Orchid (Cymbidium floribundum) Attracts the Japanese Honeybee (Apis cerana japonica) with a Mixture of 3-Hydroxyoctanoic Acid and 10-Hydroxy- (E)-2-Decenoic Acid." Zoological Science 30, no. 2 (2013): 99–104. http://dx.doi.org/10.2108/zsj.30.99.

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44

Alqarni, Abdulaziz, Mohammed Hannan, Ayman Owayss, and Michael Engel. "The indigenous honey bees of Saudi Arabia (Hymenoptera, Apidae, Apis mellifera jemenitica Ruttner): Their natural history and role in beekeeping." ZooKeys 134 (October 6, 2011): 83–98. https://doi.org/10.3897/zookeys.134.1677.

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<i>Apis mellifera jemenitica</i> Ruttner (= <i>yemenitica auctorum</i>: <i>vide</i> Engel 1999) has been used in apiculture throughout the Arabian Peninsula since at least 2000 BC. Existing literature demonstrates that these populations are well adapted for the harsh extremes of the region. Populations of <i>A</i>.<i> m</i>. <i>jemenitica</i> native to Saudi Arabia are far more heat tolerant than the standard races often imported from Europe. Central Saudi Arabia has the highest summer temperatures for the Arabian Peninsula, and it is in this region where only <i>A</i>. <i>m</i>. <i>jemenitica
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45

Wang, Xiangping, Meihong Wen, Mingsong Wu, and Dianxiang Zhang. "Cordia subcordata (Boraginaceae), a distylous species on oceanic coral islands, is self-compatible and pollinated by a passerine bird." Plant Ecology and Evolution 153, no. 3 (2020): 361–72. http://dx.doi.org/10.5091/plecevo.2020.1757.

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Background and aims – Distyly is usually rare on oceanic islands, which is probably due to the difficulty for distylous plants to colonize those islands. However, Cordia subcordata was observed to be distylous with short- and long-styled morphs on the Xisha Islands in the South China Sea. To characterize the reproduction system of Cordia subcordata and to understand how this distylous species maintains itself on these islands, we studied its reproductive and pollination biology.Methods – Seed set and pollen tube growth under manipulated intermorph, intramorph, and self-pollination were examine
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46

Wang, Xiangping, Meihong Wen, Mingsong Wu, and Dianxiang Zhang. "Cordia subcordata (Boraginaceae), a distylous species on oceanic coral islands, is self-compatible and pollinated by a passerine bird." Plant Ecology and Evolution 153, no. (3) (2020): 361–72. https://doi.org/10.5091/plecevo.2020.1757.

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<b>Background and aims</b> – Distyly is usually rare on oceanic islands, which is probably due to the difficulty for distylous plants to colonize those islands. However, <em>Cordia subcordata</em> was observed to be distylous with short- and long-styled morphs on the Xisha Islands in the South China Sea. To characterize the reproduction system of <em>Cordia subcordata</em> and to understand how this distylous species maintains itself on these islands, we studied its reproductive and pollination biology.<b>Methods</b> – Seed set and pollen tube growth under manipulated intermorph, intramorph, a
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47

Yokoi, Kakeru, Masatsugu Hatakeyama, Seigo Kuwazaki, et al. "Comprehensive expression data for two honey bee species, Apis mellifera and Apis cerana japonica." Scientific Data 12, no. 1 (2025). https://doi.org/10.1038/s41597-025-05279-z.

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Abstract Comprehensive expression datasets were constructed for Apis mellifera and Apis cerana japonica. Firstly, we obtained RNA-Seq data of the samples prepared: post-oviposition day 6 to day 58 samples of A. mellifera workers (larva to adult), and day 9, 10, 12, and 13 samples of A. mellifera queen (larva to pupa), and day 9 to day 18 samples of A. cerana japonica workers (larva to adult). For A. cerana japonica, reference transcript sequence, predicted amino acid sequence, and functional annotation data were generated based on the genome sequence and RNA-Seq data. Using the transcript sequ
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48

Liu, Wenping, Sicheng Huang, Youjin Hao, et al. "Pollination and pollen plant diversity by Apis cerana cerana during olive flowering based on DNA metabarcoding." Journal of Applied Entomology, May 16, 2024. http://dx.doi.org/10.1111/jen.13267.

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AbstractTo understand the role of Apis cerana cerana in olive tree (Olea europaea L.) pollination, pollinators and pollen carried by bees were collected from 11 experimental plots during the flowering period. The abundance and diversity of pollen plant species were investigated using DNA metabarcoding. A total of 583 pollinators were collected and A. cerana cerana accounts for 46.83%. Further analysis revealed a total of 56 families, 136 genera and 195 plant species in bee pollens. O. europaea is the dominant species accounting for 42.02 ± 34.89% and then followed by Sedum japonicum (8.70 ± 16
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49

Suzuki, Akihiko, Nobuyoshi Nakajima, and Yoshiko Sakamoto. "Draft genome sequences of Pantoea sp. strains QMID1-QMID4 isolated from the midgut of Japanese honey bee ( Apis cerana japonica )." Microbiology Resource Announcements, July 26, 2023. http://dx.doi.org/10.1128/mra.00010-23.

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ABSTRACT We report the draft genome sequences of Pantoea sp. strains QMID1-QMID4 that were recovered from the midgut of Japanese honey bee ( Apis cerana japonica ). The strains possess the carotenoid biosynthetic gene cluster. The genome information expands our knowledge of their potential use as probiotics and/or prebiotics in honey bees.
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Hosaka, Yuki, Yuto Kato, Shinya Hayashi, Madoka Nakai, Seth M. Barribeau, and Maki N. Inoue. "The effects of Nosema ceranae (Microspora: Nosematidae) isolated from wild Apis cerana japonica (Hymenoptera: Apidae) on Apis mellifera." Applied Entomology and Zoology, March 29, 2021. http://dx.doi.org/10.1007/s13355-021-00735-9.

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