Journal articles on the topic 'Bonamia'

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1

Moreira, André Luiz Da Costa, Rosângela Simão-Bianchini, and Taciana Cavalcanti. "Lectotypification and a new synonym of Bonamia sericea (Convolvulaceae): Endemic species from Argentina." Boletín de la Sociedad Argentina de Botánica 55, no. 1 (March 25, 2020): 45–51. http://dx.doi.org/10.31055/1851.2372.v55.n1.24823.

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Background and aims: Bonamia Thoaurs (Convolvulaceae) comprises about 70 species with a tropical and subtropical distribution. Morphological and molecular studies in Bonamia were carried out to clarify relationships in and out of the genus and throughout this work it was detected the need for re-limit the circumscription of some taxa. This paper contributes to the circumscription and lectotypification of Bonamia sericea (Griseb.) Hallier f., an endemic species from northern Argentina. M&M: Morphological analysis of Bonamia sericea, were made based on a study of specimens of herbaria, including the type-material, digital type images and other herbaria website. Results: A new synonym for B. sericea is proposed. The lectotype of B. sericea is here designated and a complete description and illustrations are presented.
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2

Buss, Jessica Jamuna, Kathryn Helen Wiltshire, James Owen Harris, and Marty Robert Deveney. "Decontamination of Bonamia exitiosa." Aquaculture 523 (June 2020): 735210. http://dx.doi.org/10.1016/j.aquaculture.2020.735210.

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3

Wood, John R. I. "Bonamia (Convolvulaceae) in Bolivia." Kew Bulletin 68, no. 2 (May 28, 2013): 249–60. http://dx.doi.org/10.1007/s12225-013-9452-2.

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4

MOREIRA, ANDRÉ LUIZ DA COSTA, ROSANGELA SIMÃO-BIANCHINI, and TACIANA BARBOSA CAVALCANTI. "Two new species of Bonamia (Convolvulaceae) endemic to the Brazilian Cerrado." Phytotaxa 361, no. 1 (July 18, 2018): 106. http://dx.doi.org/10.11646/phytotaxa.361.1.9.

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Two new endemic species of Bonamia Thours (Convolvulaceae) are described from the Brazilian Cerrado: Bonamia austinii A.Moreira & Sim.-Bianch., and Bonamia krapovickasii A.Moreira & Sim.-Bianch. Both species grow in Campo Limpo (savanna grassland with few scattered trees) and have small tomentose leaves and white flowers. They are easily distinguished from each other and from other species of the genus by their habit and inflorescence. The new taxa are illustrated and their characteristics are compared with morphologically similar species.
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MOREIRA, ANDRÉ LUIZ DA COSTA, GUILHERME MEDEIROS ANTAR, ROSÂNGELA SIMÃO-BIANCHINI, and TACIANA BARBOSA CAVALCANTI. "Contribution to the knowledge of Bonamia (Convolvulaceae) in Brazil: a new species and a new occurrence." Phytotaxa 306, no. 2 (May 9, 2017): 146. http://dx.doi.org/10.11646/phytotaxa.306.2.4.

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A new species, Bonamia campestris A.Moreira & Sim.-Bianch., from the Jalapão region in the state of Tocantins, Brazil, is described and illustrated. It is compared with morphologically similar species. Additional collections of the recently described Bonamia rosiewiseae J.R.I.Wood extend its range from two locations in eastern Bolivia to Mato Grosso do Sul in southwest Brazil.
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6

Austin, Daniel F. "A New Bonamia (Convolvulaceae) from Nicaragua." Novon 4, no. 4 (1994): 319. http://dx.doi.org/10.2307/3391437.

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7

R. Kottaimuthu, R. Kottaimuthu, and N. Vasudevan N. Vasudevan. "Range Extension of Bonamia evolvuloides (Choisy) Raiz. in Tamil Nadu." Paripex - Indian Journal Of Research 3, no. 7 (January 1, 2012): 1–2. http://dx.doi.org/10.15373/22501991/july2014/6.

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8

Oraić, Dražen, Relja Beck, Željko Pavlinec, Ivana Giovanna Zupičić, Ljupka Maltar, Tihana Miškić, Žaklin Acinger-Rogić, and Snježana Zrnčić. "Bonamia exitiosa in European Flat Oyster (Ostrea edulis) on the Croatian Adriatic Coast from 2016 to 2020." Journal of Marine Science and Engineering 9, no. 9 (August 27, 2021): 929. http://dx.doi.org/10.3390/jmse9090929.

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The annual production of European flat oysters (Ostrea edulis) in Croatia is about 50 to 65 tons, and it has a long tradition. All Croatian oyster farms are subjected to the national surveillance program aiming to detect the presence of Bonamia ostreae and Marteilia refringens according to the Council Directive 2006/88/EC. Within the surveillance program, the first findings of the parasite Bonamia spp. occurred in 2016 in two production areas in the north and south of the Eastern Adriatic coast. The repeated findings of the parasite were noted up to 2020 but also on two additional sites in the north. The parasite was detected by cytological analysis of stained heart smears, histological examination, and PCR. PCR positive samples were sequenced for SSU rDNA gene, and BLAST analysis confirmed infection with Bonamia exitiosa. Attempts to prove the Pacific oyster as a putative vector of the parasite failed. The infection prevalence from 2016 until 2020 ranged from 3.3 to 20% in different sites. No mortalities were reported from the infected sites, and it seemed that infection of flat oysters with B. exitiosa did not affect their health. The study has not shown the source and way of infection spread, which imposes the need for more comprehensive molecular and epidemiological studies.
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9

Friedman, Carolyn S., and Frank O. Perkins. "Range extension of Bonamia ostreae to Maine, U.S.A." Journal of Invertebrate Pathology 64, no. 3 (November 1994): 179–81. http://dx.doi.org/10.1016/s0022-2011(94)90075-2.

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10

McArdle, John F., Frank McKiernan, Helen Foley, and David Hugh Jones. "The current status of Bonamia disease in Ireland." Aquaculture 93, no. 3 (March 1991): 273–78. http://dx.doi.org/10.1016/0044-8486(91)90239-4.

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11

Elston, R. A., M. L. Kent, and M. T. Wilkinson. "Resistance of Ostrea edulis to Bonamia ostreae infection." Aquaculture 64, no. 3 (July 1987): 237–42. http://dx.doi.org/10.1016/0044-8486(87)90328-0.

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12

LÓPEZ-FLORES, I., V. N. SUÁREZ-SANTIAGO, D. LONGET, D. SAULNIER, B. CHOLLET, and I. ARZUL. "Characterization of actin genes in Bonamia ostreae and their application to phylogeny of the Haplosporidia." Parasitology 134, no. 14 (August 3, 2007): 1941–48. http://dx.doi.org/10.1017/s0031182007003307.

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SUMMARYBonamia ostreae is a protozoan parasite that infects the European flat oyster Ostrea edulis, causing systemic infections and resulting in massive mortalities in populations of this valuable bivalve species. In this work, we have characterized B. ostreae actin genes and used their sequences for a phylogenetic analysis. Design of different primer sets was necessary to amplify the central coding region of actin genes of B. ostreae. Characterization of the sequences and their amplification in different samples demonstrated the presence of 2 intragenomic actin genes in B. ostreae, without any intron. The phylogenetic analysis placed B. ostreae in a clade with Minchinia tapetis, Minchinia teredinis and Haplosporidium costale as its closest relatives, and demonstrated that the paralogous actin genes found in Bonamia resulted from a duplication of the original actin gene after the Bonamia origin.
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13

CARNEGIE, RYAN B., EUGENE M. BURRESON, P. MIKE HINE, NANCY A. STOKES, CORINNE AUDEMARD, MELANIE J. BISHOP, and CHARLES H. PETERSON. "Bonamia perspora n. sp. (Haplosporidia), a Parasite of the Oyster Ostreola equestris, is the First Bonamia Species Known to Produce Spores." Journal of Eukaryotic Microbiology 53, no. 4 (July 2006): 232–45. http://dx.doi.org/10.1111/j.1550-7408.2006.00100.x.

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14

Kraft, Carola, Kristina Jenett-Siems, Inga Köhler, Britta Tofern-Reblin, Karsten Siems, Ulrich Bienzle, and Eckart Eich. "Antiplasmodial activity of sesquilignans and sesquineolignans from Bonamia spectabilis." Phytochemistry 60, no. 2 (May 2002): 167–73. http://dx.doi.org/10.1016/s0031-9422(02)00101-2.

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15

Corbeil, S., I. Arzul, M. Robert, FCJ Berthe, N. Besnard-Cochennec, and MSJ Crane. "Molecular characterisation of an Australian isolate of Bonamia exitiosa." Diseases of Aquatic Organisms 71 (July 11, 2006): 81–85. http://dx.doi.org/10.3354/dao071081.

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16

Hine, PM, RB Carnegie, MA Kroeck, A. Villalba, MY Engelsma, and EM Burreson. "Ultrastructural comparison of Bonamia spp. (Haplosporidia) infecting ostreid oysters." Diseases of Aquatic Organisms 110, no. 1 (July 24, 2014): 55–63. http://dx.doi.org/10.3354/dao02747.

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17

Lohrmann, KB, PM Hine, and M. Campalans. "Ultrastructure of Bonamia sp. in Ostrea chilensis in Chile." Diseases of Aquatic Organisms 85 (July 23, 2009): 199–208. http://dx.doi.org/10.3354/dao02093.

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18

Laing, I., P. Dunn, EJ Peeler, SW Feist, and M. Longshaw. "Epidemiology of Bonamia in the UK, 1982 to 2012." Diseases of Aquatic Organisms 110, no. 1 (July 24, 2014): 101–11. http://dx.doi.org/10.3354/dao02647.

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19

Carnegie, Ryan B., Kristina M. Hill, Nancy A. Stokes, and Eugene M. Burreson. "The haplosporidian Bonamia exitiosa is present in Australia, but the identity of the parasite described as Bonamia (formerly Mikrocytos) roughleyi is uncertain." Journal of Invertebrate Pathology 115 (January 2014): 33–40. http://dx.doi.org/10.1016/j.jip.2013.10.017.

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20

Bradley, TL, JA Mercer, JD Humphrey, NJG Moody, and JC Hunnam. "Bonamia exitiosa in farmed native oysters Ostrea angasi in Australia: optimal epidemiological qPCR cut-point and clinical disease risk factors." Diseases of Aquatic Organisms 140 (August 6, 2020): 151–65. http://dx.doi.org/10.3354/dao03501.

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Bonamiosis has developed as a problem in Australian native oysters Ostrea angasi since the parasite Bonamia spp. was first detected in Port Phillip Bay, Victoria, in the early 1990s. At that time, large-scale mortalities in both farmed and wild oysters saw the demise of the pilot native oyster culture industry. More recent attempts to farm the species resulted in subclinical infections that progressed over time to clinical disease. The aim of this work was to establish what environmental factors result in the clinical manifestation of disease; determine the diagnostic sensitivity and diagnostic specificity of histopathological examination and a quantitative polymerase chain reaction (qPCR) test for the diagnosis of B. exitiosa infection in clinically diseased farmed native oysters; and calculate the optimal qPCR threshold cycle (CT) epidemiological cut-point for classification of positive and negative cases. After applying a range of stressors to tank-held oysters, results indicated a 58% increased risk (95% CI: 16%, 99%) of a Bonamia-infected oyster dying if the oyster was held at a higher temperature (p = 0.048). Starving and tumbling oysters, in isolation, was not significantly associated with clinical bonamiosis, but a Bonamia-infected oyster was at the greatest risk of death when increased water temperature was combined with both starvation and increased motion (p = 0.02; odds ratio = 3.47). The diagnostic sensitivity and specificity of the World Organisation for Animal Health qPCR protocol were calculated for increasing CT value cut-points from ≤25 to ≤40, with an optimal cut-point identified at ≤34.5 (specificity: 92.2; 95% posterior credible intervals [PCI]: 76.2, 99.8; Sensitivity: 93.5; 95% PCI: 84.7, 99.1).
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21

Cochennec-Laureau, N., KS Reece, FCJ Berthe, and PM Hine. "Mikrocytos roughleyi taxonomic affiliation leads to the genus Bonamia (Haplosporidia)." Diseases of Aquatic Organisms 54 (2003): 209–17. http://dx.doi.org/10.3354/dao054209.

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22

Cochennec, Nathalie, Frédérique Le Roux, Franck Berthe, and André Gerard. "Detection of Bonamia ostreae Based on Small Subunit Ribosomal Probe." Journal of Invertebrate Pathology 76, no. 1 (July 2000): 26–32. http://dx.doi.org/10.1006/jipa.2000.4939.

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23

Buss, Jessica J., Kathryn H. Wiltshire, Thomas A. A. Prowse, James O. Harris, and Marty R. Deveney. "Bonamia in Ostrea angasi : Diagnostic performance, field prevalence and intensity." Journal of Fish Diseases 42, no. 1 (October 16, 2018): 63–74. http://dx.doi.org/10.1111/jfd.12906.

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24

Buss, Jessica Jamuna, Kathryn Helen Wiltshire, James Owen Harris, Jason Elliot Tanner, and Marty Robert Deveney. "Infection dynamics of Bonamia exitiosa on intertidal Ostrea angasi farms." Journal of Fish Diseases 43, no. 3 (January 9, 2020): 359–69. http://dx.doi.org/10.1111/jfd.13134.

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25

LYNCH, S. A., E. ABOLLO, A. RAMILO, A. CAO, S. C. CULLOTY, and A. VILLALBA. "Observations raise the question if the Pacific oyster, Crassostrea gigas, can act as either a carrier or a reservoir for Bonamia ostreae or Bonamia exitiosa." Parasitology 137, no. 10 (April 14, 2010): 1515–26. http://dx.doi.org/10.1017/s0031182010000326.

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SUMMARYThis study investigated the ability of the Pacific oyster, Crassostrea gigas, to act as a carrier or reservoir of the protistan Bonamia ostreae. Studies were carried out independently in Ireland and in Spain. Naïve C. gigas were exposed to B. ostreae both in the field and in the laboratory via natural exposure or experimental injection. Naïve flat oysters, Ostrea edulis, were placed in tanks with previously exposed C. gigas. Oysters were screened for B. ostreae by examination of ventricular heart smears and by polymerase chain reaction (PCR) screening of tissue samples (gill and/or heart) and shell cavity fluid. PCR-positive oysters were further screened using histology and in situ hybridization (ISH). B. ostreae DNA was detected in the tissues and/or shell cavity fluid of a small number of C. gigas in the field and in the laboratory. B. ostreae-like cells were visualized in the haemocytes of 1 C. gigas and B. ostreae-like cells were observed extracellularly in the connective tissues of 1 other C. gigas. When C. gigas naturally exposed to B. ostreae were held with naïve O. edulis, B. ostreae DNA was detected in O. edulis; however, B. ostreae cells were not visualized. In Spain, B. exitiosa DNA was also detected in Pacific oyster tissues. The results of this study have important implications for C. gigas transfers from B. ostreae-endemic areas to uninfected areas and highlight B. ostreae and B. exitiosa's ability to survive extracellularly and in other non-typical hosts.
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Lopes, Edizon Veiga, Hercules Bezerra Dias, Zelina Estevam dos Santos Torres, Francisco Célio Maia Chaves, Antonio Carlos Siani, and Adrian Martin Pohlit. "Coumarins, triterpenes and a hemiterpene from Bonamia ferruginea (Choisy) Hallier f." Biochemical Systematics and Ecology 61 (August 2015): 67–69. http://dx.doi.org/10.1016/j.bse.2015.04.034.

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27

Austin, Daniel F., and George W. Staples. "Petrogenia as a Synonym of Bonamia (Convolvulaceae), with Comments on Allied Species." Brittonia 37, no. 3 (July 1985): 310. http://dx.doi.org/10.2307/2806081.

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Moreira, André Luiz da Costa, Ana Carolina Mezzonato-Pires, Francisco de Assis Ribeiro Santos, and Taciana Barbosa Cavalcanti. "Pollen morphology in the genus Bonamia Thouars (Convolvulaceae) and its taxonomic significance." Review of Palaeobotany and Palynology 264 (May 2019): 11–23. http://dx.doi.org/10.1016/j.revpalbo.2019.02.008.

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29

Hine, PM, N. Cochennec-Laureau, and FCJ Berthe. "Bonamia exitiosus n.sp. (Haplosporidia) infecting flat oysters Ostrea chilensis in New Zealand." Diseases of Aquatic Organisms 47 (2001): 63–72. http://dx.doi.org/10.3354/dao047063.

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30

Carnegie, RB, BJ Barber, and DL Distel. "Detection of the oyster parasite Bonamia ostreae by fluorescent in situ hybridization." Diseases of Aquatic Organisms 55 (2003): 247–52. http://dx.doi.org/10.3354/dao055247.

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31

Corbeil, S., I. Arzul, B. Diggles, M. Heasman, B. Chollet, FCJ Berthe, and MSJ Crane. "Development of a TaqMan PCR assay for the detection of Bonamia species." Diseases of Aquatic Organisms 71 (July 11, 2006): 75–80. http://dx.doi.org/10.3354/dao071075.

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32

Buss, Jessica Jamuna, James Owen Harris, Jason Elliot Tanner, Kathryn Helen Wiltshire, and Marty Robert Deveney. "Rapid transmission of Bonamia exitiosa by cohabitation causes mortality in Ostrea angasi." Journal of Fish Diseases 43, no. 2 (November 21, 2019): 227–37. http://dx.doi.org/10.1111/jfd.13116.

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33

Hine, PM, and B. Wesney. "Interaction of phagocytosed Bonamia sp. (Haplosporidia) with haemocytes of oysters Tiostrea chilensis." Diseases of Aquatic Organisms 20 (1995): 219–29. http://dx.doi.org/10.3354/dao020219.

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34

Feng, C., X. Lin, F. Wang, Y. Zhang, J. Lv, C. Wang, J. Deng, L. Mei, S. Wu, and H. Li. "Detection and characterization of Bonamia ostreae in Ostrea edulis imported to China." Diseases of Aquatic Organisms 106, no. 1 (September 24, 2013): 85–91. http://dx.doi.org/10.3354/dao02631.

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35

Cigarría, J., and R. Elston. "Independent introduction of Bonamia ostreae, a parasite of Ostrea edulis, to Spain." Diseases of Aquatic Organisms 29 (1997): 157–58. http://dx.doi.org/10.3354/dao029157.

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Fernández-Boo, S., O. Gervais, M. Prado-Alvarez, B. Chollet, S. Claverol, C. Lecadet, C. Dubreuil, and I. Arzul. "Is pallial mucus involved in oyster defense against the parasite Bonamia ostreae?" Fish & Shellfish Immunology 91 (August 2019): 443. http://dx.doi.org/10.1016/j.fsi.2019.04.215.

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37

Van Banning, P. "Further results of the Bonamia ostreae challenge tests in Dutch oyster culture." Aquaculture 67, no. 1-2 (December 1987): 191–94. http://dx.doi.org/10.1016/0044-8486(87)90025-1.

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Audemard, Corinne, Ryan B. Carnegie, Nancy A. Stokes, Melanie J. Bishop, Charles H. Peterson, and Eugene M. Burreson. "Effects of Salinity on Bonamia sp. Survival in the Asian Oyster Crassostrea ariakensis." Journal of Shellfish Research 27, no. 3 (May 2008): 535–40. http://dx.doi.org/10.2983/0730-8000(2008)27[535:eosobs]2.0.co;2.

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Arzul, Isabelle, Aimé Langlade, Bruno Chollet, Maeva Robert, Sylvie Ferrand, Emmanuelle Omnes, Sophie Lerond, et al. "Can the protozoan parasite Bonamia ostreae infect larvae of flat oysters Ostrea edulis?" Veterinary Parasitology 179, no. 1-3 (June 2011): 69–76. http://dx.doi.org/10.1016/j.vetpar.2011.01.060.

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Cochennec, N., T. Renault, P. Boudry, B. Chollet, and A. Gerard. "Bonamia-like parasite found in the Suminoe oyster Crassostrea rivularis reared in France." Diseases of Aquatic Organisms 34 (1998): 193–97. http://dx.doi.org/10.3354/dao034193.

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Sas, Hein, Brenda Deden, Pauline Kamermans, Philine S. E. zu Ermgassen, Bernadette Pogoda, Joanne Preston, Luke Helmer, et al. "Bonamia infection in native oysters ( Ostrea edulis ) in relation to European restoration projects." Aquatic Conservation: Marine and Freshwater Ecosystems 30, no. 11 (November 2020): 2150–62. http://dx.doi.org/10.1002/aqc.3430.

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Engelsma, MY, SC Culloty, SA Lynch, I. Arzul, and RB Carnegie. "Bonamia parasites: a rapidly changing perspective on a genus of important mollusc pathogens." Diseases of Aquatic Organisms 110, no. 1 (July 24, 2014): 5–23. http://dx.doi.org/10.3354/dao02741.

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Hine, PM, and B. Wesney. "The functional cytology of Bonamia sp. (Haplosporidia) infecting oysters Tiostrea chilensis:an ultracytochemical study." Diseases of Aquatic Organisms 20 (1995): 207–17. http://dx.doi.org/10.3354/dao020207.

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44

Fernández-Boo, Sergio, Ophélie Gervais, Maria Prado-Alvarez, Bruno Chollet, Stéphane Claverol, Cyrielle Lecadet, Christine Dubreuil, and Isabelle Arzul. "Is pallial mucus involved in Ostrea edulis defenses against the parasite Bonamia ostreae?" Journal of Invertebrate Pathology 169 (January 2020): 107259. http://dx.doi.org/10.1016/j.jip.2019.107259.

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45

Prado-Alvarez, M., S. A. Lynch, A. Kane, G. Darmody, B. G. Pardo, P. Martínez, J. Cotterill, T. Wontner-Smith, and S. C. Culloty. "Oral immunostimulation of the oyster Ostrea edulis: Impacts on the parasite Bonamia ostreae." Fish & Shellfish Immunology 45, no. 1 (July 2015): 43–51. http://dx.doi.org/10.1016/j.fsi.2015.01.019.

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Morga, B., T. Renault, N. Faury, and I. Arzul. "New insights in flat oyster Ostrea edulis resistance against the parasite Bonamia ostreae." Fish & Shellfish Immunology 32, no. 6 (June 2012): 958–68. http://dx.doi.org/10.1016/j.fsi.2012.01.026.

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47

Prado-Alvarez, M., B. Chollet, N. Faury, M. Robert, B. Morga, D. J. Ibara, C. Lupo, T. Renault, and I. Arzul. "Interactions between Ostrea edulis galectin (OE-GAL) and the protozoan parasite Bonamia ostreae." Fish & Shellfish Immunology 34, no. 6 (June 2013): 1674. http://dx.doi.org/10.1016/j.fsi.2013.03.123.

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48

Staples, G. "(1890) Proposal to conserve the name Bonamia menziesii (Convolvulaceae ) with a conserved type." TAXON 58, no. 2 (May 2009): 649–51. http://dx.doi.org/10.1002/tax.582031.

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Buril, Maria Teresa, and Marccus Alves. "Flora da Usina São José, Igarassu, Pernambuco: Convolvulaceae." Rodriguésia 62, no. 1 (March 2011): 93–105. http://dx.doi.org/10.1590/2175-7860201162107.

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Resumo Convolvulaceae é uma família predominantemente tropical e compreende entre 1600 e 1700 espécies. O Brasil é um importante centro de endemismo do grupo, mas sua diversidade ainda é pouco conhecida e subestimada no país. A flora de Convolvulaceae da Usina São José, aqui apresentada, portanto, incrementa o conhecimento sobre a diversidade da família no Nordeste. Foram registradas doze espécies e cinco gêneros de Convolvulaceae na região: Bonamia maripoides, Evolvulus nummularius, Ipomoea bahiensis, I. hederifolia, I. nil, I. philomega, I. quamoclit, I. tiliacea, Jacquemontia glaucescens, J. sphaerostigma, Merremia macrocalyx e M. umbellata. O tratamento conta com chave de identificação, descrições, ilustrações e comentários para os táxons.
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Montes, J., R. Anadón, and C. Azevedo. "A Possible Life Cycle for Bonamia ostreae on the Basis of Electron Microscopy Studies." Journal of Invertebrate Pathology 63, no. 1 (January 1994): 1–6. http://dx.doi.org/10.1006/jipa.1994.1001.

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