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1

Brunetti, Riccardo, and Francesco Mastrototaro. "The non-indigenous stolidobranch ascidian Polyandrocarpa zorritensis in the Mediterranean: description, larval morphology and pattern of vascular budding." Zootaxa 528, no. 1 (2004): 1–8. https://doi.org/10.11646/zootaxa.528.1.1.

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Brunetti, Riccardo, Mastrototaro, Francesco (2004): The non-indigenous stolidobranch ascidian Polyandrocarpa zorritensis in the Mediterranean: description, larval morphology and pattern of vascular budding. Zootaxa 528 (1): 1-8, DOI: 10.11646/zootaxa.528.1.1, URL: https://biotaxa.org/Zootaxa/article/view/zootaxa.528.1.1
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2

BRUNETTI, RICCARDO, and FRANCESCO MASTROTOTARO. "The non-indigenous stolidobranch ascidian Polyandrocarpa zorritensis in the Mediterranean: description, larval morphology and pattern of vascular budding." Zootaxa 528, no. 1 (2004): 1. http://dx.doi.org/10.11646/zootaxa.528.1.1.

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The stolidobranch ascidian Polyandrocarpa zorritensis was detected, for the third time in the Mediterranean, in the harbour of Taranto (South Italy). Colonies develop vigorously on all hard substrata in shallow water and now represent one of the most important elements of the local fouling community. In this article specimens of the Mediterranean populations of the species are described. The morphology of the larva, which differs from that of other Polyzoinae, and a vascular budding mechanism of replication, similar to that known to occur in the Botryllinae, were both observed for the first ti
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Mastrototaro, F., G. D'Onghia, and A. Tursi. "Spatial and seasonal distribution of ascidians in a semi-enclosed basin of the Mediterranean Sea." Journal of the Marine Biological Association of the United Kingdom 88, no. 5 (2008): 1053–61. http://dx.doi.org/10.1017/s0025315408001392.

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A total of 25 species of ascidians were collected in the Mar Piccolo of Taranto, a semi-enclosed Mediterranean basin. Three are non-indigenous for the Mediterranean Sea: Microcosmus squamiger, Polyandrocarpa zorritensis and Distaplia bermudensis. The substrate features, season and depth affect the distribution of ascidians in the study area. Some species, such as Pyura dura and Pyura microcosmus, were found only on artificial substrates, while Ascidiella aspersa was almost exclusively recovered on natural bottoms. Seasonal variation in the ascidian distribution and abundance seems to be due ma
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Aiello, Anna, Ernesto Fattorusso, Concetta Imperatore, et al. "Zorrimidazolone, a Bioactive Alkaloid from the Non-Indigenous Mediterranean Stolidobranch Polyandrocarpa zorritensis." Marine Drugs 9, no. 6 (2011): 1157–65. http://dx.doi.org/10.3390/md9061157.

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5

Vazquez, Elsa, and Craig M. Young. "Ontogenetic changes in phototaxis during larval life of the Ascidian Polyandrocarpa zorritensis ()." Journal of Experimental Marine Biology and Ecology 231, no. 2 (1998): 267–77. http://dx.doi.org/10.1016/s0022-0981(98)00094-x.

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6

Stabili, Loredana, Margherita Licciano, Caterina Longo, Marco Lezzi, and Adriana Giangrande. "The Mediterranean non-indigenous ascidian Polyandrocarpa zorritensis : Microbiological accumulation capability and environmental implications." Marine Pollution Bulletin 101, no. 1 (2015): 146–52. http://dx.doi.org/10.1016/j.marpolbul.2015.11.005.

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7

Sumida, Paulo Yukio Gomes, Arthur Ziggiatti Güth, and Miguel Mies. "Pressure tolerance of tadpole larvae of the Atlantic ascidian Polyandrocarpa zorritensis: potential for deep-sea invasion." Brazilian Journal of Oceanography 63, no. 4 (2015): 515–20. http://dx.doi.org/10.1590/s1679-87592015100606304.

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Abstract How deep-sea fauna evolved is a question still being investigated. One of the most accepted theories is that shallow water organisms migrated to deeper waters and gave origin to the deep-sea communities. However, many organisms are prevented from performing long vertical migrations by the increasing hydrostatic pressure. Tadpole larvae of the ascidian Polyandrocarpa zorritensis were submitted to pressure treatments of 1, 50, 100 and 200 atm. Survival, settlement and metamorphosis rates were verified after 24 hour incubation in a pressure chamber. The majority of larvae settled (84%, 6
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Caicci, Federico, Valentina Degasperi, Fabio Gasparini, et al. "Variability of hair cells in the coronal organ of ascidians (Chordata, Tunicata)." Canadian Journal of Zoology 88, no. 6 (2010): 567–78. http://dx.doi.org/10.1139/z10-036.

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The tunicate ascidians are nonvertebrate chordates that possess mechanoreceptor cells in the coronal organ in the oral siphon, which monitor the incoming water flow. Like vertebrate hair cells, the mechanoreceptor–coronal cells are secondary sensory (axonless) cells accompanied by supporting cells and they exhibit morphological diversities of apical specialisations: they are multiciliate in ascidians of the order Enterogona, whereas they are more complex and possess one or two cilia accompanied by stereovilli, also graded in length, in ascidians of the order Pleurogona. In morphology, embryoni
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Nichols, Claire L., Gretchen Lambert, and Marie L. Nydam. "Continued persistence of non-native ascidians in Southern California harbors and marinas." Aquatic Invasions 18, no. 1 (2023): 1–22. http://dx.doi.org/10.3391/ai.2023.18.1.101962.

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Non-native ascidians have long dominated the artificial structures in southern California’s (United States) marinas and harbors. To determine the change in ascidian abundance and community composition over the last several decades, in 2019–2020 we replicated surveys from 1994–2000. We then created nMDS plots using the abundance data collected in the 1994–2000 and 2019–2020 surveys to compare the two groups. Range and average abundance per species were analyzed to determine trends and changes in ascidian community composition. Of the species used for comparison, four are native, three are crypt
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Nichols, Claire L., Gretchen Lambert, and Marie L. Nydam. "Continued persistence of non-native ascidians in Southern California harbors and marinas." Aquatic Invasions 18, no. (1) (2023): 1–22. https://doi.org/10.3391/ai.2023.18.1.101962.

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Non-native ascidians have long dominated the artificial structures in southern California's (United States) marinas and harbors. To determine the change in ascidian abundance and community composition over the last several decades, in 2019–2020 we replicated surveys from 1994–2000. We then created nMDS plots using the abundance data collected in the 1994–2000 and 2019–2020 surveys to compare the two groups. Range and average abundance per species were analyzed to determine trends and changes in ascidian community composition. Of the species used for comparison, four are native, three are crypt
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11

Stabili, Loredana, Margherita Licciano, Maria Flavia Gravina, and Adriana Giangrande. "Filtering activity on a pure culture of Vibrio alginolyticus by the solitary ascidian Styela plicata and the colonial ascidian Polyandrocarpa zorritensis: a potential service to improve microbiological seawater quality economically." Science of The Total Environment 573 (December 2016): 11–18. http://dx.doi.org/10.1016/j.scitotenv.2016.07.216.

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12

Mastrototaro, Francesco. "Polyandrocarpa zorritensis." CABI Compendium CABI Compendium (January 7, 2022). http://dx.doi.org/10.1079/cabicompendium.108975.

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13

Tobias-Santos, Vitoria, Rita Andreoni-Pham, Dany El Gharbi, Marie Lebel, Stefano Tiozzo, and Alexandre Alié. "Salinity-mediated limitation of asexual reproduction in the colonial ascidian Polyandrocarpa zorritensis." Frontiers in Ecology and Evolution 12 (February 15, 2024). http://dx.doi.org/10.3389/fevo.2024.1332780.

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Ascidians are among the most common invasive marine invertebrates worldwide. Many species of non-indigenous ascidians (NIAs) have successfully colonized the Mediterranean Sea, notably within anthropized coastal lagoons and harbors. Although invasive species are generally characterized by their broad ecological tolerance, different ascidian species exhibit varied responses to biotic and abiotic environmental stressors, including temperature and salinity. Acquiring a better understanding about of the impact of such parameters on ascidian life history is crucial for predicting the invasive potent
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14

Hiebert, Laurel S., Marta Scelzo, Alexandre Alié, Anthony W. De Tomaso, Federico D. Brown, and Stefano Tiozzo. "Comparing dormancy in two distantly related tunicates reveals morphological, molecular, and ecological convergences and repeated co-option." Scientific Reports 12, no. 1 (2022). http://dx.doi.org/10.1038/s41598-022-16656-8.

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AbstractMany asexually-propagating marine invertebrates can survive extreme environmental conditions by developing dormant structures, i.e., morphologically simplified bodies that retain the capacity to completely regenerate a functional adult when conditions return to normal. Here, we examine the environmental, morphological, and molecular characteristics of dormancy in two distantly related clonal tunicate species: Polyandrocarpa zorritensis and Clavelina lepadiformis. In both species, we report that the dormant structures are able to withstand harsher temperature and salinity conditions com
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15

Scelzo, Marta, Alexandre Alié, Sophie Pagnotta, et al. "Novel budding mode in Polyandrocarpa zorritensis: a model for comparative studies on asexual development and whole body regeneration." EvoDevo 10, no. 1 (2019). http://dx.doi.org/10.1186/s13227-019-0121-x.

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