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Journal articles on the topic 'Polygordiidae'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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1

Avery, Lynda, Patricia A. Ramey, and Robin S. Wilson. "New Polygordiidae (Polychaeta) from the Australian region." Zootaxa 2068 (December 31, 2009): 59–68. https://doi.org/10.5281/zenodo.187027.

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2

Vishnudattan, Naduvilakkandy, Paravanparambil Rajakumar Jayachandran, and Sivasankaran Bijoy Nandan. "Note on rare knot worm, Polygordius madrasensis Aiyar and Alikunhi, 1944 (Polychaeta, Polygordiidae) from India." Records of the Zoological Survey of India 122, no. 3 (2022): 267–73. https://doi.org/10.26515/rzsi/v122/i3/2022/167818.

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Vishnudattan, Naduvilakkandy, Jayachandran, Paravanparambil Rajakumar, Nandan, Sivasankaran Bijoy (2022): Note on rare knot worm, Polygordius madrasensis Aiyar and Alikunhi, 1944 (Polychaeta, Polygordiidae) from India. Records of the Zoological Survey of India 122 (3): 267-273, DOI: 10.26515/rzsi/v122/i3/2022/167818
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3

AVERY, LYNDA, PATRICIA A. RAMEY, and ROBIN S. WILSON. "New Polygordiidae (Polychaeta) from the Australian region." Zootaxa 2068, no. 1 (2009): 59–68. http://dx.doi.org/10.11646/zootaxa.2068.1.4.

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The interstitial polychaete family Polygordiidae is recorded from Australia for the first time, based on two new species: Polygordius arafura sp. nov. from continental shelf depths in the Arafura Sea, northern Australia, and Polygordius kiarama sp. nov. from the continental shelf and slope off southeastern Australia. Polygordius kiarama sp. nov., found at slope depths up to 1650 m, is the deepest record to date for the family, which has previously been recorded from intertidal habitats, shallow coastal waters and continental shelf depths.
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4

Lehmacher, Christine, Patricia A. Ramey-Balci, Lena I. Wolff, Dieter Fiege, and Günter Purschke. "Ultrastructural differences in presumed photoreceptive organs and molecular data as a means for species discrimination in Polygordius (Annelida, Protodriliformia, Polygordiidae)." Organisms Diversity & Evolution 16, no. 3 (2016): 559–76. https://doi.org/10.1007/s13127-016-0272-8.

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Lehmacher, Christine, Ramey-Balci, Patricia A., Wolff, Lena I., Fiege, Dieter, Purschke, Günter (2016): Ultrastructural differences in presumed photoreceptive organs and molecular data as a means for species discrimination in Polygordius (Annelida, Protodriliformia, Polygordiidae). Organisms Diversity & Evolution (New York, N.Y.) 16 (3): 559-576, DOI: 10.1007/s13127-016-0272-8, URL: http://dx.doi.org/10.1007/s13127-016-0272-8
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5

Hay-Schmidt, Anders. "The Larval Nervous System ofPolygordius lacteusScheinder, 1868 (Polygordiidae, Polychaeta): Immunocytochemical Data." Acta Zoologica 76, no. 2 (1995): 121–40. http://dx.doi.org/10.1111/j.1463-6395.1995.tb00987.x.

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6

Ramey-Balcı, Patricia, Dieter Fiege, and Torsten H. Struck. "Molecular phylogeny, morphology, and distribution of Polygordius (Polychaeta: Polygordiidae) in the Atlantic and Mediterranean." Molecular Phylogenetics and Evolution 127 (October 2018): 919–30. http://dx.doi.org/10.1016/j.ympev.2018.06.039.

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7

Pereira de Souza-Santos, Lilia. "Un ensayo experimental sobre la ecofisiología del poliqueto intersticial Polygordius eschaturus (Annelida: Polygordiidae)." Scientia Marina 81, no. 4 (2017): 509. http://dx.doi.org/10.3989/scimar.04666.07b.

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Specimens of Polygordius eschaturus from a reflective sandy beach were tested in the laboratory for tolerance to salinity and temperature and for their response to light, gravity and oxygen tension. After 192 h at 10°C, almost all specimens died at salinities of 10, 20 and 50 psu and were slow moving from 30 to 40. At 20°C and 30°C, all specimens died when salinity was 10; few showed abnormal behaviour at 50 and all presented normal behaviour from 20 to 40. At 40°C, all specimens died within 24 h. In our experimental conditions, the observed migration patterns corresponded to photonegative geo
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8

Cañete, Juan I., Carlos S. Gallardo, Álvaro Medina, Javier Díaz-Ochoa, Carlos Olave, and Tania Figueroa. "Abundance and spatial distribution of Polygordius (Polychaeta: Polygordiidae) neustonic exolarvae in estuaries from southern Chile." Anales del Instituto de la Patagonia 47, no. 2 (2019): 19–33. http://dx.doi.org/10.4067/s0718-686x2019000200019.

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9

Ramey, Patricia A., Dieter Fiege, and Brian S. Leander. "A new species of Polygordius (Polychaeta: Polygordiidae): from the inner continental shelf and in bays and harbours of the north-eastern United States." Journal of the Marine Biological Association of the United Kingdom 86, no. 5 (2006): 1025–34. http://dx.doi.org/10.1017/s0025315406014007.

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A new species of Polygordiidae, Polygordius jouinae sp. nov., along with its distribution, habitat, and reproduction is described. Polygordius jouinae sp. nov., the first North American Polygordius, is a dominant member of macrofaunal communities on the inner continental shelf, and in bays and harbours from Massachusetts to southern New Jersey. It is distinguished from most other Polygordius species by its non-inflated, heavily ciliated pygidium, absence of pygidial glands, and a conical (rather than rounded) prostomium. The 18S SSU rDNA from P. jouinae sp. nov. was sequenced and represents th
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10

Worsaae, Katrine, Alexandra Kerbl, Maikon Di Domenico, Brett C. Gonzalez, Nicolas Bekkouche, and Alejandro Martínez. "Interstitial Annelida." Diversity 13, no. 2 (2021): 77. http://dx.doi.org/10.3390/d13020077.

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Members of the following marine annelid families are found almost exclusively in the interstitial environment and are highly adapted to move between sand grains, relying mostly on ciliary locomotion: Apharyngtidae n. fam., Dinophilidae, Diurodrilidae, Nerillidae, Lobatocerebridae, Parergodrilidae, Polygordiidae, Protodrilidae, Protodriloididae, Psammodrilidae and Saccocirridae. This article provides a review of the evolution, systematics, and diversity of these families, with the exception of Parergodrilidae, which was detailed in the review of Orbiniida by Meca, Zhadan, and Struck within this
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11

Lehmacher, Christine, Patricia A. Ramey-Balci, Lena I. Wolff, Dieter Fiege, and Günter Purschke. "Ultrastructural differences in presumed photoreceptive organs and molecular data as a means for species discrimination in Polygordius (Annelida, Protodriliformia, Polygordiidae)." Organisms Diversity & Evolution 16, no. 3 (2016): 559–76. http://dx.doi.org/10.1007/s13127-016-0272-8.

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12

Ramey-Balcı, Patricia A., and Julie W. Ambler. "Distribution and seasonal abundance of Polygordius spp. (Class: Polychaeta; Family: Polygordiidae) exo- and endolarvae in the southern Mid-Atlantic Bight, USA." Marine Biology 161, no. 7 (2014): 1565–81. http://dx.doi.org/10.1007/s00227-014-2441-7.

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13

Pagliosa, Paulo Roberto, João Gabriel Doria, Giorgia Freitas Alves, et al. "Polychaetes from Santa Catarina State (southern Brazil): checklist and remarks on species distribution." Zootaxa 3486 (December 31, 2012): 1–49. https://doi.org/10.5281/zenodo.213667.

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Pagliosa, Paulo Roberto, Doria, João Gabriel, Alves, Giorgia Freitas, Almeida, Tito Cesar Marques De, Lorenzi, Luciano, Netto, Sergio Antonio, Lana, Paulo Da Cunha (2012): Polychaetes from Santa Catarina State (southern Brazil): checklist and remarks on species distribution. Zootaxa 3486: 1-49, DOI: 10.5281/zenodo.213667
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14

Ribas, Julia, and Pat Hutchings. "Lizard Island Polychaete Workshop: sampling sites and a checklist of polychaetes." Zootaxa 4019, no. 1 (2015): 7–34. https://doi.org/10.11646/zootaxa.4019.1.4.

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15

Mikac, Barbara. "A sea of worms: polychaete checklist of the Adriatic Sea." Zootaxa 3943, no. 1 (2015): 1–172. https://doi.org/10.11646/zootaxa.3943.1.1.

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16

Salazar-Vallejo, Sergio I., Luis F. Carrera-Parra, Alexander I. Muir, Jesús Angel De León-González, Christina Piotrowski, and Masanori Sato. "Polychaete species (Annelida) described from the Philippine and China Seas." Zootaxa 3842, no. 1 (2014): 1–68. https://doi.org/10.11646/zootaxa.3842.1.1.

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Salazar-Vallejo, Sergio I., Carrera-Parra, Luis F., Muir, Alexander I., León-González, Jesús Angel De, Piotrowski, Christina, Sato, Masanori (2014): Polychaete species (Annelida) described from the Philippine and China Seas. Zootaxa 3842 (1): 1-68, DOI: 10.11646/zootaxa.3842.1.1
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17

Vishnudattan, Naduvilakkandy, Paravanparambil Rajakumar Jayachandran, and Sivasankaran Bijoy Nandan. "Note on rare knot worm, <i>Polygordius madrasensis</i> Aiyar and Alikunhi, 1944 (Polychaeta, Polygordiidae) from India." Records of the Zoological Survey of India, September 2, 2022, 267–73. https://doi.org/10.26515/rzsi/v122/i3/2022/167818.

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Polygordius species is a clade of smooth bodied marine annelids, which are the main inhabitants of sandy intertidal sediments. They are well adapted for life in interstitial habitats. They have a habit of tying themselves in knots when collected, giving rise to the common name “knot worm”. Due to comparative morphological appearances among Polygordius species and its resemblance with nematodes and nemerteans made its taxonomy more challenging and required more advanced microscopic and molecular techniques. Only two species and a subspecies, primarily restricted to the south coast, have bee
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