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    Halecium lightbourni Calder 1990

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    Halecium lightbourni Calder, 1990 [1991a] Fig. 19a Halecium lightbourni Calder, 1990 [1991a]: 19, figs. 10, 11. Type locality. Bermuda: Flatts Inlet, 0.5 m (Calder 1990 [1991a]: 19). Material examined. Fort Myers Beach, on stranded Idiellana pristis, 01 March 2013, one colony, 3 mm high, without gonophores, coll. D. Calder, ROMIZ B4377. Remarks. Halecium lightbourni Calder, 1990 [1991a] is an infrequently reported and poorly known species, originally described from Bermuda. It has subsequently been reported from Panama (Calder & Kirkendale 2005), Martinique (Galea & Ferry 2015), and Cuba (Castellanos et al. 2018) in the western North Atlantic, and from Brazil (Nogueira et al. 1997; Grohmann et al. 2003; Oliveira et al. 2016) in the western South Atlantic. Hydroids of H. lightbourni resemble those of H. nanum Alder, 1859 in habit and in colony size (<1 cm high), but they differ most notably in lacking zooxanthellae. Among other characters differentiating H. lightbourni, colonies are less shrubby, hydrothecae tend to be narrower at the margin (129–160 μm vs. 147–182 μm), internodes of hydrocauli and branches are more slender at the nodes (65–86 μm vs. 84–89 μm), and large nematocysts (now considered pesudostenoteles rather than euryteles) are larger (8.3–8.9 μm long x 3.8–4.7 μm wide vs. 6.7–7.4 μm long x 3.1–3.8 μm wide) and somewhat different in shape (Calder 1990 [1991a]). The species has not been reported from pelagic Sargassum, a common substrate of H. nanum. The cnidome of H. lightbourni comprises microbasic mastigophores and small pseudostenoteles in addition to large pseudostenoteles (Calder 1990 [1991a]; Galea & Ferry 2015). When originally described (Calder 1990 [1991a]), only trophosomes of H. lightbourni were available for study. Gonosomes were discovered and described in material from Martinique by Galea & Ferry (2015). From their account, female gonothecae are sac-shaped to reniform, with a lateral aperture for two gonothecal hydranths. They thus differ from those of H. nanum, which have a disto-lateral aperture at the end of two adnate, finely annulated tubes. Male gonothecae are clavate, as in many other species of the genus Halecium Oken, 1815. Gonothecae of the two sexes were found by Galea & Ferry on different colonies. Reported distribution. Gulf coast of Florida. First record. Elsewhere in western North Atlantic. Bermuda: Flatts Inlet, 0.5–1.0 m, on Pennaria disticha and algae + Harrington Sound, Cripplegate Cave, at entrance, 0.5 m, on Dynamena crisioides + Great Sound, on channel buoy, 2.5 m, on ascidians and Pennaria disticha (Calder 1990 [1991a]: 19).— Panama: Bocas del Toro, Boca del Drago, 0-3 m (Calder & Kirkendale 2005: 481).—French Lesser Antilles: Martinique, Saint Pierre, Tombant de la Galère, 14.75144, -61.18236, 10–15 m, on Thyroscyphus marginatus (Galea & Ferry 2015: 224).— Cuba: Havana, coral reef system west of the city (Castellanos et al. 2018: Supplementary Table S2).Published as part of Calder, Dale R., 2019, On a collection of hydroids (Cnidaria, Hydrozoa) from the southwest coast of Florida, USA, pp. 1-141 in Zootaxa 4689 (1) on pages 67-68, DOI: 10.11646/zootaxa.4689.1.1, http://zenodo.org/record/351904

    Hebellopsis communis Calder 1991

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    Hebellopsis communis Calder, 1991a Fig. 5c Hebellopsis communis Calder, 1991a: 42, Figs. 26 a, b. Type locality. Bermuda: 2 km off Castle Roads (Calder 1991a). Voucher material. Bethel Shoal off Vero Beach, 27°42.6’N, 80°06.8’W, 24 m, on Thyroscyphus marginatus, 18.ii.1976, Johnson-Sea-Link, JSL 328, diver lockout, one colony, without gonothecae, coll. S. Nelson, ROMIZ B1100. Remarks. Hebellopsis communis Calder, 1991a resembles H. scandens (Bale, 1888), but differs in having: (1) hydrothecae that are deeper (>500 µm vs. <500 µm) and deeply campanulate rather than cylindrical and often markedly curved, (2) hydrothecal pedicels that are spirally annulated and of varied length (up to 400 µm long) rather than smooth and short (up to 130 µm long), and (3) hydrothecal orifices with larger openings (diameter 256– 280 µm vs. 160–191 µm). Hydrothecae resemble those of Hebella furax Millard, 1957 but lack a rounded annular ring basally. Hebellopsis gigas (Pieper, 1884) is also similar, but it has longer pedicels and hydrothecae with a more pronounced distal flare. This species, usually epizoic on other hydroids (especially Thyroscyphus marginatus Allman, 1877), is known only from the warm western Atlantic (Calder 1991a, 2000; Castellanos Iglesias et al. 2011; Oliveira et al. submitted). Its gonophores have yet to be described. Reported distribution. Atlantic coast of Florida. First record. Western Atlantic. Bermuda (Calder 1991a) to Brazil (Oliveira et al. submitted).Published as part of Calder, Dale R., 2013, Some shallow-water hydroids (Cnidaria: Hydrozoa) from the central east coast of Florida, USA, pp. 1-72 in Zootaxa 3648 (1) on page 19, DOI: 10.11646/zootaxa.3648.1.1, http://zenodo.org/record/526436

    Plicatotheca anitae Calder & Vervoort 1986

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    &lt;i&gt;Plicatotheca anitae&lt;/i&gt; Calder &amp; Vervoort, 1986 &lt;p&gt;Fig. 2c, d&lt;/p&gt; &lt;p&gt; &lt;i&gt;Plicatotheca anitae&lt;/i&gt; Calder &amp; Vervoort, 1986: 2022, figs. 1&ndash;4.&lt;/p&gt; &lt;p&gt; &lt;b&gt;Type locality.&lt;/b&gt; Bermuda: 2 km southeast of Castle Roads, 60&ndash;90 m (Calder &amp; Vervoort 1986).&lt;/p&gt; &lt;p&gt; &lt;b&gt;Voucher material.&lt;/b&gt; Off Sebastian Inlet, 27&deg;52.5&rsquo;N, 79&deg;57.5&rsquo;W, 75&ndash;98 m, 28.ii.1974, Smith-McIntyre grab, R/ V &lt;i&gt;Gosnold&lt;/i&gt; Station 222/274D, six colony fragments, up to 1.5 cm high, with two gonothecae, ROMIZ B1072.&lt;/p&gt; &lt;p&gt; &lt;b&gt;Remarks&lt;/b&gt;. &lt;i&gt;Plicatotheca anitae&lt;/i&gt; Calder &amp; Vervoort, 1986 appears to be widely distributed, having been reported from the Pacific and Indian oceans as well as the western and eastern Atlantic. Although Bermuda is the type locality of the species, this is only the second record of it in the western Atlantic. It is a species of deeper waters, having a reported bathymetric distribution of 60&ndash;1480 m (Vervoort 2006). Specimens examined here were collected at the upper end of this range, on the outer edge of the continental shelf off the east coast of Florida.&lt;/p&gt; &lt;p&gt; Gonothecae of &lt;i&gt;Plicatotheca anitae&lt;/i&gt; are reported here for the second time. They correspond with the description of Gili &lt;i&gt;et al&lt;/i&gt;. (1989), based on material from Guinea Bissau, western Africa, in being laterally flattened and triangular in shape. As with the specimens of Gili &lt;i&gt;et al&lt;/i&gt;., gonothecae observed here were empty and the nature of the gonophore could not be determined.&lt;/p&gt; &lt;p&gt; &lt;i&gt;Plicatotheca anitae&lt;/i&gt; resembles &lt;i&gt;Campanulina denticulata&lt;/i&gt; Clarke, 1907, originally described from abyssal depths (2845 fathoms = 5203 m) off Peru. In addition to trophosomal differences between the two noted earlier (Calder 1991a), the gonotheca of &lt;i&gt;P. anitae&lt;/i&gt; is now known to be triangular rather than long and irregularly cylindrical as in &lt;i&gt;C. denticulata&lt;/i&gt;. &lt;i&gt;Campanulina indivisa&lt;/i&gt; Fraser, 1948 from 267&ndash;347 fathoms (488&ndash;634 m) off Catalina Island, California, regarded as conspecific with &lt;i&gt;C. denticulata&lt;/i&gt; by Vervoort (1966), was referred to &lt;i&gt;Plicatotheca&lt;/i&gt; Calder &amp; Vervoort, 1986 by Calder &lt;i&gt;et al&lt;/i&gt;. (2009). That generic assignment is doubtful if gonothecae of &lt;i&gt;C. indivisa&lt;/i&gt;, presently unknown, prove identical with those of &lt;i&gt;C. denticulata&lt;/i&gt;.&lt;/p&gt; &lt;p&gt; &lt;b&gt;Reported distribution.&lt;/b&gt; Atlantic coast of Florida. First record.&lt;/p&gt; &lt;p&gt;Western Atlantic. Bermuda (Calder 1991a) to Florida (this study).&lt;/p&gt; &lt;p&gt;Elsewhere. Atlantic and Indo-Pacific regions, from deeper neritic to bathyal depths (Vervoort 2006).&lt;/p&gt;Published as part of &lt;i&gt;Calder, Dale R., 2013, Some shallow-water hydroids (Cnidaria: Hydrozoa) from the central east coast of Florida, USA, pp. 1-72 in Zootaxa 3648 (1)&lt;/i&gt; on pages 14-15, DOI: 10.11646/zootaxa.3648.1.1, &lt;a href="http://zenodo.org/record/5264362"&gt;http://zenodo.org/record/5264362&lt;/a&gt

    Sertularella unituba Calder 1991

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    Sertularella unituba Calder, 1991a Fig. 9a, b Sertularella gayi unituba Calder, 1991a: 103, fig. 54. Type locality. Bermuda: 2 km southeast of Castle Roads (Calder 1991a). Voucher material. Off St. Lucie Inlet, 27°11.6’N, 80°00.7’W, 41 m, 18.v.1976, Johnson-Sea-Link, JSL 2048, two colony fragments, up to 2.3 cm high, without gonophores, coll. J. Reed, ROMIZ B1093.— Bethel Shoal off Vero Beach, 27°42.6’N, 80°06.8’W, 24 m, 18.ii.1976, Johnson-Sea-Link, JSL 328, diver lockout, five colonies and colony fragments, up to 4 cm high, two with gonothecae, coll. S. Nelson, ROMIZ B1099. Remarks. Originally described as Sertularella gayi unituba by Calder (1991a), the subspecific name was elevated to specific rank by Medel & Vervoort (1998). Their taxonomic judgment was followed by Vervoort (2006) and is accepted here. Its recognition as a species distinct from S. gayi Lamouroux, 1821 is supported by the molecular studies of Moura et al. (2011). Sertularella unituba has been regarded as likely conspecific with hydroids that Allman (1888) initially described under the name Sertularia exigua (not Sertularia exigua Allman, 1877; not Sertularella exigua Thompson, 1879), and on discovering the homonymy renamed in a plate caption as Sertularia laxa (not Sertularia laxa Lamarck, 1816) (see Medel & Vervoort 1998; Vervoort 2006). Inasmuch as both S. laxa and S. exigua are invalid junior primary homonyms, they do not threaten the name Sertularella unituba. As noted above in remarks on Sertularella conica Allman, 1877, questions remain over the identity of that species, and whether it and S. unituba may be conspecific. Reported distribution. Atlantic coast of Florida. First record. Western Atlantic. Bermuda (Calder 1991a) to the Dry Tortugas (Van Gemerdeen-Hoogeveen 1965, as Sertularella conica). Elsewhere. Eastern Atlantic (Allman 1888, as Sertularella exigua; Medel & Vervoort 1998; Vervoort 2006).Published as part of Calder, Dale R., 2013, Some shallow-water hydroids (Cnidaria: Hydrozoa) from the central east coast of Florida, USA, pp. 1-72 in Zootaxa 3648 (1) on page 30, DOI: 10.11646/zootaxa.3648.1.1, http://zenodo.org/record/526436

    Calder, M M H, VX36750

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    This record was harvested from a previous catalogue system and will be withdrawn in 2025. Information in this record may be superseded or incomplete. Visit this record in UMA's new catalogue at: https://archives.library.unimelb.edu.au/nodes/view/375422Surname: CALDER Given Name(s) or Initials: M M H Military Service Number or Last Known Location: VX36750 Missing, Wounded and Prisoner of War Enquiry Card Index Number: 16661188123 Item: [2016.0049.07730] "Calder, M M H, VX36750

    CALDER: Cryogenic light detectors for background-free searches

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    CALDER is a R&D project for the development of cryogenic light detectors with an active surface of 5x5cm2 and an energy resolution of 20 eV RMS for visible and UV photons. These devices can enhance the sensitivity of next generation large mass bolometric detectors for rare event searches, providing an active background rejection method based on particle discrimination. A CALDER detector is composed by a large area Si absorber substrate with superconducting kinetic inductance detectors (KIDs) deposited on it. The substrate converts the incoming light into athermal phonons, that are then sensed by the KIDs. KID technology combine fabrication simplicity with natural attitude to frequency-domain multiplexing, making it an ideal candidate for a large scale bolometric experiments. We will give an overview of the CALDER project and show the performances obtained with prototype detectors both in terms of energy resolution and efficiency

    Calder, J E M, NX423

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    This record was harvested from a previous catalogue system and will be withdrawn in 2025. Information in this record may be superseded or incomplete. Visit this record in UMA's new catalogue at: https://archives.library.unimelb.edu.au/nodes/view/375418Surname: CALDER Given Name(s) or Initials: J E M Military Service Number or Last Known Location: NX423 Missing, Wounded and Prisoner of War Enquiry Card Index Number: 16805188119 Item: [2016.0049.07726] "Calder, J E M, NX423

    Harry M. Calder

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    Sertularella affinicostata Calder and Faucci 2021

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    Sertularella affinicostata Calder and Faucci, 2021 (Figure 6e, f) Sertularella affinicostata Calder and Faucci, 2021: 23, figs 7a–e, 8 Type locality Ecuador: Galápagos Islands, Isla Darwin (Calder and Faucci 2021). Material examined Chatham Bay, 5.56126, −87.04516, 1 colony, 2 mm high, without gonothecae, coll. I. Keith, #253534. –Chatham Bay, 5.56216, −87.04516, 9 colony fragments, to 6 mm high, without gonothecae, coll. I. Keith, #240612. –Wafer Bay, 5.5456, −87.06235, 9 colony fragments, to 2 mm high, without gonothecae, coll. G. Ashton, #240597. –Wafer Bay, 5.5456, −87.06235, 2 colonies, on two barnacles, to 2 mm high, without gonothecae, coll. G. Ashton, #240591. –Wafer Bay, 5.5456, −87.06235, 6 colony fragments, to 3 mm high, without gonothecae, coll. G. Ashton, #240592. –Wafer Bay, 5.54535, −87.06185, 4 colony fragments, to 2.5 mm high, without gonothecae, coll. G. Ashton, #240636. –Wafer Bay, 5.54535, −87.06185, 1 colony, on a barnacle, 4 mm high, without gonothecae, coll. G. Ashton, #240629. –Wafer Bay, 5.54535, −87.06185, 1 colony fragment, 4 mm high, without gonothecae, coll. G. Ashton, #240630. –Chatham Bay, 5.56126, −87.04516, 2 colony fragments, to 5 mm high, without gonothecae, coll. I. Keith, #307712. –Chatham Bay, 5.56126, −87.04516, 1 colony fragment, 3 mm high, without gonothecae, coll. I. Keith, #307711. –Chatham Bay, dock 004, no coordinates, 1 colony fragment, 2 mm high, without gonothecae, coll. G. Ashton, #266336. Remarks Sertularella affinicostata Calder and Faucci, 2021 was first reported, as S. costata Leloup, 1940, from the two northernmost and warmest of the Galápagos Islands, Wolf and Darwin (Calder et al. 2003). It was discovered a second time in a collection from French Frigate Shoals in the Northwestern Hawaiian Islands (Calder and Faucci 2021) and recognised therein as an undescribed species. Calder and Faucci (2021) also provide records of previously unreported material from Cousin Rock and Marchena Island in the Galápagos. The present record from Cocos Island constitutes the third record of this tiny but morphologically striking hydroid species. Hydroids of S. affinicostata are noteworthy in having a series of sharp-edged horizontal ridges that ring walls of its hydrothecae. Trophosomes of the species differ in part from those of S. costata, originally described from Sagami Bay, Japan, in having fewer (10–14) ridges instead of about 20 (Leloup 1940; Hirohito 1983, 1995). Hydrothecae also differ in being barrel-shaped rather than distinctly tapered distally, and a neck region lacking ridges below the rim is noticeably longer. The proximal end of the hydrocaulus is typically short rather than extending as a long, slender peduncle as in S. costata, and internodes of the hydrocaulus are shorter and thicker. The original account of S. affinicostata in Calder and Faucci (2021) was based on specimens from both the Galápagos Islands and the Northwestern Hawaiian Island. The holotype, from Darwin Island in the Galápagos archipelago, was selected as being the only fertile colony in the two collections. The species was well represented in our Cocos samples. It was present in 11 of the 42 samples (26%) of hydroids in the collection, although all of the specimens were sterile. Hydroids of S. affinicostata are minute, with colonies from Cocos Island ranging between 2 and 6 mm in height. Indeed, the holotype was merely 1.5 mm high. A substrate generalist, the species has been reported from barnacles, a sponge, calcareous rubble, algae and a hydroid stem (Calder and Faucci 2021). Specimens examined here were removed from fouling panels exposed at Chatham Bay and Wafer Bay. While S. affinicostata is certainly a species of shallow waters, its overall bathymetric range is not yet well known. Specimens from the Galápagos were collected at depths of 6 m off Wolf Island (Calder et al. 2003), and from 10 m off Cousin Rock and 8 m off Marchena Island (Calder and Faucci 2021). Collections from Cocos Island were on panels exposed at depths of 0.5– 3 m. A description and additional comments on S. affinicostata are provided by Calder and Faucci (2021). We treat S. affinicostata as cryptogenic in the Cocos, Galapagos and Hawaiian Islands. While potentially a member of a naturally transpacific fauna, its occurrence in shallow water, and particularly on biofouling panels in Cocos, do not exclude it from shipmediated transport. As we discuss below, an increasing number of invasions are recognised from open-ocean environments (such as in the Galapagos and the French Frigate Shoals), thus not excluding this species from being potentially introduced, even if its home port remains unknown at this time. Reported distribution Cocos Island: first record. Elsewhere: Galápagos Islands (Calder et al. 2003, as Sertularella costata); Northwestern Hawaiian Islands (Calder and Faucci 2021).Published as part of Calder, Dale R., Carlton, James T., Keith, Inti, Ashton, Gail V., Larson, Kristen, Ruiz, Gregory M., Herrera, Esteban & Golfin, Geiner, 2022, Biofouling hydroids (Cnidaria: Hydrozoa) from a Tropical Eastern Pacific island, with remarks on their biogeography, pp. 565-606 in Journal of Natural History 56 (9 - 12) on pages 588-590, DOI: 10.1080/00222933.2022.2068387, http://zenodo.org/record/701248

    N. M. Calder, Monumenta Asiae Minoris antiqua.

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    Cumont F. N. M. Calder, Monumenta Asiae Minoris antiqua.. In: Revue belge de philologie et d'histoire, tome 7, fasc. 3, 1928. pp. 1113-1114
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