Published May 21, 2020 | Version v1
Taxonomic treatment Open

Zygophylax infundibulum Millard 1958

  • 1. Programa de Pós-Graduação em Biologia Animal, Departamento de Zoologia, Centro de Biociências, Universidade Federal de Pernambuco. Av. Professor Moraes Rego, 1235, Recife, Pernambuco, Brazil. CEP: 50670 - 420
  • 2. Programa de Pós-Graduação em Biologia Animal, Departamento de Zoologia, Centro de Biociências, Universidade Federal de Pernambuco. Av. Professor Moraes Rego, 1235, Recife, Pernambuco, Brazil. CEP: 50670 - 420 & Núcleo de Biologia, Centro Acadêmico de Vitória, Universidade Federal de Pernambuco, Vitória de Santo Antão, Pernambuco, Brazil. jazintheking @ gmail. com; https: // orcid. org / 0000 - 0002 - 0866 - 1183
  • 3. Dipartimento di Scienze della Vita e dell'Ambiente, Università Politecnica delle Marche. Via Brecce Bianche, 60131 Ancona, Italy s. puce @ staff. univpm. it; https: // orcid. org / 0000 - 0002 - 8163 - 1554
  • 4. Departamento de Zoologia, Instituto de Biociências, Universidade de São Paulo, São Paulo, Brazil

Description

Zygophylax infundibulum Millard, 1958

Plate 4 A–F

Zygophylax infundibulum Millard, 1958: 180–181, fig. 4b–c; Millard, 1968: 266; Millard, 1973: 32; Millard, 1975: 197–198, fig. 65d–e; Millard, 1978: 200; Millard, 1979: 140; Millard, 1980: 131, 143–144, fig. 4d; Rees & Vervoort, 1987: 84; Calder & Vervoort, 1998: 28; Vervoort & Watson, 2003: 69; Miranda et al., 2015: 506.

Type Series. Holotype—Several stems and two whole mounts, without gonophores (SAM H36) (Millard, 1979).

Type Locality. Coll. Pieter Faure, St. 10781, Natal coast, Durban, South Africa, 29°53’S 31°11’E, 155 m, 17 December 1900.

Material examined. Coll. T. Mortensen Exp. 1929, St. 24, near Durban coast, South Africa, 29°48’30’’S 31°18’E, 219 m, 22 August 1929, det. N.H.A. Millard, small colonial fragments, without gonophores (ZMUC-HYD 271); Coll. Benthedi, St. S 93, Indian Ocean, off northern Madagascar, 11°32.3’S 47°16’E, 400–556 m, 07 April 1977, without gonophores (RMNH-Coel. slide 253); Coll. Marion Dufresne, St. FA 117, as Z. cf. infundibulum, La Réunion, 20°57’S 54°08’E, 470–540 m, 31 August 1982, without gonophores (RMNH-Coel. slide 261).

Description of additional material. (ZMUC-HYD 271) Stem rectilineous, mostly polysiphonic with only distamost part monosiphonic, not divided into nodes; hydrothecae facing one side of the colony. Hydrocladia polysiphonic proximally and monosiphonic distally (Pl. 4A), divided into transversal nodes, each internode with three hydrothecae; hydrocladia with axillary hydrotheca on axial apophyses, with subopposite arrangement, planar; hydrothecal apophyses developed, separated from hydrocladia by septum and constricton of perisarc. Hydrothecae tubular, slightly sigmoid, adcauline wall concave under rim, abcauline wall convex (Pl. 4C–D), pedicel long, rectilineous, slightly wrinkled (Pl. 4B), diaphragm thick, convex. Nematothecae tubular on hydrothecal apophysis (Pl. 4E–F).

Measurements. Stem: distance between two subsequent hydrothecae 156–390 µm; diameter 182–442 µm; distance between subsequent hydrocladia at the same side 1.7–1.8 mm. Hydrocladia: lenght 5.1–7.4 mm; diameter at base 130–156 µm. Hydrothecae: length of adcauline wall from rim to diaphragm 350–370 µm; lenght from base budding of the axis to rim 540–610 µm; diameter at rim 130–150 µm; diameter at diaphragm 70 µm; diameter of pedicel on adcauline side 240–270 µm; diameter at apophysis 50 µm. Nematothecae: lenght 40–160 µm; diameter at rim 20–30 µm.

Diagnosis of reproductive structures. “Gonothecae not adpressed, narrow at base and widening distally, then divided into two outwardly curved necks bearing the terminal apertures. Protective tubular structures numerous, arising amongst the gonothecae and rising above them, completely obscuring them and forming a bristly coat to the coppinia; each branching irregularly and bearing many nematothecae similar to those to the trophosome. Each gonothecae apparently arising from the base of one of the tubular structures” (Millard, 1980: 143–144).

Geographical distribution. southern Brazil (Miranda et al., 2015); off Natal, South Africa, 115–219 m (Millard, 1975); off northern Madagascar, 400–556 m (present study).

Remarks. Zygophylax infundibulum Millard, 1958 is known from the Indian coast of South Africa (Millard, 1958, 1975, 1979, 1980), recently also recorded for Brazil by (Miranda et al., 2015) and now for Madagascar (this study). The gonosome of the species was subsequently described (Millard, 1980). We did not have access to any of the materials deposited in the South African Museum (SAM). The species may be diagnosed by the triangular shape of gonothecae with two short projections with apertures, the coppinia with numerous protective tubes, the hydrothecae curved at the distamost third and facing one side of the colony, and the long pedicels on well-demarcated apophyses.

Zygophylax infundibulum has similarities with Z. unilateralis, such as the sigmoid hydrothecae, hydrothecae oriented towards one side of the colony, distinct apophyses, non-adnate elongated gonothecae widening basally, and the many protective tubes in the coppinia. However, Z. unilateralis differs by the larger and thicker hydrothecae, globular to bi or trilobate nematothecae on hydrothecal apophyses, hydrocladia and secondary axial tubes, pedicel varying from totally smooth to slightly wrinkled or even segmented throughout its extension (e.g., in the holotype BMNH 29.10.28.77), and the 2–3 processes in the gonothecae of Z. unilateralis.

Millard (1980) also reported trophosomal and gonosomal similarities between Z. infundibulum and Zygophylax sibogae Billard, 1918, like the curved hydrothecae resembles of Z. infundibulum similar to those of young colonies of Z. sibogae (e.g., RMNH-Coel. slide 258), the shape of the gonothecae, and of the high density of protective tubes in the coppinia, although Z. sibogae has more elongated projections facing to opposite directions. Other characters listed above also help to differentiate between the species.

Colonies of Z. infundibulum undertake regeneration processes leading to the segmentation of the apophyses, the pedicels or even the hydrothecae, by the duplication of the diaphragms (Millard, 1958). We observed pedicels slightly segmented or wrinkled in some specimens (ZMUC-HYD 271, South Africa; RMNH-Coel. slide 253, Madagascar). This regeneration process and the resulted pedicelar annulations differ from those of Z. naomiae sp. nov. (see above). In the same specimen, regeneration processes also alter the number of renovations on rim (up to 11), increasing significantly the length, as well as the nematothecae of the secondary axial tubes of the stem vary from tubular to extremely thin and elongated, with a widened apex with one aperture.

Notes

Published as part of Campos, Felipe Ferreira, Pérez, Carlos Daniel, Puce, Stefania & Marques, Antonio Carlos, 2020, A new species of Zygophylax (Quelch, 1885) (Cnidaria, Hydrozoa) from South Africa, with taxonomic notes on the southern African species of the genus, pp. 535-552 in Zootaxa 4779 (4) on pages 545-547, DOI: 10.11646/zootaxa.4779.4.5, http://zenodo.org/record/3839510

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Linked records

Additional details

Biodiversity

Collection code
SAM
Event date
1900-12-17 , 1977-04-07 , 1982-08-31
Family
Lafoeidae
Genus
Zygophylax
Kingdom
Animalia
Material sample ID
H36
Order
Leptothecata
Phylum
Cnidaria
Scientific name authorship
Millard
Species
infundibulum
Taxon rank
species
Type status
holotype
Verbatim event date
1900-12-17 , 1977-04-07 , 1982-08-31
Taxonomic concept label
Zygophylax infundibulum Millard, 1958 sec. Campos, Pérez, Puce & Marques, 2020

References

  • Millard, N. A. H. (1958) Hydrozoa from the coasts of Natal and Portuguese East Africa. Part I. Calyptoblastea. Annals of the South African Museum, 44 (5), 165 - 226.
  • Millard, N. A. H. (1968) South African hydroids from Dr. Th. Mortensen's Java-South Africa expedition, 1929 - 1930. Videnskalbelige. Meddelelser fra Dansk Naturhistorisk. Forening i Kjobenhavn, 131, 251 - 288.
  • Millard, N. A. H. (1973) Auto-epizoism in South African hydroids. In: Recent trends in research in coelenterate biology. Proceedings of The Second International Symposium on Cnidaria, Publications of the Seto Marine Biological Laboratory, 20, 23 - 34. https: // doi. org / 10.5134 / 175792
  • Millard, N. A. H. (1975) Monograph on the Hydroida of Southern Africa. Annals of the South African Museum, 68, 1 - 513.
  • Millard, N. A. H. (1978) The geographical distribution of southern African hydroids. Annals of the South African Museum, 74, 159 - 200.
  • Millard, N. A. H. (1979) Type specimens of Hydroida (Coelenterata) in the South African Museum. Annals of the South African Museum, 77 (8), 133 - 150.
  • Millard, N. A. H. (1980) Hydroida. The South African Museum's Meiring Naude cruises. Part 11. Annals of the South African Museum, 82 (4), 129 - 153.
  • Rees, W. J. & Vervoort, W. (1987) Hydroids from the John Murray Expedition to the Indian Ocean, with revisory notes on Hydrodendron, Abietinella, Cryptolaria and Zygophylax (Cnidaria: Hydrozoa). Zoologische Verhandelingen, 237, 1 - 209.
  • Calder, D. R. & Vervoort, W. (1998) Some hydroids (Cnidaria: Hydrozoa) from the Mid-Atlantic Ridge, in the North Atlantic Ocean. Zoologische Verhandelingen, 319, 1 - 65.
  • Vervoort, W. & Watson, J. E. (2003) The Marine Fauna of New Zealand: Leptothecata (Cnidaria: Hydrozoa) (Thecate Hydroids). NIWA Biodiversity Memoir, 119, 1 - 538.
  • Miranda, T. P., Genzano, G. N. & Marques, A. C. (2015) Areas of endemism in the Southwestern Atlantic Ocean based on the distribution of benthic hydroids (Cnidaria: Hydrozoa). Zootaxa, 4033 (4), 484 - 506. https: // doi. org / 10.11646 / zootaxa. 4033.4.2
  • Billard, Α. (1918) Notes sur quelques especes d'hydroides de l'expedition du Siboga. Archives de Zoologie experimentale et generale, 57 (2), 21 - 27.