1860 Haliomma trinacrium - Haeckel p. 815
1862 Actinomma trinacrium - Haeckel p. 441; pl. 24, figs. 6-8
1887 Actinomma trinacrium - Haeckel p. 254
1887 Echinomma trinacrium - Haeckel p. 258
1900 Echinomma trinacrium - Jørgensen p. 56-57
1905 Echinomma trinacrium - Jørgensen p. 116
1909 Echinomma trinacrium - Schröder p. 29; fig. 18
1998 Actinomma trinacria - Cortese and Bjørklund p. 153-154; pl. 3, figs. 20-22
From Suzuki Paleotax db:
1861 Haliomma (Actinomma) trinacrium n. sp. Haeckel p. 815-816
1862 Actinomma trinacrium (Haeckel) Haeckel p. 441, pl. 24, figs. 6-8
1887 Actinomma (Actinommetta) trinacrium (Haeckel) Haeckel p. 254
1887 Echinomma (Echinommura) trinacrium (Haeckel) Haeckel p. 258-259
1899 Echinomma trinacrium (Haeckel) Jörgensen p. 56-67
1905 Echionomma trinacrium (Haeckel) Jörgensen p. 116
1910 Echinomma trinacrium (Haeckel) Mast p. 170
1969 Echinomma trinacrium (Haeckel) Petrushevskaya p. 124
1973 Echinomma trinacrium (Haeckel) Bjørklund pl. 1, fig. h
1974 Actinomma trinacrium (Haeckel) Caulet p. 227, pl. 4, figs. 1-2
1998 Actinomma trinacria (Haeckel) [sic] Cortese & Bjørklund p. 153-154, pl. 3, figs. 20-22
Catalog entries: Haliomma trinacrium
Original description: Rindenschale kugelig, mit zwanzig symmetrischen, dreikantigen, starken Hauptstacheln von der Länge des Schalenradius, und dazwischen mehr als 20 ähnlichen, aber halb so langen und starken Nebenstacheln. Maschen dazwischen rundlich, ungleich, von 1/15--1/5des Schalendurchmessers. Die inneren Verlängerungen der Hauptstacheln setzen sich verschmälert an die äufsere Markschale an, welche 1/3 so grofsen Durchmesser, 1/3 so breite Maschen und Balken hat als die Rindenschale. Sie verhält sich zu dieser in allen Stücken, wie die innerezur äufseren Markschale. Centralkapsel roth.
[Cortical shell spherical, with twenty symetrical, three-sided, robust main spines as long as the shell radius, and more than 20 secondary spines similar, but half as long and robust as the main spines. Pores circular of different sizes, from 1/15 to 1/5 of the shell diameter. The internal extremities of the main spines are linked to the outer medullary shell whose diameter, pores, and bars are as large as the third of their equivalents in the cortical shell. The inner medullary shell is in the same proportions with the outer medullary shell. entral capsule red. (In German. Translation by J.P.C.)]
Remarks on original description: Haeckel (1861) listed Haliomma trinacrium under the subgeneric name Actinomma, but did not include the subgeneric name in the species name.
The species is often cited as Haliomma trinacrium Haeckel 1860, but the correct publication date is 1861
Haeckel 1887 - Haliomma trinacrium (p. 254): Cortical shell as well as both medullary shells thin walled, with subregular, circular pores, twice as broad as the bars. Radial proportion of the three spheres = 1: 3: 9; radial beams between them twenty, prolonged outside into strong, three-sided pyramidal spines, as long as the radius; between them, on the surface, numerous similar spines. Sometimes the latter remain smaller, the pores more irregular, and then this species corresponds to Echinomma trinacrium. Diameter of the outer shell 0.09, middle 0.03, inner 0.01; cortical pores 0.008, bars 0.004; length of the spines 0.04, basal breadth 0.01. Habitat: Mediterranean (Messina, Corfu, Haeckel), surfaces. Haeckel 1887 - Haliomma trinacrium (p. 258): Cortical shell thin walled, roundish pores, twice to three times as broad as the bars. Both medullary shells with regular, circular pores. Radial proportion of the three spheres 1:3:9. On the surface about twenty three-sided pyramidal main spines, as long as the radius, and numerous (forty to sixty) by-spines of half length. (Compare with this species Actinomma trinacrium, with which it is connected by transitional forms).Diameter of the outer shell 0.09, middle 0.03, inner 0.01; cortical pores 0.008 to 0.012, bars 0.004; length of the spines 0.02 to 0.05, basal breadth 0.01. Habitat: Mediterranean (Messina). Jørgensen 1905 - Haliomma trinacrium (p. 116):The forms which I have tabulated under this name are somewhat uncertain. They are distinguished from the forgoing species by a strong, rather think outer shell, more numerous and stronger byspines, as well as by a different construction of the inmost shell, which is in most respects like the middle one. There is nevertheless on the one side a considerable agreement with Chromyechinus borealis, only that the outside shell (the fourth) is wanting, on the other side a considerable resemblance to younger forms of Drymyomma elegans, where the characteristic branched byspines are still wanting or are branchless needles. To this must be added that different forms of E. leptodermum may also have rather strong outer shells and more numerous spines. As a rule, though, the forms of Chromyechinus borealis may easily be recognized by the transverse processes on the radial spines, which here, as in E. leptodermum and Hexacontium enthacanthum suggest the beginnings of the still undeveloped outer shell. The forms of Drymyomma elegans have characteristic long slender main spines and narrow byspines. Yet, I am not sure if there be not still another species, most nearly answering to E. trinacrium, but with long, narrow principal spines and byspines, the latter always being branchless. It is difficult to examine the inmost shell. I have not yet succeeded in ascertaining with certainty whether such a firmly constructed inner shell with which E. trinacrium is depicted by HAECKEL (1862, pl. 24, f. 6-8) is also characteristic of Chromyechinus borealis and Drymyomma elegans. I have, however, seen such a shell. As I have already suggested in a previous paper (JRGENSEN, 1900, p. 57) it is not impossible that what I have called E. trinacrium may be certain young forms of Chromyechinus borealis, where the above mentioned transverse processus on the radial spines are wanting. On the other hand, it is just as likely that there may be with us another species differing from both Drymyomma elegans and Echinomma trinacrium, to which the supposed intermediate forms belong. This species would be comparatively frequent on the northern coast of Norway. Until this is made evident, it will be best to keep to the species which are always easily recognized, viz. Echinomma leptodermum, Chromyechinus borealis and Drymyomma elegans. Occurs in the plankton like the foregoing species. Cortese and Bjørklund 1998 - Haliomma trinacrium Haeckel (1887) described two species Actinomma trinacrium (recte trinacria) and Echinomma trinacrium (recte trinacria), and we will quote his descriptions. Actinomma trinacrium:Cortical shell as well as both medullary shells thin walled, with subregular, circular pores, twice as broad as the bars. Radial proportion of the three spheres = 1:3:9; radial beams between them twenty, prolonged outside into strong, three-sided pyramidal spines, as long as the radius; between them, on the surface, numerous similar spines. Sometimes the latter remain smaller, the pores more irregular, and then this species corresponds to Echinomma trinacrium. Echinomma trinacrium:Cortical shell thin walled, roundish pores, twice to three times as broad as the bars. Both medullary shells with regular, circular pores. Radial proportion of the three spheres 1:3:9. On the surface about twenty three-sided pyramidal main spines, as long as the radius, and numerous (forty to sixty) by-spines of half length. (Compare with this species Actinomma trinacrium, with which it is connected by transitional forms). In our material both forms are present, but the majority are transitional forms, and it is not possible to assign these forms to either Actinomma trinacria or Echinomma trinacria. We regard Echinomma trinacria as a junior subjective synonym of Actinomma trinacria, since this name has priority according to the rules of ICZN. As we already have pointed out, the juvenile stage of the long-spined form of Actinomma boreale, when only three shells have developed, strongly resembles A. trinacria. Very few typical adult and well developed A. trinacria have been observed, while A. boreale is rather common. We therefore assume that most of our transitional forms should be classified as A. boreale, which was also suggested by Jørgensen (1905). Furthermore, he stated: As a rule, though, the forms of Cromyechinus borealis may easily be recognized by the transverse processes on the radial spines, which here, as in E. leptodermum, suggest the beginning of the still undeveloped outer shell. The forms of Drymyomma elegans have characteristic long slender main spines and narrow byspines. Yet, I am not sure if there be not still another species, most nearly answering to E. trinacrium, but with long, narrow principal spines and byspines, the latter always being branchless.
Published descriptions
Distribution - To be found at the west coast of Norway in the deeper water layers (Schröder, 1909). Fairly common, but never in great numbers. Also found in the Mediterranean Sea (Haeckel, 1887).
Geological Range:
Last occurrence (top): Extant. Data source: Lazarus et al. 2015 - "R age group"
First occurrence (base): within Quaternary Period (0.00-2.59Ma, base in Gelasian stage). Data source: Lazarus et al. 2015 - "R age group"
Plot of occurrence data:
Cortese, G. & Bjørklund, K. R. (1998b). The taxonomy of boreal Atlantic Ocean Actinommida (Radiolaria). Micropaleontology. 44(2): 149-160. gs Haeckel, E (1861b). Uber neue, lebende Radiolarien des Mittelmeeres und legte die dazu gehorigen Abbildungen. Monatsberichte der Koniglichen Preussische Akademie der Wissenschaften zu Berlin. 1860: 794-817. gs Haeckel, E (1862). Die Radiolarien (Rhizopoda Radiaria). Eine Monographie. Georg Reimer, Berlin. 1-572. gs O Haeckel, E (1887). Report on the Radiolaria collected by H.M.S. Challenger during the years 1873-1876. Report on the Scientific Results of the Voyage of H.M.S. Challenger during the years 1873-1876. 18: 1-1803. gs O Jørgensen, E (1900). Protophyten und Protozoen im Plankton aus der norwegischen Westkuste. Bergens Museums Aarbog. 1899(6): 51-95. gs O Jørgensen, E (1905). The protist plankton and diatoms in bottom samples: Radiolaria. In, Nordgaard (ed.) Hydrographical and biological investigation in Norwegian Fjord. 49-151. gs O Schröder, O. (1909a). Die nordischen Spumellarian. In, Brandt, K. & Apstein, C. (eds) Nordisches Plankton. Lipsius und Tischer, Kiel and Leipzig, Germany (17): 1-66. gs O Missing or ambiguous references: Haeckel 1860; References:
Actinomma trinacria compiled by the radiolaria@mikrotax project team viewed: 12-10-2024
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