Printer Friendly

The ultrastructure of calcareous cirratulid (Polychaeta, Annelida) tubes/Tsirratuliidide (Polychaeta, Annelida) skeleti peenstruktuurid.

INTRODUCTION

Among annelids, calcareous tubes occur in the families of Serpulidae, Sabellidae, and Cirratulidae. The skeletons of serpulids are exclusively calcareous in contrast to a single recent calcareous sabellid species (Glomerula piloseta (Perkins, 1991)) and a few recent calcareous cirratulid species (e.g. Dodecaceria coralii (Leidi, 1855), D. fistulicola Ehlers, 1901, and D. caulleryi Dehorne, 1933) (Fischer et al. 2000; Vinn 2005). The earliest calcareous tubes in cirratulids (Diplochaetetes mexicanus Wilson, 1986) are known from the Oligocene of Mexico (Fischer et al. 2000). The tube structure and ultrastructure is relatively well known in serpulids (Sanfilippo 1996; Vinn 2007, 2008; Vinn et al. 2008a, 2008b, 2008c, 2008d) and sabellids (Vinn et al. 2008c), based on the scanning electronmicroscopy (SEM) studies of ample recent and fossil material. The tube microstructure of cirratulids, however, has been studied recently by mainly using the optical light microscopy (Wilson 1986; Fischer et al. 1989, 2000). According to Fischer et al. (2000), cirratulid tubes are composed of micritic peloidal lamellae. They form a stromatolitic fabric with intercalated lenses of fibrous calcite/aragonite (Fischer et al. 2000). In their study of cirratulid biomineralization Fischer et al. (2000) hypothesized that these worms precipitate their hard parts by a method, hitherto unknown in eumetazoan animals. They recognized two mechanisms: (1) outside the soft tissue within a [Ca.sup.2+] binding mucus, excreted by an exotissue (basal layer), from which calcified lamellae are produced; (2) calcification of remains of biofilms and bacterial rods, which is not controlled by the animal itself. The last mechanism produces fibrous cement rims and peloidal aggregates (Fischer et al. 2000). The ultrastructure of such unusual biomineralization is not known and detailed SEM studies of cirratulid skeletal ultrastructures are necessary for proper comparison with the structures of erpulids and sabellids as well as of other invertebrates.

The aim of the paper is (1) to find structural support or the supposed unique biomineralization system of cirratulids, (2) to compare cirratulid skeletal structures with phylogenetically close sabellids and serpulids n order to find similarities, and (3) to find whether he skeletal ultrastructures of cirratulids have evolved ince the Oligocene. The collection is housed at the Zoological Museum, University of Amsterdam (ZMA), and at the Museum of Natural History, University of Tartu (TUG).

MATERIAL AND METHODS

Three cirratulid species (Diplochaetetes mexicanus, Dodecaceria coralii, and D. caulleryi) and one sabellid species (Glomerula piloseta) were selected for the study of their skeletal ultrastructures (Table 1). Cirratulid tubes were cut using a small electrical saw. A piece of worm colonies of each species with the size of 10 mm x 10 mm was then oriented and mounted in Canada balsam for grinding. A tube fragment of G. piloseta was also cut in longitudinal section in Canada balsam. Sections of tubes were polished and treated with a 1 : 1 mixture of 25% glutaraldehyde and 1% acetic acid, to which alcian blue was added (Mutvei solution) before performing the SEM study (Schone et al. 2005). All preparations were gold-sputtered prior to SEM investigation. The SEM studies were performed on a Hitachi S-4300 SEM, equipped with an Inca EDX system, at the Swedish Museum of Natural History, Stockholm.

RESULTS

Tube structure and ultrastructure are similar in Recent Dodecaceria and Oligocene Diplochaetetes. The entire tube wall of Dodecaceria caulleryi and D. coralii is composed of numerous thin calcareous lamellae (1.5-3.0 [micro]m) with a spherulitic prismatic ultrastructure (Fig. 1A-E). In some parts of the tube wall the boundaries between the calcareous lamellae are more heavily calcified than the interior of the lamellae in D. caulleryi (Fig. 1C). The calcareous spherulitic prisms in D. caulleryi and D. coralii are not epitaxially continuous through several growth lamellae. In Diplochaetetes mexicanus the tube structure is also lamellar and mostly with a spherulitic prismatic ultrastructure (Fig. 1F, H). However, there are also lamellae with a homogeneous structure composed of unoriented calcareous rods in the tube wall of Dip. mexicanus (Fig. 1F, G). In Dip. mexicanus spherulitic prisms can be epitaxially continuous through several growth lamellae (Fig. 1F, H). Spherulites were occasionally found in the tube walls of all studied species. However, they do not form distinct layers but occur within the lamellae of a spherulitic prismatic structure (Fig. 1I). The lithic fragments were found trapped in the tube walls in D. caulleryi, as described and figured in Fischer et al. (2000) for cirratulids. Tabulae in D. caulleryi have a spherulitic prismatic ultrastructure similar to the ultrastructure of the tube wall (Fig. 1D). The lamellar tube walls of cirratulids with a spherulitic prismatic ultrastructure are not unique among polychaetes and invertebrates in general.

DISCUSSION AND CONCLUSIONS

It is difficult to estimate whether the biomineralization process of cirratulids is unique only on the basis of the studied SEM preparations. The spherulitic prismatic structure occurs also in other calcareous polychaetes (Vinn 2007; Vinn et al. 2008c, 2008d; e.g. sabellids and serpulids) and molluscs (Mutvei 1989). Spherulites form an external tube layer in Glomerula piloseta (Sabellidae). They occur in serpulids too, but similarly to cirratulids, they do not form distinct layers. However, the tube ultrastructure of cirratulids shows the strongest similarity to that of sabellids. The tube wall of cirratulids and G. piloseta is lamellar, with lamellae differing from chevron-shaped lamellae of serpulids. Spherulitic prisms are oriented perpendicular to the growth lamellae, separated by organic films both in sabellids (Fig. 1J) and cirratulids (Fig. 1A-F, H). Spherulitic prisms can be epitaxially continuous through several growth lamellae both in Diplochaetetes mexicanus and G. piloseta. The epitaxially continuous spherulitic prismatic sectors are directed towards the tubes lumen both in Dip. mexicanus (Fig. 1F, H) and G. piloseta (Fig. 1J), indicating a similar accretion direction of the shell material. Based on the above listed similarities in the tube ultrastructure of these polychaetes, I hypothesize that biomineralization systems of sabellids and cirratulids are similar. Thus, the secretion process in tube formation of sabellids (Vinn et al. 2008c) and probably also in cirratulids resembles the one seen in molluscs and many other invertebrate phyla, in which the skeleton is formed by extracellular mineralization, mediated and controlled by an organic matrix that is secreted together with calcium ions by a secretory epithelium (Addadi & Weiner 1992). However, the homogeneous structure composed of irregularly oriented calcareous rods in Dip. mexicanus does not have exact analogy in other calcareous polychaetes. Fischer et al. (2000) hypothesized that some cirratulid structures can be formed due to calcification of bacterial rods, not controlled by the worm itself. If this presumption is correct, then the homogeneous structure of Dip. mexicanus can be the one formed of calcified bacterial rods.

The biomineralization system of serpulids is most evolved among annelids (Vinn et al. 2008d). Their earliest representatives are known from the Middle Triassic. Recent serpulids possess the diverse fabrics of complex oriented tube ultrastructures which appeared presumably already in the Cretaceous or in the Early Cenozoic at the latest (Vinn 2008; Vinn & Furrer 2008). In contrast to serpulids, the biomineralization system of cirratulids has not evolved since the appearance of calcareous tubes in the Oligocene. In this respect cirratulids are also similar to sabellids, in which the tube structures have remained unchanged from the Early Jurassic when they first began to calcify (Vinn et al. 2008c).

[FIGURE 1 OMITTED]

In conclusion, I found that (1) cirratulid ultrastructure is not unique among calcareous polychaetes and invertebrates in general, (2) cirratulid skeletal ultrastructures show the strongest similarity to that of sabellids, and (3) skeletal ultrastructures of cirratulids have not evolved since the appearance of calcareous tubes in the Oligocene.

Acknowledgements. I am grateful to H. A. ten Hove, Zoological Museum, University of Amsterdam, for making identified cirratulid material available for my study. Dodecaceria caulleryi was donated for the study by R. N. Hughes, University of Wales. I am grateful to H. Mutvei and K. Kirsimae for the constructive reviews. I acknowledge the financial support of projects NL-TAF-111 and SE-TAF-113 by SYNTHESYS and grant No. 6623 of the Estonian Science Foundation.

Received 27 April 2009, accepted 30 April 2009

REFERENCES

Addadi, L. & Weiner, S. 1992. Control and design principles in biological mineralization. Angewandte Chemie International Edition, 31, 153-169.

Dehorne, A. 1933. La schizometamerie et les segmentes tetragemmes de Dodecaceria caulleryi sp.n. Bulletin Biologique de la France et de la Belgique, 67, 298-326.

Ehlers, E. 1901. Die Polychaeten des magellanischen und chilenischen Strandes. Ein faunistischer Versuch. Festschrift zur 150 Jahrigen Bestehens der Konigliche Gesellschaft fur Wissenschaften Gottingen, 232 pp.

Fischer, R., Galli Oliver, C. & Reitner, J. 1989. Skeletal structure, growth, and paleoecology of the patch reef-building polychaete worm Diplochaetetes mexicanus Wilson, 1986 from the Oligocene of Baja California (Mexico). Geobios, 22, 761-775.

Fischer, R., Pernet, B. & Reitner, J. 2000. Organomineralization of cirratulid annelid tubes--fossil and recent examples. Facies, 42, 35-50.

Leidi, J. 1855. Contributions towards a knowledge of the marine invertebrate fauna of the coasts of Rhode Island and New Jersey. Journal of the Academy of Natural Sciences of Philadelphia, 3, 135-152.

Mutvei, H. 1989. Structure of molluscan prismatic shell layers. In Origin, Evolution, and Modern Aspects of Biomineralization in Plants and Animals (Crick, R. E., ed.), pp. 137-151. Plenum Press, New York.

Perkins, T. H. 1991. Calcisabella piloseta, a new genus and species of Sabellinae (Polychaeta: Sabellidae). Bulletin of Marine Science, 48, 261-267.

Sanfilippo, R. 1996. Micromorphology, microstructure and functional morphology of the Josephella marenzelleri (Polychaeta Serpulidae) tube. In Autoecology of Selected Organisms: Achievements and Problems (Cherchi, A., ed.), Bolletino della Societa Paleontologica Italiana, Special Volume, 3, 205-211.

Schone, B. R., Dunca, E., Fiebig, J. & Pfeifer, M. 2005. Mutvei.s solution: an ideal agent for resolving microgrowth structures of biogenic carbonates. Paleogeography, Paleoclimatology and Paleoecology, 228, 149-166.

Vinn, O. 2005. A new cornulitid genus from the Silurian of Gotland, Sweden. GFF, 127, 205-210.

Vinn, O. 2007. Taxonomic implications and fossilization of tube ultrastructure of some Cenozoic serpulids (Annelida, Polychaeta) from Europe. Neues Jahrbuch fur Geologie und Palaontologie, Abhandlungen, 244, 115-128.

Vinn, O. 2008. Tube ultrastructure of the fossil genus Rotularia Defrance, 1827 (Polychaeta, Serpulidae). Journal of Paleontology, 82, 206-212.

Vinn, O. & Furrer, H. 2008. Tube structure and ultrastructure of serpulids from the Jurassic of France and Switzerland, its evolutionary implications. Neues Jahrbuch fur Geologie und Palaontologie, Abhandlungen, 250, 129-135.

Vinn, O., Jager, M. & Kirsimae, K. 2008a. Microscopic evidence of serpulid affinities of the problematic fossil tube "Serpula" etalensis from the Lower Jurassic of Germany. Lethaia, 41, 417-421.

Vinn, O., Mutvei, H., ten Hove, H. A. & Kirsimae, K. 2008b. Unique Mg-calcite skeletal ultrastructure in the tube of the serpulid polychaete Ditrupa. Neues Jahrbuch fur Geologie und Palaontologie, Abhandlungen, 248, 79-89.

Vinn, O., ten Hove, H. A. & Mutvei, H. 2008c. On the tube ultrastructure and origin of calcification in sabellids (Annelida, Polychaeta). Palaeontology, 51, 295-301.

Vinn, O., ten Hove, H. A., Mutvei, H. & Kirsimae, K. 2008d. Ultrastructure and mineral composition of serpulid tubes (Polychaeta, Annelida). Zoological Journal of the Linnean Society, 154, 633-650.

Wilson, E. C. 1986. The first Tertiary sclerosponge from the Americas. Palaeontology, 29, 577-583.

Olev Vinn

Department of Geology, University of Tartu, Vanemuise 46, 51014 Tartu, Estonia; olev.vinn@ut.ee
Table 1. Age and locality information of the samples studied

Species                    Collection number   Age, locality

Diplochaetetes mexicanus   ZMA.V.Pol. 3808     Oligocene, Baja
                                               California, Mexico
Dodecaceria coralii        ZMA.V.Pol. 3803     Recent, Mexico, Yucatan,
                                               Chicxulub Puerto
Dodecaceria caulleryi      TUG 1232-3          Recent, Atlantic coast
                                               of South Africa
Glomerula piloseta         ZMA.V.Pol. 3744     Recent, Australia,
                                               Queensland, Lizard
                                               Island; paratypes
COPYRIGHT 2009 Estonian Academy Publishers
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2009 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Author:Vinn, Olev
Publication:Estonian Journal of Earth Sciences
Article Type:Report
Geographic Code:4EXES
Date:Jun 1, 2009
Words:1892
Previous Article:Tube ultrastructure of Pomatoceros americanus (Polychaeta, Serpulidae): implications for the tube formation of serpulids/Pomatoceros americanus'e...
Next Article:Stocks of organic carbon in Estonian soils/Orgaanilise susiniku varud Eesti muldades.
Topics:

Terms of use | Privacy policy | Copyright © 2022 Farlex, Inc. | Feedback | For webmasters |