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A microscopical study of the “chlorophylloid” pigment cells of the marine polychaete Eulalia viridis (L.)

Published online by Cambridge University Press:  06 August 2013

P.M. Costa
Affiliation:
IMAR – Instituto do Mar, Departamento de Ciências e Engenharia do Ambiente, Faculdade de Ciências e Tecnologia da Universidade Nova de Lisboa, 2829–516 Caparica, Portugal ([email protected])
F. Carrapiço
Affiliation:
Universidade de Lisboa, Faculdade de Ciências, Departamento de Biologia Vegetal, Centro de Biologia Ambiental. Bloco C2 Campo Grande, 1749–016 Lisboa, Portugal
A.P. Alves de Matos
Affiliation:
Anatomia Patológica, Centro Hospitalar de Lisboa Central - HCC, Rua da Beneficência 8, 1069-166 Lisboa, Portugal; Centro de Estudos do Ambiente e do Mar (CESAM/FCUL) – Faculdade de Ciências da Universidade de Lisboa and Centro de Investigação Interdisciplinar Egas Moniz (CiiEM), Quinta da Granja, Monte de Caparica, 2829-511 Caparica, Portugal
M.H. Costa
Affiliation:
IMAR – Instituto do Mar, Departamento de Ciências e Engenharia do Ambiente, Faculdade de Ciências e Tecnologia da Universidade Nova de Lisboa, 2829–516 Caparica, Portugal ([email protected])

Abstract

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Animal skin pigments, often of undisclosed biochemical nature, have many functions besides signalling and camouflage: they also play a protective role against environmental stressors, from radiation and oxidative stress–inducers to predators and parasites. Most pigments are not fully synthetized by animals but rather acquired from vegetable feed and often biotransformed. These intriguing pigments called the attention of researchers in the past, such as the awkward green “chlorophylloid” pigments of the marine invertebrate Bonellia, first described in the 19th century. For decades, however, research has come to a stand–still. The marine annelid Eulalia viridis (Phyllodocidae: Polychaeta), although common throughout NW Europe, has so far received little attention to the origin and function of its bright green colouration. In fact, with the exception of part of its digestive system even the basic histological description of this animal is absent, as for marine annelids in general.

Adult wild E. viridis were subjected to a comprehensive microscopy study employing several fixation and staining techniques for bright–field (BF), transmission electron (TEM) and UV–epifluorescence microscopy in order to disclose the pigment cells’ microanatomy and arrangement and to infer the potential origin of the pigments. Stains for bright–field microscopy included Haematoxylin and Eosin (HE), Alcian Blue–Periodic Acid/Schiff’s–Haematoxylin (AB–PAS–H) and Bronner’s Sudan Black. Samples were either embedded in paraffin (BF and UV microscopy) or LR White resin (BF and TEM).

The high complexity of the animals’ integument was confirmed, in accordance to the scarcely known polychaete microanatomy. The green colouration is chiefly caused by the presence of specialized skin cells containing minute pigment vesicles (Fig. 1A). These pigment cells are compressed between multiple types of skin cells and possess microvilli that protrude through the integument’s polysaccharide–based cuticle. The vesicles themselves appear attached to the cells’ tonofilaments (Fig. 1B). The vesicles are densely packed within pigment cells (Fig. 2A) and are not fluorescent, which should exclude the existence of active chlorophyll within (Fig. 2B). From this data is may be inferred that the pigments are chlorophyll–derived substances (chlorins/pheophorbides), similar to what was observed in the polychaete Chaetopterus variopedatus. Oddly enough, while the latter is a filter–feeder, thus able to sequester microalgae from the water column, E. viridis is a foraging scavenger that feeds mostly on the flesh of other invertebrates. Furthermore, the animal inhabits nude rocky shores and not algal beds where its green colour would be a clear advantage, which renders further intriguing the adaptative value of this feature, however, due to some known biocidal properties of these pigments; defence should not be overruled.

P.M. Costa acknowledges the Portuguese Science and Technology Foundation (FCT) for the grant SFRH/BPD/72564/2010. The authors also thank L. Ascensão (FCUL) for the important assistance.

Type
Life Sciences
Copyright
Copyright © Microscopy Society of America 2013