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Journal of Marine Biology
Volume 2012 (2012), Article ID 382498, 5 pages
Raphides in the Uncalcified Siphonous Green Seaweed, Codium minus (Schmidt) P. C. Silva
Dauer Electron Microscopy Laboratory, Department of Biology, The University of Miami, P.O. Box 249118, Coral Gables, FL 33124, USA
Received 17 February 2012; Revised 12 April 2012; Accepted 16 April 2012
Academic Editor: Wen-Xiong Wang
Copyright © 2012 Jeffrey S. Prince. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
The vacuole of utricles, the outermost cell layer of the siphonous green seaweed, Codium minus, had numerous single needles and needle bundles. The crystals composing each needle appeared arranged in a twisted configuration, both ends were pointed, and each needle was contained in a matrix or membrane; bundles of needles appeared enclosed by a matrix. Chemical and electron diffraction analysis indicated that the needles consisted of calcium oxalate. This is the first paper on terrestrial plant-like raphides in an alga.
Bundles of acicular crystals of calcium oxalate formed in specialized cells, idioblasts, are termed raphides in embryophytes [1–3]. Only one bundle of needles occurs per idioblast; the needles are long; needle length from several key pacific economic plants had a mean minimum length of 43 μm . Each needle in a bundle is enclosed in a membrane, the crystal chamber [5–7], and bundles are enclosed by a water-soluble organic matrix, termed the vacuolar matrix [5, 8]. Raphides can burst through mature idioblasts due to swelling of the large amounts of mucilage contained in the cell . Single needles do not occur in terrestrial plants but only as a bundle of needles [9, 10]. Individual needles, raphide, are found as microfossils in soils .
Abundant evidence supports the role of these needles in deterring vertebrate and invertebrate herbivory [1, 3, 7, 11, 12]. Raphides abrade the mouth and digestive tract of terrestrial herbivores causing edema; in addition, grooves in the needles may inject noxious plant metabolites and bacteria into these grazers .
Defense against herbivory in the marine environment generally involves calcification of the outer surface of green, red, and brown seaweeds . This hard outer surface of calcium carbonate not only increases the difficulty of getting to the soft inner tissue, but consumption of the hard outer matrix can also alter the digestive pH, a deterrent for several herbivores [1, 13]. No alga has been found to have raphides. Where needles (acicular crystals) have been found, they appear singly, not in bundles of needles; they are surrounded by a vacuolar membrane or crystal chamber but not both, are generally very small, or reside individually in the cytoplasm and not the cell vacuole [14–18]. Single needles also occur in the cell vacuole of both lightly calcified parts of otherwise heavily calcified seaweeds [19–21].
We provide the first report of calcium oxalate crystals with all the characteristics that typify raphides of terrestrial plants. Large numbers of single needles and raphides (bundles of them) were found in the cell vacuole of an uncalcified green seaweed. The crystals in each acicular needle appeared twisted; individual needles were enclosed in a matrix or membrane, while bundles of needles were surrounded by a matrix. Single needles and raphides were located within the central cell vacuole and against the peripheral cytoplasmic layer.
2. Materials and Methods
Codium minus was collected on 13 July, 2003 from the Izu Peninsula, Honshu, Japan, fixed in copious 4% neutral formalin in sea water for several days, loosely wrapped in paper toweling saturated with fixative, placed in Ziploc bags, and shipped to the USA. Digital light micrographs of whole utricles were taken with an Olympus BX60. For scanning electron microscopy (SEM), utricles were rinsed in distilled water, and their contents were isolated onto stubs, air dried, and then visualized uncoated with a Jeol 5600LV scanning electron microscope.
For elemental analysis, samples with a similar preparation as above were analyzed uncoated using a Link/Oxford ISIS 300 (EDS) system ancillary to a Philips/FEI XL30 ESEM-FEG scanning electron microscope (SEM) operated in the environmental mode (1 to 10 torr.). Needles were analyzed so as to minimize beam interaction with the stub (an aluminum alloy containing copper, Figure 2).
For transmission electron microscopy (TEM), utricles were first rinsed in distilled water, and their contents were squeezed onto formvar-coated grids and examined, unstained with a Philips 300 electron microscope at 60 kV. Electron diffraction ring patterns were also obtained with the Philips 300 at 80 kV and 0 tilt.
Solubilities of the needles were tested by exposing whole specimens to 1.0 N hydrochloric acid, 5.25% sodium hypochlorite (commercial bleach), or 67% aqueous acetic acid [16, 19, 22]. The Yasue  method for calcium oxalate localization was done according to that described by Pueschel  using dithiooxamide (Sigma Chemical) which results in calcium oxalate inclusions staining densely black.
The thallus of Codium minus, a pulvinate Codiaceae, had a mean diameter of 30 mm (, 21; SD, N; Figure 1(A)). Needles and raphides (needle bundles) were found in all terminal utricles in such numbers that they caused a glistening hue to the utricle under low magnification (Figure 1(B)). They were absent from the medullary filaments that compose the mass of the central portion of the thallus. Both ends of the needles were drawn out into a point. Sizes ranged from 31 to 72 μm long (; 12 mean, SD, N) by 0.5 to 1.3 μm (; 12 mean, SD, N) wide (Figures 1(B), 1(C), and 1(D)). All needles in needle bundles, raphides, were oriented in the same direction, forming a large compound needle (Figures 1(D) and 1(G)). Optical section found that individual needles and bundles were located throughout the large central vacuole of the utricle as well as against the cytoplasm lining the cell wall. Light microscopy of raphides found a membrane or matrix surrounding the entire structure (Figure 1(D)). TEM showed a membrane-like matrix surrounding the tips of individual needles (Figure 1(F)); this membrane became obscure in the needle body. Crystalline globular material that composed the needle appeared to be arranged in a helical pattern (Figure 1(E), brackets). Under the SEM, however, the needles appeared smooth and uniform, and no globular substructure was apparent (Figure 1(C)).
Chemical tests found that needles failed to dissolve after 2 hrs in cold or warm (70°C) acetic acid (67%) or Clorox (5.25%). Hydrochloric acid (1 N) dissolved the needles in 5 to 10 min but without release of any gas. The Yasue [16, 22] method for localization of calcium oxalate found both single and compound needles outside of the utricles stained densely (Figure 1(G)), at times with a precipitate about them; needles within utricles did not stain.
EDS-SEM of the needles found strong signals for calcium, while signals for copper and aluminum appeared to originate from the stub (Figure 2). Electron diffraction patterns for the needles appeared to more closely match, those for calcium oxalate than those for calcium carbonate (Table 1).
This is the first paper on embryophyte-type raphides (bundles of acicular needles) in an alga. Raphides apparently dissociated within the vacuole of the utricle forming quantities of single needles. Single needles and needle bundles were found in the vacuole of utricles of Codium minus in such numbers that these cells glisten under low magnification. EDS-SEM found strong signals for calcium, while electron diffraction analysis suggested that the needles consisted of calcium oxalate. This was further supported by various chemical tests. Needles were found only in the utricles (the outer most, green layer of Codium species) and were not found in the internal portion of the plant composed of colorless intertwined medullary filaments. But in this group of seaweeds, there are no cross-walls; thus, utricles and medullary filaments share a common cytoplasm .
Raphides in embryophytes are formed in idioblasts, specialized cells that form crystals of various size, morphology and composition . Idioblasts that form raphides are located in all portions of terrestrial plants and have an enlarged nucleus, a dense cytoplasm, and a small to absent vacuole [4, 7]. A small vacuole appears and is the site for crystal nucleation; the vacuole membrane and cell itself markedly expand during growth of the crystal . The vacuole membrane, vacuolar matrix, appears granular at maturity under the scanning electron microscope and is apparently water soluble . Idioblasts that give rise to raphides produce a single bundle of multiple, parallel-aligned, needle-like crystals [5, 11]. In some cases, needles within a bundle can be disorganized . Each needle of a bundle, raphide, is contained within an additional membrane, the crystal chamber, which apparently dictates both the shape and precipitation of the crystal itself . Raphides at maturity are often contained in very large cells, the raphides consuming most of the idioblast, while mucilage frequently fills the remaining available space [9, 10]. Swelling of the mucilage causes the cell to burst ejecting the raphides to the outside of the plant . A single needle, raphide, furthermore, refers to needles outside the plant or microfossils found in soils [3, 4].
The definition of raphides as described above for embryophytes, therefore, requires the presence of several traits: needles developing in a specialized cell (idioblast) with an enlarged nucleus and dense cytoplasm; needles occurring in bundles; large needle size, one bundle per cell; a crystal chamber about each needle; a vacuolar matrix about a bundle of needles. As mentioned above, no paper on raphides in marine or fresh water algae meets these requirements including those found in C. minus, the current paper. But the needles in C. minus do meet the following traits for raphides: they have a mean length greater than the minimum mean length of raphides in many pacific economic plants ; they are composed of calcium oxalate; the needles occur in bundles, each bundle surrounded by a matrix (vacuolar matrix?); a crystal chamber apparently surrounds each needle. But raphides in embryophytes occur singly per cell, while each utricle has several needle bundles. But the whole thallus of Codium minus is a single cell as cross-walls are absent. The traits of C. minus, that do not meet the definition of terrestrial raphides are, therefore, several bundles per cell, the cell also being multinucleate. Is there a connection between production of needle bundles in the multinucleate, siphonous alga, C. minus, and evolution of raphides in land plants?
Dawes  and Leliaert and Coppejans  found abundant calcium oxalate needles (35–55 μm in length) in the vacuole of all cells in the endemic Australian coenocytic green alga, Apjohnia laetevirens Harvey. Calcium oxalate crystals have been recorded for other noncalcified algae. Pueschel  found small, cruciate crystals in the peripheral cytoplasm but not within the vacuole of the fresh water green alga, Spirogyra. Antithamnion, a marine red alga, had single needles up to 30 μm in length in the peripheral cytoplasm [15, 18]. The length of the needles in Antithamnion, though shorter than those in C. minus, suggested that they may adversely affect herbivores , but the bipyramidal morphology of crystals (apparently surrounded by an organic matrix = the vacuolar membrane?) in Chaetomorpha, a marine green seaweed, probably negates their role in grazer defense . Other papers [14, 15, 17] also describe needles, in some cases more than 100 μm long. All of these papers describe, however, only single needles, not bundles of them and, in addition, may describe the presence of a crystal chamber or vacuolar matrix but not both.
The acicular shape of raphides appears to be a critical component of plant defense against herbivory [7, 11]. These acicular crystals may also bear barbs or grooves . Arnott and Webb  found that raphides in grape (Vitis) are twinned (indicated by one end being forked, the opposite pointed), the twinning occurs along the long axis of the raphide, and the crystal lattice rotates around the twin axis. This rotation of the crystal lattice structure is thought to enhance crystal stability and growth . The calcium oxalate needles described for C. minus share similarities to raphides described for grape. (1) Needles in C. minus and those in grape have a similar range in length, but those in C. minus were approximately half as wide. Raphides in grape, as mentioned above, are twinned crystals, and the width of one twin is approximately, that of the nontwinned needle in C. minus (both ends of which were pointed). (2) The crystals composing the needle appear to be twisted (twisting in C. minus, however, appeared to occur at a greater frequency than that in grape). (3) Each needle in C. minus, as mentioned above, is enclosed in a crystal chamber, a bundle of needles in a vacuolar matrix.
The crystal chamber surrounding each needle in a bundle appears to share many similarities with the silicalemma of diatoms . Both are single-membrane sacks, each apparently provides an internal surface for crystal nucleation and deposition, and both determine the mature crystal morphology . The silicalemma deposits the highly characteristic, taxonomically important, silicon frustule of diatoms, while the crystal chamber appears to be involved with calcium deposition as either carbonate or oxalate in the shape of a needle or more elaborate shape.
Raphides within noncalcified green seaweeds is one possible mechanism for defense against herbivory. Another is the lack of the production of a chemical attractant for grazers. Prince and Leblanc  found that Codium fragile did not produce an attractant for Strongylocentrotus droebachiensis, the green sea urchin. Green sea urchins would graze on C. fragile only if they happen to come across it. On the other hand, the brown kelp, Laminaria saccharina, produces a strong attractant for green sea urchins resulting in urchin barrens where once kelp beds were dominant .
The author would like to thank Dr. Cynthia Trowbridge for collecting Codium minus, Dr. Matt Lynn who provided the electron diffraction patterns and elemental analysis of the needles, and Dr. Barbara Whitlock for her comments on the paper.
- M. E. Hanley, B. B. Lamont, M. M. Fairbanks, and C. M. Rafferty, “Plant structural traits and their role in anti-herbivore defence,” Perspectives in Plant Ecology, Evolution and Systematics, vol. 8, no. 4, pp. 157–178, 2007.
- S. Lev-Yadun and M. Halpern, “External and internal spines in plants insert pathogenic microorganisms into herbivore's tissue for defense,” in Microbial Ecology Research Trends, T. Van Dijk, Ed., pp. 155–168, Nova Science Pubs., Inc., New York, NY, USA, 2008.
- G. G. Coté, “Diversity and distribution of idioblasts producing calcium oxalate crystals in Dieffenbachia seguine (Araceae),” American Journal of Botany, vol. 96, no. 7, pp. 1245–1254, 2009.
- A. Crowther, “Morphometric analysis of calcium oxalate raphides and assessment of their taxonomic value for archeological microfossils,” in Archeological Science Beneath the Microscope: Studies in Residue and Ancient DNÅ Analysis in Honor of Thomas H. Loy, H. Haslam, G. Robertson, A. Crowther, S. Nugent, and L. Kirkwood, Eds., pp. 102–210, Australian National University Press, Canberra, Australia, 2009.
- M. A. Webb, J. M. Cavaletto, N. C. Carpita, L. E. Lopez, and H. J. Arnott, “The intravacuolar organic matrix associated with calcium oxalate crystals in leaves of Vitis,” Plant Journal, vol. 7, no. 4, pp. 633–648, 1995.
- C. J. Prychid, R. S. Jabaily, and P. J. Rudall, “Cellular ultrastructure and crystal development in Amorphophallus (Araceae),” Annals of Botany, vol. 101, no. 7, pp. 983–995, 2008.
- V. R. Franceschi and P. A. Nakata, “Calcium oxalate in plants: formation and function,” Annual Review of Plant Biology, vol. 56, pp. 41–71, 2005.
- V. R. Franceschi and H. T. Horner, “Calcium oxalate crystals in plants,” The Botanical Review, vol. 46, no. 4, pp. 361–427, 1980.
- K. Esau, Plant Anatomy, John Wiley & Sons, New York, NY, USA, 1965.
- C. R. Metcalf and L. Chalk, Anatomy of Dicotyledons, Leaves, Stem, and Wood in Relation to Taxonomy with Notes on Economic Uses, vol. 1-2, Claredon Press, Oxford, UK, 1950.
- H. J. Arnott and M. A. Webb, “Twinned raphides of calcium oxalate in grape (Vitis): implications for crystal stability and function,” International Journal of Plant Sciences, vol. 161, no. 1, pp. 133–142, 2000.
- J. M. Kingsbury, Poisonous Plants of the United States and Canada, Prentice-Hall Inc., Englewood Cliffs, NJ, USA, 1964.
- M. E. Hay, Q. E. Kappel, and W. Fenical, “Synergisms in plant defenses against herbivores: interactions of chemistry, calcification, and plant quality,” Ecology, vol. 75, no. 6, pp. 1714–1726, 1994.
- D. Menzel, “Fine structure of vacuolar inclusions in the siphonous green alga Chlorodesmis fastigiata (Udoteaceae, Caulerpales) and their contribution to plug formation,” Phycologia, vol. 26, no. 2, pp. 205–221, 1987.
- C. M. Pueschel, “Calcium oxalate crystals in the red alga Antithamnion kylinii (Ceramiales): cytoplasmic and limited to indeterminate axes,” Protoplasma, vol. 189, no. 1-2, pp. 73–80, 1995.
- C. M. Pueschel, “Calcium oxalate crystals in the green alga Spirogyra hatillensis (Zygnematales, Chlorophyta),” International Journal of Plant Sciences, vol. 162, no. 6, pp. 1337–1345, 2001.
- C. M. Pueschel, “Calcium oxalate crystals in the green alga Spirogyra hatillensis (Zygnematales, Chlorophyta),” Journal of Phycology, vol. 32, s. 3, pp. 55–56, 2002.
- C. M. Pueschel and J. A. West, “Effects of ambient calcium concentration on the deposition of calcium oxalate crystals in Antithamnion (Ceramiales, Rhodophyta),” Phycologia, vol. 46, no. 4, pp. 371–379, 2007.
- E. I. Friedmann, W. C. Roth, J. B. Turner, and R. S. Mcewen, “Calcium oxalate crystals in the aragonite-producing green alga Penicillus and related genera,” Science, vol. 177, no. 4052, pp. 891–893, 1972.
- J. B. Turner and E. I. Friedmann, “Fine structure of capitular filaments in the coenocytic green alga Penicillus,” Journal of Phycology, vol. 10, no. 2, pp. 125–134, 1974.
- L. Bohm and D. Futterer, “Algal calcification in some Codiaceae (Chlorophyta): ultrastructure and location of skeletal deposits,” Journal of Phycology, vol. 14, no. 4, pp. 486–493, 1978.
- T. Yasue, “Histochemical identification of calcium oxalate,” Acta Histochemistry and Cytochemistry, vol. 2, no. 3, pp. 83–95, 1969.
- R. E. Lee, Phycology, Cambridge University Press, New York, NY, USA, 1980.
- C. J. Dawes, “A study of the ultrastructure of a green alga, Apjohnia laetevirens Harvey with emphasis on the cell wall structure,” Phycologia, vol. 8, no. 2, pp. 77–84, 1969.
- F. Leliaert and E. Coppejans, “Crystalline cell inclusions: a new diagnostic character in the Cladophorophyceae (Chlorophyta),” Phycologia, vol. 43, no. 2, pp. 189–203, 2004.
- C. M. Pueschel and J. A. West, “Cellular localization of calcium oxalate crystals in Chaetomorpha coliformis (Cladophorales; Chlorophyta): evidence of vacuolar differentiation,” Phycologia, vol. 50, no. 4, pp. 430–435, 2011.
- W. S. Sakai, S. S. Shiroma, and M. A. Nagao, “Study of Raphide Microstructure in Relation to Irritation,” Scanning Electron Microscopy, pt. 2, pp. 979–986, 1984.
- J. S. Prince and W. G. Leblanc, “Comparative feeding preference of Strongylocentrotus droebachinesis (Echinoidea) for the invasive green seaweed Codium fragile ssp. tomemtosoides (Chlorophyceae) and four other seaweeds,” Marine Biology, vol. 113, no. 1, pp. 159–163, 1992.