TY - JOUR
T1 - Physiological axopodial activity of Rhizosphaera trigonacantha Haeckel (a spheroidal radiolarian, Polycystina, Protista)
AU - Suzuki, Noritoshi
N1 - Funding Information:
I wish to thank the staff of the Sesoko Tropical Biosphere Research Center, University of the Ryukyus. In particular, I am greatly indebted to Yoshikatsu Nakao for his kind hospitality and great help with sampling work. This research is a result of the 5th Observation Tour of Living Radiolarians at Sesoko Island, presided by Atsushi Matsuoka (Niigata University). I also express my hearty thanks to him for his direction and great help on the tour and valuable advice throughout the study. I extend my appreciation to Kiyoshi Kawabata (Osaka City Museum) for his kind permission to use the microscopic system. I would like to acknowledge all the participants of the tour for their kind help with daily laboratory work and for valuable discussion. Salinity was kindly measured by Katsunori Kimoto (Mutsu Institute for Oceanography, Japan Agency for Marine-Earth Science and Technology). The manuscript significantly benefited from comments and suggestions by two reviewers, O. Roger Anderson and Giuseppe Cortese, and Ellen Thomas provided a very useful final edit of the manuscript. I am partly supported by the 21st Century Center-Of-Excellence program, “Advanced Science and Technology Center for the Dynamic Earth” of Tohoku University.
PY - 2005/3
Y1 - 2005/3
N2 - Plankton samples containing specimens of the Polycystine radiolarian Rhizosphaera trigonacantha Haeckel were collected from surface ocean waters influenced by the warm Kuroshio Current at a locality approximately 2 km south of Sesoko Island (Okinawa, Southwest Japan). The axopodial activity of one R. trigonacantha individual was observed for 3 days by continuously recording with two video systems. This individual possessed an inner, dark grayish-red spherical part and an outer pale liver-brown part with numerous radiating axopodia. Axopodia are radially elongated, exceed 1.2 mm in length, and may be divided distinguished into two types: proximally observable fine axopodia (Type I), and distinct, thick axopodia (Type II). Most axopodia are Type I; few Type II axopodia radiate from the ectoplasm. Rhizosphaera trigonacantha lacks chlorophyll-bearing symbionts, as shown by autofluorescent microscopy with UV-excitation. The video recordings show that most axopodia remain elongated for hours, but a few Type II axopodia show intermittent, irregular contraction, and extension. The movement of Type II axopodia can be divided into four phases based on the state of the axopodia and movement of axopodial particles: a short phase (S-phase), an extension phase (E-phase), a long phase (L-phase), and a contraction phase (C-phase). The C-phase is divided into two subphases, CI and CII. The systematic extension and contraction of axopodia is easily disrupted by external disturbance. The function of axopodia in R. trigonacantha is not well understood, but three hypotheses are proposed: (1) the immobile phase of most axopodia is associated with the planktonic lifestyle and the maintenance of buoyancy; (2) the sudden contraction provides escape, e.g., against attack; and (3) axopodial extension and contraction on a limited part of the ectoplasm serves in predation.
AB - Plankton samples containing specimens of the Polycystine radiolarian Rhizosphaera trigonacantha Haeckel were collected from surface ocean waters influenced by the warm Kuroshio Current at a locality approximately 2 km south of Sesoko Island (Okinawa, Southwest Japan). The axopodial activity of one R. trigonacantha individual was observed for 3 days by continuously recording with two video systems. This individual possessed an inner, dark grayish-red spherical part and an outer pale liver-brown part with numerous radiating axopodia. Axopodia are radially elongated, exceed 1.2 mm in length, and may be divided distinguished into two types: proximally observable fine axopodia (Type I), and distinct, thick axopodia (Type II). Most axopodia are Type I; few Type II axopodia radiate from the ectoplasm. Rhizosphaera trigonacantha lacks chlorophyll-bearing symbionts, as shown by autofluorescent microscopy with UV-excitation. The video recordings show that most axopodia remain elongated for hours, but a few Type II axopodia show intermittent, irregular contraction, and extension. The movement of Type II axopodia can be divided into four phases based on the state of the axopodia and movement of axopodial particles: a short phase (S-phase), an extension phase (E-phase), a long phase (L-phase), and a contraction phase (C-phase). The C-phase is divided into two subphases, CI and CII. The systematic extension and contraction of axopodia is easily disrupted by external disturbance. The function of axopodia in R. trigonacantha is not well understood, but three hypotheses are proposed: (1) the immobile phase of most axopodia is associated with the planktonic lifestyle and the maintenance of buoyancy; (2) the sudden contraction provides escape, e.g., against attack; and (3) axopodial extension and contraction on a limited part of the ectoplasm serves in predation.
KW - entactinaria
KW - living radiolaria
KW - physiological ecology
KW - polycystine
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U2 - 10.1016/j.marmicro.2004.08.005
DO - 10.1016/j.marmicro.2004.08.005
M3 - Article
AN - SCOPUS:14644425972
SN - 0377-8398
VL - 54
SP - 141
EP - 153
JO - Marine Micropaleontology
JF - Marine Micropaleontology
IS - 3-4
ER -