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radiolaria - Marum

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Radiolaria 14 Bibliography - 1989<br />

Bibliography 1989-1994<br />

Luis O'Dogherty<br />

Since Radiolaria 13, almost four years of bibliographical silence have passed. This compilation intends to cover this<br />

time span. I am perfectly aware of the impossibility to compile a complete bibliography including all existing references.<br />

Therefore, you are kindly requested to notify any mistake or omitted reference. In this place, I wish to express my most<br />

sincere thanks to all those colleagues that sending their articles had collaborated and made possible this bibliography. Thanks<br />

to everybody.<br />

Adachi, M. 1989. Discovery of Late Triassic <strong>radiolaria</strong>ns<br />

from the Ino Formation, central Shikoku. J. geol. Soc. Japan,<br />

95/1, 81-83. (in Japanese)<br />

Adams, K.E. & Siok, J.P. 1989. Permian stratigraphy<br />

in the Atigun Gorge area; a transition between the Echooka<br />

and Siksikpuk formations. In: Dalton Highway, Yukon River<br />

to Prudhoe Bay, Alaska; bedrock geology of the eastern<br />

Koyukuk Basin, central Brooks Range, andeastcentral Arctic<br />

Slope. Guidebook. (Mull, C.G. et al., Eds.), vol. 7. Alaska<br />

Division of geological and geophysical Surveys, Report, pp.<br />

267-276.<br />

Alexandrovich, J.M. 1989. Radiolarian biostratigraphy<br />

of ODP Leg 111, Site 677, eastern equatoria6l Pacific, Late<br />

Miocene through Pleistocene. In: Proceedings of the Ocean<br />

Drilling Program, Scientific Results. (Becker, K., Sakai, H. et<br />

al., Eds.), vol. 111. College Station, TX (Ocean Drilling<br />

Program), pp. 245-262.<br />

Well-preserved late Miocene through Pleistocene age<br />

<strong>radiolaria</strong>n assemblages were recovered during ODP Leg 111 at Site<br />

677, on the southern flank of the Costa Rica Rift in the eastern<br />

equatorial Pacific. Radiolarian "event" biostratigraphy (first and last<br />

morphotypic appearances) was established for Holes 677A and<br />

677B using 21 species yielding 24 reliable datum levels. The cold<br />

upwelling waters above this site have prevented many typical<br />

tropical Pacific stratigraphic <strong>radiolaria</strong>ns from being useful age<br />

indicators. Biostratigraphic datum levels were assigned absolute<br />

ages based on previous work and were used to date the cores.<br />

Sedimentation rates varied from 3.7 cm/1000 yr. in the late<br />

Pleistocene to 6.0 cm/1000 yr. in the late Miocene. The age of the<br />

oldest sediments at this site is estimated as 5.89-6.37 Ma, which<br />

indicates that Site 677 is between magnetic anomalies 3A and 4. A<br />

total of 67 taxa were assessed for stratigraphic relevance at this<br />

site and are listed in the Appendix. One previously unknown Pliocene<br />

<strong>radiolaria</strong>n stratigraphic indicator, Botryostrobus euporus<br />

(Ehrenberg), is identified.<br />

Alexandrovich, J.M. & Hays, J.D. 1989. Highresolution<br />

stratigraphic correlation of ODP Leg 111 Holes<br />

677A and 677B and DSDP Leg 69 Hole 504. In: Proceedings<br />

of the Ocean Drilling Program, Scientific Results. (Becker,<br />

K., Sakai, H. et al., Eds.), vol. 111. College Station, TX<br />

(Ocean Drilling Program), pp. 263-276.<br />

The recovery of continuous sedimentary sequences has been<br />

and is a high-priority goal of the Ocean Drilling Program, yet its<br />

success has not been determined. We test the stratigraphic<br />

continuity of continuously cored sequences from ODP Leg 111 Holes<br />

677A and 677B and DSDP Leg 69 Hole 504. The two holes at Site<br />

677 and Hole 504 are correlated using high-resolution<br />

biostratigraphy, tephra stratigraphy, and time series of opaline silica<br />

and calcium carbonate. The correlation coefficient between the time<br />

series is maximized through an inverse correlation procedure.<br />

Changes in slope of the mapping function that relates the two<br />

sections indicate gaps or changes in the accumulation rate between<br />

sections. We assume as a first approximation that the sedimentary<br />

sequences are identical in each hole, given their close proximity.<br />

Slope changes of the mapping functions therefore result from errors<br />

introduced by coring. This assumption is justified by the fact that<br />

most mapping function slope changes occur at core breaks. Having<br />

identified missing sections in one site, it is possible to fill these<br />

gaps with the appropriate section from the adjacent site, thereby<br />

improving continuity. This is possible only where the sediment gaps<br />

identified at core breaks in one hole do not correspond to core break<br />

levels in the other hole. Results show that in the upper 100 m of the<br />

stratigraphic column, 3.1°70 and 4.6°70 were unsampled in Holes<br />

1989<br />

- 23 -<br />

677A and 677B, respectively, and 15°70 of the Pliocene portion of<br />

Hole 504 was not sampled by the hydraulic piston corer. This<br />

indicates that even in relatively calm seas, double or triple coring is<br />

required in order to ensure that gaps and doubly sampled intervals of<br />

the stratigraphic column which occur at core breaks are recognized<br />

and sampled at least once.<br />

Anderson, O.R. 1989. Some observations of feeding<br />

behavior, growth, and test particlemorphology of a silicasecreting<br />

testae Amoeba Netzelia tuberculata (Wallich)<br />

(Rhizopoda, Testacea) grown in laboratory culture. Arch.<br />

Protistenkunde, 137, 211-221.<br />

Netzelia tuberculata (WALLICH) fed with Iyophilized yeast in<br />

laboratory culture grows more rapidly (mean doubling time = 1.7 d)<br />

and produces siliceous test particles that are more smooth,<br />

spheroidal and regularly arranged than those fed with Spirogyra<br />

(mean doubling time = 3 1 d). The change in test particle morphology<br />

is observable during test secretion of the daughter cell in the first<br />

generation after transfer into a yeast medium. Successive<br />

generations exhibit increasingly more smooth and regularly arranged<br />

spheroidal test particles. N. tuberculata grown in a medium<br />

containing only soluble silicate (21 µM sodium silicate) reproduced<br />

and secreted siliceous test particles. Hence, a particulate source of<br />

silicate is not necessary for test particle synthesis. These results<br />

give further evidence of the ecophenotypic variation in test particle<br />

morphology of Netzelia tuberculata, in this case induced by<br />

variations in kind of food, and suggest that additional research is<br />

warranted on the cellular processes that determine the morphology<br />

of biomineralized products in these testate amoebae.<br />

Anderson, O.R., Bennett, P. & Bryan, M. 1989a.<br />

Experimental and observational studies of <strong>radiolaria</strong>n<br />

physiological ecology: 1. Growth, abundance and opal<br />

productivity of the spongiose <strong>radiolaria</strong>n Spongaster tetras<br />

tetras. Mar. Micropaleontol., 14/4, 257-266.<br />

The mean growth, longevity and percent of S. tetras tetras<br />

producing swarmers in laboratory-cultures were examined as a<br />

function of variations in water temperature, salinity and the<br />

intensity of illumination. Radiolaria were grown as individuals in<br />

optically clear glass vials maintained in environmentally controlled<br />

water baths and observed daily by light microscopy. The optimum<br />

growth and longevity occurred at moderately warmer temperatures<br />

and higher salinities (e.g. 27.5°C and 40‰ salinity) where maximum<br />

survival was 23 days compared to 4 days at a temperature of 21°C<br />

and 30‰ salinity. At higher temperatures of 33°C and 36°C, the<br />

maximum longevity was 2 and zero days respectively. Light was<br />

required for production of reproductive swarmers, but not for<br />

growth. At temperatures near or below 15°C, the axopodia became<br />

aggregated together or remained permanently withdrawn<br />

incumbering food gathering. Few individuals produced reproductive<br />

swarmers at 15°C and none produced swarmers at a temperature of<br />

10°C. These data indicate that S. tetras tetras may be restricted to<br />

warmer temperature water masses with an upper limit near 31°C.<br />

They survive better with higher salinity and warmer water (c. 28°C).<br />

Cold water and particularly dark conditions that occur at great<br />

depth, may not support large populations of S. tetras tetras since<br />

swarmer release is inhibited and, among other factors, food<br />

gathering is suppressed due to axopodial impairment.<br />

Anderson, O.R., Bennett, P., Angel, D. & Bryan,<br />

M. 1989b. Experimental and observational studies of<br />

<strong>radiolaria</strong>n physiological ecology: 2. Trophic activity and<br />

symbiont primary productivity of Spongaster tetras tetras<br />

with comparative data on predatory activity of some<br />

Nassellarida. Mar. Micropaleontol., 14/4, 267-273.

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