radiolaria - Marum
radiolaria - Marum
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.