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Thalassia

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Journal Article
Published: 01 September 1987
Journal of Sedimentary Research (1987) 57 (5): 901–906.
...M. N. Almasi; C. M. Hoskin; J. K. Reed; J. Milo Abstract Sediment traps were used to measure the rate of deposition in a Thalassia seagrass meadow and in an adjacent (sandy) grass-free area. The average depositional rate of mud in the Thalassia bed was 4.96 g trap (super -1) week (super -1...
Journal Article
Published: 01 September 1986
Journal of Sedimentary Research (1986) 56 (5): 622–628.
... Spirobis sp. live as epibionts on the leaves of Thalassia testudinum, the extensive marine grass. The lime mud produced by the epibionts was estimated by quantifying 1) the life span of Thalassia ; 2) the abundance of Thalassia ; and 3) the average amount of epibiont calcium carbonate per blade...
Journal Article
Published: 01 September 1972
Journal of Sedimentary Research (1972) 42 (3): 687–689.
...David G. Patriquin Abstract An estimate of the carbonate mud production by epibionts on Thalassia at Barbados, 2800 g/m 2 year for a typical stand, is 16 times Land's estimate for Jamaican Thalasia beds. The difference is considered in part real, and in part due to Land's estimate being somewhat...
Journal Article
Published: 01 December 1970
Journal of Sedimentary Research (1970) 40 (4): 1361–1363.
...Lynton S. Land Abstract Epibiotic growth of coralline red algae and serpulid worms on the marine turtle grass Thalassia testudinum is sufficient to produce carbonate mud at rates comparable to the rates of accumulation of ancient platform carbonates. GeoRef, Copyright 2008, American Geological...
Journal Article
Journal: AAPG Bulletin
Published: 01 September 1969
AAPG Bulletin (1969) 53 (9): 2033.
...Wayne D. Bock The marine grass Thalassia testudinum König is distributed throughout the West Indian region and the island of Bermuda. Its distribution is controlled by temperature, salinity, turbulence, and depth. It supplies a substrate for many organisms including benthonic Foraminifera. Sixty...
Image
Autocorrelograms for selected measures on Thalassia rhizomes (A–D) and Penicillus capitulae (E–H). A, E, information function H on (A) Thalassia and (E) Penicillus, respectively; B, F, Guild 1 on (B) Thalassia and (F) Penicillus; C, G, Guild II on (C) Thalassia and (G) Penicillus; D, H, Guild III on (D) Thalassia and (H) Penicillus.
Published: 01 October 2010
F igure 7. Autocorrelograms for selected measures on Thalassia rhizomes (A–D) and Penicillus capitulae (E–H). A , E , information function H on (A) Thalassia and (E) Penicillus , respectively; B , F , Guild 1 on (B) Thalassia and (F) Penicillus ; C , G , Guild II on (C
Image
—Dense Thalassia bed binding sediment in Thalassia-Halimeda zone of Isla Perez northeast reef. Mound of sand was formed by burrowing worm.
Published: 01 May 1962
Fig. 11. —Dense Thalassia bed binding sediment in Thalassia-Halimeda zone of Isla Perez northeast reef. Mound of sand was formed by burrowing worm.
Image
Crustose coralline algae (Porolithon fragilis) that encrust Thalassia seagrass blades, Almirante Bay, Panama. A) Detail of crustose coralline patches on Thalassia blade. B) SEM photomicrograph of this coralline algae showing very distinctive cellular pattern.
Published: 01 January 2006
Figure 8 Crustose coralline algae ( Porolithon fragilis ) that encrust Thalassia seagrass blades, Almirante Bay, Panama. A) Detail of crustose coralline patches on Thalassia blade. B) SEM photomicrograph of this coralline algae showing very distinctive cellular pattern.
Journal Article
Published: 01 October 2010
Journal of Foraminiferal Research (2010) 40 (4): 327–343.
...F igure 7. Autocorrelograms for selected measures on Thalassia rhizomes (A–D) and Penicillus capitulae (E–H). A , E , information function H on (A) Thalassia and (E) Penicillus , respectively; B , F , Guild 1 on (B) Thalassia and (F) Penicillus ; C , G , Guild II on (C...
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Graphs showing population densities over time: A Long Haul Bay, foraminiferal recovery per gram of detritus (Thalassia rhizomes, Penicillus capitulae) and per gram of dried Thalassia leaf and detritus; B Mosquito Bay, foraminiferal recovery per gram of detritus from all substrates.
Published: 01 July 2007
F igure 4. Graphs showing population densities over time: A Long Haul Bay, foraminiferal recovery per gram of detritus ( Thalassia rhizomes, Penicillus capitulae) and per gram of dried Thalassia leaf and detritus; B Mosquito Bay, foraminiferal recovery per gram of detritus from all
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Published: 01 May 2016
Table 2.— Vegetation densities ( Thalassia seagrass and Halimeda algae) in experimental subenvironments .
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 Figure 6. A: Dense rhizome and rootlet system of Thalassia exposed off Eleuthera Island, Bahamas, following a hurricane. Dive knife handle in center of image for scale. Photograph courtesy of N.P. James. B: Rhizoliths exposed along edge of rock reef at Key Biscayne, Florida. Morphology, size, and orientation of fossilized root casts compare favorably to mature turtle grass (Thalassia testudinum)
Published: 01 March 2002
Figure 6. A: Dense rhizome and rootlet system of Thalassia exposed off Eleuthera Island, Bahamas, following a hurricane. Dive knife handle in center of image for scale. Photograph courtesy of N.P. James. B: Rhizoliths exposed along edge of rock reef at Key Biscayne, Florida. Morphology, size
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Time series for various measures on Thalassia rhizomes. A, the information function H; B, equitability index E; C, percentage abundance of the total assemblage in each sample as Guild I; D, percentage abundance as Guild II; E, percentage abundance as Guild III. Grey stipple marks the impact of Hurricanes Luis and Marilyn, vertical dotted lines mark boundaries between temporal abundance biozones. and arrows indicate trends within temporal abundance biozones.
Published: 01 October 2010
F igure 4. Time series for various measures on Thalassia rhizomes. A , the information function H ; B , equitability index E ; C , percentage abundance of the total assemblage in each sample as Guild I; D , percentage abundance as Guild II; E , percentage abundance as Guild III. Grey
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Cross-correlations of selected measures on Thalassia rhizomes and Penicillus capitulae for September 1994 to August 1994. A, information function H; B, equitability index E.
Published: 01 October 2010
F igure 6. Cross-correlations of selected measures on Thalassia rhizomes and Penicillus capitulae for September 1994 to August 1994. A , information function H ; B , equitability index E .
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 Figure 5. Drawing of turtle grass (Thalassia testudinum) showing general size and plant morphology. Mature plant compares favorably to distant smaller rhizomes and pneumatophores of black mangrove (Avicennia germinans). Modified from Zieman and Zieman (1989, Fig. 2)
Published: 01 March 2002
Figure 5. Drawing of turtle grass ( Thalassia testudinum ) showing general size and plant morphology. Mature plant compares favorably to distant smaller rhizomes and pneumatophores of black mangrove ( Avicennia germinans ). Modified from Zieman and Zieman (1989 , Fig. 2 )
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Subsurface sediments from Thalassia grass bed (A, B, C) and Callianassa-bioturbated sites (D, E, F) in the back-reef. A) General view of subsurface sediment from Site T. Note extensive microboring of most grains, typical "dirty" surface texture, and the abundance of fine detrital sediment debris. Scale equals 500 μm. B) Heavily bored surface of a foraminifer grain, with micrite and fine sediments on the grain surface associated with biofilm calcification and sediment trapping. Site T. Scale equals 10 μm. C) Surface of Halimeda showing well preserved peripheral utricle structure and micrite and fine sediment coating the grain surface and filling utricles. Diatoms and desiccated mucus threads are visible. Site T. Scale equals 10 μm. D) General view of subsurface sediment from Site C. Note rounding of grains, the lack of fine skeletal debris, and the clean grain surface texture. Scale equals 500 μm. E) Extensive microboring evident on the surface of a mollusc fragment, but note how the process has not resulted in complete alteration of surface ornamentation. Site C. Scale equals 50 μm. F)Halimeda fragment showing evidence of extensive dissolution. The outer cortex has been removed, and utricles of the inner cortex are exposed. Site C. Scale equals 10 μm.
Published: 01 May 2000
Figure 11 Subsurface sediments from Thalassia grass bed (A, B, C) and Callianassa -bioturbated sites (D, E, F) in the back-reef. A) General view of subsurface sediment from Site T. Note extensive microboring of most grains, typical "dirty" surface texture, and the abundance of fine detrital
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—Distribution of Thalassia and turbidity in Términos Lagoon (after Ayala-Castañares, 1963).
Published: 01 December 1971
Fig. 8 —Distribution of Thalassia and turbidity in Términos Lagoon (after Ayala-Castañares, 1963 ).
Journal Article
Journal: Paleobiology
Published: 21 January 2018
Paleobiology (2018) 44 (1): 155–170.
... in the local biota. Here, we provide evidence that dense, Thalassia -rich seagrass beds preserve a stratigraphic record of biotic variation because their dense root–rhizome mats inhibit mixing. We sampled benthic mollusk assemblages at seven localities in Thalassia -rich beds around St. Croix, USVI, collecting...
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Series: SEPM Special Publication
Published: 01 January 2009
DOI: 10.2110/sepmsp.093.083
EISBN: 9781565762978
.... 4. —Hierarchical cluster analysis of A) the vegetation taxa at each site, and B) the foraminiferal sediment assemblage, total, at each site. Note the lack of agreement between the two diagrams. Taphonomic Data Fig. 5. —Foraminiferal density versus Thalassia density at each...
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Journal Article
Journal: Geology
Published: 01 August 1990
Geology (1990) 18 (8): 790–794.
... excursion toward heavy-isotope values records the first establishment of Thalassia seagrass upon open-marine flooding. A multitracer approach, combining biofacies, lithofacies, and stable-isotope analysis of TOC confirms that the dramatic +17‰ shift observed in δ 13 C was a direct result of sea-level rise...