scholarly journals Diet-dependent δ13C and δ15N fractionation among sea urchin Lytechinus variegatus tissues: implications for food web models

2012 ◽  
Vol 462 ◽  
pp. 175-190 ◽  
Author(s):  
P Prado ◽  
RH Carmichael ◽  
SA Watts ◽  
J Cebrian ◽  
KL Heck
Keyword(s):  
Food Web ◽  
Sea Urchin ◽  
Lytechinus Variegatus ◽  
Δ13c And Δ15n

The effect of dietary protein on consumption, survival, growth and production of the sea urchin Lytechinus variegatus

Aquaculture ◽  
2006 ◽  
Vol 254 (1-4) ◽  
pp. 483-495 ◽  
Author(s):  
Hugh Hammer ◽  
Stephen Watts ◽  
Addison Lawrence ◽  
John Lawrence ◽  
Renee Desmond
Keyword(s):  
Sea Urchin ◽  
Dietary Protein ◽  
Lytechinus Variegatus

scholarly journals The influence of fish cage culture on δ13C and δ15N of filter-feeding Bivalvia (Mollusca)

2013 ◽  
Vol 73 (4) ◽  
pp. 743-746
Author(s):  
E. Benedito ◽  
L. Figueroa ◽  
A.M Takeda ◽  
GI. Manetta
Keyword(s):  
Food Web ◽  
Native Species ◽  
Corbicula Fluminea ◽  
Cage Culture ◽  
Aquatic Food Web ◽  
Δ13c And Δ15n ◽  
Value Analysis ◽  
Fine Powders ◽  
Before And After ◽  
Aquatic Food

The objective of this study was to evaluate the effect of Oreochromis niloticus cage culture promoted variations in the δ13C and δ15N in Corbicula fluminea (Mollusca; Bivalvia) and in the sediment of an aquatic food web. Samples were taken before and after net cage installation in the Rosana Reservoir (Paranapanema River, PR-SP). Samples of specimens of the bivalve filterer C. fluminea and samples of sediment were collected using a modified Petersen grab. All samples were dried in an oven (60 °C) for 72 hours, macerated to obtain homogenous fine powders and sent for carbon (δ13C) and nitrogen (δ15N) isotopic value analysis in a mass spectrometer. There were significant differences in the δ13C and δ15N values of the invertebrate C. fluminea between the beginning and the end of the experiment. There were no differences between the δ13C and δ15N values of sediment. These results indicate that the installation of fish cage culture promoted impacts in the isotopic composition of the aquatic food web organisms, which could exert influence over the native species and the ecosystem.

Stable isotope analysis reveals partitioning in prey use by Kajikia audax (Istiophoridae), Thunnus albacares, Katsuwonus pelamis, and Auxis spp. (Scombridae) in the Eastern Tropical Pacific of Ecuador

2021 ◽  
Vol 19 (4) ◽  
Author(s):  
Rigoberto Rosas-Luis ◽  
Nancy Cabanillas-Terán ◽  
Carmen A. Villegas-Sánchez
Keyword(s):  
Stable Isotope ◽  
Food Web ◽  
Stable Isotope Analysis ◽  
Trophic Ecology ◽  
Isotope Analysis ◽  
Middle Level ◽  
Food Sources ◽  
Thunnus Albacares ◽  
Katsuwonus Pelamis ◽  
Δ13c And Δ15n

Abstract Kajikia audax, Thunnus albacares, Katsuwonus pelamis, and Auxis spp. occupy high and middle-level trophic positions in the food web. They represent important sources for fisheries in Ecuador. Despite their ecological and economic importance, studies on pelagic species in Ecuador are scarce. This study uses stable isotope analysis to assess the trophic ecology of these species, and to determine the contribution of prey to the predator tissue. Isotope data was used to test the hypothesis that medium-sized pelagic fish species have higher δ15N values than those of the prey they consumed, and that there is no overlap between their δ13C and δ15N values. Results showed higher δ15N values for K. audax, followed by T. albacares, Auxis spp. and K. pelamis, which indicates that the highest position in this food web is occupied by K. audax. The stable isotope Bayesian ellipses demonstrated that on a long time-scale, these species do not compete for food sources. Moreover, δ15N values were different between species and they decreased with a decrease in predator size.

Transcription of the Spec 1-like gene of Lytechinus is selectively inhibited in response to disruption of the extracellular matrix

Development ◽  
1989 ◽  
Vol 106 (2) ◽  
pp. 355-365 ◽  
Author(s):  
G.M. Wessel ◽  
W. Zhang ◽  
C.R. Tomlinson ◽  
W.J. Lennarz ◽  
W.H. Klein
Keyword(s):  
Extracellular Matrix ◽  
Sea Urchin ◽  
Cdna Clone ◽  
Lytechinus Variegatus ◽  
Gene Products ◽  
Lytechinus Pictus ◽  
Collagenous Matrix ◽  
Cell Type Specific ◽  
Differential Gene ◽  
And Control

The influence of the extracellular matrix (ECM) on differential gene expression during sea urchin development was explored using cell-type-specific cDNA probes. The ECM of three species of sea urchin, Strongylocentrotus purpuratus, Lytechinus variegatus and Lytechinus pictus, was disrupted with the lathrytic agent beta-aminopropionitrile (BAPN), which inhibits collagen deposition in the ECM and arrests gastrulation (Wessel & McClay, Devl Biol. 121: 149, 1987). The levels of several mRNAs (Spec 1, Spec 2, CyIIa actin, CyIIIa actin and collagen in S. purpuratus, and metallothionine, ubiquitin and LpS3 in L. pictus and L. variegatus) were compared in BAPN-treated and control embryos. These mRNAs accumulated normally during BAPN treatment, even though the embryos did not gastrulate. To determine if the expression of any gene product is sensitive to ECM disruption, a differential cDNA screen compared poly (A+) RNA from BAPN-arrested and control embryos in Lytechinus. A cDNA clone was isolated from this screen that represented a 2.1 kb mRNA that did not accumulate during BAPN treatment. Removal of BAPN resulted in the accumulation of this transcript coincident with the onset of gastrulation. This cDNA clone encodes a L. variegatus homologue of LpS1, recently demonstrated to be an ancestral homologue of the aboral ectoderm-specific Spec 1-Spec 2 gene family in S. purpuratus. Nuclear run-on assays in L. pictus suggested that transcriptional activity of LpS1 was selectively inhibited by BAPN treatment. Thus, although the accumulation of many gene products occurred independently of the embryonic collagenous matrix, the accumulation of LpS1 and LvS1 appeared to be mediated by the ECM.

Tracing sewage-derived organic matter into a shallow groundwater food web using stable isotope and fluorescence signatures

2011 ◽  
Vol 62 (2) ◽  
pp. 119 ◽  
Author(s):  
Adam Hartland ◽  
Graham D. Fenwick ◽  
Sarah J. Bury
Keyword(s):  
Organic Matter ◽  
Stable Isotope ◽  
Food Web ◽  
Sewage Treatment ◽  
Sewage Treatment Plant ◽  
Treatment Plant ◽  
Shallow Groundwater ◽  
Organic Pollution ◽  
Food Sources ◽  
Δ13c And Δ15n

Little is known about the feeding modes of groundwater invertebrates (stygofauna). Incorporation of sewage-derived organic matter (OM) into a shallow groundwater food web was studied using fluorescence and stable isotope signatures (δ13C and δ15N). Organic pollution was hypothesised to limit sensitive species’ abundances along the contamination gradient and isotope signatures of stygofauna consuming sewage-derived OM were expected to be enriched in δ15N. Stygofauna communities near a sewage treatment plant in New Zealand were sampled over 4 months and microbial biofilms were incubated in situ on native gravel for 1 month. As anticipated, OM stress-subsidy gradients altered stygofauna composition: the biomass of oligochaetes and Paraleptamphopus amphipods increased in OM-enriched groundwater (higher dissolved organic carbon (DOC) and tryptophan-like fluorescence), whereas other, probably less-tolerant taxa (e.g. ostracods, Dytiscidae) were absent. Isotopic signatures for stygofauna from polluted groundwater were consistent with assimilation of isotopically enriched sewage-N (δ15N values of 7–16‰), but highly depleted in δ13C relative to sewage. Negative 13C discriminations probably occur in Paraleptamphopus amphipods, and may also occur in oligochaetes and Dytiscidae, a finding with implications for the application of δ13C for determining food sources in groundwaters. Organic pollution of groundwaters may have serious repercussions for stygofauna community structure with potentially irreversible consequences.

scholarly journals Microinjection of fluorescent tubulin into dividing sea urchin cells.

1983 ◽  
Vol 97 (4) ◽  
pp. 1249-1254 ◽  
Author(s):  
P Wadsworth ◽  
R D Sloboda
Keyword(s):  
Sea Urchin ◽  
Daughter Cell ◽  
Fluorescent Protein ◽  
Living Cells ◽  
Lytechinus Variegatus ◽  
Linear Polymers ◽  
Spindle Poles ◽  
Image Intensification ◽  
Fluorescent Polymer

To follow the dynamics of microtubule (MT) assembly and disassembly during mitosis in living cells, tubulin has been covalently modified with the fluorochrome 5-(4,6-dichlorotriazin-2-yl)aminofluorescein and microinjected into fertilized eggs of the sea urchin Lytechinus variegatus. The changing distribution of the fluorescent protein probe is visualized in a fluorescence microscope coupled to an image intensification video system. Cells that have been injected with fluorescent tubulin show fluorescent linear polymers that assemble very rapidly and radiate from the spindle poles, coincident with the position of the astral fibers. No fluorescent polymer is apparent in other areas of the cytoplasm. When fluorescent tubulin is injected near the completion of anaphase, little incorporation of fluorescent tubulin into polymer is apparent, suggesting that new polymerization does not occur past a critical point in anaphase. These results demonstrate that MT polymerization is very rapid in vivo and that the assembly is both temporally and spatially regulated within the injected cells. Furthermore, the microinjected tubulin is stable within the sea urchin cytoplasm for at least 1 h since it can be reutilized in successive daughter cell spindles. Control experiments indicate that the observed fluorescence is dependent on MT assembly. The fluorescence is greatly diminished upon treatment of the cells with cold or colchicine agents known to cause the depolymerization of assembled MT. In addition, cells injected with fluorescent bovine serum albumin or assembly-incompetent fluorescent tubulin do not exhibit fluorescence localized in the spindle but rather appear diffusely fluorescent throughout the cytoplasm.

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