Changes in sea urchin populations after the destruction of kelp beds

1976 ◽  
Vol 36 (4) ◽  
pp. 321-326 ◽  
Author(s):  
C. Lang ◽  
K. H. Mann
Keyword(s):  
Sea Urchin ◽  
Kelp Beds

Destructive Grazing of Kelp by Sea Urchins in Eastern Canada

1976 ◽  
Vol 33 (6) ◽  
pp. 1278-1283 ◽  
Author(s):  
P. A. Breen ◽  
K. H. Mann
Keyword(s):  
Nova Scotia ◽  
Sea Urchin ◽  
Sea Urchins ◽  
Large Contribution ◽  
Eastern Canada ◽  
Kelp Beds ◽  
Urchin Grazing

Destruction of kelp beds by sea urchins has been documented in St. Margaret’s Bay, Nova Scotia, and also appears to be taking place in other parts of eastern Canada. Continued sea urchin settlement onto grazed areas prevents the return of kelp and other algae for long periods. Because of the large contribution of kelp beds to coastal productivity, the disappearance of kelp from large areas is alarming. Dynamics of sea urchin grazing are discussed.

The Relation Between Lobster Abundance, Sea Urchins, and Kelp Beds

1972 ◽  
Vol 29 (5) ◽  
pp. 603-605 ◽  
Author(s):  
K. H. Mann ◽  
P. A. Breen
Keyword(s):  
Sea Urchin ◽  
Food Supply ◽  
Sea Urchins ◽  
Critical Density ◽  
Eastern Canada ◽  
Kelp Beds ◽  
Key Species

When subtidal communities are disturbed and sea urchin populations expand, they frequently overgraze their food supply, eliminating large seaweeds from considerable areas. The hypothesis is advanced that the lobster is a key species, controlling sea urchin populations in eastern Canada, and that reduction of lobster populations below a critical density has led to overgrazing of seaweeds in many places.

Disease as a control of sea urchin populations in Nova Scotian kelp beds

2014 ◽  
Vol 500 ◽  
pp. 149-158 ◽  
Author(s):  
CJ Feehan ◽  
RE Scheibling
Keyword(s):  
Sea Urchin ◽  
Kelp Beds ◽  
Nova Scotian

Destructive grazing, epiphytism, and disease: the dynamics of sea urchin - kelp interactions in Nova Scotia

1999 ◽  
Vol 56 (12) ◽  
pp. 2300-2314 ◽  
Author(s):  
Robert E Scheibling ◽  
Allan W Hennigar ◽  
Toby Balch
Keyword(s):  
Nova Scotia ◽  
Sea Urchin ◽  
Canopy Cover ◽  
Strongylocentrotus Droebachiensis ◽  
Exposed Site ◽  
Membranipora Membranacea ◽  
Kelp Beds ◽  
Sheltered Site ◽  
Kelp Canopy ◽  
Over Time

We measured the rate of advance of urchin (Strongylocentrotus droebachiensis) feeding aggregations (fronts) as they destructively grazed kelp beds (Laminaria longicruris) at both a wave-exposed site and a sheltered site in Nova Scotia over 3.5 years. The grazing fronts were composed of high densities of large adults (up to 98 and 70 per 0.25 m2 at the exposed and sheltered sites, respectively). Urchins in the recently formed barrens, or in adjacent kelp beds, occurred at much lower densities and consisted mainly of juveniles. The fronts moved onshore into shallower water at each site, but their rate of advance varied markedly between sites and over time at each site, ranging from 0 to 4 m·month-1. The rate of advance of a front was related to the biomass of urchins; fronts did not advance below a threshold biomass of ~2 kg·m-2. Infestations of kelp by an epiphytic bryozoan (Membranipora membranacea) caused marked reductions in kelp canopy cover and biomass during winter, but the canopy regenerated through recruitment of juvenile sporophytes in spring. A localized outbreak of disease decimated S. droebachiensis at the exposed site in 1993, which enabled kelp to recolonize the barrens. Surviving urchins gradually reaggregated and resumed destructive grazing after ~1.5 years. A recurrence of disease in 1995 eliminated urchins at both sites and terminated the transition from kelp beds to barrens on a coastal scale. Our findings have important implications for the management of the urchin fishery, which targets grazing fronts for harvesting.

Immunogold and immunoblot studies on a cell surface protein found in primary mesenchyme cells and in the cortical secretory vesicles of the sea urchin egg

1987 ◽  
Vol 45 ◽  
pp. 832-833
Author(s):  
G.L. Decker ◽  
M.C. Valdizan
Keyword(s):  
Cell Surface ◽  
Sea Urchin ◽  
Surface Protein ◽  
Egg Cell ◽  
Secretory Vesicles ◽  
Cell Surface Protein ◽  
Surface Complexes ◽  
Mesenchyme Cells ◽  
Lowicryl K4m ◽  
Primary Mesenchyme Cells

A monoclonal antibody designated MAb 1223 has been used to show that primary mesenchyme cells of the sea urchin embryo express a 130-kDa cell surface protein that may be directly involved in Ca2+ uptake required for growth of skeletal spicules. Other studies from this laboratory have shown that the 1223 antigen, although in relatively low abundance, is also expressed on the cell surfaces of unfertilized eggs and on the majority of blastomeres formed prior to differentiation of the primary mesenchyme cells.We have studied the distribution of 1223 antigen in S. purpuratus eggs and embryos and in isolated egg cell surface complexes that contain the cortical secretory vesicles. Specimens were fixed in 1.0% paraformaldehyde and 1.0% glutaraldehyde and embedded in Lowicryl K4M as previously reported. Colloidal gold (8nm diameter) was prepared by the method of Mulpfordt.

The extracellular matrix of echinoderm and amphibian eggs: Visualization in quick-frozen, deep-etched, and rotary-shadowed specimens

1990 ◽  
Vol 48 (3) ◽  
pp. 60-61
Author(s):  
Barry Bonnell ◽  
Carolyn Larabell ◽  
Douglas Chandler
Keyword(s):  
Extracellular Matrix ◽  
Plasma Membrane ◽  
Sea Urchin ◽  
Crystalline Structure ◽  
Cortical Granule ◽  
Two Dimensional ◽  
Small Peptides ◽  
Deep Etching ◽  
Quick Freezing ◽  
Acrosomal Reaction

Eggs of many species including those of echinoderms, amphibians and mammals exhibit an extensive extracellular matrix (ECM) that is important both in the reception of sperm and in providing a block to polyspermy after fertilization.In sea urchin eggs there are two distinctive coats, the vitelline layer which contains glycoprotein sperm receptors and the jelly layer that contains fucose sulfate glycoconjugates which trigger the acrosomal reaction and small peptides which act as chemoattractants for sperm. The vitelline layer (VL), as visualized by quick-freezing, deep-etching, and rotary-shadowing (QFDE-RS), is a fishnet-like structure, anchored to the plasma membrane by short posts. Orbiting above the VL are horizontal filaments which are thought to anchor the thicker jelly layer to the egg. Upon fertilization, the VL elevates and is transformed by cortical granule secretions into the fertilization envelope (FE). The rounded casts of microvilli in the VL are transformed into angular peaks and the envelope becomes coated inside and out with sheets of paracrystalline protein having a quasi-two dimensional crystalline structure.

Introductory Remarks

1980 ◽  
Vol 38 ◽  
pp. 598-599
Author(s):  
H. Mohri
Keyword(s):  
Muscle Contraction ◽  
Experimental Evidence ◽  
Sea Urchin ◽  
Constant Length ◽  
Thin Filaments ◽  
Bridge Formation ◽  
Thick Filaments ◽  
Sliding Mechanism ◽  
Radial Spokes ◽  
Cilia And Flagella

In 1959, Afzelius observed the presence of two rows of arms projecting from each outer doublet microtubule of the so-called 9 + 2 pattern of cilia and flagella, and suggested a possibility that the outer doublet microtubules slide with respect to each other with the aid of these arms during ciliary and flagellar movement. The identification of the arms as an ATPase, dynein, by Gibbons (1963)strengthened this hypothesis, since the ATPase-bearing heads of myosin molecules projecting from the thick filaments pull the thin filaments by cross-bridge formation during muscle contraction. The first experimental evidence for the sliding mechanism in cilia and flagella was obtained by examining the tip patterns of molluscan gill cilia by Satir (1965) who observed constant length of the microtubules during ciliary bending. Further evidence for the sliding-tubule mechanism was given by Summers and Gibbons (1971), using trypsin-treated axonemal fragments of sea urchin spermatozoa. Upon the addition of ATP, the outer doublets telescoped out from these fragments and the total length reached up to seven or more times that of the original fragment. Thus, the arms on a certain doublet microtubule can walk along the adjacent doublet when the doublet microtubules are disconnected by digestion of the interdoublet links which connect them with each other, or the radial spokes which connect them with the central pair-central sheath complex as illustrated in Fig. 1. On the basis of these pioneer works, the sliding-tubule mechanism has been established as one of the basic mechanisms for ciliary and flagellar movement.

Sign in / Sign up

Export Citation Format

Share Document