Elasmobranch (sharks and rays) interaction with plastic pollution from global and local perspectives, via entanglement within anthropogenic debris and synthetic fibre ingestion

Plastic pollution is a known threat to a host of marine organisms across the world. Research in recent years has exposed numerous negative impacts on some of the world’s most threatened marine species, including turtles, cetaceans and pinnipeds. The impact of plastic pollution on elasmobranchs, however, has been relatively understudied. Sharks and rays are widely accepted to be two of the most threatened marine species in the oceans, most notably due to anthropogenic impacts including direct fisheries and bycatch. Their relationship with plastic pollution is only now being investigated in further detail. Previous studies have alluded to damaging effects on sharks and rays as a result of plastic pollution but have lacked in wide synthesis of existing information and empirical evidence. In this thesis, the impact of entanglement within and ingestion of plastic is highlighted for sharks and rays both globally and locally in the North-East Atlantic. Chapter one aimed to collect existing information on the occurrence and distribution of elasmobranch entanglement events, using a systematic literature review and novel data collection from social media site “Twitter”. Our results highlighted ghost fishing gear to be the most common entangling material for sharks and rays globally, consistent with previous studies on other marine species. The review also highlighted the lack of standardised reporting for elasmobranch entanglement and therefore resulted in the creation of an online entanglement report form for sharks and rays (ShaREN), allowing citizen scientists across the world to report entanglement incidents quickly and efficiently. Chapter two investigated the presence of microplastics and synthetic contaminant particles in four species of demersal shark found in the North-East Atlantic. Almost 70% of sharks analysed contained at least one contaminant particle, 2 however no significant relationship between size/weight and number of contaminants was identified, although further analysis was recommended. The study highlighted the ubiquity of synthetic fibres such as rayon and viscose, commonly found in clothing items, as contaminants in the marine environment. Chapter two presents the first empirical evidence of microplastic ingestion by UK shark species and highlights the pervasive nature of microplastic pollution off the English coast. While these two threats are unlikely to have significant population impacts on sharks and rays globally, similar to that of direct fisheries and bycatch, they are identified to be of clear animal welfare concern for these species. Entanglement within and ingestion of plastic is symptomatic of a degraded marine environment and highlights the need for policy-makers, scientists and stakeholders to work together to mitigate this issue for all marine species

Supply chain analysis in the Australian lamb processing industry

During the last decade, supply chain management has played an important role in enabling many agribusinesses to succeed in their business goals, gain competitive advantage, and improve their business performance. As the result, there has been extensive research into strategic supply chain management with the aim of improving agribusiness performance at each stage of the supply chain. This is because in the current agribusiness world, supply chain activities are crucial in influencing many companies to continuously adapt proper supply chain management practices. The objective of this research was to analyse supply chain performance indicators among Australian lamb processors by using survey data and empirical models. Based on the results of these analyses, alternative configurations for these supply chains were suggested to help enhance the performance of the businesses concerned. The results indicate that food quality and efficiency are significant indicators of competitive advantage for lamb processors

Annexin XIIIb: a novel epithelial specific annexin is implicated in vesicular traffic to the apical plasma membrane

The sorting of apical and basolateral proteins into vesicular carriers takes place in the trans-Golgi network (TGN) in MDCK cells. We have previously analyzed the protein composition of immunoisolated apical and basolateral transport vesicles and have now identified a component that is highly enriched in apical vesicles. Isolation of the encoding cDNA revealed that this protein, annexin XIIIb, is a new isoform of the epithelial specific annexin XIII sub-family which includes the previously described intestine-specific annexin (annexin XIIIa; Wice, B. M., and J. I, Gordon. 1992. J. Cell Biol. 116:405-422). Annexin XIIIb differs from annexin XIIIa in that it contains a unique insert of 41 amino acids in the NH2 terminus and is exclusively expressed in dog intestine and kidney, Immunofluorescence microscopy demonstrated that annexin XIIIb was localized to the apical plasma membrane and underlying punctate structures. Since annexins have been suggested to play a role in membrane-membrane interactions in exocytosis and endocytosis, we investigated whether annexin XIIIb, is involved in delivery to the apical cell surface. To this aim we used permeabilized MDCK cells and a cytosol-dependent in vitro transport assay. Antibodies specific for annexin XIIIb significantly inhibited the transport of influenza virus hemagglutinin from the TGN to the apical plasma membrane while the transport of vesicular stomatitis virus glycoprotein to the basolateral cell surface was unaffected. We propose that annexin XIIIb, plays a role in vesicular transport to the apical plasma membrane in MDCK cells

Regulated internalization of caveolae

Caveolae are specialized invaginations of the plasma membrane which have been proposed to play a role in diverse cellular processes such as endocytosis and signal transduction. We have developed an assay to determine the fraction of internal versus plasma membrane caveolae. The GPI-anchored protein, alkaline phosphatase, was clustered in caveolae after antibody-induced crosslinking at low temperature and then, after various treatments, the relative amount of alkaline phosphatase on the cell surface was determined. Using this assay we were able to show a time- and temperature-dependent decrease in cell-surface alkaline phosphatase activity which was dependent on antibody-induced clustering. The decrease in cell surface alkaline phosphatase activity was greatly accelerated by the phosphatase inhibitor, okadaic acid, but not by a protein kinase C activator. Internalization of clustered alkaline phosphatase in the presence or absence of okadaic acid was blocked by cytochalasin D and by the kinase inhibitor staurosporine. Electron microscopy confirmed that okadaic acid induced removal of caveolae from the cell surface. In the presence of hypertonic medium this was followed by the redistribution of groups of caveolae to the center of the cell close to the microtubule-organizing center. This process was reversible, blocked by cytochalasin D, and the centralization of the caveolar clusters was shown to be dependent on an intact microtubule network. Although the exact mechanism of internalization remains unknown, the results show that caveolae are dynamic structures which can be internalized into the cell. This process may be regulated by kinase activity and require an intact actin network

On the cohomology of some exceptional symmetric spaces

This is a survey on the construction of a canonical or "octonionic K\"ahler" 8-form, representing one of the generators of the cohomology of the four Cayley-Rosenfeld projective planes. The construction, in terms of the associated even Clifford structures, draws a parallel with that of the quaternion K\"ahler 4-form. We point out how these notions allow to describe the primitive Betti numbers with respect to different even Clifford structures, on most of the exceptional symmetric spaces of compact type.Comment: 12 pages. Proc. INdAM Workshop "New Perspectives in Differential Geometry" held in Rome, Nov. 2015, to appear in Springer-INdAM Serie

Supply Chain Performance Indicators for Australian Beef Industry: An Empirical Analysis

Abstract: This research presents and analyses supply chain performance indicators for Australian beef producers, processors and retailers/wholesalers based on an empirical approach. The survey results showed that: 1. for producers, competitive advantage was significantly influenced by the supply chain performance components food quality, flexibility and responsiveness 2. for processors, competitive advantage was significantly influenced by the supply chain performance components food quality and responsiveness 3. at the retail/wholesale level, competitive advantage was significantly influenced by food quality, flexibility, responsiveness and efficiency 4. a significant problem affecting the overall performance of the Australian beef supply chain was unskilled and inexperienced staff. Various statistical tests confirmed the validity and reliability of the results. Keywords: supply chain performance indicators, food quality, flexibility, responsiveness, efficiency

Transcytosis in MDCK cells: identification of glycoproteins transported bidirectionally between both plasma membrane domains.

MDCK cells display fluid-phase transcytosis in both directions across the cell. Transcytosis of cell surface molecules was estimated by electron microscopic analysis of streptavidin-gold-labeled frozen sections of biotinylated cells. Within 3 h, approximately 10% of the surface molecules, biotinylated on the starting membrane domain, were detected on the opposite surface domain irrespective of the direction of transcytosis. This suggests that the transcytosis rates for surface molecules are equal in both directions across the cell as shown previously for fluid-phase markers

Axonal and dendritic endocytic pathways in cultured neurons

The endocytic pathways from the axonal and dendritic surfaces of cultured polarized hippocampal neurons were examined. The dendrites and cell body contained extensive networks of tubular early endosomes which received endocytosed markers from the somatodendritic domain. In axons early endosomes were confined to presynaptic terminals and to varicosities. The somatodendritic but not the presynaptic early endosomes were labeled by internalized transferrin. In contrast to early endosomes, late endosomes and lysosomes were shown to be predominantly located in the cell body. Video microscopy was used to follow the transport-t of internalized markers from the periphery of axons and dendrites back to the cell body. Labeled structures in both domains moved unidirectionally by retrograde fast transport. Axonally transported organelles were sectioned for EM after video microscopic observation and shown to be large multivesicular body-like structures. Similar structures accumulated at the distal side of an axonal lesion. Multivesicular bodies therefore appear to be the major structures mediating transport of endocytosed markers between the nerve terminals and the cell body. Late endocytic structures were also shown to be highly mobile and were observed moving within the cell body and proximal dendritic segments. The results show that the organization of the endosomes differs in the axons and dendrites of cultured rat hippocampal neurons and that the different compartments or stages of the endocytic pathways can be resolved spatially

Regulation of caveolin and caveolae by cholesterol in MDCK cells

We have examined the expression of caveolin in MDCK cells under conditions that vary cellular cholesterol concentration. Caveolin mRNA levels dropped to one-sixth of control levels after treatment with simvastatin, an inhibitor of cholesterol synthesis, or beta-trimethyl cyclodextrin (CD), a cholesterol sequestering drug. Both simvastatin and CD treatment decreased total cellular cholesterol levels to about 50% of control values. The potent activator of the sterol regulatory element, 25-hydroxycholesterol, showed no direct regulation of caveolin mRNA levels. Caveolin protein concentration was also decreased to 50% of control values in cholesterol-depleted cells, giving rise to a severe attenuation of caveolin expression detected by indirect immunofluorescence labeling. Quantitative electron microscopy showed a total loss of morphologically recognizable invaginated caveolae after these cholesterol depletion treatments. When the number of invaginated caveolae per cell was expressed as a function of the cellular cholesterol content, a threshold phenomenon was observed, suggesting that caveolae only form when the steady state cellular cholesterol is above 50% of control values. These findings indicate that caveolins, and caveolae, may play an important part in cellular cholesterol homeostasis