Range extension and reproduction of the barnacle Balanus perforatus in the eastern English Channel

The distribution of the warm-water barnacle, Balanus perforatus, was surveyed along the south coast of England and the north-east coast of France between 1993 and 2001, repeating work carried out between the 1940s and 1960s. The species has recovered from catastrophic mortality during the severe winter of 1962–1963 and was found over 120 km (UK) and 190 km (France) east of previous records on both sides of the Channel. The presence of the species in the eastern Channel refutes suggestions in the 1950s that larvae, and hence adults, would not be found east of the Isle of Wight because of reproductive sterility close to the limits of distribution. Brooding of specimens translocated to Bembridge, Isle of Wight, commenced in May, earlier than previously observed in British waters, and continued until September. The stage of embryo development at Bembridge in mid-August was comparable to that of the large population at Lyme Regis, Dorset 100 km further west. However the size of brood per standard body weight was greater at Lyme Regis. Factors influencing the rate of colonization and further geographic range extension of the species as a possible result of climate change, are discussed

Antigenic variation in <i>Trypanosoma brucei</i>: joining the DOTs

African trypanosomes, such as &lt;i&gt;Trypanosoma brucei&lt;/i&gt;, are protistan parasites that cause sleeping sickness. Though first described more than a century ago, trypanosomes remain a blight on the health of the human population and on the economy of sub-Saharan Africa. &lt;i&gt;T. brucei&lt;/i&gt; replicates in the bloodstream of infected mammals and traverses the blood-brain barrier to enter the central nervous system in the late, frequently fatal, stages of the disease. Because of its extracellular lifestyle, &lt;i&gt;T. brucei&lt;/i&gt; is continuously exposed to antibody challenge. To circumvent this, the parasite uses antigenic variation of a surface protein named the variant surface glycoprotein (VSG). Around 107 VSG molecules are expressed on the parasite's cell surface, creating a dense coat that prevents adaptive immunity from detecting or accessing invariant antigens. However, antibodies against the expressed VSG are generated, and periodic switches to an immunologically distinct VSG coat are necessary for parasite survival. Such switches are pre-emptive of the immune response and contribute to the pattern of trypanosome growth seen in an infected host (Figure 1): parasite numbers increase, but then drop as VSG-specific antibodies are raised by the host. Cells that have switched to another VSG coat survive this killing and seed the outgrowth of a subsequent peak of parasites, which is again decimated by anti-VSG immune killing. As a survival strategy, antigenic variation succeeds by prolonging the time that the parasite

Composition and temporal distribution of cirripede larvae in Southampton Water, England, with particular reference to the secondary production of Elminius modestus

Southampton Water, an estuary on the south coast of England, has been the focus of a number of studies to determine the seasonality and productivity of its pelagic community. Although recognized as important in previous studies, the meroplankton component and, in particular, the cirripedes have been largely ignored, though they rank second to the Copepoda in abundance. In order to estimate the contribution of barnacle larvae to the pelagic community, 42 quantitative zooplankton samples were collected from a fixed station within the estuary during a period of 19 months ( from 12 January 2001 until 16 July 2002). As expected, barnacles were the second most abundant group averaging 13% of the total population, and accounting for up to 60% on some occasions. Eight barnacle species were identified: Elminius modestus, Balanus improvisus, Balanus crenatus, Semibalanus balanoides, Verruca stroemia, Chthamalus stellatus, Sacculina carcini, and Peltogaster paguri. Of these E. modestus was the most abundant and frequent, dominating the Cirripedia fraction throughout the year, but being outnumbered by B. crenatus from February to May. Secondary production was calculated for E. modestus and mean daily rates of 0.077 mg Cm 3 d 1 (28.08 mg Cm 3 yr 1) were found

Mapping replication dynamics in Trypanosoma brucei reveals a link with telomere transcription and antigenic variation

Survival of Trypanosoma brucei depends upon switches in its protective Variant Surface Glycoprotein (VSG) coat by antigenic variation. VSG switching occurs by frequent homologous recombination, which is thought to require locus-specific initiation. Here, we show that a RecQ helicase, RECQ2, acts to repair DNA breaks, including in the telomeric site of VSG expression. Despite this, RECQ2 loss does not impair antigenic variation, but causes increased VSG switching by recombination, arguing against models for VSG switch initiation through direct generation of a DNA double strand break (DSB). Indeed, we show DSBs inefficiently direct recombination in the VSG expression site. By mapping genome replication dynamics, we reveal that the transcribed VSG expression site is the only telomeric site that is early replicating – a differential timing only seen in mammal-infective parasites. Specific association between VSG transcription and replication timing reveals a model for antigenic variation based on replication-derived DNA fragility

Structure, institutions and NGOisation: a critical realist approach to normative change in Myanmar civil society

Following several decades of suppression under authoritarian military rule, Myanmar’s civil society has played an important role in shaping the process and the impact of recent political reforms. Constitutional and legislative change favourable for civil society has been accompanied by an expansion of initiatives by international development agencies to build the capabilities of civic actors and to strengthen their influence in governance and policy making. Together, these are claimed to have enhanced the freedom, security and opportunity, or the space, for civil society to build from its rich history of social and political action and better mobilise for future protection and fulfilment of political and human rights objectives. This thesis argues that normative change in civil society can only be fully assessed, explained and understood through analysis which critiques rather than repeats conceptualisations of civil society as an autonomous zone of freedom, and the state as an apparatus of coercion. Notions of an ‘expanding space’ or an ‘improved enabling environment’ conceal structural and cultural forces which affect the collective agency and normative orientation of civic actors by shaping the political terrain on which they act, enabling and constraining actors’ form and political objectives. I analyse these changes in Myanmar using critical realism and the thought of Antonio Gramsci, and show how the reorganisation of state power and contractual, legal and ethical relations between state and civil society have led to the emergence of an institution of organisation. Tendencies towards professionalisation, formalisation and depoliticisation arise as legitimate activity comes to centre around the hegemonic form of the non-governmental organisation (NGO), with significant implications for the radical transformative potential of both civil society and human rights. Case studies reveal how the impact of these institutional forces varies according to contingencies in circumstance, resistance and the qualities and histories of actors

Faster growth with shorter antigens can explain a VSG hierarchy during African trypanosome infections:a feint attack by parasites

The parasitic African trypanosome, Trypanosoma brucei, evades the adaptive host immune response by a process of antigenic variation that involves the clonal switching of variant surface glycoproteins (VSGs). The VSGs that come to dominate in vivo during an infection are not entirely random, but display a hierarchical order. How this arises is not fully understood. Combining available genetic data with mathematical modelling, we report a VSG-length-dependent hierarchical timing of clonal VSG dominance in a mouse model, consistent with an inverse correlation between VSG length and trypanosome growth-rate. Our analyses indicate that, among parasites switching to new VSGs, those expressing shorter VSGs preferentially accumulate to a detectable level that is sufficient to trigger a targeted immune response. This may be due to the increased metabolic cost of producing longer VSGs. Subsequent elimination of faster-growing parasites then allows slower-growing parasites with longer VSGs to accumulate. This interaction between the host and parasite is able to explain the temporal distribution of VSGs observed in vivo. Thus, our findings reveal a length-dependent hierarchy that operates during T. brucei infection. This represents a ‘feint attack’ diversion tactic utilised by these persistent parasites to out-maneuver the host adaptive immune system

Lineage-specific proteins essential for endocytosis in trypanosomes

Clathrin-mediated endocytosis (CME) is the most evolutionarily ancient endocytic mechanism known, and in many lineages the sole mechanism for internalisation. Significantly, in mammalian cells CME is responsible for the vast bulk of endocytic flux and has likely undergone multiple adaptations to accommodate specific requirements by individual species. In African trypanosomes, we previously demonstrated that CME is independent of the AP-2 adaptor protein complex, that orthologues to many of the animal and fungal CME protein cohort are absent, and that a novel, trypanosome-restricted protein cohort interacts with clathrin and drives CME. Here, we used a novel cryomilling affinity isolation strategy to preserve transient low-affinity interactions, giving the most comprehensive trypanosome clathrin interactome to date. We identified the trypanosome AP-1 complex, Trypanosoma brucei (Tb)EpsinR, several endosomal SNAREs plus orthologues of SMAP and the AP-2 associated kinase AAK1 as interacting with clathrin. Novel lineage-specific proteins were identified, which we designate TbCAP80 and TbCAP141. Their depletion produced extensive defects in endocytosis and endomembrane system organisation, revealing a novel molecular pathway subtending an early-branching and highly divergent form of CME, which is conserved and likely functionally important across the kinetoplastid parasites

Interannual differences in larval haddock survival : hypothesis testing with a 3D biophysical model of Georges Bank

Author Posting. © The Author(s), 2014. This is the author's version of the work. It is posted here by permission of John Wiley & Sons for personal use, not for redistribution. The definitive version was published in Fisheries Oceanography 23 (2014): 521–553, doi:10.1111/fog.12087.The ultimate goal of early life studies of fish over the past century has been to better understand recruitment variability. As evident in the Georges Bank haddock (Melanogrammus aeglefinus) population, there is a strong relationship between recruitment success and processes occurring during the planktonic larval stage. This research sought new insights into the mechanisms controlling the recruitment process in fish populations by using biological-physical modeling methods together with laboratory and field data sets. We created the first three-dimensional model of larval haddock on Georges Bank by coupling models of hydrodynamics, lower trophic levels, a single copepod species, and larval haddock. Interactions between feeding, metabolism, growth, vertical behavior, advection, predation, and the physical environment of larval haddock were quantitatively investigated using the coupled models. Particularly, the model was used to compare survival over the larval period and the sources of mortality in 1995 and 1998, two years of disparate haddock recruitment. The results of model simulations suggest that the increased egg hatching rates and higher food availability, which reduced starvation and predation, in 1998 contributed to its larger year-class. Additionally, the inclusion of temperature-dependent predation rates produced model results that better agreed with observations of the mean hatch date of survivors. The results from this biophysical model imply that food-limitation and its related losses to starvation and predation, especially from hatch to 7 mm, may be responsible for interannual variability in recruitment and larval survival outside of the years studied.Financial support was provided by a WHOI Watson Fellowship, a WHOI Coastal Ocean Institute Student Research Proposal Award, and GLOBEC grants NA17RJ1223 (NOAA) and OCE0815838 (NSF).2015-11-1