The foraging behaviour of Chinstrap Penguins Pygoscelis antarctica at Ardley Island, Antarctica

The foraging behaviour of 20 Chinstrap Penguins Pygoscelis antarctica breeding at Ardley Island, King George Island, Antarctica was studied during the austral summers of 1991/2 and 1995/6 using stomach temperature loggers (to determine feeding patterns), depth recorders and multiple channel loggers. The multiple channel loggers recorded dive depth, swim speed and swim heading which could be integrated using vectors to determine the foraging tracks. Half the birds left the island to forage between 02h00 and 10h00. Mean time at sea was 10.6 h. Birds generally executed a looping type course with most individuals foraging within 20 km of the island. Maximum foraging range was 33.5 km. Maximum dive depth was 100.7 m although 80% of all dives had depth maxima less than 30 m. The following dive parameters were positively related to maximum depth reached during the dive: total dive duration, descent duration, duration at the bottom of the dive, ascent duration, descent angle, ascent angle, rate of change of depth during descent and rate of change of depth during ascent. Swim speed was unrelated to maximum dive depth and had mean values of 2.6, 2.5 and 2.2 m/s for the descent, bottom and ascent phases of the dive. The sequence of maximum depths reached in a dive series was not random, tending to be concentrated at a particular depth, irrespective of whether the penguins were feeding at that depth or not. Generally, sequential dives to a specific depth were abruptly terminated by a single dive to another depth which was characteristic in having no bottom phase and unusually steep descent and ascent angles. The maximum depth reached during this dive was then adhered to in the next dive sequence. There were peaks in feeding activity between 06h00 and 09h00 and 14h00 and 22h00. Although foraging effort and relative success decreased around midnight when light intensity was lowest, birds did dive up to 22 m at this time, considerably deeper than sympatric Adélie P. adeliae or Gentoo P. papua Penguins. These findings indicate that, in accordance with their small body size, Chinstrap Penguins forage inshore close to the surface during the chick-rearing phase. Apparent short-comings in the volume of water searched compared to sympatric congeners can be made good by intense diving activity during the period at sea, with no inter-bout rests, higher swim speeds and an apparent ability to be able to forage at lower light intensities which enables Chinstrap Penguins to forage better under twilight conditions

Structural steel columns subjected to localised fires

In large open spaces within modern buildings, the application of standard compartment fire curves based on small compartments may be inappropriate for assessing the potential thermal actions imposed on structural members in fires. Instead, a localised fire approach should be considered for determining the fire protection requirements for steel structural elements in these situations. A series of experiments using real waste bin fires or controlled gas burners placed next to I-section steel columns is described. The goal of the research was to test the validity of the widely applied lumped thermal mass assumption, and potentially to propose alternative approaches. The experimental results show that steep temperature gradients developed both along the column length and over its crosssection, confirming that conventional thermal and mechanical analysis may be inappropriate for design. For the waste bin fires the maximum steel temperatures were controlled primarily by the burning duration

A Strategic Institutional Response to Micro-Credentials: Key Questions for Educational Leaders

This article responds to the rise of the micro-credential movement. It evidences the heightened attention politicians, policy-makers and educational leaders are giving to micro-credentials by framing the discussion in several recent high-level policy developments, an exponential growth in the number of academic publications and the increasing level of interest shown by popular media. It follows that micro-credentials appear to be high on the change agenda for many higher education institutions (HEIs), especially in the post-COVID-19 environment. However, the emergence of the micro-credential raises several crucial questions for educational leaders, set against fear of missing out. Importantly, the paper identifies a significant gap in the literature regarding leadership and strategic institutional responses to micro-credentials. Indeed, there is a dearth of literature. Leadership is crucial to the success of any educational change or innovation, so five key questions are presented for institutional leaders. They challenge institutions to make strategic decisions around how they engage with and position micro-credentials. If micro-credentials are part of an HEI’s change agenda, then serious consideration needs to be given to the type of leadership and internal structures required to develop and execute a successful micro-credential strategy. Consideration must also be given to fit-for-purpose business models and how to mitigate potential risks. We hope to bring these strategic questions to the table as institutions plan, envision and develop their micro-credential strategies

A tropical bird in the Artic (The Cormorant paradox)

Seabirds, like all marine endotherms, have to compensate for the extensive cooling effect of water when diving. Alone among them, cormorants (Phalacrocoracidae) have a wettable plumage and are predicted to require disproportionately large amounts of food to balance heat losses. These piscivorous birds are thus thought to have a detrimental impact on fish stocks. However, we show here that even in great cormorants from Greenland, which dive in water at 3 to 7°C, daily food intake is lower than for well-insulated European seabirds. Despite their wettable plumage, cormorants thus appear to manage their energy budgets in a remarkably efficient way. Nevertheless, the specific foraging strategies which enable this performance make cormorants dependent on high prey density areas, a feature that should be taken into account by future management plans

Dynamic Innate Immune Responses of Human Bronchial Epithelial Cells to Severe Acute Respiratory Syndrome-Associated Coronavirus Infection

Human lung epithelial cells are likely among the first targets to encounter invading severe acute respiratory syndrome-associated coronavirus (SARS-CoV). Not only can these cells support the growth of SARS-CoV infection, but they are also capable of secreting inflammatory cytokines to initiate and, eventually, aggravate host innate inflammatory responses, causing detrimental immune-mediated pathology within the lungs. Thus, a comprehensive evaluation of the complex epithelial signaling to SARS-CoV is crucial for paving the way to better understand SARS pathogenesis. Based on microarray-based functional genomics, we report here the global gene response of 2B4 cells, a cloned bronchial epithelial cell line derived from Calu-3 cells. Specifically, we found a temporal and spatial activation of nuclear factor (NF)κB, activator protein (AP)-1, and interferon regulatory factor (IRF)-3/7 in infected 2B4 cells at 12-, 24-, and 48-hrs post infection (p.i.), resulting in the activation of many antiviral genes, including interferon (IFN)-β, -λs, inflammatory mediators, and many IFN-stimulated genes (ISGs). We also showed, for the first time, that IFN-β and IFN-λs were capable of exerting previously unrecognized, non-redundant, and complementary abilities to limit SARS-CoV replication, even though their expression could not be detected in infected 2B4 bronchial epithelial cells until 48 hrs p.i. Collectively, our results highlight the mechanics of the sequential events of antiviral signaling pathway/s triggered by SARS-CoV in bronchial epithelial cells and identify novel cellular targets for future studies, aiming at advancing strategies against SARS

Gene expression analysis of Canine demodicosis; a milieu promoting immune tolerance

Canine demodicosis is a common skin disease seen in companion animal practice that results from an overpopulation of the commensal Demodex mite species. Common predisposing factors to the development of canine demodicosis include immunosuppressive diseases, such as neoplasia and hypothyroidism, and administration of immunosuppressive therapies, such as corticosteroids. Despite this, the pathogenesis of development of canine demodicosis remains unclear. Previous studies have implicated a role for increased expression of toll like receptor 2 (TLR2), increased production of interleukin (IL)-10) and T cell exhaustion. Here, we investigate gene expression of formalin fixed paraffin embedded skin samples from twelve cases of canine demodicosis in comparison to twelve healthy controls, using a 770 gene panel (NanoString Canine IO Panel). Results show an increase in the T cell population, specifically Th1 and Treg cells in dogs with demodicosis. In addition, while there is an upregulation of immunosuppressive cytokines such as IL-10 and IL-13, there is also an upregulation of immune check point molecules including PD-1/PD-L1 and CTLA-4. These findings suggest that Demodex spp. mites are modulating the host immune system to their advantage through upregulation of several immune tolerance promoting pathways

Association between usual dietary intake of food groups and DNA methylation and effect modification by metabotype in the KORA FF4 cohort

Associations between diet and DNA methylation may vary among subjects with different metabolic states, which can be captured by clustering populations in metabolically homogenous subgroups, called metabotypes. Our aim was to examine the relationship between habitual consumption of various food groups and DNA methylation as well as to test for effect modification by metabotype. A cross-sectional analysis of participants (median age 58 years) of the population-based prospective KORA FF4 study, habitual dietary intake was modeled based on repeated 24-h diet recalls and a food frequency questionnaire. DNA methylation was measured using the Infinium MethylationEPIC BeadChip providing data on >850,000 sites in this epigenome-wide association study (EWAS). Three metabotype clusters were identified using four standard clinical parameters and BMI. Regression models were used to associate diet and DNA methylation, and to test for effect modification. Few significant signals were identified in the basic analysis while many significant signals were observed in models including food group-metabotype interaction terms. Most findings refer to interactions of food intake with metabotype 3, which is the metabotype with the most unfavorable metabolic profile. This research highlights the importance of the metabolic characteristics of subjects when identifying associations between diet and white blood cell DNA methylation in EWAS

An ACAT inhibitor suppresses SARS-CoV-2 replication and boosts antiviral T cell activity

The severity of disease following infection with SARS-CoV-2 is determined by viral replication kinetics and host immunity, with early T cell responses and/or suppression of viraemia driving a favourable outcome. Recent studies uncovered a role for cholesterol metabolism in the SARS-CoV-2 life cycle and in T cell function. Here we show that blockade of the enzyme Acyl-CoA:cholesterol acyltransferase (ACAT) with Avasimibe inhibits SARS-CoV-2 pseudoparticle infection and disrupts the association of ACE2 and GM1 lipid rafts on the cell membrane, perturbing viral attachment. Imaging SARS-CoV-2 RNAs at the single cell level using a viral replicon model identifies the capacity of Avasimibe to limit the establishment of replication complexes required for RNA replication. Genetic studies to transiently silence or overexpress ACAT isoforms confirmed a role for ACAT in SARS-CoV-2 infection. Furthermore, Avasimibe boosts the expansion of functional SARS-CoV-2-specific T cells from the blood of patients sampled during the acute phase of infection. Thus, re-purposing of ACAT inhibitors provides a compelling therapeutic strategy for the treatment of COVID-19 to achieve both antiviral and immunomodulatory effects. Trial registration: NCT04318314