Body temperature and territory selection by males of the speckled wood butterfly (Pararge aegeria): what makes a forest sunlit patch a rendezvous site?

1. Insects locate mobile resources like prey items or mates using either sit‐and‐wait (‘perching’) or active (‘patrolling’) searching strategies. The sit‐and‐wait strategy can be accompanied by defending and monopolising a site through territorial behaviour. 2. The present study focuses on the territorial perching behaviour in males of the speckled wood butterfly (Pararge aegeria L.). Recent studies suggested that the selection of territories (i.e. sunlit patches on the forest floor) is driven by structural characteristics of the site that affect male visual detection. However, given that adult butterflies are heliothermic organisms and that forests provide a diverse array of light environments, it seems likely that thermal aspects may also be used for territory selection. 3. We tested whether used and unused sunlit patches differed in thermal profile under field conditions in a Belgian woodland. We also used dummy butterflies to quantify variation in operative thoracic temperature and to calculate heating rates within (i.e. different vegetation structures) and between patches. 4. Sunlit patches occupied by a territorial male were larger, and were more frequently characterised by low vegetation structures compared with empty sunlit patches. It took longer to reach optimal thorax temperature (starting from a fixed suboptimal body temperature) in small patches compared with large patches. 5. We suggest that aspects of visual detection need to be combined with thermal aspects to fully understand territory selection in the speckled wood butterfly, as synergetic and/or trade‐off effects of ambient temperature, solar radiation, and canopy/vegetation structure may be involved.     

Degradation of pectic substances in green flax fibre by Erwinia carotovora

In this paper, we report that Erwinia carotovora can perform controlled biological pectinolysis of green flax fibre. The degradation of pectic substances is considered a key step during this process and is estimated by determining the cation exchange capacity (CEC). A CEC characteristic of a ‘good retting degree’, is reached after 20 h incubation, whatever the tested temperature and initial pectate lyase activity of the bacterial culture. Similar results are obtained after only 4 h, at a temperature of 45°C and the pectate lyase activity is greater than 2 nmol ml^-1 min^-1. The linear relationship between the CEC and the weight loss of green fibre which is established, allows us to estimate an equivalent weight of 1000 g eq^-1 for the solubilised polymers.     

Stem Cell Factor Regulates Human Melanocyte-Matrix Interactions

Stem cell factor (SCF) is hypothesized to play a critical role in the migration of melanocytes during embryogenesis because mutations in either the SCF gene, or its ligand, c-kit, result in defects in coat pigmentation in mice and in skin pigmentation in humans. In this report we directly show that SCF alters the adhesion and migration of human melanocytes to extracellular matrix (ECM) ligands and regulates integrin expression at the protein level. SCF decreased adhesion of neonatal and fetal cells to collagen IV, and increased attachment of fetal cells to laminin. Attachment of fetal cells to fibronectin was decreased, but was unchanged in neonatal cells. Flow cytometry analysis of neonatal melanocytes showed that SCF down-regulated the expression of the α2 receptor, and up-regulated the expression of the α3, α5 and β1 integrin receptors. SCF down-regulated expression of α2, α5 and β1 integrins by fetal melanocytes, and up-regulated expression of the αv and α3 integrin receptors. Analysis of melanocyte migration using time-lapse videomicroscopy showed that SCF significantly increased migration of neonatal, but not fetal, melanocytes on fibronectin (FN). We conclude that SCF regulates integrin expression at the protein level and that SCF has pleiotropic effects on melanocyte attachment and migration on ECM ligands. We suggest that this may be one mechanism by which SCF regulates melanocyte migration during development of the skin.