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Gautier, G.

Publications and source records attributed to Gautier, G..

6 recordsLinked to original sources

Maps of historical forests in France and their temporal continuity since the first half of the 19th century

AbstractIntegrating environmental history is essential for understanding present-day ecosystem dynamics and guiding modern conservation strategies, particularly under the EU Biodiversity Strategy for 2030. This data paper presents the nationwide digitisation and vectorisation of the French General Ordnance survey map (1818-1866), capturing the countrys forest cover at its historical minimum (a pivotal moment known as the "forest transition"). The original manuscript sheets surveyed at a 1:40,000 scale (976 sheets) were scanned, georeferenced and vectorised. They offer higher thematic accuracy than the older Cassini map and are far more feasible for nationwide vectorisation than the highly detailed Napoleonic cadastre. The area-weighted mean survey date is 1843, and the dataset covers 99.6% of modern mainland France. To correct for paper deformation, historical surveying errors and coordinate system transformations, a rigorous workflow was established. This shifted from a global 6-parameter affine transformation (root mean square error of 60 m) to a local elastic transformation based on thousands of control points, for 21% of the territory, which reduced the positioning error to 34 m. We assessed data quality by comparing the General Ordnance Survey maps with the Napoleonic cadastre--the standard reference for 19th-century land-use data--across more than 600 municipalities. The correlation between the two sources regarding forest cover percentages was exceptionally high (r>0.9). Because forests formed large, compact blocks of significant strategic interest to military engineers, they were mapped with high precision. Localised inaccuracies were primarily found in remote areas, most notably in the mountains. The resulting historical vector layer was intersected with contemporary forest data (BD Foret(R) v2, 2005-2019). Historical polygons smaller than 0.5 ha were filtered out to comply with modern FAO forest definitions. This spatial overlay generated a new dataset detailing four distinct land-use trajectories: . ancient forests (44.8% of present day forest): land classified as forest in both the 19th century and the present day (indicating maximum temporal continuity). . recent forests (55.2% of present day forest): land that was non-forested in the 19th century but has since undergone reforestation. . deforested areas (18.9% of 19th-century forest): land recorded as forest in the 19th century but subsequently converted to other land uses. . stable non-forest areas: land that has remained unforested across both periods. Our results suggest that the forest area of mainland France at its historical minimum should be revised upward to 9.9 million ha. A preliminary analysis further indicates that current spatial variation in forest cover is explained more by land-use dynamics occurring since the forest transition than by the initial extent of forest cover. These two open-access national datasets (the 19th-century forest layer and the land-use transition map) open the door to a better understanding of present-day forests : e.g. their biodiversity, soil quality, tree growth and belowground water quality. Furthermore, they provide decision-support tools for conservation planning. Key messageIn this data paper, we provide a map of 19th-century forests in France based on the digitisation of the military topographic map (1818-1866). By overlaying this historical source with the present-day forest map, we built a second map which allows the identification of ancient forests, recent forests, and deforestation. These maps offer avenues for historical ecology and the design of conservation strategies.

ecology↗

Parallel cases of ring speciation within a rapid adaptive radiation of cichlid fishes

Speciation often emerges from the complex interplay of geography, demography, ecology, and sexual selection, yet disentangling their relative contributions remains a challenge. In this study, we examine two species complexes of rock-dwelling Lake Victoria cichlids in the genera Pundamilia and Neochromis that are distributed along a continuous geographic gradient of rocky shores. Using morphometric analyses and male nuptial coloration data, we reveal clinal craniofacial divergence following an isolation by distance model of evolution, punctuated by strong local effects. While the Pundamilia cline exhibited modular shifts in craniofacial anatomy linked to diet-specific morphology, variation in the Neochromis cline was dominated by allometric constraints, suggesting different evolutionary processes at play. At the single site where the terminal populations of both clines co-occur, each pair of sister species showed pronounced divergence in morphology and male nuptial coloration, consistent with ecological and sexual character displacement facilitating co-existence. Our findings highlight that clinal morphological variation in parapatry and more abrupt shifts in sympatry interact to generate and maintain species. These rocky shore cichlids provide a rare opportunity to investigate the speciation continuum in one of the worlds youngest adaptive radiations.

evolutionary biology↗

Immune sensing of food allergens promotes aversive behaviour

In addition to its canonical function in protecting from pathogens, the immune system can also promote behavioural alterations1-3. The scope and mechanisms of behavioural modifications by the immune system are not yet well understood. Using a mouse food allergy model, here we show that allergic sensitization drives antigen-specific behavioural aversion. Allergen ingestion activates brain areas involved in the response to aversive stimuli, including the nucleus of tractus solitarius, parabrachial nucleus, and central amygdala. Food aversion requires IgE antibodies and mast cells but precedes the development of gut allergic inflammation. The ability of allergen-specific IgE and mast cells to promote aversion requires leukotrienes and growth and differentiation factor 15 (GDF15). In addition to allergen-induced aversion, we find that lipopolysaccharide-induced inflammation also resulted in IgE-dependent aversive behaviour. These findings thus point to antigen-specific behavioural modifications that likely evolved to promote niche selection to avoid unfavourable environments.

immunology↗

Involvement of an IgE/Mast cell/B cell amplification loop in abdominal aortic aneurysm progression

AimsIgE type immunoglobulins and their specific effector cells, mast cells (MCs), are associated with abdominal aortic aneurysm (AAA) progression. In parallel, immunoglobulin-producing B cells, organised in tertiary lymphoid organs (TLOs) within the aortic wall, have also been linked to aneurysmal progression. We aimed at investigating the potential role and mechanism linking local MCs, TLO B cells, and IgE production in aneurysmal progression. Methods and ResultsThrough histological assays conducted on human surgical samples from AAA patients, we uncovered that activated MCs were enriched at sites of unhealed haematomas, due to subclinical aortic wall fissuring, in close proximity to adventitial IgE+ TLO B cells. Remarkably, in vitro the IgEs deriving from these samples enhanced MC production of IL-4, a cytokine which favors IgE class-switching and production by B cells. Finally, the role of MCs in aneurysmal progression was further analysed in vivo in ApoE-/- mice subjected to angiotensin II infusion aneurysm model, through MC-specific depletion after the establishment of dissecting aneurysms. MC-specific depletion improved intramural haematoma healing and reduced aneurysmal progression. ConclusionsOur data suggest that MC located close to aortic wall fissures are activated by adventitial TLO B cell-produced IgEs and participate to their own activation by providing support for further IgE synthesis through IL-4 production. By preventing prompt repair of aortic subclinical fissures, such a runaway MC activation loop could precipitate aneurysmal progression, suggesting that MC-targeting treatments may represent an interesting adjunctive therapy for reducing AAA progression.

pathology↗

Digital ischemia: Etiologies and long-term follow up. A cohort study of 323 patients

Introduction Introduction Material and Methods Results Discussion Conclusion References Upper extremity digital ischemia (UEDI) is a persistent peripheral vascular disease. Diagnosis remains a real challenge to identify and consequently evaluation of etiologies and determination of therapeutic strategies has proved difficult. The incidence of UEDI is about 2 cases per 100,000 persons per year (1,2) with symptomatic ischemia of the upper extremity being encountered less frequently than lower extremity vascular insufficiency.\n\n\n\nThe main causes generally identified in literature are cardiac or arterial embolism, local thrombosis, systemic autoimmune connective tissue diseases (especially systemic sclerosis), vasculitis or traumatic injury (3).\n\nPast lite ...

pathology↗

The molecular basis of genetic interaction diversity in a metabolic pathway

Our ability to predict the impact of mutations on traits relevant for disease and evolution remains severely limited by the dependence of their effects on the genetic background and environment. Even when molecular interactions between genes are known, it is unclear how these translate to organism-level interactions between alleles. We therefore characterized the interplay of genetic and environmental dependencies in determining fitness by quantifying ~4,000 fitness interactions between expression variants of two metabolic genes, in different environments. We detect a remarkable variety of environment-dependent interactions, and demonstrate they can be quantitatively explained by a mechanistic model accounting for catabolic flux, metabolite toxicity and expression costs. Complex fitness interactions between mutations can therefore be predicted simply from their simultaneous impact on a few connected molecular phenotypes.

genetics↗