Reconciling safe planetary targets and planetary justice: Why should social scientists engage with planetary targets?

As human activity threatens to make the planet unsafe for humanity and other life forms, scholars are identifying planetary targets set at a safe distance from biophysical thresholds beyond which critical Earth systems may collapse. Yet despite the profound implications that both meeting and transgressing such targets may have for human wellbeing, including the potential for negative trade-offs, there is limited social science analysis that systematically considers the justice dimensions of such targets. Here we assess a range of views on planetary justice and present three arguments associated with why social scientists should engage with the scholarship on safe targets. We argue that complementing safe targets with just targets offers a fruitful approach for considering synergies and trade-offs between environmental and social aspirations and can inform inclusive deliberation on these important issues

Earth system boundaries and Earth system justice: Sharing the ecospace

This is the author accepted manuscriptThe literature on planetary and Earth system boundaries calls on humans to live within those boundaries. Sharing such limited ecospace raises questions of justice. Global environmental assessments and scholarship are increasingly paying attention to justice issues, yet inadequately define how to share the limited ecospace. Against this background we ask: how can global environmental assessments’ concerns for justice be enhanced through an Earth system justice (ESJ) framework that guides how the global community could share and flourish within the limited ecospace? Based on an analysis of how justice concerns are addressed in the Assessment of Assessments and global environmental change projects, we build an Earth system justice framework that discusses how ecospace can be shared fairly through the setting of Earth system boundaries and the provision of minimum resource needs for all, and how this can be achieved through an equitable redistribution of resources, rights, and responsibilities focused on addressing inequality, overconsumption, and harmful accumulation.Rockefeller Philanthropy AdvisorsEuropean Research Counci

Epigenetic change induced by in utero dietary challenge provokes phenotypic variability across multiple generations of mice

Transmission of epigenetic information between generations occurs in nematodes, flies and plants, mediated by specialised small RNA pathways, histone H3K9me3, H3K27me3, H4K16ac and DNA methylation 1-3 . In higher vertebrates, epidemiological and experimental evidence supports similar trans-generational effects 4,5 although the mechanisms that underpin these are incompletely understood 6-9 . We generated a luciferase reporter knock-in mouse for the imprinted Dlk1 locus, to visualise and track epigenetic fidelity across generations. We showed that exposure to high-fat diet (HFD) in pregnancy provokes sustained re-expression of the normally silent maternal Dlk1 allele in offspring, coincident with increased DNA methylation at the Dlk1 sDMR . Interestingly, maternal Dlk1 mis-expression was also evident in the next generation (F2), exclusively in animals derived from F1-exposed females. Oocytes from these females showed altered microRNA and gene expression, without any major changes in underlying DNA methylation, and correctly imprinted Dlk1 expression resumed in subsequent generations (F3 onwards). Our results reveal how canonical and non-canonical imprinting mechanisms enable the foetal epigenome to adapt to in utero challenge to modulate the properties of two successive generations of offspring

Earth system justice needed to identify and live within Earth system boundaries

Living within planetary limits requires attention to justice as biophysical boundaries are not inherently just. Through collaboration between natural and social scientists, the Earth Commission defines and operationalizes Earth system justice to ensure that boundaries reduce harm, increase well-being, and reflect substantive and procedural justice. Such stringent boundaries may also affect ‘just access’ to food, water, energy and infrastructure. We show how boundaries may need to be adjusted to reduce harm and increase access, and challenge inequality to ensure a safe and just future for people, other species and the planet. Earth system justice may enable living justly within boundaries

Impacts of meeting minimum access on critical earth systems amidst the Great Inequality

The Sustainable Development Goals aim to improve access to resources and services, reduce environmental degradation, eradicate poverty and reduce inequality. However, the magnitude of the environmental burden that would arise from meeting the needs of the poorest is under debate—especially when compared to much larger burdens from the rich. We show that the ‘Great Acceleration’ of human impacts was characterized by a ‘Great Inequality’ in using and damaging the environment. We then operationalize ‘just access’ to minimum energy, water, food and infrastructure. We show that achieving just access in 2018, with existing inequalities, technologies and behaviours, would have produced 2–26% additional impacts on the Earth’s natural systems of climate, water, land and nutrients—thus further crossing planetary boundaries. These hypothetical impacts, caused by about a third of humanity, equalled those caused by the wealthiest 1–4%. Technological and behavioural changes thus far, while important, did not deliver just access within a stable Earth system. Achieving these goals therefore calls for a radical redistribution of resources

Safe and just Earth system boundaries.

This is the final version. Available from Nature Research via the DOI in this record. Data availability The data supporting Figs. 2 and 3 are available at https://doi.org/10.6084/m9.figshare.22047263.v2 and https://doi.org/10.6084/m9.figshare.20079200.v2, respectively. We rely on other published datasets for the climate boundary16, N boundary72 (model files are at https://doi.org/10.5281/zenodo.6395016), phosphorus73,74 (scenario breakdowns are at https://ora.ox.ac.uk/objects/uuid:d9676f6b-abba-48fd-8d94-cc8c0dc546a2, and a summary of agricultural sustainability indicators is at https://doi.org/10.5281/zenodo.5234594), current N surpluses129,130 (the repository at https://dataportaal.pbl.nl/downloads/IMAGE/GNM) with the critical N surplus limit72 subtracted, and estimated subglobal P concentration in runoff based on estimated P load to freshwater131 and local runoff data132,133. Current functional integrity is calculated from the European Space Agency WorldCover 10-metre-resolution land cover map (https://esa-worldcover.org/en). The safe boundary and current state for groundwater are derived from the Gravity Recovery And Climate Experiment (http://www2.csr.utexas.edu/grace/RL06_mascons.html) and the Global Land Data Assimilation System (https://disc.gsfc.nasa.gov/datacollection/GLDAS_NOAH025_3H_2.1.html). More information is available in ‘Code availability’ and Supplementary Methods. Source data for Fig. 2 are provided with this paper.Code availability: The code used to produce Figs. 2 and 3 are available at https://doi.org/10.6084/m9.figshare.22047263.v2 and https://doi.org/10.6084/m9.figshare.20079200.v2, respectively. The code used to make the nutrient Earth system boundary layers in Fig. 3 is available at https://doi.org/10.5281/zenodo.7636716. The code used to make the surface water layer in Fig. 3 and derive the subglobal Earth system boundaries for surface water is available at https://doi.org/10.5281/zenodo.7674802. The code to estimate current functional integrity is available at https://figshare.com/articles/software/integrity_analysis/22232749/2. The code to derive the groundwater layer in Fig. 3 and derive the total annual groundwater recharge is available at https://doi.org/10.5281/zenodo.7710540.The stability and resilience of the Earth system and human well-being are inseparably linked1-3, yet their interdependencies are generally under-recognized; consequently, they are often treated independently4,5. Here, we use modelling and literature assessment to quantify safe and just Earth system boundaries (ESBs) for climate, the biosphere, water and nutrient cycles, and aerosols at global and subglobal scales. We propose ESBs for maintaining the resilience and stability of the Earth system (safe ESBs) and minimizing exposure to significant harm to humans from Earth system change (a necessary but not sufficient condition for justice)4. The stricter of the safe or just boundaries sets the integrated safe and just ESB. Our findings show that justice considerations constrain the integrated ESBs more than safety considerations for climate and atmospheric aerosol loading. Seven of eight globally quantified safe and just ESBs and at least two regional safe and just ESBs in over half of global land area are already exceeded. We propose that our assessment provides a quantitative foundation for safeguarding the global commons for all people now and into the future.Stockholm Universit

Epigenetic changes induced by in utero dietary challenge result in phenotypic variability in successive generations of mice

Transmission of epigenetic information between generations occurs in nematodes, flies and plants, mediated by specialised small RNA pathways, modified histones and DNA methylation. Similar processes in mammals can also affect phenotype through intergenerational or trans-generational mechanisms. Here we generate a luciferase knock-in reporter mouse for the imprinted Dlk1 locus to visualise and track epigenetic fidelity across generations. Exposure to high-fat diet in pregnancy provokes sustained re-expression of the normally silent maternal Dlk1 in offspring (loss of imprinting) and increased DNA methylation at the somatic differentially methylated region (sDMR). In the next generation heterogeneous Dlk1 mis-expression is seen exclusively among animals born to F1-exposed females. Oocytes from these females show altered gene and microRNA expression without changes in DNA methylation, and correct imprinting is restored in subsequent generations. Our results illustrate how diet impacts the foetal epigenome, disturbing canonical and non-canonical imprinting mechanisms to modulate the properties of successive generations of offspring

Achieving a nature- and people-positive future

Despite decades of increasing investment in conservation, we have not succeeded in “bending the curve” of biodiversity decline. Efforts to meet new targets and goals for the next three decades risk repeating this outcome due to three factors: neglect of increasing drivers of decline; unrealistic expectations and time frames of biodiversity recovery; and insufficient attention to justice within and between generations and across countries. Our Earth system justice approach identifies six sets of actions that when tackled simultaneously address these failings: (1) reduce and reverse direct and indirect drivers causing decline; (2) halt and reverse biodiversity loss; (3) restore and regenerate biodiversity to a safe state; (4) raise minimum wellbeing for all; (5) eliminate over-consumption and excesses associated with accumulation of capital; and (6) uphold and respect the rights and responsibilities of all communities, present and future. Current conservation campaigns primarily address actions 2 and 3, with urgent upscaling of actions 1, 4, 5, and 6 needed to help deliver the post-2020 global biodiversity framework

Epigenetic changes induced by in utero dietary challenge result in phenotypic variability in successive generations of mice.

Transmission of epigenetic information between generations occurs in nematodes, flies and plants, mediated by specialised small RNA pathways, modified histones and DNA methylation. Similar processes in mammals can also affect phenotype through intergenerational or trans-generational mechanisms. Here we generate a luciferase knock-in reporter mouse for the imprinted Dlk1 locus to visualise and track epigenetic fidelity across generations. Exposure to high-fat diet in pregnancy provokes sustained re-expression of the normally silent maternal Dlk1 in offspring (loss of imprinting) and increased DNA methylation at the somatic differentially methylated region (sDMR). In the next generation heterogeneous Dlk1 mis-expression is seen exclusively among animals born to F1-exposed females. Oocytes from these females show altered gene and microRNA expression without changes in DNA methylation, and correct imprinting is restored in subsequent generations. Our results illustrate how diet impacts the foetal epigenome, disturbing canonical and non-canonical imprinting mechanisms to modulate the properties of successive generations of offspring