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Chapter 8 evaluates the challenge of SDG 2: Zero Hunger, which aims to meet the food needs of an increasing global population while safeguarding the food needs of the poor and promoting sustainable agricultural land use. The interaction between rural poverty, natural resource degradation, and food insecurity in developing countries is a vicious cycle. Increasing agricultural production to meet the rising global food demand is constrained by the limited availability of fertile agricultural land suitable for expansion. It requires significant increases in production per unit of agricultural land already in use rather than expanding the land under agricultural production. However, the high costs associated with agricultural intensification make increasing sustainable agricultural production a real challenge. Removing or re-orientating environmentally harmful subsidies in agriculture and identifying new and innovative policies to boost sustainable agricultural intensification is required, especially in developing countries with fragile and limited fertile agricultural land.
Chapter 7 explains the range of policy tools decision-makers can use to correct incentives for an oversupply of environmental “bads” and an undersupply of environmental “goods” in markets. There are two critical steps to address the underlying causes of environmental mismanagement. Step 1 involves removing existing policy distortions. Step 2 explains how policy options can be used to correct market failures and compares and contrasts these options. Market-based instruments provide incentives for producers and consumers to reduce or eliminate negative environmental externalities through markets, prices, and other economic means, e.g., Coase Bargaining solutions, cap and trade, taxes, and subsidies. Regulatory-based (command and control) instruments rely on setting a standard, such as emissions or technology adopted, backed by penalties to modify economic behavior. In the absence of government intervention to correct market failures, private sector measures, such as liability, information disclosure, and voluntary agreements, have a role in correcting environmental problems.
Chapter 6 discusses the “cost-benefit analysis” (CBA) framework for decision-making, aiding project and policy selection and acceptance. Environmental impacts may occur today, over several years, and sometimes well into the future, requiring discounting future costs and benefits, which raises important ethical considerations. Often, the environmental impacts of projects and policy decisions are not known for certain, and there may be uncertainty about the incidence, scale of the effects, and the probability of their occurrence. Thus, adopting or rejecting a project or policy requires addressing the uncertainty and risk surrounding environmental impacts. Equity issues can also be considered in CBA, as the distributional effects on those who bear the costs and receive the benefits of a project or policy decision are often different. Successfully adopting and implementing projects and policies, in the long run, relies on how costs and benefits are distributed among the stakeholders impacted by them. A case study of mangrove conversion for shrimp farms in Thailand illustrates the implementation of CBA in the real world.
Chapter 15 evaluates the challenge of SDG 17: Partnership for the Goals, which aims to address global issues related to sustainable economic development and reviews how alternative indicators reflect progress toward global sustainability. Although there have been recent advances in areas such as development aid, remittance flows, and technology access, international development funding remains a significant challenge. Global challenges like institutional inertia and vested interests, alongside private sector opportunities for sustainable economic development, are examined. Economics plays a vital role in acknowledging critical planetary limits and boundaries. This requires establishing global partnerships and international environmental agreements, improving how we secure and invest wealth from natural resource exploitation using Sovereign Wealth Funds, creating and correcting global markets, and raising funding for global public goods. Additionally, economics can help analyze ways to stimulate global innovation, increase private sector involvement, and implement safety nets like Universal Basic Income to reduce extreme poverty during environmental crises.
Chapter 10 evaluates the challenges of SDG 7: Affordable and Clean Energy, which aims to ensure access to affordable, reliable, sustainable, and modern energy for all. The scarcity of non-renewable minerals and energy resources presents a critical global challenge that could constrain economic growth and well-being. Various ways to measure natural resource scarcity are evaluated, and an economic analysis of the optimal extraction of exhaustible resources over time is established. Policies to address future demands for mineral and energy resources while balancing the environmental impacts of extraction and use are discussed. For example, substituting non-renewable energy with renewable energy sources poses economic and environmental challenges. Concerns over supply constraints and reliance on critical minerals have prompted calls for self-sufficiency, reducing reliance on imports of essential raw materials, and creating incentives to enhance recycling, recovery, and reuse, especially of rare earth elements. In addition, developing new technologies to improve end-use efficiency can support the decoupling of dependency on non-renewable resources from economic growth.
Life-history traits such as dispersal affect population attributes like gene flow, which can have consequences for speciation and extinction rates over macroevolutionary timescales. Here we use the Cheilostomatida, a monophyletic order of marine bryozoans, to test whether a life-history trait, larval brooding, affected the origination and extinction rates of genera throughout their fossil record. Cheilostome lineages that brood their larvae have shorter larval dispersal distances than non-brooding lineages, which has led to the hypothesis that the evolution of larval brooding decreased gene flow, increased origination, and drove their Cretaceous diversification. Brooding cheilostomes are far more diverse than non-brooding cheilostomes today, but it remains to be shown that brooding lineages have a higher origination rate than non-brooders. We fit time-varying Pradel seniority capture–mark–recapture models to look at the effect of brooding on origination and extinction rates during the Cretaceous cheilostome diversification, the Cretaceous/Paleogene mass extinction and recovery, and through the Cenozoic. Our results support the hypothesis that brooding affects origination rate, but only in the Cenomanian to Campanian. Extinction rates do not differ between brooding and non-brooding genera, and there is no regime shift specific to the Cretaceous/Paleogene mass extinction. Our work illustrates the importance of using fossil occurrences and time-varying models, which can detect interval-specific diversification differentials.
Mixing-induced reactions play an important role in a wide range of porous media processes. Recent advances have shown that fluid flow through porous media leads to chaotic advection at the pore scale. However, how this impacts Darcy-scale reaction rates is unknown. Here, we measure the reaction rates in steady mixing fronts using a chemiluminescence reaction in index-matched three-dimensional porous media. We consider two common mixing scenarios for reacting species, flowing either in parallel in a uniform flow or towards each other in a converging flow. We study the reactive properties of these fronts for a range of Péclet numbers. In both scenarios, we find that the reaction rates significantly depart from the prediction of hydrodynamic dispersion models, which obey different scaling laws. We attribute this departure to incomplete mixing effects at the pore scale, and propose a mechanistic model describing the pore-scale deformations of the front triggered by chaotic advection and their impact on the reaction kinetics. The model shows good agreement with the effective Darcy-scale reaction kinetics observed in both uniform and converging flows, opening new perspectives for upscaling reactive transport in porous media.
Studying deep-water shark species presents inherent challenges stemming from the difficulty in accessing their habitats, coupled with factors such as low population densities, intricate behaviours, and complex biological attributes. The integration of citizen scientists, particularly fishers, offers a valuable avenue to make use of their life-long insights and expertise, thus facilitating the acquisition of crucial data that can effectively enhance the realm of shark research. Our collaborative engagement with fishers since 2017 has yielded an extensive documentation concerning elasmobranchs in the Caribbean region of Puerto Rico providing a unique opportunity to formally record species hitherto unreported. This is exemplified by the first documentation of the smalltooth sandtiger shark (Odontaspis ferox (Risso, 1810)). Despite its broad geographic range and widespread distribution in temperate and tropical marine environments, there is a lack of comprehensive scientific understanding and limited available knowledge regarding this species. A noteworthy finding on December 30, 2020, near Rincón (northwest coast) in Puerto Rico, disclosed a large shark that an experienced fisher had captured as an unidentified by-catch at a depth of 325 m. Through an interdisciplinary approach using molecular (355 bp, Cytochrome Oxidase Subunit 1) and morphological techniques, we successfully confirmed the identity of the specimen as a female smalltooth sandtiger shark. Given the limited information available (e.g., diversity, abundance, behaviour, reproduction, distribution) on shark species in the coastal and deep waters of Puerto Rico, this report provides valuable new data that can significantly contribute to the conservation efforts to protect these enigmatic yet ecologically vital predators.
Early Miocene land mammals from eastern North America are exceedingly rare. Over the past several decades a small, but significant, vertebrate fauna has been recovered by paleontologists and citizen scientists from the Belgrade Formation at the Martin Marietta Belgrade Quarry in eastern North Carolina. This assemblage has 12 land mammal taxa, including beaver (Castoridae), stem lagomorph, carnivorans (Mustelidae, Ailuridae), horses (Equidae), rhinoceros (Rhinocerotidae), tapir (Tapiridae), peccary (Tayassuidae), anthracothere (Anthracotheriidae), entelodont (Entelodontidae), and protoceratid (Protoceratidae). Taken together, the biochronology of this Maysville Local Fauna indicates a late Arikareean (Ar3/Ar4) to early Hemingfordian (He1) North American Land Mammal Age (NALMA). This interval, which includes the Runningwater Chronofauna, documents numerous important Holarctic immigrants, including Amphictis, Craterogale, and cf. Menoceras found at this locality. Strontium isotope stratigraphy (SIS) of shark teeth collected in situ from the Belgrade Formation yield an age of 21.4 ± 0.13 Ma, which validates the age of interbedded land mammals within this unit. It also is consistent with the late Arikareean (Ar3/Ar4) biochronology and Aquitanian Neogene marine stage. New SIS analyses of oysters (Striostrea gigantissima) and clams (Chione) from this mine, previously assigned to late Oligocene or Late Miocene, are significantly older (28.0 ± 0.22 Ma and 27.6 ± 0.26 Ma, respectively) than the land mammals. Depending upon stratigraphic interpretations, these may confirm an older marine facies within the Belgrade Formation. This locality is important because of its marine and terrestrial tie-ins that facilitate intercalibration of both NALMAs and Cenozoic marine stages.
We present new unconstrained simulations and constrained experiments of a pair of pitching hydrofoils in a leader–follower in-line arrangement. Free-swimming simulations with matched pitching amplitudes show self-organisation into stable formations at a constant gap distance without any control. Over a wide range of phase synchronisation, amplitude and Lighthill number typical of biology, we discover that the stable gap distance scales with the actual wake wavelength of an isolated foil rather than the nominal wake wavelength. A scaling law for the actual wake wavelength is derived and shown to collapse data across a wide Reynolds number range of $200 \leqslant Re \leqslant 59\,000$. Additionally, vortex analysis uncovers that the leader’s wake wavelength-to-chord ratio, $\lambda /c$, is the key dimensionless variable to maximise the follower’s/collective efficiency. When $\lambda /c \approx 2$ it ensures that the follower’s leading edge suction force and the net force from a nearby vortex pair act in the direction with the foil’s motion thereby reducing the follower’s power. Moreover, in both simulations and experiments mismatched foil amplitudes are discovered to increase the efficiency of hydrofoil schools by 70 % while maintaining a stable formation without closed-loop control. This occurs by (i) increasing the stable gap distance between foils to push them into a high-efficiency zone and (ii) raising the level of efficiency in these zones. This study bridges the gap between constrained and unconstrained studies of in-line schooling by showing that constrained-foil measurements can map out the potential efficiency benefits of schooling. These findings can aid in the design of high-efficiency biorobot schools.
Over the interval 2008–2023 a large number of studies have been published testing various aspects of punctuated equilibria, including the prevalence of stasis, and also the extent to which most evolutionary change is concentrated at cladogenesis. In the vast majority of studies, punctuated equilibria continued to be strongly validated, as widespread evidence for stasis accumulated, with only some rare incidences of gradual change found. Support for the importance of cladogenetic change has increased, and new analytical approaches to study punctuated equilibria have been developed. Over this time period, there has also been an increase in the number of studies that have concentrated on extant taxa to test for punctuated equilibria, and these have also corroborated its widespread presence. In this respect, punctuated equilibria has served as an important bridge between neontological and paleontological approaches to evolutionary biology. From 2008 to 2023, there has also been some drift in how stasis is defined, such that, in certain studies, the definition diverged from the original 1972 definition in important respects. Notably, it is the few studies that have most changed the definition of what stasis constitutes that have most challenged the validity of punctuated equilibria, indicating it is morphing interpretations and definitions rather than the discovery of data compatible with phyletic gradualism that are most responsible for divergent results.
We describe the findings of cyclidans from the unpublished collection of the famous paleontologist B.I. Chernyshev (1888–1950) in the storage of the Academician F.N. Chernyshev Central Scientific Research Geological Survey Museum (CNIGR museum, St. Petersburg, Russia). These cyclidans were discovered by various researchers in the Carboniferous and Permian of the Urals. They are represented by the following taxa: Oonocarcinus uralicus new species, Uralocyclus feldmanni new species, Ambocyclus capidulum (Chernyshev, 1933), and Magnitocyclus (?) sp. indet. The discovery of the new species Oonocarcinus uralicus n. sp. greatly expands the geographic and stratigraphic interval of the genus Oonocarcinus Gemmellaro, 1890, previously known from the Middle Permian and Triassic. The discovery of Uralocyclus feldmanni n. sp. in the Mississippian deposits of the Chelyabinsk Oblast indicates a wide distribution of the genus Uralocyclus Mychko and Alekseev, 2018 in the Early Carboniferous, because Carboniferous representatives of this genus were previously known only from Ireland and England. The paper provides an up-to-date list of all known cyclidan occurrences and taxa in Russia.
The Paragaricocrinidae is an enigmatic late Paleozoic family of camerate crinoids that retained a robustly constructed calyx more typical of Devonian to Early Mississippian crinoids. The discovery of the oldest member of this family, Tuscumbiacrinus madisonensis n. gen. n. sp., initiated a phylogenetic investigation of the Paragaricocrinidae and consideration of its diversification and paleobiogeographic distribution. Phylogenetic analyses demonstrate the need to describe Tuscumbiacrinus n. gen and conduct revisions to preexisting taxa, resulting in the description of Palenciacrinus mudaensis n. gen. n. sp.; Pulcheracrinus n. gen.; Nipponicrinus hashimotoi n. gen. n. sp.; and Nipponicrinus akiyoshiensis n. gen. n. sp. Megaliocrinus exotericus Strimple is reassigned to Pulcheracrinus n. gen. In addition to having an anachronistic morphology, relatively few specimens are known through the ca. 76-million-year duration of this family. This pattern is unlikely to have resulted from low fossil sampling alone, and instead likely reflects low abundance and/or taxonomic richness of a long-lived waning clade. From its apparent origination in Laurussia during the Mississippian, the Paragaricocrinidae diversified into a cosmopolitan clade. Following a diversity drop during the Pennsylvanian, the Paragaricocrinidae persisted but exemplified characteristics of a dead clade walking until its eventual extinction during the middle Permian (Wordian).