This study presents recently collected data examining the organic petrology, palynology, mineralogy and geochemistry of the Gray Hawk coal bed. From the Early Pennsylvanian, Langsettian substage, Gray Hawk coal has been mined near the western edge of the eastern Kentucky portion of the Central Appalachian coalfield. While the coal is thin, rarely more than 0.5-m thick, it has a low-ash yield and a low-S content, making it an important local resource. The Gray Hawk coal palynology is dominated by Lycospora spp., and contains a diverse spectrum of small lycopods, tree ferns, small ferns, calamites, and gymnosperms. The maceral assemblages show an abundance of collotelinite, telinite, vitrodetrinite, fusinite, and semifusinite. Fecal pellet-derived macrinite, albeit with more compaction than is typically seen in younger coals, was observed in the Gray Hawk coal. The minerals in the coal are dominated by clay minerals (e.g., kaolinite, mixed-layer illite/smectite, illite), and to a lesser extent, pyrite, quartz, and iron III hydroxyl-sulfate, along with traces of chlorite, and in some cases, jarosite, szomolnokite, anatase, and calcite. The clay minerals are of authigenic and detrital origins. The occurrence of anatase as cell-fillings also indicates an authigenic origin. With the exception of Ge and As, which are slightly enriched in the coals, the concentrations of other trace elements are either close to or much lower than the averages for world hard coals. Arsenic and Hg are also enriched in the top bench of the coal and probably occur in pyrite. The elemental associations (e.g., Al₂O₃/TiO₂, Cr/Th-Sc/Th) indicate a sediment-source region with intermediate and felsic compositions. Rare metals, including Ga, rare earth elements and Ge, are highly enriched in the coal ashes, and the Gray Hawk coals have a great potential for industrial use of these metals. The rare earth elements in the samples are weakly fractionated or are characterized by heavy-REE enrichment, indicating an input of natural waters or probably epithermal solutions.

Non-pollen palynomorphs (NPPs) are ‘extra’ microfossils often found in palynology slides. These include remains of organisms within the size range of pollen grains ( c. 10–250 µm), resistant to laboratory treatments used for the preparation of palynological samples. NPPs are a large and taxonomically heterogeneous group of remains of organisms living in diverse environments. Taxonomically, they belong to a wide variety of groups such as cyanobacteria, algae, vascular plants, invertebrates and fungi. The aim of this chapter is to provide a general overview of NPP groups observed in palynology slides. It includes more than 40 of the most common groups starting with acritarcha, cyanobacteria and algae, moving through transitional groups to animals and fungi and finishing with human-made objects such as textile fibres. Although far from complete, it provides an updated overview of taxonomical diversity of NPPs and their indicator values. Further works on NPP identifications are of great importance to improve our current knowledge. Since NPPs occur in all kinds of sediments, their analysis is a powerful tool for reconstructing environmental changes over time. Further detailed studies of specific NPP groups and their indicator values will open the way for new fields of study.

Thermal stress on the biosphere during the extreme warmth of the Paleocene–Eocene Thermal Maximum (PETM) was most severe at low latitudes, with sea surface temperatures at some localities exceeding the 35 ^∘C at which marine organisms experience heat stress. Relatively few equivalent terrestrial sections have been identified, and the response of land plants to this extreme heat is still poorly understood. Here, we present a new record of the PETM from the peak ring of the Chicxulub impact crater that has been identified based on nannofossil biostratigraphy, an acme of the dinoflagellate genus Apectodinium, and a negative carbon isotope excursion. Geochemical and microfossil proxies show that the PETM is marked by elevated TEX${}_{\mathrm{86}}^{\mathrm{H}}$ -based sea surface temperatures (SSTs) averaging ∼37.8 ^∘C, an increase in terrestrial input and surface productivity, salinity stratification, and bottom water anoxia, with biomarkers for green and purple sulfur bacteria indicative of photic zone euxinia in the early part of the event. Pollen and plants spores in this core provide the first PETM floral assemblage described from Mexico, Central America, and the northern Caribbean. The source area was a diverse coastal shrubby tropical forest with a remarkably high abundance of fungal spores, indicating humid conditions. Thus, while seafloor anoxia devastated the benthic marine biota and dinoflagellate assemblages were heat-stressed, the terrestrial plant ecosystem thrived.

This chapter synthesizes the most common processing techniques applied to palynomorphs and their known issues. We primarily focus on non-pollen palynomorphs (NPPs), but include studies on pollen grains where the information might be relevant. An overview of recent (2017–19) NPP publications is used to connect the most common techniques to known taphonomic issues. Finally, general recommendations are made to minimize processing bias and maximize NPP recovery.

Neogene sediments in the UK are ideally situated for understanding the early development of hydrological dynamics and atmospheric circulation that led to the modern oceanic climate of northwest Europe. Onshore Neogene fossiliferous deposits in the UK are limited to the solution pipe fills at Trwyn y Parc in Anglesey (Middle Miocene), the Brassington Formation of Derbyshire (Serravallian‐Tortonian), and the Coralline Crag Formation (latest Zanclean‐earliest Piacenzian) and Red Crag Formation (Piacenzian‐Gelasian) in southeast England. Palynoflora from these localities can be used to provide snapshots into the climate at the time of deposition, however, palaeobotanical‐based reconstructions are typically lacking in their poor estimation of error. Therefore, we present the first pre‐Quaternary application of two terrestrial climate reconstruction techniques: CREST (Climate Reconstruction SofTware) and CRACLE (Climate Reconstruction Analysis using Coexistence Likelihood Estimation), that use Bayesian and likelihood estimation probability respectively to generate a new palaeoclimate reconstruction, and compare this to Co‐existence Approach reconstructions from the UK and continental Europe. Our study shows how Mean Annual Temperature (MAT) declines by 3°–6°C, Mean Annual Precipitation (MAP) declines by 480–600 mm and Precipitation Seasonality approximately halves throughout the Neogene. CREST and CRACLE reconstructions overlap with the Co‐exisence Approach and have the advantage of providing uncertainty, rather than ranges. The UK appears to have had a milder, wetter, and less seasonal climate than continental Europe. This is likely due to the buffering effects of the Atlantic Ocean and North Sea ameliorating the UK Neogene climate despite regional and global changes in atmospheric and oceanic circulation.

The middle Miocene Climate Optimum (MMCO) was the warmest interval of the last 23 million years and is one of the best analogs for proposed future climate change scenarios. Fungi play a key role in the terrestrial carbon cycle as dominant decomposers of plant debris, and through their interactions with plants and other organisms as symbionts, parasites, and endobionts. Thus, their study in the fossil record, especially during the MMCO, is essential to better understand biodiversity changes and terrestrial carbon cycle dynamics in past analogous environments, as well as to model future ecological and climatic scenarios. The fossil record also offers a unique long-term, large-scale dataset to evaluate fungal assemblage dynamics across long temporal and spatial scales, providing a better understanding of how ecological factors influenced assemblage development through time. In this study, we assessed the fungal diversity and community composition recorded in two geological sections from the middle Miocene from the coal mines of Thailand and Slovakia. We used presence-absence data to quantify the fungal diversity of each locality. Spores and other fungal remains were identified to modern taxa whenever possible; laboratory codes and fossil names were used when this correlation was not possible. This study represents the first of its kind for Thailand, and it expands existing work from Slovakia. Our results indicate a total of 281 morphotaxa. This work will allow us to use modern ecological data to make inferences about ecosystem characteristics and community dynamics for the studied regions. It opens new horizons for the study of past fungal diversity based on modern fungal ecological analyses. It also sheds light on how global variations in fungal species richness and community composition were affected by different climatic conditions and under rapid increases of temperature in the past to make inferences for the near climatic future.