The geologic setting of the Ziegler Reservoir fossil site is somewhat unusual — the sediments containing the Pleistocene fossils were deposited in a lake on top of a ridge. The lake basin was formed near Snowmass Village, Colorado (USA) when a glacier flowing down Snowmass Creek Valley became thick enough to overtop a low point in the eastern valley wall and entered the head of Brush Creek Valley. When the glacier retreated at about 155–130 ka, near the end of Marine Oxygen Isotope Stage 6, the Brush Creek Valley lobe left behind a moraine that impounded a small alpine lake. The lake was initially ~ 10 m deep and appears to have been highly productive during most of its existence, based on the abundant and exquisitely preserved organic material present in the sediments. Over time, the basin slowly filled with (mostly) eolian sediment such that by ~ 87 ka it contained a marsh or wetland rather than a true lake. Open-water conditions returned briefly between ~ 77 and 55 ka before the impoundment was finally breached to the east, establishing ties with the Brush Creek drainage system and creating an alpine meadow that persisted until historic times.

Studies of terrestrial biotic and environmental dynamics of Marine Oxygen Isotope Stage (MIS) 5, also called the Last Interglacial Period, provide insight into the effects of long-term climate change on Pleistocene ecosystems. In North America, however, there are relatively few fossil sites that definitively date to MIS 5. Even fewer contain multiple ecosystem components (vertebrates, invertebrates, plants) that have been studied in detail, and none are located at high elevation. Thus, our view of North American ecosystems during MIS 5 is, at best, an incomplete composite view, and alpine ecosystems are entirely undocumented.

In North America, terrestrial records of biodiversity and climate change that span Marine Oxygen Isotope Stage (MIS) 5 are rare. Where found, they provide insight into how the coupling of the ocean–atmosphere system is manifested in biotic and environmental records and how the biosphere responds to climate change. In 2010–2011, construction at Ziegler Reservoir near Snowmass Village, Colorado (USA) revealed a nearly continuous, lacustrine/wetland sedimentary sequence that preserved evidence of past plant communities between ~140 and 55 ka, including all of MIS 5. At an elevation of 2705 m, the Ziegler Reservoir fossil site also contained thousands of well-preserved bones of late Pleistocene megafauna, including mastodons, mammoths, ground sloths, horses, camels, deer, bison, black bear, coyotes, and bighorn sheep. In addition, the site contained more than 26,000 bones from at least 30 species of small animals including salamanders, otters, muskrats, minks, rabbits, beavers, frogs, lizards, snakes, fish, and birds. The combination of macro- and micro-vertebrates, invertebrates, terrestrial and aquatic plant macrofossils, a detailed pollen record, and a robust, directly dated stratigraphic framework shows that high-elevation ecosystems in the Rocky Mountains of Colorado are climatically sensitive and varied dramatically throughout MIS 5.

Leaf mass per area (MA) is a central ecological trait that is intercorrelated with leaf life span, photosynthetic rate, nutrient concentration, and palatability to herbivores. These coordinated variables form a globally convergent leaf economics spectrum, which represents a general continuum running from rapid resource acquisition to maximized resource retention. Leaf economics are little studied in ancient ecosystems because they cannot be directly measured from leaf fossils. Here we use a large extant data set (65 sites; 667 species-site pairs) to develop a new, easily measured scaling relationship between petiole width and leaf mass, normalized for leaf area; this enables MA estimation for fossil leaves from petiole width and leaf area, two variables that are commonly measurable in leaf compression floras. The calibration data are restricted to woody angiosperms exclusive of monocots, but a preliminary data set (25 species) suggests that broad-leaved gymnosperms exhibit a similar scaling. Application to two well-studied, classic Eocene floras demonstrates that MA can be quantified in fossil assemblages. First, our results are consistent with predictions from paleobotanical and paleoclimatic studies of these floras. We found exclusively low-MA species from Republic (Washington, U.S.A., 49 Ma), a humid, warm-temperate flora with a strong deciduous component among the angiosperms, and a wide MA range in a seasonally dry, warm-temperate flora from the Green River Formation at Bonanza (Utah, U.S.A., 47 Ma), presumed to comprise a mix of short and long leaf life spans. Second, reconstructed MA in the fossil species is negatively correlated with levels of insect herbivory, whether measured as the proportion of leaves with insect damage, the proportion of leaf area removed by herbivores, or the diversity of insect-damage morphotypes. These correlations are consistent with herbivory observations in extant floras and they reflect fundamental trade-offs in plant-herbivore associations. Our results indicate that several key aspects of plant and plant-animal ecology can now be quantified in the fossil record and demonstrate that herbivory has helped shape the evolution of leaf structure for millions of years.

We present a quantitative analysis of megafloral turnover across the Cretaceous/Paleogene boundary (K/T) based on the most complete record, which comes from the Williston Basin in southwestern North Dakota. More than 22,000 specimens of 353 species have been recovered from 161 localities in a stratigraphic section that is continuous across and temporally calibrated to the K/T and two paleomagnetic reversals. Floral composition changes dynamically during the Cretaceous, shifts sharply at the K/T, and is virtually static during the Paleocene. The K/T is associated with the loss of nearly all dominant species, a significant drop in species richness, and no subsequent recovery. Only 29 of 130 Cretaceous species that appear in more than one stratigraphic level (non-singletons) cross the K/T. Only 11 non-singletons appear first during the Paleocene. The survivors, most of which were minor elements of Cretaceous floras, dominate the impoverished Paleocene floras. Confidence intervals show that the range terminations of most Cretaceous plant taxa are well sampled. We infer that nearly all species with last appearances more than about 5 m below (approximately 70 Kyr before) the K/T truly disappeared before the boundary because of normal turnover dynamics and climate changes; these species should not be counted as K/T victims. Maxima of last appearances occur from 5 to 3 m below the K/T. Interpretation of these last appearances at a fine stratigraphic scale is problematic because of local facies changes, and megafloral data alone, even with confidence intervals, are not sufficient for precise location of an extinction horizon. For this purpose, we rely on high-resolution palynological data previously recovered from continuous facies in the same sections; these place a major plant extinction event precisely at the K/T impact horizon. Accordingly, we interpret the significant cluster of last appearances less than 5 m below the K/T as the signal of a real extinction at the K/T that is recorded slightly down section. A maximum estimate of plant extinction, based on species lost that were present in the uppermost 5 m of Cretaceous strata, is 57%. Palynological data, with higher stratigraphic but lower taxonomic resolution than the megafloral results, provide a minimum estimate of a 30% extinction. The 57% estimate is significantly lower than previous megafloral observations, but these were based on a larger thickness of latest Cretaceous strata, including most of a globally warm interval, and were less sensitive to turnover before the K/T. The loss of one-third to three-fifths of plant species supports a scenario of sudden ecosystem collapse, presumably caused by the Chicxulub impact.

We document evidence of endophytic oviposition on fossil compression/impression leaves from the early Eocene Laguna del Hunco and middle Eocene Rio Pichileufu floras of Patagonia, Argentina. Based on distinctive morphologies and damage patterns of elongate, ovoid, lens-, or teardrop-shaped scars in the leaves, we assign this insect damage to the ichnogenus Paleoovoidus, consisting of an existing ichnospecies, P. rectus, and two new ichnospecies, P. arcuatum and P. bifurcatus. In P. rectus, the scars are characteristically arranged in linear rows along the midvein; in P. bifurcatus, scars are distributed in double rows along the midvein and parallel to secondary veins; and in P. arcuatum, scars are deployed in rectilinear and arcuate rows. In some cases, the narrow, angulate end of individual scars bear a darkened region encompassing a circular hole or similar feature indicating ovipositor tissue penetration. A comparison to the structure and surface pattern of modern ovipositional damage on dicotyledonous leaves suggests considerable similarity to certain zygopteran Odonata. Specifically, members of the Lestidae probably produced P. rectus and P. bifurcatus, whereas species of Coenagrionidae were responsible for P. arcuatum. Both Patagonian localities represent an elevated diversity of potential fern, gymnosperm, and especially angiosperm hosts, the targets of all observed oviposition. However, we did not detect targeting of particular plant families. Our results indicate behavioral stasis for the three ovipositional patterns for at least 50 million years. Nevertheless, synonymy of these oviposition patterns with mid-Mesozoic ichnospecies indicates older origins for these distinctive modes of oviposition.