Abstract Chickies Rock rises abruptly from the east bank of the Susquehanna River at Columbia, Pennsylvania, where it breaks through a ridge held up by massively bedded quartzite. Here in the 1830s, Samuel Haldeman recognized long straight tubes that he later described as Skolithos linearis , penetrating the quartzite. Uncertain about the nature of these cylindrical ‘vermiform or linear’, unbranched ‘stems’, Haldeman first treated them as a subgenus of Fucoides , to which root-like traces were then often assigned. By the time James Hall first illustrated the species in 1847, Haldeman was sure they were burrows of a worm-like animal, as the name he had chosen implied. Since 1960, Donald Wise has developed a detailed analysis of structural deformation of the Chickies Anticline, using the Skolithos burrows as ‘plumb-bobs’ against which Taconic rotation of the rock fabric can be measured. Wise showed that later Alleghanian deformation produced prominent folds with external rotation up to twice as great as that of the rock fabric itself. Now conserved as a county park, Chickies Rock attracts many visitors. Its cliff-top is a superb viewpoint from which to contemplate progressive westward migration of the Appalachian drainage divide, ongoing since the late Jurassic opening of the Atlantic Ocean.

Shallow to deeply penetrating bioturbation by organisms on carbonate shelves can alter the original depositional texture of carbonate sediments, rearrange and modify the primary porosity and permeability patterns, and effectively increase the overall flow properties in multiple intervals. To explore the impact of bioturbation on reservoir quality and its spatial and vertical patterns, this study examined sedimentologically, ichnologically, and geostatistically ubiquitous bioturbated strata throughout outcrops of the Middle Jurassic Tuwaiq Mountain Formation and Upper Jurassic Hanifa Formation in central Saudi Arabia. Each lithofacies within the studied intervals had an ichnofabric index (ii) range from nonbioturbated (ii1) to beds completely homogenized by bioturbation (ii6). Most important was the occurrence of laterally extensive (>5 km) Glossifungites Ichnofacies, which represent firmgrounds with ii2 to ii5. These Glossifungites Ichnofacies are composed of complex and deep, three-dimensional Thalassinoides burrow networks (TBN) in mud-dominated lithofacies. These TBN have pore systems that consist of (1) open and partially open macropores (size of several centimeters), and (2) interparticle and moldic pores within the burrow filling, which consists of peloids, skeletal grains, and coated grains in a grain-dominated packstone texture. The TBN pore system, which typically penetrates the entire extent of the mud-dominated bioturbated beds, provides permeability pathways in an otherwise less permeable medium. Outcrop data and three-dimensional models suggest that these permeable pathways can contribute to overall reservoir flow in three ways: (1) TBN beds contribute to the overall reservoir flow as a single flow unit if bound above and below by impermeable beds (e.g., lateral flow in vertical well). (2) TBN breach the bed boundaries and, thus, connect above and below into more porous, more permeable grainy beds, providing overall reservoir connectivity for the carbonate reservoir and contributing to vertical and lateral flow. (3) TBN beds connect otherwise laterally compartmentalized reservoirs and contribute to vertical flow. Controls on the lateral and vertical variability of the TBN in the study area can be attributed to changes in water chemistry of the depositional environments, which are likely linked to global and local controls. This spatial and temporal relationship impacts the lateral and vertical distribution of flow properties of TBN strata in bioturbated reservoirs. Understanding such relationships is critical for secondary and tertiary recovery of oil by water flooding because such relationships can provide a prediction about the trend of vertical and lateral flow properties.