On several occasions at paleontology-, geology-, and stratigraphy-related meetings during the past years, I noticed that many colleagues, even micropaleontologists, are not (anymore!) aware of the fundamental application potential of pre-Quaternary, fresh- and brackish-water ostracode fossils. Ostracodes, aquatic crawling or swimming microcrustaceans with a calcified bivalved shell and high fossilization potential, have rarely been considered as a major tool in biostratigraphy, fading mostly into the background compared to other fossil groups in the marine realm. In the continental realm, however, ostracodes are often the most common and abundant fossils, whether in freshwater or saline deposits. Yet, supraregional and intercontinental biostratigraphy based on aquatic organisms sounds absurd. It is not, however! Fresh- and brackish-water ostracodes have developed different strategies and mechanisms to facilitate their adaptation to temporary habitats and dispersal in such settings. Recent fresh- and brackish-water ostracodes, just as did their fossil counterparts, have a high potential to be passively distributed over long distances and across migration barriers by wind and larger animals, particularly owing to the desiccation- and freeze-resistant resting eggs of major groups (e.g., Horne and Martens, 1998) and, therefore, are a strong candidate for biostratigraphic application. Dealing with biostratigraphy of Lower Cretaceous continental deposits, it is important to understand that in most regions, except western Europe, we are not necessarily talking about high-resolution biostratigraphy. For example, many publications to-date on such deposits in Central Asia, South America, and Africa only provide an age of Early Cretaceous without further subdivision, and no attribution to stages. In the North American Western Interior foreland basin, Lower Cretaceous continental deposits are widely regarded to be of pre-middle Albian age, or to range from Aptian to Albian, sometimes Barremian–Albian in age (e.g., Cobban and Reeside, 1952; Peck, 1959; Mateer et al., 1992; Dyman et al. 1994; Way et …