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Developing effective monitoring methods for elusive, rare, or patchily distributed species requires extra considerations, such as imperfect detection. Although detection is frequently modeled, the opportunity to assess it empirically is rare, particularly for imperiled species. We used Pecos assiminea (Assiminea pecos), an endangered semiaquatic snail, as a case study to test detection and accuracy issues surrounding quadrat searches. Quadrats (9 × 20 cm; n = 12) were placed in suitable Pecos assiminea habitat and randomly assigned a treatment, defined as the number of empty snail shells (0, 3, 6, or 9). Ten observers rotated through each quadrat, conducting 5-min visual searches for shells. The probability of detecting a shell when present was 67.4 ± 3.0%, but it decreased with the increasing litter depth and fewer number of shells present. The mean (± SE) observer accuracy was 25.5 ± 4.3%. Accuracy was positively correlated to the number of shells in the quadrat and negatively correlated to the number of times a quadrat was searched. The results indicate quadrat surveys likely underrepresent true abundance, but accurately determine the presence or absence. Understanding detection and accuracy of elusive, rare, or imperiled species improves density estimates and aids in monitoring and conservation efforts. [ABSTRACT FROM AUTHOR]

Overall descriptors of the information (determinicity) and entropy (uncertainty) content of complex molecular states are reexamined. These resultant concepts combine the classical (probability) contributions of Fisher and Shannon, and the relevant nonclassical supplements due to the state phase/current. The information-theoretic principles determining equilibria in molecules and their fragments are explored and the nonadditive part of the global entropy is advocated as a descriptor of the classical index of the quantum entanglement of molecular subsystems. Affinities associated with the probability and phase fluxes are identified and the criterion of vanishing overall information-source is shown to identify the system stationary electronic states. The production of resultant density of the gradient-information is expressed in terms of the conjugate affinities (forces, perturbations) and fluxes (currents, responses). The Schrödinger dynamics of probability and phase components of molecular electronic states is used to determine the temporal evolution of the overall gradient information and complex entropy. The global sources of the resultant information/entropy descriptors are shown to be of purely nonclassical origin, thus identically vanishing in real electronic states, e.g., the nondegenerate ground state of a molecule. [ABSTRACT FROM AUTHOR]