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1.
Ecol Evol ; 12(2): e8600, 2022 Feb.
Article in English | MEDLINE | ID: mdl-35222967

ABSTRACT

Spatial capture-recapture (SCR) analysis is now used routinely to inform wildlife management and conservation decisions. It is therefore imperative that we understand the implications of and can diagnose common SCR model misspecifications, as flawed inferences could propagate to policy and interventions. The detection function of an SCR model describes how an individual's detections are distributed in space. Despite the detection function's central role in SCR, little is known about the robustness of SCR-derived abundance estimates and home range size estimates to misspecifications. Here, we set out to (a) determine whether abundance estimates are robust to a wider range of misspecifications of the detection function than previously explored, (b) quantify the sensitivity of home range size estimates to the choice of detection function, and (c) evaluate commonly used Bayesian p-values for detecting misspecifications thereof. We simulated SCR data using different circular detection functions to emulate a wide range of space use patterns. We then fit Bayesian SCR models with three detection functions (half-normal, exponential, and half-normal plateau) to each simulated data set. While abundance estimates were very robust, estimates of home range size were sensitive to misspecifications of the detection function. When misspecified, SCR models with the half-normal plateau and exponential detection functions produced the most and least reliable home range size, respectively. Misspecifications with the strongest impact on parameter estimates were easily detected by Bayesian p-values. Practitioners using SCR exclusively for density estimation are unlikely to be impacted by misspecifications of the detection function. However, the choice of detection function can have substantial consequences for the reliability of inferences about space use. Although Bayesian p-values can aid the diagnosis of detection function misspecification under certain conditions, we urge the development of additional custom goodness-of-fit diagnostics for Bayesian SCR models to identify a wider range of model misspecifications.

2.
Muscle Nerve ; 13(8): 704-7, 1990 Aug.
Article in English | MEDLINE | ID: mdl-2385255

ABSTRACT

We report a patient who presented with involvement of multiple cranial nerves associated with otherwise typical neuralgic amyotrophy. This syndrome of unknown etiology is not limited to the brachial plexus. Simultaneous involvement of cranial nerves IX, X, XI, and XII is a unique presentation. The electrophysiological data indicate the presence of a multifocal neuropathy.


Subject(s)
Brachial Plexus Neuritis/physiopathology , Brachial Plexus/physiopathology , Cranial Nerve Diseases/physiopathology , Muscles/physiopathology , Brachial Plexus Neuritis/complications , Brachial Plexus Neuritis/diagnosis , Cranial Nerve Diseases/complications , Cranial Nerve Diseases/diagnosis , Electrophysiology , Humans , Male , Middle Aged , Muscles/pathology , Neural Conduction/physiology
3.
Reg Anesth ; 14(5): 251-2, 1989.
Article in English | MEDLINE | ID: mdl-2486649

ABSTRACT

Guillain Barre Syndrome (GBS) occurred 24 hours post-partum following an obstetrical epidural anesthetic (OEA) procedure. Clinical diagnosis was confirmed by cerebrospinal fluid (CSF) findings and nerve conduction velocity studies. GBS is an immune mediated process. Because of short latency between the onset of symptoms and the performance of the epidural block, a cause and effect relationship between epidural block and GBS in this patient is unlikely.


Subject(s)
Analgesia, Epidural/adverse effects , Analgesia, Obstetrical/adverse effects , Labor, Obstetric , Polyradiculoneuropathy/etiology , Adult , Bupivacaine , Epinephrine/administration & dosage , Female , Fentanyl , Humans , Pregnancy
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