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PubMed1999

Subjective probability of disjunctive hypotheses: local-weight models for decomposition of evidential support.

When the probability of a single member of a set of mutually exclusive and exhaustive possibilities is judged, its alternatives are evaluated as a composite "residual" hypothesis. Support theory (Rottenstreich & Tversky, 1997; Tversky & Koehler, 1994) implies that the process of packing alternatives together in the residual reduces the perceived evidential support for the set of alternatives and consequently inflates the judged probability of the focal hypothesis. Previous work has investigated the global weights that determine the extent to which the overall evidential support for the alternatives is discounted by this packing operation (Koehler, Brenner, & Tversky, 1997). In the present investigation, we analyze this issue in greater detail, examining the local weights that measure the specific contribution of each component hypothesis included implicitly in the residual. We describe a procedure for estimating local weights and introduce a set of plausible properties that impose systematic ordinal relationships among local weights. Results from four experiments testing these properties are reported, and a local-weight model is developed that accounts for nearly all of the variance in the probability judgments in these empirical tests. Local weights appear to be sensitive both to the individual component with which they are associated and to the residual hypothesis in which the component resides.

Cognition↗
PubMed1996

A disjunct Californian strain of Entomophaga aulicae infecting Orgyia vetusta.

Fungal epizootics occurred in abundant Orgyia vetusta (western tussock moth; Lepidoptera: Lymantriidae) populations on Lupinus arboreus bushes growing on the Pacific coast north of San Francisco, California. The causative pathogen was isolated and identified as Entomophaga aulicae, Group II, based on RFLPs using rDNA and PCR-amplified rDNA products. Inability of this fungus to infect the lymantriid Lymantria dispar (gypsy moth) confirmed its distinction from Entomophaga maimaiga, the only other member of this species complex which predominantly infects lymantriids. Later instar wandering by O. vetusta in outbreak populations and close proximity of larvae in dense populations are characteristics most probably promoting development of E. aulicae epizootics; these life history patterns are also typical of Lymantria dispar populations experiencing epizootics of E. maimaiga.

Animals↗
PubMed1999

Divergence of a linear and a circular plasmid in disjunct natural isolates of the fungus Neurospora.

It is known from DNA hybridization and other studies that Neurospora plasmids are widely distributed across species of this genus. However few comparisons have been performed of the structure of apparently identical plasmids in widely differing geographical and biological locations. We compare pairs of circular and linear mitochondrial plasmids from distant geographical locations. The circular plasmids (LaBelle and Harbin-1) were from different ecotypes of N. intermedia and the linear plasmids (maranhar and Harbin-3) were from different species (N. crassa and N. intermedia). The structures are highly similar at the sequence level showing that they are closely related. Most of the differences are outside the presumptive genes (coding for polymerases). Furthermore, most of the proposed functional motifs have been retained. Sequence divergence is compatible with a distribution model by vertical descent from a common ancestor, but horizontal transmission cannot be ruled out.

Amino Acid Sequence↗
PubMed1996

Cranial disjunction and visual failure in a slit ventricle syndrome with patent shunt.

A 6.5-year-old child who received a shunt at 3 weeks of age for triventricular hydrocephalus related to his congenital toxoplasmosis developed symptoms of intracranial hypertension and papilloedema. Computed tomographic scan demonstrated slit ventricles. The shunt device was shown to be patent on isotope transit study. Spontaneously the cranial sutures widened and headaches disappeared, but loss of vision occurred and did not reverse despite optic nerve sheath fenestration. We suspect that a rapid drop in intracranial pressure played a role in the pathogenesis of our patient's blindness. This possible complication should be taken into account when calvarial expansion is planned in a patient with an intracranial hypertension syndrome with papilloedema in the presence of slit ventricles and a patent shunt.

Blindness↗
PubMed1981

Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families.

A syndrome due to 3:1 meiotic segregation of balanced 11/22 translocation is defined from nine personally observed patients and 22 cases from the literature with apparently the same aberration. Frequent findings include a characteristic face with deep-set eyes, flat nose, prominent upper lip, receding mandible and preauricular pits or tags, male genital hypoplasia, anal atresia or other anomalies of the anus, cleft palate, and congenital heart defect. Less frequent are severe reduction of the auricles, an additional pair of ribs, and hypoplasia of the diaphragm. Perinatal mortality is high. Growth is usually and psychomotor development is invariably and severely delayed. Balanced 11/22 translocations are apparently disproportionally frequent; as the balanced rearrangement is not easy to detect, it is important to be aware of it at the family investigation of cases with extra chromosomes similar to a No. 22 or 22q-. The unbalanced products are most probably trisomic for both a segment of 22 (22q-) and a distal segment of 11q; the exact determination of the breakpoints is not possible at present due to the similar banding characteristics of the two segments involved in the translocation.

Abnormalities, Multiple↗
PubMed1984

Use of a chromosome 21 cloned DNA probe for the analysis of non-disjunction in Down syndrome.

A recombinant clone was isolated containing a sequence which occurs only on human chromosome 21 and defines a two-allele restriction fragment length polymorphism showing Mendelian inheritance. Forty seven percent of the London population are heterozygous for the polymorphism. The chromosomal location of the DNA sequence homologous to the probe was confirmed using rodent-human somatic cell hybrids. DNA from persons with Down syndrome and from their parents was analysed. It was possible to confirm trisomy 21 by dosage hybridisation to Southern blots, and to determine the origin of the supernumerary chromosome. The technique will be of use for determination of the paternal or maternal origin of nondisjunction in cases of Down syndrome which are not informative using existing markers.

Adult↗
PubMed1986

Evidence for the repeated primary non-disjunction of chromosome 21 as a result of premature centromere division (PCD).

A clinically normal 28-year-old woman had three conceptuses with trisomy 21 and one normal child. She showed minimal cytogenetic evidence of mosaicism: 4% of her blood cells and 6% of skin fibroblasts had trisomy 21. Also, 7% of her blood cells showed aneuploidy of the X chromosome which was associated with premature centromere division (PCD,X); 6% of fibroblasts showed trisomy 18, 10% of fibroblasts showed PCD,21, and 1% PCD,18. It is unlikely that this woman is a constitutional mosaic for trisomies X, 18, and 21, all at low levels. We suggest that she has a predisposition to irregular centromere separation and that chromosomes X, 18, and 21 are most susceptible to its action.

Adult↗
PubMed1987

Disjunctive models of Boolean category learning.

Four connectionistic/neural models which are capable of learning arbitrary Boolean functions are presented. Three are probably convergent, but of differing generalization power. The fourth is not necessarily convergent, but its empirical behavior is quite good. The time and space characteristics of the four models are compared over a diverse range of functions and testing conditions. These include the ability to learn specific instances, to effectively generalize, and to deal with irrelevant or redundant information. Trade-offs between time and space are demonstrated by the various approaches.

Brain↗