Is the way an oil spill response is reported in the media important for the final perception of the clean-up?

This research investigates the media coverage during the C/V Rena grounding in New Zealand (NZ), in 2011, to analyze if information reported in printed media is important for the final perception of the overall oil spill response. We took all articles available from NZ's largest circulated newspaper and the regional newspaper closest to the incident and analyzed the themes within each article; the article's tone (positive, neutral or negative); the time of the report relative to incident events and any differences between the regional and national papers. This analysis indicates that oil spills are reported and perceived as inherently negative incidents. However, along with coordinating an effective spill response, fast, factual and frequent media releases and increased effect in media liaison in areas of response with high public intrinsic value such as oiled wildlife response can significantly influence tone of media coverage and likely overall public perception.

Pathogen presence in feral pigs and their movement around two commercial piggeries in Queensland, Australia.

Feral pigs are wild animal reservoirs of infectious pathogens transmissible to other species, all of which are transmissible to domestic pigs. The objective of this study was to detect the presence of harmful production-limiting pathogens; Brucella suis, Leptospira species, Lawsonia intracellularis, Mycoplasma hyopneumoniae and Actinobacillus pleuropneumoniae in a feral pig population within a 10 km radius of two large-scale commercial piggeries in Southern Queensland, Australia. The movement pattern of six pigs within the feral population was also investigated using geographic positioning system collars. All pathogens were present in the feral pig population except for A pleuropneumoniae. The true seroprevalence (TP) from 83 serum samples was 10.5 per cent for B suis, 48.6 per cent for Leptospira species, 100 per cent for L intracellularis and 42.1 per cent for M hyopneumoniae. Of 72 lung samples, 27.6 per cent were positive for M hyopneumoniae. Serum samples from 86 domestic sows within the study region were positive for Leptospira species (TP 2.1 per cent), L intracellularis (TP 100 per cent) and M hyopneumoniae (TP 100 per cent). The majority of feral pig movement was within 5 km of the piggeries, with one approaching to 100 m of the free-range piggery. The presence of pathogens in feral pigs in such close proximity to commercial piggeries could pose a biosecurity risk.

Capacity of the retinogeniculate pathway to reorganize following ablation of visual cortical areas in developing and mature cats.

The purpose of the present study was to determine the pattern and density of retinal projections to the dorsal lateral geniculate nucleus (dLGN) following ablation of visual cortical areas in developing cats of different postnatal ages and in mature cats. The terminations of retinal projections to the dLGN were evaluated following the injection of tritiated amino acids into one eye. Regardless of age, a visual cortical ablation of areas 17 and 18 induces massive death of neurons within the regions of the dLGN that are linked topographically to the cortical areas removed. However, the pattern of retinal projections to these degenerated regions of the dLGN differs depending upon whether the cortical lesion is incurred early in postnatal life or in adulthood. Following ablation on the day of birth (P1), virtually all surviving cells were found in the C-complex of dLGN with only a token number in the A-laminae. Correspondingly, retinal projections were maintained to the C-complex of the nucleus and were barely detectable in the degenerated A-laminae. However, in cats in which areas 17 and 18 had been removed in adulthood (> or = 6 months of age) retinal projections were maintained to the A-laminae even though nearly all neurons in those laminae had degenerated. Moreover, a subgroup of animals that incurred area 17 and 18 ablations at P1 showed that the modification of retinal projections to the A-laminae occurs within the first postnatal month, and an additional subgroup showed that retinal projections become increasingly resistant to the degenerative events in the dLGN that follow ablation of areas 17 and 18 at progressively older ages during the first postnatal month. Furthermore, retinal inputs also respond, in an age-dependent way, to degeneration of neurons in the C-complex induced by extension of the cortical ablation to include extrastriate visual areas.

Microglial invasion and activation in response to naturally occurring neuronal degeneration in the ganglion cell layer of the postnatal cat retina.

Retinae of kittens between postnatal (P) days 2 and 10 were examined for the presence of degenerating neuronal profiles, normal nucleoli and microglia. Comparison of the numbers of degenerating profiles with numbers of axons lost from the optic nerve suggest that the majority of these profiles result from the degeneration of retinal ganglion cells. Analysis of local densities of the different profiles revealed different rates of cell loss, occurring at different times in central and peripheral retina. The period of rapid cell loss occurred between P2 and P3 in central retina compared to between P8 and P10 in peripheral retina. At both locations, these periods of rapid cell loss were accompanied by a decrease in the ratio of microglia to dying cells even though the absolute densities of microglia increased. However, calculation of the clearance times of cellular debris indicate that the speed of removal of degeneration products is greater during rapid cell loss, which suggests that cellular degeneration serves to activate the phagocytic process.

Tritiated uridine uptake in the retinal ganglion cell layer of the cat during normal development and after visual cortex ablation.

The short-term metabolic response of immature retinal ganglion cells to destruction of their target cells in the dorsal lateral geniculate nucleus (dLGN) was assessed in newborn cats. Retrograde degeneration of virtually all dLGN cells was induced by ablation of the 13 contiguous areas of visual cortex on the day of birth. The metabolic response of retinal ganglion cells to this loss of target cells in dLGN was determined by exposing the ganglion cell layer to tritiated uridine, a precursor of RNA. Control measurements were made from unoperated littermates. Following sectioning and processing of the retinae from both groups of kittens for autoradiography, silver grain densities overlying the cellular profiles in the ganglion cell layer were calculated. These calculations revealed levels of uridine incorporation at Postnatal Day 4 in both groups of kittens significantly higher than at either Postnatal Day 2 or 7, but no significant differences between the two groups on any day examined. These results show that the level of RNA synthesis in retinal ganglion cells increases temporarily during the first postnatal week and that this synthesis is unaffected by the death of target cells in the dLGN. The temporary increase may be related to the establishment of synaptic connections on retinal ganglion cells by their afferent bipolar and amacrine neurons in the inner nuclear layer.

Atrophy and degeneration of ganglion cells in central retina following loss of postsynaptic target neurons in the dorsal lateral geniculate nucleus of the adult cat.

Selective degeneration of neurons in the dorsal lateral geniculate nucleus (dLGN) of the adult cat was produced by in situ injection of kainic acid. This rapid degeneration mimics the loss of lateral geniculate neurons seen after neonatal visual cortex ablation. Following survivals of 2, 4, or 6 months, the geniculate was injected with horseradish peroxidase (HRP) and the retinas were examined for the presence of retrogradely labeled, as well as unlabeled, cells. Total ganglion cell density in central nasal retina was not different from that of controls at 2 or 4 months, but by 6 months had decreased to 68% of control values. The proportion of cells labeled with HRP did not change at 2 months, but decreased from 84% in controls to less than 1% by 4 months, and none were labeled at 6 months. Surviving ganglion cells in central retina showed atrophy of the cell body, a finding not apparent in data from the retinal periphery. Shrinkage occurred in the few cells labeled with HRP surviving at 4 months, as well as among the unlabeled cells surviving at 4 and 6 months. These results show that the survival of central retinal ganglion cells in the cat continues to depend on intact target neurons beyond the period of development. Mature ganglion cells in central retina respond to loss of appropriate targets first by axon terminal retraction and then by atrophy and cell death. However, when compared to the response of cells located in far peripheral retina following dLGN neuron loss, central ganglion cells take longer to undergo axonal retraction and a greater proportion of the central ganglion cells, although atrophied, survive after 6 months.

Gliosis and ganglion cell death in the developing cat retina during hydrocephalus and after decompression.

Even after surgical decompression, infantile hydrocephalus often results in permanent neurological symptoms, including visual deficits. However, little is known about the cellular changes that may be responsible for these effects. The present study was designed to analyze the retinae of normal, mildly hydrocephalic, severely hydrocephalic and surgically decompressed kittens to determine if changes occur in the density and size of retinal ganglion cells. Hydrocephalus was induced in 10 day old kittens by intra-cisternal injection of kaolin. Kittens were allowed to survive from 7 to 28 days after injection. Animals that were decompressed received ventriculoperitoneal shunts 10-15 days after the induction of hydrocephalus and were sacrificed 10-14 days after shunt placement. The density and area of neuronal and glial cells were determined within a sample area in peripheral nasal retina. Total cell density was significantly increased in mildly and severely hydrocephalic animals but returned to normal following decompression. This change represents a significant increase in the glial population. In addition, there was a significant loss of ganglion cells in both the severely hydrocephalic and the shunted groups. Based on these findings, we conclude that gliosis occurs as a result of cell death in the retina following severe hydrocephalus, and decompression is unable to reverse these effects. Furthermore, gliosis occurs in mild cases of hydrocephalus, and may be an early indication that cellular degeneration will follow.

Retinal ganglion cell degeneration following loss of postsynaptic target neurons in the dorsal lateral geniculate nucleus of the adult cat.

Kainic acid was used to produce selective degeneration of neurons in the dorsal lateral geniculate nucleus of the adult cat. This degeneration mimics the rapid loss of geniculate neurons seen after visual cortex ablation in the neonate. Following survivals of 2, 4, or 6 months, the geniculate was injected with horseradish peroxidase and the retinae were examined for the presence of retrogradely labeled cells. Analysis of ganglion cell density in peripheral nasal retina revealed a 58% loss of cells overall at 6 months. The proportion of cells labeled with horseradish peroxidase decreased more rapidly, until none were labeled at 6 months. Separate analysis of small, medium, and large ganglion cell populations revealed that only medium-sized cells were lost at 2 months whereas both medium and large cells were lost at 4 and 6 months. By 6 months, 92% of medium cells and 65% of large cells had degenerated. These results show that mature retinal ganglion cells in the cat maintain a dependence on target integrity for their continued survival. When the appropriate target is lost, the ganglion cells respond first by axon terminal retraction and then by cell death.

Response of retinal terminals to loss of postsynaptic target neurons in the dorsal lateral geniculate nucleus of the adult cat.

We have used the neurotoxin kainic acid to produce rapid degeneration of neurons in the dorsal lateral geniculate nucleus (dLGN) of the adult cat. This degeneration mimics the rapid loss of geniculate neurons seen after visual cortex ablation in the neonate. Subsequent anterograde transport of horseradish peroxidase injected into the eye was used to reveal the projection patterns of retinal ganglion cell axons at different survival periods after the kainic acid injection. The density of retinal projections to the degenerated regions of the geniculate was reduced considerably at 4 and 6 months survival, but at 2 months was not significantly different from normal. The laminar pattern of projections to degenerated regions of the geniculate did not change in any animals studied, even when an adjacent lamina contained surviving cells. Electron microscopic examination of degenerated dLGN revealed intact retinal (RLP) and RSD terminals at all survival times, although the density of terminals appeared much reduced when compared to controls. Some RLP terminals exhibited the "dark reaction" of degeneration and these degenerating terminals were most numerous at 2 months survival. These findings demonstrate that, in response to degeneration of their usual target cells, mature retinal ganglion cells with withdraw their axon terminals from these regions of degeneration. We conclude that mature retinal ganglion cells continue to be dependent on target integrity for the maintenance of a normal axonal arborization.

Selectivity of kainic acid as a neurotoxin within the dorsal lateral geniculate nucleus of the cat: a model for transneuronal retrograde degeneration.

In situ injections of the cytotoxin kainic acid were used to make localized lesions of the dorsal lateral geniculate nucleus in the adult cat to produce a model for studying the effects of postsynaptic target loss. Kainic acid has been used extensively to produce lesions of neuronal cell bodies within the central nervous system. However, the selectivity of kainic acid has been questioned, as it may also affect afferent terminals or axons of passage. Retinal projections to degenerated geniculate nuclei were visualized 1 week after kainate injection using anterograde labelling with horseradish peroxidase and electron microscopy. The results demonstrate the presence of afferent terminals within regions of neuronal loss, and hence the selectivity of kainic acid for intrinsic geniculate neurons.

Consequences of visual deprivation in the absence of binocular competitive mechanisms in Siamese cat area 17.

The Siamese cat is a mutant with abnormally crossed visual pathways, which provides a model for studying the effects of visual deprivation in the absence of binocular competitive interactions. Siamese cats are known to be resistant to the effects of monocular eyelid suture. To further explore the nature of this resistance, the receptive field properties of neurons in area 17 of monocularly (MD) and binocularly (BD) deprived Siamese cats were studied. Neither condition produced a loss of cortical responsiveness, which is a characteristic result of binocular deprivation in normally pigmented cats. Somewhat more units in the deprived hemisphere of MD Siamese cats were orientation-selective, and many more units were direction-selective than in BD Siamese cats. This difference may be due to an effect of visual attentional mechanisms, which can function in MD but not BD Siamese cats. To test whether the resistance to the effects of visual deprivation in Siamese cats might be a more general phenomenon. Siamese and normally pigmented cats were raised in an 8-Hz stroboscopically illuminated environment. Both groups showed a severe loss of direction selectivity. Some of the normally pigmented cats also showed a loss of binocularity, which appeared to be secondary to strabismus.

Neocortical connections in fetal cats.

The major extrinsic projections to and from visual and auditory areas of cerebral cortex were examined in fetal cats between 46 and 60 days of gestation (E46-E60) using axonal transport of horseradish peroxidase either alone or in combination with tritiated proline. Projections to visual cortex from the dorsal lateral geniculate nucleus and lateral-posterior/pulvinar complex exist by E46, and those from the contralateral hemisphere, claustrum, putamen, and central lateral nucleus of the thalamus are present by E54-E56. In addition, cells in the medial geniculate nucleus project to auditory cortex by E55. At E54-E56 efferent cortical projections reach the contralateral hemisphere, claustrum, putamen, lateral-posterior/pulvinar complex and reticular nucleus of the thalamus. Cells in visual cortex also project to the dorsal and ventral lateral geniculate nuclei, pretectum, superior colliculus and pontine nuclei, and cells in auditory cortex project to the medial geniculate nucleus. Except for interhemispheric projections, all pathways demonstrated are ipsilateral, and projections linking cerebral cortex with claustrum, dorsal lateral geniculate nucleus and lateral-posterior/pulvinar complex are reciprocal. The reciprocal projections formed with the dorsal lateral geniculate nucleus, lateral-posterior/pulvinar complex and the claustrum show a greater degree of topological organization compared to the projections formed with the contralateral hemisphere and superior colliculus, which show little or no topological order. Therefore, the results of the present study show that the major extrinsic projections of the cat's visual and auditory cortical areas with subcortical structures are present by the eighth week of gestation, and that the origins and terminations of many of these projections are arranged topologically.

The effects of neonatal monocular enucleation on the organization of ipsilateral and contralateral retinothalamic projections in the rabbit.

Autoradiographic methods were used to compare the ipsilateral and contralateral retinothalamic projections in pigmented Dutch-Belted rabbits that had neonatal monocular enucleation with the projections found in normally reared rabbits. In the normal adult rabbit, there is dense label throughout the dorsal lateral geniculate nucleus (LGd) except for a decreased label density in the region corresponding to the ipsilateral input. Following neonatal monocular enucleation, the contralateral projection fills in the part of the LGd corresponding to the ipsilateral input. Our data indicate that following monocular enucleation, two processes occur: an arrest of the segregation process and an expansion of the contralateral projection into the space normally containing the terminals of the ipsilateral projection. In addition, this filling in of the terminal space occurs relatively rapidly and is completed by day 14. No changes, however, were observed in the ipsilateral projection to the LGd. Unlike the LGd, the ventral lateral geniculate nucleus and the intergeniculate leaflet showed increases in the size of the ipsilateral projection region, and no changes in the contralateral projection. The present findings suggest that there may be different mechanisms governing whether alterations in the distribution of retinothalamic projections will occur in either the ipsilateral or contralateral nucleus.

Role of corpus callosum in functional organization of cat striate cortex.

The short-term (3-51 days) and long-term (31-42 wk) effects of corpus callosum transection on the receptive-field properties of neurons were assessed at the single-cell, architectural, and topographical levels of organization in the cat striate cortex. Corpus callosum transection decreased the proportion of neurons that could be activated from both eyes. In short-term animals, the reduction in binocularity was restricted to the representation of a vertical strip of visual space extending from the vertical meridian to at least 12 degrees lateral. In the long-term animals, the reduction in binocularity was restricted to the representation of visual space 4 degrees lateral to the vertical meridian. Therefore, the reduction in the representation of 4-12 degrees was only temporary. In both groups, the reduction in binocularity was less in the representation of area centralis than at other retinal locations in the same vertical strip. The region of area 17 affected permanently by the transection receives fibers from the contralateral hemisphere in normal animals. The region affected temporarily by the transection contains callosal cells but does not contain callosal terminals. Binocularity was assessed separately for simple I, simple II, and complex receptive-field types. The reduction in binocularity in the 12 degrees strip in short-term animals and in the 4 degrees strip in long-term animals was accounted for mainly by a reduction in binocularity of simple I and complex cells. As in normal animals, complex cells in callosum-transected cats were always more binocular than the other cell types. An analysis of the effects of corpus callosum transection on different cortical layers showed that a greater proportion of cells in the supragranular layers II and III showed a reduction in binocularity than in the infragranular layers V and VI. The proportion of binocular neurons in layer IV was not significantly different from normal. The major decreases in binocularity occurred in layers II, III, and VI for simple I and simple II cells and in layers II, III, and V for complex cells. The binocularity of simple II cells in layer IV and complex cells in layer VI was not affected. The effects of the transection on the columnar organization of the cortex were assessed by making electrode tracks that passed in the radial or laminar dimensions of the cortex. Reconstructions of the radial tracks showed that cells within one radial column tended to be dominated by the same eye. In adjacent columns, cells tended to be dominated by different eyes.(ABSTRACT TRUNCATED AT 400 WORDS)

Deafferentation and axotomy of neurons in cat striate cortex: time course of changes in binocularity following corpus callosum transection.

Single neurons were recorded in the callosal terminal and cell zones of area 17 in the cat to assess the time course of changes in the proportion of binocular neurons produced by corpus callosum transection. The callosal terminal zone contains all the degenerating terminals in area 17 after corpus callosum transection. The callosal cell zone contains all the cells in area 17 which contribute axons to the corpus callosum. The cell zone is larger than, and partially overlaps, the callosal terminal zone. After corpus callosum transection there was an initial change in ocular dominance of neurons in both callosal zones. This initial change was followed by a reduction in the proportion of binocular neurons in both zones. This reduction became maximal 2-4 weeks after transection. In the callosal terminal zone, binocularity did not recover even at the longest postoperative periods examined (31-42 weeks). In the part of the callosal cell zone outside of the callosal terminal zone, the proportion of binocular neurons began to recover after 5 weeks and was at normal levels at the longest survival periods studied. Corpus callosum transection deafferents and axotomizes cells in the callosal terminal zone and, since central neurons do not regenerate their long-ranging axons, the combined effects of deafferentation and axotomy in this zone are permanent. The callosal cell zone outside of the callosal terminal zone contains axotomized cells and no degenerating terminals following transection. The recovery of binocularity in this region may be attributed to the transient changes which axotomized cells undergo. The zone which contains no callosal cells or terminals is unaffected by transection of the corpus callosum.

Transneuronal degeneration of beta retinal ganglion cells in the cat.

Transneuronal retrograde degeneration of retinal ganglion cells was investigated following neonatal visual cortex ablation in the cat. After a survival time of at least 18 months, retinal ganglion cells projecting to the thalamus were labelled by retrograde transport of horseradish peroxidase. Filled ganglion cells were classified into alpha, beta and gamma types on the basis of dendritic morphology. In normal cats, alpha cells made up 8-10% of the total population in the sample area, beta cells made up 64-67% and gamma cells made up 23-27%. In retinae of visual cortex-ablated cats, normal numbers of alpha and gamma cells were present, but the beta cell population was depleted by 90% of normal. Thalamic projections of surviving retinal ganglion cells were investigated by anterograde transport of tritiated proline injected into the eye. In these animals, ablation of visual cortex resulted in almost complete degeneration of laminae A and A1 of the dorsal lateral geniculate nucleus. In the radioautographic material, projections from the retina to the degenerated parts of laminae A and A1 were barely detectable. Survival of some ganglion cell populations and death of others after neonatal visual cortex ablation may be explained in terms of the pattern of projections of the different cell types. We conclude that the majority of beta cells degenerate following visual cortex ablation because of removal of cells in the dorsal lateral geniculate nucleus which form their sole or principal target. Alpha and gamma cells and 10% of beta-cells survive because of extensive collateral projections to targets other than cells of the laminae A and A1 of dorsal lateral geniculate nucleus.

Effects of stroboscopic rearing on the response properties and laminar distribution of single units in the rabbit superior colliculus.

Single neurons were recorded from the superior colliculus of rabbits reared in a stroboscopically illuminated environment, and data were compared with recordings made from the superior colliculus of normally reared rabbits. Some of the consequences of strobe rearing were observed in all laminae of the superior colliculus: direction selectivity was abolished, receptive field size was increased and there was an increase in the proportion of cells responding more strongly to the offset than to the onset of light. Other consequences of strobe-rearing were observed selectively in specific laminae of the superior colliculus. Among cells influenced by a stroboscopic stimulus, cells in SGSu were more often responsive to the strobe stimulus, whereas cells in SGS1 were more often strobe inhibited. In layers deep to SO, equal numbers of cells showed strobe responsivity and strobe inhibition. Inhibitory surround organization was more strongly affected by strobe rearing in the deep layers, and external inhibition was abolished in layers deep to SO. The results indicate that strobe rearing has significant effects on responsivity to stroboscopic illumination, and on several other receptive field characteristics including direction selectivity, receptive field size, surround inhibition and responsivity to light offset. The data are discussed with reference to the role of the cortico-collicular projection.

Frequency specific effects of stroboscopic rearing in the visual cortex of the rabbit.

Rearing animals in stroboscopic illumination deprives those animals of the experience of visual motion. In the rabbit, stroboscopic rearing produces a significant alteration in the response properties of cells in the visual cortex, demonstrating that the rabbit visual system is susceptible to environmental manipulation during early postnatal life. Response properties were determined for single units recorded in the primary visual cortex of 3 groups of rabbits. One group had been reared from birth to 2 months of age at a stroboscopic flash frequency of 8 Hz, a second group was raised at a flash frequency of 4 Hz and a third was reared normally. Compared to normal rabbits, rabbits reared at 8 Hz showed a reduction in the proportion of orientation selective cells which were also direction-selective, and there was an increase in the proportion of cells responsive to stroboscopic flashes. There was no reduction, however, in the overall proportion of orientation-selective cells. This contrasts with the finding for the rabbits raised at a flash frequency of 4 Hz. In addition, cortical cells in the rabbits raised at 8 Hz responded to frequencies of stroboscopic flashes which were significantly higher than the frequencies found for cells in the rabbits raised at 4 Hz. The effects of stroboscopic rearing on the rabbit visual cortex are dependent, therefore, on the flash frequency experienced by the rabbits during development.

Critical periods in development for susceptibility to the effects of stroboscopic rearing in the rabbit visual cortex.

Previous studies have shown that rearing rabbits in a stroboscopically illuminated environment results in a decrease in orientation and direction selectivity and an increase in responsivity to stroboscopic stimuli among neurons in area 17. In the present study, the critical period for susceptibility to these effects was studied by varying the time of onset of the deprivation. Groups of Dutch belted rabbits were reared normally and then placed in a stroboscopically illuminated environment at ages 1, 2 or 3 months, and response characteristics of visual cortical neurons were compared with those obtained from normal rabbits and from rabbits reared in a stroboscopic environment from birth. Results show that the different effects of strobe rearing have different critical periods. Increased responsivity to stroboscopic stimuli was seen only in rabbits deprived from birth. The effects of strobe rearing on both direction and orientation selectivity decreased with increasing age at the time of onset of the deprivation. However, only direction selectivity was modified by deprivation beginning at 3 months of age.