How to consider history in landscape ecology: patterns,processes, and pathways

Landscape Ecology - Landscape ecology early on developed the awareness that central objects of investigation are not stable over time and therefore the historical dimension must be included, or at...     

Survival of tanoak (Lithocarpus densiflorus) and Pacific madrone (Arbutus menziesii) seedlings in forests of southwestern Oregon

Survival of tanoak (Lithocarpus densiflorus) and Pacific madrone (Arbutus menziesii) seedlings was studied in order to interpret succession in conifer hardwood forests and to determine ways to suppress establishment of these species. Seed protected from rodents and birds, and unprotected seed was sown in clearcuts and in conifer stands 40 to 200+ years old. Second-year survival rates of tanoak seedlings were high (50–70%) in exposed clearcuts and conifer stands. Seed predators appear to be of prime importance in limiting tanoak establishment. Survival rates of Pacific madrone seedlings on the same sites as the tanoak were low (0–8%), and many factors caused mortality. Seedlings of both species grew slowly; after 3 years, average tanoak height was only 6.0 to 14.0 cm, average madrone height 2.0 to 6.0 cm.     

An integrative approach for analysing landscape dynamics in diverse cultivated and natural mountain areas

Our landscape can be regarded as a development process that is affected and subsequently shaped by a series of different environmental and human-induced factors. However, to date, concrete data about the impact of each of these factors are still missing. One key reason for this is that methods of acquisition and evaluation of these factors inherently have differences, thereby preventing meaningful comparative analyses. This study presents an integrative methodical approach that bridges many of these gaps. Our approach also has the advantages of being generally applicable while delivering easily interpretable results that also allow comparisons between diverse geographical regions. The indicators used enable all major features of landscape change, e.g. changes in land use, landscape structuring, habitat settings, and urban sprawl, to be accurately monitored and provide high-quality realistic results that were validated in our study site, South Tyrol (North Italy). Indicators were selected for both their further subdivision, e.g. monocrops and different features of mixed crops, and their easy to ascertain hierarchically structured feature classification, e.g. land cover. Furthermore, our use of ecoregions enables better comparison of aspects of landscape development for geographical regions having diverse socio-economic and ecological conditions. Our methodical approach can be used as a basis not only for creating landscape change scenarios, but also for determining the environmental and human-induced factors involved and being able to list them in order of importance. Further the detected striking difference between the mapped land-use data and the official census data suggests a validation of the methodical approach in context of the national agriculture census.     

Response of old-growth conifers to reduction in stand density in western Oregon forests

The positive growth response of healthy young trees to density reduction is well known. In contrast, large old trees are usually thought to be intrinsically limited in their ability to respond to increased growing space; therefore, density reduction is seldom used in stands of old-growth trees. We tested the null hypothesis that old-growth trees are incapable of responding with increased growth following density reduction. The diameter growth response of 271 Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco), ponderosa pine (Pinus ponderosa Dougl. ex Laws) and sugar pine (Pinus lambertiana Dougl.) trees ranging in age from 158 to 650 years was examined 20 to 50 years after density reduction. Density reduction involved either light thinning with removal of less vigorous trees, or shelterwood treatments in which overstory trees were not removed. Ratios of basal area growth after treatment to basal area growth before treatment, and several other measures of growth, all indicated that the old trees sometimes benefited and were not harmed by density reduction. Growth increased by 10% or more for 68% of the trees in treated stands, and nearly 30% of trees increased growth by over 50%. This growth response persisted for at least 20 years. During this 20-year period, only three trees in treated stands (1.5%) exhibited a rapid decrease in growth, whereas growth decreased in 64% of trees in untreated stands. The length of time before a growth response to density reduction occurred varied from 5 to 25 years, with the greatest growth response often occurring 20 to 25 years after treatment. These results have important implications both for the basic biology of aging in woody plants as well as for silvicultural practices in forests with old-growth trees.     

Observed dynamics of ponderosa pine (<Emphasis Type="Italic">Pinus ponderosa</Emphasis> var. <Emphasis Type="Italic">ponderosa</Emphasis> Dougl. ex Laws.) seedling recruitment in the Cascade Range,USA

An observational study of early seedling establishment (first 1–2 summers after emergence) was conducted in four ponderosa pine (Pinus ponderosa var. ponderosa Dougl. ex Laws.) stands east of the Cascade Range crest in central Oregon, USA. Newly emerged ponderosa pine seedlings were identified at the start of summer and were monitored through their second summer; a subsequent cohort of seedlings was identified and monitored for one summer. About 3% of the viable seed that was produced resulted in new seedlings. Mortality was substantial immediately following emergence. Most seedlings emerged without shading from understory vegetation, but few survived. Most seedlings alive after one year had emerged beneath live cover; by the end of two summers only shaded seedlings were alive. 63–85% of new seedlings initiated in clusters attributed to rodent caching, and seedlings originating in clusters remained a substantial proportion of the cohort (60%) after two seasons. Results suggest that understory vegetation in these types of stands facilitates the recruitment of ponderosa pine seedlings, most likely by buffering them against environmental stressors during the seedling establishment phase. They also reveal that seed caching rodents are highly active in seed redistribution and can exert a lasting influence on seedling recruitment.     

In vivo measurement of central corneal thickness in normal chicks (Gallus gallus domesticus) with the optical low-coherence reflectometer

Objective To determine the practicability and accuracy of central corneal thickness (CCT) measurements in living chicks utilizing a noncontact, high‐speed optical low‐coherence reflectometer (OLCR) mounted on a slit lamp. Animals studied Twelve male chicks (Gallus gallus domesticus). Procedures Measurements of CCT were obtained in triplicate in 24 eyes of twelve 1‐day‐old anaesthetized chicks using OLCR. Every single measurement taken by OLCR consisted of the average result of 20 scans obtained within seconds. Additionally, corneal thickness was determined histologically after immersion fixation in Karnovsky’s solution alone (20 eyes) or with a previous injection of the fixative into the anterior chamber before enucleation (4 eyes). Results Central corneal thickness measurements using OLCR in 1‐day‐old living chicks provide a rapid and feasible examination technique. Mean CCT measured with OLCR (189.7 ± 3.34 μm) was significantly lower than histological measurements (242.1 ± 47.27 μm) in eyes with fixation in Karnovsky’s solution (P = 0.0005). In eyes with additional injection of Karnovsky’s fixative into the anterior chamber, mean histologically determined CCT was 195.2 ± 8.25 μm vs. 191.9 ± 8.90 μm with OLCR. A trend for a lower variance was found compared to the eyes that had only been immersion fixed. Conclusion Optical low‐coherence reflectometry is an accurate examination technique to measure in vivo CCT in the eye of newborn chicks. The knowledge of the thickness of the chick cornea and the ability to obtain noninvasive, noncontact measurements of CCT in the living animal may be of interest for research and development of eye diseases in chick models.     

Recruitment of ponderosa pine seedlings in the Cascade Range

Abiotic stresses on seedling regeneration in xeric ecosystems are great, hence recruitment processes can be facilitated by stand factors that ameliorate the germinant-scale microenvironment. An experiment was conducted on the eastern slope of the Cascade Range to test the effects of shrub cover, simulated seed caching, and substrate on the recruitment of Pacific ponderosa pine (Pinus ponderosa var. ponderosa Dougl. ex Laws.) seedlings. Failure rates of seeds sowed in exclosures were large, with less than 30% emerging as germinants in the spring following fall sowing. Simulated seed caching improved emergence rates by more than sevenfold and was responsible for 88% of all spring germinants. Emergence rates were lowest from uncached seeds on litter. Just 16% of the crop survived the summer and fall to the month of November, or less than 5 months after emergence. Shrub cover did not affect emergence rates, but establishment rates were higher: seedlings beneath shrubs succumbed to desiccation at a slower rate than unshaded seedlings. By August there were 2.3 times more survivors at shrub-shaded sites than unshaded sites, and by the end of fall, when seedlings were considered established, more than 78% existed beneath shrubs. This study provides evidence that the natural recruitment of ponderosa pine seedlings is facilitated by the occurrence of the species’ common shrub associates.