The delay of flowering time in almond: a review of the combined effect of adaptation,mutation and breeding

Regulation of flowering time in almond, as in other Prunus species, is a complex process involving both chill and heat requirements. Following exposure to appropriate consecutive periods of cold and warm temperatures, the buds break dormancy and sprout or flower depending on bud type. To maximize flowering and subsequent vegetative growth and fruit set, chilling and ensuing warm temperature requirements have to be fully satisfied. Because of its potential for very early flowering, flowering time in almond is a major determinant of its adaptation to new environments. In colder regions, Late-flowering is often necessary to avoid frost damage during and just after flowering. Consequently, the selection of delayed flowering times remains an important objective in almond improvement programs. Flowering time is considered a quantitative though highly heritable trait. In addition, a dominant gene (Late flowering, Lb), originally identified in a spontaneous mutation of the Californian almond cultivar ‘Nonpareil’, was also described. The objective of this review is a comparative analysis of the effects of regional adaptation, breeding and mutation on the delay of flowering time in new almond cultivars. Findings indicate that the adaptation of almonds from the Mediterranean basin to colder regions in Northern Europe and America has been mainly achieved through delayed flowering. These adapted late-flowering cultivars have usually been developed by selecting desired quantitative genes within each regional germplasm. Additional progress thus appears achievable with a more comprehensive understanding of the quantitative and qualitative genetics controlling this trait. The use of molecular markers for the early selection of genes conferring late flowering, including both spontaneous mutations as well as unique regional germplasm, should allow development of even later cultivars including ultra-late cultivars flowering as into April.     

Evaluation of potato clones for their adaptation to medium altitude conditions in the tropics

Potato is one of the most important crops in the world, including in the tropics. Potato requires low temperatures or cool climate for optimum tuber yield, which in the tropics, can be obtained mostly in high altitude growing areas. The limitation of land availability for potato production in highland areas of some tropical countries has steered the recent development of potato production to medium altitude areas. The objective of our study is to identify potato accessions with promising levels of heat resistance in laboratory and with good adaptation to medium altitude in the field. We used in vitro assay to screen a number of potato clones with possible resistance to heat stress on the basis literature and database of the International Potato Center, supplemented with the collection of Bogor Agricultural University. We then continued with verification of selected clones using field test in high altitude (1300 m above sea level) and medium altitude (700 m above sea level) areas. Our result showed that there is considerable variation of S. tuberosum for their adaptation to medium altitude areas in the tropics that can be exploited in breeding programs. We identified one genotype PKHT 2013-06 that was superior for its ability to produce tubers under extreme conditions. Thus, it might be very suitable to be used in a breeding program to develop tolerant varieties of potato to medium altitude areas in the tropics.     

Using landscape graphs to delineate ecologically functional areas

Context

Landscape graphs are widely used to model connectivity and to support decision-making in conservation planning. Compartmentalization methods applied to such graphs aim to define clusters of highly interconnected patches. Recent studies show that compartmentalization based on modularity is suitable, but it applies to non-weighted graphs whereas most landscape graphs involve weighted nodes and links.

Objectives

We propose to adapt modularity computation to weighted landscape graphs and to validate the relevance of the resulting compartments using demographic or genetic data about the patches.

Methods

A weighted adjacency matrix was designed to express potential fluxes, associating patch capacities and inter-patch distances. Eight weighting scenarios were compared. The statistical evaluation of each compartmentalization was based on Wilks’ Lambda. These methods were performed on a grassland network where patches are documented by annual densities of water voles in the Jura massif (France).

Results

The scenarios in which patch capacity is assigned a small weight led to the more relevant results, giving high modularity values and low Wilks’ Lambda values. When considering a fixed number of compartments, we found a significant negative correlation between these two criteria. Comparison showed that compartments are ecologically more valid than graph components.

Conclusions

The method proposed is suitable for designing ecologically functional areas from weighted landscape graphs. Maximum modularity values can serve as a guide for setting the parameters of the adjacency matrix.

     

Landscape dynamics of floral resources affect the supply of a biodiversity-dependent cultural ecosystem service

Context

Cultural ecosystem services, many of which depend on biodiversity, are recognized as important but seldom quantified biophysically across landscapes. Furthermore, many ecosystem service models are static, and the supply of cultural ecosystem services may be misrepresented if seasonal shifts in biotic communities are ignored.

Objectives

We modeled landscape dynamics of wildflower blooms in a temperate montane landscape to determine (1) how floral resources (wildflower species richness, abundance, timing, and presence of charismatic species) changed over the growing season, (2) how projected wildflower viewing hotspots varied over space and time, and (3) how spatial shifts in floral resources affected potential public access to wildflower viewing.

Methods

Data were collected at 63 sites across a rural-to-urban gradient in the Southern Appalachian Mountains (USA). Generalized linear models were used to identify factors affecting floral resources at two temporal scales. Floral resources were projected across the landscape and hotspots of wildflower viewing were quantified using overlay analysis.

Results

Floral resources were affected by topoedaphic conditions, climate, and surrounding building density and changed seasonally. Seasonal models revealed locational shifts in ecosystem service hotspots, which changed the proportion of hotspots accessible to the public and identified wildflower-viewing opportunities unnoticed by static models.

Conclusion

Relationships between landscape gradients, biodiversity, and ecosystem service supply varied seasonally, and our models identified cultural ecosystem service hotspots otherwise obscured by simple proxies. Landscape models of biodiversity-based cultural ecosystem services should include seasonal dynamics of biotic communities to avoid under- or over-emphasizing the importance of particular locations in ecosystem service assessments.

     

Grassland songbird occurrence on remnant prairie patches is primarily determined by landscape characteristics

Context

North American grassland songbird populations have declined significantly due to habitat loss and fragmentation. Understanding the influence of the surrounding landscape on prairie fragment occupancy is vital for predicting the fate of grassland birds in these heavily altered landscapes.

Objectives

We examined the relative importance of local and landscape variables on grassland bird occupancy of prairie fragments using a focal-patch study. We also investigated the spatial scale at which landscape variables were most influential.

Methods

We surveyed birds on 29 unplowed prairie fragments in western Minnesota and eastern North and South Dakota. We quantified local habitat on the fragment using vegetation surveys and aerial photographs and the landscape surrounding the fragment out to 4 km using aerial photographs. We analyzed occupancy using multi-model approaches applied to multiple logistic regression.

Results

Of 38 species encountered, nine were neither too rare nor too abundant to be analyzed. Predictors of patch occupancy were unique for each bird species, yet general patterns emerged. For eight species, landscape variables were more important than local variables. Mostly, those landscape variables measured configuration (e.g., edge density) and not composition (e.g., percent cover of a particular matrix element). Landscape effects were mostly from variables measured at the greatest extents from the prairie fragment.

Conclusions

Using a focal-patch study design we demonstrated the importance of the surrounding landscape, often out to 4 km from the fragment edge, on prairie occupancy by grassland birds. Effective management of grassland songbirds will require attention to the landscape context of prairie fragments.

     

Spatial relationship between biodiversity and geodiversity across a gradient of land-use intensity in high-latitude landscapes

Context

‘Conserving Nature’s stage’ has been advanced as an important conservation principle because of known links between biodiversity and abiotic environmental diversity, especially in sensitive high-latitude environments and at the landscape scale. However these links have not been examined across gradients of human impact on the landscape.

Objectives

To (1) analyze the relationships between land-use intensity and both landscape-scale biodiversity and geodiversity, and (2) assess the contributions of geodiversity, climate and spatial variables to explaining vascular plant species richness in landscapes of low, moderate and high human impact.

Methods

We used generalized additive models (GAMs) to analyze relationships between land-use intensity and both geodiversity (geological, geomorphological and hydrological richness) and plant species richness in 6191 1-km² grid squares across Finland. We used linear regression-based variation partitioning (VP) to assess contributions of climate, geodiversity and spatial variable groups to accounting for spatial variation in species richness.

Results

In GAMs, geodiversity correlated negatively, and plant species richness positively, with land-use intensity. Both relationships were non-linear. In VP, geodiversity best accounted for species richness in areas of moderate to high human impact. These overall contributions were mainly due to variation explained jointly with climate, which dominated the models. Independent geodiversity contributions were highest in pristine environments, but low throughout.

Conclusions

Human action increases biodiversity but may reduce geodiversity, at landscape scale in high-latitude environments. Better understanding of the connections between biodiversity and abiotic environment along changing land-use gradients is essential in developing sustainable measures to conserve biodiversity under global change.

     

Spatial resilience of forested landscapes under climate change and management

Context

Resilience, the ability to recover from disturbance, has risen to the forefront of scientific policy, but is difficult to quantify, particularly in large, forested landscapes subject to disturbances, management, and climate change.

Objectives

Our objective was to determine which spatial drivers will control landscape resilience over the next century, given a range of plausible climate projections across north-central Minnesota.

Methods

Using a simulation modelling approach, we simulated wind disturbance in a 4.3 million ha forested landscape in north-central Minnesota for 100 years under historic climate and five climate change scenarios, combined with four management scenarios: business as usual (BAU), maximizing economic returns (‘EcoGoods’), maximizing carbon storage (‘EcoServices’), and climate change adaption (‘CCAdapt’). To estimate resilience, we examined sites where simulated windstorms removed >70% of the biomass and measured the difference in biomass and species composition after 50 years.

Results

Climate change lowered resilience, though there was wide variation among climate change scenarios. Resilience was explained more by spatial variation in soils than climate. We found that BAU, EcoGoods and EcoServices harvest scenarios were very similar; CCAdapt was the only scenario that demonstrated consistently higher resilience under climate change. Although we expected spatial patterns of resilience to follow ownership patterns, it was contingent upon whether lands were actively managed.

Conclusions

Our results demonstrate that resilience may be lower under climate change and that the effects of climate change could overwhelm current management practices. Only a substantial shift in simulated forest practices was successful in promoting resilience.