How Neutral is Ecology?

Neutral ecological theory comes in two flavors—a two-stage model with space implicit and a spatially explicit version. Reconciliation of the two flavors has proven problematic. Panmixis, an implicit assumption of the two-stage model, is neither realistic for nor supported by tropical forest trees. However, in spatially explicit versions, stochastic species input in local communities is still necessary to retain high species richness. A unified theory of biodiversity must include both stochasticity and relevant ecological mechanisms.     

Is Restoration Ecology Practical?

2 E. Brown-Weiss, Environment, April 1990.

     

Holism vs. Reductionism: Do Ecosystem Ecology and Landscape Ecology Clarify the Debate?

The holism-reductionism debate, one of the classic subjects of study in the philosopy of science, is currently at the heart of epistemological concerns in ecology. Yet the division between holism and reductionism does not always stand out clearly in this field. In particular, almost all work in ecosystem ecology and landscape ecology presents itself as holistic and emergentist. Nonetheless, the operational approaches used rely on conventional reductionist methodology.From an emergentist epistemological perspective, a set of general 'transactional' principles inspired by the work of J. Dewey and J.K. Feibleman are proposed in an effort to develop a coherent ontological and methodological semantics.     

Ecology – a science put to use

There is no lack of pretext for reviewing historically how ecologists have striven to gain the respect of scholars in their own and other fields, and to demonstrate the wider public-utility of their science. If self-serving, in terms of securing the scope and resources required to advance their studies in ecology, such activities have also been encouraged, and indeed commissioned, in the belief that a greater awareness and understanding of the natural world is essential for human wellbeing. Illustrative material is drawn from the British experience.     

Ecology and evolution of plant�Cpollinator interactions

Background

Some of the most exciting advances in pollination biology have resulted from interdisciplinary research combining ecological and evolutionary perspectives. For example, these two approaches have been essential for understanding the functional ecology of floral traits, the dynamics of pollen transport, competition for pollinator services, and patterns of specialization and generalization in plant–pollinator interactions. However, as research in these and other areas has progressed, many pollination biologists have become more specialized in their research interests, focusing their attention on either evolutionary or ecological questions. We believe that the continuing vigour of a synthetic and interdisciplinary field like pollination biology depends on renewed connections between ecological and evolutionary approaches.

Scope

In this Viewpoint paper we highlight the application of ecological and evolutionary approaches to two themes in pollination biology: (1) links between pollinator behaviour and plant mating systems, and (2) generalization and specialization in pollination systems. We also describe how mathematical models and synthetic analyses have broadened our understanding of pollination biology, especially in human-modified landscapes. We conclude with several suggestions that we hope will stimulate future research. This Viewpoint also serves as the introduction to this Special Issue on the Ecology and Evolution of Plant–Pollinator Interactions. These papers provide inspiring examples of the synergy between evolutionary and ecological approaches, and offer glimpses of great accomplishments yet to come.Key words: Floral traits, generalization and specialization, global change, male fitness, mating systems, multiple paternity, plant–pollinator networks, pollen and gene dispersal, pollinator behaviour, pollination syndromes, pollination webs, self-fertilization     

What Can Ecology Teach Us About Cancer?

In 2008, Pienta et al. (Transl Oncol. 2008;1:158-164) introduced the term ecological therapy for cancer treatment and, in particular, emphasized that destruction of the tumor microenvironment would be more effective than just killing the cells that inhabit it. Proposed here is an expansion on the idea of ecological therapy of cancer, incorporating 1) literature on species invasion, i.e., a right cancerous clone needs to be at the right place at the right time to actually invade its environment, and 2) the literature on niche construction, that is, the idea that once a tumor is formed, cancer cells they modify their microenvironment (niche construction) by changing pH through glycolysis, secreting growth factors and recruiting tumor-associated macrophages to promote cell growth, activating fibroblasts, evading predation from immune system, making the cancer that much more difficult to eradicate. Paleontological literature suggests that the largestmass extinctions occurred when environmental stress that would weaken the population was coupled with some pulse destructive event that caused extensive mortality. To have the same effect on cells in the tumor, rather than, or at least in addition to, killing the cells, one would also need to target the niche that they created for themselves.     

Homogenization of Large-Scale Movement Models in Ecology

A difficulty in using diffusion models to predict large scale animal population dispersal is that individuals move differently based on local information (as opposed to gradients) in differing habitat types. This can be accommodated by using ecological diffusion. However, real environments are often spatially complex, limiting application of a direct approach. Homogenization for partial differential equations has long been applied to Fickian diffusion (in which average individual movement is organized along gradients of habitat and population density). We derive a homogenization procedure for ecological diffusion and apply it to a simple model for chronic wasting disease in mule deer. Homogenization allows us to determine the impact of small scale (10–100 m) habitat variability on large scale (10–100 km) movement. The procedure generates asymptotic equations for solutions on the large scale with parameters defined by small-scale variation. The simplicity of this homogenization procedure is striking when compared to the multi-dimensional homogenization procedure for Fickian diffusion,and the method will be equally straightforward for more complex models.     

How "Molecular Ecology" Should be Defined?

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Animal Personality： Ecology,Behavior, and Evolution

The past decade has seen an extraordinary rise in the number of papers devoted to the study of consistent individual differences in behavior, termed variably as ＂personality＂, ＂behavioral types＂, ＂temperament＂, ＂cor related phenotypes＂, and/or ＂behavioral syndromes＂. In earnest, the acceleration of this field was initiated by a handful of reviews that focused on the ecological and evolutionary implications of personality,     

CEOHAB- Ecology and Oceanography of HarmfulAlgal Blooms in China

HarmfulAlgalBloom (HAB) ,aworld wideseriousmarineenvironmentalproblemandecologicaldisaster ,hasbeendrawngreatattentioninChina .About 4 0 0HABeventshavebeenrecordedsince 1970’s ,andthenum berofitsyearlyoutbreakisincreasingdramatically .LargescaleHABhashitChangjiangEstuaryanditsadjacentseaareasinEastChinaSeaineachSpringsince 1998.TheHABcausedbythesamespecies ,Prorocentrumdonghaiense ,couldreach 70 0 0km2 andlastformorethanonemonth .Atthesametime ,moreandmoreothertoxicandharmfulHABspec…     

Can You Sequence Ecology? Metagenomics of Adaptive Diversification

Few areas of science have benefited more from the expansion in sequencing capability than the study of microbial communities. Can sequence data, besides providing hypotheses of the functions the members possess, detect the evolutionary and ecological processes that are occurring? For example, can we determine if a species is adapting to one niche, or if it is diversifying into multiple specialists that inhabit distinct niches? Fortunately, adaptation of populations in the laboratory can serve as a model to test our ability to make such inferences about evolution and ecology from sequencing. Even adaptation to a single niche can give rise to complex temporal dynamics due to the transient presence of multiple competing lineages. If there are multiple niches, this complexity is augmented by segmentation of the population into multiple specialists that can each continue to evolve within their own niche. For a known example of parallel diversification that occurred in the laboratory, sequencing data gave surprisingly few obvious, unambiguous signs of the ecological complexity present. Whereas experimental systems are open to direct experimentation to test hypotheses of selection or ecological interaction, the difficulty in “seeing ecology” from sequencing for even such a simple system suggests translation to communities like the human microbiome will be quite challenging. This will require both improved empirical methods to enhance the depth and time resolution for the relevant polymorphisms and novel statistical approaches to rigorously examine time-series data for signs of various evolutionary and ecological phenomena within and between species.     

Dispersal Ecology: Where Have All the Seeds Gone?

How effective are different animals at dispersing seeds? A new study has traced seeds sampled in faeces to their mother of origin and concluded that carnivorous mammals can be better dispersers than birds.     

Pollination Ecology of Caesalpinia crista （Leguminosae： Caesalpinioideae）

The flowering phenology, pollination ecology and breeding system of Caesa/pinia crista L.were studied in Dinghushan Nature Reserve, Guangdong, China. The species started blooming in Februaryor March, then last till late April. It took about one week from first flower appearance to its full blooming,which lasted for 2-4 d. The pollen-ovule ratio was 18 000~500. The breeding system was self-incompatible,and protogynous xenogamy. Hymenoptera constituted the major group of pollinators. The pollination typeis ambophily, the species could be pollinated by wind if the pollinators were unavailable: this is the firstrecord of ambophily in the genus Caesalpinia. The floral structure adaptation to the pollinating behavior ofcarpenter bees was described. The influences of artificial treatments in pollination biological studies onthe flowering and fruiting of the plants were also discussed.