破碎景观建立保护区面积-数量模式界定

由于生境丧失日益严重,很难找到一片未被破坏的生境建立自然保护区,因而在设计保护区时,必须处理生境丧失带来的影响。在一个已经遭受过生境丧失的景观上,选取一片正方形的区域,并调整区域的面积以保证其中未被破坏生境的面积为一个固定常数,探讨将未被破坏的生境建设成大量小保护区还是少量大保护区。结果表明:(1)随机的生境丧失下,生境丧失比例越高,少量大保护区模式的优势越明显。(2)即使生境丧失比例恒定,被破坏生境的空间分布形式也有重要影响——被破坏生境的空间聚集程度越高,大量小保护区模式的优势越明显。(3)增加扩散率或降低扩散死亡率可导致从少量大保护区更有利于物种到大量小保护区更有利的转变,且被破坏生境的聚集程度越高,转变的程度越高。以上结论为自然保护区设计提供了理论依据。     

Cortical pattern formation during visual hallucinations

We theoretically investigate pattern formation during simple visual hallucinations caused by epileptic activity. To this end we analyze the activator-inhibitor model of Ermentrout and Cowan [1]. In contrast to these authors we focus on a different disease mechanism: According to experimental findings (cf. [2]) we decrease the influence of the inhibitor on the activator. This causes spontaneous pattern formation due to a bifurcation. The model parameters determine whether one or two or four modes become unstable. By means of the center manifold theorem, in all cases the order parameter equation is derived, the stability of the solution is proofed, and the bifurcating activity pattern is calculated explicitely in lowest order. Taking into account terms up to third order in all cases the order parameter equation has a potential. For the two-modes and the four-modes instability this potential causes a winner-takes all dynamics. We integrate the order parameter equation numerically and plot the visual hallucinations which result from the bifurcating cortical activity. The theoretically derived hallucinations correspond to clinically observed visual hallucinations (cf. [3, 4]), which are, for instance, well-known from petit mal epilepsy [5].Finally we investigate the influence of noise on the activity patterns as well as the visual hallucinations.     

Young children spontaneously invent wild great apes’ tool-use behaviours

The variety and complexity of human-made tools are unique in the animal kingdom. Research investigating why human tool use is special has focused on the role of social learning: while non-human great apes acquire tool-use behaviours mostly by individual (re-)inventions, modern humans use imitation and teaching to accumulate innovations over time. However, little is known about tool-use behaviours that humans can invent individually, i.e. without cultural knowledge. We presented 2- to 3.5-year-old children with 12 problem-solving tasks based on tool-use behaviours shown by great apes. Spontaneous tool use was observed in 11 tasks. Additionally, tasks which occurred more frequently in wild great apes were also solved more frequently by human children. Our results demonstrate great similarity in the spontaneous tool-use abilities of human children and great apes, indicating that the physical cognition underlying tool use shows large overlaps across the great ape species. This suggests that humans are neither born with special physical cognition skills, nor that these skills have degraded due to our species’ long reliance of social learning in the tool-use domain.     

Biological trade and markets

Cooperation between organisms can often be understood, like trade between merchants, as a mutually beneficial exchange of services, resources or other ‘commodities’. Mutual benefits alone, however, are not sufficient to explain the evolution of trade-based cooperation. First, organisms may reject a particular trade if another partner offers a better deal. Second, while human trade often entails binding contracts, non-human trade requires unwritten ‘terms of contract’ that ‘self-stabilize’ trade and prevent cheating even if all traders strive to maximize fitness. Whenever trading partners can be chosen, market-like situations arise in nature that biologists studying cooperation need to account for. The mere possibility of exerting partner choice stabilizes many forms of otherwise cheatable trade, induces competition, facilitates the evolution of specialization and often leads to intricate forms of cooperation. We discuss selected examples to illustrate these general points and review basic conceptual approaches that are important in the theory of biological trade and markets. Comparing these approaches with theory in economics, it turns out that conventional models—often called ‘Walrasian’ markets—are of limited relevance to biology. In contrast, early approaches to trade and markets, as found in the works of Ricardo and Cournot, contain elements of thought that have inspired useful models in biology. For example, the concept of comparative advantage has biological applications in trade, signalling and ecological competition. We also see convergence between post-Walrasian economics and biological markets. For example, both economists and biologists are studying ‘principal–agent’ problems with principals offering jobs to agents without being sure that the agents will do a proper job. Finally, we show that mating markets have many peculiarities not shared with conventional economic markets. Ideas from economics are useful for biologists studying cooperation but need to be taken with caution.     

Evolution of risk assessment strategies for food and feed uses of stacked GM events

Data requirements are not harmonized globally for the regulation of food and feed derived from stacked genetically modified (GM) events, produced by combining individual GM events through conventional breeding. The data required by some regulatory agencies have increased despite the absence of substantiated adverse effects to animals or humans from the consumption of GM crops. Data from studies conducted over a 15‐year period for several stacked GM event maize (Zea mays L.) products (Bt11 ×  GA21, Bt11 ×  MIR604, MIR604 ×  GA21, Bt11 ×  MIR604 ×  GA21, Bt11 ×  MIR162 ×  GA21 and Bt11 ×  MIR604 ×  MIR162 ×  GA21), together with their component single events, are presented. These data provide evidence that no substantial changes in composition, protein expression or insert stability have occurred after combining the single events through conventional breeding. An alternative food and feed risk assessment strategy for stacked GM events is suggested based on a problem formulation approach that utilizes (i) the outcome of the single event risk assessments, and (ii) the potential for interactions in the stack, based on an understanding of the mode of action of the transgenes and their products.     

Citrus replant problem in Iraq I. Possible role of soil fungi and nematodes

The role of soil fungi and nematodes in citrus replant problems was investigated. Several pathogenic and non-pathogenic fungi and the nematodeTylenchulus semipenetrans were isolated in about equal abundance from soils which displayed or did not display replant problems. However, in almost all trees showing evidence of decline, infection by the fungusPhytophthora citrophthora had advanced through the roots until it had reached the tree crown. Fumigation of old citrus soil with methyl bromide greatly increased the growth of sour organe. The application of Nemacure, Benomyl and Ridomil 5G confirmed the important role of pathogenic and non-pathogenic fungi and nematodes in the citrus replant problem. Inoculation of methyl bromide-treated soil with the pathogenic and non-pathogenic fungi separately or in combination further confirmed the previous experiments and also revealed an important role ofP. citrophthora andFusarium solani when replanting citrus in old citrus orchards.