Ants can sort their brood without a gaseous template

A fundamental issue of collective intelligence is whether the collective pattern or process is based on environmental information that explicitly codes for it or arises through self-organization of the individuals. Sometimes, these alternatives occur together. Adaptive systems may also be capable of utilizing different types of mechanism under different conditions. Sendova-Franks et al. (Anim Behav 68:1095–1106, 2004) demonstrated evidence for a self-organization mechanism of brood sorting in the ant Temnothorax albipennis, where the brood are sorted in a series of bands or concentric annuli that increase in size with distance from the colony centre. The work by Cox and Blanchard (J Theor Biol 204:223-238, 2000) suggests an alternative or complementary mechanism whereby the brood pattern is specified by the template of a CO₂ gradient. Here, we test for a gaseous template as a necessary condition for brood sorting. Under the experimental condition, we pumped the air out of the nest continuously to prevent the accumulation of any gaseous substances. We compared the brood pattern between the experimental and control conditions according to four characteristics: mean distance from centre, mean nearest-neighbour distance, shape and area. Under the experimental condition, the order of brood types according to the first two characteristics was the same as in the control. The area of the brood pattern was smaller, and its shape elongated under the experimental condition. As expected on the basis of these differences, mean distance from centre was greater and mean nearest-neighbour distance was smaller under the experimental condition (although not statistically significantly) and by the expected amount. We found evidence that ants avoid placing brood in the strongest airflow stream. This could explain the reduced area and elongated shape of the brood pattern under the experimental condition. We conclude that a gaseous template is not a necessary condition for brood sorting. Electronic supplementary material Supplementary material is available in the online version of this article at and is accessible for authorized users.     

Sublittoral epifaunal communities at Signy Island,Antarctica. I. The ice-foot zone

Photographs were taken every 0.5 m along three transects of 5.5 m length on shallow rock faces at Signy Island, Antarctica, during the austral summer of 1991/1992. The percentage cover of substratum ranged from 0 to 100% and the colonising communities included representatives of ten phyla. The zone from mean low-water neap level to 1.5 m depth was mostly devoid of organisms as a result of the seasonal formation of the encrusting ice foot. Coralline and macroalgae dominated from 2 to 3 m, and animal groups from 3.5 to 5.5 m. Bryozoans, and to a lesser extent sponges, were the most abundant animal phyla. Within the bryozoans a succession of colonisation of different species was observed, the most abundant two of which occupied >80% of substratum in places. Substratum type seemed to be the main factor influencing community development in the shallow sublittoral at Signy Island, although ice impact prevents community development in the top 1.5 m and limits it over the rest of the transect down to 5.5 m. Depth and profile of substratum also influenced communities within this depth range (particularly taxonomic composition).     

Spatial and social connectivity of fish-eating “Resident” killer whales (Orcinus orca) in the northern North Pacific

The productive North Pacific waters of the Gulf of Alaska, Aleutian Islands and Bering Sea support a high density of fish-eating “Resident” type killer whales (Orcinus orca), which overlap in distribution with commercial fisheries, producing both direct and indirect interactions. To provide a spatial context for these interactions, we analyzed a 10-year dataset of 3,058 whale photo-identifications from 331 encounters within a large (linear ~4,000 km) coastal study area to investigate the ranging and social patterns of 532 individually identifiable whales photographed in more than one encounter. Although capable of large-scale movements (maximum 1,443 km), we documented ranges generally <200 km, with high site fidelity across summer sampling intervals and also re-sightings during a winter survey. Bayesian analysis of pair-wise associations identified four defined clusters, likely representing groupings of stable matrilines, with distinct ranging patterns, that combined to form a large network of associated whales that ranged across most of the study area. This provides evidence of structure within the Alaska stock of Resident killer whales, important for evaluating ecosystem and fisheries impacts. This network included whales known to depredate groundfish from longline fisheries, and we suggest that such large-scale connectivity has facilitated the spread of depredation.     

Open Corridors Appear to Facilitate Dispersal by Ringlet Butterflies (Aphantopus hyperantus) between Woodland Clearings

We studied the ringlet butterfly (Aphantopus hyperantus) in an area of woodland in eastern England. A. hyperantus occurs in open fields, rides (grassy tracks), and glades within the woodland. Mark-recapture methods showed that exchange rates of adult A. hyperantus between fields and glades can be predicted better by distance-via-rides than by direct distance. Behavioral observations showed that A. hyperantus readily moved from glades into rides but rarely moved from glades into dense woodland. The rides are likely to be corridors that act as conduits between fields and glades. In the A. hyperantus system, connectivity could reduce local extinctions and increase rates of recolonization in the event of local extinction.     

Metapopulation dynamics in the butterfly Hipparchia semele changed decades before occupancy declined in The Netherlands

The survival of many species in human-dominated, fragmented landscapes depends on metapopulation dynamics, i.e., on a dynamic equilibrium of extinctions and colonizations in patches of suitable habitat. To understand and predict distributional changes, knowledge of these dynamics can be essential, and for this, metapopulation studies are preferably based on long-time-series data from many sites. Alas, such data are very scarce. An alternative is to use opportunistic data (i.e., collected without applying standardized field methods), but these data suffer from large variations in field methods and search intensity between sites and years. Dynamic site-occupancy models offer a general approach to adjust for variable survey effort. These models extend classical metapopulation models to account for imperfect detection of species and yield estimates of the probabilities of occupancy, colonization, and survival of species at sites. By accounting for detection, they fully correct for among-year variability in search effort. As an illustration, we fitted a dynamic site-occupancy model to 60 years of presence-absence data (more precisely, detection-nondetection) of the heathland butterfly Hipparchia semele in The Netherlands. Detection records were obtained from a database containing volunteer-based data from 1950-2009, and nondetection records were deduced from database records of other butterfly species. Our model revealed that metapopulation dynamics of Hipparchia had changed decades before the species' distribution began to contract. Colonization probability had already started to decline from 1950 onward, but this was counterbalanced by an increase in the survival of existing populations, the result of which was a stable distribution. Only from 1990 onward was survival not sufficient to compensate for the further decrease of colonization, and occupancy started to decline. Hence, it appears that factors acting many decades ago triggered a change in the metapopulation dynamics of this species, which ultimately led to a severe decline in occupancy that only became apparent much later. Our study emphasizes the importance of knowledge of changes in survival and colonization of species in modern landscapes over a very long time scale. It also demonstrates the power of site-occupancy modeling to obtain important population dynamics information from databases containing opportunistic sighting records.     

Ecology of subtropical hermit crabs in S.W. Madagascar: cluster structure and function

The Madagascar coast (both) has a higher density and diversity of hermit crabs than is known from any other locality in the western Indian Ocean. Of the 20 species occurring at Anakao (S.W. Madagascar), 11 aggregated into clusters, including all but one of the species above the subtidal zone. The mean number of hermit crabs and species in clusters varied with several spatial parameters and time. Over 80% of the community clustered in certain habitats in particular tidal zones, whilst as low as 3% clustered in others. The highest intensity of clustering with shore zone was coincident with peak numbers of hermit crabs. The initiation and duration of clusters of hermit crabs above the eulittoral was driven by circadian rhythms, whilst those in the eulittoral were governed by tidal state. Clusters above and below the eulittoral were longer in duration, and those in the subtidal were more temporally variable than those above it. Certain pairs of species showed positive correlations of occurrence and (more rarely) of abundance, and all the correlations (of occurrence) of one, Clibanarius eurysternus, were negative. Positive correlations of occurrence were related to the degree of shell-use commonality between species pairs. Eulittoral species clustered with other individuals of approximately similar size and exchanged shells upon cluster disintegration. There was evidence of a dehydration-reduction function to shell clustering in addition to shell-exchange facilitation. The highly variable species-specific strategies of clustering may be important in alleviating both intra- and interspecific competition in assemblages of similar and highly abundant species.     

在线富集HTLC/MS/MS分析环境水资源中多种抗生素

<正>人们日益关注环境水资源中抗生素的存在情况.这迫使环境和政府实验室开发新的液相色谱/质谱(LC/MS)方法,以监测水资源中抗生素的存在状况.然而,环境水资源中含有的抗生素通常是很痕量的,往往需要大量的水样进行富集和净化.在液相色谱/质谱(LC/MS)分析之前,需要对大约100—1000ml水样进行富集和清理,以达到被测物质的检测限。     

Seasonality of polypide recycling and sexual reproduction in some erect Antarctic bryozoans

The seasonality of polypide cycling has been investigated for three species of erect bryozoans from Antarctica: Isoseculiflustra rubefacta (Kluge, 1914), Nematoflustra flagellata (Waters, 1904) and Himantozoum antarcticum (Calvet, 1905). Approximately ten colonies of each species were collected monthly by SCUBA divers over a 14 mo period during 1992/1993, and the status of each individual zooid was classified as differentiating/regenerating, active (feeding autozooids), degenerate (brown body) or sexually reproductive (ovicells present, or zooid containing a larva). Polypide cycling in all three species was distinctly seasonal. New zooids formed at the growth margin and typically contained actively feeding polypides for ≃9 mo before these polypides degenerated into brown bodies in the austral winter (June). Very few polypides were active in the period from June to August, when water-column food levels were at their lowest; after this period new polypides differentiated. Individual zooids typically underwent a total of five (I. rubefacta and N. flagellata), or at least four (H. antarcticum) complete polypide cycles before becoming senescent. Polypide lifetimes generally became shorter as the age of the zooid increased. Sexual reproduction was also distinctly seasonal in these species, with bands of ovicells or sexually reproductive zooids being formed each year in late summer once a given colony had grown to a threshold size (or age). Larvae were then brooded for ≃10 mo before being released in January/February (N. flagellata) or February/March (H. antarcticum). The seasonal patterns of polypide cycling are related clearly to the variations in food availability, and these species appear to have the longest zooid lifetime (≃5 yr) and the slowest polypide cycling (once per year with polypide lifetimes up to 10 mo) reported for any bryozoan so far. Received: 7 May 1995 / Accepted: 19 November 1997