37 research outputs found

    Congruent biogeographical disjunctions at a continent-wide scale: Quantifying and clarifying the role of biogeographic barriers in the Australian tropics

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    AIM: To test whether novel and previously hypothesized biogeogaphic barriers in the Australian Tropics represent significant disjunction points or hard barriers, or both, to the distribution of plants. LOCATION: Australian tropics: Australian Monsoon Tropics and Australian Wet Tropics. METHODS: The presence or absence of 6,861 plant species was scored across 13 putative biogeographic barriers in the Australian Tropics, including two that have not previously been recognised. Randomizations of these data were used to test whether more species showed disjunctions (gaps in distribution) or likely barriers (range limits) at these points than expected by chance. RESULTS: Two novel disjunctions in the Australian Tropics flora are identified in addition to eleven putative barriers previously recognized for animals. Of these, eleven disjunction point (all within the Australian Monsoon Tropics) were found to correspond to range-ending barriers to a significant number of species, while neither of the two disjunctions found within the Australian Wet Tropics limited a significant number of species' ranges. MAIN CONCLUSIONS: Biogeographic barriers present significant distributional limits to native plant species in the Australian Monsoon Tropics but not in the Australian Wet TropicsThe authors would like to thank the ‘Coopers and Cladistics’ systematics discussion group at the ANU for comments on early versions of the manuscript. They would also like to acknowledge the University of Queensland for supporting RDE via a Postgraduate Research Scholarship, and the Australian Research Council for supporting LGC and MDC via Discovery Grants during data collection, analysis and manuscript preparatio

    Dust Devil Tracks

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    Dust devils that leave dark- or light-toned tracks are common on Mars and they can also be found on the Earth’s surface. Dust devil tracks (hereinafter DDTs) are ephemeral surface features with mostly sub-annual lifetimes. Regarding their size, DDT widths can range between ∼1 m and ∼1 km, depending on the diameter of dust devil that created the track, and DDT lengths range from a few tens of meters to several kilometers, limited by the duration and horizontal ground speed of dust devils. DDTs can be classified into three main types based on their morphology and albedo in contrast to their surroundings; all are found on both planets: (a) dark continuous DDTs, (b) dark cycloidal DDTs, and (c) bright DDTs. Dark continuous DDTs are the most common type on Mars. They are characterized by their relatively homogenous and continuous low albedo surface tracks. Based on terrestrial and martian in situ studies, these DDTs most likely form when surficial dust layers are removed to expose larger-grained substrate material (coarse sands of ≥500 μm in diameter). The exposure of larger-grained materials changes the photometric properties of the surface; hence leading to lower albedo tracks because grain size is photometrically inversely proportional to the surface reflectance. However, although not observed so far, compositional differences (i.e., color differences) might also lead to albedo contrasts when dust is removed to expose substrate materials with mineralogical differences. For dark continuous DDTs, albedo drop measurements are around 2.5 % in the wavelength range of 550–850 nm on Mars and around 0.5 % in the wavelength range from 300–1100 nm on Earth. The removal of an equivalent layer thickness around 1 μm is sufficient for the formation of visible dark continuous DDTs on Mars and Earth. The next type of DDTs, dark cycloidal DDTs, are characterized by their low albedo pattern of overlapping scallops. Terrestrial in situ studies imply that they are formed when sand-sized material that is eroded from the outer vortex area of a dust devil is redeposited in annular patterns in the central vortex region. This type of DDT can also be found in on Mars in orbital image data, and although in situ studies are lacking, terrestrial analog studies, laboratory work, and numerical modeling suggest they have the same formation mechanism as those on Earth. Finally, bright DDTs are characterized by their continuous track pattern and high albedo compared to their undisturbed surroundings. They are found on both planets, but to date they have only been analyzed in situ on Earth. Here, the destruction of aggregates of dust, silt and sand by dust devils leads to smooth surfaces in contrast to the undisturbed rough surfaces surrounding the track. The resulting change in photometric properties occurs because the smoother surfaces have a higher reflectance compared to the surrounding rough surface, leading to bright DDTs. On Mars, the destruction of surficial dust-aggregates may also lead to bright DDTs. However, higher reflective surfaces may be produced by other formation mechanisms, such as dust compaction by passing dust devils, as this may also cause changes in photometric properties. On Mars, DDTs in general are found at all elevations and on a global scale, except on the permanent polar caps. DDT maximum areal densities occur during spring and summer in both hemispheres produced by an increase in dust devil activity caused by maximum insolation. Regionally, dust devil densities vary spatially likely controlled by changes in dust cover thicknesses and substrate materials. This variability makes it difficult to infer dust devil activity from DDT frequencies. Furthermore, only a fraction of dust devils leave tracks. However, DDTs can be used as proxies for dust devil lifetimes and wind directions and speeds, and they can also be used to predict lander or rover solar panel clearing events. Overall, the high DDT frequency in many areas on Mars leads to drastic albedo changes that affect large-scale weather patterns

    Niche differentiation and spatial partitioning in the evolution of two Australian monsoon tropical tree species

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    Aim: Geographical and climatic barriers to organismal dispersal and distribution play a major role in speciation. We use a sister-pair of widespread savanna trees (Melaleuca argentea and M. fluviatilis) to test the influence of putative barriers on dive

    Investigating the chemical pathway to the formation of a single biofilm using infrared spectroscopy

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    Diagnosing biofilm infections has remained a constant challenge for the last 50 years. Existing diagnostic methods struggle to identify the biofilm phenotype. Moreover, most methods of biofilm analysis destroy the biofilm making the resultant data interpretation difficult. In this study we introduce Fourier Transform Infra-Red (FTIR) spectroscopy as a label-free, non-destructive approach to monitoring biofilm progression. We have utilised FTIR in a novel application to evaluate the chemical composition of bacterial biofilms without disrupting the biofilm architecture. S. epidermidis (RP62A) was grown onto calcium fluoride slides for periods of 30 min–96 h, before semi-drying samples for analysis. We report the discovery of a chemical marker to distinguish between planktonic and biofilm samples. The appearance of new proteins in biofilm samples of varying maturity is exemplified in the spectroscopic data, highlighting the potential of FTIR for identifying the presence and developmental stage of a single biofilm

    Recent changes in the distribution of a marine gastropod, <i>Patella rustica</i> Linnaeus, 1758, and their relationship to unusual climatic events

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    Aim: Recent colonization of northern Portuguese shores by Patella rustica Linnaeus, 1758, led to the bridging of a historical gap in the distribution known since the 1900s. Long-term oceanographic data collected over the last half-century were examined in order to detect possible mechanisms for the observed change in its distribution.Location: This study was carried out along the entire Portuguese coastline, from 41°50' to 37°06' N. Time-series of hydrographical variables (sea surface temperature and salinity) were derived for the Atlantic coast of the Iberian Peninsula.Methods: Abundance and size-frequency distributions of the newly observed limpet populations were compared with those from well-established populations in southern Portugal. Anomalies were computed for sea surface temperature (1950–2000) and sea surface salinity (1958–2001) data, covering the whole Atlantic coast of the Iberian Peninsula. An upwelling index (1967–2005) was derived for a single location within the distributional gap of P. rustica. Split moving window analysis was performed to detect significant discontinuities in hydrographical data sets.Results: Patella rustica has gradually been expanding in northern Iberia, and in the late 1990s the historical gap in distribution in northern Portugal was bridged. Size-frequency distribution differed between historical and recent populations, the latter lacking small-sized individuals. At the same time, several anomalous oceanographic events occurred off the Portuguese coast and were probably related to this expansion.Main conclusions: Although sea surface temperature might be a major determinant of the reproductive success of P. rustica and hence its dispersal potential, it is more likely that a coincidence of several factors occurring in the late 1990s provided exceptional conditions that allowed the geographical expansion of this species

    Population consequences of mutual attraction between settling and adult barnacles

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    1. Spatial patterns of recruitment were compared between populations of the rocky shore barnacles (Crustacea: Cirripedia) Semibalanus balanoides, an obligate cross-fertilizer, and Chthamalus montagui, which can self-fertilize. We tested the hypothesis that recruitment depends on a behaviourally mediated interaction at settlement between the effects of adult background density and adult spacing, which limit free space for settlement and mating opportunities, respectively. Recruitment to patches of cleared rock (10- or 30-cm diameter) was compared between replicate shores with background densities of adult barnacles classed as low (?20 per 25 cm2) and high (&gt;4× low). Replicate patches were cleared of all barnacles surrounding a remnant cluster, comprising 0, 1, 2, 4, 8, 16 or 32 adults.2. For S. balanoides, settlement and subsequent recruitment over 5 months varied in direct proportion to remnant cluster size, except on the shore with the highest background density where recruitment was inversely proportional to cluster size. We interpret this inversion to indicate attraction to potential mates at low adult densities (positive density dependence, an Allee effect) switching to attraction to free space at high density (negative density dependence). The strengths and slopes of the regressions increased from shores with the lowest to the highest overall recruitment of barnacles, but retained significance over a five-fold range in recruitment. Positive effects of cluster size on recruitment were consistent between consecutive years, despite considerable variation in recruitment densities. In contrast, recruitment of C. montagui was generally more weakly proportional to cluster size, except for a strong positive correlation at the shore with the highest recruitment.3. Dispersion of recruits within treatment patches was accurately modelled by a computer simulation that allowed each barnacle to settle at random between fixed minimum and maximum distances from the nearest other settled barnacle. The model estimated threshold distances by maximum likelihood fit to observed recruitment into concentric annuli around the central adult cluster. Upper thresholds of separation corresponded to penis length for 65% of S. balanoides and 42% of C. montagui patches. Lower thresholds were ?2× cyprid length for 75% of S. balanoides patches, but were larger than this for C. montagui patches
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