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        <title>Frontiers in Zoology - Most accessed articles</title>
        <link>http://www.frontiersinzoology.com</link>
        <description>The most accessed research articles published by Frontiers in Zoology</description>
        <dc:date>2010-03-01T00:00:00Z</dc:date>
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                                <rdf:li rdf:resource="http://www.frontiersinzoology.com/content/6/1/28" />
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        <item rdf:about="http://www.frontiersinzoology.com/content/6/1/28">
        <title>Functional chloroplasts in metazoan cells - a unique evolutionary strategy in animal life</title>
        <description>Background:
Among metazoans, retention of functional diet-derived chloroplasts (kleptoplasty) is known only from the sea slug taxon Sacoglossa (Gastropoda: Opisthobranchia). Intracellular maintenance of plastids in the slug&apos;s digestive epithelium has long attracted interest given its implications for understanding the evolution of endosymbiosis. However, photosynthetic ability varies widely among sacoglossans; some species have no plastid retention while others survive for months solely on photosynthesis. We present a molecular phylogenetic hypothesis for the Sacoglossa and a survey of kleptoplasty from representatives of all major clades. We sought to quantify variation in photosynthetic ability among lineages, identify phylogenetic origins of plastid retention, and assess whether kleptoplasty was a key character in the radiation of the Sacoglossa.
Results:
Three levels of photosynthetic activity were detected: (1) no functional retention; (2) short-term retention lasting about one week; and (3) long-term retention for over a month. Phylogenetic analysis of one nuclear and two mitochondrial loci revealed reciprocal monophyly of the shelled Oxynoacea and shell-less Plakobranchacea, the latter comprising a monophyletic Plakobranchoidea and paraphyletic Limapontioidea. Only species in the Plakobranchoidea expressed short- or long-term kleptoplasty, most belonging to a speciose clade of slugs bearing parapodia (lateral flaps covering the dorsum). Bayesian ancestral character state reconstructions indicated that functional short-term retention arose once in the last common ancestor of Plakobranchoidea, and independently evolved into long-term retention in four derived species.
Conclusion:
We propose a sequential progression from short- to long-term kleptoplasty, with different adaptations involved in each step. Short-term kleptoplasty likely arose as a deficiency in plastid digestion, yielding additional energy via the release of fixed carbon. Functional short-term retention was an apomorphy of the Plakobranchoidea, but the subsequent evolution of parapodia enabled slugs to protect kleptoplasts against high irradiance and further prolong plastid survival. We conclude that functional short-term retention was necessary but not sufficient for an adaptive radiation in the Plakobranchoidea, especially in the genus Elysia which comprises a third of all sacoglossan species. The adaptations necessary for long-term chloroplast survival arose independently in species feeding on different algal hosts, providing a valuable study system for examining the parallel evolution of this unique trophic strategy.</description>
        <link>http://www.frontiersinzoology.com/content/6/1/28</link>
                <dc:creator>Katharina Haendeler</dc:creator>
                <dc:creator>Yvonne Grzymbowski</dc:creator>
                <dc:creator>Patrick Krug</dc:creator>
                <dc:creator>Heike Waegele</dc:creator>
                <dc:source>Frontiers in Zoology 2009, 6:28</dc:source>
        <dc:date>2009-12-01T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1742-9994-6-28</dc:identifier>
        <prism:publicationName>Frontiers in Zoology</prism:publicationName>
        <prism:issn>1742-9994</prism:issn>
        <prism:volume>6</prism:volume>
        <prism:startingPage>28</prism:startingPage>
        <prism:publicationDate>2009-12-01T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.frontiersinzoology.com/content/7/1/3">
        <title>Blood feeding patterns of mosquitoes: random or structured?
</title>
        <description>Background:
The foraging behavior of blood-sucking arthropods is the defining biological event shaping the transmission cycle of vector-borne parasites. It is also a phenomenon that pertains to the realm of community ecology, since blood-feeding patterns of vectors can occur across a community of vertebrate hosts. Although great advances in knowledge of the genetic basis for blood-feeding choices have been reported for selected vector species, little is known about the role of community composition of vertebrate hosts in determining such patterns.Methods &amp; ResultsHere, we present an analysis of feeding patterns of vectors across a variety of locations, looking at foraging patterns of communities of mosquitoes, across communities of hosts primarily comprised of mammals and birds. Using null models of species co-occurrence, which do not require ancillary information about host abundance, we found that blood-feeding patterns were aggregated in studies from multiple sites, but random in studies from a single site. This combination of results supports the idea that mosquito species in a community may rely primarily on host availability in a given landscape, and that contacts with specific hosts will be influenced more by the presence/absence of hosts than by innate mosquito choices. This observation stresses the importance of blood-feeding plasticity as a key trait explaining the emergence of many zoonotic mosquito transmitted diseases.DiscussionFrom an epidemiological perspective our observations support the idea that phenomena promoting synchronization of vectors and hosts can promote the emergence of vector-borne zoonotic diseases, as suggested by observations on the linkages between deforestation and the emergence of several human diseases.</description>
        <link>http://www.frontiersinzoology.com/content/7/1/3</link>
                <dc:creator>Luis Chaves</dc:creator>
                <dc:creator>Laura Harrington</dc:creator>
                <dc:creator>Carolyn Keogh</dc:creator>
                <dc:creator>Andy Nguyen</dc:creator>
                <dc:creator>Uriel Kitron</dc:creator>
                <dc:source>Frontiers in Zoology 2010, 7:3</dc:source>
        <dc:date>2010-01-21T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1742-9994-7-3</dc:identifier>
        <prism:publicationName>Frontiers in Zoology</prism:publicationName>
        <prism:issn>1742-9994</prism:issn>
        <prism:volume>7</prism:volume>
        <prism:startingPage>3</prism:startingPage>
        <prism:publicationDate>2010-01-21T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.frontiersinzoology.com/content/1/1/4">
        <title>The structure of biodiversity - insights from molecular phylogeography</title>
        <description>DNA techniques, analytical methods and palaeoclimatic studies are greatly advancing our knowledge of the global distribution of genetic diversity, and how it evolved. Such phylogeographic studies are reviewed from Arctic, Temperate and Tropical regions, seeking commonalities of cause in the resulting genetic patterns. The genetic diversity is differently patterned within and among regions and biomes, and is related to their histories of climatic changes. This has major implications for conservation science.</description>
        <link>http://www.frontiersinzoology.com/content/1/1/4</link>
                <dc:creator>Godfrey Hewitt</dc:creator>
                <dc:source>Frontiers in Zoology 2004, 1:4</dc:source>
        <dc:date>2004-10-26T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1742-9994-1-4</dc:identifier>
        <prism:publicationName>Frontiers in Zoology</prism:publicationName>
        <prism:issn>1742-9994</prism:issn>
        <prism:volume>1</prism:volume>
        <prism:startingPage>4</prism:startingPage>
        <prism:publicationDate>2004-10-26T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.frontiersinzoology.com/content/7/1/8">
        <title>Visual acuity in larval zebrafish: behavior and histology</title>
        <description>Background:
Visual acuity, the ability of the visual system to distinguish two separate objects at a given angular distance, is influenced by the optical and neuronal properties of the visual system. Although many factors may contribute, the ultimate limit is photoreceptor spacing. In general, at least one unstimulated photoreceptor flanked by two stimulated ones is needed to perceive two objects as separate. This critical interval is also referred to as the Nyquist frequency and is according to the Shannon sampling theorem the highest spatial frequency where a pattern can be faithfully transmitted. We measured visual acuity in a behavioral experiment and compared the data to the physical limit given by photoreceptor spacing in zebrafish larvae.
Results:
We determined visual acuity by using the optokinetic response (OKR), reflexive eye movements in response to whole field movements of the visual scene. By altering the spatial frequency we determined the visual acuity at approximately 0.16 cycles/degree (cpd) (minimum separable angle = 3.1degrees). On histological sections we measured the retinal magnification factor and the distance between double cones, that are thought to mediate motion perception. These measurements set the physical limit at 0.24 cpd (2.1degrees)
Conclusion:
The maximal spatial information as limited by photoreceptor spacing can not be fully utilized in a motion dependent visual behavior, arguing that the larval zebrafish visual system has not matured enough to optimally translate visual information into behavior. Nevertheless behavioral acuity is remarkable close to its maximal value, given the immature state of young zebrafish larvae.</description>
        <link>http://www.frontiersinzoology.com/content/7/1/8</link>
                <dc:creator>Marion Haug</dc:creator>
                <dc:creator>Oliver Biehlmaier</dc:creator>
                <dc:creator>Kaspar Mueller</dc:creator>
                <dc:creator>Stephan Neuhauss</dc:creator>
                <dc:source>Frontiers in Zoology 2010, 7:8</dc:source>
        <dc:date>2010-03-01T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1742-9994-7-8</dc:identifier>
        <prism:publicationName>Frontiers in Zoology</prism:publicationName>
        <prism:issn>1742-9994</prism:issn>
        <prism:volume>7</prism:volume>
        <prism:startingPage>8</prism:startingPage>
        <prism:publicationDate>2010-03-01T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.frontiersinzoology.com/content/7/1/4">
        <title>Sexual dimorphism and population divergence in the Lake Tanganyika cichlid fish genus Tropheus</title>
        <description>Background:
With about 120 colour morphs currently assigned to six nominal species, the genus Tropheus is an ideal model to study evolutionary divergence of populations in allopatry. The morphology of Tropheus has been described as relatively static, but reproductive constraints are sexually dimorphic due to mouthbrooding in females. We analysed phenotypic variation in six populations of T. moorii and one population of T. polli using geometric morphometrics to assess morphological differences among sexes in relation to the differentiation of populations and species.
Results:
The mean shapes differed significantly between sexes, populations, and species even though within-sex variation exceeded the divergence among populations. The first principal component of Procrustes shape coordinates revealed differences between populations and species in mouth position and ventral head shape. The second principal component reflected sex-specific shape differences, mainly comprising a relatively larger female viscerocranium and, in particular, a larger buccal area. While shape variation between populations and between sexes was primarily located in the cranial region, within-sex variation was relatively uniform across all landmarks.
Conclusions:
Deviations of the between-population and between-sex pattern of shape variation from that within sex indicate that the differences in head shape likely result from both adaptations to female mouthbrooding and population-specific foraging strategies.</description>
        <link>http://www.frontiersinzoology.com/content/7/1/4</link>
                <dc:creator>Juergen Herler</dc:creator>
                <dc:creator>Michaela Kerschbaumer</dc:creator>
                <dc:creator>Philipp Mitteroecker</dc:creator>
                <dc:creator>Lisbeth Postl</dc:creator>
                <dc:creator>Christian Sturmbauer</dc:creator>
                <dc:source>Frontiers in Zoology 2010, 7:4</dc:source>
        <dc:date>2010-01-22T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1742-9994-7-4</dc:identifier>
        <prism:publicationName>Frontiers in Zoology</prism:publicationName>
        <prism:issn>1742-9994</prism:issn>
        <prism:volume>7</prism:volume>
        <prism:startingPage>4</prism:startingPage>
        <prism:publicationDate>2010-01-22T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.frontiersinzoology.com/content/7/1/7">
        <title>Trapped in freshwater: the internal anatomy of the entoproct Loxosomatoides sirindhornae</title>
        <description>Background:
Entoprocta is a small phylum of tentacle-bearing spiralian lophotrochozoans that comprises mainly marine representatives, with only two known freshwater species. One of them, Loxosomatoides sirindhornae Wood, 2005 was only recently described, and detailed information on its morphology including adaptations to life in freshwater are unknown. We analyzed the internal anatomy of L. sirindhornae using serial semi-thin sections, 3D reconstruction, as well as immunocytochemistry and confocal laserscanning microscopy.
Results:
The nephridial system shows high complexity, strikingly similar to that of Urnatella gracilis, the only other known freshwater entoproct. It is composed of 105-120 large flame-bulb terminal organs that occur in the stalk and calyx. In the stalk they terminate in the epidermis, whereas efferent ducts in each terminal organ in the calyx lead to large, paired terminal ducts that fuse close to the central nervous system and open into the atrium by a nephridiopore. Compared to other stolonate entoprocts, L. sirindhornae shows a different stalk-calyx junction by possessing only a single, multicellular canopy instead of a stack of star cells. A sphincter muscle is situated below the diaphragm of the stalk. The remaining musculature is concentrated in the stalk, while the calyx musculature is sparsely developed. The central nervous system is dumbbell-shaped as in basal entoprocts.
Conclusions:
The nephridial system probably has mainly osmoregulatory function. Previous studies have shown that L. sirindhornae is unable to cope with higher salinities, suggesting that its adaptation to freshwater has reached such a high degree that it is unable to &apos;turn off&apos; the nephridial system in higher salinities. The current data available show that the architecture of internal organ systems such as the musculature or the calyx-stalk junction hold more promising information for taxonomic and perhaps even evolutionary inferences in Entoprocta than external characters such as spination. Contrary to previous investigations, the longitudinal calyx musculature of the genus Loxosomatoides should not be classified as generally strong or conspicuous, since its extent and site of insertion differs between species.</description>
        <link>http://www.frontiersinzoology.com/content/7/1/7</link>
                <dc:creator>Thomas Schwaha</dc:creator>
                <dc:creator>Timothy Wood</dc:creator>
                <dc:creator>Andreas Wanninger</dc:creator>
                <dc:source>Frontiers in Zoology 2010, 7:7</dc:source>
        <dc:date>2010-02-04T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1742-9994-7-7</dc:identifier>
        <prism:publicationName>Frontiers in Zoology</prism:publicationName>
        <prism:issn>1742-9994</prism:issn>
        <prism:volume>7</prism:volume>
        <prism:startingPage>7</prism:startingPage>
        <prism:publicationDate>2010-02-04T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.frontiersinzoology.com/content/7/1/6">
        <title>Of tests, trochs, shells, and spicules: development of the basal mollusk Wirenia argentea (Solenogastres) and its bearing on the evolution of trochozoan larval key features </title>
        <description>Background:
The phylogenetic status of the aplacophoran mollusk taxon Solenogastres (Neomeniomorpha) is controversially discussed. Some authors propose the clade to represent the most basal branch within Mollusca, while others claim aplacophoran mollusks (Solenogastres and Caudofoveata) to be derived. Larval characters are central in these discussions, specifically the larval test (calymma, apical cap), the ontogeny of the epidermal scleritome, and the proposed absence of larval protonephridia. To date, developmental data are available for five solenogaster species, but most reports are incomplete and need confirmation.
Results:
Wirenia argentea deposit small batches of uncleaved embryos that are tightly enclosed by a smooth and transparent egg hull. Cleavage is spiral and unequal. The ciliated larvae hatch about 45 hours after deposition and swim actively in the water column. Within 48-60 hours after hatching they become mushroom-shaped with a pronounced apical cap partly enclosing a posterior trunk. The cells covering the apical cap are large and cleavage arrested. On the apical cap there is a prominent prototrochal band of compound cilia and an apical ciliary tuft and the trunk bears a terminal ciliary band (telotroch). Obscured by the apical cap, a ciliary band originates in the stomodaeal pore and surrounds the trunk. As development is proceeding, the trunk elongates and becomes covered by cuticle with the exception of a ventral ciliary band, the future foot. The larvae have a pair of protonephridia. At 5 days after hatching they begin to settle and within the following 7-9 days the apical cap is gradually reduced. Scattered epidermal sclerites form under the cuticle. Wirenia argentea lack iterated groups of sclerites at any developmental stage. At 40 days after hatching, the postlarvae have a fully developed foregut, but the midgut and hindgut are not yet interconnected.
Conclusions:
Solenogastres develop via a trochophore-like lecitotrophic larva with a preoral apical cap that at least partly represents an enlarged prototrochal area. Homology of this larval type (pericalymma larva) to test cell larvae of other spiralian clades is doubtful. The ontogeny of W. argentea does not provide any evidence for a derived status of Solenogastres within Mollusca.</description>
        <link>http://www.frontiersinzoology.com/content/7/1/6</link>
                <dc:creator>Christiane Todt</dc:creator>
                <dc:creator>Andreas Wanninger</dc:creator>
                <dc:source>Frontiers in Zoology 2010, 7:6</dc:source>
        <dc:date>2010-01-26T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1742-9994-7-6</dc:identifier>
        <prism:publicationName>Frontiers in Zoology</prism:publicationName>
        <prism:issn>1742-9994</prism:issn>
        <prism:volume>7</prism:volume>
        <prism:startingPage>6</prism:startingPage>
        <prism:publicationDate>2010-01-26T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.frontiersinzoology.com/content/7/1/2">
        <title>Dichlorvos exposure impedes extraction and amplification of DNA from insects in museum collections</title>
        <description>Background:
The insecticides dichlorvos, paradichlorobenzene and naphthalene have been commonly used to eradicate pest insects from natural history collections. However, it is not known how these chemicals affect the DNA of the specimens in the collections. We thus tested the effect of dichlorvos, paradichlorobenzene and naphthalene on DNA of insects (Musca domestica) by extracting and amplifying DNA from specimens exposed to insecticides in two different concentrations over increasing time intervals.
Results:
The results clearly show that dichlorvos impedes both extraction and amplification of mitochondrial and nuclear DNA after relatively short time, whereas paradichlorobenzene and naphthalene do not.
Conclusion:
Collections treated with paradichlorobenzene and naphthalene, are better preserved concerning DNA, than those treated with dichlorvos. Non toxic pest control methods should, however, be preferred due to physical damage of specimens and putative health risks by chemicals.</description>
        <link>http://www.frontiersinzoology.com/content/7/1/2</link>
                <dc:creator>Marianne Espeland</dc:creator>
                <dc:creator>Martin Irestedt</dc:creator>
                <dc:creator>Kjell Arne Johanson</dc:creator>
                <dc:creator>Monika Akerlund</dc:creator>
                <dc:creator>Jan-Erik Bergh</dc:creator>
                <dc:creator>Mari Kallersjo</dc:creator>
                <dc:source>Frontiers in Zoology 2010, 7:2</dc:source>
        <dc:date>2010-01-18T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1742-9994-7-2</dc:identifier>
        <prism:publicationName>Frontiers in Zoology</prism:publicationName>
        <prism:issn>1742-9994</prism:issn>
        <prism:volume>7</prism:volume>
        <prism:startingPage>2</prism:startingPage>
        <prism:publicationDate>2010-01-18T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.frontiersinzoology.com/content/7/1/5">
        <title>Neuromuscular development of Aeolidiella stephanieae Valdez, 2005 (Mollusca, Gastropoda, Nudibranchia)</title>
        <description>Background:
Studies on the development of the nervous system and the musculature of invertebrates have become more sophisticated and numerous within the last decade and have proven to provide new insights into the evolutionary history of organisms. In order to provide new morphogenetic data on opisthobranch gastropods we investigated the neuromuscular development in the nudibranch Aeolidiella stephanieae Vald&#233;z, 2005 using immunocytochemistry as well as F-actin labelling in conjunction with confocal laser scanning microscopy (cLSM).
Results:
The ontogenetic development of Aeolidiella stephanieae can be subdivided into 8 stages, each recognisable by characteristic morphological and behavioural features as well as specific characters of the nervous system and the muscular system, respectively. The larval nervous system of A. stephanieae includes an apical organ, developing central ganglia, and peripheral neurons associated with the velum, foot and posterior, visceral part of the larva. The first serotonergic and FMRFamidergic neural structures appear in the apical organ that exhibits an array of three sensory, flask-shaped and two non-sensory, round neurons, which altogether disappear prior to metamorphosis. The postmetamorphic central nervous system (CNS) becomes concentrated, and the rhinophoral ganglia develop together with the anlage of the future rhinophores whereas oral tentacle ganglia are not found. The myogenesis in A. stephanieae begins with the larval retractor muscle followed by the accessory larval retractor muscle, the velar or prototroch muscles and the pedal retractors that all together degenerate during metamorphosis, and the adult muscle complex forms de novo.
Conclusions:
Aeolidiella stephanieae comprises features of the larval and postmetamorphic nervous as well as muscular system that represent the ground plan of the Mollusca or even the Trochozoa (e. g. presence of the prototrochal or velar muscle ring). On the one hand, A. stephanieae shows some features shared by all nudibranchs like the postmetamorphic condensation of the CNS, the possession of rhinophoral ganglia and the lack of oral tentacle ganglia as well as the de novo formation of the adult muscle complex. On the other hand, the structure and arrangement of the serotonergic apical organ is similar to other caenogastropod and opisthobranch gastropods supporting their sister group relationship.</description>
        <link>http://www.frontiersinzoology.com/content/7/1/5</link>
                <dc:creator>Alen Kristof</dc:creator>
                <dc:creator>Annette Klussmann-Kolb</dc:creator>
                <dc:source>Frontiers in Zoology 2010, 7:5</dc:source>
        <dc:date>2010-01-22T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1742-9994-7-5</dc:identifier>
        <prism:publicationName>Frontiers in Zoology</prism:publicationName>
        <prism:issn>1742-9994</prism:issn>
        <prism:volume>7</prism:volume>
        <prism:startingPage>5</prism:startingPage>
        <prism:publicationDate>2010-01-22T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <title>Smells like home: Desert ants, Cataglyphis fortis, use olfactory landmarks to pinpoint the nest</title>
        <description>Background:
Cataglyphis fortis ants forage individually for dead arthropods in the inhospitable salt-pans of Tunisia. Locating the inconspicuous nest after a foraging run of more than 100 meters demands a remarkable orientation capability. As a result of high temperatures and the unpredictable distribution of food, Cataglyphis ants do not lay pheromone trails. Instead, path integration is the fundamental system of long-distance navigation. This system constantly informs a foraging ant about its position relative to the nest. In addition, the ants rely on visual landmarks as geocentric navigational cues to finally pinpoint the nest entrance.
Results:
Apart from the visual cues within the ants&apos; habitat, we found potential olfactory landmark information with different odour blends coupled to various ground structures. Here we show that Cataglyphis ants can use olfactory information in order to locate their nest entrance. Ants were trained to associate their nest entrance with a single odour. In a test situation, they focused their nest search on the position of the training odour but not on the positions of non-training odours. When trained to a single odour, the ants were able to recognise this odour within a mixture of four odours.
Conclusion:
The uniform salt-pans become less homogenous if one takes olfactory landmarks into account. As Cataglyphis ants associate environmental odours with the nest entrance they can be said to use olfactory landmarks in the vicinity of the nest for homing.</description>
        <link>http://www.frontiersinzoology.com/content/6/1/5</link>
                <dc:creator>Kathrin Steck</dc:creator>
                <dc:creator>Bill Hansson</dc:creator>
                <dc:creator>Markus Knaden</dc:creator>
                <dc:source>Frontiers in Zoology 2009, 6:5</dc:source>
        <dc:date>2009-02-27T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1742-9994-6-5</dc:identifier>
        <prism:publicationName>Frontiers in Zoology</prism:publicationName>
        <prism:issn>1742-9994</prism:issn>
        <prism:volume>6</prism:volume>
        <prism:startingPage>5</prism:startingPage>
        <prism:publicationDate>2009-02-27T00:00:00Z</prism:publicationDate>
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