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113 results for “pipefish”

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Fig. 1 in Collaborative monitoring of the ornamental trade of seahorses and pipefishes (Teleostei: Syngnathidae) in Brazil: Bahia State as a case study

Fig. 1. Map showing the Baía de Todos os Santos, the main area of collection of live syngnathids in Salvador, Bahia State, NE Brazil.

opencc-by-4.0Jun 2006View details →
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Fig. 3. a in Collaborative monitoring of the ornamental trade of seahorses and pipefishes (Teleostei: Syngnathidae) in Brazil: Bahia State as a case study

Fig. 3. a) Specimen of Micrognathus sp., Baía de Todos os Santos, Bahia State, Brazil. b) Specimen of Cosmocampus albirostris, Baía de Todos os Santos, Bahia State, Brazil. Photos: Cláudio L. S. Sampaio.

opencc-by-4.0Jun 2006View details →
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Fig. 4 in Collaborative monitoring of the ornamental trade of seahorses and pipefishes (Teleostei: Syngnathidae) in Brazil: Bahia State as a case study

Fig. 4. Hooka-diver using hand-nets to collect marine ornamental fishes. Baía de Todos os Santos, Bahia State, Brazil. Photo: Leo Dutra.

opencc-by-4.0Jun 2006View details →
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Fig. 1 in Diet composition and feeding strategy of the southern pipefish Syngnathus folletti in a Widgeon grass bed of the Patos Lagoon Estuary, RS, Brazil

Fig. 1. Relationship between mouth gape (a) and prey size (b) with total length (in mm) of female (open circles) and male (dots) individuals of the southern pipefish Syngnathus folletti.

opencc-by-4.0Sep 2005View details →
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Fig. 3 in Diet composition and feeding strategy of the southern pipefish Syngnathus folletti in a Widgeon grass bed of the Patos Lagoon Estuary, RS, Brazil

Fig. 3. Conceptual diagram showing the microhabitat distribution within the Widgeon grass bed of some benthic macroinvertebrates consumed by Syngnathus folletti. Gastropoda: 1. Heleobia australis; Tanaidacea: 2. Kalliapseudes schubartii, 3. Tanais stanfordi; Isopoda: 4. Dies fluminensis, 5. Uromunna peterseni; Amphipoda: 6. Mellita mangrovi.

opencc-by-4.0Sep 2005View details →
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Fig. 4 in Kyonemichthys rumengani (Teleostei: Syngnathidae) is Sister Taxon to the Pipefish Genus Urocampus: Genetic and Morphological Evidence

Fig. 4. Maximum likelihood (ML) tree of 74 syngnathid species based on mitochondrial DNA sequences from 12S, 16S, and CO1. Numbers on branches are ML bootstrap values; those below 50% are not shown.

opencc-by-4.0Oct 2022View details →
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Fig. 1 in Kyonemichthys rumengani (Teleostei: Syngnathidae) is Sister Taxon to the Pipefish Genus Urocampus: Genetic and Morphological Evidence

Fig. 1. Photograph of preserved specimen of Kyonemichthys rumengani (OCF-P 10439, 25.6 mm SL) collected from Okinawa Island, Ryukyu Islands.

opencc-by-4.0Oct 2022View details →
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Figure 7 in A new pipefish, Stigmatopora narinosa (Syngnathidae) from South Australia

Figure 7. Known locations (•) of the Southern Gulf Pipefish Stigmatopora narinosa sp. nov. in South Australia. The range of S. narinosa extends from south-eastern Spencer Gulf, along the lower half of western Gulf St.Vincent with a localised population in eastern Gulf St Vincent.

opencc-by-4.0Dec 2007View details →
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Figure 6. A in A new pipefish, Stigmatopora narinosa (Syngnathidae) from South Australia

Figure 6. A side (a) and dorsal (b) view of S. nigra (upper; Kaup 1853) and also of S. argus (lower, b,c; Richardson 1840) from South Australia. Both species have a relatively longer more tubular snout than S. narinosa, with S. argus having a longer snout than S. nigra.

opencc-by-4.0Dec 2007View details →
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Figure 5. A in A new pipefish, Stigmatopora narinosa (Syngnathidae) from South Australia

Figure 5. A side (a) and dorsal (b) view of Stigmatopora nigra (upper; Kaup, 1853) and also of S. argus (lower, b,c; Richardson, 1840) from South Australia. Both species have a relatively longer more tubular snout than S. narinosa, with S. argus having a longer snout than S. nigra.

opencc-by-4.0Dec 2007View details →
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Figure 1. S in A new pipefish, Stigmatopora narinosa (Syngnathidae) from South Australia

Figure 1. S. narinosa sp. nov. from Port Victoria, Spencer Gulf, with its prehensile tail coiled around macroalgae. The parasite is an isopod which is also commonly found on the leafy seadragon (Phycodurus equis). Image Graham Short.

opencc-by-4.0Dec 2007View details →
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Figure 3 in A new pipefish, Stigmatopora narinosa (Syngnathidae) from South Australia

Figure 3. Side view of Stigmatopora narinosa sp. nov. (Paratype SAM F10195). The tail tapers to a point without a caudal fin.

opencc-by-4.0Dec 2007View details →
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Data from: Population genomics reveals multiple drivers of population differentiation in a sex-role-reversed pipefish

Open the record for dataset details and reuse information.

publicJun 2022View details →
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The population genomics of repeated freshwater colonizations by Gulf Pipefish

<p class="abstract_para">How organisms adapt to the novel challenges imposed by the colonization of a new habitat has long been a central question in evolutionary biology. When multiple populations of the same species independently adapt to similar environmental challenges, the question becomes whether the populations have arrived at their adaptations through the same genetic mechanisms. In recent years, genetic techniques have been used to tackle these questions by investigating the genome‐level changes underlying local adaptation. Here, we present a genomic analysis of colonization of freshwater habitats by a primarily marine fish, the Gulf pipefish (<em>Syngnathus scovelli</em>). We sample pipefish from four geographically distinct freshwater locations and use double‐digest restriction site associated DNA sequencing to compare them to 12 previously studied saltwater populations. The two most geographically distant and isolated freshwater populations are the most genetically distinct, although demographic analysis suggests that these populations are experiencing ongoing migration with their saltwater neighbours. Additionally, outlier regions were found genome‐wide, showing parallelism across ecotype pairs. We conclude that these multiple freshwater colonizations involve similar genomic regions, despite the large geographical distances and different underlying mechanisms. These similar patterns are probably facilitated by the interacting effects of intrinsic barriers, gene flow among populations and ecological selection in the Gulf pipefish.</p>

opencc-zeroJun 2021View details →
dryad36/100

Reduced sexual size dimorphism in a pipefish population where males do not prefer larger females

<p><span>Within a species' distribution, populations are often exposed to diverse environments and may thus experience different sources of both natural and sexual selection. These differences are likely to impact the balance between costs and benefits to individuals seeking reproduction, thus entailing evolutionary repercussions. Here, we look into an unusual population (Baltic Sea) of the broadnosed pipefish, <i>Syngnathus typhle</i>, where males do not seem to select females based on size and hypothesise that this pattern may derive from a reduction of direct benefits to the male. We further hypothesise that if larger females do not persistently secure a higher reproductive success, either through pre- or post-copulatory sexual selection, a decrease in sexual size dimorphism in the Baltic population should be apparent, especially when contrasted with a well-studied population, inhabiting similar latitudes (Swedish west coast), where males prefer larger females.</span></p> <p>We found that, in the Baltic population, variation in female quality is low. We were unable to find differences in abortion rates or protein concentration in oocytes produced by females of contrasting sizes. Direct benefits from mating with large partners seem, thus, reduced in the Baltic population. We also found no evidence of any post-copulatory mechanism that could favour larger mothers as embryo development was unrelated to female size. While female size can still be selected through intrasexual competition or fecundity selection, the pressure for large female body size seems to be lower in the Baltic. Accordingly, we found a noticeable decrease in sexual size dimorphism in the Baltic population. We conclude that, although far from negating the significance of other selective process, sexual selection seems to have a decisive role in supporting pipefish sexual size asymmetries.</p>

opencc-zeroOct 2022View details →
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Figure 3 in Preliminary report of a biometric analysis of greater pipefish Syngnathus acus Linnaeus, 1758 for the western Black Sea

Figure 3. Length–weight relationship of S. acus from catches in the western Black Sea.

opencc-by-4.0Feb 2015View details →
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Figure 2 in Preliminary report of a biometric analysis of greater pipefish Syngnathus acus Linnaeus, 1758 for the western Black Sea

Figure 2. Diagram of morphometric measurements of pipefishes.

opencc-by-4.0Feb 2015View details →
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Figure 1 in Preliminary report of a biometric analysis of greater pipefish Syngnathus acus Linnaeus, 1758 for the western Black Sea

Figure 1. Sampling stations.

opencc-by-4.0Feb 2015View details →
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Figure 1 in Syngnathus chihiroe, a new species of pipefish (Syngnathidae) from southern Japan

Figure 1. – Preserved specimen of Centrogenys vaigiensis [FAKU 103752, 73.7 mm SL, Mauritius].

opencc-by-4.0Dec 2017View details →
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Fig. 3 in Kyonemichthys rumengani (Teleostei: Syngnathidae) is Sister Taxon to the Pipefish Genus Urocampus: Genetic and Morphological Evidence

Fig. 3. Aquarium photograph of Kyonemichthys rumengani (OCF-P 10439, 25.6 mm SL).

opencc-by-4.0Oct 2022View details →

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