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24 results for “Syngnathus”
Figure 3 in Syngnathus chihiroe, a new species of pipefish (Syngnathidae) from southern Japan
Figure 3. – Distributional map of Centrogenys vaigiensis. The star indicates locality of FAKU 103752 (Mauritius). Shaded area indicates previously recorded distributional range.
Figure 2 in Syngnathus chihiroe, a new species of pipefish (Syngnathidae) from southern Japan
Figure 2. – Head of Centrogenys vaigiensis [FAKU 103752, 73.7 mm SL, Mauritius]. Arrowheads indi- cate antrorse spines on preopercle margin.
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.
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.
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.
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.
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.
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].
Syngnathus scovelli band iridescence measurements
<p>This is the raw data that corresponds to the manuscript "The development of a quantification method for measuring iridescence using sexually selected traits in the Gulf pipefish (<em>Syngnathus scovelli</em>)" (DOI: <a href="https://doi.org/10.3389/fmars.2023.1127790">10.3389/fmars.2023.1127790</a>). The two datasets contain the iridescence measurements for each individual band on the pipefish for each study outlined in the manuscript.</p> <ol> <li><strong>iridescence_across_lighting_RAW</strong>: contains every iridescence measurements for the study about lighting conditions, to see if lighting has any affect on the amount of iridescence measured from a photo.</li> <li><strong>pipefish_measures_iridescence_RAW</strong>: contatins all of the other iridescence measurements for the geographic study, for females from two Texas populations and two Florida populations, and the estrogen study, where we measured the development of iridescence on male pipefish in response to synthetic estrogen.</li> </ol>
FIGURE 4 in Syngnathus chihiroe, a new species of pipefish (Syngnathidae) from southern Japan
FIGURE 4. Preserved specimen of Syngnathus schlegeli, BSKU 47138 (1 of 9 specimens), 79.4 mm SL, East China Sea.
FIGURE 2 in Syngnathus chihiroe, a new species of pipefish (Syngnathidae) from southern Japan
FIGURE 2. Semi-schematic drawings of (A) lateral and (B) dorsal views of head; (C) lateral and (D) dorsolateral views of trunk-tail portion in holotype of Syngnathus chihiroe sp. nov., NSMT-P 106296, 92.0 mm SL. AR: anal ring; DE: dorsal-fin base end; DO: dorsal-fin base origin; ITAR: inferior tail ridge; ITR: inferior trunk ridge; LTAR: lateral tail ridge; LTR: lateral trunk ridge; STAR: superior tail ridge; STR: superior trunk ridge. Dorsal-fin not illustrated in (C) and (D), except for 1st and last rays in (D). Bars indicate 3 mm.
FIGURE 5 in Syngnathus chihiroe, a new species of pipefish (Syngnathidae) from southern Japan
FIGURE 5. Relationships between snout length (% HL) (A); snout depth (% HL) (B); anal ring depth (% HL); and snout depth (% snout length) (D) to head length (mm) in Syngnathus chihiroe sp. nov. (blue triangle) and S. schlegeli (red circles).
FIGURE 1 in Syngnathus chihiroe, a new species of pipefish (Syngnathidae) from southern Japan
FIGURE 1. Holotype of Syngnathus chihiroe sp. nov., NSMT-P 106296, female, 92.0 mm SL, southwest of Yakushima Island, Kagoshima Prefecture, Japan. (A) Lateral view of body; (B) lateral and (C) dorsal views of head.
Syngnathus floridae SPAdes preassembly
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Syngnathus floridae decontaminated FSCR
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Syngnathus floridae decontaminated gx
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Data from: Genetic evidence for polygynandry in the black-striped pipefish Syngnathus abaster: a microsatellite-based parentage analysis
Open the record for dataset details and reuse information.
FIGURE 86. Syngnathus abaster Risso 1827 in The marine ichthyofauna of Lebanon: an annotated checklist, history, biogeography, and conservation status
FIGURE 86. Syngnathus abaster Risso 1827, Beirut, 28 April 2009 (female below) and 21 May 2011 (male above), AUBM (OS3836, OS3969).
FIGURE 3 in Syngnathus chihiroe, a new species of pipefish (Syngnathidae) from southern Japan
FIGURE 3. Type locality of Syngnathus chihiroe sp. nov. (red star).
Data from: Sexual selection on female ornaments in the sex-role-reversed Gulf pipefish (Syngnathus scovelli)
Understanding how selection acts on traits individually and in combination is an important step in deciphering the mechanisms driving evolutionary change, but for most species, and especially those in which sexual selection acts more strongly on females than on males, we have no estimates of selection coefficients pertaining to the multivariate sexually selected phenotype. Here, we use a laboratory-based mesocosm experiment to quantify pre- and post-mating selection on female secondary sexual traits in the Gulf pipefish (Syngnathus scovelli), a sexually dimorphic, sex-role-reversed species in which ornamented females compete for access to choosy males. We calculate selection differentials and gradients on female traits, including ornament area, ornament number and body size for three episodes of selection related to female reproductive success (number of mates, number of eggs transferred and number of surviving embryos). Selection is strong on both ornament area and ornament size, and the majority of selection occurs during the premating episode of selection. Interestingly, selection on female body size, which has been detected in previous studies of Gulf pipefish, appears to be indirect, as evidenced by a multivariate analysis of selection gradients. Our results show that sexual selection favours either many bands or larger bands in female Gulf pipefish.
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