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Keywords = ultrasonic clicks

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9 pages, 1028 KB  
Article
How Do Moth Clicks Decrease the Capture Success of Horseshoe Bats?
by Yinli Hu, Jiqian Li, Maojun Zhong and Aiqing Lin
Diversity 2023, 15(7), 804; https://doi.org/10.3390/d15070804 - 24 Jun 2023
Cited by 2 | Viewed by 2316
Abstract
Moths are among the most diverse and abundant animals. They have evolved a suite of acoustic defenses, such as producing ultrasound to guard against predation by low-duty-cycle bats. Recently, we found that the ultrasonic clicks of several moth species can also help decrease [...] Read more.
Moths are among the most diverse and abundant animals. They have evolved a suite of acoustic defenses, such as producing ultrasound to guard against predation by low-duty-cycle bats. Recently, we found that the ultrasonic clicks of several moth species can also help decrease the capture success of high-duty-cycle bats. We tested whether moth clicks could advertise moth toxicity and/or jam the echolocation calls of high-duty-cycle bats. We examined the acoustic response of a hawkmoth (Cechenena minor) and a tiger moth (Creatonotos transiens) to free-flying horseshoe bats, Rhinolophus osgoodi. C. minor and C. transiens produced anti-bat ultrasonic clicks with an average duty cycle of 22.3% and 4.9%, respectively. The clicks of C. minor overlapped spectrally with the echolocation calls of R. osgoodi. C. minor occasionally emitted clicks immediately after the end of bat feeding buzzes. The clicks of C. transiens did not overlap spectrally with the echolocation calls of R. osgoodi. More than half the click sequences of C. transiens were produced before the emergence of bat feeding buzzes and did not overlap temporally with the feeding buzzes. Moreover, we found that C. minor was palatable and C. transiens was unpalatable to R. osgoodi. These results suggest that C. minor might be capable of jamming R. osgoodi and might also use ultrasonic clicks as warning signals. The clicks of C. transiens probably function to advertise moth toxicity. This study highlights the diversity of moth anti-bat sounds and illustrates the potential mechanisms of moth acoustic defense against high-duty-cycle bats. Full article
(This article belongs to the Section Animal Diversity)
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19 pages, 4441 KB  
Article
An Injectable Click-Crosslinked Hydrogel that Prolongs Dexamethasone Release from Dexamethasone-Loaded Microspheres
by Ji Yeon Heo, Jung Hyun Noh, Seung Hun Park, Yun Bae Ji, Hyeon Jin Ju, Da Yeon Kim, Bong Lee and Moon Suk Kim
Pharmaceutics 2019, 11(9), 438; https://doi.org/10.3390/pharmaceutics11090438 - 1 Sep 2019
Cited by 33 | Viewed by 5774
Abstract
Our purpose was to test whether a preparation of injectable formulations of dexamethasone (Dex)-loaded microspheres (Dex-Ms) mixed with click-crosslinked hyaluronic acid (Cx-HA) (or Pluronic (PH) for comparison) prolongs therapeutic levels of released Dex. Dex-Ms were prepared using a monoaxial-nozzle ultrasonic atomizer with an [...] Read more.
Our purpose was to test whether a preparation of injectable formulations of dexamethasone (Dex)-loaded microspheres (Dex-Ms) mixed with click-crosslinked hyaluronic acid (Cx-HA) (or Pluronic (PH) for comparison) prolongs therapeutic levels of released Dex. Dex-Ms were prepared using a monoaxial-nozzle ultrasonic atomizer with an 85% yield of the Dex-Ms preparation, encapsulation efficiency of 80%, and average particle size of 57 μm. Cx-HA was prepared via a click reaction between transcyclooctene (TCO)-modified HA (TCO-HA) and tetrazine (TET)-modified HA (TET-HA). The injectable formulations (Dex-Ms/PH and Dex-Ms/Cx-HA) were fabricated as suspensions and became a Dex-Ms-loaded hydrogel drug depot after injection into the subcutaneous tissue of Sprague Dawley rats. Dex-Ms alone also formed a drug depot after injection. The Cx-HA hydrogel persisted in vivo for 28 days, but the PH hydrogel disappeared within six days, as evidenced by in vivo near-infrared fluorescence imaging. The in vitro and in vivo cumulative release of Dex by Dex-Ms/Cx-HA was much slower in the early days, followed by sustained release for 28 days, compared with Dex-Ms alone and Dex-Ms/PH. The reason was that the Cx-HA hydrogel acted as an external gel matrix for Dex-Ms, resulting in the retarded release of Dex from Dex-Ms. Therefore, we achieved significantly extended duration of a Dex release from an in vivo Dex-Ms-loaded hydrogel drug depot formed by Dex-Ms wrapped in an injectable click-crosslinked HA hydrogel in a minimally invasive manner. In conclusion, the Dex-Ms/Cx-HA drug depot described in this work showed excellent performance on extended in vivo delivery of Dex. Full article
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