skip to main content


Title: Benthic jellyfish dominate water mixing in mangrove ecosystems

Water mixing is a critical mechanism in marine habitats that governs many important processes, including nutrient transport. Physical mechanisms, such as winds or tides, are primarily responsible for mixing effects in shallow coastal systems, but the sheltered habitats adjacent to mangroves experience very low turbulence and vertical mixing. The significance of biogenic mixing in pelagic habitats has been investigated but remains unclear. In this study, we show that the upside-down jellyfishCassiopeasp. plays a significant role with respect to biogenic contributions to water column mixing within its shallow natural habitat (<2m deep). The mixing contribution was determined by high-resolution flow velocimetry methods in both the laboratory and the natural environment. We demonstrate thatCassiopeasp. continuously pump water from the benthos upward in a vertical jet with flow velocities on the scale of centimeters per second. The volumetric flow rate was calculated to be 212 L⋅h-1for average-sized animals (8.6 cm bell diameter), which translates to turnover of the entire water column every 15 min for a median population density (29 animals per m2). In addition, we foundCassiopeasp. are capable of releasing porewater into the water column at an average rate of 2.64 mL⋅h−1per individual. The release of nutrient-rich benthic porewater combined with strong contributions to water column mixing suggests a role forCassiopeasp. as an ecosystem engineer in mangrove habitats.

 
more » « less
Award ID(s):
1930451 1829945
PAR ID:
10279506
Author(s) / Creator(s):
; ; ;
Publisher / Repository:
Proceedings of the National Academy of Sciences
Date Published:
Journal Name:
Proceedings of the National Academy of Sciences
Volume:
118
Issue:
30
ISSN:
0027-8424
Page Range / eLocation ID:
Article No. e2025715118
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Abstract

    Upside-down jellyfish, genusCassiopea(Péron and Lesueur, 1809), are found in shallow coastal habitats in tropical and subtropical regions circumglobally. These animals have previously been demonstrated to produce flow both in the water column as a feeding current, and in the interstitial porewater, where they liberate porewater at rates averaging 2.46 mL h−1. Since porewater inCassiopeahabitat can be nutrient-rich, this is a potential source of nutrient enrichment in these ecosystems. This study experimentally determines that porewater release byCassiopeasp. jellyfish is due to suction pumping, and not the Bernoulli effect. This suggests porewater release is directly coupled to bell pulsation rate, and unlike vertical jet flux, should be unaffected by population density. In addition, we show that bell pulsation rate is positively correlated with temperature, and negatively correlated with animal size. As such, we would predict an increase in the release of nutrient-rich porewater during the warm summer months. Furthermore, we show that, at our field site in Lido Key, Florida, at the northernmost limit ofCassiopearange, population densities decline during the winter, increasing seasonal differences in porewater release.

     
    more » « less
  2. A<sc>bstract</sc>

    In this paper we exploreppW±(±ν)γto$$ \mathcal{O}\left(1/{\Lambda}^4\right) $$O1/Λ4in the SMEFT expansion. Calculations to this order are necessary to properly capture SMEFT contributions that grow with energy, as the interference between energy-enhanced SMEFT effects at$$ \mathcal{O}\left(1/{\Lambda}^2\right) $$O1/Λ2and the Standard Model is suppressed. We find that there are several dimension eight operators that interfere with the Standard Model and lead to the same energy growth, ~$$ \mathcal{O}\left({E}^4/{\Lambda}^4\right) $$OE4/Λ4, as dimension six squared. While energy-enhanced SMEFT contributions are a main focus, our calculation includes the complete set of$$ \mathcal{O}\left(1/{\Lambda}^4\right) $$O1/Λ4SMEFT effects consistent with U(3)5flavor symmetry. Additionally, we include the decay of theW±→ ℓ±ν, making the calculation actually$$ \overline{q}{q}^{\prime}\to {\ell}^{\pm}\nu \gamma $$q¯q±νγ. As such, we are able to study the impact of non-resonant SMEFT operators, such as$$ \left({L}^{\dagger }{\overline{\sigma}}^{\mu }{\tau}^IL\right)\left({Q}^{\dagger }{\overline{\sigma}}^{\nu }{\tau}^IQ\right) $$Lσ¯μτILQσ¯ντIQBμν, which contribute to$$ \overline{q}{q}^{\prime}\to {\ell}^{\pm}\nu \gamma $$q¯q±νγdirectly and not to$$ \overline{q}{q}^{\prime}\to {W}^{\pm}\gamma $$q¯qW±γ. We show several distributions to illustrate the shape differences of the different contributions.

     
    more » « less
  3. A<sc>bstract</sc>

    A comprehensive study of the local and nonlocal amplitudes contributing to the decayB0K*0(→K+π)μ+μis performed by analysing the phase-space distribution of the decay products. The analysis is based onppcollision data corresponding to an integrated luminosity of 8.4 fb1collected by the LHCb experiment. This measurement employs for the first time a model of both one-particle and two-particle nonlocal amplitudes, and utilises the complete dimuon mass spectrum without any veto regions around the narrow charmonium resonances. In this way it is possible to explicitly isolate the local and nonlocal contributions and capture the interference between them. The results show that interference with nonlocal contributions, although larger than predicted, only has a minor impact on the Wilson Coefficients determined from the fit to the data. For the local contributions, the Wilson Coefficient$$ {\mathcal{C}}_9 $$C9, responsible for vector dimuon currents, exhibits a 2.1σdeviation from the Standard Model expectation. The Wilson Coefficients$$ {\mathcal{C}}_{10} $$C10,$$ {\mathcal{C}}_9^{\prime } $$C9and$$ {\mathcal{C}}_{10}^{\prime } $$C10are all in better agreement than$$ {\mathcal{C}}_9 $$C9with the Standard Model and the global significance is at the level of 1.5σ. The model used also accounts for nonlocal contributions fromB0→ K*0[τ+τ→ μ+μ] rescattering, resulting in the first direct measurement of thebsττvector effective-coupling$$ {\mathcal{C}}_{9\tau } $$C9τ.

     
    more » « less
  4. Abstract

    Decreases in shallow-water habitat area (SWHA) in the Lower Columbia River and Estuary (LCRE) have adversely affected salmonid populations. We investigate the causes by hindcasting SWHA from 1928 to 2004, system-wide, based on daily higher high water (HHW) and system hypsometry. Physics-based regression models are used to represent HHW along the system as a function of river inflow, tides, and coastal processes, and hypsometry is used to estimate the associated SWHA. Scenario modeling is employed to attribute SWHA losses to levees, flow regulation, diversion, navigational development, and climate-induced hydrologic change, for subsidence scenarios of up to 2 m, and for 0.5 m fill. For zero subsidence, the system-wide annual-average loss of SWHA is 55 ± 5%, or 51 × 105 ha/year; levees have caused the largest decrease ($${54}_{-14}^{+5}$$54-14+5%, or ~ 50 × 105 ha/year). The loss in SWHA due to operation of the hydropower system is small, but spatially and seasonally variable. During the spring freshet critical to juvenile salmonids, the total SWHA loss was$${63}_{-3}^{+2}$$63-3+2%, with the hydropower system causing losses of 5–16% (depending on subsidence). Climate change and navigation have caused SWHA losses of$${5}_{-5}^{+16}$$5-5+16% and$${4}_{-6}^{+14}$$4-6+14%, respectively, but with high spatial variability; irrigation impacts have been small. Uncertain subsidence causes most of the uncertainty in estimates; the sum of the individual factors exceeds the total loss, because factors interact. Any factor that reduces mean or peak flows (reservoirs, diversion, and climate change) or alters tides and along-channel slope (navigation) becomes more impactful as assumed historical elevations are increased to account for subsidence, while levees matter less.

     
    more » « less
  5. A<sc>bstract</sc>

    We report the first measurement of the inclusivee+e$$ b\overline{b} $$bb¯$$ {D}_s^{\pm } $$Ds±Xande+e$$ b\overline{b} $$bb¯→ D0/$$ {\overline{D}}^0 $$D¯0Xcross sections in the energy range from 10.63 to 11.02 GeV. Based on these results, we determineσ(e+e$$ {B}_s^0{\overline{B}}_s^0 $$Bs0B¯s0X) andσ(e+e$$ B\overline{B} $$BB¯X) in the same energy range. We measure the fraction of$$ {B}_s^0 $$Bs0events at Υ(10860) to befs= ($$ {22.0}_{-2.1}^{+2.0} $$22.02.1+2.0)%. We determine also the ratio of the$$ {B}_s^0 $$Bs0inclusive branching fractions$$ \mathcal{B} $$B($$ {B}_s^0 $$Bs0→ D0/$$ {\overline{D}}^0 $$D¯0X)/$$ \mathcal{B} $$B($$ {B}_s^0 $$Bs0$$ {D}_s^{\pm } $$Ds±X) = 0.416 ± 0.018 ± 0.092. The results are obtained using the data collected with the Belle detector at the KEKB asymmetric-energye+ecollider.

     
    more » « less