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• W2098982899 abstract "Drilling predation is one of the most studied biotic interactions in the fossil record and potentially controls biodiversity, but its history may be confounded by natural patchiness across environments. This aspect has been inconsistently evaluated. The current study contributes to our understanding of drilling predation in the Northern Adriatic, which has been previously classified as a low-predation setting, and examines the roles of environment, patchiness, and ecology of prey organisms in modern seas. Nearly 49,000 molluscs from two intertidal and six sublittoral bulk samples along a transect in the Gulf of Trieste were analysed for drill frequency (DF) and prey effectiveness (PE), a measure of prey's ability to resist predatory attacks. DF across all samples was 20.6%, but varied between the intertidal (1.4%) and sublittoral (27.4%). Among the latter, DF differed between the delta foreset beds (18.1%) and level bottom muds and sands (∼ 28% each). PE was low in the intertidal (1.1%) and sublittoral (4.5%). Overall DF and PE among the three mud samples varied by nearly 10%, while that within the two sand samples varied little; however, significantly different DFs were observed only among the families Nuculidae, Galeommatidae and Corbulidae in level bottom mud and Cerithiidae in level bottom sand samples. Only Corbulidae displayed significant variation in PE among level bottom mud samples (16.5–43.7%). PE varied significantly between level bottom sand samples only within the families Cerithiidae and Trochidae. Suspension-feeding bivalves and gastropods had the highest DFs (24.3% and 39.1%, respectively), and the value of epifaunal bivalves (32.0%) was nearly twice as high as that of infaunal bivalves (17.9%). DFs of cementing (43.0%) and byssate (27.0%) bivalves were higher than that of recliners (9.9%). Considering their cryptic life habits, parasitic gastropods (20.3%) and commensal bivalves (40.6%) had exceptionally high DF. For each ecological category, PE was highest on suspension-feeding (11.1%), infaunal (15.8%) and cementing (10.5%) bivalves, and on parasitic gastropods (11.9%). DF did not correlate with diversity indices or predator abundance in the sublittoral; therefore, drilling predation probably does not control diversity on the local scale here. DFs support paleoecological theory relating predation to changes in ecological guilds through the Phanerozoic. DFs were highest on suspension feeders, parasites and sessile prey, and were lowest on predators, recliners, and endobenthic molluscs. While cementation likely reduces bivalve susceptibility to durophages, it apparently does not to impede drilling predators. Finally, DF did not vary across size classes in any species examined except Venerupis rhomboides, where the smallest fraction was drilled more often. Additionally, as the proportion of large individuals in our samples was small, disparities in DF across size classes probably did not influence our results. With respect to predation intensity the relatively high DF in the sublittoral, as well as high DF and PE for various taxa and guilds, places the Northern Adriatic Sea among typical Cenozoic shelf environments." @default.
• W2098982899 created "2016-06-24" @default.
• W2098982899 creator A5049462681 @default.
• W2098982899 creator A5050433640 @default.
• W2098982899 date "2010-01-01" @default.
• W2098982899 modified "2023-09-25" @default.
• W2098982899 title "Intensities of drilling predation of molluscan assemblages along a transect through the northern Gulf of Trieste (Adriatic Sea)" @default.
• W2098982899 cites W129132970 @default.
• W2098982899 cites W1831162637 @default.
• W2098982899 cites W1965120508 @default.
• W2098982899 cites W1968383871 @default.
• W2098982899 cites W1968935812 @default.
• W2098982899 cites W1973688100 @default.
• W2098982899 cites W1974825338 @default.
• W2098982899 cites W1977505995 @default.
• W2098982899 cites W1977725268 @default.
• W2098982899 cites W1978377499 @default.
• W2098982899 cites W1985309843 @default.
• W2098982899 cites W1985689124 @default.
• W2098982899 cites W1989127551 @default.
• W2098982899 cites W1994939355 @default.
• W2098982899 cites W1995094187 @default.
• W2098982899 cites W1996164831 @default.
• W2098982899 cites W1997193098 @default.
• W2098982899 cites W2001171746 @default.
• W2098982899 cites W2001671958 @default.
• W2098982899 cites W2008127067 @default.
• W2098982899 cites W2009191502 @default.
• W2098982899 cites W2010560578 @default.
• W2098982899 cites W2011328557 @default.
• W2098982899 cites W2017656786 @default.
• W2098982899 cites W2020306944 @default.
• W2098982899 cites W2038996818 @default.
• W2098982899 cites W2043156007 @default.
• W2098982899 cites W2044035301 @default.
• W2098982899 cites W2044239708 @default.
• W2098982899 cites W2044941590 @default.
• W2098982899 cites W2051486427 @default.
• W2098982899 cites W2053461229 @default.
• W2098982899 cites W2053997500 @default.
• W2098982899 cites W2054637019 @default.
• W2098982899 cites W2055601147 @default.
• W2098982899 cites W2056594928 @default.
• W2098982899 cites W2058009600 @default.
• W2098982899 cites W2058782676 @default.
• W2098982899 cites W2063251273 @default.
• W2098982899 cites W2063547148 @default.
• W2098982899 cites W2065658121 @default.
• W2098982899 cites W2066983174 @default.
• W2098982899 cites W2074034424 @default.
• W2098982899 cites W2076771682 @default.
• W2098982899 cites W2078100847 @default.
• W2098982899 cites W2079676167 @default.
• W2098982899 cites W2082371743 @default.
• W2098982899 cites W2084722111 @default.
• W2098982899 cites W2088915887 @default.
• W2098982899 cites W2093252897 @default.
• W2098982899 cites W2095229089 @default.
• W2098982899 cites W2098222425 @default.
• W2098982899 cites W2103160001 @default.
• W2098982899 cites W2105460985 @default.
• W2098982899 cites W2106038550 @default.
• W2098982899 cites W2108052723 @default.
• W2098982899 cites W2108198193 @default.
• W2098982899 cites W2108988331 @default.
• W2098982899 cites W2115166983 @default.
• W2098982899 cites W2115186425 @default.
• W2098982899 cites W2133482591 @default.
• W2098982899 cites W2133868171 @default.
• W2098982899 cites W2133877679 @default.
• W2098982899 cites W2139045477 @default.
• W2098982899 cites W2141340161 @default.
• W2098982899 cites W2148556666 @default.
• W2098982899 cites W2149184561 @default.
• W2098982899 cites W2162706765 @default.
• W2098982899 cites W2163632159 @default.
• W2098982899 cites W2166722801 @default.
• W2098982899 cites W2167456258 @default.
• W2098982899 cites W2171562752 @default.
• W2098982899 cites W2176334850 @default.
• W2098982899 cites W2182573603 @default.
• W2098982899 cites W2186305985 @default.
• W2098982899 cites W2186813831 @default.
• W2098982899 cites W2190271654 @default.
• W2098982899 cites W2201387843 @default.
• W2098982899 cites W2276297734 @default.
• W2098982899 cites W2318712142 @default.
• W2098982899 cites W2326396900 @default.
• W2098982899 cites W2336345527 @default.
• W2098982899 cites W2488896796 @default.
• W2098982899 cites W2497888800 @default.
• W2098982899 cites W2506697899 @default.
• W2098982899 cites W4245961073 @default.
• W2098982899 cites W4251871516 @default.
• W2098982899 cites W2004982109 @default.
• W2098982899 doi "https://doi.org/10.1016/j.palaeo.2009.11.007" @default.
• W2098982899 hasPublicationYear "2010" @default.
• W2098982899 type Work @default.

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