Magdy El-Hedeny’s research while affiliated with Alexandria University and other places

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Publications (56)


A palaeoenvironmental reconstruction of the Campanian‒lower Palaeocene succession of the Dakhla Oasis (Western Desert, Egypt): Insights from integrated sequence stratigraphy, macrobenthos, and trace fossil analyses
  • Article

March 2025

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122 Reads

Journal of African Earth Sciences

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Magdy El-Hedeny

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The palaeoenvironments of the Campanian‒lower Palaeocene composite succession in the Dakhla Oasis, Egypt, are interpreted based on the integration of sequence-stratigraphy, macrobenthic associations, and trace fossils. This succession comprises six rock units, corresponding to several transgression-regression cycles. These rock units include the Quseir Formation, the Duwi Formation, and the Mawhoob, Beris, Lower Kharga, and Upper Kharga members of the Dakhla Formation. Six unconformities delineate seven 3rd-order depositional sequences, including the lower‒middle Campanian DS-Q1, the upper Campanian DS-D1 and DS-D2, the lower Maastrichtian DS-Dk1, the upper Maastrichtian DS-Dk2 and DS-Dk3, and the lower Danian DS-Dk4. The invertebrate macrobenthic elements sporadically occurred throughout the studied succession, representing three bivalve associations: the late Campanian Nicaisolopha-Plicatula association, the late Maastrichtian Exogyra overwegi association, and an early Danian Venericardia association. At least 12 ichnotaxa have been identified, representing two ichnoassemblages: the late Campanian Thalassinoides-Psilonichnus and the latest Maastrichtian‒early Danian Rhizocorallium jenense-Tisoa siphonalis, both belonging to the Glossifungites Ichnofacies. Sequences characteristics indicate palaeoenvironments ranging from brackish, littoral, and near-shore to inner and outer neritic settings, reflecting the influence of syn-sedimentary tectonics combined with sea-level fluctuations, which resulted in varied depositional features. The distribution and the trophic structure of the body and trace fossil assemblages confirm the role of several environmental parameters, such as substrate characteristics, bathymetry, water energy, productivity level, sedimentation rates, and oxygen availability, in shaping the occurrence of different elements within these faunal assemblages.


Symbiotic endobionts in tabulate corals from the Late Ordovician and Silurian of Estonia

January 2025

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42 Reads

GFF

Four new symbiotic associations between worms and tabulate corals have been described from the Hirnantian to Ludfordian of Estonia. Chaetosalpinx csp. occurs in Palaeofavosites porkuniensis from the Hirnantian of northern Estonia. Chaetosalpinx ferganensis occurs in Favosites hisingeri from the Telychian, with an infestation rate of about 18%. Chaetosalpinx siberiensis occurs in the Favosites forbesi from the Ludfordian of Estonia, with an infestation rate of about 33%. Endobiotic Cornulites sp . was discovered from the Ludfordian Favosites terrae-novae. Our data suggest that Chaetosalpinx trace makers exhibited a significantly broader parasitic behavior, infesting a wider variety of coral species during the Silurian in the Baltica. The discovery of cornulitid within the corallum of Favosites indicates that the symbiotic relationship between cornulitids and tabulates spanned a broad stratigraphic range, extending from the late Katian to the Ludfordian during the early Paleozoic in Estonia.


Fig. 1. Simplified geological map of the Fayum Depression (modified after Beadnell, 1905; Said, 1962; Gingerich, 1992) with indication of the measured section in the Wadi El-Hitan area; Fm. – Formation.
Fig. 2. Lithological description of the middle‒upper Eocene succession at the Sandouk El-Borneta section with occurrences of vertebrate fossils.
Fig. 3. Some field aspects of the section studied. (A) The upper Eocene Birket Qarun Formation is unconformably underlain by the middle Eocene Gehannam Formation. (B) A well preserved basilosaurid remains of Basilosaurus isis from the study area. (C) A complete whale bones of B. isis from the Wadi El-Hitan area.
Fig. 4. Taphonomic aspects of some studied bone specimens. (A) Bone specimen of the whale Basilosaurus isis with Osedax borings displaying wide and isolated circular to elliptical pits and rounded boreholes. (B) Lateral side of mesosternum element of the whale Dorudon atrox illustrating abundant Osedax borings. (C) Maeandropolydora isp. (yellow arrow) preserving its producer (black arrow) at the termination of the trace. (D) A cluster of Hydroides sp. tubes (arrows). (E) A large S-shaped serpulid tube worm (arrows) characterised by its wide basal seams or basal flanges assigned as Spirobranchus sp. (F) Long, irregularly coiled or slightly curved and sometimes straight serpulid tubes, with more or less circular cross-section (arrows), assigned to ?Serpula sp. (G) Dense clusters of small calcareous tube-dwelling encrusting polychaetes ?Serpula sp. (black arrows) on a whale bone specimen; bryozoans are represented by small, sheet‐like cheilostome type (green arrows); a well preserved serpulid tube worm with a single median longitudinal keel (yellow arrow), is assigned to Spirobranchus sp. (H) Conical calcareous tubeworms, with flaring peristomes along their extension, colonise an extensively bored whale bone specimen with the siboglinid Osedax. (I) A vertebral epiphysis specimen encrusted with a cluster of Balanus sp. (J) Poorly preserved cheilostome bryozoan sheets encrusted a whale bone specimen. (K) Small scleractinian corals (arrows) on basilosaurid remains of Basilosaurus isis. Scale bars equal 0.5 cm, except for (B‒D, I, K), which are 1 cm.
Fig. 5. Scanning of whale bone, showing networks of the Osedax borings; borehole (bh), root lobe (rl), trabecular bone (tb), and solid bone (sb). Scale bar equals 1 cm.

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Shallow-water whale-fall communities: Evidence from the middle‒late Eocene basilosaurid whale bones, Wadi El-Hitan, Fayum, Egypt

January 2025

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686 Reads

Palaeoworld

The present study examines the basilosaurid whale bone specimens collected from the Sandouk El-Borneta section, Wadi El-Hitan (Valley of Whales), Fayum, Egypt. These specimens are embedded in highly fossiliferous calcareous sandstones of the middle Eocene Gehannam and the upper Eocene Birket Qarun formations. These whale bones display some post-mortem alterations, representing good signs of at least three distinct stages in what is called the whale fall. The co-occurrence of shark, ray, and crocodile fossil specimens with the examined whale bones may indicate the first mobile-scavenger stage. Borings of the siboglinid polychaete genus Osedax represent the most common worm type that deeply bioeroded the whale bones, contributing to their rapid degradation, and representing the enrichment-opportunist stage. These fossil traces of the bone-eating worm Osedax represent the first record in the Eocene Epoch regionally and inter-regionally, filling the gap between the Late Cretaceous and the Oligocene occurrences. Subsequently, the studied whale bones served as hard substrates for some calcareous tube-dwelling encrusting polychaetes, balanoid barnacles, sheet‐like cheilostome bryozoans, and scleractinian corals. Furthermore, a bioerosion structure produced by polychaete annelids was also observed. The presence of these sclerobionts assemblage confirms the well-developed final reef stage with prolonged exposure and colonisation of these whale bones prior to final burial. Based on the recorded post-mortem alterations, together with other sedimentological and palaeontological data, the studied whale bones were deposited in a shallow open marine bay to sheltered gulf environments, which were characterised by low depositional energy, low to moderate rate of sedimentation, and high surface water productivity.


Figure 1. Location of Nõmmküla quarry and Hosholm, NW Estonia.
Figure 3. A-B, Kenophyllum subcylindricum from the Katian of NW Estonia with multiple Chaetosalpinx siberiensis in transverse section from Vormsi Regional Stage (Katian) (GIT 80-8). Scale bars = 1 mm.
First record of Chaetosalpinx bioclaustrations in the rugose corals from the Late Ordovician of Baltica
  • Article
  • Full-text available

December 2024

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65 Reads

Revista Brasileira de Paleontologia

Bioclaustrations are extremely rare in the rugose corals from the Ordovician of Estonia. A specimen of Kenophyllum subcylindricum from the Vormsi Regional Stage (Katian) contains multiple shafts of Chaetosalpinx siberiensis?. The latter bioclaustration also occurs in the Pirgu Regional Stage (Katian). The growth lines of the host coral show a reaction to the infesting organism, suggesting that the shafts in the calyx are bioclaustrations and not post-mortem borings (Trypanites). The worm-like Chaetosalpinx tracemaker initially caused damage to the coral's soft tissues and used the coral's resources to build its domicile, resulting in a negative impact. The symbiotic worms benefited from having a domicile and protection against predators from the host's nematocysts. Chaetosalpinx siberiensis?-Kenophyllum subcylindricum association was likely parasitic. RESUMO: Bioclaustrações são extremamente raros nos corais rugosos do Ordoviciano da Estonia. Um espécime de Kenophyllum subcylindricum do estágio regional Vormsi (Katiano) contém eixos múltiplos de Chaetosalpinx siberiensis?. Essa última bioclaustração também ocorre no estágio regional de Pirgu (Katiano). As linhas de crescimento do coral hospedeiro mostram uma reação ao organismo infestante, sugerindo que os eixos no cálice são bioclaustrações e não perfurações post-mortem (Trypanites). O Chaetosalpinx tracemaker, semelhante a um verme, inicialmente causou danos aos tecidos moles do coral e usou os recursos do coral para construir seu domicílio, resultando em um impacto negativo. Os vermes simbióticos se beneficiaram do fato de terem um domicílio e proteção contra predadores dos nematocistos do hospedeiro. A associação Chaetosalpinx siberiensis?-Kenophyllum subcylindricum foi provavelmente parasitária.

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Fig. 1. Locality map. The Silurian and Devonian Basin of Bohemia. Silurian and Devonian (orange), Cambrian (green). Modified after Chlup� a� c et al. (1980).
Fig. 2. Schematic line drawing of Styliolina showing the general morphology. Modified after Farsan (2005).
Shell microstructure of Styliolina clavulus (Tentaculita) from the Middle Devonian of Czech Republic: implications for phylogenetic affinities and biomineralization of thin-walled tentaculitids

May 2024

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113 Reads

Alcheringa An Australasian Journal of Palaeontology

Based on shell microstructure, pelagic tentaculitids have been affiliated with molluscs in the past. Species of the genus Styliolina were among the most important pelagic tentaculitids in the Devonian. The shell wall of Styliolina clavulus is single-layered and composed of thin calcareous lamellae that are parallel to the wall of the shell. The thickness of individual lamellae varies about two times but the thickness of each lamella in the shell wall is constant. The structure is clearly laminar and is similar to bryozoan, brachiopod and molluscan calcitic regularly foliated structures. Based on the structure of S. clavulus alone and the reinterpretation of published SEM images, it is impossible to rule out molluscan affinities for styliolinids, as both regularly foliated and semi-nacreous structures are known in molluscs. However, considering the whole shell structure spectrum of tentaculitoids, one should conclude that the structure of S. clavulus fits well within the group of tentaculitoids and lophophorates in general. The biomineralization of styliolinids was likely advanced and organic matrix controlled; the secreting epithelium was located within the shell and secretion likely took place lamella by lamella.


Taphonomy of the middle Miocene regular echinoid spines from Cairo-Suez District, Egypt: Palaeoecological and palaeoenvironmental interpretations

April 2024

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399 Reads

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1 Citation

Palaeoworld

The palaeoecology and palaeoenvironment of a dense cluster of regular echinoid spines that occur in an oyster-rich limestone layer are interpreted based on detailed taphonomic study. The paucispecific macrobenthic assemblage associated with these echinoid spines have been studied in the middle Miocene Geniefa Formation, Gebel Gharra, Cairo-Suez District of Egypt. Both echinoid spines and macrobenthic assemblages are dominated by moderately to well-preserved, moderately packed, highly disarticulated, moderately to poorly sorted, re-oriented, and moderately to highly fragmented specimens, confirming parautochthonous nature of this assemblage. The spines are commonly encrusted and bored. At least four taxonomic groups of encrusters are identified, including juvenile oysters, sheet-like cheilostome bryozoans, serpulids, and balanoid barnacles. The diversity of bioerosional ichnotaxa is moderate and includes Gastrochaenolites, Entobia, Maeandropolydora, Trypanites, and Spirolites. Moreover, some echinoid spines display distinct biting traces of fish, representing the first recorded of fish tooth bite marks on remains of regular echinoid spines from the Miocene deposits of Egypt. The faunal composition and trophic structure of the studied faunal assemblage indicate fully oxygenated and euhaline shallow-marine environment with meso- to eutrophic productivity level. The controlling environmental parameters include substrate consistency, bathymetry, water energy, surface-water productivity, and rate of sedimentation. Furthermore, two scenarios for sclerobionts colonisation and development of fish bite marks have been proposed. In the first syn vivo scenario, predatory fish either focused on the encrusting organisms attached to the spines or attacked the echinoid as a food source, resulting in the separation of spines from their original test during the echinoid’s life. In the second post-mortem scenario, disarticulated spines serve as a hard substrate for the colonisation of sclerobionts. Once again, the spines became subject to attacks by fish that fed on the encrusters, resulting in additional bite marks.


Fig. 1. Geographical and geological framework of the study area. A, geographical overview. B, simplified geological map of the study area (modified after Mandic & Piller 2001) with the location of the measured section at Gebel Gharra.
Fig. 4. Distribution and occurrences (percentage) of the observed bioerosion structures and encrusting organisms in the five shell concentrations of the Miocene succession in the study area.
Fig. 5. Endobionts on oyster shells. A-C, Entobia cateniformis. A, represents the growth phase ' A' (arrows) (Gh9O18). B, natural mould, and apertures (yellow and black arrows, respectively) of E. cateniformis (Gh9O33). C, an irregular maze of E. cateniformis (arrows) with T-and L-elongated chambers (Gh22O200). D-F, Entobia laquea. D, tunnel systems and chambers (arrows) (Gh9O1). E, E. laquea (yellow arrows) associated with curved tunnels of Talpina ramose (black arrow) (Gh22O201). F, E. laquea (circle) showing growth phase 'B' and 'C' , stenomorphic (Gh22O212). G, subcylindrical gallery of E. megastoma growth phase 'C-D' showing branching via bifurcation and swollen at nodal points (yellow arrows) with merging of several galleries (black arrows) (Gh22O243). H-L, circular to subcircular apertures of Entobia isp on surface of some oyster shells (Gh22O213, Gh9O4, Gh9O3, Gh9O27, and Gh22O237, respectively). Scale bars equal 1 cm, except for D and K, which are 2 cm.
Palaeoenvironmental analysis of bivalve-dominated concentrations from the lower‒middle Miocene succession, Gebel Gharra, Cairo-Suez District, Egypt

March 2024

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515 Reads

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1 Citation

Lethaia

The most conspicuous feature of the lower‒middle Miocene deposits of Gebel Gharra, Cairo-Suez District of Egypt, is the presence of three pectinid- and two oyster shell concentrations. They are paucispecific to polyspecific macrobenthic biotopes. Their shells were significantly colonised by abundant endobionts and common epibionts, characterising the Entobia ichnofacies, and representing successive phases of colonisation and bioerosion on stable substrates with a low sedimentation rate in high energy, shallow marine environments. Four types of shell concentrations have been distinguished. Pectinid-shell concentration of bed 2 is interpreted as a simple transgressive lag concentration that formed by reworking of previous deposited sediments in a shoal environment. Pectinid-shell concentration of bed 13 represents a coquina of high and moderately convex, sub-horizontally oriented to chaotic, and highly disarticulated and fragmented pectinid valves. It is interpreted as a remnant of previously deposited sediments that have been reworked by a single storm event without major transport of shells, and deposition in a lagoon environment. Pectinid-shell concentration of bed 14b is characterised by completely disarticulated, highly fragmented, moderately to densely packed, and re-oriented pectinid shells. It represents a composite concentration that was originated in a lagoon environment by sporadic high-energy events. Oyster-dominated concentrations of beds 9 and 22 represent “within-habitat” environmentally condensed assemblages, and formed by densely fossiliferous deposits with highly disarticulated, convex-up oysters along with articulated specimens preserved in life position, and with a moderate to high grades of bioerosion and encrustation. They were deposited by several high-energy events in supratidal and lagoonal environments, respectively.


Figure 1. The location of the ASIOP structure in the longitudinal section of the C. zygophora tube.
New Type of SIOP Structure in Serpulidae: Formation and Evolutionary Implications

March 2024

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18 Reads

Minerals

There is a controversy involved in the models of the formation of serpulid tube microstruc-tures, which either have been formed in similar ways to molluscan structures or in an alternative, unique serpulid way. A scanning electron microscope (SEM) study of the tube microstructure of Crucigera zygophora has been performed. A new serpulid tube microstructure, an aggregative SIOP, has been discovered in C. zygophora, herein termed ASIOP. During the first phase of crystallization, the sparsely located nuclei of the ASIOP structure formed, and in the second phase of crystal growth, the nucleation of spherultic sectors took place on the surface of preformed nuclei. The ASIOP structure differs from SIOP by more sparsely located crystallisation centres (nuclei) and the slower formation (i.e., crystallisation) of basic units. The formation of the ASIOP structure cannot be fully explained by the classical carbonate slurry model. Future comparative studies should show whether molluscan crossed spindle-like structures and serpulid SIOP structures are structural analogues.


Citations (35)


... Several studies have systematically identified the diversity of epizoans and epiphytes found on presentday cidaroid spines, which include algae, foraminifera, sponges, hydrozoans, corals, polychaetes (including tubed serpulids and spirorbids), bryozoans, barnacles, isopods, brachiopods, molluscs, and other echinoderms (Steinbeck and Ricketts, 1941;Brusca, 1973Brusca, , 1980Salazar-Vallejo and Loṕez-Muraira, 1983;Gutt and Schickan, 1998;Heteŕier et al., 2004Heteŕier et al., , 2008Linse et al., 2008;David et al., 2009;Gonzaĺez and Borrero-Peŕez, 2020). Of these associations, calcifying encrusting organisms have a robust fossil record (Rashwan et al., 2024), while evidence of soft-bodied or non-cemented epizoa is reliant on exceptional preservation quality (e.g., Schneider et al., 2010). ...

Reference:

Quaternary intensification of spine epibiosis in the cidaroid echinoid Eucidaris: implications for anthropogenic impacts
Taphonomy of the middle Miocene regular echinoid spines from Cairo-Suez District, Egypt: Palaeoecological and palaeoenvironmental interpretations
  • Citing Article
  • April 2024

Palaeoworld

... Cephalopods, bivalves and gastropods are represented by several genera and species (Sinitsyna and Mironova 1978;Kiselev et al. 1990). The fossils of trilobites are also common; the (Vinn et al. 2023). Rare macroscopic vertebrate fossils such as shields of the heterostracan Tolypelepis undulata, plates of the osteichthyan Lophosteus superbus Pander 1856; and jaw bones of acanthodians can be found at Ohesaare Cliff (Märss and Nestor 2014). ...

Tentaculitids from the Silurian of Estonia
  • Citing Article
  • August 2023

Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen

... Lower Kharga Shale Member (bed 66); abundant simple, vertical, U-shaped burrows having closely appressed limbs, basal part of "U" rarely preserved; hence, specimens consist typically of two parallel tubes shallow marine anoxic condition (Glossifungites Ichnofacies) (Knaust, 2017(Knaust, , 2019El-Refaiy et al., 2023) to deep marine environments (Nereites ichnofacies) (Knaust, 2017(Knaust, , 2019 Tisoa is regarded as a dwelling structure (domichnia) of tube-dwelling polychaetes (Knaust, 2017(Knaust, , 2019 marine salinity and weakly reducing conditions along with low rate of sedimentation (e.g., McRae, 1972). In general, several previous studies suggested that the Quseir Formation deposited in fluvial to brackish environment (Barthel and Herrmann-Degen, 1981;Hermina, 1990;Said, 1990;Mahmoud, 2003;Sallam et al., 2016). ...

Stratigraphical, microfacies, and ichnological characteristics and depositional environments of the Permo‒Carboniferous Aheimer Formation, western side of the Gulf of Suez, Egypt

Facies

... In general, the trace maker polychaete worms of Maeandropolydora ichnogenus are common in the lower intertidal and upper subtidal environments (e.g., Wilson and Taylor, 2001;El Hedeny and El-Sabbagh, 2007). On the other hand, epibionts, including serpulids, balanoid barnacles, and bryozoans, typically occur in shallow marine environments (Fig. 6B; Taylor and Wilson, 2003;Mandor et al., 2022Mandor et al., , 2023. ...

Calcareous tube-dwelling encrusting polychaetes from a lower‒middle Miocene sedimentary succession, Cairo-Suez District, Egypt
  • Citing Article
  • March 2022

Bulletin of Geosciences

... This biological process, well known for other marine invertebrates, particularly for molluscs (e.g. Lescinsky et al., 2002;Rashwan et al., 2022;Taylor, 1979;Taylor & Wilson, 2003), is in general the result of articulated taphonomic pathways involving phases of prolonged exposure and stable orientation and the formation of shelly grounds which could involve also boring epibionts (see Taylor & Wilson, 2003 for an overview; Nebelsick et al., 1997 and references cited therein for irregular, burrowing echinoids; and Garilli et al., 2021 for molluscs). Also, fossil and Recent echinoids are known to have played an important role in the colonization of several epibionts, encrusters and bioeroders (Belaustegui et al., 2013;Borszcz et al., 2013;Nebelsick et al., 1997). ...

Taphonomy and its significant role in palaeoenvironmental reconstruction of the upper Turonian actaeonellid gastropod concentrations of Abu Roash, Western Desert, Egypt

Lethaia

... Sediments of bed 18 have been deposited in a shallow lagoonal environment on an inner ramp setting (Mandor et al., 2023). Apparently, the abundant epifaunal elements may indicate a relatively stable low-stress environment (Fü rsich, 1981;Fü rsich et al., 2012;El-Sabbagh et al., 2021;Mandor et al., 2023). The common occurrence of corals indicates euhaline conditions probably within the shallow photic zone (e.g., Ayoub-Hannaa and Fü rsich, 2012). ...

Palaeoecological and palaeoenvironmental analyses of Cenomanian–early Turonian macrobenthic faunas from the northern Eastern Desert of Egypt
  • Citing Article
  • April 2021

Cretaceous Research

... Shell concentrations are characteristic features in most shelf and coastal areas (e.g. Kidwell et al. 1986;Fürsich 1995;Bressan & Palma 2010;Kassab et al. 2021;Rashwan et al. 2022). They can provide significant palaeoecological information in addition to detailed data on the palaeoenvironment of their desposition (e.g. ...

Late Eocene marginal marine deposits and paleoenvironment characterisation from the Maadi Formation (Northern Eastern Egypt)
  • Citing Article
  • July 2021

Proceedings of the Geologists Association

... In general, the numerous occurrences of sclerobionts (both endo-and epibionts) on macrofauna have been described from Cenozoic of Egypt (e.g. El-Shazly et al. 2016;El Hedeny et al. 2021a;Kassab et al. 2021). However, only few studies have previously been devoted to Miocene sclerobiont communities (e.g. ...

Paleoecology and taphonomy of a Middle Miocene domical cheilostome bryozoan, Siwa Oasis, the northern Western Desert of Egypt
  • Citing Article
  • April 2021

Lethaia

... Geographic distribution: Coniacian-Santonian of France, Spain and Morocco. It has been also recorded from the Campanian of Iran (Hashmie et al., 2020). ...

Facies development, palaeoecology, and palaeoenvironment of the Seymareh (Lopha Limestone) Member of the Gurpi Formation (Upper Campanian), Lurestan Province, SW Iran
  • Citing Article
  • March 2020

... (3) evidence of mortality due to overgrowth (e.g., bryozoans overgrown mollusks that in turn have overgrown polychaetes, forming layers, where polychaetes are basal) or predation (e.g., ophiuroids and crustaceans within barnacles at the end of the study). Bryozoans are considered superior competitors to polychaetes and barnacles (El Hedeny et al. 2021). Although bryozoans exhibited lower calcification rates compared to barnacles and mollusks, bryozoans and CCA had the greatest substrate coverage (especially in IES) (Figure 4). ...

Epi-and endobiont faunal communities on an Egyptian Mediterranean rocky shore: species composition and their competition for space
  • Citing Article
  • January 2021

Chinese Journal of Oceanology and Limnology