ABSTRACTS

 

 

Anne C. Cohen, Louis S. Kornicker, and Thomas M. Iliffe, 2000, Jimmorinia, a new genus of myodocopid ostracoda (Cypridinidae) from the Bahamas, Jamaica, Honduras, and Panama:  Smithsonian Contributions to Zoology, 605: 1-46.

 

A new genus and two new species of marine Ostracoda (Myodocopina: Cypridinidae), collected mostly from baited traps in the waters of the Bahamas and Caribbean Sea, are described and illustrated.  Jimmorinia gunnari, the type species, is non-luminescent, and was captured at 88-99 m depth on a submarine escarpment in Exuma Sound near Lee Stocking Island and Great Exuma island, Exuma Cays, Great Bahama Bank, Bahamas, and from shallower depths (3-15 m) off Discovery Bay, Jamaica, Roatan Island, Honduras, and the San Blas Islands, Panama, whereas J. gamma was collected only near Lee Stocking Island.  Descriptions for adult females are given for both species, and descriptions of adult males and some juvenile stages are given for J. gunnari.  Some sexual and geographic variation is described.  A table of generic comparisons is presented.  Some specimens of the new genus were tested and found to be non-luminescent.  Jimmorinia has an upper lip with fewer glandular processes (nozzles) than are present on the lips of Caribbean bioluminescent species.,  This paucity of nozzles may be related to a lack of bioluminescent capacity.  The reduced number of ommatidia, very unusual in a cypridinid from shallow depths, may be related to the lack of luminosity, or perhaps it indicates an ancestral relationship to cypridinids from greater depths or from an anchialine cave.

 

 

Sanad A. Al-Khashab, Lower Cretaceous Ostracoda from selected boreholes in Central Iraq.

 

Ostracoda of Zangura, Garagu, Ratawi, and Zubair Formations from boreholes Makhul-2, Balad-2 and East Baghdad-1 have been studied in detail.  One hundred and siz species and subspecies belonging to 28 genera are described, including 5 new species and one species were renamed.  These 28 genera are:  Asciocythere, Bairdia, Candoniella, Centrocythere, Curfsina, Cythereis, Cytherella, Cytherelloidea, Dolocytheridea, Eocytheropteron, Euryitcythere, Indet. Gen., Isocythereis, Macrocypris, Matronella, Metacytheropteron, Neocythere, Paijenborchellina, Paracypris, Pontocyprella, Protobuntonia, Pseudophanasymmetrica, Pterygocythere, Rehacythereis, Schuleridea, Spinoleberis, Strigosocythere, Veenia.

 

Three biozones (assemblage biozones) were established on the basis of the ostracod species occurrence.  These are:

            1—Schuleridea cf. punctatula Biozone (Zangura Formation) which confirmed late Berriasian-Early Valanginian age

in the studied section;

            2—Schuleridea cf. obtabilis Biozone (Garagu and Ratawi Formations) which confirmed Late Valanginian-

Hauterivian age in the studied section;

            3—Cythereis libanensis Biozone (Zubair Formation) which confirmed Barremian-Early Albian age in the studied

sections.

The paleoecology of Zangura Formation is shallow marine environment with interference of brackish representing littoral to inner sublittoral environments, warm water under normal sea water salinity.  Garagu Formation representing by shallow marine environment with warm water and normal salinity.  Ratawi Formation indicates an inner platform with redox environment.  While Zubair Formation representing different types of deltaic environment.  The ostracode genera migrated from east to west as well as from west to east and we concluded that the Trans-Sahara seaway has been present since Pre-Albian age, and some of the genera use the deep-sea barrier to migrate between Iberia and North Africa.  The affinities of the described species are discussed from a paleogeographical viewpoint, indicating that there are three bio-provinces in south Europe, north Africa, and the Middle East (Iraq and Iran).