Relevant bibliographies by topics / Golgo 13

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Academic literature on the topic 'Golgo 13'

Author: Grafiati
Published: 4 June 2021
Last updated: 13 February 2022

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Journal articles on the topic "Golgo 13"

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Casey, Carol, Paul Thomes, Sonia Manca, and Armen Petrosyan. "Giantin Is Required for Post-Alcohol Recovery of Golgi in Liver Cells." Biomolecules 8, no. 4 (November 16, 2018): 150. http://dx.doi.org/10.3390/biom8040150.

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In hepatocytes and alcohol-metabolizing cultured cells, Golgi undergoes ethanol (EtOH)-induced disorganization. Perinuclear and organized Golgi is important in liver homeostasis, but how the Golgi remains intact is unknown. Work from our laboratories showed that EtOH-altered cellular function could be reversed after alcohol removal; we wanted to determine whether this recovery would apply to Golgi. We used alcohol-metabolizing HepG2 (VA-13) cells (cultured with or without EtOH for 72 h) and rat hepatocytes (control and EtOH-fed (Lieber–DeCarli diet)). For recovery, EtOH was removed and replenished with control medium (48 h for VA-13 cells) or control diet (10 days for rats). Results: EtOH-induced Golgi disassembly was associated with de-dimerization of the largest Golgi matrix protein giantin, along with impaired transport of selected hepatic proteins. After recovery from EtOH, Golgi regained their compact structure, and alterations in giantin and protein transport were restored. In VA-13 cells, when we knocked down giantin, Rab6a GTPase or non-muscle myosin IIB, minimal changes were observed in control conditions, but post-EtOH recovery was impaired. Conclusions: These data provide a link between Golgi organization and plasma membrane protein expression and identify several proteins whose expression is important to maintain Golgi structure during the recovery phase after EtOH administration.
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Loizaga de Castro, Rocío, Fabiana Saporiti, Damián G. Vales, Néstor A. García, Luis Cardona, and Enrique A. Crespo. "Feeding ecology of dusky dolphins Lagenorhynchus obscurus : evidence from stable isotopes." Journal of Mammalogy 97, no. 1 (November 9, 2015): 310–20. http://dx.doi.org/10.1093/jmammal/gyv180.

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Abstract The dusky dolphin Lagenorhynchus obscurus occurs in the Southern Hemisphere, where it is restricted to coastal temperate areas. This study aimed to characterize the feeding ecology of dusky dolphins inhabiting northern and central Patagonia by using δ 13 C and δ 15 N stable isotope ratios in skin samples. We searched for evidence of geographical and seasonal variation in diet and we explored dietary differences between sexes. Significant differences in the stable isotope ratios of dusky dolphins were found among the 4 gulfs under study. Skin samples from Golfo San Matías and Golfo San Jorge were 13 C-enriched and 15 N-depleted compared to those from Golfo Nuevo and Golfo San José. There was no seasonality in the diet at Golfo Nuevo, and no differences in the diet between sexes in any gulf. Furthermore, Bayesian ellipses of males and females were similar in size and the overlap was mostly symmetrical in Golfo San José and Golfo San Jorge, while in the Golfo San Matías and Golfo Nuevo, females had wider ranges of δ 15 N, suggesting the exploitation of a wider trophic niche. Finally, pelagic fishes and demersal pelagic squids were identified as the main prey for this species of dolphin, although the proportion of each prey varied regionally. El delfín oscuro Lagenorhynchus obscurus se distribuye ampliamente en el Hemisferio Sur, donde prefiere áreas templadas costeras. Este estudio tuvo como objetivo caracterizar la ecología trófica de delfines oscuros que habitan en el norte y centro de la Patagonia mediante el uso de isótopos estables de δ 13 C y δ 15 N en muestras de piel. Específicamente, buscamos evidencia de variación geográfica y estacional en la dieta de los delfines y exploramos la diferencia de dieta entre sexos. Se encontraron diferencias significativas en los valores de isótopos estables de los delfines entre los cuatro golfos bajo estudio. Las muestras de piel de Golfo San Matías y Golfo San Jorge se encuentran enriquecidas en 13 C y deprimidas en 15 N en comparación con las muestras del Golfo Nuevo y Golfo San José. No hubo estacionalidad en la dieta en el Golfo Nuevo, y no hay diferencias en la dieta entre sexos en ningún golfo. Además, las elipses bayesianas de machos y hembras fueron similares en tamaño y la superposición fue mayormente simétrica en el Golfo San José y el Golfo San Jorge, mientras que en el Golfo San Matías y el Golfo Nuevo, las hembras tienen rangos más amplios de δ 15 N, lo que sugiere la explotación de un nicho trófico más amplio. Por último, los peces pelágicos y los calamares demersales pelágicos fueron identificados como la presa principal de esta especie de delfín, aunque la contribución de cada presa varió regionalmente.
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Zhou, Z., M. M. Mogensen, P. P. Powell, S. Curry, and T. Wileman. "Foot-and-Mouth Disease Virus 3C Protease Induces Fragmentation of the Golgi Compartment and Blocks Intra-Golgi Transport." Journal of Virology 87, no. 21 (August 28, 2013): 11721–29. http://dx.doi.org/10.1128/jvi.01355-13.

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Sengupta, Prabuddha, Prasanna Satpute-Krishnan, Arnold Y. Seo, Dylan T. Burnette, George H. Patterson, and Jennifer Lippincott-Schwartz. "ER trapping reveals Golgi enzymes continually revisit the ER through a recycling pathway that controls Golgi organization." Proceedings of the National Academy of Sciences 112, no. 49 (November 23, 2015): E6752—E6761. http://dx.doi.org/10.1073/pnas.1520957112.

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Whether Golgi enzymes remain localized within the Golgi or constitutively cycle through the endoplasmic reticulum (ER) is unclear, yet is important for understanding Golgi dependence on the ER. Here, we demonstrate that the previously reported inefficient ER trapping of Golgi enzymes in a rapamycin-based assay results from an artifact involving an endogenous ER-localized 13-kD FK506 binding protein (FKBP13) competing with the FKBP12-tagged Golgi enzyme for binding to an FKBP-rapamycin binding domain (FRB)-tagged ER trap. When we express an FKBP12-tagged ER trap and FRB-tagged Golgi enzymes, conditions precluding such competition, the Golgi enzymes completely redistribute to the ER upon rapamycin treatment. A photoactivatable FRB-Golgi enzyme, highlighted only in the Golgi, likewise redistributes to the ER. These data establish Golgi enzymes constitutively cycle through the ER. Using our trapping scheme, we identify roles of rab6a and calcium-independent phospholipase A2 (iPLA2) in Golgi enzyme recycling, and show that retrograde transport of Golgi membrane underlies Golgi dispersal during microtubule depolymerization and mitosis.
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Jin, Di, Jun Tao, Dan Li, Yanan Wang, Li Li, Zhongdong Hu, Zhenzhen Zhou, Xiuli Chang, Chunfeng Qu, and Hongbing Zhang. "Golgi protein 73 activation of MMP-13 promotes hepatocellular carcinoma cell invasion." Oncotarget 6, no. 32 (September 10, 2015): 33523–33. http://dx.doi.org/10.18632/oncotarget.5590.

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Chao, Daniel S., Jesse C. Hay, Shawn Winnick, Rytis Prekeris, Judith Klumperman, and Richard H. Scheller. "SNARE Membrane Trafficking Dynamics In Vivo." Journal of Cell Biology 144, no. 5 (March 8, 1999): 869–81. http://dx.doi.org/10.1083/jcb.144.5.869.

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The ER/Golgi soluble NSF attachment protein receptor (SNARE) membrin, rsec22b, and rbet1 are enriched in ∼1-μm cytoplasmic structures that lie very close to the ER. These appear to be ER exit sites since secretory cargo concentrates in and exits from these structures. rsec22b and rbet1 fused to fluorescent proteins are enriched at ∼1-μm ER exit sites that remained more or less stationary, but periodically emitted streaks of fluorescence that traveled generally in the direction of the Golgi complex. These exit sites were reused and subsequent tubules or streams of vesicles followed similar trajectories. Fluorescent membrin- enriched ∼1-μm peripheral structures were more mobile and appeared to translocate through the cytoplasm back and forth, between the periphery and the Golgi area. These mobile structures could serve to collect secretory cargo by fusing with ER-derived vesicles and ferrying the cargo to the Golgi. The post-Golgi SNAREs, syntaxin 6 and syntaxin 13, when fused to fluorescent proteins each displayed characteristic patterns of movement. However, syntaxin 13 was the only SNARE whose life cycle appeared to involve interactions with the plasma membrane. These studies reveal the in vivo spatiotemporal dynamics of SNARE proteins and provide new insight into their roles in membrane trafficking.
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Corse, Emily, and Carolyn E. Machamer. "The Cytoplasmic Tail of Infectious Bronchitis Virus E Protein Directs Golgi Targeting." Journal of Virology 76, no. 3 (February 1, 2002): 1273–84. http://dx.doi.org/10.1128/jvi.76.3.1273-1284.2002.

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ABSTRACT We have previously shown that the E protein of the coronavirus infectious bronchitis virus (IBV) is localized to the Golgi complex when expressed exogenously from cDNA. Here, we report that neither the transmembrane domain nor the short lumenal domain of IBV E is required for Golgi targeting. However, an N-terminal truncation containing only the cytoplasmic domain (CTE) was efficiently localized to the Golgi complex, and this domain could retain a reporter protein in the Golgi. Thus, the cytoplasmic tail of the E protein is necessary and sufficient for Golgi targeting. The IBV E protein is palmitoylated on one or two cysteine residues adjacent to its transmembrane domain, but palmitoylation was not required for proper Golgi targeting. Using C-terminal truncations, we determined that the IBV E Golgi targeting information is present between tail amino acids 13 and 63. Upon treatment with brefeldin A, both the E and CTE proteins redistributed to punctate structures that colocalized with the Golgi matrix proteins GM130 and p115 instead of being localized to the endoplasmic reticulum like Golgi glycosylation enzymes. This suggests that IBV E is associated with the Golgi matrix through interactions of its cytoplasmic tail and may have interesting implications for coronavirus assembly in early Golgi compartments.
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WESTERMANN, Peter, Maria KNOBLICH, Olaf MAIER, Carsten LINDSCHAU, and Hermann HALLER. "Protein kinase C bound to the Golgi apparatus supports the formation of constitutive transport vesicles." Biochemical Journal 320, no. 2 (December 1, 1996): 651–58. http://dx.doi.org/10.1042/bj3200651.

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Constitutive secretion of heparan sulphate proteoglycans (HSPGs) was stimulated in human hepatoma HepG2 cells by phorbol 12-myristate 13-acetate (PMA) and inhibited by calphostin C, a specific inhibitor of protein kinase C (PKC). To delineate more closely the site of PKC action, the packaging in vitro of 35SO4-labelled HSPGs into transport vesicles was investigated. Formation of transport vesicles at the trans-Golgi network was stimulated by PMA and inhibited by calphostin C or Ro 31-8220 by using a post-nuclear supernatant. Treatment of either isolated Golgi-enriched membranes or cytosolic proteins with calphostin C provided evidence that membrane-bound PKC forms strongly supported vesicle formation, whereas cytosolic PKC forms showed a marginal effect. The PKC isoforms PKC-α and PKC-ζ were attached to highly purified Golgi membranes, as shown by Western blotting. Both isoforms were localized by confocal immunofluorescence microscopy in the Golgi area of HepG2 cells. Immunoelectron microscopy of ultrathin cryosections of HepG2 cells showed that PKC-ζ predominantly attaches to the trans-Golgi region, whereas PKC-α binds to the cis- and trans-Golgi area.
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Tantra, M., L. Guo, J. Kim, N. Zainolabidin, V. Eulenburg, G. J. Augustine, and A. I. Chen. "Conditional deletion of Cadherin 13 perturbs Golgi cells and disrupts social and cognitive behaviors." Genes, Brain and Behavior 17, no. 6 (March 15, 2018): e12466. http://dx.doi.org/10.1111/gbb.12466.

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Johnston, P. A., A. Stieber, and N. K. Gonatas. "A hypothesis on the traffic of MG160, a medial Golgi sialoglycoprotein, from the trans-Golgi network to the Golgi cisternae." Journal of Cell Science 107, no. 3 (March 1, 1994): 529–37. http://dx.doi.org/10.1242/jcs.107.3.529.

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We have reported that MG160, an intrinsic membrane sialoglycoprotein of the Golgi apparatus (GA), resides in the medial cisternae of the organelle (Gonatas et al. (1989) J. Biol. Chem. 264, 646–653). In order to resolve the question whether MG160 acquires sialic acid residues in the trans cisternae or trans-Golgi network (TGN) prior to its retrograde transport, we have examined the effects of brefeldin A (BFA) on the post-translational processing of MG160, and the distribution of internalized wheat germ agglutinin covalently linked with HRP (WGA-HRP), which labels the TGN (Gonatas et al. (1977) J. Cell Biol. 73, 1–13). In BFA-treated PC12 cells, MG160 acquires resistance to endo H, but fails to be sialylated. This effect occurs in parallel with the redistribution of MG160 into an ER compartment dispersed throughout the cytoplasm including the nuclear envelope, and the collapse of the WGA-HRP-labelled TGN into vesicles and tubules surrounding the centriole. These results suggest that MG160 is not sialylated in BFA-treated cells because it is sequestered from the sialyltransferase enzyme(s), presumably located in the TGN, and provide evidence supporting the hypothesis for a retrograde transport pathway that recycles resident GA proteins, including MG160, between the Golgi cisternae and the TGN. To examine further the above hypothesis we studied cells treated with BFA and then allowed to recover from the effect of the drug for various lengths of time. After 15 minutes of recovery, cisternae of the Golgi apparatus, typically found in the pericentriolar region, are labeled by both MG160 and WGA-HRP.(ABSTRACT TRUNCATED AT 250 WORDS)
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Books on the topic "Golgo 13"

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Encuentro Regional de Investigación Científica y Tecnológica del Golfo de México (6th 1994 Tamaulipas, Mexico). Memoria del VI Encuentro Regional de Investigación Científica y Tecnológica del Golfo de México: 12 y 13 de mayo de 1994. [Tamaulipas, México]: Universidad Autónoma de Tamaulipas, 1994.

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Compute's Guide to Nintendo Games. Greensboro, USA: Compute Books, 1989.

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Tom, Badgett, ed. Ultimate unauthorized Nintendo game strategies: Winning Strategies for 100 Top Games. New York: Bantam Books, 1989.

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Inc, Game Counselor. Game Counselor's Answer Book for Nintendo Players. Redmond, USA: Microsoft Pr, 1991.

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Sepowski, Stephen J., ed. The Ultimate Hint Book. Old Saybrook, CT: The Ultimate Game Club Ltd., 1991.

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Saito, Takao. Golgo 13, Vol. 13 (Golgo 13). VIZ Media LLC, 2008.

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Saitō, Takao. Gogo 13, Volume 8 (Golgo 13). VIZ Media LLC, 2007.

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Saito, Takao. Golgo 13 Vol. 12 (Golgo 13). VIZ Media LLC, 2007.

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Saito, Takao. Golgo 13 Vol. 11 (Golgo 13). VIZ Media LLC, 2007.

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Saito, Takao. Golgo 13, Volume 5 (Golgo 13). VIZ Media LLC, 2006.

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Book chapters on the topic "Golgo 13"

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Kam, Peter, Ian Power, Michael J. Cousins, and Philip J. Siddal. "Muscle Spindles, Golgi Tendon Organs and Spinal Reflexes." In Principles of Physiology for the Anaesthetist, 81–84. Fourth edition. | Boca Raton : CRC Press, Taylor & Francis Group, 2020.: CRC Press, 2020. http://dx.doi.org/10.1201/9780429288210-13.

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TORRES, ANTONIO OLGUÍN. "El Golfo de México en caso de un derrame petrolero:." In Lecturas sobre derecho del medio ambiente Tomo XIX, 309–36. Universidad del Externado de Colombia, 2019. http://dx.doi.org/10.2307/j.ctv1k03pmb.13.

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"Bibliografía." In Aprovechamiento de vertebrados terrestres por las poblaciones humanas que habitaron la costa del Golfo San Matías (Río Negro, Argentina) durante el Holoceno tardío, 233–72. Archaeopress Publishing Ltd, 2018. http://dx.doi.org/10.2307/j.ctv1zcm0sq.13.

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Wuestehube, Linda J., and Randy W. Schekman. "[13] Reconstitution of transport from endoplasmic reticulum to golgi complex using endoplasmic reticulum-enriched membrane fraction from yeast." In Reconstitution of Intracellular Transport, 124–36. Elsevier, 1992. http://dx.doi.org/10.1016/0076-6879(92)19015-x.

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Koch, Christof. "Dendritic Spines." In Biophysics of Computation. Oxford University Press, 1998. http://dx.doi.org/10.1093/oso/9780195104912.003.0018.

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Dendritic spines, sometimes also called dendritic thorns, are tiny, specialized protoplasmic protuberances that cover the surface of many neurons. First described by Ramón y Cajal (1909; 1991) in light-microscopic studies of Golgi stained tissue, they are among the most striking subneuronal features of many neurons. Indeed, the presence of a high density of dendritic spines allows the unambiguous classification of neuronal types into spiny and aspiny, sparsely spiny, or smooth neurons. Over 90% of all excitatory synapses that occur in the cortex are located on dendritic spines. Spines can be found in all vertebrates as well as in invertebrates (e.g., the dendrites of Kenyon cells in the mushroom bodies in the olfactory system of the insect brain). The intimate association of spines with synaptic traffic suggests some crucial role in synaptic transmission and plasticity. Because of their submicrometer size (see below), physiological hypotheses as to the function of dendritic spines have only very recently become accessible to the experimentalist. For the previous two decades, spine properties have been investigated through analytical and computational studies based on morphological data, providing a very fertile ground for the crosspollination of theory and experiment. (For a very readable historical account of this see Segev et al., 1995.) The recent technical advances in the direct visualization of calcium dynamics in dendrites and spines are now permitting direct tests of some of these theoretical inferences (Guthrie, Segal, and Kater, 1991; Müller and Connor, 1991; Yuste and Denk, 1995; Denk, Sugimori, and Llinás, 1995; Svoboda, Tank, and Denk, 1996). As discussed in this chapter and, more extensively, in Chap. 19, the theoretical models that have endowed spines with active properties giving rise to all-or-none behavior (Perkel and Perkel, 1985; Shepherd et al., 1985; Segev and Rail, 1988; Baer and Rinzel, 1991) have, in general, been confirmed experimentally. Historically, the possibility of implementing synaptic memory by modulating the electroanatomy of spines was recognized early on (Chang, 1952) and was subsequently analyzed in depth by Rail (1970, 1974, 1978) and many others. Because small changes in the spine morphology can lead to large changes in the amplitude of the EPSP induced by the excitatory synapse on the spine, spines have been considered to contribute to the modulation of synaptic “weight” during long-term potentiation (see Chap. 13).
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Conference papers on the topic "Golgo 13"

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Ponge, Julien, Frédéric Le Mouël, and Nicolas Stouls. "Golo, a dynamic, light and efficient language for post-invokedynamic JVM." In PPPJ '13: virtual machines, languages, and tools. New York, NY, USA: ACM, 2013. http://dx.doi.org/10.1145/2500828.2500844.

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Grice, D., H. Faddy, P. Kenny, G. Monteith, and S. Roberts-Thomson. "The Golgi Associated Calcium Pumps in Human Breast Cancer." In Abstracts: Thirty-Second Annual CTRC‐AACR San Antonio Breast Cancer Symposium‐‐ Dec 10‐13, 2009; San Antonio, TX. American Association for Cancer Research, 2009. http://dx.doi.org/10.1158/0008-5472.sabcs-09-1129.

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Hernández Noguera, Luis Adrian, Rosa Soto Rojas, and Jose Vega Alpízar. "Descripción de la pesquería del pez dorado (Coryphaena hippurus) en las zonas 12, 13 y 14 del Área Marina de Pesca Responsable (AMPR) Paquera-Tambor, Golfo de Nicoya, Costa Rica." In I Congreso Internacional de Ciencias Exactas y Naturales. Universidad Nacional, 2019. http://dx.doi.org/10.15359/cicen.1.27.

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El pez dorado Coryphaena hippurus es una de las especies de mayor importancia co­mercial capturada en el Golfo de Nicoya. De noviembre del 2017 a enero del 2019, se analizaron 379 especímenes, correspondientes al stock distribuido en las zonas 12,13 y 14 del AMPR Paquera-Tambor. La relación longitud total-peso total para esta especie indica un crecimiento isométrico, tanto para hembras Pt= 0.0091Lt2.83, como para machos Pt= 0.0034Lt3.03. La talla media de captura para hembras fue de 111 cm Lt y de 115 cm Lt para machos; se estimó que el 94% de la captura se encuentra sexualmente madura, con un periodo máximo de reproducción comprendido de noviembre a enero. La fecundidad absoluta en hembras varió de 16243 a 598688 ovocitos; mientras que la fecundidad relativa osciló de 1 a 147 ovocitos por gramo/pez. Los análisis de hábitos alimenticios sugieren que esta población es generalista con preferencias por los peces.
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