[54] Golüke S, Bischof H-J, Engelmann J, Caspers B A and Mayer U. Social odour activates the hippocampal formation in zebra finches (Taeniopygia guttata) Behavioural Brain Research: 364, 2019, 41-49. doi.org/10.1016/j.bbr.2019.02.013.
[53] R Perrone, F Pedraja, G Valiño, B Tassin and A Silva. Non-breeding territoriality and the effect of territory size on aggression in the weakly electric fish, Gymnotus omarorum acta ethologica, 2019. 1-11. doi.org/10.1007/s10211-019-00309-7.
[52] Wolf-Homeyer S, Engelmann J and Schneider A. Application of reduced sensor movement sequences as a precursor for search area partitioning and a selection of discrete EEV-contour-ring fragments for active electrolocation Bioinspiration & Biomimetics. 13(6):066008. doi: 10.1088/1748-3190/aae23f.
[51] Nagel R, Kirschbaum F, Hofmann V, Engelmann J, Tiedemann R. Electric pulse characteristics can enable species recognition in African weakly electric fish species Scientific Reports. 10799 (2018)
[50] Fechner S, Grant K, von der Emde G, Engelmann J. Physiological evidence of sensory integration in the electrosensory lateral line lobe of Gnathonemus petersii Plos One. 13(4): e0194347.
[49] Nagel R, Kirschbaum F, Engelmann J, Hofmann V, Pawelzik F, Tiedemann R. Male-mediated species recognition among African weakly electric fishes Royal Society Open Science.
5(2): 170443.
[48] F Pedraja, V Hofmann, K M. Lucas, C Young, J Engelmann and J E. Lewis. Motion parallax in electric sensing. PNAS 2018 January, 115 (3) 573-577.
[47] Chagnaud B., Engelmann J, Fritzsch B, Glover JC and H Straka. Sensing external and self-motion with hair cells. A comparison of the lateral line and vestibular systems from a developmental and evolutionary perspective. Brain Behav Evol. 2017;90(2):98-116.
  
[46] Pedraja F, Perrone R, Silva A, Budelli R. Passive and active electroreception during agonistic encounters in the weakly electric fish Gymnotus omarorum. (2016) Bioinspir. Biomim. 11, doi:10.1088/1748-3190/11/6/065002  
[45] Hofmann V, Sanguinetti-Scheck J, Gómez-Sena L and Engelmann J. Sensory flow as a basis for a novel distance cue in freely behaving electric fish. J. Neuroscience (2017);37(2):302-312  
[44] Hollmann V, Engelmann J  and Gómez-Sena L. A quest for excitation: theoretical arguments and immunohistochemical evidence of excitatory granular cells in the ELL of Gnathonemus petersii. J. Physiol., Paris 2016 (16)
   
[43] Engelmann J, Walther T, Grant K, Chicca E and Gómez-Sena L. Modeling latency code processing in the electric sense: from the biological template to its VLSI implementation. Bioinspiration & Biomimetics, Bioinspir. Biomim. (2016) 11:(5), 055007  
[42] Wolf-Homeyer, S, Engelmann J and Schneider A. Electrolocation of objects in fluids by means of active sensor movements based on discrete EEVs. Bioinspiration & Biomimetics, 2016, 11(5)  
[42] Hollmann V, Hofmann V and Engelmann J. A somatotopic map of the active electrosensory sense in the midbrain of the mormyrid Gnathonemus petersii. J Comp. Neurology 5;524(12):2479-91.
[41] Hollmann V, Lucks V, Kurtz R and Engelmann J. Adaptation-induced modification of motion selectivity tuning in visual tectal neurons of adult zebrafish | Journal of Neurophysiology 114: 2893–2902, 2015.  
[40] Paul C, Mamonekene V, Vater M, Feulner P, Engelmann P, Tiedemann R and Kirschbaum R. Comparative histology of the adult electric organ among four species of the genus Campylomormyrus (Teleostei: Mormyridae) | Journal of Comp Physiol A,201(4):357-74
[39] Amey-Özel M, von der Emde G, Engelmann J and  Grant K. More a finger than a nose: the trigeminal motor and sensory innervation of the Schnauzenorgan in the elephant-nose fish, Gnathonemus petersii | Journal of Comp Neurology, 523(5):769-89  
[38] Hofmann V, Guerten B, Sanguinetti-Scheck J, Gomez-Senna  and Engelmann J.  Motor patterns during active electrosensory acquisition  | Frontiers in Behav. Neuroscience, 8 http://www.frontiersin.org/files/Articles/92855/fnbeh-08-00186-r2/image_m/fnbeh-08-00186-g003.jpg
[37] Francke, M. Kreysing, A.Mack, J. Engelmann, A. Karl, F. Makarov, J. Guck, M. Kolle, H. Wolburg and A. Reichenbach. Grouped Retinae and Tapetal Cups in some Teleostian Fish: Occurrence, Structure, and Function | Progress in Retinal and Eye Research, 38, p. 43 – 69 
[36] R. Pusch, H-J Wagner, G. von der Emde and J. Engelmann. Spatial resolution of an eye containing a grouped retina: ganglion cell morphology and tectal physiology in the weakly electric fish Gnathonemus petersii. | J Comp Neuro,1;521(17):4075-93
[35] V. Kassing, J. Engelmann and R. Kurtz, Monitoring of single- cell responses in the optic tectum of adult zebrafish with dextran-coupled calcium dyes delivered via local electroporation | PLoS ONE 8(5): e62846
[34] V. Hofmann, J. Sanguinetti-Scheck; Silke Künzel; Bart Geurten; Leonel Gómez-Sena, J. Engelmann. Sensory flow shaped by active sensing: sensormotor strategies in electric fish. | JExpBiol 216 (2013), 2487-2500
[33] V. Hofmann, J. Sanguinetti-Scheck; L. Gómez-Sena, J. Engelmann. From static electric images to electric flow: towards dynamic perceptual cues in active electroreception. | J. Physiol., Paris, Vol. 107/1-2 (2013) 95-106
[32] Pusch R, Kassing V, Riemer U, Wagner HJ, Emde GV, Engelmann J. A grouped retina provides high temporal resolution in the weakly electric fish Gnathonemus petersii. | J. Physiol., Paris, Vol. 107/1-2 (2013) 84- 94 image description
[31] Kreysing et al. (2012) Photonic Crystal Light Collectors in Fish Retina Improve Vision in Turbid Water“, | Science Vol. 336 no. 6089 pp. 1700-1703 DOI: 10.1126/science.1218072 image description
[30] Goulet, van Hemmen, Jung, Chagnaud, Scholz and Engelmann (2012) Temporal precision and reliability in the velocity regime of a hair-cell sensory system: the mechanosensory lateral line of goldfish, Carassius auratus . | J Neurophysiology,107: 2581-2593. Cover
[29] von der Emde G. and Engelmann J. (2011) Active Electrolocation. In: Farrell A.P., (ed.), Encyclopedia of Fish Physiology: From Genome to Environment, volume 1, pp. 375–386. San Diego: Academic Press Encyclopedia Fish Physiol
[28] J. Engelmann, S. Gertz, J. Goulet, A. Schuh, and G. von der Emde (2010) Coding of Stimuli by Ampullary Afferents in Gnathonemus petersii. | J Neurophysiol 104: 1955-1968, 2010
[27] von der Emde G, Behr K, Bouton B, Engelmann J, Fetz S and Folde C (2010) 3-dimensional scene perception during active electrolocation in a weakly electric pulse fish. | Front. Behav. Neurosci. 4:26. doi:10.3389/fnbeh.2010.00026
[26] Engelmann J., Nöbel S., Röver T., von der Emde G. (2009) The Schnauzenorgan-response of Gnathonemus petersii. | Frontiers in Zoology 6:21
[25] Hagedorn, J.A.H., Engelmann J., Franosch, J.-M.P., Goulet, J. and van Hemmen J.L. (2009) Wake Tracking and the Detection of Vortex Rings by the Canal Lateral Line of Fish | Physical Review Letters 103(7), e78102

[24] Feulner P D.G., Plath M., Engelmann J., Kirschbaum K and R. Tiedemann (2009) Magic trait Electric Organ Discharge (EOD): Dual function of electric signals promotes speciation in African weakly electric fish. | Communicative and Integrative Biology 2008, 2 (4)
[23] P.G.D. Feulner, M. Plath, J. Engelmann , F. Kirschbaum and R. Tiedemann. Electrifying love: Electric fish use species-specific discharge for mate choice. | Biology Letters, doi:10.1098/rsbl.2008.0566

[22] Moritz T, von der Emde G, Engelmann J and K. E. Linsenmair (2009) The electric organ discharges of the Petrocephalus species (Teleostei: Mormyridae) of the Upper Volta System. | J Fish Physio. 74: 54-76

[21] Engelmann J, Bacelo J, de Rujter M, Grant K and Sugawara Y. (2008)  Dendritic backpropagation and synaptic plasticity in the mormyrid electrosensory lobe | J. Physiol Paris, 102 (2):233-245

  

[20] von der Emde G, Amey M, Engelmann J, Fetz F, Folde C, Hollmann M, Metzen M and Pusch R. (2008) Active electrolocation in G. petersii. Behaviour, Sensory performance and Receptor Systems. | J. Physiol Paris, 102(2):279-290

  

[19] Engelmann J, Pusch R and von der Emde G (2008) Active sensing: pre-receptor mechanisms and behaviour in electric fish.| Communicative and Integrative Biology: Vol. 1(1)
 

[18] Metzen MG, Engelmann J and Gerhard von der Emde. (2008) Size, structure, and distribution of receptive fields of neurons in the electrosensory lateral line lobe of the weakly electric fish, Gnathonemus petersii. | J Comp Physiol A. DOI 10.1007/s00359-008-0377-4.
 

[17] Bacelo J, Engelmann J, Hollmann M, von der Emde G and K. Grant. (2008) Peripheral distribution and central representation of electroreceptors in Gnathonemus petersii indicate functional foveae. | J Comp Neurol 511(3):342-359 
 

[16] Hollmann M, Engelmann J and von der Emde G. (2008) Distribution, density and morphology of electroreceptor organs in mormyrid electric fish: anatomical investigations of a receptor mosaic. | Journal of Zoology. DOI 10.1111/j.-1469- 7998.2008.00465.x 
 

[15] Engelmann J, Bacelo J, Metzen M, Pusch R, Bouton B, Migliaro A, Caputi A, Budelli R, Grant K and Gerhard von der Emde. (2008) Electric imaging through active electrolocation: Implication for the analysis of complex scenes. | Biological Cybernetics. DOI 10.1007/s004224-088-0213-5
 

[14] Pusch R, von der Emde G, Hollmann M, Nöbel S, Bacelo J and J. Engelmann. (2008) Active Sensing in a Mormyrid Fish – Electric Images and Peripheral Modifications of the Signal Carrier give Evidence of Dual Foveation. | J Exp Biol 2008 211: 921- 934.
 

[13] Goulet J, Engelmann J, Chagnaud B, Franosch JM, Suttner MD and JL van Hemmen. (2007) Object localization through the lateral line system of fish: Theory and experiment. | J. Comp Physiol A. 194(1): 1-17
 

[12] van den Burg EH, Engelmann J, Bacelo J, Gomez L and Grant K. (2007) Etomidate reduces initiation of backpropagating dendritic action potentials: implications for sensory processing and synaptic plasticity during anesthesia. | J Neurophysiol. 2007 Mar;97(3):2373-84. 
 

[11] Chagnaud BP, Bleckmann H, Engelmann J. (2006) Neural responses of goldfish lateral line afferents to vortex motions. | J Exp Biol.; 209: 327-42.
 

[10] Engelmann J, Bacelo J, van den Burg EH and Grant K (2005) The sensory and motor effects of etomidate anaesthesia. | J Neurophysiol. 2005; doi:10.1152/jn.00405.2005
 
[09] Engelmann J and Bleckmann H (2004) Effects of running water on lateral line responses to moving objects. Zoology 107 (2):135-151
 

[08] Bleckmann H, Mogdans J, Engelmann J, Kröther S, Hanke W (2004) Wie Fische Wasser fuehlen: Das Seitenliniensystem. | BIUZ. Vol. 34(6): 358-365
 

[07] Engelmann J and Bleckmann H (2004) Effects of running water on lateral line responses to moving objects. | Zoology 107 (2):135-151
 

[06] Mogdans J, Kröther S, Engelmann J (2004) Neurobiology of the fish lateral line: adaptations for the detection of hydrodynamic stimuli in running water. In: von der Emde G., Mogdans J., Kapoor B.G. (eds) The Senses of Fish. Adaptations for the reception of natural stimuli. Narosa Publishing House, New Delhi: 265- 287
 

[05]  Mogdans J, Engelmann J, Hanke W, Kröther S (2003) The fish lateral line: how to detect hydrodynamic stimuli. In: Barth FG, Humphrey JAC, Secomb TW (eds) Sensors and Sensing in Biology and Engineering. Springer, Wien New York: 173-185


 

[04]Engelmann J, Kröther S, Mogdans J, Bleckmann H (2003) Effects of running water on lateral line responses to moving objects. | Brain Behaviour and Evolution 61: 195-212
 
[03]  Engelmann J, Hanke W, Bleckmann H (2002) Lateral line reception in still- and running water. | J Comp Physiol A 188: 513-526.
 
[02] Engelmann J, Kröther S, Mogdans J, Bleckmann H (2002) Responses of primary and secondary lateral line units to dipole stimuli under still and running water conditions. | Bioacustics 12: 158-161
 
[01]  Engelmann J, Hanke W, Mogdans J, Bleckmann H (2000) Coding of hydrodynamic signals by the fish lateral line in still and running water. | Nature 408: 52-53
 
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