Electromagnetic Modeling of the Propagation Characteristics of Satellite Communications Through Composite Precipitation Layers Science and Technology, 8 (2003) 97-106 © 2003 Sultan Qaboos University Some Aspects of the Anatomy and Histology of Digestive Tracts in Two Sympatric Species of Freshwater Fishes Taher Ba-Omar, Reginald Victor and Daniel Tobias Department of Biology, College of Science, Sultan Qaboos University, P.O.Box 36, Al Khod 123, Muscat, Sultanate of Oman, Email: Taher@squ.edu.om. بعض الجوانب التشريحية والنسيجية للجهاز الهضمي لنوعين من أسماك المياه العذبة دانيال توباز طاهر بن عبدالرحمن باعمر، ريجنالد فيكتور و من Aphanius dispar and Garra barreimiaeدراسة مقارنة للجهاز الهضمي لنوعين من أسماك المياه العذبة : خالصة كما تم تقييم العالقة . والقناة الهضمية وعدد عكنات المعدة وارتفاعها األسماكتم قياس كل من طول . منظور تشريحي ونسيجي سوف . كذلك تم توصيف ومقارنة أنسجة الجهاز الهضمي لكال السمكتين . أعاله إليها المشار واألجزاءبين طول هاتين السمكتين . تملك معدة حقيقيةاألسماكه كانت هذإذا نتائج هذه الدراسة لمناقشة ما تستخدم ABSTRACT: Comparative anatomy and histology of the digestive tracts of two sympatric species of freshwater fish, Aphanius dispar (Cyprinodontidae) and Garra barreimiae (Cyprinidae) are studied. Morphometric measurements of alimentary canal such as length and the number and height of rugae in sections have been made for both species. Relationships between these morphometric characters and the total length of fish have been evaluated. The ratio between the length of alimentary canal and total length of fish in both species reflects their feeding habits. Histology of the ‘stomach’ and ‘intestine’ of these two species as shown by light microscopy has been described and compared. Results of this study are used to discuss the query whether these species have true stomachs. KEYWORDS: Aphanius; Garra; Fish; Anatomy; Histology; Stomach; Intestine 1. Introduction Several studies have been carried out on the digestive tracts of teleost fishes (Grau et al. 1992; Osman and Caceci 1991; Gargiulo et al. 1997;1998). Recently, we have studied the structure and ultrastructure of the stomach of Aphanius dispar (Rüppell 1828), a cyprinodont fish with special reference to stress from starvation (Ba-Omar et al. 1998; Ba-Omar and Victor, 2000). What is referred to as ‘stomach’ in these studies is the morphologically distinct, enlarged sac-like portion of the gut separated from intestine by a constriction (Ba-Omar and Victor, 2000). However, it is well known that many fish including cyprinids and cyprinodonts lack a ‘true’ stomach, that is a portion of the digestive tube with a typically acid secretion and a distinctive epithelial lining different from that of the intestine (Lagler et al. 1977). From our work so far on A. dispar, the 'stomach' we describe could well be a ‘stomach-like’ pouch, a hollow organ covered by an intestinal mucosa. Despite being different in gross anatomy, this portion of the alimentary canal could well be the same as that of 'true' intestine both histologically and functionally. Therefore, it is necessary to describe and compare sections of alimentary canal above and below the constriction that seemingly separates 'stomach' from that of 'intestine' in A. dispar. In this study, we also compare the anatomy and histology of the alimentary canal of another cyprinid, Garra barreimiae that is sympatric with A. dispar in the freshwaters of Oman. These two species occupy different feeding niches. The cyprinid, is a benthic herbivore, while A. dispar 97 TAHER BA-OMAR, REGINALD VICTOR and DANIEL TOBIAS is an ubiquitous omnivore. Both species have ‘stomachs’ and ‘intestines’ sensu Ba-Omar and Victor (2000). The descriptions of alimentary canals provided here are of value in their own right because very little is known about the biology of these species. However, we also use the results to address the existence of ‘stomachs’ in these species. 2. Materials and methods Specimens of Aphanius dispar and Garra barreimiae were collected from Wadi Al-Khod near Sultan Qaboos University, Sultanate of Oman (Lat. 23ο 30' N; Long. 58ο 40' E). Both species are sympatric in the temporary and permanent pools of the same wadi (i.e. seasonal river) system. Most often they are mutually exclusive in the same pools. G. barreimiae, however, regularly shares its habitat with another cyprinid Cyprinion microphthalmum. All fishes for this study were collected in freshwater, although A. dispar also lives in brackish waters of the coastal lagoons and estuaries. The fishes were kept in an aerated holding tank in the laboratory and were fed with the commercial Tetramin flakes ad libitum daily. For each species 11 specimens irrespective of sex were killed and the entire alimentary canal was removed from each fish. The total length of the fish and the entire gut length were measured in mm. The size ranges of A. dispar and G. barreimiae were 30 – 48 and 29 – 69 mm, respectively. Ten percent buffered formalin (pH 7.3) at room temperature was used to fix the gut. The entire gut was processed, embedded in paraffin with an anterior-posterior orientation and serially sectioned at 5 µm. Serially numbered paraffin sections were stained using Mayer’s hematoxylin – eosin for examination under routine light microhoscopy. The histological topography was studied separately for the ‘stomach’ and ‘intestine’ regions under low and high magnifications (100 – 400 x). All measurements of rugae ( i.e. internal folds) were made on 25 randomly chosen representative sections. In each section five randomly chosen rugae were measured making up a total of 125 measurements for each region. Measurements in µm were made using an ocular meter calibrated with a stage micrometer. Data transformations were made wherever necessary. All statistical analyses were performed using SYSTAT (Version 7.0) and all graphs were generated using SYGRAPH (Version 7.0). 3. Results 3.1 Aphanius dispar In the alimentary canal of Aphanius dispar two distinct parts, an anterior dilated segment, presumably the ‘stomach’, and a posterior tubular segment, presumably the ‘intestine’, are recognized (Figure 1A). The anterior segment is shorter than the posterior segment, which is approximately five times longer. The mean alimentary canal length of A. dispar is approximately twice the total length (TL) of the fish (Table 1). Figure 2 shows the positive relationship between the total length (TL) and the length of alimentary canal in A. dispar irrespective of sex. The regression equation describing this relationship, length of alimentary canal = - 58.483 (TL) is significant (n = 11; ANOVA , F = 10.609; r = 0.736; P < 0.01). Figure 3 shows the histological organization of the ‘stomach’. It is composed of four different layers, mucosa, submucosa, muscularis and serosa. The four layers differ in their thickness and the mucosa is thrown into rugae. These rugae vary in length and width. They are made of columnar epithelial cells with the nuclei located at the basal side. Figure 4 presents the histology of the ‘intestine’. It is not different from that of the 'stomach'. Part of the mucosa is thrown into rugae while the rest is flat. The heights of the rugae are shorter than those found in the ‘stomach’. Table 1 shows the number and the mean heights of rugae in the ‘stomach’ and in the ‘intestine’. The number of rugae in the ‘stomach’ was significantly higher than those in the intestine (t-test, t = 4.912; p < 0.001). There is no correlation between the number 98 ANATOMY AND HISTOLOGY OF DIGESTIVE TRACTS of rugae in the ‘stomach’ and in the ‘intestine’(n = 11; r = - 0.148; p > 0.05). Similarly, the height of rugae in the ‘stomach’ (Figure 5) is significantly greater than that in the intestine (paired t-test, t = 19.162; p < 0.001). There is no correlation between rugae heights of the ‘stomach’ and those of the ‘intestine’( n = 125; r = -0.157; p > 0.05). Figure 1A. Aphanius dispar and its alimentary canal; stomach (large arrow) and intestine (small arrow). Figure 1B. Garra barriemiae and its alimentary canal; stomach (large arrow) and intestine (small arrow). 99 TAHER BA-OMAR, REGINALD VICTOR and DANIEL TOBIAS Figure 2. Relationship between total length and alimentary canal length in Aphanius dispar. Table 1: Morphometric measurements comparing alimentary canals of Aphanius dispar and Garra barreimiae; n = number of measurements; values given or mean ± standard deviation; * indicates significant differences within species at P<0.001. Character n A. dispar G. barriemiae Total length (mm) 11 39.1 ± 3.4 49.6 ± 10.7 Canal length (mm) 11 77.3 ± 16.6 371.1 ± 134.3 Stomach – No. of rugae 62 32 ± 6* 15 ± 4* Intestine – No. of rugae 62 25 ± 6* 12 ± 2* Stomach – rugae height (µm) 125 21.1 ± 9.3* 10.3 ± 3.0* Intestine – rugae height (µm) 125 4.3 ± 2.0* 1.4 ± 0.7* 3.2 Garra barreimiae The external morphology of the alimentary canal is characterized by a ‘stomach’ and an ‘intestine’. The ‘stomach’ is short and poorly dilated. (Figure 1B). The alimentary canal of Garra barreimiae is a long tube with a narrow lumen. Its length is nearly 7.5 times the total length (TL) of the fish (Table 1). The positive relationship between the total length (TL) and the length of the alimentary canal (Figure 6) described by the equation, length of alimentary canal = -210.46 (TL) is significant (n = 11; ANOVA, F =83.492; r = 0.950; p < 0.001). 100 ANATOMY AND HISTOLOGY OF DIGESTIVE TRACTS Figure 3. Light micrograph of a transverse section showing histological organization of the ‘stomach’ of Aphanius dispar fish; folds (rugae) (Large open arrowheads), mucosa (M), submucosa (Sm), muscularis (small arrow). Bar = 25 mµ . Figure 4. Light micrograph of a transverse section showing histological organization of the intestine of Aphanius dispar fish; mucosa (M) and muscularis (small arrows). Bar = 25 µm. 101 TAHER BA-OMAR, REGINALD VICTOR and DANIEL TOBIAS Figure 5. Box plots showing the fold length in Aphanius dispar and Garra barriemiae (Ad = Aphanius dispar intestine, Ad-S = Aphanius dispar stomach, Ga = Garra barriemiae intestine and Ga-S = Garra barriemiae stomach). Figure 6. Relationship between total length and alimentary canal length in Garra barriemiae. 102 ANATOMY AND HISTOLOGY OF DIGESTIVE TRACTS igure 7. Light micrograph of a transverse section showing the histological organization of the he histology of the ‘stomach’ is shown in Figure 7. It is composed of four different layers, muc the histology of the ‘intestine’. Its basic structure is the same as that of the ‘stom s well as their heights in these two regio ach other in the gross anatomy of the alimentary cana F ‘stomach’ of Garra barriemiae fish; rugae (folds) (large open arrowheads), mucosa (M), submucosa (Sm), muscularis (small arrows). Bar = 25 µm. T osa, submucosa, muscularis and serosa all characterised by varying thickness. The mucosa is thrown into rugae with variable heights and widths. These are made of columnar epithelial cells with basal nuclei. Figure 8 shows ach’. The rugae heights are variable and shorter than those of the ‘stomach’. The structure of the columnar epithelium is the same as that in the ‘stomach’. Numbers of rugae in the ‘stomach’ and the ‘intestine’ a ns are given in Table 1 and Figure 5. Both the numbers (t-test, t = 3.950; p < 0.001) and rugae heights (paired t-test, t = 32.726; p < 0.001) are significantly different. There are no correlations between the numbers of rugae (n = 25; r = 0.320; p > 0.05) or between the heights of rugae (n = 125; r = 0.055; p > 0.05) in the ‘stomach’ and in the ‘intestine’. 3.3 Comparison of A. dispar and G. barreimiae A. dispar and G. barreimiae do not resemble e l. The histological organization of the ‘stomach’ and ‘intestine’ show very close resemblances. Table 1 shows the morphometric measurements of the ‘stomach’ and ‘intestine’ of both species. The ratio of the total length of fish to the length of alimentary canal in adult fish ( total length / alimentary canal length) is different in both species. In A. dispar this ratio ranged from 0.40 to 0.66, while in G. barreimiae it ranged from 0.12 to 0.17. These ratios were significantly different (t-test on arcsin transformed data, t = 17.346; df = 20; p < 0. 001). The mean numbers of rugae in both the ‘stomach’ and ‘intestine’ of A. dispar were significantly higher than those of G. barreimiae (Table 1). 103 TAHER BA-OMAR, REGINALD VICTOR and DANIEL TOBIAS igure 8. Light micrograph of a transverse section showing the histological organization of the 4. Discussion The anatomical structure of the intestine, its relative length in particular, depends on the nature of fo remarkably similar desp ussion on the histology of the ‘stomach’ of A.dispar has been provided elsew F intestine of the Garra barriemiae fish; mucosa (M) and muscularis (small arrows). Bar = 25 µm. od eaten by fishes (Kapoor et al. 1975; Anderson, 1986; Kuperman and Kuz'mina 1994). The length of the disgestive tracts in general not only increases from carnivorous to herbivorous diet, but their looping is more complex in herbivores than in carnivores and omnivores (Al- Hussainy 1949; Lagler et al. 1977). The gross anatomy of alimentary canals in Aphanius dispar and Garra barreimiae further confirms these findings. A. dispar, with a relatively short alimentary canal and a simpler loop is an omnivore which includes live animal food, while G. barreimiae with its extremely long alimentary canal and a complex loop is a herbivorous benthophage feeding on epilithic and epipsammic algae. The ratio of the total length of the fish to the total length of the alimentary canal in adult fish seems to be a good indicator of the feeding habits. The omnivorous A. dispar had a significantly higher ratio than the herbivorous G. barreimiae. The histologies of the ‘stomach’ and ‘intestine’ of these two species are ite morphometric differences. It has been reported earlier that the height of microvilli decreased from the anterior to the posterior part of the fish intestine (Yamamoto 1966; Kayanja et al. 1975; Stroband 1977; Noaillac-Depeyre and Gas 1979; Anderson 1986). The number of rugae and the height of rugae significantly decreased from the anterior 'stomach' to the posterior 'intestine' in both species (Table 1). It appears that the columnar epithelial cells forming the brush- border along the margins of rugae are larger in the anterior 'stomach' region than in the posterior 'intestine' region. Adequate disc here (Ba-Omar et al. 1998; Ba-Omar and Victor, 2000). The histology of the alimentary canal of G. barreimiae has been provided for the first time in this study. Comparisons of the number and the height of rugae in both species are significantly different both in the 'stomach' and in the 'intestine' (Table 1). The total length (TL) ranges of A. dispar and G. barreimiae studied 104 ANATOMY AND HISTOLOGY OF DIGESTIVE TRACTS overlapped (Table 1). Therefore, the differences in histological measurements can not be explained by the differences in size range alone. The internal epithelia of the 'stomach' and the 'intestine' in both species have goblet cells and columnar cells with microvilli that appear as a brush border. These characters are similar to those reported for other cyprinids, but special cellular nests reported in the intestinal epithelia of some cyprinids were absent in these species (Al-Hussainy 1949). Whether the columnar cells with microvilli are equally absorptive in both 'stomach' and 'intestine' regions of both species requires histochemical verification. The histological organization of the ‘stomachs’ described for both species here raises the ques light and electron microscopy did not show the pres References AL-HUSSAINI, A.H. 1949. On the functional morphology of the alimentary tract of some fish in ANDERSON, T.A. 1986. Histological and cytological structure of the gastrointestinal tract of the BA-OMAR, T.A., VICTOR, R. and TOBIAS, D.B. 1998. Histology of the stomach of Aphanius BA- 00. Ultrastructural changes in the epithelium of The stomach GARGIULO, A.M., CECCARELLI, P., DALL’ AGELIO, C. and PEDINI, V. 1997. GARGIULO, A.M., CECCARELLI, P., DALL’ AGELIO, C. and PEDINI, V. 1998. Histology and GRAU, A., CRESPO, S., SARASQUETE, M.C., GONZALEZ, D.E. and CANALES, M.L. 1992. tion whether these are true ‘stomachs’. Several cyprinids have earlier been described as stomachless (Al-Hussainy 1949; Lagler et al. 1997). The 'stomach' in both species studied here is not as distinct as those described for freshwater fishes like pike, burbot and sunfish (Williams and Nickol 1989; Kuperman and Kuz'mina 1994), but nevertheless it is a morphological entity separated from the 'intestine' by a constriction. Histological studies in A. dispar using ence of gastric glands ((Ba-Omar et al. 1998; Ba-Omar and Victor, 2000). Also gastric glands were not seen in the ‘stomach’ of G. barreimiae. It is often argued that the presence of gastric glands and their function are essential for defining a ‘true’ stomach. Stomachs store ingested food and by contraction facilitate the movement of food down the alimentary canal. Therefore, the absence of gastric glands alone need not qualify the absence of a ‘stomach’. Both A. dispar and G. barreimiae have ‘stomachs’ in the morphological sense and terms like ‘stomach-like pouch’ and ‘intestinal bulb’ are not necessary for their description. The histological organization of ‘stomach’ in both A. dispar and G. barreimiae indicates a greater surface area than that of ‘intestine’. It is quite likely that the ‘stomachs’ of these species play an important role in the absorption of food. Again the conventional thinking that the‘intestine’ is the only place where absorption of digested food takes place has to be readdressed. Based on the available evidence, this paper prefers to maintain that the cyprinodont A. dispar and the cyprinid G. barreimiae have demarcated ‘stomach’ and ‘intestine’. relation to differences in their feeding habits: cytology and physiology. Quart. J. Micros. Sci. 90: 323-354. luderick, Gerilla tricuspidata (Pisces, Kuphosidae), in relation to diet. J. Morph. 190: 109- 119. dispar (Ruppell 1828), a cyprinodont fish, with emphasis on changes caused by stress from starvation. Trop. Zool. 11:11-17. OMAR, T.A. and VICTOR, R. 20 of Aphanius dispar (Cyprinodontidae), due to stress from starvation. SQU J. Scientific. Res. - Science and Tech., 5:1-9. Ultrastructural study on the stomach of Tilapia spp. (Teleostei). Anat. Histol. and Embryol. 26: 331-336. ultrastructure of the gut of the tilapia (Tilapia spp), hybrid teloest. Anat. Histol. And Embryol. 27: 89-94. The tract of the amberjack Seriola dumerili, Risso: a light and scanning electron microscope study. J. Fish Biol. 41: 287-303. 105 TAHER BA-OMAR, REGINALD VICTOR and DANIEL TOBIAS KAPOOR, B.G., SMITH, H. and VERIGHINA, I.A. 1975. The alimentary canal and digestion in teleosts, pp109-239. In: Russell F.S & Young M., edits. Advances in Marine Biology. Vol III, London: Academic Press. KAYANJA, F.J.B., MALOIY, G.M.O. and REITE, O.B. 1975. The fine structure of the intestinal epithelium of the Tilapia grahami. Anat. Anz. 138: 451-462. KUPERMAN, B.I. and KUZ’MINA, V.V. 1994. The ultrastructure of the intestinal epithelium in fishes with different types of feeding. J. Fish Biol. 44: 181-193. LAGLER, K.F., BARDACH, J.E., MILLER, R.R., and PASSINO, D.R.M. 1977. Icthyology (2nd Edition). New York: John Wiley. NOAILLAC-DEPEYRE, J. and GAS, N. 1979. Structure and function of the intestinal epithelial cells in the Perch (Perca fluviatilis L.). Anat. Rec. 195: 621-640. OSMAN, A.H.K. and CACECI, T. 1991. Histology of the stomach of Tilapia nilotica (Linnaeus, 1758) from the River Nile. J. Fish Biol. 38: 211-223. STROBAND, H.W.J. 1977. Growth and diet dependent structural adaptations of the digestive tract in juvenile grass carp (Ctenopharingodon idelle Val.). J. Fish. Biol. 11: 167-174. WILLIAMS, J.A. and NICKOL, B.B. 1989. Histological structure of the intestine and pyloric caeca of the green sunfish, Lepomis cyanellus Rafinesque. J. Fish Biol. 35: 359-372. YAMAMOTO, T. 1966. An electron microscope study of the columnar epithelial cell in the intestine of fresh water teleosts: gold fish (Carassius auratus) and rainbow trout (Salmo irideus). Zeit. fur Zellf. 72: 66-87. Received 11 February 2003 Accepted 4 September 2003 106 Some Aspects of the Anatomy and Histology of Digestive Tracts in Two Sympatric Species of Freshwater Fishes Taher Ba-Omar, Reginald Victor and Daniel Tobias Department of Biology, College of Science, Sultan Qaboos University, P.O.Box 36, Al Khod 123, Muscat, Sultanate of Oman, Email: Taher@squ.edu.om. ØÇåÑ Èä ÚÈÏÇáÑÍãä ÈÇÚãÑ¡ ÑíÌäÇáÏ� KEYWORDS: Aphanius; Garra; Fish; Anatomy; Histology; Stomach; Intestine S everal studies have been carried out on the diges In this study, we also compare the anatomy and histology of the alimentary canal of another cyprinid, Garra barreimiae that is sympatric with A. dispar in the freshwaters of Oman. These two species occupy different feeding niches. The cyprinid, is a be Materials and methods 3. Results 3.1 Aphanius dispar Character A. dispar G. barriemiae 3.2 Garra barreimiae 4. Discussion The anatomical structure of the intestine, its relative length in particular, depends on the nature of food eaten by fishes (Kapoor et al. 1975; Anderson, 1986; Kuperman and Kuz'mina 1994). The length of the disgestive tracts in general not only incre References KAPOOR, B.G., SMITH, H. and VERIGHINA, I.A. 1975. The alimentary canal and digestion in teleosts, pp109-239. In: Russell F.S & Young M., edits. Advances in Marine Biology. Vol III, London: Academic Press. KAYANJA, F.J.B., MALOIY, G.M.O. and REITE, O.B. 1975. The fine structure of the intestinal epithelium of the Tilapia grahami. Anat. Anz. 138: 451-462. NOAILLAC-DEPEYRE, J. and GAS, N. 1979. Structure and function of the intestinal epithelial cells in the Perch (Perca fluviatilis L.). Anat. Rec. 195: 621-640. OSMAN, A.H.K. and CACECI, T. 1991. Histology of the stomach of Tilapia nilotica (Linnaeus, 1758) from the River Nile. J. Fish Biol. 38: 211-223. STROBAND, H.W.J. 1977. Growth and diet dependent structural adaptations of the digestive tract in juvenile grass carp (Ctenopharingodon idelle Val.). J. Fish. Biol. 11: 167-174.