The reproductive seasonality is a phenomenon influenced mainly by annual variations in the photoperiod, which increase the proportionally to latitude such that reproductive and non-reproductive seasons are well defined among seasonal species (Abecia et al., 2012). However, in tropical regions, other ambient factors such as ambient temperature, relative air humidity, rain distribution, and nutrition also seem to have effects on reproductive physiology in seasonal animals (Rosa and Bryant, 2003).

The seasonal characteristics of reproduction are expressed with high intensity in females that have a period during which they are apt for reproduction (reproductive season) or are not apt for reproduction (non-reproductive season) (Goodman and Inskeep, 2006), while spermatogenesis and sexual activity are constant in males (Pelletier and Almeida, 1987). Among the main characteristics with seasonal changes that can be observed in males are the changes in sexual behavior (libido), testicular size, spermatogenesis, and hormonal secretion (Kafi et al., 2004; Zamiri and Khodaei, 2005).

Exploring the influence of variations in the ambience on dairy goat breeds, such as Alpine, Saanen, Toggenburg, and Anglo-Nubiana, is necessary, because they are the main breeds from temperate regions that are utilized in tropical regions (Gonçalves et al., 2001). In relation to male goats, greater knowledge of their reproductive variations during the year can help with breeding and husbandry decisions. Thus, it can define the period of the year during which the semen has the best parameters for cryopreservation (Zamiri et al., 2010), which can consequently increase reproductive indexes while maintaining an adequate male:female proportion and also allow for a decrease in the maintenance costs associated with a reduction in the number of breeding (Roca et al., 1992; Barkawi et al., 2006). Moreover, males with better sexual behaviors in high temperature conditions can be selected for the development of breeds that are adapted to tropical climates (Pacheco and Quirino, 2010).

The objective of this study was to analyze the seasonal variation in testicular biometry, semen parameters, concentration of testosterone, follicle-stimulating (FSH) and luteinizing (LH) hormones, as well as the sexual behavior of male Alpine goats in tropical climate conditions and possible interference with fertility.

All procedures of animal handling were approved by the local Ethics Committee for Animal Use (case no. 32/2013) and were performed according to the Ethics principles of animal experimentation as established by the Brazilian Animal Experimentation College and the current law.

The animals were housed in Viçosa, Minas Gerais, Brazil (649 m of altitude, under the latitude of 20°45'20"S and longitude 42°52'40"W). The average annual temperature is 20.9 °C, with an average annual precipitation index of 1,221 mm³ and a highland tropical climate, Cwa type (dry winter and wet summer), based on the weather classification of Köeppen-Geiger. The experimental period was 12 months (from March 2012 to March 2013) and was comprised of the four seasons of the year - autumn (from 20th March to 20th June), winter (from 21th June to 21th September), spring (22th September to 20th December), and summer (21th December to 19th March).

Four clinically healthy male Alpine goats with an average age of 3.4±1.9 years were selected and maintained under natural lighting conditions. The animals were housed in covered individual pens with an uncovered exercise area (solarium) where they had free access to solar radiation. The animals received corn silage, a protein and energy concentrate, as well as free access to mineral salt and water, thereby meeting the nutritional requirements of goats according to the National Research Council (NRC, 2007).

The values for brightness from the region where the experiment was performed were acquired from the National Observatory (ON 2013) and the maximum and minimum ambient temperatures (°C) were measured every day at 17.00 h using a maximum and minimum digital thermo hygrometer (Incoterm^®), which was installed at half the height of the animals.

Blood samples were collected every fortnight at 7.00 h by jugular venipuncture in 10-mL tubes without anticoagulant, which were then immediately centrifuged at 1500 × g over 10 min, and the blood serum was then stored at –20°C. The assays for dosage of testosterone (ng/mL), FSH (mUI/mL), and LH (mUI/mL) were performed by chemiluminescence through the immune-enzymatic technique while using the commercial kits Beckman Coulter^® (Beckman Coulter, USA) and the Access^® equipment (Beckman Coulter, USA) according to specifications of the manufacturer.

The testicles of the goats were measured every fortnight during the experimental period with animals in breeding period before semen collection. The testicles were gently pulled by the distal portion of the scrotum and, with a flexible tape, the scrotum circumference (cm) was measured at the largest longitudinal region. There was no correction made for the scrotal skin thickness. The width (medium-side; cm) and the length (dorsoventral; cm) of each testicle were measured with a caliper rule while excluding the head, body, and tail of the epididymis. The testicular volumes were obtained using the following formula: TV = 0.5236(TL)(TW)², based on the equation by Bailey et al. (1998), in which TV = testicular volume, TL = testicular length, and TW = testicular width.

Sexual behavior during semen collection was observed while considering the following variables: reaction time (period between the introduction of the goat in the collection room with its observation of the female in estrus and ejaculation in the artificial vagina); act of smelling and licking the non-genital region of the female; Flehmen reflex; act of knocking and scraping the hull on the floor; kicking and knocking of the female; emission of characteristic sounds; externalization and retraction of the tongue; penis erection and exhibition; breeding reflex (followed by contraction of the posterior region of the male with or without penis exposure); number of false breeding; and sexual interest after breeding (service). Service was defined as a breeding followed by introduction of the penis in the artificial vagina and ejaculation characterized by a pelvic impulse with head thrown back, followed or not by a short period during which time the goat did not show an interest in the female (refractory period).

Semen collection of the animals was performed every fortnight, always in the morning, during all experimental periods using an artificial vagina with water at 40-42 °C. In a squeeze chute for goats, females in natural or induced estrus during the non-reproductive season were used as dummies. The collection tube (15 mL) was plastic, transparent, conic, graduated, and protected from the light with aluminum foil.

Two collections from each animal were performed in an interval of ten minutes and after the formation of a pool, the semen was taken immediately to the laboratory for analysis. In all ejaculates, the volume (mL), appearance (1 = creamy, 2 = milky, and 3 = aqueous), coloration (1 = white, 2 = white-yellowish, and 3 = yellowish), turbulence or mass movement (0 to 5), progressive spermatic motility (0 to 100%), spermatic force (0 to 5), concentration (spermatozoids/mL), and spermatic pathologies were evaluated. In the collection tubes, volume, aspect, and coloration were verified macroscopically immediately after the collection according to Ax et al. (2004). The evaluation of turbulence was performed by depositing a drop of semen (10 µL) in a pre-warmed blade (37 °C), with subsequent observation achieved by using a phase contrast optical microscope at 100X to classify the sample on a scale from 0 to 5, in which 0 was the absence of wave movements and 5 was the maximum value of this parameter. To perform the evaluation of spermatic motility and force, 10 µL of semen were homogenized with 100 µL of Botubov^® diluent (Botupharma) and a 10-µL aliquot was removed. The observation was made by using a phase contrast optical microscope at 200X, while also using pre-warmed blades and coverslips (37 °C). For motility, subjective percentage grades from 0 to 100% were attributed to the samples in relation to the amount of total mobile spermatozoids. While for force, values from 0 to 5 were attributed to the samples according to the intensity and speed of movement. The concentration of spermatozoids in the collected semen was determined by using the Neubauer chamber after dilution (1:200) of the sample, while the spermatic morphology was determined by evaluating 100 spermatozoids while using a phase contrast optical microscope (1000X) according to criteria adopted by Blom (1973) for total abnormalities.

Semen samples were diluted in a commercial kit TRIS-egg yolk containing glycerol (Botubov^®, Botupharma), which was pre-warmed (37 °C) and had a final concentration of 2.00×10⁶ spermatozoids/mL. Afterwards, the diluted semen was packed in 0.25-mL plastic straws (IMV^®), which were maintained in a freezer at 5°C for 3 h.

After the cooling period, the straws were placed over the liquid nitrogen vapor in a horizontal position in a stainless steel support grid (Botupharma^®). The straws remained at 5 cm from liquid nitrogen for 20 min and then they were immersed in liquid nitrogen and packed in identified racks to be stored in cryogenic containers until further evaluation.

The straws were thawed in a water bath at 37 °C for 30 min and the content was transferred to a 1.5- mL plastic tube (Eppendorf^®), from which a 10-µL aliquot was removed for analysis of spermatic motility and spermatic force parameters according to the methods described for fresh semen. For the performance of the hypoosmotic test, which evaluates the functionality of the plasmatic membrane, a 50-µL aliquot of thawed semen was removed and transferred to a 1.5-mL plastic tube (Eppendorf^®) containing 1 mL of hypoosmotic solution (fructose solution at 100 mOsm/L), and was then incubated in a water bath at 37 °C for 30 min. After the end of the incubation, 500 µL of saline formaldehyde was added for subsequent counting of 100 cells by using an optical microscope with a magnification of 1000X. Spermatozoids with functional membranes were considered those that suffered tail folding during incubation (Bittencourt et al., 2005).

Data were analyzed by the SAS software (Statistical Analysis System, version 9.0). The quantitative variables were evaluated by variance analysis while considering the effect of animal and while using the PROC GLM; the averages were compared by the Ryan-Einot-Gabriel-Welsh test. The qualitative variables were analyzed by the Kruskal-Wallis test and the PROC NPAR1WAY. Data of sexual behavior were compared between the reproductive (March to August) and the non-reproductive seasons (September to February) by the exact Fisher test (PROC FREQ). The correlations among quantitative variables were evaluated by simple Pearson correlation and the Spearman correlation (PROC CORR) was utilized among the qualitative variables. Data were presented as mean ± standard error of the mean and the adopted significance was α = 0.05.

The average difference in the incidence of light between months with greater (December) and less (June) amounts of light was 2.48 h (Figure 1). This means that there is an increased luminous period during periods of spring and summer and a decrease in autumn and winter (ON, 2013). Goats and some sheep breeds are considered short-day seasonally polyestrous breeders, because the females start their sexual activity (reproductive season) in response to the decreasing length of day, while an increasing length of day ceases the reproductive period (non-reproductive season) (Abecia et al., 2012). The average difference in the incidence of light of 2.48 h was enough to allow for seasonality in goats in the region studied. In the region, we verified that the reproductive season of females occurs from March to August, which is comprised of the end of summer, autumn, and the beginning of winter.

Figure 1

The scrotal circumference (cm) presented a positive correlation with the maximum temperature (r = 0.48) and thus, there were greater values from September to February (P<0.05), which comprise spring and summer (non-reproductive season) (Table 1 and Figure 2). Barkawi et al. (2006), when working in Egypt (30° 1' N), also found greater values for scrotal circumference during spring and summer, while Coloma et al. (2011) and Santiago-Moreno et al. (2013), when working in higher latitudes (40° 25' N - Spain), found greater values during summer and autumn, which overlap the reproductive season of females. Also, a gradual increase in the measurements of the left and right testicular volumes were observed in this study in September (P<0.05), during which we observed the absence of females in estrus.

Table 1

Period	Fresh semen								Thawed semen
	Volume (mL)	Coloration (1-3)1	Appearance (1-3)2	Turbulence (0-5)	Spermatic motility (0-100%)	Spermatic force (0-5)	Concentration (×109 SPTZ/mL)	Total abnormalities	Spermatic motility (0-100%)	Spermatic force (0-5)	Hypoosmotic test (%)
March/12	1.6±0.3cd	1.9±0.2	2.2±0.2	2.7±0.3	85.8±1.5	3.4±0.2	3.2±0.4ab	38.3±4.6	45.4±2.4	3.4±0.1ab	42.9±4.6
April/12	1.2±0.2d	2.0±0.2	2.3±0.2	2.7±0.3	84.4±1.8	3.3±0.1	2.7±0.5ab	31.3±5.8	45.0±4.1	3.7±0.2ab	44.4±5.8
May/12	1.9±0.3bcd	2.0±0.2	2.1±0.1	3.4±0.3	85.0±1.9	3.8±0.1	2.3±0.2b	43.6±4.8	46.3±3.9	3.8±0.1a	33.9±2.8
June/12	2.7±0.5abc	1.6±0.2	1.6±0.2	3.4±0.3	83.8±1.6	3.8±0.1	2.5±0.4b	30.1±6.5	40.6±4.0	3.4±0.2ab	42.6±5.2
July/12	2.8±0.5abc	1.6±0.2	2.0±0.0	2.9±0.3	80.7±2.0	3.4±0.2	2.7±0.6ab	40.6±5.9	41.4±6.0	3.2±0.2bc	42.5±4.4
August/12	1.8±0.2bcd	1.5±0.2	1.9±0.2	3.1±0.3	84.6±1.8	3.6±0.1	3.5±0.4ab	27.7±4.6	43.2±4.9	3.3±0.2b	41.2±6.0
September/12	2.4±0.3abcd	1.4±0.2	2.3±0.2	3.0±0.5	84.4±2.7	3.6±0.2	4.2±0.8ab	33.4±4.0	41.9±2.7	3.3±0.1b	38.9±5.9
October/12	2.9±0.3abc	1.6±0.2	2.1±0.1	3.3±0.3	82.5±2.8	3.5±0.2	4.5±0.7a	22.4±4.1	43.8±3.8	3.2±0.2bc	43.4±4.0
November/12	3.2±0.3a	1.6±0.3	2.1±0.1	2.6±0.3	80.0±2.1	3.6±0.1	4.1±0.5ab	32.3±4.4	35.6±3.7	2.8±0.1c	37.3±5.1
December/12	3.1±0.3ab	2.0±0.3	2.4±0.2	2.1±0.4	80.0±2.5	3.3±0.2	3.7±0.7ab	36.1±6.3	36.3±4.2	3.1±0.1bc	41.1±6.6
January/13	3.0±0.3ab	2.0±0.2	2.1±0.1	2.5±0.3	79.6±2.1	3.5±0.1	3.8±0.5ab	39.3±4.6	41.7±3.0	3.3±0.1b	42.4±5.3
February/13	2.4±0.2abcd	2.4±0.2	2.4±0.2	2.8±0.4	85.0±2.5	3.7±0.2	3.1±0.5ab	28.6±6.3	48.1±3.8	3.4±0.2ab	47.8±5.5

SE - standard error.

Table 2

Period	FSH (mUI/mL)	LH (mUI/mL)	Testosterone (ng/mL)
March/12	0.45±0.16ab	1.29±0.42ab	14.17±0.88ab
April/12	0.13±0.05b	0.40±0.24bc	16.95±0.65a
May/12	0.10±0.05b	0.37±0.25bc	9.54±1.43bcd
June/12	0.16±0.07b	0.54±0.25bc	5.62±1.01cde
July/12	0.07±0.03b	0.38±0.25bc	3.46±1.25e
August/12	0.14±0.03b	0.23±0.10c	2.03±0.24e
September/12	0.06±0.02b	0.25±0.16bc	3.07±0.58de
October/12	0.10±0.04b	0.36±0.17bc	2.83±0.49e
November/12	0.10±0.04b	0.41±0.20bc	4.75±1.34cde
December/12	0.12±0.07b	0.32±0.20bc	3.89±1.26de
January/13	0.10±0.04b	0.35±0.15bc	10.22±1.83bc
February/13	0.54±0.19a	1.64±0.55a	14.37±1.81ab

FSH - follicle-stimulating hormone; LH - luteinizing hormone; SE - standard error.

Figure 2

The macroscopic (volume, coloration, and appearance) and microscopic parameters (turbulence, spermatic motility, spermatic force, concentration, and total abnormalities) of the semen can help with the analysis of semen parameters for processing and in the decision regarding the use of in vivo or in vitro.

The semen volume of goats is 1.0 mL on average, varying from 0.5 to 1.2 mL (Ax et al., 2004). The average volume that was obtained by Santos et al. (2006) for adult Alpine animals and recommended by the Colégio Brasileiro de Reprodução Animal (CBRA, 2013) is 0.8 mL. Karagiannidis et al. (2000) worked with Alpine goats and verified a difference in the semen volume of 0.33 mL between the reproductive (1.42 mL) and non-reproductive seasons (1.09 mL). In this study, a pool of two successive semen collections with an interval of 10 min was created and the lowest values of semen volume were observed during the reproductive season (Figure 3), with average correlations of r = 0.35 and r = 0.33 for scrotal circumference and testicular volume, respectively (P<0.05).

Figure 3

The semen coloration and appearance did not present differences among the monthly averages (P>0.05) and, according to Mies Filho (1987) and Ax et al. (2004), when analyzed together, these parameters can be indicators of spermatic concentration in ruminants. The greatest semen dilution is due to greater semen plasma production, which for goats naturally has as a yellowish coloration (Ax et al., 2004). In this study, we observed that the more intense the yellowish coloration (more semen plasma), the greater the aqueous aspect (r = 0.40) and the lower the spermatic concentration (r = –0.43) of the collected semen. Moreover, the observation of spermatic coloration can help diagnose pathology in the male reproductive system based on the presence of blood, pus, and urine in the newly collected semen (Ax et al., 2004).

The turbulence, or mass movement (0 to 5), that occurs in fresh semen of ruminants is characterized by movements such as waves; in this study, these movements correlated positively with the motility (r = 0.62), the spermatic force (r = 0.55), and spermatic concentration (r = 0.38). The monthly averages did not present differences during this experiment and were close to the minimum value recommended by the CBRA (2013) and that has been verified by Nunes et al. (1983), which are 3.0 and 3.5 respectively. Yet, it can be highlighted that there were negative correlations obtained between the turbulence and other semen parameters: volume (r = –0.20), appearance (r = –0.33), and coloration (r = –0.41). Thus, with a greater dilution, the aqueous aspect and the yellowish coloration were more intense and there was a greater amount of semen plasma in relation to the amount of spermatozoids, which caused lower turbulence.

The progressive rectilinear spermatic motility is represented by the percentage of total mobile progressive spermatozoids, while the spermatic force is the quality (intensity) of the movement of spermatic cells (Castelo et al., 2008). In this study, the progressive motility (0-100%) and the force (0-5) did not present differences (P>0.05) among the monthly means and were within the minimum values recommended by the CBRA (2013) for fresh semen of goats, which is 80% for motility and 3 for spermatic force. The same finding was verified by Coloma et al. (2011), who did not observe differences among the evaluated months either, although they were greater than the values obtained by Santiago-Moreno et al. (2013). The motility and spermatic force are the main and most common parameters utilized in semen evaluation to predict semen quality because of their positive correlation with semen fertilization (Correa et al., 1997).

The average monthly values verified in this study for the spermatic concentration during the experimental period were similar to those observed by Castelo et al. (2008) and Aller et al. (2012), who described a concentration varying from 2.5 to 5.0 × 10⁹ spermatozoids/mL for goats as standard. These values were also above the minimum recommended by the CBRA (2013) of 2 × 10⁹ spermatozoids/mL.

The progressive rectilinear spermatic motility (0-100%) of thawed semen did not present differences (P<0.05) among the average monthly values, varying from 36.3 to 48.1%. This was different from the spermatic force (0-5), which varied from 2.8 to 3.8 after the thawing process (P>0.05). The values obtained for these parameters were greater than those verified by Coloma et al. (2011) and also above those recommended by the CBRA (2013) with the minimum of 30% for motility and 2 for force; however, the values were lower than those obtained by Bitencourt et al. (2005).

The processes for semen cryopreservation (dilution, freezing, and thawing) are responsible for important lesions in the spermatozoids, mainly in the plasmatic membranes (Holt, 2000). The injuries that occurred in the spermatic cells from effects of temperature and/or osmolarity result in a 50% decrease of motility in fresh semen (Amman and Pickett, 1987; Thomas et al., 1998), which was observed in this study. Moreover, the morphological and biochemical changes in the semen can also alter the metabolism and production of adenosine triphosphate in the mitochondria of the intermediate piece of the spermatozoid, and thus affect the spermatic force.

Of the ambient variables, high ambient temperatures are those that can influence semen quality the most because they alter the epididymal maturation process, thereby compromising the structures of the plasmatic membrane of the spermatozoids (Huang et al., 2000) and thus decreasing the semen quality after thawing. The hypoosmotic test (%) evaluates the functionality of plasmatic membranes of spermatozoids and has a positive correlation with progressive spermatic motility, as observed by Martins et al. (2006) and Lodhi et al. (2008), who found r = 0.28 and r = 0.65, respectively. In this study, the hypoosmotic test results (33.9-47.8%) of thawed semen did not present a difference among the monthly averages and were close to those verified by Santos et al. (2006), but were greater than those obtained by Bittencourt et al. (2005), which were 39 and 17%, respectively. Thus, based on the absence of significant changes in the averages of progressive spermatic motility and the hypoosmotic test during all months of the year, it can be inferred that the ambient did not change the spermatic plasmatic membranes or lead to a decrease in semen quality.

In the analyzes of the sperm morphology of fresh semen (total abnormalities) no difference was found between the months (P>0.05) during the experimental period (Table 1). However, Coloma et al. (2011) and Santiago-Moreno et al. (2013) verified differences along the year, during which autumn and spring had the lowest (30 and 24.1%) and the greatest (80 and 61.5%) spermatic pathology percentages, respectively. According to Sarlós et al. (2013), this difference can occur because there is a negative correlation between seasonality and spermatic abnormalities (r = –0.55). In other words, during the reproductive season, there is a lower occurrence of defective spermatozoid indexes, which can compromise spermatic quality and affect the efficiency of fertilization. However, these studies were conducted in higher latitude regions (>40° N), where the seasonality of the photoperiod has a large influence on reproductive physiology, which is different from the regions where this study was conducted (20° S).

The seasonal reproductive characteristics are expressed more intensely in goats such as Alpines from latitudes higher than 35° N or 35° S (Avdi et al., 2004; Sarlós et al., 2013). These animals from temperate climates have reproductive seasons during lower light intensity periods, i.e., during the end of summer, autumn, and winter (Abecia et al., 2012). In males, these reproductive changes are lower and do not contribute to an interruption in gametogenesis and sexual activity, as is the case in females (Pelletier and Almeida, 1987).

According to Baril et al. (1993), the testicles of a male adult goat are influenced by breed, season, and nutritional status. In this experiment, animals from the same breed were utilized and the feeding did not suffer from changes during the experimental period, with the photoperiod as the unique variable modified along the year (Figure 1). The majority of the testicular and semen parameters did not present differences (P>0.05) among the evaluated months and therefore, in males, the reproductive seasonality influenced by photoperiod was not observed with greater intensity, as was the case for females, which had the expression of estrus only between March and August. Thus, we suppose that the changes observed from March to August (reproductive season) in the form of decreasing scrotal circumference, testicular volume, and spermatic concentration could be due to the increased number of coverage performed by breeding the herd during this period. However, it is possible that the photoperiod has also influenced the accessory glands, which are responsible for seminal plasma production, and could thus have increased the seminal volume during the reproductive season and decreased the spermatic concentration from May to June (Figure 3).

However, high ambient temperatures can influence morphological and seminal changes in the breeding due to the increase in seminiferous tubules and, consequently, also affect the testicular volume and scrotal circumference (Amman, 1962). In this study, the maximum ambient temperatures were higher in the period from September to February, which is the period when an increase in seminal volume and concentration were also observed, as well as scrotal circumference and testicular volume (P<0.05). These animals from temperate climate regions can adapt their reproductive physiology to highland tropical climates and thus, the reference values of some parameters, such as scrotal circumference, should be evaluated differently and according to the ambient where they live.

The greatest plasmatic concentrations (P<0.05) of FSH and LH occurred in February and March and of testosterone, from February to April, or during periods that comprise summer and autumn. The concentrations of these hormones can be influenced mainly by annual photoperiod and proximity of the reproductive season of goats in the regions of the experiment (latitude 20 °S), which occurred from March to August. The LH and testosterone presented a negative correlation with light. In other words, the decreasing photoperiod stimulated LH synthesis and, consequently, stimulated testosterone synthesis. Barkawi et al. (2006), Zarazaga et al. (2009), and Coloma et al. (2011), when working with goats in regions with latitudes of 30° N, 37° N, and 36° N, respectively, also verified greater values of these hormones during the end of the summer and autumn, which are periods with decreasing photoperiods.

With the reduction in the photoperiod from January (P<0.05) (Figure 1), melatonin probably began to be synthesized in greater amounts by the pineal gland (Abecia et al., 2012). In goats, this hormone induces the hypothalamus to release the gonadotropin-releasing hormone via pulsatile secretion, which acts on the anterior pituitary and leads to the release of greater amounts of the gonadotropins FSH and LH (Brackett, 2006). In testicles, the follicle-stimulating hormone is responsible for the functionality of the Sertoli cells, which are located inside of the seminiferous tubules and provide structural, nutritional, and functional support for the differentiation and proliferation of germ cells (Sharpe et al., 2003; Brackett, 2006). The LH acts on Leydig cells, which are located in the intertubular tissue and synthesize androgens as their main function (Gardner and Hafez, 2004; Brackett, 2006). Testosterone is the main male hormone and stimulates the final stages of spermatogenesis, contributes to the extension of the life of spermatozoids in the epididymis, and stimulates the development of reproductive organs, secondary sexual characteristics, and libido (Gardner and Hafez, 2004; Brackett, 2006).

The increase in the synthesis of the pituitary hormone and testosterone occurred in advance of the reproductive period of females (Thiéry et al., 2002), which happens at the end of summer, autumn, and at the beginning of winter (from March to August). This early stimulation begins 1 to 1.5 months before females are due to begin their cyclic period, at which time the males have already reached sexual activity and spermatic production. This differential sensitivity to photoperiod is important because, while females in anestrus ovulate a few days after the beginning of hormonal stimulation, males need around 54 days to complete spermatogenesis (Rosa and Bryant, 2003).

According to Sharpe et al. (2003) and Barkawi et al. (2006), the increased testicular volume in the period prior to and during the reproductive season is due to the increase in the area occupied by seminiferous tubules, which is influenced by the hormones FSH and LH and that are secreted in association with the reduction in the photoperiod, as observed by Coloma et al. (2011) and Santiago-Moreno et al. (2013). In this study, despite the annual variation in the concentrations of FSH, LH, and testosterone (P<0.05) (Figure 4), changes were not observed in seminal quality (Table 1; Figure 3) and testicular volume (Figure 2), which are related to these hormones but are also related to greater or lower use of the animals for breeding in coverage.

Figure 4

Salles (2010) reported an increase in the testosterone concentrations during the period of the year with higher ambient temperatures, although Coelho et al. (2008) showed that male goats in heat stress do not present variations in testosterone plasmatic concentrations. According to Barbosa et al. (1999), it is not yet known whether the changes in hormonal synthesis are only influenced by photoperiod or by a combination of other ambient factors (temperature, humidity, etc.).

According to Chemineau et al. (1991), the sexual behaviors of adult males depend mainly on hormonal secretions based on social interactions. Nevertheless, Azevêdo et al. (2008) stated that the intensity and frequency of male sexual behavior can also be influenced by ambient factors and not exclusively by sexual hormones.

The real reproductive ability of males can be indirectly determined by libido, which is the degree of interest of the male to copulate (Chenoweth, 1981). According to the classification of Chemineau et al. (1991), for small ruminants, libido can be evaluated by reaction time (seconds). In other words, libido can be evaluated based on the elapsed time between presentation of females to the male and the subsequent ejaculation on a female in estrus; it can be classified as excellent (30 s), good (31 to 60 s), average (61 to 120 s), or tolerable (longer than 120 s). Thus, as verified by Souza et al. (2007), the libido of the animals in this experiment can be considered good for the reproductive and non-reproductive seasons.

According to Azevêdo et al. (2008), in tropical climate countries, the libido of small ruminants generally reveals little variation, although it can be influenced by ambient variables such as temperature, rainfall, relative air humidity, insulation, or by a change in the feed offered. Godfrey et al. (1998), when working with sheep from temperate climates in heat stress conditions, observed that there were no changes in behavioral parameters, which reveals the adaptability of breeds to tropical climates. However, in temperate latitude regions, the sexual activity is greater from October (autumn), when there is a decrease in the amount of light, as it stimulates males to synthesize androgens and females to reset their estrous cycle and produce pheromones (Barkawi et al., 2006; Zarazaga et al., 2009).

According to Chemineau et al. (1991), after the male identifies and approaches a female, it evaluates the female receptivity. If the female is in estrus (immobility), the male continues its sequence of pre-coital behavior (courtship) that culminates in copulation. In this study, the sexual behavior showed a seasonal variation only in the act of beating and scraping of the hull on the floor, in externalizing and retracting the tongue, and in the breeding reflex (Table 3). These behaviors in males can be caused by the pheromones of goats in natural estrus, therefore allowing for greater excitations and the act of pre-copulatory courtship. The presence of the majority of the sexual behaviors during the non-reproductive season can be also due to the fact that the animals were already conditioned to people, the locale, and handling for collection using an artificial vagina, or were adapted to the tropical climate.

Table 3

Behavior	Period
	Reproductive season (%)	Non-reproductive season (%)
Act of smelling and licking the non-genital region of females	96.4 (53/55)a	98.1 (51/52)a
Flehmen reflex	18.2 (10/55)a	7.7 (4/52)a
Act of beating and scraping the hull floor	32.7 (18/55)a	15.4 (8/52)b
Kicking and knocking of female	12.7 (7/55)a	9.6 (5/52)a
Emission of characteristic sounds	20.0 (11/55)a	17.3 (9/52)a
Externalization and retraction of the tongue	52.7 (29/55)a	26.9 (14/52)b
Penis erection and exposure	54.6 (30/55)a	59.6 (31/52)a
Breeding reflex	76.4 (42/55)a	40.4 (21/52)b
Breeding without service (or false breeding)	14.6 (8/55)a	5.8 (3/52)a
Sexual interest after breeding (service)	47.3 (26/55)a	42.3 (22/52)a

SE - standard error.

Therefore, the greater the latitude of the region, the greater the variation in reproductive parameters of seasonal species will be between reproductive and non-reproductive seasons (Aguirre et al., 2007) (Figure 5) due to the influence of annual photoperiods. When these animals are raised in tropical regions, some physiological characteristics sensitive to decreasing photoperiods, such as the synthesis of gonadotropin hormones, can remain. However, as observed in this study, the proximity to the Ecuador line and consequently, the occurrence of shorter photoperiod variations during the year did not significantly change the seminal quality. Thus, we can consider that the reproductive physiology of animals from temperate regions is adapted to the tropical climate. The occurrence of some variations in seminal quantity and quality, hormone profile, and some sexual behaviors during courtship and copulation should not be considered as an obstacle in the decision on whether to use male Alpine goats in reproductive handling along the year. As verified in other studies (Roca et al., 1992; Karagiannidis et al., 2000; Kafi et al., 2004; Aguirre et al., 2007; Sarlós et al., 2013), the variation in some physiological parameters of male Alpine goats in highland tropical climates (Viçosa, MG - Brazil) throughout the year did not compromise their capacity for fertilization.

Figure 5

The existence of variations during the breeding seasons in testicular biometry, some seminal parameters (volume and concentration), sexual hormone synthesis, and sexual behavior of male Alpine goats raised in tropical climate conditions should not be considered as an obstacle in the decision to use these animals for breeding throughout the year. These variations may be correlated with the coverage frequency of females and/or the influence of photoperiod, and do not change the semen in a way that could compromise the capacity of fertilization of these animals.