Next Article in Journal
Estimates of Direct and Maternal Genetic Effects on Birth and Weaning Weights in Salem Black Goats from India
Previous Article in Journal
Impact of Algae Species from the Baltic Sea Region on Ruminal Fermentation Parameters and Methane Mitigation Using an In Vitro Gas Production System
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Effect of Calving Season and Timing Within Season on Performance and Economics of Cow-Calf Production in Southwest Missouri

by
Briana VerPloeg
,
Phillip A. Lancaster
and
Elizabeth Walker
*
William H. Darr College of Agriculture, Missouri State University, 901 S. National Ave, Springfield, MO 66897, USA
*
Author to whom correspondence should be addressed.
Ruminants 2026, 6(1), 19; https://doi.org/10.3390/ruminants6010019
Submission received: 12 January 2026 / Revised: 2 March 2026 / Accepted: 13 March 2026 / Published: 18 March 2026

Simple Summary

Cow-calf operations are the first step in beef production. The sustainability of cow-calf operations is greatly influenced by producers’ ability to plan management strategies that function most efficiently around variables such as weather, forage quality, and market conditions. These factors fluctuate semi-consistently throughout the year and can affect the performance of a cow and her calf, determining operational profitability. The purpose of this study was to evaluate the effect of the time of calving on cow and calf performance and, ultimately, net monetary returns. Cow and calf records were analyzed in conjunction with feed and forage data and market records to determine not only calf marketability but also cow efficiency and performance as affected by the timing of calving. Results indicated that later calving periods in spring negatively affected cow reproductive performance, calf weaning weight, total costs, and net returns compared with fall calving.

Abstract

A multitude of factors affect the optimum calving season, requiring site-specific systems analysis. The objective of this study was to determine the effects of the calving season (S1 and S2) and the timing of calving within the season on production parameters and economics in southwest Missouri. A five-year study was conducted from 2014 to 2018 using field data recorded for 1979 Hereford cow–calf pairs. Cows were categorized by calving season and 21 d calving periods within season (Periods 1–5) in which they calved. Data were analyzed under a completely randomized design with effects of season, period, calf sex, and two and three-way interactions with the calving year as a random effect. The Cattle Value Discovery System (CVDS) beef cow model was used to estimate required cow feed and feed intake. Historical cattle market prices were used, along with total feed costs, to calculate net returns. Calving in later periods reduced the pregnancy percentage in S1 but not S2. Cows calving earlier in both seasons weaned heavier calves. Feed costs were greater in S2, but replacement heifer costs were greater in S1, especially in later calving periods. Overall, net returns were not different between S1 and S2 cows, but net returns declined in later calving periods in S1, whereas there was no difference in S2. In conclusion, at the latitude of southwest Missouri for a forage species with a bimodal growth curve, the calving period affected cow productivity and profitability in Season 1 but less so in Season 2 cows, with no difference in profitability between calving seasons.

1. Introduction

The choice of calving season is based on many factors, such as the environment, availability of feed resources, availability of labor, market timing, and tradition [1]. The environment is most likely the single largest factor to consider and varies by latitude and longitude across the U.S. such that optimal calving season is not the same throughout the nation. For example, extreme cold affects neonatal calf survival [2]. At northern latitudes, late-spring calving is more advantageous than early-spring or fall calving [3,4], but fall calving is more advantageous in southern latitudes [5,6].
The chosen calving season dictates the timing of other aspects of the production cycle—specifically, the breeding season, which must be taken into consideration. Environmental conditions such as temperature and humidity influence heat and cold stress experienced by cattle during the breeding season and can have negative effects on male [6,7] and female [8,9] fertility. The breed affects the reproductive response to environmental stress and the photoperiod length [10], and the photoperiod affects puberty in heifers and postpartum anestrus in cows [11,12], which are critical to maintaining a 365-day calving interval. Additionally, beef heifers that calve early in their first calving season remain in the herd longer and have greater lifetime productivity [13,14,15] than those calving later in the season. Cows that calve early in the calving season generally wean heavier calves and have a greater pregnancy percentage than cows calving later in the calving season [16,17].
Calf prices fluctuate throughout the year with changes in supply and demand [18], impacting prices received when marketing calves born in different seasons and born at different times within a calving season. Labor supply affects the ability to monitor cows during calving and utilize advanced reproductive technologies in integrated crop and livestock operations during the growing season [19].
Nutrient requirements of beef cows are greatest during early lactation, leading up to the breeding season [20], and maintaining cows in adequate body condition (BCS ≥ 5; range = 1 to 9) during this time is critical to ensure maximum pregnancy percentages [21]. However, environmental factors including temperature, precipitation, soil type, latitude, and topography can affect forage species suited to the region and the timing of optimally nutritious forage availability [22], and the availability of feed resources interacts with mature size and milk production [23] to affect the optimum time to calve beef cows.
Milk production of beef cows is affected by energy intake such that the cow balances milk production with mobilization of body reserves [23,24]. Additionally, the calf becomes more reliant on nutrients from forage in mid and late lactation as milk production declines. Thus, aligning the calving season to coincide with the availability of grazed forage of greater nutritive value during early lactation and breeding can reduce supplemental feed costs [25]. However, having high-quality forage available in late lactation can increase calf growth [26,27]. All cows do not calve at the same time within the calving season, and alignment of nutrient demands of the cow and calf with the nutritive value of forage varies among cows.
Consequently, determining the optimum calving season is difficult due to the myriad factors involved and the site-specific nature of cow-calf production systems [28]. Additionally, timing of calving within a calving season impacts cow productivity due to the age of the calf and alignment of nutrient requirements with the nutritive value of forage. However, little research has evaluated the optimal calving season and timing within a calving season in central latitudes without extreme winters and summers or bimodal (spring and fall) forage growth curves. Thus, we hypothesized (1) that spring and fall calving seasons would be equally productive but that fall calving cows would be more profitable at the central latitude of southwest Missouri and (2) that cows calving earlier in the calving season would be more productive and profitable. The objective of this study was to determine the effects of the calving season and the timing of calving within the calving season on production parameters and economics of cow-calf systems in southwest Missouri.

2. Materials and Methods

A research protocol was submitted for approval by the Missouri State University Institutional Animal Care and Use Committee (Protocol #16-035.0); however, the committee deemed that a protocol was not necessary, since data collected on cows and calves were generally accepted as production data. The care and use of animals followed the Guide for the Care and Use of Agricultural Animals in Research and Teaching.

2.1. Cow/Calf Performance Traits

2.1.1. General Management

Research was conducted at Missouri State University’s Leo Journagan Ranch, located south of Mountain Grove, MO (36.993897, −92.258733). The five-year study, which was conducted from 2014 to 2018, utilized field data from Hereford cow–calf pairs (2222 calvings). Cows and calves were managed on 16 to 65 ha pastures year-round and divided into approximately 30-cow groups. Some groups continuously grazed a single pasture, and others were minimally rotated to alternate pastures throughout the year as grazing necessitated based on forage availability. The major forage species was Tall Fescue (Festuca arundinacea), along with other cool- and warm-season grasses and legumes. The full list is available in the Supplemental Material. Hay of similar plant species was produced on the ranch and fed during winter months (generally, December–April). Pasture management included fertilization every third year with urea, and hay pastures were fertilized every year.
Cows were managed as either spring or fall calving herds (Season 1 or Season 2, respectively). Season 1 cows gave birth in late January through early July, and Season 2 cows gave birth in late August through early December. The months composing Season 1 and Season 2 were determined based on the calf weaning date, as calves born January through July were usually weaned the following October/November and calves born August through December were usually weaned the following June. Most cows were bred via natural service, but about 100 cows/year (mostly heifers) were bred via artificial insemination. Bulls were released into pastures on April 1 for Season 1 and on November 1 for Season 2, then removed at weaning.
Cows were provided with supplemental feed during the winter and respective breeding seasons. Season 1 cows were supplemented 0.91 kg/hd/day from late January through March and 0.70 kg/week from April through June. Season 2 cows were supplemented with 1.13 kg/hd/d from August through December and 0.91 kg/hd/day from January through April. Season 2 calves were provided with creep feed from March until weaning (usually in May) via a self-feeder. Target creep feed intake at weaning was 2.27–3.63 kg as-fed/calf/day. The same grain mix was used for cow supplement and calf creep feed (Table S1).

2.1.2. Data Collection

Performance data were recorded by ranch employees as a part of normal production practices in a beef cattle seedstock operation. Collected cow data included American Hereford Association (AHA) registration number, dam tag ID, Body Condition Score (BCS) at calving and weaning, mature cow weight, and pregnancy status. Body condition scores were collected from 2016 to 2018 by visual appraisal using methods described in [29]. At weaning, the mature cow weight was recorded, and the pregnancy status was checked via palpation. Calf data collected included calf AHA registration number, date of birth, calf sex, birth weight, weaning weight, and weaning date. The calf birth weight was recorded within 24 h of parturition using a weight tape. Collected records were used to calculate the calving interval, calf weaning age, and 205-day adjusted weaning weight. Due to use of field data, data collection was partially incomplete; in these cases, some data gaps were able to be filled using the AHA online registry records. A total of 1979 complete records were used in data analysis.

2.2. Model Outputs

2.2.1. Forage and Supplement Sampling

Forage samples were collected monthly from all pastures in which study cows were residing from 2016 to 2018. Hay core samples were collected once a year from approximately 10% of total hay inventory in such a manner as to ensure all cuttings and fields were included in the yearly sample. Monthly pasture samples consisted of 4 to 6 combined sub-samples per pasture collected from locations chosen by observing the grazing patterns of cattle. Hay and pasture forage samples were dried in a forced-air oven at 55 °C, ground using a Cyclone Sample Mill (UDY Corporation, Fort Collins, CO, USA), and stored in plastic air-tight bags. Ground samples were analyzed for crude protein (CP), neutral detergent fiber (NDF), and acid detergent fiber (ADF) using near-infrared spectroscopy (NIRS SpectraStar, Unity Scientific, Milford, MA, USA). The total digestible nutrients measure (TDN) was calculated using Equation (S1) [30]. Metabolizable energy (ME) was calculated from TDN using Equation (S2) [20]. Samples of supplemental feed were collected from each load delivered to the ranch from 2016 to 2018. Samples were analyzed by Dairy One Forage Laboratory (Ithaca, NY, USA) for moisture, CP, NDF, ADF, and calculated TDN. The metabolizable energy concentration was computed using Equation (S3) [31]. Forage, hay, and supplement nutrient compositions are reported in Tables S2 and S3.
Forage metabolizable energy concentration (MEC) values were averaged for all pastures for each month of collection during the study for input into the model. The years of the study that preceded the forage collection period used a monthly average across all years of the forage collection period as the input forage ME values. Hay vs. pasture forage consumption was estimated based on ranch management practices. Consumption estimates were as follows: December to March = 100% hay, April = 75% pasture and 25% hay, and May to November = 100% pasture. A modification to the model was made to account for creep feed consumption by Season 2 calves. The model was modified to substitute 45% of non-milk intake with creep feed while assuming the other 55% of non-milk intake consisted of forage and that the calf would consume the entire daily milk yield of the cow. A rate of 45% was chosen because it gave an average creep intake for the group that matched the estimated intake of 1.81 kg/(calf/day) set by the ranch manager and accounted for variance in intake amount based on varying calf body weight.

2.2.2. Model Calculations

The Cattle Value Discovery System (CVDS) beef cow model was used to estimate nutrient requirements of cow–calf pairs, hay and supplemental feed consumption, and cow efficiency [32]. Performance inputs required for this model were cow weight at weaning, calf date of birth, birth weight, weaning weight, sex, weaning date, and date of cow weight. Values were obtained from performance data collected for the calf crops of 2014–2018. Other inputs included the estimated calf-equivalent shrunk body weight at harvest (ESBW), and relative milk production (RMP); these were applied to all cows as follows: ESBW = 550 kg and RMP = 5 (on a 1–9 scale). These values were chosen because they are average values for beef cattle in the USA, as actual values were unknown.
From performance and forage/feed inputs, the model calculated values for ME required for maintenance, gestation, and lactation throughout the production cycle. The net energy requirement for maintenance was based on cow weight at weaning using a net energy for maintenance (NEm) requirement of 77 kcal/kg shrunk body weight.75 [20]. The net energy requirement was converted to the metabolizable energy requirement by calculating the efficiency of ME use for maintenance of the diet as diet NEm concentration divided by the diet ME concentration. The net energy requirement for gestation was computed from calf birth weight and day of conception, assuming 283 d gestation [20]. The net energy required for gestation was converted to ME required for gestation using an efficiency of ME use for conceptus of 0.13 [20]. The net energy requirement for lactation was computed from milk yield, which was calculated using the equation of Tedeschi et al. [32] and the National Academies of Science, Engineering and Medicine [20] milk yield equation based on the day of lactation by iteratively solving for the peak milk yield (PKM) such that predicted calf weaning weight matched the observed calf weaning weight. The net energy for lactation was converted to ME required for lactation assuming an efficiency of ME use for lactation of 0.64 [33]. The total ME required (MER) was calculated as the sum of ME required for maintenance, gestation, and lactation. The equations to predict milk yield also predict calf non-milk ME required (forage and/or creep feed).
The predicted ME intake was computed using the National Academies of Science, Engineering and Medicine [20] dry-matter intake equations for beef cows multiplied by the MEC of the forage (grazed and/or hay) plus supplemental ME intake. The energy balance was calculated for each day of the production cycle as ME intake minus MER and, as such, represents the deficiency of forage alone to meet energy requirements. The energy-balance nadir (EBN) is the lowest value during the production cycle. The time of EBN during the production cycle was calculated as days since parturition at energy-balance nadir (DSPN) and day of the year at energy-balance nadir (DOYN). Cow efficiency was evaluated using the energy efficiency index (EEI), which is calculated as the ratio of MER to calf weaning weight (Mcal/kg) based on cow MER alone (EEI1) or cow plus calf MER (EEI2).
The CVDS beef cow model uses cow weight, milk energy yield, and calf birth weight to compute the ME required for maintenance, lactation, and gestation, respectively, which are important variables that explain at least 85% of the variation in energy intake of beef cows [34,35]. An evaluation of the CVDS beef cow model using an independent dataset of drylot-fed cows found that MER explained 74% of the variation in observed ME intake, with a mean bias of 1671 Mcal (17% underprediction) over the entire production cycle [36]. Additionally, the predicted milk energy yield explained 25% of the variation in observed milk energy yield, with a mean bias of 105 Mcal (10% underprediction) over 240 d lactation, and EEI1 explained 39% of the variation in observed cow biological efficiency, with a mean bias of 5.35 Mcal MER/kg WW (17% underprediction). Thus, the CVDS beef cow model gives a reasonable estimation of cow energy consumption, milk yield, and biological efficiency.

2.3. Economic Outputs

Historic prices for weaned calves and cull cows were used to determine revenue. Prices for weaned calves and cull cows were obtained from USDA market report archives (https://www.ams.usda.gov/market-news/search-market-news, accessed on 17 September 2019). Weaned calf prices were from the USDA-MO Dept. of Ag Market News Feeder Cattle Reports for Joplin Regional Stockyards (report code jc_ls758), Springfield Livestock Marketing Center (report code jc_ls771), and Ozarks Regional Stockyard (report code jc_ls763), using the Medium and Large 1–2 feeder cattle grades. Calf revenue (CaREV) was calculated as the weaning weight multiplied by the calf price. Cull cow prices were from the USDA-MO Dept. of Ag Market News Slaughter/Replacement Cattle Reports for Joplin Regional Stockyards (report code jc_ls174) and Springfield Livestock Marketing Center (report code jc_ls140). Boner price was used for cows with a weaning BCS 5–7, and lean price was used for cows with a weaning BCS of less than 5. Cull cow revenue (CoREV) was calculated as cow weight at weaning multiplied by cull cow price.
Hay prices were gathered from USDA market report archives of the Missouri Weekly Hay Summary(report code jc_gr310) for June and July when hay was harvested. Cow supplement and creep-feed prices ($/ton) were collected from invoice records from South Central MFA Agri Services (Mountain Grove, MO, USA). Cow feed costs were calculated as predicted hay consumed multiplied by hay price plus supplemental feed fed multiplied by feed price and summed for the entire production cycle. Calf feed costs were computed as predicted calf ME required as hay or creep feed multiplied by the respective price and summed for the entire production cycle. Total feed cost (TFC) was computed as cow feed costs plus calf feed costs. Replacement heifer cost (RHC) data were collected from Show Me Select heifer sales at Joplin Regional Stockyards in the spring and fall of each year. It was assumed that all open cows were sold at weaning for this analysis. Spring replacement heifer prices were used for Season 2 cows, and fall replacement heifer prices were used for Season 1 cows. Revenue from the sale of calves and open cows and costs for feed and replacement heifers were used to compute returns to land, labor, and management (RET).

2.4. Statistical Analysis

For data analysis, cows were categorized as Season 1 or Season 2 and were grouped into calving periods based on 21 d periods to reflect cow estrus cycle length, starting with the date of birth for the first calf in a given calving season and year. Cows were grouped into 5 calving periods; period 5 included all calvings following period 4 due to low numbers in Season 2. Performance, model output, and economic data were analyzed using the mixed-model function (lmer in lmerTest package) in R statistical software (ver. 4.5.1, [37]). The model included the fixed effects of calving season, calving-period category, and calf sex, as well as the random effect of calving year. The Tukey–Kramer method was used to generate probabilities and standard errors for differences of least-square means between levels of each factor using the predictemeans function in R. Pregnancy and calf survival percentage were analyzed using the glmer function with the same fixed and random effects using a binary response distribution for least-square means. Means were considered significant at p ≤ 0.05. Treatment means of all variables are presented for all 2- and 3-way interactions to allow the reader to make inferences of animal biology, even though all variables do not have significant 2- and 3-way interactions and only the significant interactions will be discussed.

3. Results

For Season 1 cows, the average starting date of calving periods 1, 2, 3, 4, and 5 was 15 January, 6 February, 28 February, 22 March, and 13 April, respectively. For Season 2 cows, the average starting date of calving periods 1, 2, 3, 4, and 5 was 18 August, 9 September, 1 October, 23 October, and 14 November, respectively. Due to the nature of an observational study, there was an uneven number of recorded cow–calf pairs between calving seasons (1620 vs. 290 in Season 1 and 2, respectively), calving periods within seasons (308, 679, 556, 264, and 173 in Periods 1, 2, 3, 4, and 5, respectively), and calf sex within calving seasons and periods (1057 vs. 923 male and female calves, respectively).

3.1. Performance Traits

3.1.1. Cow Weight and Condition

The mature cow weight recorded at weaning (MCW) and body condition score at calving (CBCS) were significantly (p ≤ 0.05) affected by the calving season (Table 1). Season 2 cows had greater (p ≤ 0.05) CBCS (6.1 vs. 5.7 ± 0.1) and were lighter (p ≤ 0.05; 570 vs. 549 ± 8 kg) at weaning than Season 1 cows (Table 2). The body condition score at weaning (WBCS) was significantly (p ≤ 0.05) affected by the interaction of calving season with calf sex such that Season 2 cows giving birth to males had lower (p ≤ 0.05) WBCS than those giving birth to females, but for Season 1 cows, WBCS was not different (p > 0.05) between cows giving birth to males and females (Table 2). Season 2 cows had more favorable temperatures (Figure S1) and greater forage nutritive values (Table S2) during late gestation than Season 1 cows. Conversely, Season 2 cows had more extreme temperatures and lower forage nutritive values during mid to late lactation than Season 1 cows.

3.1.2. Cow Reproduction

Cows giving birth to males had greater (p ≤ 0.05) pregnancy percentages than those giving birth to females (87 vs. 83 ± 3%), regardless of calving season or calving period. A calving season × calving period interaction was evident (p ≤ 0.05) for pregnancy percentage, with no difference (p > 0.05) among calving periods in Season 2 cows; but in Season 1, cows calving in period 1 had greater (p ≤ 0.05) pregnancy percentages than those calving in periods 3 and 5, with pregnancy percentages in Season 1, period 5 being lower than in all other periods (p < 0.05; Table 3). There was no effect (p > 0.05) of calving season, calving period, calf sex, or two- and three-way interactions on calf survival from birth to weaning (Table 1).
The calving interval (CAINT) differed (p ≤ 0.05) between calving periods, with cows giving birth in calving periods 1 and 2 having greater (p ≤ 0.05) CAINT values than those giving birth in calving periods 3, 4, and 5 (392, 383, 365, 348, and 348 ± 7 d, respectively). Additionally, the interaction of calving season and calf sex affected (p ≤ 0.05) CAINT; Season 1 cows giving birth to females had greater (p ≤ 0.05) CAINT values than Season 2 cows giving birth to females, but there was no difference (p > 0.05) in cows giving birth to males (Table 2).
In the current study, Season 1 cows giving birth in calving period 5 had lower pregnancy percentages and shorter calving intervals, suggesting that fewer cows became pregnant due to having fewer estrous cycles prior to the end of breeding, but cows that did become pregnant had shorter calving intervals because of a shorter anestrus period after calving. Season 2 cows giving birth in calving period 5 also had shorter calving intervals than those giving birth in earlier calving periods, but pregnancy percentage was not reduced.

3.1.3. Calf Growth

There was a significant (p ≤ 0.05) calving season × calving period × calf sex interaction for birth weight (BW), weaning weight (WW), and weaning age (WAGE) but not (p > 0.05) 205 d adjusted WW (AWW; Table 1). Females born in Season 2 in calving period 1 had lower (p ≤ 0.05) BWs than females born in Season 2 during calving periods 2 and 3; however, calving period did not (p > 0.05) affect the BW of females born in Season 1 or that of males born in Season 1 or Season 2 (Table 4). Heat stress during late gestation, as would have been experienced by Season 2 cows in this study (Figure S1), decreases placental blood flow and reduces birth weight in dairy and beef cattle [38,39,40,41,42].
Females born in Season 2 during calving periods 1 and 2 had greater (p ≤ 0.05) WWs than those born in calving period 5 but not (p > 0.05) calving period 3 or 4, whereas Season 1 females born in calving periods 1 and 2 had greater (p ≤ 0.05) WWs than females born in other Season 1 calving periods. Males born in Season 2 during calving periods 1 and 2 had greater (p ≤ 0.05) WWs than those born in calving periods 3 and 4 but not (p > 0.05) calving period 5, whereas Season 1 males born in calving period 1 had greater (p ≤ 0.05) WWs than those born in calving periods 3, 4 and 5. These trends in WW are likely due to differences in age, as WAGE follows a similar pattern and the three-way interaction for AWW was not significant. Calves born in Season 2 consumed hay with lower CP and TDN than calves born in Season 1 consuming summer pasture (Tables S2 and S3).
In the current study, both calving period and calf sex interacted with calving season to affect (p ≤ 0.05) AWW (Table 1). Although the F-test was significant for the calving season × calving period interaction for AWW, there were no differences (p > 0.05) among treatment means; however, numerically, AWW increased 26 kg from calving period 1 to 5 in Season 2 calves but only 9 kg from calving period 1 to 5 in Season 1 calves, which likely caused the significant interaction (Table 3). Similarly, the AWW of Season 2 females was 25 kg less (p ≤ 0.05) than that of males, whereas the AWW of Season 1 females was only 7 kg less (p ≤ 0.05) than that of males (Table 2).

3.2. Model Outputs

3.2.1. Energy Required

Season 1 cows had greater (p ≤ 0.05) metabolizable energy required (MER) than Season 2 cows (7922 vs. 7626 ± 45 Mcal), and cows giving birth to males had greater (p ≤ 0.05) MER than cows giving birth to females (7877 vs. 7671 ± 96 Mcal), likely due to differences in peak milk yield and metabolizable energy required for lactation (Table 1 and Table 4). There was a calving season × calf sex interaction for peak milk yield (PKM) such that Season 2 cows giving birth to males produced 1.1 kg greater (p ≤ 0.05) PKM than those giving birth to females, whereas Season 1 cows giving birth to males produced 0.4 kg greater (p ≤ 0.05) PKM than those giving birth to females (Table 2). Given that fall forage and hay consumed by Season 2 calves had lower CP and TDN values than spring and summer forage available to Season 1 calves, the CVDS Beef Cow Model estimated greater PKM required for males to gain faster than females, achieving a greater difference in AWW in Season 2 (25 kg) compared with Season 1 (7 kg; Tables S2 and S3).

3.2.2. Energy Balance

For energy-balance nadir (EBN), there was a significant (p ≤ 0.05) calving season × calving period × calf sex interaction (Table 1). Season 1 cows that gave birth to males in calving period 4 had lower (p ≤ 0.05) EBN values than those that gave birth to males in periods 1 and 2, whereas, Season 2 cows giving birth to males in period 5 had lower (p ≤ 0.05) EBN values than in other periods, and those giving birth to males in calving period 3 had greater (p ≤ 0.05) EBN values than in calving periods 1 and 2 (Table 4). For cows giving birth to females, Season 1 cows in period 4 had lower (p ≤ 0.05) EBN values than in periods 1 and 2, with periods 3 and 5 being intermediate, but Season 2 cows in period 3 had greater (p ≤ 0.05) EBN values than in period 1, with other periods being intermediate. The interaction for EBN is likely due to the greater predicted PKM for cows giving birth to males and the timing of calving relative to forage nutritive value. In Season 1, cows giving birth in period 4 had lower forage nutritive values during mid lactation in May and June than cows giving birth in periods 1 and 2, with mid lactation occurring in April and May (Table S2). In contrast, in Season 2, cows giving birth in period 5 had lower forage and hay nutritive values in mid lactation in January than cows giving birth in previous periods, with mid lactation occurring in November and December (Tables S2 and S3).
Days since parturition at energy-balance nadir (DSPN) were not different (p > 0.05) between calving periods or calf sexes in Season 1 cows, indicating that energy requirement is the affecting variable, since EBN occurred at the same DSPN, regardless of changing forage nutritive value (Table 4). In Season 2 cows, DSPN decreased (p ≤ 0.05) progressively from calving period 1 through 4, with period 5 not being different from period 4, indicating that changing forage nutritive value affected the time in the production cycle when cows experienced EBN. This effect of changing forage nutritive value is confirmed by the calving season × calving period interaction (p ≤ 0.05) for day of the year at energy-balance nadir (DOYN; Table 1). In Season 1 cows, DOYN increased (p ≤ 0.05) for each successive calving period, which, again, indicates that energy requirement was the driving factor causing energy-balance nadir; but in Season 2 cows, DOYN decreased (p ≤ 0.05) from periods 1 and 2 to periods 3, 4 and 5, although not consistently (Table 3). The fact that the change in DOYN across calving periods in Season 2 cows is less than 21 days indicates that forage nutritive value affects the timing of energy-balance nadir, but the fact that the change in DOYN across calving periods is not 0 days indicates that energy requirement also affects the timing of energy-balance nadir.

3.2.3. Cow Efficiency

Calf sex interacted (p ≤ 0.05) with calving season to affect cow efficiency (energy efficiency index, EEI; Table 1) when based on metabolizable energy required for the cow (EEI1) or metabolizable energy required for the cow and calf (EEI2). A lesser EEI value indicates greater cow efficiency, as the cow requires less metabolizable energy per kg of weaned calf. In Season 1 cows, EEI1 and EEI2 were not different (p > 0.05) between cows giving birth to males and females, but in Season 2 cows, those giving birth to males had lower (p ≤ 0.05) EEI1 and EEI2 values compared to those giving birth to females (Table 2).
Additionally, calving period interacted (p ≤ 0.05) with calving season to affect EEI1 and EEI2 (Table 1). In Season 1 cows, EEI1 increased successively (p ≤ 0.05) from calving periods 1 through 5, and those giving birth in calving periods 1 and 2 had lower (p ≤ 0.05) EEI2 values than those giving birth in calving periods 3, 4 and 5, which then also increased successively (p ≤ 0.05). However, in Season 2 cows, those giving birth in calving periods 1 and 2 had lower (p ≤ 0.05) EEI1 and EEI2 values than those giving birth in calving periods 3 and 4 but not (p > 0.05) calving period 5 (Table 3).

3.3. Economics

3.3.1. Revenue

Calf revenue (CaREV) was affected (p ≤ 0.05) by calving season × calving period, calving season × calf sex, and calving period × calf sex interactions (Table 1). In Season 1 cows, CaREV was greater (p ≤ 0.05) for those giving birth in calving period 1 than those giving birth in calving periods 4 and 5, with calving periods 2 and 3 being intermediate, whereas in Season 2 cows, CaREV was greater (p ≤ 0.05) for those giving birth in calving period 2 than those giving birth in calving periods 3 and 5, with calving periods 1 and 4 being intermediate (Table 3). In Season 2 cows, CaREV was greater (p ≤ 0.05) for cows giving birth to males than females, but there was no difference (p > 0.05) in CaREV between calf sexes in Season 1 cows (Table 2). For cows giving birth to males, CaREV did not change (p > 0.05) across calving periods, but CaREV tended to decrease from calving period 1 to 5 for cows giving birth to females, with calving periods 1 and 2 being greater than calving periods 3 and 5 (p ≤ 0.05) and calving period 4 being intermediate (Table 5).
There was a calving season × calving period × calf sex interaction (p ≤ 0.05) for cull cow revenue per cow (CoREV; Table 1), corresponding to a function of pregnancy percentage and timing of marketing of open cows. In Season 1 cows, CoREV was greater (p ≤ 0.05) for cows that gave birth to males in calving period 5 than in calving periods 1 and 3, whereas CoREV for cows that gave birth to females in calving period 5 was greater (p ≤ 0.05) than in calving periods 1 and 2 (Table 4). In Season 2 cows, there was no difference (p > 0.05) across calving periods for cows giving birth to males or females.
Total revenue (TREV) was affected by calving season × calving period, calving season × calf sex, and calving period × calf sex interactions and followed a pattern similar to that for CaREV, likely due to CaREV being a large proportion (87.5% on average) of TREV (Table 1). When comparing the same calving period in alternate calving seasons, cows giving birth in calving period 2 had greater (p ≤ 0.05) TREV values for Season 2 than Season 1 cows, but there were no differences (p > 0.05) between other calving periods (Table 3). There were no differences (p > 0.05) among treatment means for the calving season × calf sex interaction for TREV (Table 2). The significant interaction is likely due to Season 1 cows giving birth to males with $14/cow lower TREV values than those giving birth to females, whereas in Season 2 cows, those giving birth to males had $126/cow greater TREV values than those giving birth to females. Similarly, there were no differences (p > 0.05) among treatment means for the calving period × calf sex interaction for TREV (Table 5). Total revenue had no discernable pattern from calving period 1 to 5 for cows giving birth to males; however, TREV numerically decreased from calving period 1 to 5 for cows giving birth to females, resulting in the significant calving period × calf sex interaction.

3.3.2. Costs

Total feed cost (TFC) was greater (p ≤ 0.05) for cows giving birth to males than those giving birth to females (212 vs. 209 ± 12 $/cow; Table 1). Additionally, TFC was greater (p ≤ 0.05) for cows giving birth in calving periods 1 and 2 than in calving period 5 in Season 2, but in Season 1 cows, the TFC was only lower in calving period 5 (p ≤ 0.05) than calving periods 2 and 3 (Table 1 and Table 5). The lack of reduced costs for cows giving birth in later Season 1 calving periods in the current study is likely due to all cows being managed for early-spring calving; thus, supplemental feed during January and February was not adjusted for the cows calving in March, April, and May (calving periods 3 to 5).
Replacement heifer cost per cow (RHC), which is a function of the pregnancy percentage and the time of year at which replacements were purchased, was affected (p ≤ 0.05) by a calving season × calving period × calf sex interaction (Table 1). In Season 1 cows, RHC increased (p ≤ 0.05) by $337/cow from calving period 1 to 5 in cows giving birth to males and by $465/cow from calving period 1 to 5 in cows giving birth to females. There was no difference (p > 0.05) in RHC among calving periods for Season 2 cows giving birth to males or females; however, RHC was numerically lower in calving periods 1 and 5 than in calving periods 2, 3 and 4 for Season 2 cows giving birth to males and numerically decreased by $482/cow from calving period 1 to 5 in Season 2 cows giving birth to females (Table 4).
Total cost (COST) followed a pattern similar to that of RHC and had (p ≤ 0.05) a calving season × calving period × calf sex interaction (Table 1). In Season 1 cows, COST increased (p ≤ 0.05) by $330/cow from calving period 1 to 5 in cows giving birth to males and by $466/cow from calving period 1 to 5 in cows giving birth to females, but there was no difference (p > 0.05) in COST among calving periods for Season 2 cows giving birth to males or females; however, COST was numerically lower in calving periods 1 and 5 than in calving periods 2, 3 and 4 for Season 2 cows giving birth to males and numerically decreased by $533/cow from calving period 1 to 5 in Season 2 cows giving birth to females (Table 4).

3.3.3. Returns

Return over feed and replacement cost (RET) was affected (p ≤ 0.05) by a calving season × calving period × calf sex interaction (Table 1). In Season 1 cows giving birth to males or females, RET was greater (p ≤ 0.05) in calving periods 1, 2, 3, and 4 than in calving period 5, but there was no difference (p > 0.05) in RET among calving periods for Season 2 cows giving birth to males or females (Table 4). However, Season 2 cows giving birth to males had the numerically lowest RET in calving period 4, whereas those giving birth to females had the numerically lowest RET in calving period 1, which likely caused the three-way interaction.

4. Discussion

4.1. Effect of Calving Season

In forage production systems with bimodal growth patterns, such as tall fescue, both spring and fall calving seasons are potentially productive and profitable. Peak forage nutritive value can align well with peak energy requirements of the cow, resulting in acceptable pregnancy percentages in both seasons. Generally, fall-calving cows would be expected to have greater body condition scores at calving than spring-calving cows [3,43,44] due to lower nutrient requirements, more favorable temperatures, and greater forage nutritive value during late gestation, as observed in the current study. Because fall-calving cows have greater body condition scores at calving than spring-calving cows, pregnancy percentage is expected to be greater [43,44], as in the current study, although this may not always be the case [3].
Reports on the effect of calving season on calving interval and pregnancy percentage are conflicting. Similar to the current study, Caldwell et al. [44] reported a longer calving interval for spring-calving cow, whereas Campbell et al. [45] reported a shorter calving interval for spring-calving cows; in both studies, cows were grazing endophyte-infected tall fescue pastures. Bagley et al. [5] reported no difference in calving interval or pregnancy percentage between spring- and fall-calving cows, but cows grazed ryegrass-overseeded bermudagrass during winter months. In contrast, King and Macleod [46] reported a shorter anestrus period postpartum and a greater percentage of cows pregnant by d 100 postpartum in fall-calving cows than spring-calving cows, which could be due to changing day length [12]; thus, latitude is likely a significant factor affecting differences in reproductive efficiency between spring- and fall-calving cows. This effect is dependent upon breed type (Bos Taurus vs. Bos indicus) [10], as Bos indicus cattle have less frequent estrus and longer periods of anestrus in months with the shortest photoperiods [8,47,48].
Early lactation through breeding is the time of greatest energy requirements during the beef cow production cycle, and matching this time with forage of high nutritive value is critical to ensuring successful rebreeding [6,28]. In the current study, only Season 1 cows were expected to be in negative energy balance during the breeding season, which may be due to a greater model-predicted PKM than Season 2 cows. Similarly, Caldwell et al. [44] reported that fall-calving cows were in positive energy balance during breeding in Arkansas, whereas spring-calving cows were in negative energy balance when grazing tall fescue pastures. However, Griffin et al. [3] reported that fall-calving cows were in negative energy balance during breeding in Nebraska when grazing native rangeland. McCarter et al. [49] reported no difference in milk yield of fall- and spring-calving cows over 6 months of lactation; however, milk yield is reduced when cow feed energy intake is reduced [23,24,50], as was likely the cause with Season 2 versus Season 1 cows in the current study.
Fall-calving cows would be expected to have lower body condition scores at weaning than spring-calving cows due to relatively greater nutrient requirements in mid lactation coupled with lower forage nutritive value and increased maintenance energy requirements during winter, as observed in the current study. In contrast to the current study, Caldwell et al. [44] reported that spring-calving cows were lighter and had lower body condition scores at weaning than fall-calving cows. The reason for the discrepancy between studies performed in such close proximity to each other is unclear but may be due to different precipitation patterns relative to the types of forage produced, genetics of the cattle, access to shade/ponds for cooling, or the effects of subclinical fescue toxicosis. For example, the majority of precipitation in the current study occurred from June to August but occurred in early spring and fall (ideal for cool season forages) in the study by Caldwell et al. [44]. The timing of rainfall, coupled with average daily temperature, may have resulted in greater availability of forage in the current study, allowing spring-calving cows to maintain their weight and condition better.
Maintenance energy requirements are affected by environmental factors (extreme temperatures, wind chill, humidity, etc.) [20,51,52,53]. At the latitude of the current study, maintenance energy requirements may be more balanced across seasons such that relative differences between energy requirements and forage nutritive value are reduced at different times of the year. Edwards et al. [54] reported no difference in body-weight nadir between low- and high-milking spring-calving cows, but high-milking cows had numerically 20 kg less body-weight nadir. In general, Season 1 cows were predicted to be in negative energy balance between calving and weaning, which agrees with the decrease in BCS between calving and weaning; however, Season 2 cows were rarely predicted to be in negative energy balance, which could partially be due to their lower PKM in Season 2. Additionally, the CVDS beef cow model does not currently adjust maintenance energy requirements for environmental effects associated with cold and heat stress as discussed by the National Academy of Science, Engineering, and Medicine [20], which likely explains the discrepancy between the positive EBN and decrease in BCS from calving to weaning of Season 2 cows.
Forage nutritive value can also align well with peak energy requirements of the cow, resulting in high milk production for calf growth in early and mid lactation, but lower forage nutritive value for fall-born calves in late lactation can result in less growth. Weaning weight is generally greater for fall-born calves than spring-born calves [5,44] due to age and nutrition. Fall-born calves are sometimes weaned at an older age (current study, [44]) to allow older calves with a functional rumen to capture the benefits of early-spring forage with greater nutritional value [55]; thus, age-adjusted weaning weight may [44,45] or may not (current study, [5]) differ. Also, fall-born calves may be creep-fed, as in the current study, to compensate for hay with lower nutritive value during winter months [56]. The effects of age and nutrition can be seen in the studies of Griffin et al. [3] and McCarter et al. [57]. August-born calves were older but had weights similar to those of March-born calves at weaning because August-born calves were not creep-fed and weaned in April prior to grazing spring pasture [3], and fall-born calves not provided creep feed and weaned at 240 d had weaning weights similar to those of spring-born calves at 205 d [57].
Calf and cull cow prices are typically greater in the spring, when fall-born calves are weaned and open dams are culled, than in the fall, when spring-born calves are weaned and open dams are culled, resulting in greater calf and total revenue for fall-calving systems [4,44,58]. However, feed costs are often greater for fall-calving cows due to increased nutrient requirements of lactating cows fed through winter and creep feed provided to calves (current study, [5]); however, Henry et al. [58] reported similar winter feed costs for spring- and fall-calving beef herds ($60.24 and $60.21/cow, respectively) in Tennessee, and Griffin et al. [4] reported lower annual feed costs for August-calving than March-calving cows in Nebraska. Shifting the calving date from early to late spring reduced winter feed usage by 52% [59] and reduced costs [4,60,61]. In the current study, calf revenue and feed costs were greater in Season 2, resulting in no difference in net returns between Season 1 and 2. In contrast, average net returns were greater for fall- than spring-calving cows in Louisiana, Nebraska, and Tennessee [4,5,58].

4.2. Effect of Calving Timing Within Season

The timing of when cows calve during a calving season can influence the alignment of forage nutritive value with peak nutrient requirements, affecting milk production, energy balance, and reproductive performance. In the current study, the timing of calving interacted with the calving season for almost all evaluated variables, which is likely due to alignment with forage nutritive value and photoperiod. Cows calving early in Season 1 would have lower forage nutritive values and shorter photoperiods through early lactation than cows calving late in Season 1, whereas cows calving early in Season 2 would have greater forage nutritive values and longer photoperiods through early lactation than cows calving late in Season 2. For example, pregnancy percentage was reduced for cows calving in later periods in Season 1 but not for cows calving in later periods in Season 2, e.g., period 5, possibly due to effects of photoperiod. Additionally, the calving interval was shorter in later calving periods in both Seasons 1 and 2.
Cows calving later in the calving season have less time to begin cycling and become pregnant prior to the end of the breeding season, which can be seen in the results of Deutscher et al. [62], who reported lower pregnancy percentages for cows allowed shorter breeding seasons. However, the time of year can also impact the resumption of estrous cycles in beef cattle [12,46]. Shorter breeding seasons had a greater impact in terms of reducing the pregnancy percentage in March-calving cows than April-calving cows in Nebraska [62], and calving in February versus June decreased pregnancy percentages in 2- and 3-yr-old cows in Montana [59]. Consistent with these results, females that calve in the first 21 days of the calving season as 2-yr-olds have longer postpartum and calving intervals, which increases pregnancy percentages and subsequently allows them to remain in the herd longer [14,15].
Additionally, the body condition score at calving and changes in body condition between calving and breeding are important factors [21,63]. Thus, cows calving shortly before or after availability of pasture with greater nutritive value in the spring, such as those calving in April to June in the northern U.S., are likely to have shorter anestrus periods and greater pregnancy percentages due to a more positive energy balance [59,62]. In contrast to the current study, several studies [3,59,62] have reported that early spring-calving cows were in greater negative energy balance than late spring-calving cows during breeding, which may be due to the timing of EBN, with Season 1 cows giving birth in calving periods 1 and 2 reaching nadir in May and June, when forage was of greater nutritive value than those giving birth in calving periods 4 and 5, reaching nadir in July and August, when forage was of moderate nutritive value. Additionally, as mentioned above, the CVDS beef cow model does not currently adjust maintenance energy requirements for environmental effects associated with cold and heat stress, as discussed by the National Academy of Science, Engineering, and Medicine [20]. The lower temperatures for cows calving in periods 1 and 2 of Season 1 would likely increase maintenance energy requirements, resulting in greater EBN than for cows calving in later calving periods and could have shifted the DSPN of cows calving in periods 1 and 2.
The timing of when cows calve during the calving season also impacts the age and weight of the calf at weaning, which impacts cow efficiency and profitability. Cows that give birth earlier in the calving season generally wean heavier calves, even when adjusted to a constant age [13,14,64]. Calves born earlier in the calving season were consistently heavier at weaning than calves born in later periods, and their dams had improved EEI. These findings support previous research indicating that cow biological efficiency is strongly correlated with calf weaning weight [35,65].
Similar to the current study, Damiran et al. [64] reported lower calf revenue for calves born later in the spring calving season, but calf revenue was greater for calves born later in the spring in studies by Stockton et al. [60] and Griffin et al. [4], although in these studies, calves were weaned at similar age rather than on a similar day of the year as in the current study. Thus, age at weaning appears to be the primary driver of differences in weaning weight and calf revenue between calves born earlier and later in the calving season. Feed costs were not different among calving periods in Season 1; thus, net returns decreased for cows calving later in Season 1. Alternatively, net returns were increased when shifting the calving season from early to late spring in Nebraska and Montana [60,61].

4.3. Interactions with Calf Sex

The effect of calf sex interacted with calving season and calving period for many outcome variables—WBCS, CAINT, BW, WW, WAGE, AWW, PKM, EBN, DSPN, EEI, CaREV, CoREV, TREV, RHC, COST, and RET. Many of these pertain to the biological differences between males and females, with females having lighter birth and weaning weights, leading to lower model-predicted milk production and negative energy balance of the cow, as well as to lower cow efficiency and net returns. These differences provide a biological understanding of the effects on cow performance, but calf sex is not a primary factor for producers to consider when deciding on a calving season.

4.4. Summary

Overall, fall calving systems have some advantages over early-spring calving systems, especially in southern latitudes, for several reasons. Fall-calving cows calve in better body condition, and it is more cost effective to maintain body condition grazing cool-season or stockpiled forage than using harvested forage. Extending the grazing season with stockpiled forage and crop residues is a successful way to reduce winter feed costs; however, these feed supplies are often exhausted in early winter, causing the bulk of harvested feed and feed costs to occur in late winter and early spring, when spring-calving cows have the greatest nutrient requirements and, therefore, need for supplemental feed. Fall-calving systems have the advantage that cows can be allowed to lose some body condition after the breeding season in late winter and early spring to reduce feed costs, knowing that summer pasture will enable cows to regain body condition prior to calving. Thus, better body condition at breeding, along with any benefit of photoperiod, results in improved (or, at least, more cost-effective) pregnancy percentages in fall-calving cows. In northern climates, late-spring calving is more advantageous than early-spring calving due to reduced feed costs when cows are able to maintain body condition while grazing pasture during early lactation, which could increase pregnancy percentages. Late-spring calving in southern climates may not be as advantageous due to the decline in forage nutritive value during early lactation (depending upon the forage species being grazed) and the negative effects of heat stress on reproduction [66,67]. Likewise, fall calving systems may not be as advantageous as late-spring calving systems in northern climates due to harsher winter weather resulting in reduced calf growth and increased winter feed costs; however, only one study has made this comparison [3,4].

4.5. Limitations and Scope

One of the limitations of this study is the observational nature of the data collection, in contrast with a prospective study where cows are randomly assigned to calving season and period. Cows in Season 1 and Season 2 could have some inherent differences, as they are essentially separate herds, and cows could have adapted to the calving season. Additionally, the calving period in which a cow calves is determined by one of two factors: (1) lack of fertility in an earlier calving period in a previous year, shifting her to the later calving period or (2) the cow being born to a dam calving in the later calving period, which could have been due to reduced fertility of the dam in the past. Calving timing and offspring performance can be the results of past events of the dam, as females that are born early in the calving season, themselves, are more likely to calve early in their first calving season as 2-yr-old cows and wean heavier calves [68]. Thus, the observational nature of this study could bias the results, as female breeding lines with later calving periods could result in breeding lines with lower fertility.
Additionally, the results of this study are applicable to cow-calf operations in the central latitudes of the USA, where winter and summer weather is not extreme. The forage base was tall fescue with a bimodal growth curve, providing highly nutritious forage in both spring and fall; therefore, the results may not be applicable to other forage species.
Model assumptions were based on equations to predict the energy requirements of the mean beef cow; however, there is considerable variability among individual cows in a herd. Furthermore, the feed costs in the economic analysis were based on estimated feed requirements from the CVDS model. Thus, model outputs and economic costs could be biased toward the center of the population.

5. Conclusions

In forage systems with a bimodal growth pattern, such as tall fescue, fall-calving cows have an advantage in reproductive performance, as the greater forage nutritive value in summer increases the body condition score at the time of calving. Additionally, the shorter days during the breeding season shorten postpartum intervals and increase fertility in fall-calving cows. In contrast, feed costs for spring-calving cows are lower, and spring-born calves have greater forage nutritive value during late lactation, leading to more cost-effective gains. However, spring-born calves wean at lighter weights and are generally sold during periods of lower calf prices. The tradeoff between lower calf revenue and feed costs for spring calving compared with greater revenue and costs associated with fall calving results in a similar net income.
The calving period affects the alignment of cow nutrient requirements with forage nutritive value and the length of time to rebreed but is highly dependent upon the calving season. Reproductive performance declined in later calving periods during spring calving but not during fall calving. Calf weaning weight declined less in later periods during fall calving, but calf revenue declined to a greater extent. Replacement female costs were lower in later fall calving periods compared to later spring calving periods due to improved reproductive performance. Thus, net returns did not decline in later calving periods for fall-calving cows, as it did for spring calving cows.
The interactions among calving season and calving period add complexity in terms of identifying the optimal calving season, warranting further study. At the latitude of the current study, using a forage species with a bimodal growth curve, fall calving resulted in improved cow reproductive performance, calf growth, and calf revenue but increased feed costs and no difference in net returns.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ruminants6010019/s1, Table S1: Ingredient composition of supplemental feed provided to Hereford cows and to calves as creep feed; Equation (S1); Equation (S2); Equation (S3); Table S2: Nutritive value (mean ± SD) of pasture forage by month for years 2016–2018 in southwest Missouri; Table S3: Nutritive value (mean ± SD) of hay and supplemental feed provided to Hereford cows and calves from 2016–2018; Figure S1: Mean (±SD) high and low temperatures by month for years 2013–2019 recorded at Wright County Missouri State University Fruit Experiment Station 17.9 km north of Journagan Ranch (36.993897, −92.258733); Figure S2: Mean (±SD) precipitation by month for years 2013–2019 recorded at Wright County Missouri State University Fruit Experiment Station 17.9 km north of Journagan Ranch (36.993897, −92.258733).

Author Contributions

Conceptualization, P.A.L., B.V., and E.W.; Methodology, P.A.L., B.V., and E.W.; Software, P.A.L.; Validation, P.A.L., B.V., and E.W.; Formal Analysis, P.A.L. and B.V.; Investigation, B.V. and P.A.L.; Resources, P.A.L.; Data Curation, B.V. and P.A.L.; Writing—Original Draft Preparation, B.V. and P.A.L.; Writing—Review and Editing, B.V., E.W., and P.A.L.; Visualization, P.A.L. and B.V.; Supervision, P.A.L.; Project Administration, P.A.L. and B.V.; Funding Acquisition, P.A.L. All authors have read and agreed to the published version of the manuscript.

Funding

Internal funding was provided by the Missouri State University Darr College of Agriculture.

Institutional Review Board Statement

The animal study protocol was submitted for approval by the Missouri State University Institutional Animal Care and Use Committee (Protocol #16-035.0). It was deemed by the committee that a protocol was not necessary, since the data collected on cows and calves were generally accepted as production data.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding author. (The datasets presented in this article are proprietary data of Leo Journagan Ranch.)

Acknowledgments

The authors would like to thank Marty Lueck and the staff at Leo Journagan Ranch for collecting all cow and calf data. We would also like to acknowledge the contribution of Jonathan Bellis in collecting forage data used in this study for 2016–2017.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Schulz, L.L.; Andresen, C.E.; Gunn, P.J. Factors Affecting Timing and Intensity of Calving Season of Beef Cow-Calf Producers in the Midwest. Prof. Anim. Sci. 2016, 32, 430–437. [Google Scholar] [CrossRef]
  2. Olson, D.P.; Papasian, C.J.; Ritter, R.C. The Effects of Cold Stress on Neonatal Calves. I. Clinical Condition and Pathological Lesions. Can. J. Comp. Med. 1980, 44, 11–18. [Google Scholar] [PubMed]
  3. Griffin, W.A.; Stalker, L.A.; Adams, D.C.; Funston, R.N.; Klopfenstein, T.J. Calving Date and Wintering System Effects on Cow and Calf Performance I: A Systems Approach to Beef Production in the Nebraska Sandhills. Prof. Anim. Sci. 2012, 28, 249–259. [Google Scholar] [CrossRef]
  4. Griffin, W.A.; Stalker, L.A.; Stockton, M.C.; Adams, D.C.; Funston, R.N.; Klopfenstein, T.J. Calving Date and Wintering System Effects on Cow and Calf Performance II: Economic Analysis. Prof. Anim. Sci. 2012, 28, 260–271. [Google Scholar] [CrossRef]
  5. Bagley, C.P.; Carpenter, J.C., Jr.; Feazel, J.I.; Hembry, F.G.; Huffman, D.C.; Koonce, K.L. Influence of Calving Season and Stocking Rate on Beef Cow-Calf Productivity. J. Anim. Sci. 1987, 64, 687–694. [Google Scholar] [CrossRef]
  6. Sprott, L.R.; Selk, G.E.; Adams, D.C. REVIEW: Factors Affecting Decisions on When to Calve Beef Females. Prof. Anim. Sci. 2001, 17, 238–246. [Google Scholar] [CrossRef]
  7. Skinner, J.D.; Louw, G.N. Heat Stress and Spermatogenesis in Bos Indicus and Bos Taurus Cattle. J. Appl. Physiol. 1966, 21, 1784–1790. [Google Scholar] [CrossRef]
  8. Plasse, D.; Warnick, A.C.; Koger, M. Reproductive Behavior of Bos Indicus Females in a Subtropical Environment. I. Puberty and Ovulation Frequency in Brahman and Brahman X British Heifers. J. Anim. Sci. 1968, 27, 94–100. [Google Scholar] [CrossRef]
  9. Biggers, B.G.; Geisert, R.D.; Wetteman, R.P.; Buchanan, D.S. Effect of Heat Stress on Early Embryonic Development in the Beef Cow. J. Anim. Sci. 1987, 64, 1512–1518. [Google Scholar] [CrossRef]
  10. McCarter, M.N.; Buchanan, D.S.; Frahm, R.R. Comparison of Crossbred Cows Containing Various Proportions of Brahman in Spring- or Fall-Calving Systems: IV. Effects of Genotype × Environment Interaction on Lifetime Productivity of Young Cows. J. Anim. Sci. 1991, 69, 3977–3982. [Google Scholar] [CrossRef]
  11. Petitclerc, D.; Chapin, L.T.; Emery, R.S.; Tucker, H.A. Body Growth, Growth Hormone, Prolactin and Puberty Response to Photoperiod and Plane of Nutrition in Holstein Heifers. J. Anim. Sci. 1983, 57, 892–898. [Google Scholar] [CrossRef] [PubMed]
  12. Schillo, K.K.; Hall, J.B.; Hileman, S.M. Effects of Nutrition and Season on the Onset of Puberty in the Beef Heifer. J. Anim. Sci. 1992, 70, 3994–4005. [Google Scholar] [CrossRef] [PubMed]
  13. Lesmeister, J.L.; Burfening, P.J.; Blackwell, R.L. Date of First Calving in Beef Cows and Subsequent Calf Production. J. Anim. Sci. 1973, 36, 1–6. [Google Scholar] [CrossRef]
  14. French, J.T.; Ahola, J.K.; Whittier, J.C.; Frasier, W.M.; Enns, R.M.; Peel, R.K. Differences in Lifetime Productivity of Beef Heifers That Conceived to First-Service Artificial Insemination (AI) or a Clean-up Bull via Natural Service (NS) as a Yearling and among Females That Were Offspring of an AI or NS Mating. Prof. Anim. Sci. 2013, 29, 57–63. [Google Scholar] [CrossRef]
  15. Damiran, D.; Larson, K.; Pearce, L.; Erickson, N.; Lardner, H.A. Effects of Heifer Calving Date on Longevity and Lifetime Productivity in Western Canada. Sustain. Agric. Res. 2018, 7, 11. [Google Scholar] [CrossRef]
  16. Bitencourt, M.F.; Cerdótes, L.; Restle, J.; Costa, P.T.; Fernandes, T.A.; Ferreira, O.G.L.; Silveira, D.D.; Vaz, R.Z. Age and Calving Time Affects Production Efficiency of Beef Cows and Their Calves. An. Acad. Bras. Ciênc. 2020, 92, e20181058. [Google Scholar] [CrossRef]
  17. Funston, R.N.; Musgrave, J.A.; Meyer, T.L.; Larson, D.M. Effect of Calving Distribution on Beef Cattle Progeny Performance. J. Anim. Sci. 2012, 90, 5118–5121. [Google Scholar] [CrossRef]
  18. Peel, D.S. Economics of Stocker Production. Vet. Clin. N. Am. Food Anim. Prac. 2006, 22, 271–296. [Google Scholar] [CrossRef]
  19. Diskin, M.G.; Kenny, D.A. Managing the Reproductive Performance of Beef Cows. Theriogenology 2016, 86, 379–387. [Google Scholar] [CrossRef]
  20. National Academies of Sciences, Engineering, and Medicine. Nutrient Requirements of Beef Cattle: Eighth Revised Edition, 8th ed.; Animal Nutrition Series; The National Academies Press: Washington, DC, USA, 2016. [Google Scholar]
  21. Hess, B.W.; Lake, S.L.; Scholljegerdes, E.J.; Weston, T.R.; Nayigihugu, V.; Molle, J.D.C.; Moss, G.E. Nutritional Controls of Beef Cow Reproduction. J. Anim. Sci. 2005, 83, E90–E106. [Google Scholar] [CrossRef]
  22. Barnes, R.F.; Miller, D.A.; Nelson, C.J. Forages: An Introduction to Grassland Agriculture, 5th ed.; Iowa State University Press: Ames, IA, USA, 1995; Volume 1. [Google Scholar]
  23. Jenkins, T.G.; Ferrell, C.L. Lactation Characteristics of Nine Breeds of Cattle Fed Various Quantities of Dietary Energy. J. Anim. Sci. 1992, 70, 1652–1660. [Google Scholar] [CrossRef]
  24. Spencer, C.M.; Bayliff, C.L.; Redden, M.D.; McGee, A.L.; Reuter, R.; Horn, G.W.; Moffet, C.A.; Lalman, D.L. Milk Production Responses to Beef Cow Energy Intakes. J. Anim. Sci. 2017, 95, 13–14. [Google Scholar] [CrossRef]
  25. Adams, D.C.; Clark, R.T.; Klopfenstein, T.J.; Volesky, J.D. Matching the Cow with Forage Resources. Rangelands 1996, 18, 57–62. [Google Scholar]
  26. Williams, M.J.; Chase, C.C.; Hammond, A.C. Performance of Cows and Their Calves Creep-Grazed on Rhizoma Perennial Peanut. Agron. J. 2004, 96, 671–676. [Google Scholar] [CrossRef]
  27. Corriher, V.A.; Hill, G.M.; Andrae, J.G.; Froetschel, M.A.; Mullinix, B.G., Jr. Cow and Calf Performance on Coastal or Tifton 85 Bermudagrass Pastures with Aeschynomene Creep-Grazing Paddocks1. J. Anim. Sci. 2007, 85, 2762–2771. [Google Scholar] [CrossRef]
  28. Funston, R.N.; Grings, E.E.; Roberts, A.J.; Tibbitts, B.T. Invited Review: Choosing a Calving Date. Prof. Anim. Sci. 2016, 32, 145–153. [Google Scholar] [CrossRef]
  29. Eversole, D.E.; Browne, M.F.; Hall, J.B.; Dietz, R.E. Body Condition Scoring Beef Cows; Virginia Cooperative Extension Service: Blacksburg, VA, USA, 2009. [Google Scholar]
  30. Davis, G.V.; Gadberry, M.S.; Troxel, T.R. Composition and Nutrient Deficiencies of Arkansas Forages for Beef Cattle. Prof. Anim. Sci. 2002, 18, 127–134. [Google Scholar] [CrossRef]
  31. Galyean, M.L.; Cole, N.A.; Tedeschi, L.O.; Branine, M.E. BOARD-INVITED REVIEW: Efficiency of Converting Digestible Energy to Metabolizable Energy and Reevaluation of the California Net Energy System Maintenance Requirements and Equations for Predicting Dietary Net Energy Values for Beef Cattle. J. Anim. Sci. 2016, 94, 1329–1341. [Google Scholar] [CrossRef]
  32. Tedeschi, L.O.; Fox, D.G.; Baker, M.J.; Long, K.L. A Model to Evaluate Beef Cow Efficiency. In Nutrient Digestion and Utilization in Farm Animals: Modelling Approaches; Kebreab, E., Dijkstra, J., Bannink, A., Gerrits, W.J.J., France, J., Eds.; CABI Publishing: Cambridge, MA, USA, 2006; pp. 84–98. [Google Scholar]
  33. Moe, P.W. Energy Metabolism of Dairy Cattle. J. Dairy Sci. 1981, 64, 1120–1139. [Google Scholar] [CrossRef] [PubMed]
  34. Lemenager, R.P.; Nelson, L.A.; Hendrix, K.S. Influence of Cow Size and Breed Type on Energy Requirements. J. Anim. Sci. 1980, 51, 566–576. [Google Scholar] [CrossRef]
  35. Dinkel, C.A.; Tucker, W.L.; Marshall, D.M. Sources of Variation in Beef Cattle Weaning Weight. Can. J. Anim. Sci. 1990, 70, 761–769. [Google Scholar] [CrossRef]
  36. Lancaster, P.A.; Tedeschi, L.O.; Buessing, Z.; Davis, M.E. Assessment of Milk Yield and Nursing Calf Feed Intake Equations in Predicting Calf Feed Intake and Weaning Weight among Breeds. J. Anim. Sci. 2021, 99, skaa406. [Google Scholar] [CrossRef]
  37. R Core Team. R: A Language and Environment for Statistical Computing; R Core Team: Vienna, Austria, 2022. [Google Scholar]
  38. Oakes, G.K.; Walker, A.M.; Ehrenkranz, R.A.; Cefalo, R.C.; Chez, R.A. Uteroplacental Blood Flow during Hyperthermia with and without Respiratory Alkalosis. J. Appl. Physiol. 1976, 41, 197–201. [Google Scholar] [CrossRef]
  39. Collier, R.J.; Doelger, S.G.; Head, H.H.; Thatcher, W.W.; Wilcox, C.J. Effects of Heat Stress during Pregnancy on Maternal Hormone Concentrations, Calf Birth Weight and Postpartum Milk Yield of Holstein Cows. J. Anim. Sci. 1982, 54, 309–319. [Google Scholar] [CrossRef] [PubMed]
  40. Tao, S.; Monteiro, A.P.A.; Thompson, I.M.; Hayen, M.J.; Dahl, G.E. Effect of Late-Gestation Maternal Heat Stress on Growth and Immune Function of Dairy Calves. J. Dairy Sci. 2012, 95, 7128–7136. [Google Scholar] [CrossRef]
  41. Monteiro, A.P.A.; Tao, S.; Thompson, I.M.; Dahl, G.E. Effect of Heat Stress during Late Gestation on Immune Function and Growth Performance of Calves: Isolation of Altered Colostral and Calf Factors. J. Dairy Sci. 2014, 97, 6426–6439. [Google Scholar] [CrossRef]
  42. Alves, M.S.; Bignardi, A.B.; Zuim, D.M.; Silva, J.A.d.; Cardoso, M.G.R.; Piccoli, M.L.; Roso, V.M.; Carvalheiro, R.; Faro, L.E.; Pereira, R.J.; et al. Thermal Stress during Late Gestation Impairs Postnatal Growth and Provides Background for Genotype-Environment Interaction in Hereford-Braford and Angus-Brangus Cattle. Livest. Sci. 2022, 263, 105027. [Google Scholar] [CrossRef]
  43. Selk, G.E.; Wettemann, R.P.; Lusby, K.S.; Oltjen, J.W.; Mobley, S.L.; Rasby, R.J.; Garmendia, J.C. Relationships among Weight Change, Body Condition and Reproductive Performance of Range Beef Cows. J. Anim. Sci. 1988, 66, 3153–3159. [Google Scholar] [CrossRef]
  44. Caldwell, J.D.; Coffey, K.P.; Jennings, J.A.; Philipp, D.; Young, A.N.; Tucker, J.D.; Hubbell, D.S., III; Hess, T.; Looper, M.L.; West, C.P.; et al. Performance by Spring and Fall-Calving Cows Grazing with Full, Limited, or No Access to Toxic Neotyphodium Coenophialum-Infected Tall Fescue1. J. Anim. Sci. 2013, 91, 465–476. [Google Scholar] [CrossRef]
  45. Campbell, B.T.; Backus, W.M.; Dixon, C.M.; Carlisle, R.J.; Waller, J.C. A Comparison of Spring- and Fall-Calving Beef Herds Grazing Tall Fescue. Prof. Anim. Sci. 2013, 29, 172–178. [Google Scholar] [CrossRef]
  46. King, G.J.; Macleod, G.K. Reproductive Function in Beef Cows Calving in the Spring or Fall. Anim. Reprod. Sci. 1984, 6, 255–266. [Google Scholar] [CrossRef]
  47. Harrison, L.M.; Hansen, T.R.; Randel, R.D. Evidence for Seasonal and Nutritional Modification of Ovarian and Pituitary Function in Crossbred Heifers and Brahman Cows. J. Anim. Sci. 1982, 55, 649–656. [Google Scholar] [CrossRef] [PubMed]
  48. Stahringer, R.C.; Neuendorff, D.A.; Randel, R.D. Seasonal Variations in Characteristics of Estrous Cycles in Pubertal Brahman Heifers. Theriogenology 1990, 34, 407–415. [Google Scholar] [CrossRef] [PubMed]
  49. McCarter, M.N.; Buchanan, D.S.; Frahm, R.R. Comparison of Crossbred Cows Containing Various Proportions of Brahman in Spring or Fall Calving Systems: II. Milk Production. J. Anim. Sci. 1991, 69, 77–84. [Google Scholar] [CrossRef]
  50. Lalman, D.L.; Williams, J.E.; Hess, B.W.; Thomas, M.G.; Keisler, D.H. Effect of Dietary Energy on Milk Production and Metabolic Hormones in Thin, Primiparous Beef Heifers. J. Anim. Sci. 2000, 78, 530–538. [Google Scholar] [CrossRef]
  51. Laurenz, J.C.; Byers, F.M.; Schelling, G.T.; Greene, L.W. Effects of Season on the Maintenance Requirements of Mature Beef Cows. J. Anim. Sci. 1991, 69, 2168–2176. [Google Scholar] [CrossRef]
  52. Thompson, W.R.; Meiske, J.C.; Goodrich, R.D.; Rust, J.R.; Byers, F.M. Influence of Body Composition on Energy Requirements of Beef Cows during Winter. J. Anim. Sci. 1983, 56, 1241–1252. [Google Scholar] [CrossRef] [PubMed]
  53. Wagner, J.J.; Lusby, K.S.; Oltjen, J.W.; Rakestraw, J.; Wettemann, R.P.; Waiters, L.E. Carcass Composition in Mature Hereford Cows: Estimation and Effect on Daily Metabolizable Energy Requirement during Winter. J. Anim. Sci. 1988, 66, 603–612. [Google Scholar] [CrossRef]
  54. Edwards, S.R.; Hobbs, J.D.; Mulliniks, J.T. High Milk Production Decreases Cow-Calf Productivity within a Highly Available Feed Resource Environment. Trans. Anim. Sci. 2017, 1, 54–59. [Google Scholar] [CrossRef]
  55. Hudson, M.D.; Winterholler, S.J.; Krehbiel, C.R.; Ward, C.E.; Lalman, D.L. Comparison of Two Weaning Dates and Two Finishing Systems on Feedlot Performance, Carcass Characteristics, and Enterprise Profitability of Fall-Born Steers. Prof. Anim. Sci. 2010, 26, 222–229. [Google Scholar] [CrossRef]
  56. Mayo, S.J.; Lalman, D.L.; Selk, G.E.; Wettemann, R.P.; Buchanan, D.S. Effect of Level of Cow Winter Nutrition and Calf Creep Feeding on Fall Calving System Productivity; Department of Animal Science Research Report; Oklahoma State University: Stillwater, OK, USA, 2002. [Google Scholar]
  57. McCarter, M.N.; Buchanan, D.S.; Frahm, R.R. Comparison of Crossbred Cows Containing Various Proportions of Brahman in Spring or Fall Calving Systems: III. Productivity as Three-, Four-, and Five-Year Olds. J. Anim. Sci. 1991, 69, 2754–2761. [Google Scholar] [CrossRef]
  58. Henry, G.W.; Boyer, C.N.; Griffith, A.P.; Larson, J.; Smith, A.; Lewis, K. Risk and Returns of Spring and Fall Calving for Beef Cattle in Tennessee. J. Agric. Appl. Econ. 2016, 48, 257–278. [Google Scholar] [CrossRef]
  59. Grings, E.E.; Short, R.E.; Klement, K.D.; Geary, T.W.; MacNeil, M.D.; Haferkamp, M.R.; Heitschmidt, R.K. Calving System and Weaning Age Effects on Cow and Preweaning Calf Performance in the Northern Great Plains. J. Anim. Sci. 2005, 83, 2671–2683. [Google Scholar] [CrossRef]
  60. Stockton, M.C.; Adams, D.C.; Wilson, R.K.; Klopfenstein, T.J.; Clark, R.T.; Carriker, G.L. Production and Economic Comparisons of Two Calving Dates for Beef Cows in the Nebraska Sandhills. Prof. Anim. Sci. 2007, 23, 500–508. [Google Scholar] [CrossRef]
  61. Kruse, R.E.; Tess, M.W.; Grings, E.E.; Short, R.E.; Heitschmidt, R.K.; Phillips, W.A.; Mayeux, H.S. Evaluation of Beef Cattle Operations Utilizing Different Seasons of Calving, Weaning Strategies, Postweaning Management, and Retained Ownership. Prof. Anim. Sci. 2008, 24, 319–327. [Google Scholar] [CrossRef]
  62. Deutscher, G.H.; Stotts, J.A.; Nielsen, M.K. Effects of Breeding Season Length and Calving Season on Range Beef Cow Productivity. J. Anim. Sci. 1991, 69, 3453–3460. [Google Scholar] [CrossRef]
  63. Rutter, L.M.; Randel, R.D. Postpartum Nutrient Intake and Body Condition: Effect on Pituitary Function and Onset of Estrus in Beef Cattle. J. Anim. Sci. 1984, 58, 265–274. [Google Scholar] [CrossRef] [PubMed]
  64. Damiran, D.; Larson, K.A.; Pearce, L.T.; Erickson, N.E.; Lardner, B.H.A. Effect of Calving Period on Beef Cow Longevity and Lifetime Productivity in Western Canada. Trans. Anim. Sci. 2018, 2, S61–S65. [Google Scholar] [CrossRef]
  65. Dinkel, C.A.; Brown, M.A. An Evaluation of the Ratio of Calf Weight to Cow Weight as an Indicator of Cow Efficiency. J. Anim. Sci. 1978, 46, 614–617. [Google Scholar] [CrossRef]
  66. Jordan, E.R. Effects of Heat Stress on Reproduction. J. Dairy Sci. 2003, 86, E104–E114. [Google Scholar] [CrossRef]
  67. Rahman, M.B.; Schellander, K.; Luceño, N.L.; Van Soom, A. Heat Stress Responses in Spermatozoa: Mechanisms and Consequences for Cattle Fertility. Theriogenology 2018, 113, 102–112. [Google Scholar] [CrossRef] [PubMed]
  68. Funston, R.N.; Martin, J.L.; Larson, D.M.; Roberts, A.J. Physiology and endocrinology symposium: Nutritional Aspects of Developing Replacement Heifers. J. Anim. Sci. 2012, 90, 1166–1171. [Google Scholar] [CrossRef]
Table 1. ANOVA results (Pr > F) for calving season (CS), calving period (CP), calf sex, and two- and three-way interactions for performance traits, model outputs, and economics of Hereford cows in southwest Missouri.
Table 1. ANOVA results (Pr > F) for calving season (CS), calving period (CP), calf sex, and two- and three-way interactions for performance traits, model outputs, and economics of Hereford cows in southwest Missouri.
Item 1CSCPSexCS × CPCS × SexCP × SexCS × CP × Sex
Performance
MCW0.010.280.430.130.540.770.44
CBCS0.010.660.950.570.710.760.76
WBCS0.760.610.250.220.010.270.17
PREG0.050.410.020.04---
SURV0.400.520.900.20---
CAINT0.080.010.220.600.040.350.12
BW0.010.010.010.070.060.030.04
WW0.010.010.010.010.010.410.04
WAGE0.010.010.100.040.440.030.01
AWW0.340.010.010.030.010.510.13
Model outputs
MER0.010.240.010.140.260.400.10
PKM0.010.010.010.020.010.350.07
EBN0.010.010.010.010.010.010.01
DSPN0.010.010.010.010.010.010.01
DOYN0.010.010.170.010.180.520.69
EEI10.010.010.010.010.010.470.18
EEI20.010.010.010.010.010.570.29
Economics
CaREV0.010.010.010.010.010.010.10
CoREV0.370.310.300.070.870.040.04
TREV0.450.140.100.010.040.010.12
TFC0.010.010.020.010.320.880.25
RHC0.390.240.240.040.920.020.04
COST0.840.310.260.030.900.020.03
RET0.370.010.010.010.130.040.04
1 MCW = mature cow weight; CBCS = body condition score at calving; WBCS = body condition score at weaning; PREG = pregnancy percentage; SURV = calf survival percentage from birth to weaning; CAINT = calving interval; BW = calf birth weight; WW = calf weaning weight; WAGE = calf age at weaning; AWW = 205 d adjusted calf weaning weight; MER = metabolizable energy required; PKM = peak milk yield; EBN = energy-balance nadir; DSPN = days since parturition at energy-balance nadir; DOYN = day of the year at energy-balance nadir; EEI1 = cow energy efficiency index; EEI2 = cow + calf energy efficiency index; CaREV = calf revenue; CoREV = cull cow revenue; TREV = total revenue; TFC = total feed cost; RHC = replacement female cost; COST = total cost; RET = returns over costs.
Table 2. Performance traits, model outputs and economics for effects of calving season (Season 1 or Season 2) and calf sex (males or females) of Hereford cows in southwest Missouri.
Table 2. Performance traits, model outputs and economics for effects of calving season (Season 1 or Season 2) and calf sex (males or females) of Hereford cows in southwest Missouri.
Season 1Season 2
Item 1MalesFemalesMalesFemalesSEM
NC920770137153
Performance
MCW5745655505499
CBCS5.75.76.16.10.1
WBCS5.5 ab5.4 ab5.0 b5.5 a0.2
PREG-----
SURV-----
CAINT370 ab374 a371 ab354 b7
BW36.234.934.532.00.3
WW253 b242 c283 a255 bc7
WAGE2172152362313
AWW242 a235 b254 a229 b6
Model outputs
MER7987785777677484106
PKM6.3 a5.9 b5.8 b4.7 c0.2
EBN−1.7 d−1.6 c0.0 b0.8 a0.1
DSPN112 c112 c175 b192 a3
DOYN1811811121186
EEI132.9 a33.5 a28.1 c31.0 b0.8
EEI236.3 ab36.9 a32.1c34.8 b0.7
Economics
CaREV951 b931 b1067 a915 b114
CoREV13616911514029
TREV1086 a1100 a1182 a1056 a113
TFC19018823422912
RHC31639626833670
COST50658450256465
RET580515680489121
1 NC = number of calves; MCW = mature cow weight, kg; CBCS = body condition score at calving (1–9); WBCS = body condition score at weaning (1–9); PREG = pregnancy percentage, %; SURV = calf survival percentage from birth to weaning, %; CAINT = calving interval, d; BW = calf birth weight, kg; WW = calf weaning weight, kg; WAGE = calf age at weaning, d; AWW = 205 d adjusted calf weaning weight, kg; MER = metabolizable energy required, Mcal; PKM = peak milk yield, kg/d; EBN = energy-balance nadir, Mcal/d; DSPN = days since parturition at energy-balance nadir, d; DOYN = day of the year at energy-balance nadir, d; EEI1 = cow energy efficiency index, Mcal/kg; EEI2 = cow + calf energy efficiency index, Mcal/kg; CaREV = calf revenue, $/cow; CoREV = cull cow revenue, $/cow; TREV = total revenue, $/cow; TFC = total feed cost, $/cow; RHC = replacement heifer cost, $/cow; COST = total cost, $/cow; RET = returns over costs, $/cow. abcd Means without a common superscript in the same row differ at p ≤ 0.05.
Table 3. Performance traits, model outputs and economics for effects of calving season (Season 1 or Season 2) and calving period (1 to 5) of Hereford cows in southwest Missouri.
Table 3. Performance traits, model outputs and economics for effects of calving season (Season 1 or Season 2) and calving period (1 to 5) of Hereford cows in southwest Missouri.
Season 1Season 2
Item 112345+12345+SEM
NC25057746423716258102922711
Performance
MCW56556356557558053656155856252911
CBCS5.55.65.75.75.96.16.16.26.25.80.1
WBCS5.25.35.55.55.75.55.65.55.54.20.2
PREG92.1 a85.1 ab82.6 b84.0 ab69.2 c84.1 ab89.0 ab89.4 ab75.9 ab90.2 ab4.9
SURV98.196.198.398.097.1100.098.093.796.591.82.0
CAINT3953843713603483903813583363479
BW35.035.935.636.135.231.233.433.634.234.00.5
WW273 bc264 cd250 e237 f214 g292 ab296 a256 de250 cdef252 bcdefg8
WAGE249 b236 c218 d200 e178 f270 a255 b230 c207 de205 de4
AWW233 a235 a239 a243 a242 a229 a244 a231 a250 a255 a7
Model outputs
MER7956790879147954787975237817762077377429127
PKM5.9 a6.0 a6.1 a6.2 a6.2 a4.6 b5.1 b4.7 b5.6 ab6.1 ab0.3
EBN−1.4 d−1.5 d−1.6 e−1.8 e−1.7 e0.2 c0.3 bc1.0 a0.8 ab−0.3 c0.1
DSPN110 e112 e113 e113 e112 e244 a223 b190 c139 d123 de3
DOYN139 e157 d178 c199 b234 a141 e135 e107 f90 f103 f6
EEI129.5 e30.9 d32.4 c34.8 b38.5 a26.6 f27.2 f31.1 cde31.8 bcde31.1 bcdef0.9
EEI233.7d34.8d35.9c37.8b41.0a31.3e31.6e35.0cd35.1bcd34.4 bcde0.8
Economics
CaREV1004 b963 bc965 bc936c836d1028 abc1131 a965 bc986 abc846 bcd117
CoREV65130159134275134989620110940
TREV1067 b1092 b1125 ab1071 b1111 ab1160 ab1228 a1062 ab1188 ab955 ab120
TFC189 cd191 c192 c189 cd185 d243 ab244 a237 ab230 b203 cd12
RHC156 c312 bc358 b322 bc633 a324 abc222 bc217 bc499 abc249 abc93
COST344 c503 bc550 b512 bc819 a567 abc465 bc454 bc728 abc451 abc90
RET725 a591 b573 b559 b291 c600 ab761 a606 ab455 abc501 abc130
1 NC = number of calves; MCW = mature cow weight, kg; CBCS = body condition score at calving (1–9); WBCS = body condition score at weaning (1–9); PREG = pregnancy percentage, %; SURV = calf survival percentage from birth to weaning, %; CAINT = calving interval, d; BW = calf birth weight, kg; WW = calf weaning weight, kg; WAGE = calf age at weaning, d; AWW = 205 d adjusted calf weaning weight, kg; MER = metabolizable energy required, Mcal; PKM = peak milk yield, kg/d; EBN = energy-balance nadir, Mcal/d; DSPN = days since parturition at energy-balance nadir, d; DOYN = day of the year at energy-balance nadir, d; EEI1 = cow energy efficiency index, Mcal/kg; EEI2 = cow + calf energy efficiency index, Mcal/kg; CaREV = calf revenue, $/cow; CoREV = cull cow revenue, $/cow; TREV = total revenue, $/cow; TFC = total feed cost, $/cow; RHC = replacement heifer cost, $/cow; COST = total cost, $/cow; RET = returns over costs, $/cow; abcdefg Means without a common superscript in the same row differ at p ≤ 0.05.
Table 4. Performance traits, model outputs and economics for effects of calving season (Season 1 or Season 2), calf sex (males or females), and calving period (1 to 5) of Hereford cows in southwest Missouri.
Table 4. Performance traits, model outputs and economics for effects of calving season (Season 1 or Season 2), calf sex (males or females), and calving period (1 to 5) of Hereford cows in southwest Missouri.
Season 1Season 2
MalesFemales MalesFemales
Item 112345+12345+SEM12345+12345+SEM
NC121311258139911292662069871-285536135304756146-
Performance
MCW579566569575581550560562574580952855255456355154356956256050819
CBCS5.65.65.75.75.95.55.65.75.75.90.16.16.16.06.26.06.26.16.36.25.60.3
WBCS5.55.45.55.65.54.95.15.55.45.80.15.15.55.45.3NA5.85.65.65.74.90.3
PREG----------------------
SURV----------------------
CAINT39638436636233939438537635835811402373364339NA37938935333231821
BW35.6 abc36.4 ab36.3 ab36.8 a35.8 abc34.4 cdef35.4 bcd34.8 cdef35.4 abcde34.5 cdef0.432.6 fg33.6 cdef33.8 cdef36.6 abcdef36.0 abcdefg29.8 g33.1 f33.4 ef31.8 defg32.1 abcdefg0.9
WW277 bce270 cdeg259 dfghi245 ijk213 l269 bcdefgh258 fhi242 jk228 kl215 l7299 ab306 a260 cdefghij260 bcdefghijk291 abcdefghijk284 abcdf285 abc251 dfghijk241 cdefghijkl213 eghijkl12
WAGE247 c237 d221 efg204 h182 i252 bc236 d215 fg196 h179 i5268 ab260 abc229 def200 ghi166 cdefgh272 a251 bc232 de214 defgh180 ghi11
AWW239240245247240227230234239243623625023626728322223922623222611
Model outputs
MER80877974800679897913782678417821791980401447506779476807886695175437843755975846595372
PKM6.26.26.36.46.25.75.85.96.16.40.34.85.34.96.26.84.34.94.55.03.80.8
EBN−1.5 efg−1.6 efg−1.8 gh−1.9 h−1.8 fgh−1.3 e−1.4 ef−1.5 efg−1.8 gh−1.9 efgh0.10.2 cd0.2 d1.0 ab0.6 abcd−1.7 efgh0.3 bcd0.5 abcd1.0 a1.0 abc1.5 abcd0.4
DSPN109 g112 fg113 fg113 fg113 fg110 fg112 fg113 fg113 fg112 fg4235 ab231 bc187 d124 efg55 fg253 a215 c192 d154 e158 ef11
DOYN140157178199220139157178198222713913410692341421361088812413
EEI129.630.431.833.737.729.431.433.035.837.51.025.926.030.630.729.627.228.431.732.937.62.4
EEI233.734.335.336.840.333.735.336.438.740.00.930.630.534.433.831.931.932.735.636.340.42.4
Economics
CaREV9939749949478691016951936925849119102511991015103386810321064914938869162
CoREV47 d133 bcd114 cd122 abcd262 ab84 cd127 bcd203 abc146 abcd287 a3143 abcd101 abcd103 abcd337 abcd−8 abcd226 abcd94 abcd89 abcd64 abcd226 abcd78
TREV103711061110106910661098107911401072112612510641300111913738631256115610051005902220
TFC1931921931891851851901911901861224324424023420224224323322619615
RHC114 d302 bcd265 cd307 abcd451 ab198 cd323 bcd452 abc335 abcd663 a11382 bcd246 abcd216 abcd814 abcd−36 abcd562 abcd197 abcd220 abcd187 abcd80 abcd336
COST306 d494 bcd457 cd497 abcd636 ab383 cd512 abcd642 abc526 abcd849 a109327 abcd488 abcd457 abcd1048 abcd166 abcd805 abcd440 abcd452 abcd411 abcd272 abcd334
RET733 a614 ab651 ab573 ab428 cd716 a567 ab495 bc546 abc276 d139747 ab806 a661 abc321 abcd704 abcd455 abcd717 ab549 abcd586 abcd611 abcd258
1 NC = number of calves; MCW = mature cow weight, kg; CBCS = body condition score at calving (1–9); WBCS = body condition score at weaning (1–9); PREG = pregnancy percentage, %; SURV = calf survival percentage from birth to weaning, %; CAINT = calving interval, d; BW = calf birth weight, kg; WW = calf weaning weight, kg; WAGE = calf age at weaning, d; AWW = 205 d adjusted calf weaning weight, kg; MER = metabolizable energy required, Mcal; PKM = peak milk yield, kg/d; EBN = energy-balance nadir, Mcal/d; DSPN = days since parturition at energy-balance nadir, d; DOYN = day of the year at energy-balance nadir, d; EEI1 = cow energy efficiency index, Mcal/kg; EEI2 = cow + calf energy efficiency index, Mcal/kg; CaREV = calf revenue, $/cow; CoREV = cull cow revenue, $/cow; TREV = total revenue, $/cow; TFC = total feed cost, $/cow; RHC = replacement heifer cost, $/cow; COST = total cost, $/cow; RET = returns over costs, $/cow. abcdefghijkl Means without a common superscript in the same row differ at p ≤ 0.05.
Table 5. Performance traits, model outputs, and economics for effects of calf sex (males or females) and calving period (1 to 5) of Hereford cows in southwest Missouri.
Table 5. Performance traits, model outputs, and economics for effects of calf sex (males or females) and calving period (1 to 5) of Hereford cows in southwest Missouri.
MalesFemales
Item 112345+12345+SEM
NC1493662941529615931326211277
Performance
MCW55455956156956654756456256754411
CBCS5.85.95.95.96.05.85.86.05.95.80.1
WBCS5.35.55.45.54.55.45.45.65.65.40.2
PREG-----------
SURV-----------
CAINT3993793653513593873873643453379
BW34.1 b35.0 ab35.1 ab36.7 a35.9 ab32.1 c34.2 b34.1 b33.6 bc33.3 bc0.5
WW2882882602532522772722462342148
WAGE257 ab249 bc225 d202 ef200 ef262 a243 c223 d205 e183 f4
AWW2372452402572622252352302362357
Model outputs
MER7795788378447939792576847842769177527383132
PKM5.55.85.66.36.85.05.45.25.55.50.3
EBN−0.7 bc−0.7 c−0.4 ab−0.7 abc−1.8 d−0.5 abc−0.5 abc−0.3 a−0.4 abc−0.3 abc0.1
DSPN172 ab171 b150 c119 e106 e182 a164 b152 c133 d128 de4
DOYN1391461421461621411461431431766
EEI127.828.231.232.233.228.329.932.434.336.40.9
EEI232.232.434.935.336.232.834.036.037.539.10.9
Economics
CaREV1009 abc1086 a1005 abc990 abc955 abc1024 ab1007 b925 c931 bc726 d117
CoREV45 a117 a109 a229 a127 a155 a111 a146 a105 a257 a43
TREV1050 a1203 a1115 a1221 a1081 a1177 a1117 a1072 a1038 a985 a120
TFC21821821621119721421721220819212
RHC99 b274 ab240 ab560 a289 ab380 ab261 ab335 ab261 ab594 ab100
COST317 b491 ab456 ab771 b484 ab594 ab476 ab547 ab468 ab786 ab97
RET739 a710 a657 ab448 bc596 abc585 ab642 ab522 bc567 abc196 c131
1 NC = number of calves; MCW = mature cow weight, kg; CBCS = body condition score at calving (1–9); WBCS = body condition score at weaning (1–9); PREG = pregnancy percentage, %; SURV = calf survival percentage from birth to weaning, %; CAINT = calving interval, d; BW = calf birth weight, kg; WW = calf weaning weight, kg; WAGE = calf age at weaning, d; AWW = 205 d adjusted calf weaning weight, kg; MER = metabolizable energy required, Mcal; PKM = peak milk yield, kg/d; EBN = energy-balance nadir, Mcal/d; DSPN = days since parturition at energy-balance nadir, d; DOYN = day of the year at energy-balance nadir, d; EEI1 = cow energy efficiency index, Mcal/kg; EEI2 = cow + calf energy efficiency index, Mcal/kg; CaREV = calf revenue, $/cow; CoREV = cull cow revenue, $/cow; TREV = total revenue, $/cow; TFC = total feed cost, $/cow; RHC = replacement heifer cost, $/cow; COST = total cost, $/cow; RET = returns over costs, $/cow. abcdef Means without a common superscript in the same row differ at p ≤ 0.05.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

VerPloeg, B.; Lancaster, P.A.; Walker, E. Effect of Calving Season and Timing Within Season on Performance and Economics of Cow-Calf Production in Southwest Missouri. Ruminants 2026, 6, 19. https://doi.org/10.3390/ruminants6010019

AMA Style

VerPloeg B, Lancaster PA, Walker E. Effect of Calving Season and Timing Within Season on Performance and Economics of Cow-Calf Production in Southwest Missouri. Ruminants. 2026; 6(1):19. https://doi.org/10.3390/ruminants6010019

Chicago/Turabian Style

VerPloeg, Briana, Phillip A. Lancaster, and Elizabeth Walker. 2026. "Effect of Calving Season and Timing Within Season on Performance and Economics of Cow-Calf Production in Southwest Missouri" Ruminants 6, no. 1: 19. https://doi.org/10.3390/ruminants6010019

APA Style

VerPloeg, B., Lancaster, P. A., & Walker, E. (2026). Effect of Calving Season and Timing Within Season on Performance and Economics of Cow-Calf Production in Southwest Missouri. Ruminants, 6(1), 19. https://doi.org/10.3390/ruminants6010019

Article Metrics

Back to TopTop