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Animal Improvement Programs Laboratory, Agricultural Research Service, USDA, Beltsville, MD 20705-2350
1 Corresponding author: mkuhn{at}aipl.arsusda.gov
| ABSTRACT |
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Key Words: days dry Jersey fertility somatic cell score
| INTRODUCTION |
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Much of the past research, as well as recent research, on days dry (DD) has focused on effects on subsequent lactation performance, and primarily effects on production. Several studies (Gulay et al., 2003; Annen et al., 2004; Rastani et al., 2005; Kuhn et al., 2006b), however, have examined subsequent lactation effects on other traits such as fertility, SCS, and fat and protein percentages, and one recent study (Kuhn et al., 2006a) examined effects on lifetime performance. Furthermore, research has been conducted on interactions of DD with previous lactation days open (DO), SCS, age at calving, and milk yield (Kuhn et al., 2005b). However, one aspect that has received little attention, if any, in either past or recent research on DD is whether breeds respond differently to variations in dry period length; virtually all research has been conducted using only Holsteins. The objectives of this research were first to characterize dry period lengths for US Jerseys and to determine the effects of DD on subsequent lactation milk, fat, and protein yields, fat and protein percentages, SCS, and DO for US Jerseys. Characterization of DD included a frequency distribution of dry period lengths as well as factors affecting US Jersey DD.
Information on the effects of DD in the subsequent lactation is a necessary first step for a complete understanding of the consequences of various dry period lengths. But cows also lose production in the previous lactation because of dry off. A further objective, then, was to determine the dry period length for Jerseys that maximizes yield across adjacent lactations. Even total yield across adjacent lactations, however, is not entirely complete information. If either short or long DD resulted in greater culling late in the lactation following the dry period, then this would be an impact on lifetime performance or value that would not be reflected in the mere total across adjacent lactations. A final objective, then, was to provide some assessment of the potential impact of varying dry period lengths on lifetime performance.
Jerseys were an optimal choice in the United States for examining DD effects in an alternative breed because, although a distant second, Jerseys rank only behind Holsteins in terms of number of cows on test. Thus, adequate sample sizes for research were more likely for Jerseys than for other breeds.
| MATERIALS AND METHODS |
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Records also had to be initiated no later than November 2004 to be included, which, given that data were extracted from the database in May of 2006, was also done to ensure complete lactations. Thus, calving dates for records included in this research spanned the period of January 1997 to November 2004. Herds were not required to be on test for the entire period; rather, they were only required to be on test continuously, up to May of 2006, after their first date of inclusion. For example, if a herd was not on test until 1999, it was still included provided it remained on test until May of 2006. This alternative resulted in larger sample sizes, compared with requiring herds to be on test continuously from 1997 to 2006.
Additional edits included exclusion of records initiated by abortion and exclusion of cows known to be donor dams, because these factors would result in unexpected or artificially abnormal dry period lengths. Donor dams can be identified from 2 sources of information in the Animal Improvement Programs Laboratory database: 1) pedigrees supplied by the breed association that identify calves as "ET" (embryo transfer) and thus their dams as donor dams; and 2) the reproductive record known as format 5, which allows reporting of donor dams. Another edit was to require actual calving dates to be within 10 d of the expected calving date, given the last reported breeding date, which ensured that the owner knew, at least at one point in time, when the cow was going to calve. Finally, any herd that had fewer than 5 cows in any year was deleted, which was done to ensure adequate sample size for adjustment of herd effects.
Actual lactational yields for milk, fat, and protein were calculated using the test-interval method (Sargent et al., 1968) and the lactation shape adjustment factors of Shook et al. (1980). The only standardization done was to a twice-daily milking basis. Records less than 305 d were not extended to 305 d, and all production beyond 305 d was included.
Factors Affecting Dry Period Length
To determine the effects of DD on performance following the dry period, the trait of interest (e.g., milk yield) would be the dependent variable and DD an independent variable in the model. However, to determine how various factors affect dry period length, the opposite is done; DD becomes the dependent variable and factors from the lactation preceding the dry period (previous lactation) are the independent variables of interest.
The linear fixed effects model used for assessment of factors affecting dry period length in US Jerseys was:
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where Herd, Yr, Mo, and parity were herd, year, month, and parity of calving in the lactation preceding the dry period; Age and DO were age at calving and DO in the previous lactation; Milk was the actual lactational milk yield in the previous lactation; and Last_SCS was the SCS on the last test-day in the previous lactation. Age, DO, milk, and Last_SCS were all fit as categorical variables. Categories for age were defined as follows: 1) 2 yr of age or younger, 2) 2 to 2.5 yr, 3) 2.5 to 3 yr, 4) 3 to 3.5 yr, 5) 3.5 to 4 yr, and 6) older then 4 yr. Categories for milk, Last_SCS, and DO were defined as follows: 1) lower third of data sorted by trait, 2) middle third of data, and 3) top third of data. Arithmetic means of milk, SCS, and DO subclasses are given in Table 1
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Analysis of DD Effects on Subsequent Lactation Performance
General Considerations and Further Description of Data.
Studies that had the capability to estimate DD effects over a basically continuous range of dry period lengths have generally found that subsequent lactation performance does not change either linearly or quadratically over a range of DD from 0 to 100 d or more. On the contrary, subsequent lactation milk yield, for example, has been reported to increase at a decreasing rate up to about 60 DD, at which point production essentially levels off (Funk et al., 1987; Makuza and McDaniel, 1996; Kuhn et al., 2005b). This implies that DD effects cannot be appropriately modeled with simple linear or quadratic covariates. Furthermore, use of any covariates necessarily dictates the nature of the relationship between the variables of interest, but the objective in this research was to discover the nature of the relationship between performance and DD; use of DD as a categorical variable allows for direct and straightforward examinations of those relationships. Thus, DD categories were formed for analysis and are presented in Table 2
. Categories used for analysis (Table 2
) represented a compromise between the desire for categories with a small range for DD, which provide the maximum amount of information with regard to how performance changes as DD changes, and the need for reasonable sample sizes for estimation.
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Several studies using Holsteins (Funk et al., 1987; Kuhn et al., 2005b) have investigated whether the effect of dry period length in the subsequent lactation depends on parity and have generally found either no or only small interactions with parity. Furthermore, even when DD effects were found to differ slightly across parities, the dry period length to maximize subsequent lactation performance was generally the same regardless of parity. Kuhn et al. (2005b), for example, found that dry periods of less than 20 d decreased subsequent lactation milk yield for Holsteins more in the second lactation than in later lactations, but 60 DD maximized yield in the following lactation regardless of parity. Preliminary results (presented graphically in the Results and Discussion section) indicated similar results for milk yield in Jerseys. Furthermore, sample sizes by parity, especially for third and fourth lactations, were rather small. Thus, the final analyses for effects of DD on subsequent lactation performance used all lactations combined in a single analysis, in contrast to separate analyses for each parity. The final number of records for each DD subclass and for each trait is given in Table 2
, along with the total number of herds for each trait. For example, a total 123,032 records from 73,797 cows in 808 herds and 44 states were used for estimation of DD effects on subsequent lactation actual milk yield.
The major factor affecting sample size was more availability of data, rather than edits (eliminating available records) per se. The requirement for herds to be on continuous test, for example, eliminated about one-third of the herds with Jersey cows. Furthermore, not all processing centers began sending complete lactation information (needed for calculation of actual records) at the same time, which meant that not all records back to 1997 could be kept for all processing centers; that is, the date of first possible inclusion had to be moved forward for some herds, depending on the processing center. This editing by the processing center eliminated approximately 300,000 records. Given a US culling rate after first lactation of about 35 to 40%, the requirement for cows to have at least 2 lactations (and thus at least 1 dry period) also had a substantial impact on the number of records available for final analysis. Methodology (described below) also imposed some data requirements, most importantly that cows had an available first lactation. Thus, in a herds first year of inclusion, only first-lactation cows would be eligible. If the milking herd size was 100 cows, for example, with 35 first-lactation cows, then only 35 cows were eligible for inclusion for that year and of those 35, only those making a second lactation could be included.
Estimation of DD Effects.
Dry period length has been found to be correlated with cow effects (Kuhn and Hutchison, 2005); cows with a higher producing ability tend to get shorter dry periods. Thus, methods for analysis must adjust for cow effects to avoid underestimation of short dry period effects (confounding with positive cow effects would tend to bias estimates of short DD effects upward). Kuhn and Hutchison (2005) showed that prior adjustment of records for cow effects, estimated from an animal model, would provide estimates of DD effects that are unbiased by cow effects. Thus, cow effects (sum of animal and permanent environmental effects) were estimated for each trait using multiple trait animal models. Multiple, rather than single, trait models were used for estimation of cow effects to improve the accuracy of estimates. Two- and 3-trait models were used for estimation of cow effects; actual milk, fat, and protein yields were analyzed simultaneously; fat and protein percentages were combined in a 2-trait model; and SCS and DO were each analyzed simultaneously with milk yield. In addition to the random animal and permanent environmental effects, the models for estimation of cow effects included the fixed effects of herd-year of calving, year-state-month of calving, age at calving, and DD fit as a categorical variable. For estimation of cow effects, cows were required to have a first-lactation record, but not a second or later lactation. First lactations needed to be included in these analyses to avoid bias in the estimates of cow effects. Because there are no DD associated with a first lactation, first-parity records were assigned their own unique DD category, which was part of the method of Kuhn and Hutchison (2005).
After adjusting for cow effects, the same linear, fixed effects model was used for analysis of all traits:
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where y* was an actual lactational milk, fat, or protein yield, fat or protein percentage, SCS, or DO record adjusted for cow effects; HY was herd-year of calving; Yr-St-Mo and parity were year-state-month and parity of calving; Age was age at calving fit as a linear and quadratic covariate; ß3x PrevRecord was a regression on the previous lactation record, the use of which has been shown to improve the accuracy of estimates (Kuhn and Hutchison, 2005), even with records adjusted for cow effects; DD was a categorical DD variable with categories as defined in Table 2
; and e was random error. Month effects were allowed to vary by year and state because climate can vary considerably from year to year in the United States and from region to region within a year. Month was fit separately from herd-year to avoid small group sizes. Overall arithmetic means for each trait are given in Table 3
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Dry Period Length to Maximize Yield Across Multiple Lactations.
This issue has been addressed in previous research with Holsteins using lifetime actual milk yield (Kuhn et al., 2006a). Analyses of lifetime yield, however, require that cows have sufficient time to complete their lifetimes, which means that data from only the earliest several years can be used, and this restriction resulted in sample sizes too small to study lifetime Jersey yield. The question at hand is whether short (or long) dry periods result in additional culling or other carryover effects that would not be detected by an analysis of sums across adjacent lactations. For example, shortened dry periods could result in essentially no milk yield loss across lactations 1 and 2, but if the shorter DD caused additional culling toward the end of lactation 2, this would not be reflected in Sum12, but it would be of economic importance. Given the potential economic importance of this question and the present interest in using shortened dry periods, some investigation on this topic would be of value, in spite of insufficient data for lifetime yield.
An alternative approach, to partly address whether DD has effects on lifetime performance, would be to use total yield across lactations 1, 2, and 3 (Sum123) in place of lifetime yield, and to examine the effects of the first dry period length (DD1) on Sum123. The Sum123 would detect detrimental or beneficial effects that DD1 had at the end of or after lactation 2. Thus, Sum123 was preadjusted for cow effects (breeding value, because each cow had only 1 record) and analyzed with a model that included the fixed effects of herd-year and year-state-month of first calving, age at first calving, and DD1. Categories for DD1 were the same as those for the subsequent lactation analyses (Table 2
). Data were restricted to cows that first calved no later than December 2002 to allow the cows adequate time to complete 3 lactations. The arithmetic means for Sum12, Sum23, and Sum123 were 14,633, 15,691, and 19,065 kg, respectively. An analysis to examine the effects of the second dry period on total yield across lactations 2, 3, and 4 (analogous to Sum123) was considered, but sample sizes were too small to make effective inferences.
| RESULTS AND DISCUSSION |
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Given that the Jersey average for SCS is about 0.3 higher than for Holsteins (AIPL, 2006), SCS might be expected to play a larger role in dry period length for Jerseys than for Holsteins; however, results for Jerseys were nearly identical to those reported by Kuhn et al. (2006b) for Holsteins. The main difference among the SCS groups was about 2.4 more DD for cows with the highest SCS, whereas there was very little difference in DD between the first 2 groups for either breed. Thus, the highest SCS group probably includes mastitic cows and, as such, represents a sort of threshold at which SCS begins to affect dry period length; cows with mastitis are dried off, but otherwise SCS has little or no effect on dry period length.
The most notable effect of parity on dry period length was for first-parity cows to average about 3 to 5 fewer DD than later parity cows. This is likely due to the greater persistency of first-lactation cows (Stanton et al., 1992). Thus, although cows produce more total milk over the entire lactation in second and later lactations, first-lactation cows actually have higher yields at the end of lactation, which in turn leads to slightly longer lactations, on average, and fewer DD.
The primary difference among years was that the last year included (2003) had a 2- to 3-d lower mean than previous years. Although there may be some trend toward shorter dry periods in Jerseys, this year effect probably reflects a slight bias in this analysis for this particular factor; for cows calving in 2004 (previous year = 2003), those with the shortest dry periods would have more of a chance to calve again, and thus be included in the data, than cows with the longest dry periods.
Effects on Subsequent Lactation Performance
Milk, Fat, and Protein Yields.
The preliminary results for actual milk yield by parity are illustrated in Figure 1
. Although the graphs are not identical for all 3 parities, Figure 1
certainly illustrates no dramatic difference in DD effects across parities for subsequent lactation production. Furthermore, standard errors were rather large for parity 3, and especially parity 4. The P-value for the parity x DD interaction was 0.0501, which, for an F-test with 24 numerator and 115,802 denominator degrees of freedom, is not particularly low (not "highly significant"). Thus, little, if any, information was lost by analysis of all parities combined.
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Not only did shortened dry periods result in lost production in the subsequent lactation, but also dry periods longer than 60 d were associated with production lower than that for 60 DD, although the reduction in subsequent lactation for DD >60 was far less than for short DD. A similar result has been reported for Holsteins (Kuhn et al., 2005b, 2006b). The reason for lower production with dry periods >60 d is unknown. Kuhn and Hutchison (2005) showed, using simulation, that the methodology used in this research provides unbiased estimates for dry periods beyond the point at which milk yield is maximized. Furthermore, Funk et al. (1987) and Schaeffer and Henderson (1972) also found lower milk yields for DD >60, using alternative methodologies; Funk et al. (1987) included only a cow effect with no relationships and Schaeffer Henderson (1972) used a sire model with no relationships. Thus, the result of lower milk yield with dry periods longer than 60 d does not appear to be caused by inadequate adjustment for cow effects or an artifact of methodology; it may be that cows become overconditioned during dry periods of more than 60 d.
Compared with results for Holsteins reported by Kuhn et al. (2005b), the absolute amount of loss in production for dry periods less than 60 d was less for Jerseys than for Holsteins. Holsteins, for example, averaged 2,214 kg less milk yield in lactations following dry periods of 20 d or less, whereas Jerseys averaged only 1,457 kg less actual milk. On a percentage basis, however (differences expressed relative to the overall arithmetic mean for each breed), losses for Jerseys were essentially the same as those for Holsteins. Production for Jerseys with 20 or fewer DD, for example, was 18.9% less than for 60 DD, whereas the corresponding loss in production for Holsteins was 19.4%. Thus, with regard to effects of DD on subsequent lactation production, there appears to be little difference between Holsteins and Jerseys. Differences among DD subclasses for 4% FCM (NRC, 1989) were similar for the 2 breeds, except that losses for DD <30 were about 400 kg larger for Holsteins than for Jerseys.
Most previous research, both past and recent, supports the general finding of lower production following dry periods of less than 60 d. Sørensen and Enevoldsen (1991) reported 3.1 kg/d lower milk yield for cows with 4- vs. 10-wk dry periods and Rémond et al. (1992) found a 4.1 kg/d loss for cows with 0 DD, compared with cows with 60 DD. Rastani et al. (2005) found a 4.5 kg/d loss for cows with 28 vs. 56 DD and an 8.6 kg/d loss for cows with no dry period. Gulay et al. (2005) also reported an 18.9% reduction in milk yield for dry periods of 30 d compared with dry periods of 70 d. Earlier research using large data sets of field records (Schaeffer and Henderson, 1972; Coppock et al., 1974; Dias and Allaire, 1982; Funk et al., 1987; Makuza and McDaniel, 1996) all reported lower yields for dry periods less than 60 d. Capuco et al. (1997) showed that a dry period was necessary to replace mammary epithelial cells, thus providing one biological basis for the lower milk yield that has been observed with shortened dry periods. Results of Annen et al. (2004) provided some indication that it may be possible to reduce or eliminate these losses with the use of bST, but given their small sample sizes, further research would be needed to confirm this. The evidence for lower yields in lactations following dry periods <60 d is substantial. Only 2 studies (Bachman, 2002; Gulay et al., 2003) have reported no loss with dry periods <60 d. Sample sizes in both of those studies were small, however, and it has been shown (Kuhn and Hutchison, 2005) that even estimates in the wrong direction are not unlikely with such small sample sizes.
Fat and Protein Percentages.
Results for fat and protein percentages are given in Table 8
. In contrast to fat and protein yields, short dry periods actually favored fat and protein percentages. Cows with less than 20 DD, for example, averaged 0.08 (fat) and 0.09 (protein) higher percentages than cows with 61 to 65 DD. In fact, lactational percentages for both fat and protein decreased with increasing DD. The higher percentages were not due to the lower milk yields associated with the shorter dry periods because when milk yield was included as a covariate for percentages, estimates were nearly identical to those without milk yield in the model.
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Kuhn et al. (2006b) reported results for Holsteins for fat and protein percentages that were similar to those in Table 8
, although fat percentage for Holsteins did not decrease as DD increased beyond 60 d. On a percentage basis, however, Holsteins had a larger increase in both fat (1.7% for Jerseys vs. 2.2% for Holsteins) and protein (2.5% for Jerseys vs. 4.0% for Holsteins) percentages for DD
20.
SCS.
Shortened dry periods had pronounced effects on Jersey SCS, especially dry periods less than 30 d (Table 8
). Cows with dry periods of 20 d or less averaged 0.31 higher SCS (10% higher than the overall mean) than cows with 61 to 65 DD. Although SCS decreased with 21 to 30 DD, cows in this DD category still averaged 0.14 higher SCS than cows with at least 60 DD. The substantial, undesirable impact on SCS is largely mitigated by dry periods of at least 45 d. The higher SCS associated with shorter dry periods were somewhat, but by no means completely, related to the lower milk yields associated with shorter dry periods. The mean differences of categories 1, 2, and 3 from category 8, for example, were 0.27, 0.10, and 0.06, respectively, when milk yield was included as a covariate for SCS.
Annen et al. (2004) reported higher SCC for dry periods less than 60 d, which is consistent with the results of this study. In contrast to the results of this study, Gulay et al. (2003) reported a lower SCC with 30 DD than with 60 DD during the first 10 wk of lactation. The comparison was not significantly different from zero and was based on a small sample. Rastani et al. (2005) also found higher SCS for cows with longer dry periods, although differences were not statistically significant. In general, results from the small number of studies that have considered effects of DD on SCS are consistent with the results of this study. The variation observed in results of previous reports almost certainly reflects the small sample sizes in those studies, for a trait subject to large environmental effects.
The biggest difference between the results in Table 8
for Jersey SCS and those presented by Kuhn et al. (2006b) for Holstein SCS was that dry periods less than 20 d had a considerably larger (undesirable) impact on Jersey SCS than on Holstein SCS. Holsteins, for example, averaged only 0.113 (3.7%) higher SCS for dry periods less than 20 d and 0.097 (3.1%) for DD between 21 and 30 d. Another difference was that Holstein SCS continued to decrease with increasing dry period length, even for DD >60, whereas Jersey SCS did not show this tendency and, in fact, were optimal at around 60 DD. Jersey producers need to be even more cautious than Holstein producers about dry periods of less than 20 or even 30 d because the value of the milk in the following lactation will be substantially lowered by higher SCS when DD are <30 d.
DO.
Results for DO are given in Table 9
. On first inspection, shorter dry periods appear to favor fertility. Cows with 40 or fewer DD averaged 4 fewer DO than cows with 61 to 65 DD. However, this apparent advantage was due entirely to the lower milk yields associated with the shorter dry periods. When DO was adjusted for milk yield, by inclusion of milk yield as a covariate in the model for analysis, short dry periods actually resulted in poorer fertility than dry periods of longer lengths. Cows with only 0 to 20 DD had 24 more DO, when DO was adjusted for yield, than cows with 61 to 65 DD; categories 2 (18 d) and 3 (10 d) still showed considerably higher DO adjusted for milk. With a minimum of about 45 DD, however, effects on fertility were small and approached 0 as DD approached 60 d.
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Using shortened dry periods to improve fertility in either breed is not likely to be of much overall benefit because the "benefit" in fertility results only from lowered milk yield. It is, first of all, questionable whether improving fertility by lowering milk yield is a prudent economic choice. However, even if improved fertility through lowered milk yield was shown to be of merit, there are almost certainly less expensive or more efficient ways to lower milk yield than by reducing dry period length, a practice that necessarily increases labor, time, and maintenance in the milking parlor, unless herd size is also reduced. Lower cost rations, for example, might lower milk yield and would simultaneously reduce costs rather than increase them, again if improved fertility through lowered milk yield was desired or found to be in some way a favorable alternative.
DD to Maximize Yield Across Lactations
Adjacent Lactations.
Results, along with sample sizes, for Sum12 and Sum23 are given in Table 10
. Although production was still lost with shortened dry periods, the losses were, of course, much less than those found for the subsequent lactation because of the mitigating effect of yield gained in the previous lactation. A wide range of dry periods can maximize total yield across adjacent lactations in Jerseys. A minimum of about 45 DD resulted in no loss for either Sum12 or Sum23, but dry periods of up to about 70 d will also maximize yields across lactations.
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Jersey DD effects for Sum12 and Sum23 generally showed patterns similar to that reported for Holsteins by Kuhn et al. (2006a). The major difference was that long dry periods were less costly for Holsteins than for Jerseys. For DD of 70 d or more, Sum12 did not show a loss in Holsteins, and the percentage loss for Jerseys was higher for Sum23 than for Holsteins. Schutz et al. (1990) reported greater persistency for Holsteins than for Jerseys in both first and second lactations, which would explain the smaller losses of Holsteins with long dry periods.
Dry Period in First Lactation to Maximize Total Yield Across Lactations 1, 2, and 3.
Results, as well as sample sizes, for Sum123 are given in Table 11
. Losses in total yield across the first 3 lactations were substantially higher for both short (<45 d) and long (>70 d) dry periods than for Sum12. The larger effect of DD1 on Sum123 than on Sum12 can be explained, at least in part, by DIM, culling, or both in the second and third lactations. The average total DIM across lactations 2 and 3, in Table 11
, illustrate that cows with either short or long dry periods after the first lactation have fewer DIM in subsequent lactations. The percentage of cows culled after the second lactation, by DD category, is also shown in Table 11
. The percentages culled show, in turn, that the fewer DIM for either short or long dry periods are due, at least in part, to greater culling. Thus, dry period length after the first lactation affects total yield across the first 3 lactations, in part by affecting DIM and culling. A minimum of about 45 DD after the first lactation is necessary to maximize total yield across lactations 1, 2, and 3. Dry periods longer than 65 d after the first lactation also result in lost lifetime yield, not only because cows with DD1 >65 have fewer total DIM, but also because of greater culling among these cows.
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| CONCLUSIONS |
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The biggest difference between Jerseys and Holsteins, with regard to DD effects in the subsequent lactation, was a much larger detrimental effect on SCS in Jerseys for dry periods of 30 d or less. Jersey SCS was 10% higher, relative to the overall mean, for dry periods of 20 d or less. Jersey producers, especially, should be skeptical of dry periods less than 30 d, because the value of the milk will be reduced in the following lactation due to substantially higher SCS.
Effects on Jersey production in the subsequent lactation were similar to previous reports for Holsteins, at least on a percentage basis. Jersey milk, fat, and protein yields in the subsequent lactation were maximized with 61 to 65 DD. Dry periods of 30 d or less resulted in especially large reductions in subsequent lactation production. With a minimum of approximately 45 DD, production losses in the following lactation were reduced to about 255 kg of milk, 9 kg of fat, and 7 kg of protein.
As previously reported for Holsteins, fat and protein percentages for Jerseys were actually favored by shortened dry periods, and this was not due to the lowered milk yield associated with shortened DD. The net effect of DD on DO was fewer DO with shorter dry periods and was less for Jerseys than the effects previously published for Holsteins. This reduction in DO, however, was due entirely to the lower milk yields associated with shortened dry periods. When adjusted for milk yield, the advantage in DO was completely nullified and, in fact, short dry periods actually resulted in poorer fertility when DO was adjusted for yield. Given that the only benefit to fertility of shortened DD is due to lower milk yield, it is unlikely that "improved" fertility is a viable reason for shortening dry periods.
Although further research would be needed in Jerseys to determine the long-term consequences of DD after second and later lactations, it is recommended that Jersey producers maintain dry periods of between 45 and 60 d, at least after the first lactation; 60 DD are at least as acceptable, in terms of performance, as are shorter dry periods. There is no benefit to production in either the short or long term of dry periods less than 45 d; furthermore, the value of milk produced following lactations with dry periods of <30 or even <45 d will be lower than for dry periods of at least 45 d because of the higher SCS.
Given the recent advocacy for shortened dry periods, it is worthwhile to emphasize that 61 to 65 DD does provide optimal production and performance, although as few as 45 DD can as well; there are no production advantages for dry periods less than 60 d. This research has also underscored the need for good fertility. Cows with long DO have longer dry periods, on average, which in turn results in substantial lost production across the lifetime of a cow. Considering, then, the need to avoid both short and long dry periods, and given some variation in gestation length, a target dry period length of 55 d will serve Jersey producers well; if cows calve even 10 d earlier (45 DD) or 10 d later (65 DD) than expected, little, if anything, will be lost.
| ACKNOWLEDGEMENTS |
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Received for publication October 24, 2006. Accepted for publication December 15, 2006.
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